A FHIRPath expression which specifies a message to put in the transform log when content matching the source rule is found.
Message to put in log if source exists (FHIRPath)
The status of the disease or symptom for the contraindication.
Indicates when the documentation of the assessment was complete.
What happens in each alternative option.
The common subject (or patient) of the resources that are in the list if there is one.
A rational number with implicit precision
The date (and optionally time) when the message definition was published. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the message definition changes.
A species specific time during which consumption of animal product is not appropriate.
The actual contact point details, in a form that is meaningful to the designated communication system (i.e. phone number or email address).
The provider which is responsible for the bill, claim pre-determination, pre-authorization.
Monetary amount associated with the code.
A short description of the action used to provide a summary to display to the user.
Substance may be used to describe a kind of substance, or a specific package/container of the substance: an instance.
If this describes a specific package/container of the substance
Canonical identifier for this contract, represented as a URI (globally unique).
This resource is primarily used for the identification and definition of a medication for the purposes of prescribing, dispensing, and administering a medication as well as for making statements about medication use.
Security label privacy tag that species the level of confidentiality protection required for this term and/or term elements.
The provider which is responsible for the claim.
Who or what the composition is about. The composition can be about a person, (patient or healthcare practitioner), a device (e.g. a machine) or even a group of subjects (such as a document about a herd of livestock, or a set of patients that share a common exposure).
Who and/or what the composition is about
The time course of drug absorption, distribution, metabolism and excretion of a medication from the body.
The maximum total quantity of formula that may be administered to a subject over the period of time, e.g. 1440 mL over 24 hours.
Upper limit on formula volume per unit of time
The dose form for a single part product, or combined form of a multiple part product.
Search parameters for implementations to support and/or make use of - either references to ones defined in the specification, or additional ones defined for/by the implementation.
A copyright statement relating to the structure definition and/or its contents. Copyright statements are generally legal restrictions on the use and publishing of the structure definition.
The type of the resource. See http://build.fhir.org/resourcelist.html.
The required consistency (e.g. honey-thick, nectar-thick, thin, thickened.) of liquids or fluids served to the patient.
The required consistency of fluids and liquids provided to the patient
If true indicates that the CommunicationRequest is asking for the specified action to *not* occur.
The current state of the request. For request groups, the status reflects the status of all the requests in the group.
draft | active | suspended | cancelled | completed | entered-in-error | unknown
Careteam applicable for this service or product line.
Whether or not the test execution performs validation on the bundle navigation links.
The impact of the content of the message.
The name of the search parameter used in the interface.
Clinical assessment of the severity of the reaction event as a whole, potentially considering multiple different manifestations.
mild | moderate | severe (of event as a whole)
The date (and perhaps time) when the prescription was written.
Provides a reference to the device that performed the guidance.
The class of information covered by this rule. The type can be a FHIR resource type, a profile on a type, or a CDA document, or some other type that indicates what sort of information the consent relates to.
A non-monetary value for example a percentage. Mutually exclusive to the amount element above.
The first dose (dose quantity) administered in humans can be specified, for a product under investigation, using a numerical value and its unit of measurement.
The date when this resource was created.
A human-readable text description of how the slicing works. If there is no discriminator, this is required to be present to provide whatever information is possible about how the slices can be differentiated.
Text description of how slicing works (or not)
Logical network location for application activity, if the activity has a network location.
The entity (e.g. person, organization, clinical information system, care team or device) which was the target of the communication. If receipts need to be tracked by individual, a separate resource instance will need to be created for each recipient. Multiple recipient communications are intended where either a receipt(s) is not tracked (e.g. a mass mail-out) or is captured in aggregate (all emails confirmed received by a particular time).
Item typification or modifiers codes, e.g. for Oral whether the treatment is cosmetic or associated with TMJ, or for medical whether the treatment was outside the clinic or out of office hours.
A contact detail (e.g. a telephone number or an email address) by which the individual may be contacted.
The interactions of the medicinal product with other medicinal products, or other forms of interactions.
Sequence of the information element which serves to provide a link.
The third-tier service adjudications for payor added services.
The entity who benefits from the performance of the service specified in the task (e.g., the patient).
Explanation of why this concept map is needed and why it has been designed as it has.
The XPath or JSONPath expression to be evaluated against the fixture representing the response received from server.
A short, descriptive, user-friendly title for the capability statement.
Name for this capability statement (human friendly)
Where a specific encounter should be classified as a part of a specific episode(s) of care this field should be used. This association can facilitate grouping of related encounters together for a specific purpose, such as government reporting, issue tracking, association via a common problem. The association is recorded on the encounter as these are typically created after the episode of care, and grouped on entry rather than editing the episode of care to append another encounter to it (the episode of care could span years).
Episode(s) of care that this encounter should be recorded against
The practitioner who is responsible for the services rendered to the patient.
Citations, references and other related documents.
Start position of the variant on the reference sequence.If the coordinate system is either 0-based or 1-based, then start position is inclusive.
Start position of the variant on the reference sequence
Rules which provide exceptions to the base rule or subrules.
Specifies a concept to be included or excluded.
available | unavailable | unsatisfactory | entered-in-error
Identifies a specific implementation instance that is described by the capability statement - i.e. a particular installation, rather than the capabilities of a software program.
Mutually exclusive with Services Provided (Item).
The capacity (volume or other measure) the container may contain.
The TestScript.rule id value this assert will evaluate.
List of Unique Device Identifiers associated with this line item.
Clause or question text (Prose Object) concerning the asset in a linked form, such as a QuestionnaireResponse used in the formation of the contract.
This provides a textual description of constraints on the intended activity occurrence, including relation to other activities. It may also include objectives, pre-conditions and end-conditions. Finally, it may convey specifics about the activity such as body site, method, route, etc.
Extra info describing activity to perform
Text, questions and other groups to be nested beneath a question or group.
Specifies the entire name as it should be displayed e.g. on an application UI. This may be provided instead of or as well as the specific parts.
Id [identifier??] of the clause or question text related to this action in the referenced form or QuestionnaireResponse.
SI unit used to report quantitative results of this observation.
Whether the initiator is deactivated right after the transaction.
If present, indicates that the order of the repeating element has meaning and describes what that meaning is. If absent, it means that the order of the element has no meaning.
Vaccine(s) or vaccine group that pertain to the recommendation.
Vaccine or vaccine group recommendation applies to
A code that identifies the component. Codes may be used to differentiate between kinds of taxes, surcharges, discounts etc.
The business identifier for the instance: invoice number, claim number, pre-determination or pre-authorization number.
An individual or organization primarily responsible for review of some aspect of the content.
Description of initial status before the process starts.
A contact detail for the person, e.g. a telephone number or an email address.
Information about why this link is of interest in this graph definition.
A legal or geographic region in which the implementation guide is intended to be used.
Intended jurisdiction for implementation guide (if applicable)
A coded value indicating the method by which the medication is intended to be or was introduced into or on the body. This attribute will most often NOT be populated. It is most commonly used for injections. For example, Slow Push, Deep IV.
Indicates whether the plan is currently being acted upon, represents future intentions or is now a historical record.
draft | active | suspended | completed | entered-in-error | cancelled | unknown
Whether multiple parameters are allowed - e.g. more than one parameter with the same name. The search matches if all the parameters match.
The date on which the resource content was approved by the publisher. Approval happens once when the content is officially approved for usage.
When the library was approved by publisher
The amount of medication expressed as a timing amount.
Amount of medication expressed as a timing amount
Contact details to assist a user in finding and communicating with the publisher.
The type of resource that all instances must conform to.
Additional information codes regarding exceptions, special considerations, the condition, situation, prior or concurrent issues. Often there are multiple jurisdiction specific valuesets which are required.
Describes the form of the item. Powder; tablets; capsule.
Identifier for a person within a particular scope.
An absolute URI that is a formal reference to where this parameter was first defined, so that a client can be confident of the meaning of the search parameter (a reference to [SearchParameter.url]). This element SHALL be populated if the search parameter refers to a SearchParameter defined by the FHIR core specification or externally defined IGs.
Describes validation requirements, source(s), status and dates for one or more elements.
The request being actioned or the resource being manipulated by this task.
Describe the undesirable effects of the medicinal product.
Security label privacy tag that species the applicable privacy and security policies governing this term and/or term elements.
Defines the selection behavior for the action and its children.
any | all | all-or-none | exactly-one | at-most-one | one-or-more
The item from the Questionnaire that corresponds to this item in the QuestionnaireResponse resource.
Pointer to specific item from Questionnaire
Action to take - permit or deny - when the rule conditions are met. Not permitted in root rule, required in all nested rules.
Associated or related knowledge about a medication.
Describes an expected sequence of events for one of the participants of a study. E.g. Exposure to drug A, wash-out, exposure to drug B, wash-out, follow-up.
Defined path through the study for a subject
A code or string that identifies the device detail being asserted.
patient | practitioner | related-person | device
Related artifacts such as additional documentation, justification, or bibliographic references.
Security labels for the identified entity.
An individual or organization primarily responsible for internal coherence of the content.
Reference to the program or plan identification, underwriter or payor.
The number of repetitions of a service or product.
Indicates the type of medication dispense (for example, where the medication is expected to be consumed or administered (i.e. inpatient or outpatient)).
The population group to which this applies.
Indicates how quickly the ServiceRequest should be addressed with respect to other requests.
The factor that has been applied on the base price for calculating this component.
Factor used for calculating this component
A human-readable formatted text, including images.
Explanation of why this event definition is needed and why it has been designed as it has.
The organization responsible for the care team.
Organization responsible for the care team
Specified maximum cardinality for the element - a number or a "*". This is optional; if present, it acts an implicit check on the input content (* just serves as documentation; it's the default value).
Specified maximum cardinality (number or *)
Indicates whether the account is presently used/usable or not.
active | inactive | entered-in-error | on-hold | unknown
A regulator which oversees the operation.
A short, descriptive user-friendly label for the study.
The name of the city, town, suburb, village or other community or delivery center.
The parameter element defines parameters used by the library.
One of the potential outcomes for the patient (e.g. remission, death, a particular condition).
Adjustment to the payment of this transaction which is not related to adjudication of this transaction.
Identifies what progress is being made for the specific activity.
not-started | scheduled | in-progress | on-hold | completed | cancelled | stopped | unknown | entered-in-error
General description of how security works.
The period over which the characteristic is tested; e.g. the patient had an operation during the month of June.
Period over which characteristic is tested
A formal identifier that is used to identify this value set when it is represented in other formats, or referenced in a specification, model, design or an instance.
Additional identifier for the value set (business identifier)
A link to an encounter, or episode of care, that identifies the particular occurrence or set occurrences of contact between patient and health care provider.
The identification of the system that provides the coded form of the unit.
The date when target is next validated, if appropriate.
The kind of operation to perform as a part of the filter criteria.
= | is-a | descendent-of | is-not-a | regex | in | not-in | generalizes | exists
A larger event of which this particular event is a component or step.
The type of item - medication, device, service, protocol or other.
The scope in which the template applies.
The patient/healthcare consumer to whom this consent applies.
An absolute URI that is used to identify this event definition when it is referenced in a specification, model, design or an instance; also called its canonical identifier. This SHOULD be globally unique and SHOULD be a literal address at which at which an authoritative instance of this event definition is (or will be) published. This URL can be the target of a canonical reference. It SHALL remain the same when the event definition is stored on different servers.
Canonical identifier for this event definition, represented as a URI (globally unique)
The fixture id (maybe new) to map to the request.
Each of the possible options in an alternative.
Additional information about how this entry should be processed as part of a transaction or batch. For history, it shows how the entry was processed to create the version contained in the entry.
Description of why this constraint is necessary or appropriate.
Why this constraint is necessary or appropriate
The version of the code system from this code was taken. Note that a well-maintained code system does not need the version reported, because the meaning of codes is consistent across versions. However this cannot consistently be assured, and when the meaning is not guaranteed to be consistent, the version SHOULD be exchanged.
Version in which this code/display is defined
If this is an actual service or product line, i.e. not a Group, then use code to indicate the Professional Service or Product supplied (e.g. CTP, HCPCS,USCLS,ICD10, NCPDP,DIN,ACHI,CCI). If a grouping item then use a group code to indicate the type of thing being grouped eg. 'glasses' or 'compound'.
The name of the operation or query. For an operation, this is the name prefixed with $ and used in the URL. For a query, this is the name used in the _query parameter when the query is called.
Name by which the operation/query is invoked
A short, descriptive, user-friendly title for the code system.
Name for this code system (human friendly)
The schedule resource that this slot defines an interval of status information.
A reference to an [ElementDefinition] that provides the details for the item.
ElementDefinition - details for the item
May be used to represent additional information that is not part of the basic definition of the element and that modifies the understanding of the element in which it is contained. Usually modifier elements provide negation or qualification. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension. Applications processing a resource are required to check for modifier extensions. Modifier extensions SHALL NOT change the meaning of any elements on Resource or DomainResource (including cannot change the meaning of modifierExtension itself).
Extensions that cannot be ignored if unrecognized
The ID of the Profile to validate against.
Profile Id of validation profile reference
An explanation or justification for why this service is being requested in coded or textual form. This is often for billing purposes. May relate to the resources referred to in supportingInformation.
Explanation/Justification for procedure or service
A Boolean value to indicate that this graph definition is authored for testing purposes (or education/evaluation/marketing) and is not intended to be used for genuine usage.
The canonical URL that identifies the structure.
Indicates who or what performed the event.
The required capability must exist and are assumed to function correctly on the FHIR server being tested.
Required capability that is assumed to function correctly on the FHIR server being tested
Distinguishes between physical addresses (those you can visit) and mailing addresses (e.g. PO Boxes and care-of addresses). Most addresses are both.
Applcations submitted to obtain a marketing authorization.
An identifier for this question or group of questions in a particular terminology such as LOINC.
Concept that represents the overall questionnaire
Codes to indicate the target population this reference range applies to. For example, a reference range may be based on the normal population or a particular sex or race.
The direction of the sort, ascending or descending.
Allows the product to be classified by various systems.
Potential clinical unwanted effects of use.
XPath or JSONPath expression to evaluate against the source fixture. When compareToSourceId is defined, either compareToSourceExpression or compareToSourcePath must be defined, but not both.
XPath or JSONPath expression to evaluate against the source fixture
Monitory amount associated with the code.
The official certifications, training, and licenses that authorize or otherwise pertain to the provision of care by the practitioner. For example, a medical license issued by a medical board authorizing the practitioner to practice medicine within a certian locality.
Certification, licenses, or training pertaining to the provision of care
Extra information about the prescription that could not be conveyed by the other attributes.
A list of alternate names that the product is known as, or was known as in the past.
The referenced rule within the external ruleset template.
For the code system, a list of versions that are supported by the server.
The identification of the code system that defines the meaning of the symbol in the code.
A description or code indicating why this task needs to be performed.
The sequence number of the addition within the line item submitted which contains the error. This value is omitted when the error is not related to an Addition.
A code that provides meaning for the action or action group. For example, a section may have a LOINC code for a the section of a documentation template.
Code representing the meaning of the action or sub-actions
Used to capture quantitative values for a variety of elements. If only limits are given, the arithmetic mean would be the average. If only a single definite value for a given element is given, it would be captured in this field.
Path plus parameters after [type]. Used to set parts of the request URL explicitly.
Minimum cardinality of the base element identified by the path.
Coded representation of the qualification.
The definition of the search parameter that describes this part.
Whether the receiver is deactivated right after the transaction.
Clinical trials or studies that this product is involved in.
If the procedure required specific follow up - e.g. removal of sutures. The followup may be represented as a simple note, or could potentially be more complex in which case the CarePlan resource can be used.
The organization requesting the service.
Organization providing the charged sevice
Who or what the set of documents is about. The documents can be about a person, (patient or healthcare practitioner), a device (i.e. machine) or even a group of subjects (such as a document about a herd of farm animals, or a set of patients that share a common exposure). If the documents cross more than one subject, then more than one subject is allowed here (unusual use case).
Indicates a category the goal falls within.
The period during which the questionnaire content was or is planned to be in active use.
When the questionnaire is expected to be used
Relevant time or time-period when this Contract Provision is applicable.
The first-tier service adjudications for payor added services.
The name of this test used for tracking/logging purposes by test engines.
If the matching elements have to occur in the same order as defined in the profile.
If elements must be in same order as slices
A specific version of a resource contained in the instance.
True positives, from the perspective of the truth data, i.e. the number of sites in the Truth Call Set for which there are paths through the Query Call Set that are consistent with all of the alleles at this site, and for which there is an accurate genotype call for the event.
True positives from the perspective of the truth data
Indicates the purpose of this bundle - how it is intended to be used.
document | message | transaction | transaction-response | batch | batch-response | history | searchset | collection
The "patient friendly language" versionof the Contract in whole or in parts. "Patient friendly language" means the representation of the Contract and Contract Provisions in a manner that is readily accessible and understandable by a layperson in accordance with best practices for communication styles that ensure that those agreeing to or signing the Contract understand the roles, actions, obligations, responsibilities, and implication of the agreement.
A label assigned to the group for human identification and communication.
The element id of the action this is related to.
The laterality of the (possibly paired) anatomic structures examined. E.g., the left knee, both lungs, or unpaired abdomen. If present, shall be consistent with any laterality information indicated in ImagingStudy.series.bodySite.
DICOM Study Instance UID, and Accession Number.
A real number that represents a multiplier used in determining the overall value of services delivered and/or goods received. The concept of a Factor allows for a discount or surcharge multiplier to be applied to a monetary amount.
Establishes the namespace for the value - that is, a URL that describes a set values that are unique.
Variable is set based either on element value in response body or on header field value in the response headers.
Goals that describe what the activities within the plan are intended to achieve. For example, weight loss, restoring an activity of daily living, obtaining herd immunity via immunization, meeting a process improvement objective, etc.
The matter of concern in the context of this provision of the agrement.
Identifies a protocol or workflow that this MessageDefinition represents a step in.
The organization that provides this healthcare service.
Facility where the services were provided.
The amount that is to be dispensed for one fill.
Amount of medication to supply per dispense
Substance introduced in the kind of container to preserve, maintain or enhance the specimen. Examples: Formalin, Citrate, EDTA.
The subject of the questionnaire response. This could be a patient, organization, practitioner, device, etc. This is who/what the answers apply to, but is not necessarily the source of information.
Describes the event of a patient consuming or otherwise being administered a medication. This may be as simple as swallowing a tablet or it may be a long running infusion. Related resources tie this event to the authorizing prescription, and the specific encounter between patient and health care practitioner.
Authorization in areas within a country.
active | cancelled | draft | entered-in-error
The specific service that is to be performed during this appointment.
The MessageHeader.id of the message to which this message is a response.
How the decision about a Contract was conveyed.
Specific benefits under this type of coverage.
This flag is used to mark the record to not be used. This is not used when a center is closed for maintenance, or for holidays, the notAvailable period is to be used for this.
Whether this HealthcareService record is in active use
Where the formal definition can be found.
A reference to a StructureMap resource that defines a transform that can be executed to produce the intent resource using the ActivityDefinition instance as the input.
Feeding provided through the gastrointestinal tract via a tube, catheter, or stoma that delivers nutrition distal to the oral cavity.
Rationale for the action to be performed or not performed. Describes why the action is permitted or prohibited.
Each resource contained in the instance.
The server where the request message originates from. Must be one of the server numbers listed in TestScript.origin section.
A broad categorization of the service that is to be performed during this appointment.
Describes the details of the manufacturer of the medication product. This is not intended to represent the distributor of a medication product.
The amount of supply that has been dispensed. Includes unit of measure.
Nested groups and/or questions found within this particular answer.
Text based condition for which the reference range is valid.
Condition associated with the reference range
A device that is implanted, removed or otherwise manipulated (calibration, battery replacement, fitting a prosthesis, attaching a wound-vac, etc.) as a focal portion of the Procedure.
Manipulated, implanted, or removed device
A code that represents types of uses of designations.
A guidance response is the formal response to a guidance request, including any output parameters returned by the evaluation, as well as the description of any proposed actions to be taken.
If the item is a node then this is the fee for the product or service, otherwise this is the total of the fees for the children of the group.
If the section is empty, why the list is empty. An empty section typically has some text explaining the empty reason.
The encounter or episode of care that establishes the context for this media.
Encounter / Episode associated with media
The TestScript.rule this assert will evaluate.
Other identifiers associated with the document manifest, including version independent identifiers.
The specific type of service that may be delivered or performed.
Type of service that may be delivered or performed
Security labels applied to this resource. These tags connect specific resources to the overall security policy and infrastructure.
Security Labels applied to this resource
A contact party (e.g. guardian, partner, friend) for the patient.
The shelf life time period can be specified using a numerical value for the period of time and its unit of time measurement The unit of measurement shall be specified in accordance with ISO 11240 and the resulting terminology The symbol and the symbol identifier shall be used.
A URL referencing an externally defined protocol, guideline, orderset or other definition that is adhered to in whole or in part by this request.
Instantiates external protocol or definition
Indicates the type of modular component such as protein, carbohydrate, fat or fiber to be provided in addition to or mixed with the base formula.
Type of modular component to add to the feeding
Human-readable name for the source system.
A set of additional dependencies for this mapping to hold. This mapping is only applicable if the specified element can be resolved, and it has the specified value.
Other elements required for this mapping (from context)
A list of implementation guides that the server does (or should) support in their entirety.
A code to indicate if the substance is actively used.
Referral Request(s) that are fulfilled by this EpisodeOfCare, incoming referrals.
The NPM package name for this Implementation Guide, used in the NPM package distribution, which is the primary mechanism by which FHIR based tooling manages IG dependencies. This value must be globally unique, and should be assigned with care.
busy | free | busy-unavailable | busy-tentative | entered-in-error.
Business idenfifier for this product. Could be an MPID.
The code specifying the type of clinical activity that resulted in placing the associated content into the DocumentManifest.
A series of links that provide context to this entry.
The name of the parameter or dot-separated path of parameter names pointing to the resource parameter that is expected to contain a reference to this resource.
The URL pointing to a FHIR-defined protocol, guideline, orderset or other definition that is adhered to in whole or in part by this NutritionOrder.
Instantiates FHIR protocol or definition
The document and format referenced. There may be multiple content element repetitions, each with a different format.
Number of participants enrolled in the plan.
A brief, natural language description of the condition that effectively communicates the intended semantics.
Natural language description of the condition
Date the educational material was given to the patient.
Broad categorization of the service that is to be provided (e.g. cardiology).
Each resource instance used by the responder.
A filter that can be used in a value set compose statement when selecting concepts using a filter.
Code indicating: Co-Pay, deductable, elegible, benefit, tax, etc.
Adjudication category such as co-pay, eligible, benefit, etc.
A code that identifies the kind of this biologically derived product (SNOMED Ctcode).
What this biologically derived product is
The date this measure report was generated.
Describes what was observed. Sometimes this is called the observation "code".
Type of component observation (code / type)
A code that identifies a property defined in the code system.
The identifier that is used to identify this version of the message definition when it is referenced in a specification, model, design or instance. This is an arbitrary value managed by the message definition author and is not expected to be globally unique. For example, it might be a timestamp (e.g. yyyymmdd) if a managed version is not available. There is also no expectation that versions can be placed in a lexicographical sequence.
Business version of the message definition
A short, descriptive, user-friendly title for the activity definition.
Name for this activity definition (human friendly)
The patient who is the focus of this episode of care.
The second-tier service adjudications for payor added services.
The authority that is specifying the regulations.
Specifies the authority of the regulation
The type of isotopic substitution present in a single substance.
An allele is one of a set of coexisting sequence variants of a gene ([SO:0001023](http://www.sequenceontology.org/browser/current_svn/term/SO:0001023)). Nucleotide(s)/amino acids from start position of sequence to stop position of sequence on the positive (+) strand of the reference sequence. When the sequence type is DNA, it should be the sequence on the positive (+) strand. This will lay in the range between variant.start and variant.end.
Number of discrete units within this product.
The amount of this biologically derived product
Id of the source fixture used as the contents to be evaluated by either the "source/expression" or "sourceId/path" definition.
Id of the source fixture to be evaluated
The characteristics, operational status and capabilities of a medical-related component of a medical device.
The role of the moiety should be specified if there is a specific role the moiety is playing.
FHIRPath expression - must be true or the mapping engine throws an error instead of completing.
Defines the required behavior for the action.
The resources controlled by this rule if specific resources are referenced.
Details concerning a service request that required a specimen to be collected.
The value of the header e.g. "application/fhir+xml".
The type of structure (e.g. Full, Partial, Representative).
The encounter or episode of care this impression was created as part of.
Commentary about the impression, typically recorded after the impression itself was made, though supplemental notes by the original author could also appear.
Comments made about the ClinicalImpression
Insurance plans, coverage extensions, pre-authorizations and/or pre-determinations that may be relevant to the Task.
A copyright statement relating to the activity definition and/or its contents. Copyright statements are generally legal restrictions on the use and publishing of the activity definition.
Information that only applies to packages (not products).
Entity or Organization having regulatory jurisdiction or accountability for enforcing policies pertaining to Consent Directives.
Capabilities that must exist and are assumed to function correctly on the FHIR server being tested.
Capabilities that are assumed to function correctly on the FHIR server being tested
The defined billing details in this resource pertain to the given product instance(s).
The NPM package name for the Implementation Guide that this IG depends on.
An absolute URI that is used to identify this activity definition when it is referenced in a specification, model, design or an instance; also called its canonical identifier. This SHOULD be globally unique and SHOULD be a literal address at which at which an authoritative instance of this activity definition is (or will be) published. This URL can be the target of a canonical reference. It SHALL remain the same when the activity definition is stored on different servers.
Canonical identifier for this activity definition, represented as a URI (globally unique)
Identifies medications, devices and any other substance used as part of the procedure.
The name of a section, the text of a question or text content for a display item.
Identifier for this instance of the anatomical structure.
Indicator for type of action performed during the event that generated the audit.
Type of action performed during the event
An internal reference to the definition of a mapping.
registered | preliminary | final | amended +
A description of how or why the filter is used.
Each rule template can take one or more parameters for rule evaluation.
A link to the FHIR specification that this test is covering.
An expression that returns true or false, indicating whether or not the condition is satisfied.
For programs which require reson codes for the inclusion, covering, of this billed item under the program or sub-program.
Program specific reason for item inclusion
The status of the narrative - whether it's entirely generated (from just the defined data or the extensions too), or whether a human authored it and it may contain additional data.
generated | extensions | additional | empty
Reference to the network that providing the type of coverage.
Specific findings or diagnoses that was considered likely or relevant to ongoing treatment.
Possible or likely findings and diagnoses
Indicates whether the asserted set of linkages are considered to be "in effect".
Whether this linkage assertion is active or not
Id [identifier??] of the clause or question text related to the requester of this action in the referenced form or QuestionnaireResponse.
An action or group of actions to be taken as part of the plan.
The legal status of supply of the medicinal product as classified by the regulator.
Identifies the broad category of service being performed or delivered.
Broad category of service being performed or delivered
If this is the default rule set to apply for the source type or this combination of types.
Identifies one of the records that is considered to refer to the same real-world occurrence as well as how the items should be evaluated within the collection of linked items.
An accident which resulted in the need for healthcare services.
Identifies the individual(s) or organization who provided the contents of the care plan.
Who provided the content of the care plan
The date (and optionally time) when the compartment definition was published. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the compartment definition changes.
Exclude one or more codes from the value set based on code system filters and/or other value sets.
Explicitly exclude codes from a code system or other value sets
Indicates the time during which this Contract ValuedItem information is effective.
The history of statuses that the EpisodeOfCare has been through (without requiring processing the history of the resource).
Past list of status codes (the current status may be included to cover the start date of the status)
The reason that the activity was taking place.
Additional representations for this item - other languages, aliases, specialized purposes, used for particular purposes, etc. These are relevant when the conditions of the expansion do not fix to a single correct representation.
Additional representations for this item
The base language in which the resource is written.
The URL pointing to an externally maintained protocol, guideline, questionnaire or other definition that is adhered to in whole or in part by this CarePlan.
A human readable string that is the recommended default way to present this concept to a user.
Identifies the facility where the activity will occur; e.g. home, hospital, specific clinic, etc.
Indicates if the medicinal product has an orphan designation for the treatment of a rare disease.
Id [identifier??] of the clause or question text about the asset in the referenced form or QuestionnaireResponse.
Describes the entity that is suspected to have caused the adverse event.
One or more sets of investigations (signs, symptoms, etc.). The actual grouping of investigations varies greatly depending on the type and context of the assessment. These investigations may include data generated during the assessment process, or data previously generated and recorded that is pertinent to the outcomes.
The function of the agent with respect to the activity. The security role enabling the agent with respect to the activity.
A patient's point-in-time set of recommendations (i.e. forecasting) according to a published schedule with optional supporting justification.
Header elements would be used to set HTTP headers.
Each operation can have one or more header elements
If the ETag values match, return a 304 Not Modified status. See the API documentation for ["Conditional Read"](http.html#cread).
The route or physiological path of administration into the patient's gastrointestinal tract for purposes of providing the formula feeding, e.g. nasogastric tube.
How the formula should enter the patient's gastrointestinal tract
Optical activity shall be captured as described in 4.7.2.
Descriptive topics related to the module. Topics provide a high-level categorization of the module that can be useful for filtering and searching.
E.g. Education, Treatment, Assessment, etc.
draft | requested | received | accepted | +
The type of role or competency of an individual desired or required to perform or not perform the action.
A finer grained suite of claim subtype codes which may convey Inpatient vs Outpatient and/or a specialty service. In the US the CMS Bill Type.
The program under which the medication is reviewed.
Program under which a medication is reviewed
Categorizes the type of clinical assessment performed.
The status of this measure. Enables tracking the life-cycle of the content.
For requests that are targeted to more than on potential recipient/target, for whom is fulfillment sought?
Documentation that describes anything special about the operation behavior, possibly detailing different behavior for system, type and instance-level invocation of the operation.
Specific details about operation behavior
Whether this represents partial or complete payment of the claim.
Number of minutes that the appointment is to take. This can be less than the duration between the start and end times. For example, where the actual time of appointment is only an estimate or if a 30 minute appointment is being requested, but any time would work. Also, if there is, for example, a planned 15 minute break in the middle of a long appointment, the duration may be 15 minutes less than the difference between the start and end.
Can be less than start/end (e.g. estimate)
Where the activity occurred, if relevant.
Quantity of time the encounter lasted. This excludes the time during leaves of absence.
Quantity of time the encounter lasted (less time absent)
User-visible prefix for the action (e.g. 1. or A.)
The nature of the relationship between a patient and the related person.
Describes what was observed. Sometimes this is called the observation "name".
The party to be reimbursed for the services.
A summary of the context and/or cause of the assessment - why / where was it performed, and what patient events/status prompted it.
Whether the request is a proposal, plan, or an original order.
proposal | plan | order | original-order | instance-order | option
When this specific batch of product will expire.
The sequential number of the interaction, e.g. 1.2.5.
The sequential number of the interaction
A suite of underwrite specific classifiers, for example may be used to identify a class of coverage or employer group, Policy, Plan.
A description of why this action is necessary or appropriate.
Characteristics for quantitative results of this observation.
The entity (e.g. person, organization, clinical information system, or device) which is to be the source of the communication.
Formal identifier for this image or other content.
Formal DICOM identifier for this instance
The administrable dose form, after necessary reconstitution.
The period that applies to the maximum number of units.
Other codes and entries contained under this entry in the hierarchy.
Alternative representation of the title for this Contract definition, derivative, or instance in any legal state., e.g., a domain specific contract number related to legislation.
Jurisdiction code for where this name applies.
Specifies the order of the results to be returned.
A reference to a resource that contains details of the request for this procedure.
Additional documentation about the resource and compartment.
Additional information codes regarding exceptions, special considerations, the condition, situation, prior or concurrent issues. Often there are mutiple jurisdiction specific valuesets which are required.
The party who is billing and responsible for the claimed good or service rendered to the patient.
An external identifier for this statement such as an IRI.
A list of key images associated with this report. The images are generally created during the diagnostic process, and may be directly of the patient, or of treated specimens (i.e. slides of interest).
Where applicable, the height can be specified using a numerical value and its unit of measurement The unit of measurement shall be specified in accordance with ISO 11240 and the resulting terminology The symbol and the symbol identifier shall be used.
Characteristics of the patient that are relevant to the administration guidelines (for example, height, weight,gender, etc).
Characteristics of the patient that are relevant to the administration guidelines
An experimental feature attribute that defines the quality of the feature in a quantitative way, such as a phred quality score ([SO:0001686](http://www.sequenceontology.org/browser/current_svn/term/SO:0001686)).
Code representing the set of handling instructions.
Specified time of day for action to take place.
Date/time(s) of when this Invoice was posted.
This modifier is used to convey Order-specific modifier about the type of oral food or oral fluids that should not be given. These can be derived from patient allergies, intolerances, or preferences such as No Red Meat, No Soy or No Wheat or Gluten-Free. While it should not be necessary to repeat allergy or intolerance information captured in the referenced AllergyIntolerance resource in the excludeFoodModifier, this element may be used to convey additional specificity related to foods that should be eliminated from the patient’s diet for any reason. This modifier applies to the entire nutrition order inclusive of the oral diet, nutritional supplements and enteral formula feedings.
Order-specific modifier about the type of food that should not be given
The name of the organization or individual that published the concept map.
Name of the publisher (organization or individual)
Identifies a specific implementation instance that is described by the terminology capability statement - i.e. a particular installation, rather than the capabilities of a software program.
For example, provides the reason for: the additional stay, or missing tooth or any other situation where a reason code is required in addition to the content.
The main (and possibly only) identifier for the coverage - often referred to as a Member Id, Certificate number, Personal Health Number or Case ID. May be constructed as the concatenation of the Coverage.SubscriberID and the Coverage.dependant.
Select concepts by specify a matching criteria based on the properties (including relationships) defined by the system. If multiple filters are specified, they SHALL all be true.
A categorical assessment of an observation value. For example, high, low, normal.
Security labels that protect the handling of information about the term and its elements, which may be specifically identified..
Identifier assigned to the resource for business purposes, outside the context of FHIR.
A formal identifier that is used to identify this structure definition when it is represented in other formats, or referenced in a specification, model, design or an instance.
Additional identifier for the structure definition
The maximum number of times this element is permitted to appear in the request or response.
A legal or geographic region in which the operation definition is intended to be used.
Intended jurisdiction for operation definition (if applicable)
Identifier for the organization that is used to identify the endpoint across multiple disparate systems.
Identifies this endpoint across multiple systems
User for example for ATC classification, or.
Additional classification of the catalog entry
A terminology code that corresponds to this group or question (e.g. a code from LOINC, which defines many questions and answers).
Corresponding concept for this item in a terminology
The actual design of the device or software version running on the device.
The value of the low bound of the reference range. The low bound of the reference range endpoint is inclusive of the value (e.g. reference range is >=5 - <=9). If the low bound is omitted, it is assumed to be meaningless (e.g. reference range is <=2.3).
The URL of a Questionnaire that this Questionnaire is based on.
If the Task.focus is a request resource and the task is seeking fulfillment (i.e. is asking for the request to be actioned), this element identifies any limitations on what parts of the referenced request should be actioned.
Which authority uses this official name.
Whether or not to implicitly send the request url in encoded format. The default is true to match the standard RESTful client behavior. Set to false when communicating with a server that does not support encoded url paths.
Whether or not to send the request url in encoded format
Codes that define how this element is represented in instances, when the deviation varies from the normal case.
xmlAttr | xmlText | typeAttr | cdaText | xhtml
When the request transitioned to being actionable.
A set of additional outcomes from this mapping to other elements. To properly execute this mapping, the specified element must be mapped to some data element or source that is in context. The mapping may still be useful without a place for the additional data elements, but the equivalence cannot be relied on.
Other concepts that this mapping also produces
An individiual or organization primarily involved in the creation and maintenance of the content.
A language the practitioner can use in patient communication.
A reference to a set of rules that were followed when the resource was constructed, and which must be understood when processing the content. Often, this is a reference to an implementation guide that defines the special rules along with other profiles etc.
A set of rules under which this content was created
Desired type of performer for doing the diagnostic testing.
The person, organization or device that created the flag.
May be a subtype or part of an offered asset.
The individual, organization, or device that initiated the request and has responsibility for its activation.
A formal identifier that is used to identify this activity definition when it is represented in other formats, or referenced in a specification, model, design or an instance.
Additional identifier for the activity definition
completed | in-progress | waiting | stopped | entered-in-error
Part of the name that is acquired as a title due to academic, legal, employment or nobility status, etc. and that appears at the end of the name.
This element contains the results for a single stratum within the stratifier. For example, when stratifying on administrative gender, there will be four strata, one for each possible gender value.
Vaccine date recommendations. For example, earliest date to administer, latest date to administer, etc.
Describes the meaning or use of this parameter.
A short, descriptive, user-friendly title for the charge item definition.
Name for this charge item definition (human friendly)
A reference to the the preferred location(s) where the procedure should actually happen. E.g. at home or nursing day care center.
For example granted, pending, expired or withdrawn.
A text equivalent of the action to be performed. This provides a human-interpretable description of the action when the definition is consumed by a system that might not be capable of interpreting it dynamically.
Static text equivalent of the action, used if the dynamic aspects cannot be interpreted by the receiving system
A resource that is part of the implementation guide. Conformance resources (value set, structure definition, capability statements etc.) are obvious candidates for inclusion, but any kind of resource can be included as an example resource.
The media type of the language for the expression.
The attribute of the sort. The specified path must be resolvable from the type of the required data. The path is allowed to contain qualifiers (.) to traverse sub-elements, as well as indexers ([x]) to traverse multiple-cardinality sub-elements. Note that the index must be an integer constant.
The name of the attribute to perform the sort
Used to define the parts of a composite search parameter.
For Composite resources to define the parts
The device, practitioner, etc. who performed or participated in the service.
An absolute URI that is used to identify this search parameter when it is referenced in a specification, model, design or an instance; also called its canonical identifier. This SHOULD be globally unique and SHOULD be a literal address at which at which an authoritative instance of this search parameter is (or will be) published. This URL can be the target of a canonical reference. It SHALL remain the same when the search parameter is stored on different servers.
Canonical identifier for this search parameter, represented as a URI (globally unique)
A human's name with the ability to identify parts and usage.
Type of plan. For example, "Platinum" or "High Deductable".
The justification of why the procedure was performed.
The justification that the procedure was performed
Captures the reason for the current state of the procedure.
The form to be used for printing the content.
Describes what will be observed. Sometimes this is called the observation "name".
Specifies the schedule of a medication in jurisdiction.
Record of the date and/or time of the onset of the Reaction.
The date on which the resource content was last reviewed. Review happens periodically after approval but does not change the original approval date.
When the event definition was last reviewed
The textual description of the kind of container.
A set of flags that defines how references are supported.
literal | logical | resolves | enforced | local
Indicates another resource whose existence justifies this Study.
Additional text about the adverse reaction event not captured in other fields.
Text about event not captured in other fields
Technical endpoints providing access to services operated for this role.
usual | official | temp | nickname | anonymous | old | maiden
The description of the resource version.
A set of rules as FHIRPath Invariants about when the extension can be used (e.g. co-occurrence variants for the extension). All the rules must be true.
FHIRPath invariants - when the extension can be used
The content was developed with a focus and intent of supporting the contexts that are listed. These terms may be used to assist with indexing and searching for appropriate questionnaire instances.
The context that the content is intended to support
A code that indicates how the page is generated.
The category of claim, e.g. oral, pharmacy, vision, institutional, professional.
The source application from which this message originated.
Fixture in the test script - by reference (uri). All fixtures are required for the test script to execute.
Fixture in the test script - by reference (uri)
A Boolean value to indicate that this charge item definition is authored for testing purposes (or education/evaluation/marketing) and is not intended to be used for genuine usage.
The individual, device, or organization for whom the change was made.
Provides a description of an individual term used within the measure.
Defined terms used in the measure documentation
The name of the organization or individual that published the library.
A selector of the type of consent being presented: ADR, Privacy, Treatment, Research. This list is now extensible.
Which of the four areas this resource covers (extensible)
The name of a search parameter that represents the link to the compartment. More than one may be listed because a resource may be linked to a compartment in more than one way,.
Search Parameter Name, or chained parameters
A curated namespace that issues unique symbols within that namespace for the identification of concepts, people, devices, etc. Represents a "System" used within the Identifier and Coding data types.
An authorization for the supply of glasses and/or contact lenses to a patient.
A series of required setup operations before tests are executed.
A relationship to another action such as "before" or "30-60 minutes after start of".
The type of relationship between the medicinal product indication or contraindication and another therapy.
Content to create because of this mapping rule.
Classes of devices, or ATC for medication.
Classification (category or class) of the item entry
Other identifiers associated with the document, including version independent identifiers.
The person to which the body site belongs.
The identifier(s) of this Ingredient that are assigned by business processes and/or used to refer to it when a direct URL reference to the resource itself is not appropriate.
The tag or value under the classification
High-level Dental, Vision, Medical, Pharmacy, Rehab etc. and detailed types of services: Dental: basic, major, ortho; Vision exam, glasses, contacts; etc.
An absolute reference to a strand. The Watson strand is the strand whose 5'-end is on the short arm of the chromosome, and the Crick strand as the one whose 5'-end is on the long arm.
A longer description of the group of operations.
The length of time between sampling times, measured in milliseconds.
A lower limit for the quantity of substance in the unit of presentation. For use when there is a range of strengths, this is the lower limit, with the presentation attribute becoming the upper limit.
An edition identifier used for business purposes to label business significant variants.
Descriptive name for this parameter that matches the external assert ruleset rule parameter name.
Parameter name matching external assert ruleset rule parameter
Diagnosis applicable for this service or product line.
The instance number of the Coverage which is the focus for adjudication. The Coverage against which the claim is to be adjudicated.
Identifiers assigned to this report by the performer or other systems.
The participation the agent had with respect to the activity.
How the element value is interpreted when discrimination is evaluated.
value | exists | pattern | type | profile
The human readable description of this supplemental data.
A collection of times the practitioner is available or performing this role at the location and/or healthcareservice.
An identifier - identifies some entity uniquely and unambiguously. Typically this is used for business identifiers.
Health Care Service Type Codes to identify the classification of service or benefits.
Whether the $closure operation is supported.
Information about the [ConceptMap/$closure](conceptmap-operation-closure.html) operation
A Boolean value to indicate that this test script is authored for testing purposes (or education/evaluation/marketing) and is not intended to be used for genuine usage.
Describes the purpose of this example amoung the set of examples.
The overall result from the execution of the TestScript.
The amount of energy (calories) that the formula should provide per specified volume, typically per mL or fluid oz. For example, an infant may require a formula that provides 24 calories per fluid ounce or an adult may require an enteral formula that provides 1.5 calorie/mL.
Amount of energy per specified volume that is required
Identifies the quantity expected to be consumed at once (per dose, per meal, etc.).
How much is administered/consumed/supplied
The reason why the supply item was requested.
Base definition for all elements that are defined inside a resource - but not those in a data type.
Base for elements defined inside a resource
Tagged value pairs for conveying additional information about the entity.
A Contract Valued Item unit valuation measure.
Contract Valued Item fee, charge, or cost
Provenance of a resource is a record that describes entities and processes involved in producing and delivering or otherwise influencing that resource. Provenance provides a critical foundation for assessing authenticity, enabling trust, and allowing reproducibility. Provenance assertions are a form of contextual metadata and can themselves become important records with their own provenance. Provenance statement indicates clinical significance in terms of confidence in authenticity, reliability, and trustworthiness, integrity, and stage in lifecycle (e.g. Document Completion - has the artifact been legally authenticated), all of which may impact security, privacy, and trust policies.
The type of container used to contain this kind of specimen.
Kind of container associated with the kind of specimen
If true, implementations that produce or consume resources SHALL provide "support" for the element in some meaningful way. If false, the element may be ignored and not supported. If false, whether to populate or use the data element in any way is at the discretion of the implementation.
A single identifier that uniquely identifies this manifest. Principally used to refer to the manifest in non-FHIR contexts.
Unique Identifier for the set of documents
The name of a resource supported by the server.
Information that may be needed by/relevant to the performer in their execution of this term action.
A Boolean value to indicate that this code system is authored for testing purposes (or education/evaluation/marketing) and is not intended to be used for genuine usage.
The date (and optionally time) when the search parameter was published. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the search parameter changes.
The party who 'owns' the insurance policy, may be an individual, corporation or the subscriber's employer.
Information about the use of the medicinal product in relation to other therapies as part of the indication.
A free text natural language description of the operation definition from a consumer's perspective.
Natural language description of the operation definition
This indicates the validity period of a prescription (stale dating the Prescription).
A free-text description of what is to be performed.
A concept from the target value set that this concept maps to.
A region or surface of the site, e.g. limb region or tooth surface(s).
A reference to an application-usable description of the identity that signed (e.g. the signature used their private key).
A plan, proposal or order that is fulfilled in whole or in part by this event.
An absolute URI that is used to identify this operation definition when it is referenced in a specification, model, design or an instance; also called its canonical identifier. This SHOULD be globally unique and SHOULD be a literal address at which at which an authoritative instance of this operation definition is (or will be) published. This URL can be the target of a canonical reference. It SHALL remain the same when the operation definition is stored on different servers.
Canonical identifier for this operation definition, represented as a URI (globally unique)
A substance used to create the material(s) of which the device is made.
Where applicable, the depth can be specified using a numerical value and its unit of measurement The unit of measurement shall be specified in accordance with ISO 11240 and the resulting terminology The symbol and the symbol identifier shall be used.
Location that identifies the physical place at which the user's session is occurring. For the purposes of context synchronization, this is intended to represent the user's workstation.
Encounter or Episode with primary association to specified term activity.
A short, descriptive, user-friendly title for the measure.
A list of the diagnostic requests that resulted in this imaging study being performed.
The license that applies to this Implementation Guide, using an SPDX license code, or 'not-open-source'.
SPDX license code for this IG (or not-open-source)
URL of Data type or Resource that is a(or the) type used for this element. References are URLs that are relative to http://hl7.org/fhir/StructureDefinition e.g. "string" is a reference to http://hl7.org/fhir/StructureDefinition/string. Absolute URLs are only allowed in logical models.
Data type or Resource (reference to definition)
The time period over which the service that is described by the document was provided.
Time of service that is being documented
An operation would involve a REST request to a server.
A code signifying whether a different drug was dispensed from what was prescribed.
Code signifying whether a different drug was dispensed from what was prescribed
Id of the referenced rule within the external ruleset template.
Id of referenced rule within the ruleset
A free text natural language description of the structure definition from a consumer's perspective.
Natural language description of the structure definition
planned | billable | not-billable | aborted | billed | entered-in-error | unknown
A participant who has attested to the accuracy of the composition/document.
Adjudication reason such as limit reached.
Unique identifier for this particular Contract Provision.
Identifies the organization or group who is responsible for ongoing maintenance of and access to the composition/document information.
Organization which maintains the composition
Code for an allergy or intolerance statement (either a positive or a negated/excluded statement). This may be a code for a substance or pharmaceutical product that is considered to be responsible for the adverse reaction risk (e.g., "Latex"), an allergy or intolerance condition (e.g., "Latex allergy"), or a negated/excluded code for a specific substance or class (e.g., "No latex allergy") or a general or categorical negated statement (e.g., "No known allergy", "No known drug allergies"). Note: the substance for a specific reaction may be different from the substance identified as the cause of the risk, but it must be consistent with it. For instance, it may be a more specific substance (e.g. a brand medication) or a composite product that includes the identified substance. It must be clinically safe to only process the 'code' and ignore the 'reaction.substance'. If a receiving system is unable to confirm that AllergyIntolerance.reaction.substance falls within the semantic scope of AllergyIntolerance.code, then the receiving system should ignore AllergyIntolerance.reaction.substance.
Code that identifies the allergy or intolerance
An organization which administer other services such as underwriting, customer service and/or claims processing on behalf of the health insurance product owner.
Indicates who or what performed the medication administration.
Who performed the medication administration
Code that specifies the property DeviceDefinitionPropetyCode (Extensible).
A natural language name identifying the graph definition. This name should be usable as an identifier for the module by machine processing applications such as code generation.
Name for this graph definition (computer friendly)
Describes the type of the metric. For example: Heart Rate, PEEP Setting, etc.
Identity of metric, for example Heart Rate or PEEP Setting
Information about an assembled implementation guide, created by the publication tooling.
The technical details of an endpoint that can be used for electronic services, such as for web services providing XDS.b or a REST endpoint for another FHIR server. This may include any security context information.
The subject of the report. Usually, but not always, this is a patient. However diagnostic services also perform analyses on specimens collected from a variety of other sources.
The subject of the report - usually, but not always, the patient
The provider who is responsible for the services rendered to the patient.
Include one or more codes from a code system or other value set(s).
Defines the grouping behavior for the action and its children.
visual-group | logical-group | sentence-group
The type of appointments that can be booked into this slot (ideally this would be an identifiable service - which is at a location, rather than the location itself). If provided then this overrides the value provided on the availability resource.
The healthcare professional responsible for authorizing the prescription.
List of contacts related to this specific healthcare service.
Contacts related to the healthcare service
A legal or geographic region in which the example scenario is intended to be used.
Intended jurisdiction for example scenario (if applicable)
The specimen imaged, e.g., for whole slide imaging of a biopsy.
Identifies an element defined elsewhere in the definition whose content rules should be applied to the current element. ContentReferences bring across all the rules that are in the ElementDefinition for the element, including definitions, cardinality constraints, bindings, invariants etc.
Reference to definition of content for the element
The content was developed with a focus and intent of supporting the contexts that are listed. These terms may be used to assist with indexing and searching for appropriate structure definition instances.
Definition of an operation or a named query together with its parameters and their meaning and type.
Provides a reason why the expected value in the element Observation.value[x] is missing.
The medication for which this is an indication.
Latitude. The value domain and the interpretation are the same as for the text of the latitude element in KML (see notes below).
Whether a treatment instruction (e.g. artificial respiration yes or no) was verified with the patient, his/her family or another authorized person.
Associated documentation about the medication.
Country - a nation as commonly understood or generally accepted.
Country (e.g. can be ISO 3166 2 or 3 letter code)
Where applicable, the external diameter can be specified using a numerical value and its unit of measurement The unit of measurement shall be specified in accordance with ISO 11240 and the resulting terminology The symbol and the symbol identifier shall be used.
The specialty of a practitioner that would be required to perform the service requested in this appointment.
The period during which the library content was or is planned to be in active use.
Whether the Medicinal Product is subject to additional monitoring for regulatory reasons.
The resource to which this actual person is associated.
The subscription resource is used to define a push-based subscription from a server to another system. Once a subscription is registered with the server, the server checks every resource that is created or updated, and if the resource matches the given criteria, it sends a message on the defined "channel" so that another system can take an appropriate action.
Fixture to evaluate the XPath/JSONPath expression or the headerField against within this variable.
Fixture Id of source expression or headerField within this variable
Indicates whether the answer value is selected when the list of possible answers is initially shown.
The content was developed with a focus and intent of supporting the contexts that are listed. These terms may be used to assist with indexing and searching for appropriate activity definition instances.
The second-tier service adjudications for submitted services.
The time period in which this catalog entry is expected to be active.
Indicates a relative path to an image that exists within the IG.
The label would be used for tracking/logging purposes by test engines.
Type of benefit (primary care; speciality care; inpatient; outpatient).
The country or countries for which the strength range applies.
Clinical stage or grade of a condition. May include formal severity assessments.
A code indicating why the administration was not performed.
List of patient diagnosis for which care is sought.
The score of an experimentally derived feature such as a p-value ([SO:0001685](http://www.sequenceontology.org/browser/current_svn/term/SO:0001685)).
Information on whether an increase or decrease in score is the preferred result (e.g., a higher score indicates better quality OR a lower score indicates better quality OR quality is within a range).
The information about where the adverse event occurred.
Notices and disclaimers regarding the use of the measure or related to intellectual property (such as code systems) referenced by the measure.
Disclaimer for use of the measure or its referenced content
text/cql | text/fhirpath | application/x-fhir-query | etc.
Set this to true if the record is saying that the service/procedure should NOT be performed.
True if service/procedure should not be performed
Exceptions, special considerations, the condition, situation, prior or concurrent issues
A short description of the test used by test engines for tracking and reporting purposes.
Tracking/reporting short description of the test
The root of the sections that make up the composition.
Completed or terminated request(s) whose function is taken by this new request.
Defines an appropriate combination of parameters to use when invoking this operation, to help code generators when generating overloaded parameter sets for this operation.
Define overloaded variants for when generating code
A human-readable description of each option.
The practitioner that holds legal responsibility for ordering the diet, nutritional supplement, or formula feedings.
Who ordered the diet, formula or nutritional supplement
The anatomical location or region of the specimen, lesion, or body structure.
Any comment can be provided in this field, if necessary.
Indicates if the dose is valid or not valid with respect to the published recommendations.
Status of the dose relative to published recommendations
The sequence number of the line item submitted which contains the error. This value is omitted when the error is elsewhere.
The organization that manages this endpoint (even if technically another organization is hosting this in the cloud, it is the organization associated with the data).
Organization that manages this endpoint (might not be the organization that exposes the endpoint)
The specific characteristic (e.g. height, weight, gender, etc).
Each resource instance used by the initiator.
Special precautions for storage, if any, can be specified using an appropriate controlled vocabulary The controlled term and the controlled term identifier shall be specified.
A request to convey information; e.g. the CDS system proposes that an alert be sent to a responsible provider, the CDS system proposes that the public health agency be notified about a reportable condition.
The language this designation is defined for.
The date at which the given status has become applicable.
Whether the device must be sterilised before use.
An identifier that links together multiple tasks and other requests that were created in the same context.
The anatomical location where this condition manifests itself.
The individual or organization that authored the Contract definition, derivative, or instance in any legal state.
A reference to a code defined by a terminology system.
Country code for where this name applies.
Allows identification of which elements have their cardinalities impacted by the constraint. Will not be referenced for constraints that do not affect cardinality.
A digital identity certificate associated with the validator.
Regulatory information about a medication.
An expression in the specified language that returns a value.
The quantity times the unit price for an additional service or product or charge. For example, the formula: unit Quantity * unit Price (Cost per Point) * factor Number * points = net Amount. Quantity, factor and points are assumed to be 1 if not supplied.
draft | active | suspended | completed | entered-in-error | cancelled
The date (and optionally time) when the terminology capabilities was published. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the terminology capabilities changes.
The full UDI carrier as the human readable form (HRF) representation of the barcode string as printed on the packaging of the device.
May include configuration or other information useful in debugging.
Indicates the reason for the substitution (or lack of substitution) from what was prescribed.
Assert rule to be used in one or more asserts within the test script.
The Implicit meaning that is to be understood when this element is missing (e.g. 'when this element is missing, the period is ongoing').
Implicit meaning when this element is missing
Unique device identifier (UDI) assigned to device label or package. Note that the Device may include multiple udiCarriers as it either may include just the udiCarrier for the jurisdiction it is sold, or for multiple jurisdictions it could have been sold.
Unique Device Identifier (UDI) Barcode string
Insurance plans, coverage extensions, pre-authorizations and/or pre-determinations that may be required for delivering the requested service.
The content was developed with a focus and intent of supporting the contexts that are listed. These terms may be used to assist with indexing and searching for appropriate concept map instances.
Provides additional information about what the account tracks and how it is used.
The Software version associated with the device, typically only used for devices with embedded software or firmware.
The Software version associated with the device
The lower limit of detection of the measured points. This is needed if any of the data points have the value "L" (lower than detection limit).
Where applicable, the color can be specified An appropriate controlled vocabulary shall be used The term and the term identifier shall be used.
A computer processable form of the unit in some unit representation system.
A description of what the value for the filter should be.
Code filters specify additional constraints on the data, specifying the value set of interest for a particular element of the data. Each code filter defines an additional constraint on the data, i.e. code filters are AND'ed, not OR'ed.
The URL pointing to an externally maintained protocol, guideline, orderset or other definition that is adhered to in whole or in part by this Procedure.
Basic is used for handling concepts not yet defined in FHIR, narrative-only resources that don't map to an existing resource, and custom resources not appropriate for inclusion in the FHIR specification.
Where applicable, the scoring can be specified An appropriate controlled vocabulary shall be used The term and the term identifier shall be used.
The capabilities supported on a device, the standards to which the device conforms for a particular purpose, and used for the communication.
A description of the scope and nature of the plan.
How the entity was used during the activity.
derivation | revision | quotation | source | removal
For referring to data content defined in other formats.
Software that is covered by this capability statement. It is used when the capability statement describes the capabilities of a particular software version, independent of an installation.
Software that is covered by this capability statement
Ranking of the diagnosis (for each role type).
Which compartment this definition describes.
Patient | Encounter | RelatedPerson | Practitioner | Device
active | recurrence | relapse | well-controlled | poorly-controlled | inactive | remission | resolved
Reason or justification for the use of this device.
The type of the Diagnosis, for example: admitting, primary, secondary, discharge.
The members of the team who provided the overall service.
One of the permitted answers for a "choice" or "open-choice" question.
The date (and optionally time) when the concept map was published. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the concept map changes.
The priority of the coverage in the context of this account.
Plan/proposal/order fulfilled by this request.
What days/times during a week is this location usually open.
A description of when the action should be triggered.
Indicates the type of performer of the administration of the medication.
Desired kind of performer of the medication administration
The display for the code. The display is only provided to help editors when editing the concept map.
A copyright statement relating to the capability statement and/or its contents. Copyright statements are generally legal restrictions on the use and publishing of the capability statement.
A simple summary of the stage such as "Stage 3". The determination of the stage is disease-specific.
Provides an explanation as to why the vaccine administration event is valid or not relative to the published recommendations.
Captures the reason for the current state of the MedicationRequest.
A Boolean value to indicate that this measure is authored for testing purposes (or education/evaluation/marketing) and is not intended to be used for genuine usage.
Batch number or expiry date of a device.
Health insurance provider network in which the participatingOrganization provides the role's services (if defined) at the indicated locations (if defined).
The total number of concepts defined by the code system. Where the code system has a compositional grammar, the basis of this count is defined by the system steward.
Adjustment for astigmatism measured in integer degrees.
Additional information about the resource type used by the system.
Additional information about the use of the resource type
A guarantor may be placed on credit hold or otherwise have their role temporarily suspended.
A human-readable narrative that contains the attested content of the section, used to represent the content of the resource to a human. The narrative need not encode all the structured data, but is required to contain sufficient detail to make it "clinically safe" for a human to just read the narrative.
Text summary of the section, for human interpretation
Points to the value set or external definition (e.g. implicit value set) that identifies the set of codes to be used.
Captures the reason for the current state of the Communication.
Descriptive name for this parameter that matches the external assert rule parameter name.
Parameter name matching external assert rule parameter
A specification of the restful capabilities of the solution for a specific resource type.
active | administratively-completed | approved | closed-to-accrual | closed-to-accrual-and-intervention | completed | disapproved | in-review | temporarily-closed-to-accrual | temporarily-closed-to-accrual-and-intervention | withdrawn
Defines input data requirements for the action.
Catalog entries are wrappers that contextualize items included in a catalog.
Allows the context of the guidance response to be provided if available. In a service context, this would likely be unavailable.
Encounter or Episode during which the response was returned
The encounter or episode of care within which the communication request was created.
Any processing of the product during collection.
A free text natural language description of the questionnaire from a consumer's perspective.
Natural language description of the questionnaire
Software that is covered by this terminology capability statement. It is used when the statement describes the capabilities of a particular software version, independent of an installation.
Software that is covered by this terminology capability statement
planned | arrived | triaged | in-progress | onleave | finished | cancelled +.
The type of enteral or infant formula such as an adult standard formula with fiber or a soy-based infant formula.
The meaning of the hierarchy of concepts as represnted in this resource.
grouped-by | is-a | part-of | classified-with
The fee for an addittional service or product or charge.
The identifier that is used to identify this version of the charge item definition when it is referenced in a specification, model, design or instance. This is an arbitrary value managed by the charge item definition author and is not expected to be globally unique. For example, it might be a timestamp (e.g. yyyymmdd) if a managed version is not available. There is also no expectation that versions can be placed in a lexicographical sequence. To provide a version consistent with the Decision Support Service specification, use the format Major.Minor.Revision (e.g. 1.0.0). For more information on versioning knowledge assets, refer to the Decision Support Service specification. Note that a version is required for non-experimental active assets.
Business version of the charge item definition
A specified substance that comprises this ingredient.
The existing physiological conditions of the specific population to which this applies.
The style of appointment or patient that may be booked in the slot (not service type).
Expresses the product of the Contract Valued Item unitQuantity and the unitPriceAmt. For example, the formula: unit Quantity * unit Price (Cost per Point) * factor Number * points = net Amount. Quantity, factor and points are assumed to be 1 if not supplied.
The identifier that is used to identify this version of the compartment definition when it is referenced in a specification, model, design or instance. This is an arbitrary value managed by the compartment definition author and is not expected to be globally unique. For example, it might be a timestamp (e.g. yyyymmdd) if a managed version is not available. There is also no expectation that versions can be placed in a lexicographical sequence.
Business version of the compartment definition
The product or brand name of the enteral or infant formula product such as "ACME Adult Standard Formula".
Product or brand name of the enteral or infant formula
Additional names for a medication, for example, the name(s) given to a medication in different countries. For example, acetaminophen and paracetamol or salbutamol and albuterol.
Logical network location for application activity
Sequence of the careTeam which serves to order and provide a link.
Name of the rule for internal references.
The description would be used by test engines for tracking and reporting purposes.
Tracking/reporting operation description
A snapshot view is expressed in a standalone form that can be used and interpreted without considering the base StructureDefinition.
Each study has one or more series of images or other content.
Each study has one or more series of instances
initial-population | numerator | numerator-exclusion | denominator | denominator-exclusion | denominator-exception | measure-population | measure-population-exclusion | measure-observation
The regulatory procedure for granting or amending a marketing authorization.
Identifies the types of resource or data type elements to which the extension can be applied.
If an extension, where it can be used in instances
Practitioner that is able to provide the defined services for the organization.
The document or URL of the document along with critical metadata to prove content has integrity.
A resource that represents the data of a single raw artifact as digital content accessible in its native format. A Binary resource can contain any content, whether text, image, pdf, zip archive, etc.
Indicates which days of the week are available between the start and end Times.
The organization that has assumed the specific responsibilities for the specified duration.
The date (and perhaps time) when the adverse event occurred.
Type of molecular weight such as exact, average (also known as. number average), weight average.
The type of deviceName. UDILabelName | UserFriendlyName | PatientReportedName | ManufactureDeviceName | ModelName.
udi-label-name | user-friendly-name | patient-reported-name | manufacturer-name | model-name | other
Identifiers assigned to this order instance by the orderer and/or the receiver and/or order fulfiller.
Describes the expected outcome for the subject.
The types on which this operation can be executed.
For draft requests, indicates the date of initial creation. For requests with other statuses, indicates the date of activation.
When request transitioned to being actionable
Physical service site on the patient (limb, tooth, etc.).
This alert is only relevant during the encounter.
Class that describes any texture modifications required for the patient to safely consume various types of solid foods.
Describes the type of performance (e.g. ordering provider, administering provider, etc.).
The number of bytes of data that make up this attachment (before base64 encoding, if that is done).
Number of bytes of content (if url provided)
Internal rule reference for shared list items.
The status of this operation definition. Enables tracking the life-cycle of the content.
Type of Party to be reimbursed: Subscriber, provider, other.
Type of party: Subscriber, Provider, other
Information about chromosome structure variation.
The status of this capability statement. Enables tracking the life-cycle of the content.
Information about how a resource is related to the compartment.
Asset context reference may include the creator, custodian, or owning Person or Organization (e.g., bank, repository), location held, e.g., building, jurisdiction.
Indicates the current state of this list.
A structured set of tests against a FHIR server or client implementation to determine compliance against the FHIR specification.
The label for this particular section. This will be part of the rendered content for the document, and is often used to build a table of contents.
The organization which is receiving the payment.
Organization which is receiving the payment
The price for a ChargeItem may be calculated as a base price with surcharges/deductions that apply in certain conditions. A ChargeItemDefinition resource that defines the prices, factors and conditions that apply to a billing code is currently under developement. The priceComponent element can be used to offer transparency to the recipient of the Invoice of how the prices have been calculated.
A description of site availability exceptions, e.g. public holiday availability. Succinctly describing all possible exceptions to normal site availability as details in the available Times and not available Times.
Additional information that supports the medication being dispensed.
Information that supports the dispensing of the medication
A short, descriptive, user-friendly title for the concept map.
Name for this concept map (human friendly)
Indicates the reason the request was initiated. This is typically provided as a parameter to the evaluation and echoed by the service, although for some use cases, such as subscription- or event-based scenarios, it may provide an indication of the cause for the response.
An abstract server used in operations within this test script in the origin element.
An abstract server representing a client or sender in a message exchange
Describes the eligibility conditions for the service.
A link to a resource representing the person whom the delivered item is for.
Clinical or Operational Relevant period of time that bounds the data controlled by this rule.
Timeframe for data controlled by this rule
Identifies the quantity expected to be consumed in a given day.
Educational material presented to the patient (or guardian) at the time of vaccine administration.
Educational material presented to patient
The equivalence between the source and target concepts (counting for the dependencies and products). The equivalence is read from target to source (e.g. the target is 'wider' than the source).
relatedto | equivalent | equal | wider | subsumes | narrower | specializes | inexact | unmatched | disjoint
A list of note references to the notes provided below.
This resource provides eligibility and plan details from the processing of an CoverageEligibilityRequest resource.
A set of criteria that define the contents of the value set by including or excluding codes selected from the specified code system(s) that the value set draws from. This is also known as the Content Logical Definition (CLD).
Content logical definition of the value set (CLD)
apply-business-version | apply-jurisdiction | path-resource | path-pages | path-tx-cache | expansion-parameter | rule-broken-links | generate-xml | generate-json | generate-turtle | html-template.
Human readable form of this Contract Offer.
The MeasureReport status. No data will be available until the MeasureReport status is complete.
Indicates the degree of conformance expectations associated with this binding - that is, the degree to which the provided value set must be adhered to in the instances.
required | extensible | preferred | example
References to message definitions for messages this system can send or receive.
The value to use in a comparison against the request URL path string.
Id of the variant in this external repository. The server will understand how to use this id to call for more info about datasets in external repository.
Id of the dataset that used to call for dataset in repository
Include additional information (for example, patient height and weight) that supports the ordering of the medication.
Information to support ordering of the medication
Identifies the patient, practitioner, device or any other resource that is the "focus" of this resource.
The Resource for the entry. The purpose/meaning of the resource is determined by the Bundle.type.
The actual configuration settings of a device as it actually operates, e.g., regulation status, time properties.
Reference of a prior response to resource which is the target or subject of this action.
The time required for any specified property (e.g., the concentration of a substance in the body) to decrease by half.
Time required for concentration in the body to decrease by half
Diet given orally in contrast to enteral (tube) feeding.
In a transaction or batch, this is the HTTP action to be executed for this entry. In a history bundle, this indicates the HTTP action that occurred.
GET | HEAD | POST | PUT | DELETE | PATCH
Payment details for the claim if the claim has been paid.
A code identifying the kind of content contained within the section. This must be consistent with the section title.
The program or plan underwriter or payor including both insurance and non-insurance agreements, such as patient-pay agreements. May provide multiple identifiers such as insurance company identifier or business identifier (BIN number).
Identifier for the plan or agreement issuer
The entity is attributed to an agent to express the agent's responsibility for that entity, possibly along with other agents. This description can be understood as shorthand for saying that the agent was responsible for the activity which generated the entity.
The frequency of occurrence of the effect.
Whether the substance is a known or suspected allergen.
The id of the fixture used as the body of a PUT or POST request.
Fixture Id of body for PUT and POST requests
The parameter whose value is to be tracked, e.g. body weight, blood pressure, or hemoglobin A1c level.
The parameter whose value is to be tracked
A list of conditions/problems/diagnoses that this episode of care is intended to be providing care for.
Conditions/problems/diagnoses this episode of care is for
The recordedDate represents when this particular Condition record was created in the system, which is often a system-generated date.
Customizations that should be applied to the statically defined resource. For example, if the dosage of a medication must be computed based on the patient's weight, a customization would be used to specify an expression that calculated the weight, and the path on the resource that would contain the result.
Reference to the parent (source) specimen which is used when the specimen was either derived from or a component of another specimen.
Specimen from which this specimen originated
Unique identifier used to reference the account. Might or might not be intended for human use (e.g. credit card number).
The payload type describes the acceptable content that can be communicated on the endpoint.
The type of content that may be used at this endpoint (e.g. XDS Discharge summaries)
The period during which the activity definition content was or is planned to be in active use.
When the activity definition is expected to be used
Item typification or modifiers codes, eg for Oral whether the treatment is cosmetic or associated with TMJ, or for medical whether the treatment was outside the clinic or out of office hours.
Text based reference range in an observation which may be used when a quantitative range is not appropriate for an observation. An example would be a reference value of "Negative" or a list or table of "normals".
Text based reference range in an observation
The canonical URL of the Implementation guide for the dependency.
Defines whether the action can be selected multiple times.
This records identifiers associated with this biologically derived product instance that are defined by business processes and/or used to refer to it when a direct URL reference to the resource itself is not appropriate (e.g. in CDA documents, or in written / printed documentation).
The list of healthcare services that this worker provides for this role's Organization/Location(s).
Identifiers assigned to this research subject for a study.
Business Identifier for research subject in a study
Specifies the criteria by which the question is enabled.
The workflow/clinical status of this composition. The status is a marker for the clinical standing of the document.
preliminary | final | amended | entered-in-error
MimeType of the binary content represented as a standard MimeType (BCP 13).
Which other rules to apply in the context of this rule.
A larger care plan of which this particular care plan is a component or step.
Description of the quality and completeness of the asset that imay be a factor in its valuation.
An action that is or was performed on or for a patient. This can be a physical intervention like an operation, or less invasive like long term services, counseling, or hypnotherapy.
The relationship of this action to the related action.
before-start | before | before-end | concurrent-with-start | concurrent | concurrent-with-end | after-start | after | after-end
Categorizes the account for reporting and searching purposes.
A description and/or code explaining the premature termination of the study.
accrual-goal-met | closed-due-to-toxicity | closed-due-to-lack-of-study-progress | temporarily-closed-per-study-design
Free text or additional instructions or information pertaining to the oral supplement.
Instructions or additional information about the oral supplement
The individual responsible for dispensing the medication, supplier or device.
List of participants involved in the appointment.
The URL pointing to an externally maintained protocol, guideline, orderset or other definition that is adhered to in whole or in part by this Communication.
The date (and optionally time) when the value set was published. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the value set changes. (e.g. the 'content logical definition').
Specifies if changes are allowed when dispensing a medication from a regulatory perspective.
Identifies the type of the data in the attachment and allows a method to be chosen to interpret or render the data. Includes mime type parameters such as charset where appropriate.
Mime type of the content, with charset etc.
The URL pointing to a FHIR-defined protocol, guideline, orderset or other definition that is adhered to in whole or in part by this DeviceRequest.
The type of study based upon the intent of the study's activities. A classification of the intent of the study.
treatment | prevention | diagnostic | supportive-care | screening | health-services-research | basic-science | device-feasibility
The URL pointing to an externally maintained protocol, guideline, orderset or other definition that is adhered to in whole or in part by this DeviceRequest.
Indicates an actual or potential clinical issue with or between one or more active or proposed clinical actions for a patient; e.g. Drug-drug interaction, Ineffective treatment frequency, Procedure-condition conflict, etc.
As new versions of a protocol or guideline are defined, allows identification of what versions are replaced by a new instance.
One or more values that should be pre-populated in the answer when initially rendering the questionnaire for user input.
When the charge item definition was approved by publisher
The code used in the URL or the parameter name in a parameters resource for this search parameter.
Abstract name given to an origin server in this test script. The name is provided as a number starting at 1.
The index of the abstract origin server starting at 1
Identifies the impact constraint violation has on the conformance of the instance.
A free text natural language description of the library from a consumer's perspective.
Natural language description of the library
Any texture modifications (for solid foods) that should be made, e.g. easy to chew, chopped, ground, and pureed.
Code to indicate how to alter the texture of the foods, e.g. pureed
The date/time validation was last completed (incl. failed validations).
The context of the activities a user is taking - why the user is accessing the data - that are controlled by this rule.
Context of activities covered by this rule
Identifies problems, conditions, issues, or concerns the goal is intended to address.
The significant Conditions (or condition) that the family member had. This is a repeating section to allow a system to represent more than one condition per resource, though there is nothing stopping multiple resources - one per condition.
Specimen conditioned in a container as expected by the testing laboratory.
URL to a particular requirement or feature within the FHIR specification.
Indicates who should participate in performing the action described.
Link to another patient resource that concerns the same actual patient.
The content was developed with a focus and intent of supporting the contexts that are listed. These terms may be used to assist with indexing and searching for appropriate message definition instances.
The fixed code to use when the mode = 'fixed' - all unmapped codes are mapped to a single fixed code.
The insurer-specific identifier for the insurer-defined network of providers to which the beneficiary may seek treatment which will be covered at the 'in-network' rate, otherwise 'out of network' terms and conditions apply.
A link to further details on the result.
Identifies a planned action to occur as part of the plan. For example, a medication to be used, lab tests to perform, self-monitoring, education, etc.
The degree to which the server supports the code search parameter on ValueSet, if it is supported.
Identify the exact boundaries of variant sequences. Each type of structure variant requires the DNA duplex to be broken and rejoined, and this creates a new sequence of bases at the rejoined sites, known as breakpoints or boundaries.
Id [identifier??] of the clause or question text related to the reason type or reference of this action in the referenced form or QuestionnaireResponse.
An indication, when true, that the value cannot be changed by a human respondent to the Questionnaire.
Amino Acid Sequence/ DNA Sequence / RNA Sequence.
A link to a resource that identifies the particular occurrence of contact between patient and health care provider.
Created during encounter / admission / stay
The status of this search parameter. Enables tracking the life-cycle of the content.
A code specifying the state of the set of dispense events.
preparation | in-progress | cancelled | on-hold | completed | entered-in-error | stopped | unknown
The clinical status of the allergy or intolerance.
A comorbidity (concurrent condition) or coinfection.
The visit, admission, or other contact between patient and health care provider during which the medication administration was performed.
Encounter or Episode of Care administered as part of
Defines whether the action should usually be preselected.
The list of people responsible for providing the service.
List of participants involved in the encounter
An amount that expresses the weighting (based on difficulty, cost and/or resource intensiveness) associated with the Contract Valued Item delivered. The concept of Points allows for assignment of point values for a Contract Valued Item, such that a monetary amount can be assigned to each point.
Contract Valued Item Difficulty Scaling Factor
Indicates how the system may be identified when referenced in electronic exchange.
A measured amount (or an amount that can potentially be measured). Note that measured amounts include amounts that are not precisely quantified, including amounts involving arbitrary units and floating currencies.
Reference range for ordinal and continuous observations.
Select codes/concepts by their properties (including relationships)
The fee for an additional service or product or charge.
The appointment that scheduled this encounter.
The person or organization that accepts overall responsibility for the contents of the message. The implication is that the message event happened under the policies of the responsible party.
A uri that identifies the source system of the resource. This provides a minimal amount of [Provenance] information that can be used to track or differentiate the source of information in the resource. The source may identify another FHIR server, document, message, database, etc.
Identifies where the resource comes from
The “real world” units in which the quantity of the manufactured item is described.
HealthCare Professional performing collection.
The operation code type that will be executed
This resource provides the adjudication details from the processing of a Claim resource.
The Reference(s) that were generated or updated by the activity described in this resource. A provenance can point to more than one target if multiple resources were created/updated by the same activity.
Target Reference(s) (usually version specific)
The name of the organization or individual that published the search parameter.
A container for a collection of resources.
Status of the validation of the target against the primary source (successful; failed; unknown).
Associated documentation about the associated medication knowledge.
Identifies the patient, group or organization for whom the goal is being established.
The number of false positives if the GQ score threshold was set to "score" field value.
The machine-readable AIDC string in base64 encoding. Can correspond to the UDI pattern in devices.
The machine-readable AIDC string in base64 encoding
A free text natural language description of the charge item definition from a consumer's perspective.
Natural language description of the charge item definition
Reference to the network included in the health insurance product.
Assessment of if the entity caused the event.
Indicates how the medication is/was or should be taken by the patient.
Details of how medication is/was taken or should be taken
Notes for special requirements such as coatings and lens materials.
The device, practitioner, etc. who initiated the request.
Identifies the computable language in which mapping.map is expressed.
Didactic or other informational resources associated with the action that can be provided to the CDS recipient. Information resources can include inline text commentary and links to web resources.
Supporting documentation for the intended performer of the action
A code (or set of codes) that specify this medication, or a textual description if no code is available. Usage note: This could be a standard medication code such as a code from RxNorm, SNOMED CT, IDMP etc. It could also be a national or local formulary code, optionally with translations to other code systems.
A label or set of text to display in place of the data.
Name of parameter to include in overload.
The intended effect, aim or strategy to be achieved by the indication.
Detailed description of the type of planned activity; e.g. what lab test, what procedure, what kind of encounter.
Identity of the Entity used. May be a logical or physical uri and maybe absolute or relative.
A description of the substance - its appearance, handling requirements, and other usage notes.
Textual description of the substance, comments
Each resource and each version that is present in the workflow.
Free-text information captured about the task as it progresses.
ProbabilityScale | Bayesian | Checklist.
Collection of specialties handled by the service site. This is more of a medical term.
Specialties handled by the HealthcareService
Set of instructions for conservation/transport of the specimen at a defined temperature interval, prior the testing process.
The status of this questionnaire. Enables tracking the life-cycle of the content.
Used when the type is "Reference" or "canonical", and identifies a profile structure or implementation Guide that applies to the target of the reference this parameter refers to. If any profiles are specified, then the content must conform to at least one of them. The URL can be a local reference - to a contained StructureDefinition, or a reference to another StructureDefinition or Implementation Guide by a canonical URL. When an implementation guide is specified, the target resource SHALL conform to at least one profile defined in the implementation guide.
If type is Reference | canonical, allowed targets
A brief description of the document or knowledge resource being referenced, suitable for display to a consumer.
Brief description of the related artifact
A legal clause or condition contained within a contract that requires one or both parties to perform a particular requirement by some specified time or prevents one or both parties from performing a particular requirement by some specified time.
A reference to the message definition that must be adhered to by this supported response.
Reference to allowed message definition response
Indicates who or what performed or participated in the charged service.
Number of SOP Instances in the Study. The value given may be larger than the number of instance elements this resource contains due to resource availability, security, or other factors. This element should be present if any instance elements are present.
Action would contain either an operation or an assertion.
A test operation or assert that was performed
The disease, symptom or procedure that is the indication for treatment.
A legal or geographic region in which the structure map is intended to be used.
Intended jurisdiction for structure map (if applicable)
Represents a request for a patient to employ a medical device. The device may be an implantable device, or an external assistive device, such as a walker.
Additional headers / information to send as part of the notification.
A copyright statement relating to the measure and/or its contents. Copyright statements are generally legal restrictions on the use and publishing of the measure.
An expression that returns true or false, indicating whether the condition is satisfied.
The marketing status describes the date when a medicinal product is actually put on the market or the date as of which it is no longer available.
Identifies traits whose presence r absence is shared by members of the group.
Include / Exclude group members by Trait
A classification of the type of episode of care; e.g. specialist referral, disease management, type of funded care.
Type/class - e.g. specialist referral, disease management
The disease, symptom or procedure for the contraindication.
A Boolean value to indicate that this concept map is authored for testing purposes (or education/evaluation/marketing) and is not intended to be used for genuine usage.
A short, descriptive, user-friendly title for the structure definition.
Name for this structure definition (human friendly)
Indicates the resource representing the current activity or proposed activity that is potentially problematic.
Only perform the operation if the Etag value matches. For more information, see the API section ["Managing Resource Contention"](http.html#concurrency).
The item that is being delivered or has been supplied.
A comment to be inserted in the diagram.
Indicates how the medication is to be used by the patient.
The clinical particulars - indications, contraindications etc. of a medicinal product, including for regulatory purposes.
Payment details such as banking details, period of payment, deductables, methods of payment.
Indicates what should be done and within what timeframe.
Indicates the type of medication request (for example, where the medication is expected to be consumed or administered (i.e. inpatient or outpatient)).
A flag to indicate that the member is no longer in the group, but previously may have been a member.
Link to a resource that concerns the same actual person.
Strength expressed in terms of a reference substance.
Risk of harmful or undesirable, physiological response which is unique to an individual and associated with exposure to a substance.
Displayable text string with hint help information to the user when entering a default value.
Hint help text for default value to enter
Indicates another resource, such as the health condition(s), whose existence justifies this request and drove the inclusion of this particular activity as part of the plan.
This may be either the same as the appointment request to confirm the details of the appointment, or alternately a new time to request a re-negotiation of the end time.
Time from appointment, or requested new end time
An ingredient of a manufactured item or pharmaceutical product.
Information about the specific installation that this capability statement relates to.
The instance number of the Coverage which is the focus for adjudication. The Coverage against which the claim was adjudicated.
The portion of the identifier typically relevant to the user and which is unique within the context of the system.
Contact details to assist a user in finding and communicating with the contributor.
Details about the admission to a healthcare service.
Contains one or more rules. Offers a way to group rules so assertions could reference the group of rules and have them all applied.
Assert ruleset used within the test script
Statement of a provision in a policy or a contract.
The specific medication, food or laboratory test that interacts.
A series of links that provide context to this bundle.
The start of the period. The boundary is inclusive.
A high-level category for the legal instrument, whether constructed as a Contract definition, derivative, or instance in any legal state. Provides additional information about its content within the context of the Contract's scope to distinguish the kinds of systems that would be interested in the contract.
Information about the entity attesting to information.
Information on the possible cause of the event.
Whether or not the test execution will validate the given capabilities of the server in order for this test script to execute.
A statement of relationships from one set of concepts to one or more other concepts - either concepts in code systems, or data element/data element concepts, or classes in class models.
The parameters to the module. This collection specifies both the input and output parameters. Input parameters are provided by the caller as part of the $evaluate operation. Output parameters are included in the GuidanceResponse.
Information about the primary source(s) involved in validation.
The ID of a fixture. Asserts that the response contains at a minimum the fixture specified by minimumId.
Indicates whether a resource instance represents a specific location or a class of locations.
Exceptions, special conditions and supporting information pplicable for this service or product line.
Applicable exception and supporting information
The subject for which the request group was created.
A concise description of what this element means (e.g. for use in autogenerated summaries).
Concise definition for space-constrained presentation
Comments made about the study by the performer, subject or other participants.
Limited to 'real' people rather than equipment.
The preference for this type of conditioned specimen.
This records identifiers associated with this appointment response concern that are defined by business processes and/ or used to refer to it when a direct URL reference to the resource itself is not appropriate.
A description of the status of the adjudication.
The maximum number of units of the medicaton that can be dispensed.
Related Resource to this DocumentManifest. For example, Order, ServiceRequest, Procedure, EligibilityRequest, etc.
Information about the use of the medicinal product in relation to other therapies described as part of the indication.
A code specifying the route or physiological path of administration of a therapeutic agent into or onto the patient. For example, topical, intravenous, etc.
Indicates how quickly the action should be addressed with respect to other actions.
The identifier that is used to identify this version of the plan definition when it is referenced in a specification, model, design or instance. This is an arbitrary value managed by the plan definition author and is not expected to be globally unique. For example, it might be a timestamp (e.g. yyyymmdd) if a managed version is not available. There is also no expectation that versions can be placed in a lexicographical sequence. To provide a version consistent with the Decision Support Service specification, use the format Major.Minor.Revision (e.g. 1.0.0). For more information on versioning knowledge assets, refer to the Decision Support Service specification. Note that a version is required for non-experimental active artifacts.
Indicates a purpose for which the contact can be reached.
Guidance on how to interpret the value by comparison to a normal or recommended range.
Provides guide for interpretation of component result
Quantity of which the charge item has been serviced.
The supplemental data criteria for the measure report, specified as either the name of a valid CQL expression within a referenced library, or a valid FHIR Resource Path.
What other data should be reported with the measure
A FHIR expression that identifies one of FHIR References to other resources.
Path in the resource that contains the link
The date and/or time that this set of answers were last changed.
The text to display to the user for this concept in the context of this valueset. If no display is provided, then applications using the value set use the display specified for the code by the system.
Text to display for this code for this value set in this valueset
Individual who recorded the record and takes responsibility for its content.
Indicates the quantity or duration for the first dispense of the medication.
Explanation of why this message definition is needed and why it has been designed as it has.
The instructions for preparing the medication.
The composition editing time, when the composition was last logically changed by the author.
Identifies coded items that were used as part of the procedure.
The identifier that is used to identify this version of the search parameter when it is referenced in a specification, model, design or instance. This is an arbitrary value managed by the search parameter author and is not expected to be globally unique. For example, it might be a timestamp (e.g. yyyymmdd) if a managed version is not available. There is also no expectation that versions can be placed in a lexicographical sequence.
Business version of the search parameter
An explanatory message associated with the result.
The serial number assigned by the organization when the device was manufactured.
Serial number assigned by the manufacturer
Defines the observations that are expected to be produced by the action.
What observations must be produced by this action
The time at which the statement was made/recorded.
Indicates when the guidance response was processed.
When the guidance response was processed
A description of the reason that a resource has been included in the implementation guide.
The type of category for the medication (for example, therapeutic classification, therapeutic sub-classification).
Sequence that was observed. It is the result marked by referenceSeq along with variant records on referenceSeq. This shall starts from referenceSeq.windowStart and end by referenceSeq.windowEnd.
The identifier that is used to identify this version of the structure definition when it is referenced in a specification, model, design or instance. This is an arbitrary value managed by the structure definition author and is not expected to be globally unique. For example, it might be a timestamp (e.g. yyyymmdd) if a managed version is not available. There is also no expectation that versions can be placed in a lexicographical sequence.
Business version of the structure definition
Formula administration instructions as structured data. This repeating structure allows for changing the administration rate or volume over time for both bolus and continuous feeding. An example of this would be an instruction to increase the rate of continuous feeding every 2 hours.
Used for example, to point to a substance, or to a device used to administer a medication.
When the activity definition was last reviewed
Indicates which type of context is being provided.
Specific amount of the drug in the packaged product. For example, when specifying a product that has the same strength (For example, Insulin glargine 100 unit per mL solution for injection), this attribute provides additional clarification of the package amount (For example, 3 mL, 10mL, etc.).
The number of true positives if the GQ score threshold was set to "score" field value.
A definition of the restful capabilities of the solution, if any.
The brief description of the appointment as would be shown on a subject line in a meeting request, or appointment list. Detailed or expanded information should be put in the comment field.
Shown on a subject line in a meeting request, or appointment list
A copyright statement relating to the concept map and/or its contents. Copyright statements are generally legal restrictions on the use and publishing of the concept map.
An absolute URI that is used to identify this library when it is referenced in a specification, model, design or an instance; also called its canonical identifier. This SHOULD be globally unique and SHOULD be a literal address at which at which an authoritative instance of this library is (or will be) published. This URL can be the target of a canonical reference. It SHALL remain the same when the library is stored on different servers.
Canonical identifier for this library, represented as a URI (globally unique)
The type of the property value. Properties of type "code" contain a code defined by the code system (e.g. a reference to another defined concept).
code | Coding | string | integer | boolean | dateTime | decimal
Contains the description about the protocol under which the vaccine was administered.
A request to supply a diet, formula feeding (enteral) or oral nutritional supplement to a patient/resident.
Minimum capabilities required of server for test script to execute successfully. If server does not meet at a minimum the referenced capability statement, then all tests in this script are skipped.
The person or organization that has primary responsibility for the substitution.
Does this service have specific eligibility requirements that need to be met in order to use the service?
Specific eligibility requirements required to use the service
Comments made about the event by the performer, subject or other participants.
Party to be reimbursed: Subscriber, provider, other.
A group of population criteria for the measure.
A natural language name identifying the compartment definition. This name should be usable as an identifier for the module by machine processing applications such as code generation.
Name for this compartment definition (computer friendly)
A detailed description of how the event definition is used from a clinical perspective.
Describes the clinical usage of the event definition
Raw data describing a biological sequence.
Processing outcome errror, partial or complete processing.
Indicates the period of time when this name was valid for the named person.
Captures constraints on each element within the resource, profile, or extension.
Definition of an element in a resource or extension
A Boolean value to indicate that this plan definition is authored for testing purposes (or education/evaluation/marketing) and is not intended to be used for genuine usage.
Chemicals may be stoichiometric or non-stoichiometric.
The content was developed with a focus and intent of supporting the contexts that are listed. These terms may be used to assist with indexing and searching for appropriate test script instances.
A reference to the original source of the constraint, for traceability purposes.
Reference to original source of constraint
Indicates an alternative material of the device.
Related resources such as additional documentation, justification, or bibliographic references.
Additional documentation, citations, etc.
Patient information, If the device is affixed to a person.
True if subsumption is supported for this version of the code system.
The human readable description of this population group.
For programs which require reason codes for the inclusion or covering of this billed item under the program or sub-program.
The mime type to send the payload in - either application/fhir+xml, or application/fhir+json. If the payload is not present, then there is no payload in the notification, just a notification.
MIME type to send, or omit for no payload
The type of relationship that this document has with anther document.
A coded value specifying the technique that is used to perform the procedure.
Identifies a particular constituent of interest in the product.
Precusory content developed with a focus and intent of supporting the formation a Contract instance, which may be associated with and transformable into a Contract.
A constraint indicating that this item should only be enabled (displayed/allow answers to be captured) when the specified condition is true.
Dosage for the medication for the specific guidelines.
Notes about the adherence/status/progress of the activity.
Comments about the activity status/progress
Pointer to next atomic sequence which at most contains one variant.
Width of the image in pixels (photo/video).
Immediate (STAT), best effort (NORMAL), deferred (DEFER).
Additional clinical information about the patient that may influence the request fulfilment. For example, this may include where on the subject's body the device will be used (i.e. the target site).
An integer associated with each note which may be referred to from each service line item.
Indicates that this coding was chosen by a user directly - e.g. off a pick list of available items (codes or displays).
If this coding was chosen directly by the user
Definition of an operation or a named query together with its parameters and their meaning and type. Consult the definition of the operation for details about how to invoke the operation, and the parameters.
Indicates how likely the outcome is (in the specified timeframe), expressed as a qualitative value (e.g. low, medium, or high).
Likelihood of specified outcome as a qualitative value
The actual narrative content, a stripped down version of XHTML.
The FHIRPath expression to be evaluated against the request or response message contents - HTTP headers and payload.
The device, practitioner, etc. who performed the action. It should be assumed that the actor is the dispenser of the medication.
Identifies other resource parameters within the operation invocation that are expected to resolve to this resource.
The category of the associated medication knowledge reference.
Which investigations support finding or diagnosis.
The interval during which the endpoint is expected to be operational.
Interval the endpoint is expected to be operational
Security label privacy tag that species the manner in which term and/or term elements are to be protected.
The principal physical location where the ImagingStudy was performed.
An expression that defines where an extension can be used in resources.
Where the extension can be used in instances
The kind of nutritional supplement product required such as a high protein or pediatric clear liquid supplement.
An activity is something that occurs over a period of time and acts upon or with entities; it may include consuming, processing, transforming, modifying, relocating, using, or generating entities.
draft | issued | balanced | cancelled | entered-in-error
The intended use of the product, e.g. prevention, treatment.
The status of this library. Enables tracking the life-cycle of the content.
Security labels that protects the asset.
Allows a flag to be divided into different categories like clinical, administrative etc. Intended to be used as a means of filtering which flags are displayed to particular user or in a given context.
Business identifiers assigned to this condition by the performer or other systems which remain constant as the resource is updated and propagates from server to server.
The name of the organization or individual that published the structure map.
An identifier that uniquely identifies this expansion of the valueset, based on a unique combination of the provided parameters, the system default parameters, and the underlying system code system versions etc. Systems may re-use the same identifier as long as those factors remain the same, and the expansion is the same, but are not required to do so. This is a business identifier.
Identifies the value set expansion (business identifier)
A parameter that controlled the expansion process. These parameters may be used by users of expanded value sets to check whether the expansion is suitable for a particular purpose, or to pick the correct expansion.
Each line item represents one charge for goods ond services rendered. Details such as date, code and amount are found in the referenced ChargeItem resource.
The type of channel to send notifications on.
rest-hook | websocket | email | sms | message
The name of the parameter (reference to the operation definition).
The location(s) that this service is available to (not where the service is provided).
Location(s) service is intended for/available to
A business identifier associated with the kind of specimen.
Business identifier of a kind of specimen
The type of questionnaire item this is - whether text for display, a grouping of other items or a particular type of data to be captured (string, integer, coded choice, etc.).
group | display | boolean | decimal | integer | date | dateTime +
The recommended display for this item in the expansion.
A free text natural language description of the plan definition from a consumer's perspective.
Natural language description of the plan definition
The set of valid coded results for the observation.
Value set of valid coded values for the observation
Time period during which the patient was present at the location.
The period of time covered by the documentation. There is no assertion that the documentation is a complete representation for this period, only that it documents events during this time.
The header for a message exchange that is either requesting or responding to an action. The reference(s) that are the subject of the action as well as other information related to the action are typically transmitted in a bundle in which the MessageHeader resource instance is the first resource in the bundle.
A shared identifier common to all service requests that were authorized more or less simultaneously by a single author, representing the composite or group identifier.
Defines the requiredness behavior for the action.
The name of the organization or individual that published the plan definition.
A description of status/issues in mapping that conveys additional information not represented in the structured data.
Name used for the account when displaying it to humans in reports, etc.
Condition(s) that this care team addresses.
The business identifier for the instance: claim number, pre-determination or pre-authorization number.
Party which is a signator to this Contract.
Describes the reason for the request group in coded or textual form.
Descriptive topics related to the content of the plan definition. Topics provide a high-level categorization of the definition that can be useful for filtering and searching.
The URL pointing to an externally maintained protocol, guideline, questionnaire or other definition that is adhered to in whole or in part by this CarePlan activity.
List of individual settlement amounts and the corresponding transaction.
If true, indicates that the resource refers to a specific group of real individuals. If false, the group defines a set of intended individuals.
Upper limit on medication per unit of time.
The category of the cost information. For example, manufacturers' cost, patient cost, claim reimbursement cost, actual acquisition cost.
Identifies a Contract Valued Item instance.
A unique name for the group for the convenience of human readers.
A single preferred label which is the text to display beside the element indicating its meaning or to use to prompt for the element in a user display or form.
Name for element to display with or prompt for element
Clinical contraindications, reasons for not giving this.
This resource provides processing status, errors and notes from the processing of a resource.
A device accompanying a medicinal product.
A list of alternate names that the location is known as or was known as in the past.
Indicates the patient or group who the condition record is associated with.
Indicates that the element is sliced into a set of alternative definitions (i.e. in a structure definition, there are multiple different constraints on a single element in the base resource). Slicing can be used in any resource that has cardinality ..* on the base resource, or any resource with a choice of types. The set of slices is any elements that come after this in the element sequence that have the same path, until a shorter path occurs (the shorter path terminates the set).
Describes the link to the Device that this DeviceMetric belongs to and that contains administrative device information such as manufacturer, serial number, etc.
A default, hard-coded, or user-defined value for this variable.
Default, hard-coded, or user-defined value for this variable
The contract number of a business agreement which describes the terms and conditions.
If true, indicates the characteristic is one that is NOT held by members of the group.
References the code system that this code system supplement is adding designations and properties to.
Code System this adds designations and properties to
The date (and perhaps time) when the prescription was initially written or authored on.
Specify whether requesting: prior authorization requirements for some service categories or billing codes; benefits for coverages specified or discovered; discovery and return of coverages for th patient; and/or validation that the specified coverage is in-force at the date/period specified or 'now' if not specified.
auth-requirements | benefits | discovery | validation
A manifestation or symptom that led to the recording of this condition.
The destination application which the message is intended for.
Extended CIGAR string for aligning the sequence with reference bases. See detailed documentation [here](http://support.illumina.com/help/SequencingAnalysisWorkflow/Content/Vault/Informatics/Sequencing_Analysis/CASAVA/swSEQ_mCA_ExtendedCIGARFormat.htm).
Extended CIGAR string for aligning the sequence with reference bases
Most elements that require a quantitative value will also have a field called amount type. Amount type should always be specified because the actual value of the amount is often dependent on it. EXAMPLE: In capturing the actual relative amounts of substances or molecular fragments it is essential to indicate whether the amount refers to a mole ratio or weight ratio. For any given element an effort should be made to use same the amount type for all related definitional elements.
An actor taking an active role in the document.
Information about the [ConceptMap/$translate](conceptmap-operation-translate.html) operation.
This records identifiers associated with this appointment concern that are defined by business processes and/or used to refer to it when a direct URL reference to the resource itself is not appropriate (e.g. in CDA documents, or in written / printed documentation).
Identifies who is responsible for adding the information to the document.
Indicates a patient's eligibility for a funding program.
Patient eligibility for a vaccination program
Identifier for the data life-cycle stage for the entity.
A central contact detail for the care team (that applies to all members).
A contact detail for the care team (that applies to all members)
How to handle the list mode for this element.
first | not_first | last | not_last | only_one
The specific person or organization who is participating/expected to participate in the care team.
Represents the date and/or time of the last known occurrence of a reaction event.
Date(/time) of last known occurrence of a reaction
A set of Security-Tag codes specifying the level of privacy/security of the Document. Note that DocumentReference.meta.security contains the security labels of the "reference" to the document, while DocumentReference.securityLabel contains a snapshot of the security labels on the document the reference refers to.
Configurations of the external repository. The repository shall store target's observedSeq or records related with target's observedSeq.
External repository which contains detailed report related with observedSeq in this resource
Additional information to support the appointment provided when making the appointment.
Additional information to support the appointment
Comments made about the {{title}} by the requester, performer, subject or other participants.
Total price of the charge overriding the list price associated with the code.
Identifier for a family of the event. For example, a menu item, program, rule, policy, function code, application name or URL. It identifies the performed function.
Additional validation information for the in parameters - a single profile that covers all the parameters. The profile is a constraint on the parameters resource as a whole.
Validation information for in parameters
Other claims which are related to this claim such as prior claim versions or for related services.
A free text natural language description of the graph definition from a consumer's perspective.
Natural language description of the graph definition
A set of rules of how FHIR is used to solve a particular problem. This resource is used to gather all the parts of an implementation guide into a logical whole and to publish a computable definition of all the parts.
The full UDI carrier of the Automatic Identification and Data Capture (AIDC) technology representation of the barcode string as printed on the packaging of the device - e.g., a barcode or RFID. Because of limitations on character sets in XML and the need to round-trip JSON data through XML, AIDC Formats *SHALL* be base64 encoded.
A security label, comprised of 0..* security label fields (Privacy tags), which define which resources are controlled by this exception.
Security Labels that define affected resources
Additional information that may be needed in the execution of the task.
The date when the first authorization was granted by a Medicines Regulatory Agency.
A relationship of two Quantity values - expressed as a numerator and a denominator.
A ratio of two Quantity values - a numerator and a denominator
Category of supply, e.g. central, non-stock, etc. This is used to support work flows associated with the supply process.
The kind of supply (central, non-stock, etc.)
If present, indicates that the frequency is a range - so to repeat between [frequency] and [frequencyMax] times within the period or period range.
Event occurs up to frequencyMax times per period
The individual, device or organization that participated in the event.
The stratifier criteria for the measure report, specified as either the name of a valid CQL expression defined within a referenced library or a valid FHIR Resource Path.
A claim, a list of completed goods and services; a preauthorization, a list or proposed goods and services; or a predetermination, a set of goods and services being considered, for which insurer adjudication is sought.
claim | preauthorization | predetermination
Comments that provide information about the mapping or its use.
The patient for which the request was processed.
Specific instances of data or objects that have been accessed.
Who reported the device was being used by the patient.
Indicates the results of processing the corresponding 'request' entry in the batch or transaction being responded to or what the results of an operation where when returning history.
A date parameter that refers to a search parameter defined on the specified type of the DataRequirement, and which searches on elements of type date, dateTime, Period, Schedule, or Timing.
Organizes the mapping into manageable chunks for human review/ease of maintenance.
A short, descriptive, user-friendly title for the implementation guide.
Name for this implementation guide (human friendly)
A compartment definition that defines how resources are accessed on a server.
Evaluates the results of previous operations to determine if the server under test behaves appropriately.
Additional representations for this concept when used in this value set - other languages, aliases, specialized purposes, used for particular purposes, etc.
Additional representations for this concept
An indication, if true, that the item may occur multiple times in the response, collecting multiple answers for questions or multiple sets of answers for groups.
The lead, assisting or supervising practitioner and their discipline if a multidisiplinary team.
The version of the FHIR specification on which this StructureDefinition is based - this is the formal version of the specification, without the revision number, e.g. [publication].[major].[minor], which is 3.5a.0. for this version.
FHIR Version this StructureDefinition targets
Data type allowed for the result of the observation.
Permitted data type for observation value
Estimate of the potential clinical harm, or seriousness, of the reaction to the identified substance.
The clinical service, such as a colonoscopy or an appendectomy, being documented.
A flag to indicate that this Coverage is the focus for adjudication. The Coverage against which the claim is to be adjudicated.
Used when the type is "Reference" or "canonical", and identifies a profile structure or implementation Guide that applies to the target of the reference this element refers to. If any profiles are specified, then the content must conform to at least one of them. The URL can be a local reference - to a contained StructureDefinition, or a reference to another StructureDefinition or Implementation Guide by a canonical URL. When an implementation guide is specified, the target resource SHALL conform to at least one profile defined in the implementation guide.
Profile (StructureDefinition or IG) on the Reference/canonical target - one must apply
A description of why this subscription is defined.
Description of why this subscription was created
A link to a resource representing the person or the group to whom the medication will be given.
What the example scenario resource is created for. This should not be used to show the business purpose of the scenario itself, but the purpose of documenting a scenario.
The purpose of the example, e.g. to illustrate a scenario
Indicates when the mitigating action was documented.
A formal computable definition of an operation (on the RESTful interface) or a named query (using the search interaction).
The method or technique used to perform the observation.
The status property covers the general availability of the resource, not the current value which may be covered by the operationStatus, or by a schedule/slots if they are configured for the location.
Comments about the test result value may include statements about significant, unexpected or unreliable results values, or information about the its source when this is relevant to its interpretation.
BasedOn refers to a higher-level authorization that triggered the creation of the task. It references a "request" resource such as a ServiceRequest, MedicationRequest, ServiceRequest, CarePlan, etc. which is distinct from the "request" resource the task is seeking to fulfill. This latter resource is referenced by FocusOn. For example, based on a ServiceRequest (= BasedOn), a task is created to fulfill a procedureRequest ( = FocusOn ) to collect a specimen from a patient.
Descriptive topics related to the content of the library. Topics provide a high-level categorization of the library that can be useful for filtering and searching.
Describes the color representation for the metric. This is often used to aid clinicians to track and identify parameter types by color. In practice, consider a Patient Monitor that has ECG/HR and Pleth for example; the parameters are displayed in different characteristic colors, such as HR-blue, BP-green, and PR and SpO2- magenta.
black | red | green | yellow | blue | magenta | cyan | white
A legal or geographic region in which the activity definition is intended to be used.
Intended jurisdiction for activity definition (if applicable)
A flag for whether the server is able to return past versions as part of the vRead operation.
System and code pertaining to the specific information regarding special conditions relating to the setting, treatment or patient for which care is sought which may influence the adjudication.
A unique identifier assigned to this observation.
The business identifier that is used to reference the MessageDefinition and *is* expected to be consistent from server to server.
Business Identifier for a given MessageDefinition
A short, descriptive, user-friendly title for the questionnaire.
Name for this questionnaire (human friendly)
The insurer may provide both the details for the requested coverage as well as details for additional coverages known to the insurer.
Identifies the general type of issue identified.
Issue Category, e.g. drug-drug, duplicate therapy, etc.
Formal constraints such as co-occurrence and other constraints that can be computationally evaluated within the context of the instance.
The name of the organization or individual that published the questionnaire.
Identifies role of subject in context of a given document
Original prescription which has been superceded by this prescription to support the dispensing of pharmacy services, medications or products. For example, a physician may prescribe a medication which the pharmacy determines is contraindicated, or for which the patient has an intolerance, and therefor issues a new precription for an alternate medication which has the same theraputic intent. The prescription from the pharmacy becomes the 'prescription' and that from the physician becomes the 'original prescription'.
Original prescription if superceded by fulfiller
The method by which the molecular weight was determined.
Characteristics e.g. a products onset of action.
Persons involved in the encounter other than the patient.
A lower limit for the strength per unitary volume (or mass), for when there is a range. The concentration attribute then becomes the upper limit.
The date of the invoice or financial resource.
A sequence that is used as a reference to describe variants that are present in a sequence analyzed.
A natural language name identifying this Contract definition, derivative, or instance in any legal state. Provides additional information about its content. This name should be usable as an identifier for the module by machine processing applications such as code generation.
Indicates where the message should be routed to.
Additional information (for example, patient height and weight) that supports the administration of the medication.
Additional information to support administration
A name given to the device to identify it.
A code that provides meaning for the action or action group. For example, a section may have a LOINC code for the section of a documentation template.
Categorization of the medication within a formulary or classification system.
An address expressed using postal conventions (as opposed to GPS or other location definition formats). This data type may be used to convey addresses for use in delivering mail as well as for visiting locations which might not be valid for mail delivery. There are a variety of postal address formats defined around the world.
An address expressed using postal conventions (as opposed to GPS or other location definition formats)
Anatomical location from which the specimen was collected (if subject is a patient). This is the target site. This element is not used for environmental specimens.
A summary of information based on the results of executing a TestScript.
The entity the action is performed or not performed on or for.
Identifies a restful operation supported by the solution.
One or more links to full details of any imaging performed during the diagnostic investigation. Typically, this is imaging performed by DICOM enabled modalities, but this is not required. A fully enabled PACS viewer can use this information to provide views of the source images.
Reference to full details of imaging associated with the diagnostic report
The lead, assisting or supervising practitioner and their discipline if a multidisciplinary team.
This resource allows for the definition of some activity to be performed, independent of a particular patient, practitioner, or other performance context.
An individual or organization responsible for officially endorsing the content for use in some setting.
An Internal id that is used to identify this mapping set when specific mappings are made.
A coded specification of the anatomic site where the medication first entered the body. For example, "left arm".
How the search parameter relates to the set of elements returned by evaluating the xpath query.
normal | phonetic | nearby | distance | other
The resource that is the target of the action (e.g. CommunicationRequest).
The HTTP header field name e.g. 'Location'.
Date/Time that the appointment is to take place.
A copyright statement relating to the code system and/or its contents. Copyright statements are generally legal restrictions on the use and publishing of the code system.
Specification of the participation type the agent played.
A code for the timing schedule (or just text in code.text). Some codes such as BID are ubiquitous, but many institutions define their own additional codes. If a code is provided, the code is understood to be a complete statement of whatever is specified in the structured timing data, and either the code or the data may be used to interpret the Timing, with the exception that .repeat.bounds still applies over the code (and is not contained in the code).
BID | TID | QID | AM | PM | QD | QOD | +
Relationships that this document has with other document references that already exist.
Documentation about text searching works.
Insurance policies which the patient has advised may be applicable for paying for health services.
Indicates the timeframe after the start of the goal in which the goal should be met.
Reference to who this agent is that was involved in the event.
Identifies the patient or group whose intended care is described by the plan.
An instant in time - known at least to the second
An absolute URI that is used to identify this graph definition when it is referenced in a specification, model, design or an instance; also called its canonical identifier. This SHOULD be globally unique and SHOULD be a literal address at which at which an authoritative instance of this graph definition is (or will be) published. This URL can be the target of a canonical reference. It SHALL remain the same when the graph definition is stored on different servers.
Canonical identifier for this graph definition, represented as a URI (globally unique)
Selects the concepts found in this value set (based on its value set definition). This is an absolute URI that is a reference to ValueSet.url. If multiple value sets are specified this includes the union of the contents of all of the referenced value sets.
Select the contents included in this value set
A network address on which the device may be contacted directly.
Describes the time last calibration has been performed.
Organization that is charged with issuing UDIs for devices. For example, the US FDA issuers include : 1) GS1: http://hl7.org/fhir/NamingSystem/gs1-di, 2) HIBCC: http://hl7.org/fhir/NamingSystem/hibcc-dI, 3) ICCBBA for blood containers: http://hl7.org/fhir/NamingSystem/iccbba-blood-di, 4) ICCBA for other devices: http://hl7.org/fhir/NamingSystem/iccbba-other-di.
A code that has the same meaning as the element in a particular terminology.
List of top level items to be re-adjudicated, if none specified then the entire submission is re-adjudicated.
Describes why the request is being made in coded or textual form.
The status of this test script. Enables tracking the life-cycle of the content.
Concepts that are in the code system. The concept definitions are inherently hierarchical, but the definitions must be consulted to determine what the meaning of the hierarchical relationships are.
The measure score for this stratum, calculated as appropriate for the measure type and scoring method, and based on only the members of this stratum.
An XPath expression of constraint that can be executed to see if this constraint is met.
The name of the organization or individual that published the example scenario.
Who or what is controlled by this rule. Use group to identify a set of actors by some property they share (e.g. 'admitting officers').
Who|what controlled by this rule (or group, by role)
Binds to a value set if this parameter is coded (code, Coding, CodeableConcept).
Whether the device is supplied as sterile.
An occurrence of information being transmitted; e.g. an alert that was sent to a responsible provider, a public health agency was notified about a reportable condition.
Whether the entry represents an orderable item.
A MessageDefinition that is superseded by this definition.
A code that indicates how the server supports conditional read.
not-supported | modified-since | not-match | full-support
If this is set to 'true', then no new versions of the content logical definition can be created. Note: Other metadata might still change.
Indicates whether or not any change to the content logical definition may occur
The maximum number of characters that are permitted in the answer to be considered a "valid" QuestionnaireResponse.
A Boolean value to indicate that this questionnaire is authored for testing purposes (or education/evaluation/marketing) and is not intended to be used for genuine usage.
A natural language name identifying the terminology capabilities. This name should be usable as an identifier for the module by machine processing applications such as code generation.
Name for this terminology capabilities (computer friendly)
The Insurer who produced this adjudicated response.
This field is set to no-version to specify that the system does not support (server) or use (client) versioning for this resource type. If this has some other value, the server must at least correctly track and populate the versionId meta-property on resources. If the value is 'versioned-update', then the server supports all the versioning features, including using e-tags for version integrity in the API.
no-version | versioned | versioned-update
A copyright statement relating to the implementation guide and/or its contents. Copyright statements are generally legal restrictions on the use and publishing of the implementation guide.
A reference to the profile that all instances must conform to.
Profile that all resources must conform to
A larger definition of which this particular definition is a component or step.
Sequence of careteam which serves to order and provide a link.
Indication of whether the diagnosis was present on admission to a facility.
List of Computable Policy Rule Language Representations of this Contract.
Indicates whether or not substitution was made as part of the dispense. In some cases substitution will be expected but does not happen, in other cases substitution is not expected but does happen. This block explains what substitution did or did not happen and why. If nothing is specified, substitution was not done.
Describes the event of a patient being administered a vaccine or a record of an immunization as reported by a patient, a clinician or another party.
An absolute URI which is a reference to the definition of a compartment that the system supports. The reference is to a CompartmentDefinition resource by its canonical URL .
Indicates the patient whose record the detected issue is associated with.
The intended or approved route of administration.
The time when this communication arrived at the destination.
Indicates the current status of the immunization event.
Indicates the level of authority/intentionality associated with the activity and where the request should fit into the workflow chain.
The contact details of communication devices available at the location. This can include phone numbers, fax numbers, mobile numbers, email addresses and web sites.
Patient Information that supports the status and recommendation. This includes patient observations, adverse reactions and allergy/intolerance information.
Patient observations supporting recommendation
Fixture to evaluate the XPath/JSONPath expression or the headerField against.
Fixture Id of source expression or headerField
The Organization which submitted the claim or financial transaction.
A plan or request that is fulfilled in whole or in part by this medication request.
The date (and optionally time) when the contract was published. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the contract changes.
Explanation of why this operation definition is needed and why it has been designed as it has.
Why this operation definition is defined
The results of the assertion performed on the previous operations.
The amount of the ingredient in the substance - a concentration ratio.
Tracking/reporting assertion description
A free text natural language description of the message definition from a consumer's perspective.
Natural language description of the message definition
The device, individual, or organization who initiated the request and has responsibility for its activation.
A Terminology Capabilities documents a set of capabilities (behaviors) of a FHIR Server that may be used as a statement of actual server functionality or a statement of required or desired server implementation.
A code that is a reference to CodeSystem.property.code.
The list of practitioners that may be facilitating this episode of care for specific purposes.
Other practitioners facilitating this episode of care
An XPath expression that returns a set of elements for the search parameter.
A [FHIRPath](fhirpath.html) expression of constraint that can be executed to see if this constraint is met.
A version-independent identifier for the Composition. This identifier stays constant as the composition is changed over time.
Version-independent identifier for the Composition
Group of properties which are applicable under the same conditions. If no applicability rules are established for the group, then all properties always apply.
Group of properties which are applicable under the same conditions
An error, warning or information message that results from a system action.
A single issue associated with the action
The date (and optionally time) when the structure definition was published. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the structure definition changes.
The number of this instance in the series
The kind of resource that must be the focus for this message.
A set of rules that describe when the event is scheduled.
Code indicating: Co-Pay, deductible, eligible, benefit, tax, etc.
Provides a mechanism to communicate additional information about the response.
The date the information was attested to.
Role of this Contract signer, e.g. notary, grantee.
A reference to a Library resource containing any formal logic used by the plan definition.
For when strength is measured at a particular point or distance.
The Insurer who is target of the request.
The product or brand name of the type of modular component to be added to the formula.
Product or brand name of the modular additive
If this is an actual service or product line, i.e. not a Group, then use code to indicate the Professional Service or Product supplied (e.g. CTP, HCPCS,USCLS,ICD10, NCPDP,DIN,RxNorm,ACHI,CCI). If a grouping item then use a group code to indicate the type of thing being grouped e.g. 'glasses' or 'compound'.
The kind of specimen conditioned for testing expected by lab.
Human-readable and/or coded description of a specific desired objective of care, such as "control blood pressure" or "negotiate an obstacle course" or "dance with child at wedding".
The logical id of the resource, as used in the URL for the resource. Once assigned, this value never changes.
The data type or resource that the value of this element is permitted to be.
This code identifies the type of the component.
base | surcharge | deduction | discount | tax | informational
Reason why a dose is considered to be subpotent.
A particular question, question grouping or display text that is part of the questionnaire.
Questions and sections within the Questionnaire
The actions, if any, produced by the evaluation of the artifact.
The patient who has the allergy or intolerance.
Identity (code or path) or the element/item that the map refers to.
A larger research study of which this particular study is a component or step.
Defines how to interpret the expression that defines what the context of the extension is.
If the concept is inactive in the code system that defines it. Inactive codes are those that are no longer to be used, but are maintained by the code system for understanding legacy data. It might not be known or specified whether an concept is inactive (and it may depend on the context of use).
If concept is inactive in the code system
A list of the formats supported by this implementation using their content types.
formats supported (xml | json | ttl | mime type)
A slot of time on a schedule that may be available for booking appointments.
The organization where the Practitioner performs the roles associated.
Organization where the roles are available
A list of service types or billable services for which bebefit details and/or an authorization prior to service delivery may be required by the payor.
The fixture id (maybe new) to map to the response.
End position of the sequence.If the coordinate system is 0-based then end is is exclusive and does not include the last position. If the coordinate system is 1-base, then end is inclusive and includes the last position.
The status of characteristic e.g. assigned or pending.
Regulatory authorization reference number.
A short, descriptive, user-friendly title for the plan definition.
Name for this plan definition (human friendly)
A string that may contain Github Flavored Markdown syntax for optional processing by a mark down presentation engine
The URL pointing to a FHIR-defined protocol, guideline, questionnaire or other definition that is adhered to in whole or in part by this CarePlan activity.
Explanation of why this compartment definition is needed and why it has been designed as it has.
Why this compartment definition is defined
A set of date ranges (potentially including times) that the appointment is preferred to be scheduled within. When using these values, the duration (usually in minutes) should be provided to indicate the length of the appointment to fill and populate the start/end times for the actual allocated time.
Potential date/time interval(s) requested to allocate the appointment within
The request method or HTTP operation code to compare against that used by the client system under test.
delete | get | options | patch | post | put
The package billing code, for example DRG, based on the assigned grouping code system.
The identifier that is used to identify this version of the structure map when it is referenced in a specification, model, design or instance. This is an arbitrary value managed by the structure map author and is not expected to be globally unique. For example, it might be a timestamp (e.g. yyyymmdd) if a managed version is not available. There is also no expectation that versions can be placed in a lexicographical sequence.
The explicit or dynamic value for the parameter that will be passed on to the external rule template.
Parameter value defined either explicitly or dynamically
A formal identifier that is used to identify this structure map when it is represented in other formats, or referenced in a specification, model, design or an instance.
Additional identifier for the structure map
Indicates the purpose for the naming system - what kinds of things does it make unique?
A Boolean value to indicate that this search parameter is authored for testing purposes (or education/evaluation/marketing) and is not intended to be used for genuine usage.
The date or date-time when the detected issue was initially identified.
Role that this diagnosis has within the episode of care (e.g. admission, billing, discharge …).
This element is a URI that refers to an [ElementDefinition] that provides information about this item, including information that might otherwise be included in the instance of the Questionnaire resource. A detailed description of the construction of the URI is shown in Comments, below. If this element is present then the following element values MAY be derived from the Element Definition if the corresponding elements of this Questionnaire resource instance have no value: * code (ElementDefinition.code) * type (ElementDefinition.type) * required (ElementDefinition.min) * repeats (ElementDefinition.max) * maxLength (ElementDefinition.maxLength) * answerValueSet (ElementDefinition.binding) * options (ElementDefinition.binding).
Number used to link this term or term element to the applicable Security Label.
An actor taking a role in an activity for which it can be assigned some degree of responsibility for the activity taking place.
A code that identifies what the overall request group is.
The modality of the instances in the series
Provides detailed dosage instructions in the same way that they are described for MedicationRequest resources.
How the entry list was prepared - whether it is a working list that is suitable for being maintained on an ongoing basis, or if it represents a snapshot of a list of items from another source, or whether it is a prepared list where items may be marked as added, modified or deleted.
If this is a composite measure, the scoring method used to combine the component measures to determine the composite score.
opportunity | all-or-nothing | linear | weighted
A business identifier assigned to a particular completed (or partially completed) questionnaire.
not-calibrated | calibration-required | calibrated | unspecified
Related Claims which may be relevant to processing this claim
Identifies the period of time over which this identifier is considered appropriate to refer to the naming system. Outside of this window, the identifier might be non-deterministic.
This slot has already been overbooked, appointments are unlikely to be accepted for this time.
An absolute URI that is used to identify this charge item definition when it is referenced in a specification, model, design or an instance; also called its canonical identifier. This SHOULD be globally unique and SHOULD be a literal address at which at which an authoritative instance of this charge item definition is (or will be) published. This URL can be the target of a canonical reference. It SHALL remain the same when the charge item definition is stored on different servers.
Canonical identifier for this charge item definition, represented as a URI (globally unique)
The practitioner is not available or performing this role during this period of time due to the provided reason.
Not available during this time due to provided reason
The content was developed with a focus and intent of supporting the contexts that are listed. These terms may be used to assist with indexing and searching for appropriate terminology capabilities instances.
This will either be a name or a description; e.g. "Aunt Susan", "my cousin with the red hair".
The individual or Organization responsible for balancing of this invoice.
Indicates another resource whose existence justifies this DeviceUseStatement.
True if the prescriber allows a different drug to be dispensed from what was prescribed.
Reference to the organization validating information.
Indicates a meaning for the stratifier. This can be as simple as a unique identifier, or it can establish meaning in a broader context by drawing from a terminology, allowing stratifiers to be correlated across measures.
Explanation of why this measure is needed and why it has been designed as it has.
Potential clinical issue with or between medication(s) (for example, drug-drug interaction, drug-disease contraindication, drug-allergy interaction, etc).
Potential clinical issue with or between medication(s)
Timing or duration information as part of the indication.
A language which may be used to communicate with the patient about his or her health.
The mime type to send the payload in - e.g. application/fhir+xml, application/fhir+json. If the mime type is not specified, then the sender could send any content (including no content depending on the connectionType).
Mimetype to send. If not specified, the content could be anything (including no payload, if the connectionType defined this)
Reference to a canonical URL of another CapabilityStatement that this software adds to. The capability statement automatically includes everything in the other statement, and it is not duplicated, though the server may repeat the same resources, interactions and operations to add additional details to them.
Canonical URL of another capability statement this adds to
Used to support catalog exchange even for unsupported products, e.g. getting list of medications even if not prescribable.
Distinguishes which item is "source of truth" (if any) and which items are no longer considered to be current representations.
Technical endpoints providing access to services operated for the practitioner with this role.
The actual content of the media - inline or by direct reference to the media source file.
An absolute URI that is used to identify this questionnaire when it is referenced in a specification, model, design or an instance; also called its canonical identifier. This SHOULD be globally unique and SHOULD be a literal address at which at which an authoritative instance of this questionnaire is (or will be) published. This URL can be the target of a canonical reference. It SHALL remain the same when the questionnaire is stored on different servers.
Canonical identifier for this questionnaire, represented as a URI (globally unique)
The specimen that was used when this observation was made.
The Operational status covers operation values most relevant to beds (but can also apply to rooms/units/chair/etc. such as an isolation unit/dialysis chair). This typically covers concepts such as contamination, housekeeping and other activities like maintenance.
The Operational status of the location (typically only for a bed/room)
What kind of device or device system this is.
The purposeOfUse (reason) that was used during the event being recorded.
A FHIRPath expression, using [the simple subset of FHIRPath](fhirpath.html#simple), that is used to identify the element on which discrimination is based.
The ISO-639-1 alpha 2 code in lower case for the language, optionally followed by a hyphen and the ISO-3166-1 alpha 2 code for the region in upper case; e.g. "en" for English, or "en-US" for American English versus "en-EN" for England English.
The date (and optionally time) when the test script was published. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the test script changes.
Reason or purpose for the action stipulated by this Contract Provision.
Indicates another resource that provides a justification for why this service is being requested. May relate to the resources referred to in supportingInformation.
Explanation/Justification for service or service
A value set can also be "expanded", where the value set is turned into a simple collection of enumerated codes. This element holds the expansion, if it has been performed.
Any additional description of the service and/or any specific issues not covered by the other attributes, which can be displayed as further detail under the serviceName.
Additional description and/or any specific issues not covered elsewhere
An entry in a bundle resource - will either contain a resource or information about a resource (transactions and history only).
Entry in the bundle - will have a resource or information
Identifies the unique identifier scheme used for this particular identifier.
A procedure that is fulfilled in whole or in part by the creation of this media.
Procedure that caused this media to be created
A description of the messaging capabilities of the solution.
Indicates the reason for the substitution, or why substitution must or must not be performed.
A goal that the study is aiming to achieve in terms of a scientific question to be answered by the analysis of data collected during the study.
A unique identifier for this particular sequence instance. This is a FHIR-defined id.
Unique ID for this particular sequence. This is a FHIR-defined id
A mime type that indicates the technical format of the target resources signed by the signature.
The technical format of the signed resources
Indicates the timestamp when the user session will expire (i.e. no longer be valid).
Each major process - a group of operations.
Identifier by which this substance is known.
The identifier that is to be associated with every Device that references this DeviceDefintiion for the issuer and jurisdication porvided in the DeviceDefinition.udiDeviceIdentifier.
The references to the policies that are included in this consent scope. Policies may be organizational, but are often defined jurisdictionally, or in law.
When the charge item definition was last reviewed
The kind of diet or dietary restriction such as fiber restricted diet or diabetic diet.
Type of oral diet or diet restrictions that describe what can be consumed orally
Questions or sub-groups nested beneath a question or group.
The quantity of this package in the medicinal product, at the current level of packaging. The outermost is always 1.
The product's name, including full name and possibly coded parts.
Deals with details of the dispense part of the supply specification.
The type of attestation the authenticator offers.
personal | professional | legal | official
Identifies the mutually agreed level of importance associated with reaching/sustaining the goal.
high-priority | medium-priority | low-priority
This is the base resource type for everything.
The category of documentation about the medication. (e.g. professional monograph, patient educaton monograph).
The date that this appointment was initially created. This could be different to the meta.lastModified value on the initial entry, as this could have been before the resource was created on the FHIR server, and should remain unchanged over the lifespan of the appointment.
The date that this appointment was initially created
A code specifying the status of the record of the family history of a specific family member.
partial | completed | entered-in-error | health-unknown
One possible path to achieve presumed immunity against a disease - within the context of an authority.
Identifier by which this moiety substance is known.
A nested sub-section within this section.
The molecular weight or weight range (for proteins, polymers or nucleic acids).
A process where a researcher or organization plans and then executes a series of steps intended to increase the field of healthcare-related knowledge. This includes studies of safety, efficacy, comparative effectiveness and other information about medications, devices, therapies and other interventional and investigative techniques. A ResearchStudy involves the gathering of information about human or animal subjects.
Defines which action to take if there is no match for the source concept in the target system designated for the group. One of 3 actions are possible: use the unmapped code (this is useful when doing a mapping between versions, and only a few codes have changed), use a fixed code (a default code), or alternatively, a reference to a different concept map can be provided (by canonical URL).
The status of this graph definition. Enables tracking the life-cycle of the content.
The specified desired performer of the medication treatment (e.g. the performer of the medication administration).
Identifies goals that this action supports. The reference must be to a goal element defined within this plan definition.
A subjective assessment of the severity of the condition as evaluated by the clinician.
Set this to true if the definition is to indicate that a particular activity should NOT be performed. If true, this element should be interpreted to reinforce a negative coding. For example NPO as a code with a doNotPerform of true would still indicate to NOT perform the action.
True if the activity should not be performed
Sub-unit of a country with limited sovereignty in a federally organized country. A code may be used if codes are in common use (e.g. US 2 letter state codes).
Factor for converting value expressed with SI unit to value expressed with customary unit.
A succinct description of the path through the study that would be followed by a subject adhering to this arm.
Contact lens power measured in dioptres (0.25 units).
The relationship of beneficiary (patient) to the subscriber.
Beneficiary relationship to the Subscriber
The coded reason why the procedure was performed. This may be coded entity of some type, or may simply be present as text.
Information about the base definition of the element, provided to make it unnecessary for tools to trace the deviation of the element through the derived and related profiles. When the element definition is not the original definition of an element - i.g. either in a constraint on another type, or for elements from a super type in a snap shot - then the information in provided in the element definition may be different to the base definition. On the original definition of the element, it will be same.
The status code returned by processing this entry. The status SHALL start with a 3 digit HTTP code (e.g. 404) and may contain the standard HTTP description associated with the status code.
The respondent's answer(s) to the question.
Reasons why the vaccine was administered.
Indicates the level of authority/intentionality associated with the NutrionOrder and where the request fits into the workflow chain.
The code for the performed procedure type.
Identifies the workflow status of the assessment.
The status of this implementation guide. Enables tracking the life-cycle of the content.
An expression that describes applicability criteria, or start/stop conditions for the action.
The maximum amount of a service item a plan will pay for a covered benefit. For examples. wellness visits, or eyeglasses.
A patient, practitioner, or organization for which this set of documents is intended.
Intended to get notified about this set of documents
Activity or service obligation to be done or not done, performed or not performed, effectuated or not by this Contract term.
Internal reference that identifies the goals that this activity is intended to contribute towards meeting.
Sequence of procedures which serves to order and provide a link.
Code that identifies the type of response to the message - whether it was successful or not, and whether it should be resent or not.
Indicates an actual or potential clinical issue with or between one or more active or proposed clinical actions for a patient; e.g. drug-drug interaction, duplicate therapy, dosage alert etc.
Parties with legal standing in the Contract, including the principal parties, the grantor(s) and grantee(s), which are any person or organization bound by the contract, and any ancillary parties, which facilitate the execution of the contract such as a notary or witness.
Transaction: error, complete, partial processing.
Type of alerts/updates the primary source can send (specific requested changes; any changes; as defined by source).
Details of the outcome or action resulting from the activity. The reference to an "event" resource, such as Procedure or Encounter or Observation, is the result/outcome of the activity itself. The activity can be conveyed using CarePlan.activity.detail OR using the CarePlan.activity.reference (a reference to a “request” resource).
An identifier for the pharmaceutical medicinal product.
Specifies the particular kind of document referenced (e.g. History and Physical, Discharge Summary, Progress Note). This usually equates to the purpose of making the document referenced.
The URL for this entry, relative to the root (the address to which the request is posted).
Contact details at the participatingOrganization relevant to this Affiliation.
Identifiers assigned to this order by the orderer or by the receiver.
The opening time of day. Note: If the AllDay flag is set, then this time is ignored.
Opening time of day (ignored if allDay = true)
Structural Variant Inner Start.If the coordinate system is either 0-based or 1-based, then start position is inclusive.
A facility in which study activities are conducted.
Facility where study activities are conducted
Identifies specific times when the event occurs.
A reference to a specific resource that defines which resources are covered by this consent.
Prescription to support the dispensing of Pharmacy or Vision products.
Prescription authorizing services or products
Details about the coverage offered by the insurance product.
The period during which the person is authorized to act as a practitioner in these role(s) for the organization.
The period during which the practitioner is authorized to perform in these role(s)
This represents the manufacturer's name of the device as provided by the device, from a UDI label, or by a person describing the Device. This typically would be used when a person provides the name(s) or when the device represents one of the names available from DeviceDefinition.
The name of the device as given by the manufacturer
The results of the series of required setup operations before the tests were executed.
Initial value(s) when item is first rendered
Method for communicating with the primary source (manual; API; Push).
The process(es) by which the target is validated
Indicates how the medication is/was taken or should be taken by the patient.
How the medication is/was taken or should be taken
A code that classifies the service for searching, sorting and display purposes (e.g. "Surgical Procedure").
Lens power measured in dioptres (0.25 units).
The code for this item in the expansion hierarchy. If this code is missing the entry in the hierarchy is a place holder (abstract) and does not represent a valid code in the value set.
Code - if blank, this is not a selectable code
List of locations where the patient has been during this encounter.
A code specifying the state of the dispense event.
in-progress | completed | abandoned | entered-in-error
The type of destination profile the test system supports.
FHIR-Server | FHIR-SDC-FormManager | FHIR-SDC-FormReceiver | FHIR-SDC-FormProcessor
Administrative Gender - the gender that the patient is considered to have for administration and record keeping purposes.
The status of the marketing authorization.
A free text natural language description of the implementation guide from a consumer's perspective.
Natural language description of the implementation guide
Comorbidity (concurrent condition) or co-infection as part of the indication.
An abstract server used in operations within this test script in the destination element.
Click and see / RESTful API / Need login to see / RESTful API with authentication / Other ways to see resource.
directlink | openapi | login | oauth | other
Identifies the minimum number of resources of this type that must be pointed to by a message in order for it to be valid against this MessageDefinition.
The identifier of a specific version of a resource.
The subject of the Products and Services
A short, descriptive, user-friendly title for the terminology capabilities.
Name for this terminology capabilities (human friendly)
The vaccine preventable disease the dose is being evaluated against.
Appointment that this response is replying to.
The encounter within which the communication was sent.
A legal or geographic region in which the message definition is intended to be used.
Intended jurisdiction for message definition (if applicable)
The class history permits the tracking of the encounters transitions without needing to go through the resource history. This would be used for a case where an admission starts of as an emergency encounter, then transisions into an inpatient scenario. Doing this and not restarting a new encounter ensures that any lab/diagnostic results can more easily follow the patient and not require re-processing and not get lost or cancelled during a kindof discharge from emergency to inpatient.
Describes the clinical encounter or type of care that the document content is associated with.
Demographics and administrative information about a person independent of a specific health-related context.
A name which details the functional use for this link - see [http://www.iana.org/assignments/link-relations/link-relations.xhtml#link-relations-1](http://www.iana.org/assignments/link-relations/link-relations.xhtml#link-relations-1).
See http://www.iana.org/assignments/link-relations/link-relations.xhtml#link-relations-1
The standard that is used to operate and communicate.
The time that the episode was in the specified class.
Category or kind of location after discharge.
A natural language name identifying the code system. This name should be usable as an identifier for the module by machine processing applications such as code generation.
Name for this code system (computer friendly)
Optional Extension Element - found in all resources.
The content was developed with a focus and intent of supporting the contexts that are listed. These terms may be used to assist with indexing and searching for appropriate event definition instances.
A group of mappings that all have the same source and target system.
The types of subjects that can be the subject of responses created for the questionnaire.
Resource that can be subject of QuestionnaireResponse
The document being referenced, represented as an attachment. This is exclusive with the resource element.
Procedures applicable for this service or product line.
Detailed definition of a medicinal product, typically for uses other than direct patient care (e.g. regulatory use).
Id of fixture used for extracting the [id], [type], and [vid] for GET requests.
List of the specific benefits under this category of benefit.
A reference to a location at which the other resource is found. The reference may be a relative reference, in which case it is relative to the service base URL, or an absolute URL that resolves to the location where the resource is found. The reference may be version specific or not. If the reference is not to a FHIR RESTful server, then it should be assumed to be version specific. Internal fragment references (start with '#') refer to contained resources.
Literal reference, Relative, internal or absolute URL
Provides additional safety characteristics about a medical device. For example devices containing latex.
A collection of documents compiled for a purpose together with metadata that applies to the collection.
Additional clinical information about the patient or specimen that may influence the services or their interpretations. This information includes diagnosis, clinical findings and other observations. In laboratory ordering these are typically referred to as "ask at order entry questions (AOEs)". This includes observations explicitly requested by the producer (filler) to provide context or supporting information needed to complete the order. For example, reporting the amount of inspired oxygen for blood gas measurements.
Provides additional information associated with the context.
Additional information about the session
The service delivery location where the vaccine administration occurred.
A real number that represents a multiplier used in determining the overall value of the Contract Valued Item delivered. The concept of a Factor allows for a discount or surcharge multiplier to be applied to a monetary amount.
Contract Valued Item Price Scaling Factor
The healthcare event (e.g. a patient and healthcare provider interaction) during which this observation is made.
Healthcare event during which this observation is made
Contact lens diameter measured in millimetres.
When the resource last changed - e.g. when the version changed.
Date classification of recommendation. For example, earliest date to give, latest date to give, etc.
The metadata about a resource. This is content in the resource that is maintained by the infrastructure. Changes to the content might not always be associated with version changes to the resource.
The version specific identifier, as it appears in the version portion of the URL. This value changes when the resource is created, updated, or deleted.
The units of time for the period in UCUM units.
s | min | h | d | wk | mo | a - unit of time (UCUM)
The findings and interpretation of diagnostic tests performed on patients, groups of patients, devices, and locations, and/or specimens derived from these. The report includes clinical context such as requesting and provider information, and some mix of atomic results, images, textual and coded interpretations, and formatted representation of diagnostic reports.
A reason for why the medication is being/was taken.
Reason for why the medication is being/was taken
Identifier of the source where the event was detected.
The identity of source detecting the event
Information on who recorded the adverse event. May be the patient or a practitioner.
The string that should be sent over the wire to identify the code system or identifier system.
The date (and optionally time) when the plan definition was published. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the plan definition changes.
A classification of the type of consents found in the statement. This element supports indexing and retrieval of consent statements.
Classification of the consent statement - for indexing/retrieval
Unique identifier for the packaged Medicinal Product.
A correction factor that is applied to the sampled data points before they are added to the origin.
Multiply data by this before adding to origin
Sites in which the contract is complied with, exercised, or in force.
Describes why the family member history occurred in coded or textual form.
Why was family member history performed?
Type of specific benefit (preventative; primary care office visit; speciality office visit; hospitalization; emergency room; urgent care).
The Path that identifies the base element - this matches the ElementDefinition.path for that element. Across FHIR, there is only one base definition of any element - that is, an element definition on a [StructureDefinition] without a StructureDefinition.base.
The type of relationship this person has to the patient (father, mother, brother etc.).
Describes why the action is to be performed or not performed in textual form.
Supporting documentation, typically for regulatory submission.
Date this version of the software was released.
The value of the HTTP response code to be tested.
This resource provides the status of the payment for goods and services rendered, and the request and response resource references.
Digital Signature - base64 encoded. XML-DSig or a JWT.
How the value should be understood and represented - whether the actual value is greater or less than the stated value due to measurement issues; e.g. if the comparator is "<" , then the real value is < stated value.
< | <= | >= | > - how to understand the value
The individual who initiated the request and has responsibility for its activation.
The amount of patient payments for various types of services/products, expressed as a percentage of the service/product cost or a fixed amount of currency.
The amount or percentage of the copayment
Allows a service to provide a unique, business identifier for the request.
The calculated hash of the data using SHA-1. Represented using base64.
The date and time this version of the observation was made available to providers, typically after the results have been reviewed and verified.
Date/Time this version was made available
registered | partial | preliminary | final +
Describes the action that was taken or the observation that was made that reduces/eliminates the risk associated with the identified issue.
The organization of which this organization forms a part.
Identifies the patient, device, practitioner, location or other object the account is associated with.
The content was developed with a focus and intent of supporting the contexts that are listed. These terms may be used to assist with indexing and searching for appropriate code system instances.
Text that is displayed above the contents of the group or as the text of the question being answered.
The date (and optionally time) when the activity definition was published. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the activity definition changes.
Account into which this ChargeItems belongs.
The value for the parameter that will be passed on to the external rule template.
The location/organization from which the patient came before admission.
Location/organization to which the patient is discharged.
A description of how the application supports or uses the specified document profile. For example, when documents are created, what action is taken with consumed documents, etc.
Date filters specify additional constraints on the data in terms of the applicable date range for specific elements. Each date filter specifies an additional constraint on the data, i.e. date filters are AND'ed, not OR'ed.
Business identifiers assigned to this health insurance product which remain constant as the resource is updated and propagates from server to server.
Information about the [ValueSet/$expand](valueset-operation-expand.html) operation.
Recognized governance framework or system operating with a circumscribed scope in accordance with specified principles, policies, processes or procedures for managing rights, actions, or behaviors of parties or principals relative to resources.
A sphere of control governed by an authoritative jurisdiction, organization, or person
A short title used to represent this page in navigational structures such as table of contents, bread crumbs, etc.
Short title shown for navigational assistance
Explanation of why this plan definition is needed and why it has been designed as it has.
The qualification which is applicable for this service.
Indicates whether this operation or named query can be invoked at the resource type level for any given resource type level (e.g. without needing to choose a specific resource id for the context).
Human-readable description of the source document. This is sometimes known as the "title".
An external specification that the content is mapped to.
Applicable for single substances that contain a radionuclide or a non-natural isotopic ratio.
Used in supporting different identifiers for the same product, e.g. manufacturer code and retailer code.
Guidelines for the administration of the medication.
Gudelines for administration of the medication
The entity that is providing the health insurance product and underwriting the risk. This is typically an insurance carriers, other third-party payers, or health plan sponsors comonly referred to as 'payers'.
Identification of the specific substance (or pharmaceutical product) considered to be responsible for the Adverse Reaction event. Note: the substance for a specific reaction may be different from the substance identified as the cause of the risk, but it must be consistent with it. For instance, it may be a more specific substance (e.g. a brand medication) or a composite product that includes the identified substance. It must be clinically safe to only process the 'code' and ignore the 'reaction.substance'. If a receiving system is unable to confirm that AllergyIntolerance.reaction.substance falls within the semantic scope of AllergyIntolerance.code, then the receiving system should ignore AllergyIntolerance.reaction.substance.
Specific substance or pharmaceutical product considered to be responsible for event
The CodeSystem resource is used to declare the existence of and describe a code system or code system supplement and its key properties, and optionally define a part or all of its content.
A copyright statement relating to the structure map and/or its contents. Copyright statements are generally legal restrictions on the use and publishing of the structure map.
Resources contained in the instance (e.g. the observations contained in a bundle).
The minimum number of times this element SHALL appear in the instance.
A code representing the patient or other source's judgment about the state of the device used that this statement is about. Generally this will be active or completed.
Some observations have multiple component observations. These component observations are expressed as separate code value pairs that share the same attributes. Examples include systolic and diastolic component observations for blood pressure measurement and multiple component observations for genetics observations.
Reference to the resource (containing the contents of the rule needed for assertions).
Results of execution (transaction/batch/history)
Explanation of why this search parameter is needed and why it has been designed as it has.
Identifies the sending system to allow the use of a trust relationship.
Substance name for each non-natural or radioisotope.
The content was developed with a focus and intent of supporting the contexts that are listed. These terms may be used to assist with indexing and searching for appropriate charge item definition instances.
The name(s) associated with the practitioner.
For assessments or prognosis specific to a particular condition, indicates the condition being assessed.
The uri that describes the actual end-point to connect to.
The technical base address for connecting to this endpoint
A name assigned to an instance of data. The instance must be provided when the mapping is invoked.
An identifier that applies to this person in this role.
An identifier for the person as this agent
A practitioner, patient, device, or related person engaged in the session.
A record of a request for a medication, substance or device used in the healthcare setting.
Mappings for an individual concept in the source to one or more concepts in the target.
Mappings for a concept from the source set
Human-readable description of the source document.
Explanation of why this structure definition is needed and why it has been designed as it has.
Why this structure definition is defined
The identifier of the request associated with this response. If an identifier was given as part of the request, it will be reproduced here to enable the requester to more easily identify the response in a multi-request scenario.
The identifier of the request associated with this response, if any
Coded identifier of the operation, supported by the system resource.
read | vread | update | patch | delete | history-instance | history-type | create | search-type
Text, attachment(s), or resource(s) to be communicated to the recipient.
The medicinal product that is being authorized.
The title of the action displayed to a user.
planned | waitlist | active | onhold | finished | cancelled.
planned | waitlist | active | onhold | finished | cancelled | entered-in-error
Additional information about the Condition. This is a general notes/comments entry for description of the Condition, its diagnosis and prognosis.
Additional information about the Condition
Specifies the type of substitution allowed.
An exception to the base policy of this consent. An exception can be an addition or removal of access permissions.
The FHIRPath expression to evaluate against the source fixture. When compareToSourceId is defined, either compareToSourceExpression or compareToSourcePath must be defined, but not both.
The FHIRPath expression to evaluate against the source fixture
The logical author of the message - the person or device that decided the described event should happen. When there is more than one candidate, pick the most proximal to the MessageHeader. Can provide other authors in extensions.
Coded representation of the context generally or of the Referenced entity, such as the asset holder type or location.
Tags applied to this resource. Tags are intended to be used to identify and relate resources to process and workflow, and applications are not required to consider the tags when interpreting the meaning of a resource.
Provides a reference to the author of the request group.
Device or practitioner that authored the request group
The symptom, condition or undesirable effect.
[Observations](observation.html) that are part of this diagnostic report.
A reference to the Measure that was calculated to produce this report.
A reference to an invariant that may make additional statements about the cardinality or value in the instance.
The organization responsible for the provisioning and upkeep of the location.
Organization responsible for provisioning and upkeep
An absolute URI that is used to identify this concept map when it is referenced in a specification, model, design or an instance; also called its canonical identifier. This SHOULD be globally unique and SHOULD be a literal address at which at which an authoritative instance of this concept map is (or will be) published. This URL can be the target of a canonical reference. It SHALL remain the same when the concept map is stored on different servers.
Canonical identifier for this concept map, represented as a URI (globally unique)
Address where the related person can be contacted or visited.
Includes information about the reaction that occurred as a result of exposure to a substance (for example, a drug or a chemical).
The person or device that performed the data entry leading to this message. When there is more than one candidate, pick the most proximal to the message. Can provide other enterers in extensions.
The date when the enclosed suite of services were performed or completed.
A coded identifier of the operation, supported by the system.
transaction | batch | search-system | history-system
A human assigned name for the resource. All resources SHOULD have a name, but the name may be extracted from the resource (e.g. ValueSet.name).
A Boolean value to indicate that this implementation guide is authored for testing purposes (or education/evaluation/marketing) and is not intended to be used for genuine usage.
Condition or observation that supports why the medication is being/was taken.
Indicates when this particular annotation was made.
A tag to add to any resource that matches the criteria, after the subscription is processed.
A page / section in the implementation guide. The root page is the implementation guide home page.
The populations that make up the population group, one for each type of population appropriate for the measure.
The maximum number of units of the medicaton that can be dispensed in a period.
Assertion about certainty associated with the propensity, or potential risk, of a reaction to the identified substance (including pharmaceutical product).
unconfirmed | confirmed | refuted | entered-in-error
The type of link between this patient resource and another patient resource.
replaced-by | replaces | refer | seealso
Amount of prism to compensate for eye alignment in fractional units.
Legally binding Contract DSIG signature contents in Base64.
Identifies the practitioner who determined the mitigation and takes responsibility for the mitigation step occurring.
Indicates whose goal this is - patient goal, practitioner goal, etc.
An explanatory or alternate title for the plan definition giving additional information about its content.
Subordinate title of the plan definition
Invoice containing collected ChargeItems from an Account with calculated individual and total price for Billing purpose.
Indicates who or what performed the medication administration and how they were involved.
The reason or justification for the communication.
List of Legal expressions or representations of this Contract.
The verification status to support the clinical status of the condition.
unconfirmed | provisional | differential | confirmed | refuted | entered-in-error
Explanation of why this code system is needed and why it has been designed as it has.
Identifies a concept from an external specification that roughly corresponds to this element.
Map element to another set of definitions
The other patient resource that the link refers to.
The other patient or related person resource that the link refers to
If field is a list, how to manage the list.
The status of this structure map. Enables tracking the life-cycle of the content.
The human-friendly name of the interaction.
Explanation of why this questionnaire is needed and why it has been designed as it has.
An attached file with the structural representation.
When the TestScript was executed and this TestReport was generated.
Anatomic location where the procedure should be performed. This is the target site.
The identifier that is used to identify this version of the event definition when it is referenced in a specification, model, design or instance. This is an arbitrary value managed by the event definition author and is not expected to be globally unique. For example, it might be a timestamp (e.g. yyyymmdd) if a managed version is not available. There is also no expectation that versions can be placed in a lexicographical sequence.
Business version of the event definition
When populated, the author is responsible for the care plan. The care plan is attributed to the author.
Characterizes how quickly the proposed act must be initiated. Includes concepts such as stat, urgent, routine.
Identification of the condition, problem or diagnosis.
The term or period of the values such as 'maximum lifetime benefit' or 'maximum annual visits'.
Specifies the applicability of the term to an asset resource instance, and instances it refers to orinstances that refer to it, and/or are owned by the offeree.
One or more Contract Provisions, which may be related and conveyed as a group, and may contain nested groups.
Significant health conditions for a person related to the patient relevant in the context of care for the patient.
Reference to a formal record of the evidence on which the staging assessment is based.
Human-readable name for the target system.
Program Names that can be used to categorize the service.
Program Names that categorize the service
The regulatory authorization of a medicinal product.
Description of the capabilities that this test script is requiring the server to support.
A period of time during which the fulfilling resources would have been created.
Condition, Observation or DiagnosticReport that supports why the immunization was administered.
The first-tier service adjudications for submitted services.
The location(s) at which the role occurs.
The name of the organization or individual that published the activity definition.
Declare at a message definition level whether a response is required or only upon error or success, or never.
Structural Variant Outer Start.If the coordinate system is either 0-based or 1-based, then start position is inclusive.
The metadata about the resource. This is content that is maintained by the infrastructure. Changes to the content might not always be associated with version changes to the resource.
Lot number assigned by the manufacturer.
Points to a message definition that identifies the messaging event, message structure, allowed responses, etc.
Indicates the mechanism used to perform the observation.
Defines children of a concept to produce a hierarchy of concepts. The nature of the relationships is variable (is-a/contains/categorizes) - see hierarchyMeaning.
Child Concepts (is-a/contains/categorizes)
The media type of the language for the expression, e.g. "text/cql" for Clinical Query Language expressions or "text/fhirpath" for FHIRPath expressions.
Indicates that this operation definition is a constraining profile on the base.
An actor taking an active role in the event or activity that is logged.
The amount of the medication given at one administration event. Use this value when the administration is essentially an instantaneous event such as a swallowing a tablet or giving an injection.
The start and expected end date of the authorization.
Indicates whether the issue indicates a variation from successful processing.
A code that details how this designation would be used.
Details how this designation would be used
The content was developed with a focus and intent of supporting the contexts that are listed. These terms may be used to assist with indexing and searching for appropriate compartment definition instances.
The encounter or episode of care with primary association to the questionnaire response.
Encounter or Episode during which questionnaire was completed
Business identifiers assigned to this communication request by the performer or other systems which remain constant as the resource is updated and propagates from server to server.
Comparators supported for the search parameter.
eq | ne | gt | lt | ge | le | sa | eb | ap
The period during which this contact person or organization is valid to be contacted relating to this patient.
Type of choice made by accepting party with respect to an offer made by an offeror/ grantee.
The maximum single dose that can be administered as per the protocol of a clinical trial can be specified using a numerical value and its unit of measurement.
Specifies descriptive properties of the medicine, such as color, shape, imprints, etc.
Quantity of the substance or specified substance present in the manufactured item or pharmaceutical product.
Official human-readable label for the composition.
A postal code designating a region defined by the postal service.
From where patient was admitted (physician referral, transfer).
The Genome Build used for reference, following GRCh build versions e.g. 'GRCh 37'. Version number must be included if a versioned release of a primary build was used.
The Genome Build used for reference, following GRCh build versions e.g. 'GRCh 37'
The time when this communication was sent.
A person who is directly or indirectly involved in the provisioning of healthcare.
The type of value a search parameter refers to, and how the content is interpreted.
number | date | string | token | reference | composite | quantity | uri | special
A free text natural language description of the test script from a consumer's perspective.
Natural language description of the test script
The reason for the assigned forecast status.
The minimum period of time that must occur between dispenses of the medication.
Minimum period of time between dispenses
The date and time the series was started.
Any special requests that have been made for this hospitalization encounter, such as the provision of specific equipment or other things.
Indicates how quickly the Medication Request should be addressed with respect to other requests.
Relevant time or time-period when this Contract is applicable.
The strength per unitary volume (or mass).
Describes how to combine the information calculated, based on logic in each of several populations, into one summarized result.
How is rate aggregation performed for this measure
Supplemental instructions to the patient on how to take the medication (e.g. "with meals" or"take half to one hour before food") or warnings for the patient about the medication (e.g. "may cause drowsiness" or "avoid exposure of skin to direct sunlight or sunlamps").
Supplemental instruction or warnings to the patient - e.g. "with meals", "may cause drowsiness"
URI of an external repository which contains further details about the genetics data.
Description of final status after the process ends.
A plan or proposal that is fulfilled in whole or in part by this request.
An actor taking an active role in the manifest.
The number of members of the population in this stratum.
The policy or plan that authorized the activity being recorded. Typically, a single activity may have multiple applicable policies, such as patient consent, guarantor funding, etc. The policy would also indicate the security token used.
Security labels that protects the offer.
The identifier that is used to identify this version of the capability statement when it is referenced in a specification, model, design or instance. This is an arbitrary value managed by the capability statement author and is not expected to be globally unique. For example, it might be a timestamp (e.g. yyyymmdd) if a managed version is not available. There is also no expectation that versions can be placed in a lexicographical sequence.
Business version of the capability statement
A specification of restful operations supported by the system.
The date on which the existence of the AdverseEvent was first recorded.
A record of an event made for purposes of maintaining a security log. Typical uses include detection of intrusion attempts and monitoring for inappropriate usage.
Details and position information for a physical place where services are provided and resources and participants may be stored, found, contained, or accommodated.
Confidentiality level of the specified substance as the ingredient.
Types of security services that are supported/required by the system.
OAuth | SMART-on-FHIR | NTLM | Basic | Kerberos | Certificates
Sub actions that are contained within the action. The behavior of this action determines the functionality of the sub-actions. For example, a selection behavior of at-most-one indicates that of the sub-actions, at most one may be chosen as part of realizing the action definition.
A setup operation or assert that was executed
A code to indicate the Professional Service or Product supplied.
Event resulting in discontinuation or termination of this Contract instance by one or more parties to the contract.
Describes the type of performance or participation(e.g. primary surgeon, anaesthesiologiest, etc.).
Any combination of letters, numerals, "-" and ".", with a length limit of 64 characters. (This might be an integer, an unprefixed OID, UUID or any other identifier pattern that meets these constraints.) Ids are case-insensitive.
An expression that describes applicability criteria or start/stop conditions for the action.
Expressions that describe applicability criteria for the billing code.
Whether or not the billing code is applicable
A Person, Location/HealthcareService or Device that is participating in the appointment.
Person, Location/HealthcareService or Device
The description of the overall patte3rn of the administration of the medication to the patient.
Overall pattern of medication administration
An organization that initiates the investigation and is legally responsible for the study.
Organization that initiates and is legally responsible for the study
A detailed description of how the library is used from a clinical perspective.
Describes the clinical usage of the library
The version of the code system that the codes are selected from, or the special version "*" for all versions.
Specific version of the code system referred to
Explanation for the non-claim adjustment
Indicates the site on the subject's body where the observation was made (i.e. the target site).
The match value may be either a code defined by the system, or a string value, which is a regex match on the literal string of the property value when the operation is 'regex', or one of the values (true and false), when the operation is 'exists'.
Code from the system, or regex criteria, or boolean value for exists
This field contains a patient's most recent marital (civil) status.
Description of the Location, which helps in finding or referencing the place.
Additional details about the location that could be displayed as further information to identify the location beyond its name
Reference of response to resource for which payment is being made.
Customary unit used to report quantitative results of this observation.
The country in which the marketing authorization has been granted.
A record of the patient's informed agreement to participate in the study.
If paging is being used, the offset at which this resource starts. I.e. this resource is a partial view into the expansion. If paging is not being used, this element SHALL NOT be present.
The reason that this appointment is being scheduled. This is more clinical than administrative.
The type of action to perform (create, update, remove).
Administrative Gender - the gender that the person is considered to have for administration and record keeping purposes.
The slots from the participants' schedules that will be filled by the appointment.
The slots that this appointment is filling
Indicates whether the goal has been reached and is still considered relevant.
proposed | accepted | planned | in-progress | on-target | ahead-of-target | behind-target | sustaining | achieved | on-hold | cancelled | entered-in-error | rejected
Date/Time that the appointment is to take place, or requested new start time.
Time from appointment, or requested new start time
A list of _include values supported by the server.
The profile that describes the use of the base resource.
The end of the period. If the end of the period is missing, it means no end was known or planned at the time the instance was created. The start may be in the past, and the end date in the future, which means that period is expected/planned to end at that time.
End time with inclusive boundary, if not ongoing
Code representing the role the entity played in the event being audited.
A brief description of the action used to provide a summary to display to the user.
The url that describes the actual end-point to send messages to.
An absolute base URL for the implementation. This forms the base for REST interfaces as well as the mailbox and document interfaces.
Additional information about the evaluation.
Whether this patient record is in active use. Many systems use this property to mark as non-current patients, such as those that have not been seen for a period of time based on an organization's business rules. It is often used to filter patient lists to exclude inactive patients Deceased patients may also be marked as inactive for the same reasons, but may be active for some time after death.
Whether this patient's record is in active use
The type of processing action being requested, for example Reversal, Readjudication, StatusRequest, PendedRequest.
Details about each adverse reaction event linked to exposure to the identified substance.
A name for the specification that is being mapped to.
The general class of the information supplied: information; exception; accident, employment; onset, etc.
Related Claims which may be revelant to processing this claim
The span of time over which the collection of a specimen occurred.
The date whose meaning is specified by dateCriterion.code.
Indicates whether the measure is used to examine a process, an outcome over time, a patient-reported outcome, or a structure measure such as utilization.
process | outcome | structure | patient-reported-outcome | composite
The list of diagnosis relevant to this encounter.
An absolute URI that identifies the code system of the dependency code (if the source/dependency is a value set that crosses code systems).
The server where the request message is destined for. Must be one of the server numbers listed in TestScript.destination section.
A brief discussion of what the parameter is for and how it is used by the module.
Identifies the purpose for the contact point.
home | work | temp | old | mobile - purpose of this contact point
Defines the characteristics of a message that can be shared between systems, including the type of event that initiates the message, the content to be transmitted and what response(s), if any, are permitted.
Which origin server these requirements apply to.
The geographic region in which a health insurance plan's benefits apply.
A label for the list assigned by the author.
Indicates the status of the detected issue.
The definition of variant here originates from Sequence ontology ([variant_of](http://www.sequenceontology.org/browser/current_svn/term/variant_of)). This element can represent amino acid or nucleic sequence change(including insertion,deletion,SNP,etc.) It can represent some complex mutation or segment variation with the assist of CIGAR string.
The name of the arm in the study the subject actually followed as part of this study.
The code that identifies this filter when it is used as a filter in [ValueSet].compose.include.filter.
The date (and optionally time) when the charge item definition was published. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the charge item definition changes.
An absolute URI that is used to identify this test script when it is referenced in a specification, model, design or an instance; also called its canonical identifier. This SHOULD be globally unique and SHOULD be a literal address at which at which an authoritative instance of this test script is (or will be) published. This URL can be the target of a canonical reference. It SHALL remain the same when the test script is stored on different servers.
Canonical identifier for this test script, represented as a URI (globally unique)
Additional comments about the appointment.
This element refers to a List of subject level MeasureReport resources, one for each subject in this population.
For subject-list reports, the subject results in this population
A care plan that is fulfilled in whole or in part by this care plan.
Refers to the value set that identifies the set of codes the binding refers to.
The reporting period for which the report was calculated.
A record of a medication that is being consumed by a patient. A MedicationStatement may indicate that the patient may be taking the medication now, or has taken the medication in the past or will be taking the medication in the future. The source of this information can be the patient, significant other (such as a family member or spouse), or a clinician. A common scenario where this information is captured is during the history taking process during a patient visit or stay. The medication information may come from sources such as the patient's memory, from a prescription bottle, or from a list of medications the patient, clinician or other party maintains. The primary difference between a medication statement and a medication administration is that the medication administration has complete administration information and is based on actual administration information from the person who administered the medication. A medication statement is often, if not always, less specific. There is no required date/time when the medication was administered, in fact we only know that a source has reported the patient is taking this medication, where details such as time, quantity, or rate or even medication product may be incomplete or missing or less precise. As stated earlier, the medication statement information may come from the patient's memory, from a prescription bottle or from a list of medications the patient, clinician or other party maintains. Medication administration is more formal and is not missing detailed information.
The status of this concept map. Enables tracking the life-cycle of the content.
The number of copies of the seqeunce of interest. (RNASeq).
Date/Time that the appointment is to conclude.
The Care Team includes all the people and organizations who plan to participate in the coordination and delivery of care for a patient.
Contains the names of any search parameters which may be chained to the containing search parameter. Chained parameters may be added to search parameters of type reference and specify that resources will only be returned if they contain a reference to a resource which matches the chained parameter value. Values for this field should be drawn from SearchParameter.code for a parameter on the target resource type.
A parameter passed to or received from the operation.
This resource provides enrollment and plan details from the processing of an Enrollment resource.
Identifies the resource (or resources) that are being addressed by the event. For example, the Encounter for an admit message or two Account records for a merge.
Ordered list of patient procedures performed to support the adjudication.
The date and time this task was created.
Indicates the type of dispensing event that is performed. For example, Trial Fill, Completion of Trial, Partial Fill, Emergency Fill, Samples, etc.
Trial fill, partial fill, emergency fill, etc.
The status of this structure definition. Enables tracking the life-cycle of the content.
This resource provides the target, request and response, and action details for an action to be performed by the target on or about existing resources.
The EpisodeOfCare may be known by different identifiers for different contexts of use, such as when an external agency is tracking the Episode for funding purposes.
Business Identifier(s) relevant for this EpisodeOfCare
Identification of the route by which the subject was exposed to the substance.
How the subject was exposed to the substance
A natural language name identifying the operation definition. This name should be usable as an identifier for the module by machine processing applications such as code generation.
Name for this operation definition (computer friendly)
active | suspended | error | off | test.
active | suspended | error | off | entered-in-error | test
A group of related requests that can be used to capture intended activities that have inter-dependencies such as "give this medication after that one".
Detailed description of the type of activity; e.g. What lab test, what procedure, what kind of encounter.
The date and time of last modification to this task.
Additional information about the general costs associated with this plan.
A name of the entity in the audit event.
The minimum number of times this parameter SHALL appear in the request or response.
Key events in the history of the request.
The type of dosage (for example, prophylaxis, maintenance, therapeutic, etc).
Describes why the family member's history is not available.
subject-unknown | withheld | unable-to-obtain | deferred
A formal identifier that is used to identify this library when it is represented in other formats, or referenced in a specification, model, design or an instance. e.g. CMS or NQF identifiers for a measure artifact. Note that at least one identifier is required for non-experimental active artifacts.
Maximum cardinality of the base element identified by the path.
A coded type for the identifier that can be used to determine which identifier to use for a specific purpose.
Description of the purpose/content, similar to a subject line in an email.
This resource identifies a type of a manufactured item that is used in the provision of healthcare without being substantially changed through that activity. The device may be a medical or non-medical device. Medical devices include durable (reusable) medical equipment, implantable devices, as well as disposable equipment used for diagnostic, treatment, and research for healthcare and public health. Non-medical devices may include items such as a machine, cellphone, computer, application, etc. This is the catalog description of a device (not the specific instance).
An expression specifying the value of the customized element.
An expression that provides the dynamic value for the customization
Defines how the compartment rule is used - whether it it is used to test whether resources are subject to the rule, or whether it is a rule that must be followed.
Diet preferences reported by the patient.
A set of ordered Quantities defined by a low and high limit.
The output parameters of the evaluation, if any. Many modules will result in the return of specific resources such as procedure or communication requests that are returned as part of the operation result. However, modules may define specific outputs that would be returned as the result of the evaluation, and these would be returned in this element.
The output parameters of the evaluation, if any
Where a Medicines Regulatory Agency has granted a marketing authorisation for which specific provisions within a jurisdiction apply, the jurisdiction can be specified using an appropriate controlled terminology The controlled term and the controlled term identifier shall be specified.
Unique identifier for this Contract or a derivative that references a Source Contract.
A free text natural language name identifying the executed TestScript.
Informal name of the executed TestScript
The value for the parameter that will be passed on to the external ruleset rule template.
A set of healthcare-related information that is assembled together into a single logical package that provides a single coherent statement of meaning, establishes its own context and that has clinical attestation with regard to who is making the statement. A Composition defines the structure and narrative content necessary for a document. However, a Composition alone does not constitute a document. Rather, the Composition must be the first entry in a Bundle where Bundle.type=document, and any other resources referenced from Composition must be included as subsequent entries in the Bundle (for example Patient, Practitioner, Encounter, etc.).
Reason the encounter takes place, as specified using information from another resource. For admissions, this is the admission diagnosis. The indication will typically be a Condition (with other resources referenced in the evidence.detail), or a Procedure.
Reason the encounter takes place (resource)
A reference to the specific base computable regulation or policy.
The URL pointing to a protocol, guideline, orderset or other definition that is adhered to in whole or in part by this NutritionOrder.
An indication of the reason that the entity signed this document. This may be explicitly included as part of the signature information and can be used when determining accountability for various actions concerning the document.
Indication of the reason the entity signed the object(s)
The type of message conveyed such as alert, notification, reminder, instruction, etc.
The status of the participants' presence at the specified location during the period specified. If the participant is is no longer at the location, then the period will have an end date/time.
The organization who produced this adjudicated response.
Controls how multiple enableWhen values are interpreted - whether all or any must be true.
Describes the calibrations that have been performed or that are required to be performed.
Whether the sequence is numbered starting at 0 (0-based numbering or coordinates, inclusive start, exclusive end) or starting at 1 (1-based numbering, inclusive start and inclusive end).
Base number of coordinate system (0 for 0-based numbering or coordinates, inclusive start, exclusive end, 1 for 1-based numbering, inclusive start, inclusive end)
Details about the specimens on which this diagnostic report is based.
A formal identifier that is used to identify this MeasureReport when it is represented in other formats or referenced in a specification, model, design or an instance.
Additional identifier for the MeasureReport
An association between a patient and an organization / healthcare provider(s) during which time encounters may occur. The managing organization assumes a level of responsibility for the patient during this time.
Type of primary source (License Board; Primary Education; Continuing Education; Postal Service; Relationship owner; Registration Authority; legal source; issuing source; authoritative source).
How the parameter is understood as a search parameter. This is only used if the parameter type is 'string'.
The valueset for the code filter. The valueSet and code elements are additive. If valueSet is specified, the filter will return only those data items for which the value of the code-valued element specified in the path is a member of the specified valueset.
If this medicine applies to human or veterinary uses.
The type of participant that can execute the task.
requester | dispatcher | scheduler | performer | monitor | manager | acquirer | reviewer
An absolute URI that identifies the source system where the concepts to be mapped are defined.
Source system where concepts to be mapped are defined
Indicates when the team did (or is intended to) come into effect and end.
Constraints to the base Consent.policyRule
Sequence of diagnosis which serves to provide a link.
When the composition was attested by the party.
A bibliographic citation for the related artifact. This text SHOULD be formatted according to an accepted citation format.
An absolute URI that is used to identify this example scenario when it is referenced in a specification, model, design or an instance; also called its canonical identifier. This SHOULD be globally unique and SHOULD be a literal address at which at which an authoritative instance of this example scenario is (or will be) published. This URL can be the target of a canonical reference. It SHALL remain the same when the example scenario is stored on different servers.
Canonical identifier for this example scenario, represented as a URI (globally unique)
The medication(s), food(s), therapy(ies), device(s) or other concerns or interventions that the study is seeking to gain more information about.
If specified, this indicates a profile that the input data must conform to, or that the output data will conform to.
What profile the value is expected to be
Reference of resource which is the target or subject of this action.
The diagnostic service that is responsible for issuing the report.
The coded value or textual component of the flag to display to the user.
Coded or textual message to display to user
The individual or set of individuals the action is being or was performed on.
Information about the entity validating information.
Indicates how the calculation is performed for the measure, including proportion, ratio, continuous-variable, and cohort. The value set is extensible, allowing additional measure scoring types to be represented.
proportion | ratio | continuous-variable | cohort
A unique business identifier for this group.
Business identifiers assigned to this procedure by the performer or other systems which remain constant as the resource is updated and propagates from server to server.
A code to indicate the Professional Service or Product supplied (e.g. CTP, HCPCS,USCLS,ICD10, NCPDP,DIN,ACHI,CCI).
Original prescription which has been superseded by this prescription to support the dispensing of pharmacy services, medications or products. For example, a physician may prescribe a medication which the pharmacy determines is contraindicated, or for which the patient has an intolerance, and therefor issues a new prescription for an alternate medication which has the same therapeutic intent. The prescription from the pharmacy becomes the 'prescription' and that from the physician becomes the 'original prescription'.
Original prescription if superseded by fulfiller
An absolute URI which is the code system in which the code for this item in the expansion is defined.
The period during which the charge item definition content was or is planned to be in active use.
When the charge item definition is expected to be used
The status of the disease or symptom for which the indication applies.
How the individual is involved in the resources content that is described in the exception.
Alternative agent Identifier. For a human, this should be a user identifier text string from authentication system. This identifier would be one known to a common authentication system (e.g. single sign-on), if available.
Describes the measurement repetition time. This is not necessarily the same as the update period. The measurement repetition time can range from milliseconds up to hours. An example for a measurement repetition time in the range of milliseconds is the sampling rate of an ECG. An example for a measurement repetition time in the range of hours is a NIBP that is triggered automatically every hour. The update period may be different than the measurement repetition time, if the device does not update the published observed value with the same frequency as it was measured.
Describes the measurement repetition time
The jurisdiction where this name applies.
Technical endpoints providing access to services operated for the organization.
A unique identifier assigned to this immunization record.
The person, animal or group on which the procedure was performed.
The location where the procedure actually happened. E.g. a newborn at home, a tracheostomy at a restaurant.
Named instance provided when invoking the map
A Boolean value to indicate that this operation definition is authored for testing purposes (or education/evaluation/marketing) and is not intended to be used for genuine usage.
Where the supply is expected to come from.
Unique instance identifiers assigned to a device by the software, manufacturers, other organizations or owners. For example: handle ID.
The identity of the authoritative source for UDI generation within a jurisdiction. All UDIs are globally unique within a single namespace with the appropriate repository uri as the system. For example, UDIs of devices managed in the U.S. by the FDA, the value is http://hl7.org/fhir/NamingSystem/fda-udi.
Legal states of the formation of a legal instrument, which is a formally executed written document that can be formally attributed to its author, records and formally expresses a legally enforceable act, process, or contractual duty, obligation, or right, and therefore evidences that act, process, or agreement.
A contributor to the content of a knowledge asset, including authors, editors, reviewers, and endorsers.
A collection of error, warning or information messages that result from a system action.
List of the costs associated with a specific benefit.
What the target is validated against (nothing; primary source; multiple sources).
The name of the organization or individual that published the charge item definition.
Additional representations for the concept - other languages, aliases, specialized purposes, used for particular purposes, etc.
Specifies descriptive properties of the medicine
Indicates how quickly the activity should be addressed with respect to other requests.
The original request, instruction or authority to perform the administration.
Request administration performed against
Additional representations for the concept
The Etag for the resource, if the operation for the entry produced a versioned resource (see [Resource Metadata and Versioning](http.html#versioning) and [Managing Resource Contention](http.html#concurrency)).
Additional information explaining the basis for the prediction.
An order or request for both supply of the medication and the instructions for administration of the medication to a patient. The resource is called "MedicationRequest" rather than "MedicationPrescription" or "MedicationOrder" to generalize the use across inpatient and outpatient settings, including care plans, etc., and to harmonize with workflow patterns.
The status of this value set. Enables tracking the life-cycle of the content.
General category of benefit (Medical; Dental; Vision; Drug; Mental Health; Substance Abuse; Hospice, Home Health).
A legal or geographic region in which the naming system is intended to be used.
Intended jurisdiction for naming system (if applicable)
References the source of pricing information, rules of application for the code this ChargeItem uses.
Defining information about the code of this charge item
Specifies a code for the concept to be included or excluded.
Official name of the health insurance product as designated by the owner.
Business identifiers assigned to this health insurance plan which remain constant as the resource is updated and propagates from server to server.
Whether this reference needs to be version specific or version independent, or whether either can be used.
Class that defines the quantity and type of nutrient modifications (for example carbohydrate, fiber or sodium) required for the oral diet.
A count of the number of resource instances that are part of the group.
The number of minutes from the event. If the event code does not indicate whether the minutes is before or after the event, then the offset is assumed to be after the event.
Reference to a Group that defines the criteria for and quantity of subjects participating in the study. E.g. " 200 female Europeans between the ages of 20 and 45 with early onset diabetes".
Identifies the user or organization responsible for asserting the linkages and who establishes the context for evaluating the nature of each linkage.
Additional details about the error. This may be a text description of the error, or a system code that identifies the error.
Explanation of why this structure map is needed and why it has been designed as it has.
A description of the risk adjustment factors that may impact the resulting score for the measure and how they may be accounted for when computing and reporting measure results.
How risk adjustment is applied for this measure
The date on which the practitioner was born
Allows a service to provide a unique, business identifier for the session.
A copyright statement relating to the event definition and/or its contents. Copyright statements are generally legal restrictions on the use and publishing of the event definition.
activating | active | suspended | closing | closed
Person who created the invoice/claim/pre-determination or pre-authorization.
Chemical substances are a single substance type whose primary defining element is the molecular structure. Chemical substances shall be defined on the basis of their complete covalent molecular structure; the presence of a salt (counter-ion) and/or solvates (water, alcohols) is also captured. Purity, grade, physical form or particle size are not taken into account in the definition of a chemical substance or in the assignment of a Substance ID.
A short label for a particular group, question or set of display text within the questionnaire used for reference by the individual completing the questionnaire.
An absolute URI that identifies the specification that this mapping is expressed to.
Indicates where the medication is expected to be consumed or administered.
The time when the dispensed product was packaged and reviewed.
A group or question item from the original questionnaire for which answers are provided.
List of input service items which this service line is intended to replace.
A free text natural language description of the structure map from a consumer's perspective.
Natural language description of the structure map
The specific version of the code system, as determined by the code system authority.
Business Identifiers that are specific to a role/location.
Another implementation guide that this implementation depends on. Typically, an implementation guide uses value sets, profiles etc.defined in other implementation guides.
Another Implementation guide this depends on
Documentation that describes how the structure is used in the mapping.
The healthcare event (e.g. a patient and healthcare provider interaction) during which this task was created.
Healthcare event during which this task originated
The encounter when the allergy or intolerance was asserted.
Encounter when the allergy or intolerance was asserted
An indication, if true, that the item must be present in a "completed" QuestionnaireResponse. If false, the item may be skipped when answering the questionnaire.
Whether the item must be included in data results
The healthcare event (e.g. a patient and healthcare provider interaction) which this DiagnosticReport per is about.
An absolute URI that is used to identify this measure when it is referenced in a specification, model, design or an instance; also called its canonical identifier. This SHOULD be globally unique and SHOULD be a literal address at which at which an authoritative instance of this measure is (or will be) published. This URL can be the target of a canonical reference. It SHALL remain the same when the measure is stored on different servers.
Canonical identifier for this measure, represented as a URI (globally unique)
Vaccine(s) which should not be used to fulfill the recommendation.
Vaccine which is contraindicated to fulfill the recommendation
Rich text representation of the entire result as issued by the diagnostic service. Multiple formats are allowed but they SHALL be semantically equivalent.
Details concerning the specimen collection.
The party(s) that contribute to payment (or part of) of the charges applied to this account (including self-pay). A coverage may only be resposible for specific types of charges, and the sequence of the coverages in the account could be important when processing billing.
The party(s), such as insurances, that may contribute to the payment of this account
A collection of times that the Service Site is available.
A structured set of questions and their answers. The questions are ordered and grouped into coherent subsets, corresponding to the structure of the grouping of the questionnaire being responded to.
The name of the organization or individual that published the capability statement.
Whether this participant is required to be present at the meeting. This covers a use-case where two doctors need to meet to discuss the results for a specific patient, and the patient is not required to be present.
An absolute URI that is used to identify this structure map when it is referenced in a specification, model, design or an instance; also called its canonical identifier. This SHOULD be globally unique and SHOULD be a literal address at which at which an authoritative instance of this structure map is (or will be) published. This URL can be the target of a canonical reference. It SHALL remain the same when the structure map is stored on different servers.
Canonical identifier for this structure map, represented as a URI (globally unique)
External identifier - FHIR will generate its own internal identifiers (probably URLs) which do not need to be explicitly managed by the resource. The identifier here is one that would be used by another non-FHIR system - for example an automated medication pump would provide a record each time it operated; an administration while the patient was off the ward might be made with a different system and entered after the event. Particularly important if these records have to be updated.
The uri of the participant. An absolute URL is preferred.
If true indicates that the provider is asking for the medication request not to occur.
inpatient | outpatient | ambulatory | emergency +.
Reference pointer to the educational material given to the patient if the information was on line.
This a list of the relevant problems/conditions for a patient.
When searching, the server's search ranking score for the entry.
Identifies a specific instance of the entity. The reference should be version specific.
Participation status of the participant. When the status is declined or tentative if the start/end times are different to the appointment, then these times should be interpreted as a requested time change. When the status is accepted, the times can either be the time of the appointment (as a confirmation of the time) or can be empty.
accepted | declined | tentative | in-process | completed | needs-action | entered-in-error
Qualifier to refine the anatomical location. These include qualifiers for laterality, relative location, directionality, number, and plane.
Additional information about the cost, such as information about funding sources (e.g. HSA, HRA, FSA, RRA).
Whether or not the test execution will produce a warning only on error for this assert.
Will this assert produce a warning only on error?
A full description of how the study is being conducted.
The quantity or "count number" of the manufactured item.
The quantity of the specified nutrient to include in diet.
Business identifiers assigned to this family member history by the performer or other systems which remain constant as the resource is updated and propagates from server to server.
The code(s) that detail the conditions under which the healthcare service is available/offered.
Conditions under which service is available/offered
The billable period for which charges are being submitted.
A code - a text symbol - that uniquely identifies the concept within the code system.
A channel that was used for this communication (e.g. email, fax).
Provides a specific type of resource the group includes; e.g. "cow", "syringe", etc.
The details of the proposed activity represented in a specific resource.
Activity details defined in specific resource
The date at which the code status is changed as part of the terminology maintenance.
The parameter whose value is being tracked, e.g. body weight, blood pressure, or hemoglobin A1c level.
The parameter whose value is being tracked
A profile to which the target of the activity definition is expected to conform.
What profile the resource needs to conform to
Comments made about the media by the performer, subject or other participants.
A code to indicate if the medication is in active use.
Sequence of coverage which serves to provide a link and convey coordination of benefit order.
The diagram title of the group of operations.
In the case of a Pre-Determination/Pre-Authorization the provider may request that funds in the amount of the expected Benefit be reserved ('Patient' or 'Provider') to pay for the Benefits determined on the subsequent claim(s). 'None' explicitly indicates no funds reserving is requested.
Which person or organization authenticates that this document is valid.
A booking of a healthcare event among patient(s), practitioner(s), related person(s) and/or device(s) for a specific date/time. This may result in one or more Encounter(s).
Indicates another resource whose existence justifies this request group.
Unique code or number identifying the location to its users.
The base64 encoding of the Signature content. When signature is not recorded electronically this element would be empty.
The actual signature content (XML DigSig. JWS, picture, etc.)
A Boolean value to indicate that this example scenario is authored for testing purposes (or education/evaluation/marketing) and is not intended to be used for genuine usage.
Reason the encounter takes place, expressed as a code. For admissions, this can be used for a coded admission diagnosis.
The person, animal or group who is/was taking the medication.
Indicates whether or not a prospective consumer will require an appointment for a particular service at a site to be provided by the Organization. Indicates if an appointment is required for access to this service.
If an appointment is required for access to this service
The linkId for the question whose answer (or lack of answer) governs whether this item is enabled.
Question that determines whether item is enabled
The actual focus of an observation when it is not the patient of record representing something or someone associated with the patient such as a spouse, parent, fetus, or donor. For example, fetus observations in a mother's record. The focus of an observation could also be an existing condition, an intervention, the subject's diet, another observation of the subject, or a body structure such as tumor or implanted device. An example use case would be using the Observation resource to capture whether the mother is trained to change her child's tracheostomy tube. In this example, the child is the patient of record and the mother is the focus.
What the observation is about, when it is not about the subject of record
A single SOP instance within the series, e.g. an image, or presentation state.
Captures constraints on each element within the resource.
Definition of elements in the resource (if no StructureDefinition)
End position of the variant on the reference sequence.If the coordinate system is 0-based then end is is exclusive and does not include the last position. If the coordinate system is 1-base, then end is inclusive and includes the last position.
End position of the variant on the reference sequence
The date when the above payment action occurred.
The name of the device / manufacturer of the device that was used to make the recording.
The content was developed with a focus and intent of supporting the contexts that are listed. These terms may be used to assist with indexing and searching for appropriate plan definition instances.
The subject, typically a patient, of the imaging study.
A researcher in a study who oversees multiple aspects of the study, such as concept development, protocol writing, protocol submission for IRB approval, participant recruitment, informed consent, data collection, analysis, interpretation and presentation.
Researcher who oversees multiple aspects of the study
The participant that should perform or be responsible for this action.
What order applies to the items in the list.
A summary, charactarization or explanation of the body structure.
Indicates the risk for this particular subject (with their specific characteristics) divided by the risk of the population in general. (Numbers greater than 1 = higher risk than the population, numbers less than 1 = lower risk.).
A description of the kind of resource the in-line definition of a care plan activity is representing. The CarePlan.activity.detail is an in-line definition when a resource is not referenced using CarePlan.activity.reference. For example, a MedicationRequest, a ServiceRequest, or a CommunicationRequest.
The mime-type contents to compare against the request or response message 'Content-Type' header.
Mime type to compare against the 'Content-Type' header
Body site where vaccine was administered.
A list of _revinclude (reverse include) values supported by the server.
_revinclude values supported by the server
Individual who is making the procedure statement.
Distinguishes the type of performer in the dispense. For example, date enterer, packager, final checker.
Who performed the dispense and what they did
Either the Grantor, which is the entity responsible for granting the rights listed in a Consent Directive or the Grantee, which is the entity responsible for complying with the Consent Directive, including any obligations or limitations on authorizations and enforcement of prohibitions.
Instructions in terms that are understood by the patient or consumer.
Patient or consumer oriented instructions
The clinical service(s) being documented
The patient or group the risk assessment applies to.
Identifies the person who picked up the Supply.
Where applicable, the nominal volume can be specified using a numerical value and its unit of measurement The unit of measurement shall be specified in accordance with ISO 11240 and the resulting terminology The symbol and the symbol identifier shall be used.
This could be a histology result, pathology report, surgical report, etc.
Details where to send notifications when resources are received that meet the criteria.
A set of security labels that define which terms are controlled by this condition.
Security Labels that define affected terms
A natural language name identifying the measure. This name should be usable as an identifier for the module by machine processing applications such as code generation.
Name for this measure (computer friendly)
Harmonic mean of Recall and Precision, computed as: 2 * precision * recall / (precision + recall).
The contract resource which may provide more detailed information.
A plan, proposal or order that is fulfilled in whole or in part by this DeviceUseStatement.
A coded value specifying the procedure used to process the specimen.
Indicates the treatment step applied to the specimen
The version of the FHIR specification on which this ImplementationGuide is based - this is the formal version of the specification, without the revision number, e.g. [publication].[major].[minor], which is 3.5a.0. for this version.
FHIR Version this Implementation Guide targets
This describes the shelf life, taking into account various scenarios such as shelf life of the packaged Medicinal Product itself, shelf life after transformation where necessary and shelf life after the first opening of a bottle, etc. The shelf life type shall be specified using an appropriate controlled vocabulary The controlled term and the controlled term identifier shall be specified.
A logical group of resources. Logical groups can be used when building pages.
Grouping used to present related resources in the IG
The Imaging Manager description of the study. Institution-generated description or classification of the Study (component) performed.
okay | created | noContent | notModified | bad | forbidden | notFound | methodNotAllowed | conflict | gone | preconditionFailed | unprocessable.
The network service providing access (e.g., query, view, or retrieval) for this series. See implementation notes for information about using DICOM endpoints. A series-level endpoint, if present, has precedence over a study-level endpoint with the same Endpoint.connectionType.
Clinical interactions with other medications or substances.
The codes that are contained in the value set expansion.
The human language of the content. The value can be any valid value according to BCP 47.
A unique identifier assigned to this particular recommendation record.
How the referenced structure is used in this mapping.
The number of sample points at each time point. If this value is greater than one, then the dimensions will be interlaced - all the sample points for a point in time will be recorded at once.
Number of sample points at each time point
Codes to indicate the what part of the targeted reference population it applies to. For example, the normal or therapeutic range.
The style of appointment or patient that has been booked in the slot (not service type).
The set of abnormal coded results for the observation.
Value set of abnormal coded values for the observation
The measure score for this population group, calculated as appropriate for the measure type and scoring method, and based on the contents of the populations defined in the group.
The party(s) that are responsible for covering the payment of this account, and what order should they be applied to the account.
Language code for the human-readable text strings produced by the device (all supported).
The length of time that the first dispense is expected to last.
The way that this statement is intended to be used, to describe an actual running instance of software, a particular product (kind, not instance of software) or a class of implementation (e.g. a desired purchase).
Roles which this practitioner is authorized to perform for the organization.
Roles which this practitioner may perform
Identifier for the List assigned for business purposes outside the context of FHIR.
Resources supporting the reason the risk assessment was performed.
Related identifier to this DocumentManifest. For example, Order numbers, accession numbers, XDW workflow numbers.
The defined billing details in this resource pertain to the given billing code.
Billing codes or product types this definition applies to
The content was developed with a focus and intent of supporting the contexts that are listed. These terms may be used to assist with indexing and searching for appropriate operation definition instances.
The practitioner who was involved in the procedure.
Whether this practitioner's record is in active use.
Administrative Gender - the gender that the contact person is considered to have for administration and record keeping purposes.
The mode of this event declaration - whether application is sender or receiver.
The teardown action will only contain an operation.
One or more teardown operations performed
Part of the name that is acquired as a title due to academic, legal, employment or nobility status, etc. and that appears at the start of the name.
Types of products or services such as visit, specialist visits, emergency, inpatient care, etc.
A link to a record of allergies or intolerances which should be included in the nutrition order.
List of the patient's food and nutrition-related allergies and intolerances
A code indicating why the medication was given.
Regulatory type, e.g. Investigational or Authorized.
The term or period of the values such as 'maximum lifetime benefit' or 'maximum annual vistis'.
Categorizes a naming system for easier search by grouping related naming systems.
e.g. driver, provider, patient, bank etc.
Identifier for the designation, or procedure number.
A differential view is expressed relative to the base StructureDefinition - a statement of differences that it applies.
Indicates who or what performed the series.
identical | matching | different | no-rule | custom.
identical | matching | different | custom
A natural language name identifying the capability statement. This name should be usable as an identifier for the module by machine processing applications such as code generation.
Name for this capability statement (computer friendly)
The period during which the activity occurred.
The URL pointing to a FHIR-defined protocol, guideline, orderset or other definition that is adhered to in whole or in part by this ServiceRequest.
Collection of characteristics (attributes).
Specific reference for finding or diagnosis, which may include ruled-out or resolved conditions.
Identification of the facility/location where the Supply was shipped to, as part of the dispense event.
The related resource, such as a library, value set, profile, or other knowledge resource.
A record of a clinical assessment performed to determine what problem(s) may affect the patient and before planning the treatments or management strategies that are best to manage a patient's condition. Assessments are often 1:1 with a clinical consultation / encounter, but this varies greatly depending on the clinical workflow. This resource is called "ClinicalImpression" rather than "ClinicalAssessment" to avoid confusion with the recording of assessment tools such as Apgar score.
FHIRPath expression - must be true or the rule does not apply.
The period of time from the activation of the flag to inactivation of the flag. If the flag is active, the end of the period should be unspecified.
The results of the series of operations required to clean up after all the tests were executed (successfully or otherwise).
The id of the element in the referencing resource that is expected to resolve to this resource.
The person (patient) who needs the nutrition order for an oral diet, nutritional supplement and/or enteral or formula feeding.
The person who requires the diet, formula or nutritional supplement
Concise and clinically contextualized summary conclusion (interpretation/impression) of the diagnostic report.
Clinical conclusion (interpretation) of test results
Start position of the sequence. If the coordinate system is either 0-based or 1-based, then start position is inclusive.
Business identifiers assigned to this communication by the performer or other systems which remain constant as the resource is updated and propagates from server to server.
Display for the code (if value is a code)
The quantity of specimen in the container; may be volume, dimensions, or other appropriate measurements, depending on the specimen type.
Business identifiers assigned to this AllergyIntolerance by the performer or other systems which remain constant as the resource is updated and propagates from server to server.
The comparator is not used on a SimpleQuantity
Details concerning processing and processing steps for the specimen.
An explanation as to why this task is held, failed, was refused, etc.
The role the participant should play in performing the described action.
Type of media involved. Used when the event is about exporting/importing onto media.
Provides a succinct statement of the need for the measure. Usually includes statements pertaining to importance criterion: impact, gap in care, and evidence.
Detailed description of why the measure exists
This subject or group impacted by the event.
Suite of processing notes or additional requirements if the processing has been held.
Processing comments or additional requirements
The path identifies the element and is expressed as a "."-separated list of ancestor elements, beginning with the name of the resource or extension.
Path of the element in the hierarchy of elements
The status of the response. If the evaluation is completed successfully, the status will indicate success. However, in order to complete the evaluation, the engine may require more information. In this case, the status will be data-required, and the response will contain a description of the additional required information. If the evaluation completed successfully, but the engine determines that a potentially more accurate response could be provided if more data was available, the status will be data-requested, and the response will contain a description of the additional requested information.
success | data-requested | data-required | in-progress | failure | entered-in-error
The content was developed with a focus and intent of supporting the contexts that are listed. These terms may be used to assist with indexing and searching for appropriate graph definition instances.
Identifies all people and organizations who are expected to be involved in the care envisioned by this plan.
The clinical context in which the document was prepared.
Unique, human-readable label for this objective of the study.
A list of profiles that represent different use cases supported by the system. For a server, "supported by the system" means the system hosts/produces a set of resources that are conformant to a particular profile, and allows clients that use its services to search using this profile and to find appropriate data. For a client, it means the system will search by this profile and process data according to the guidance implicit in the profile. See further discussion in [Using Profiles](profiling.html#profile-uses).
Flag indicating if the coverage provided is inforce currently if no service date(s) specified or for the whole duration of the service dates.
Indicates the degree of importance associated with the identified issue based on the potential impact on the patient.
If true, the value of this element affects the interpretation of the element or resource that contains it, and the value of the element cannot be ignored. Typically, this is used for status, negation and qualification codes. The effect of this is that the element cannot be ignored by systems: they SHALL either recognize the element and process it, and/or a pre-determination has been made that it is not relevant to their particular system.
If this modifies the meaning of other elements
A code specifying the current state of the order. Generally, this will be active or completed state.
active | on-hold | cancelled | completed | entered-in-error | stopped | draft | unknown
Information about the use of the medicinal product in relation to other therapies described as part of the contraindication.
A medicinal product in a container or package.
The outcome of the procedure - did it resolve reasons for the procedure being performed?
Allows data conveyed by a message to be addressed to a particular person or department when routing to a specific application isn't sufficient.
Intended "real-world" recipient for the data
The entity responsible for deciding what the contents of the list were. Where the list was created by a human, this is the same as the author of the list.
Who and/or what defined the list contents (aka Author)
Number of SOP Instances in Study. This value given may be larger than the number of instance elements this resource contains due to resource availability, security, or other factors. This element should be present if any instance elements are present.
Specifies a preferred order in which to use a set of contacts. ContactPoints with lower rank values are more preferred than those with higher rank values.
Specify preferred order of use (1 = highest)
Specifies the entire address as it should be displayed e.g. on a postal label. This may be provided instead of or as well as the specific parts.
Describes the link to the Device that this DeviceMetric belongs to and that provide information about the location of this DeviceMetric in the containment structure of the parent Device. An example would be a Device that represents a Channel. This reference can be used by a client application to distinguish DeviceMetrics that have the same type, but should be interpreted based on their containment location.
Text that can be used to describe the constraint in messages identifying that the constraint has been violated.
Indicates who performed the immunization event.
Whether this practitioner role record is in active use.
The type of extra detail provided in the value.
The identifier that is used to identify this version of the graph definition when it is referenced in a specification, model, design or instance. This is an arbitrary value managed by the graph definition author and is not expected to be globally unique. For example, it might be a timestamp (e.g. yyyymmdd) if a managed version is not available. There is also no expectation that versions can be placed in a lexicographical sequence.
Business version of the graph definition
Canonical URL of value set that contains the entire code system.
Canonical URL for value set with entire code system
Whether the parameter is input or output for the module.
General information detailing this substance.
The period of time for which payments have been gathered into this bulk payment for settlement.
The channel on which to report matches to the criteria
Calculated precision if the GQ score threshold was set to "score" field value.
Transaction status: error, complete, held.
The set of critical coded results for the observation.
Value set of critical coded values for the observation
Specifies the units by which the Contract Valued Item is measured or counted, and quantifies the countable or measurable Contract Valued Item instances.
The vaccine administration event being evaluated.
A free text natural language description of the capability statement from a consumer's perspective. Typically, this is used when the capability statement describes a desired rather than an actual solution, for example as a formal expression of requirements as part of an RFP.
Natural language description of the capability statement
The patient the recommendation(s) are for.
Clinical symptoms and/or signs that are observed or associated with the adverse reaction event.
Clinical symptoms/signs associated with the Event
The code-valued attribute of the filter. The specified path SHALL be a FHIRPath resolveable on the specified type of the DataRequirement, and SHALL consist only of identifiers, constant indexers, and .resolve(). The path is allowed to contain qualifiers (.) to traverse sub-elements, as well as indexers ([x]) to traverse multiple-cardinality sub-elements (see the [Simple FHIRPath Profile](fhirpath.html#simple) for full details). Note that the index must be an integer constant. The path must resolve to an element of type code, Coding, or CodeableConcept.
The jurisdiction to which the deviceIdentifier applies.
The name of the organization or individual that published the operation definition.
Descriptive topics related to the content of the activity. Topics provide a high-level categorization of the activity that can be useful for filtering and searching.
Information about the system's restful capabilities that apply across all applications, such as security.
This element is for traceability of why the element was created and why the constraints exist as they do. This may be used to point to source materials or specifications that drove the structure of this element.
Unique instance identifiers assigned to a device by manufacturers other organizations or owners.
A free text natural language description of the concept map from a consumer's perspective.
Natural language description of the concept map
A natural language name identifying the activity definition. This name should be usable as an identifier for the module by machine processing applications such as code generation.
Name for this activity definition (computer friendly)
Details of what's changed (or not changed).
A structured set of questions intended to guide the collection of answers from end-users. Questionnaires provide detailed control over order, presentation, phraseology and grouping to allow coherent, consistent data collection.
Indicates whether this operation or named query can be invoked at the system level (e.g. without needing to choose a resource type for the context).
Whether this hospitalization is a readmission and why if known.
The type of hospital re-admission that has occurred (if any). If the value is absent, then this is not identified as a readmission
Business identifiers assigned to this flag by the performer or other systems which remain constant as the resource is updated and propagates from server to server.
The amount of the nutritional supplement to be given.
To indicate if this proces is commercially confidential.
Trade name of the device, where applicable.
The insurer assigned ID for the Subscriber.
How the medication is to be used by the patient or administered by the caregiver
Other resources that pertain to this communication and to which this communication should be associated.
Resources that pertain to this communication
If this code is found in an instance, then the rule applies.
e.g. LOINC or SNOMED CT code, etc. in the content
Label for the page intended for human display.
Reference to the id of the pack this resource appears in.
When this Contract Provision was issued.
The type of revenue or cost center providing the product and/or service.
A Pointer to another Sequence entity as reference sequence.
The stage in the progression of a therapy from initial experimental use in humans in clinical trials to post-market evaluation.
n-a | early-phase-1 | phase-1 | phase-1-phase-2 | phase-2 | phase-2-phase-3 | phase-3 | phase-4
Indicates how quickly the request should be addressed with respect to other requests.
A Boolean value to indicate that this compartment definition is authored for testing purposes (or education/evaluation/marketing) and is not intended to be used for genuine usage.
Whether additional slices are allowed or not. When the slices are ordered, profile authors can also say that additional slices are only allowed at the end.
The kind of staging, such as pathological or clinical staging.
A legal or geographic region in which the terminology capabilities is intended to be used.
Intended jurisdiction for terminology capabilities (if applicable)
Target entity type about which the term may be concerned.
Technical endpoints providing access to services operated for the specific healthcare services defined at this resource.
Technical endpoints providing access to services operated for the location
The recommended maximum wear period for the lens.
An identifier assigned to a drug at the point of manufacturing and repackaging (at the package or pallet level), sufficient to facilitate the identification, validation, authentication, and tracking and tracking of drugs.
Identifier assigned to a drug at the time of manufacture
The legal framework against which this authorization is granted.
A series of operations required to clean up after all the tests are executed (successfully or otherwise).
A natural language name identifying the example scenario. This name should be usable as an identifier for the module by machine processing applications such as code generation.
Name for this example scenario (computer friendly)
The date when the Medicinal Product is placed on the market by the Marketing Authorisation Holder (or where applicable, the manufacturer/distributor) in a country and/or jurisdiction shall be provided A complete date consisting of day, month and year shall be specified using the ISO 8601 date format NOTE “Placed on the market” refers to the release of the Medicinal Product into the distribution chain.
The status of the RiskAssessment, using the same statuses as an Observation.
A provider issued list of services and products provided, or to be provided, to a patient which is provided to an insurer for payment recovery.
The name of the organization or individual that published the measure.
Reference to the formal meaning of the property. One possible source of meaning is the [Concept Properties](codesystem-concept-properties.html) code system.
A reference to a Bundle containing the Resources that were used in the calculation of this measure.
What data was used to calculate the measure score
The status of this example scenario. Enables tracking the life-cycle of the content.
The status of this code system. Enables tracking the life-cycle of the content.
Named context for field, if a field is specified.
The period during which the measure content was or is planned to be in active use.
The time period and frequency at which the diet should be given. The diet should be given for the combination of all schedules if more than one schedule is present.
The Absolute URL for the resource. The fullUrl SHALL NOT disagree with the id in the resource - i.e. if the fullUrl is not a urn:uuid, the URL shall be version-independent URL consistent with the Resource.id. The fullUrl is a version independent reference to the resource. The fullUrl element SHALL have a value except that: * fullUrl can be empty on a POST (although it does not need to when specifying a temporary id for reference in the bundle) * Results from operations might involve resources that are not identified.
URI for resource (Absolute URL server address or URI for UUID/OID)
An encounter that provides additional context in which this request is made.
A summary of the events of interest that have occurred, such as when the dispense was verified.
The name of the organization or individual that published the naming system.
The number of product units the package would contain if fully loaded.
Additional diagnostic information about the issue. Typically, this may be a description of how a value is erroneous, or a stack dump to help trace the issue.
Additional diagnostic information about the issue
Identifies all people and organizations who are expected to be involved in the care team.
The total number of concepts in the expansion. If the number of concept nodes in this resource is less than the stated number, then the server can return more using the offset parameter.
A kind of specimen with associated set of requirements.
Guidance specific to the implementation of this operation, such as 'delete is a logical delete' or 'updates are only allowed with version id' or 'creates permitted from pre-authorized certificates only'.
Anything special about operation behavior
Whether the element should be included if a client requests a search with the parameter _summary=true.
A formal identifier that is used to identify this questionnaire when it is represented in other formats, or referenced in a specification, model, design or an instance.
Additional identifier for the questionnaire
The maximum dose per treatment period that can be administered as per the protocol referenced in the clinical trial authorisation.
Completed or terminated care plan whose function is taken by this new care plan.
The validation status of the target (attested; validated; in process; requires revalidation; validation failed; revalidation failed).
attested | validated | in-process | req-revalid | val-fail | reval-fail
The recordedDate represents when this particular AllergyIntolerance record was created in the system, which is often a system-generated date.
Immunization event history and/or evaluation that supports the status and recommendation.
Past immunizations supporting recommendation
Indicates what types of messages may be sent as an application-level response to this message.
Indicates current operational state of the device. For example: On, Off, Standby, etc.
The content of the library as an Attachment. The content may be a reference to a url, or may be directly embedded as a base-64 string. Either way, the contentType of the attachment determines how to interpret the content.
Contents of the library, either embedded or referenced
The name of the organization or individual that published the terminology capabilities.
A code that identifies the type of context being specified by this usage context.
The organization that is primarily responsible for this Encounter's services. This MAY be the same as the organization on the Patient record, however it could be different, such as if the actor performing the services was from an external organization (which may be billed seperately) for an external consultation. Refer to the example bundle showing an abbreviated set of Encounters for a colonoscopy.
The organization (facility) responsible for this encounter
The position of the questionnaire response within its overall lifecycle.
in-progress | completed | amended | entered-in-error | stopped
While Appointment.comment contains information for internal use, Appointment.patientInstructions is used to capture patient facing information about the Appointment (e.g. please bring your referral or fast from 8pm night before).
Detailed information and instructions for the patient
Longitude. The value domain and the interpretation are the same as for the text of the longitude element in KML (see notes below).
Indicated the rendered service that caused this charge.
Which rendered service is being charged?
The organization attesting to information.
Ordered list of patient diagnosis for which care is sought.
The mime-type to use for RESTful operation in the 'Accept' header.
Mime type to accept in the payload of the response, with charset etc.
Whether multiple values are allowed for each time the parameter exists. Values are separated by commas, and the parameter matches if any of the values match.
Allow multiple values per parameter (or)
Formula feeding instruction as structured data
Comments on the slot to describe any extended information. Such as custom constraints on the slot.
Specifies how many (or how much) of the items there are in this Medication. For example, 250 mg per tablet. This is expressed as a ratio where the numerator is 250mg and the denominator is 1 tablet.
A reference to an ActivityDefinition that describes the action to be taken in detail, or a PlanDefinition that describes a series of actions to be taken.
Description of the activity to be performed
True if the indicated class of service is excluded from the plan, missing or False indicated the service is included in the coverage.
A description of when the locations opening ours are different to normal, e.g. public holiday availability. Succinctly describing all possible exceptions to normal site availability as detailed in the opening hours Times.
The target document of this relationship.
Identifies the outcome at the point when the status of the activity is assessed. For example, the outcome of an education activity could be patient understands (or not).
Textual instructions regarding the light exposure of the specimen prior testing.
The Patient Information as known when the document was published. May be a reference to a version specific, or contained.
The current focus of the user's session. Common values are a reference to a Patient, Encounter, ImagingStudy, etc.
These resources do not have an independent existence apart from the resource that contains them - they cannot be identified independently, and nor can they have their own independent transaction scope.
An absolute URI that is used to identify this compartment definition when it is referenced in a specification, model, design or an instance; also called its canonical identifier. This SHOULD be globally unique and SHOULD be a literal address at which at which an authoritative instance of this compartment definition is (or will be) published. This URL can be the target of a canonical reference. It SHALL remain the same when the compartment definition is stored on different servers.
Canonical identifier for this compartment definition, represented as a URI (globally unique)
The URL pointing to a FHIR-defined Contract Definition that is adhered to in whole or part by this Contract.
The gestational age at which this reference range is applicable, in the context of pregnancy.
Applicable gestational age range, if relevant
The period during this EpisodeOfCare that the specific status applied.
Duration the EpisodeOfCare was in the specified status
Identifies who is responsible for the information in the composition, not necessarily who typed it in.
Who and/or what authored the composition
Idenifying type for this part of the name (e.g. strength part).
Indicates the category of the observation generation process. A DeviceMetric can be for example a setting, measurement, or calculation.
measurement | setting | calculation | unspecified
Describes why the event occurred in coded or textual form.
The name of the moiety shall be provided.
The number of frames in a photo. This is used with a multi-page fax, or an imaging acquisition context that takes multiple slices in a single image, or an animated gif. If there is more than one frame, this SHALL have a value in order to alert interface software that a multi-frame capable rendering widget is required.
The part of a name that links to the genealogy. In some cultures (e.g. Eritrea) the family name of a son is the first name of his father.
Identifies a code system that is supported by the server. If there is a no code system URL, then this declares the general assumptions a client can make about support for any CodeSystem resource.
Contact for the organization for a certain purpose.
A human-readable narrative that contains a summary of the resource and can be used to represent the content of the resource to a human. The narrative need not encode all the structured data, but is required to contain sufficient detail to make it "clinically safe" for a human to just read the narrative. Resource definitions may define what content should be represented in the narrative to ensure clinical safety.
Text summary of the resource, for human interpretation
The quantity of specimen collected; for instance the volume of a blood sample, or the physical measurement of an anatomic pathology sample.
A legal or geographic region in which the structure definition is intended to be used.
Intended jurisdiction for structure definition (if applicable)
Links to Provenance records for past versions of this Task that identify key state transitions or updates that are likely to be relevant to a user looking at the current version of the task.
Whether this is an input or an output parameter.
XPath or JSONPath to evaluate against the fixture body. When variables are defined, only one of either expression, headerField or path must be specified.
XPath or JSONPath against the fixture body
The actual data of the message - a reference to the root/focus class of the event.
The anatomic structures examined. See DICOM Part 16 Annex L (http://dicom.nema.org/medical/dicom/current/output/chtml/part16/chapter_L.html) for DICOM to SNOMED-CT mappings. The bodySite may indicate the laterality of body part imaged; if so, it shall be consistent with any content of ImagingStudy.series.laterality.
The id of the clause or question text of the offer in the referenced questionnaire/response.
Legally enforceable, formally recorded unilateral or bilateral directive i.e., a policy or agreement.
An absolute base URL for the implementation.
A physical, countable instance of an item, for example one box or one unit.
Coverage (read depth or depth) is the average number of reads representing a given nucleotide in the reconstructed sequence.
Average number of reads representing a given nucleotide in the reconstructed sequence
Indicates the type of function performed at the location.
Identifies the type of library such as a Logic Library, Model Definition, Asset Collection, or Module Definition.
logic-library | model-definition | asset-collection | module-definition
A free text natural language description of the code system from a consumer's perspective.
Natural language description of the code system
Length if the receiver's reliable messaging cache in minutes (if a receiver) or how long the cache length on the receiver should be (if a sender).
Id of the clause or question text related to the context of this valuedItem in the referenced form or QuestionnaireResponse.
A list of the messaging transport protocol(s) identifiers, supported by this endpoint.
Indicates who or what performed the series and how they were involved.
Given names (not always 'first'). Includes middle names
The period of time that the slots that are attached to this Schedule resource cover (even if none exist). These cover the amount of time that an organization's planning horizon; the interval for which they are currently accepting appointments. This does not define a "template" for planning outside these dates.
The nutrient that is being modified such as carbohydrate or sodium.
A list of the patch formats supported by this implementation using their content types.
A natural language name identifying the structure map. This name should be usable as an identifier for the module by machine processing applications such as code generation.
Name for this structure map (computer friendly)
A formally or informally recognized grouping of people or organizations formed for the purpose of achieving some form of collective action. Includes companies, institutions, corporations, departments, community groups, healthcare practice groups, payer/insurer, etc.
The location where the item is phisically located.
The priority of the appointment. Can be used to make informed decisions if needing to re-prioritize appointments. (The iCal Standard specifies 0 as undefined, 1 as highest, 9 as lowest priority).
Used to make informed decisions if needing to re-prioritize
The version of the IG that is depended on, when the correct version is required to understand the IG correctly.
The nature of the relationship between the patient and the contact person.
A mode or state of being that describes the nature of the specimen.
The path to the element to be customized. This is the path on the resource that will hold the result of the calculation defined by the expression.
The path to the element to be set dynamically
Organization that is the custodian of the patient record.
Benefits and optionally current balances by Category or Service.
A time period defined by a start and end date and optionally time.
Time range defined by start and end date/time
Defines the outputs of the action, if any.
Condition or observation that supports why the medication was ordered.
Condition or observation that supports why the prescription is being written
The actual cost value. (some of the costs may be represented as percentages rather than currency, e.g. 10% coinsurance).
Is this always available? (hence times are irrelevant) e.g. 24 hour service.
Can convey versions of multiple systems in situations where a message passes through multiple hands.
The text of the annotation in markdown format.
The annotation - text content (as markdown)
A plan, proposal or order that is fulfilled in whole or in part by this event. For example, a MedicationRequest may require a patient to have laboratory test performed before it is dispensed.
A coded value that represents the technical details of the usage of this endpoint, such as what WSDLs should be used in what way. (e.g. XDS.b/DICOM/cds-hook).
Protocol/Profile/Standard to be used with this endpoint connection
An alternate organizational reference to the case or file to which this particular claim pertains - e.g. Property/Casualty insurer claim # or Workers Compensation case # .
An integer with a value that is positive (e.g. >0)
The TestScript.ruleset this assert will evaluate.
A pointer to an Observation containing variant information.
A Boolean value to indicate that this structure map is authored for testing purposes (or education/evaluation/marketing) and is not intended to be used for genuine usage.
Assessment whether this event was of real importance.
Additional information about how to use this operation or named query.
A record of a device being used by a patient where the record is the result of a report from the patient or another clinician.
Describes the context of the request group, if any.
Encounter or Episode for the request group
Indicates the level of authority/intentionality associated with the request and where the request fits into the workflow chain.
A legal or geographic region in which the library is intended to be used.
Intended jurisdiction for library (if applicable)
Another Encounter of which this encounter is a part of (administratively or in time).
Another Encounter this encounter is part of
A legal or geographic region in which the value set is intended to be used.
Intended jurisdiction for value set (if applicable)
The preferred name to be used when reporting the results of this observation.
The duration of the recording in seconds - for audio and video.
A short, descriptive, user-friendly title for the message definition.
Name for this message definition (human friendly)
Link to another patient resource that concerns the same actual person
The manufactured item as contained in the packaged medicinal product.
A natural language name identifying the naming system. This name should be usable as an identifier for the module by machine processing applications such as code generation.
Name for this naming system (computer friendly)
Explanation of why this capability statement is needed and why it has been designed as it has.
Why this capability statement is defined
The manufacture or preparation date and time. Times are necessary for several examples - for example biologically derived products, prepared or coumpounded medication, rapidly decaying isotopes.
The manufacture or preparation date and time
The final score (percentage of tests passed) resulting from the execution of the TestScript.
The number of false positives where the non-REF alleles in the Truth and Query Call Sets match (i.e. cases where the truth is 1/1 and the query is 0/1 or similar).
False positives where the non-REF alleles in the Truth and Query Call Sets match
food | medication | environment | biologic
Additional execution information (transaction/batch/history)
Indication if a dose is considered to be subpotent. By default, a dose should be considered to be potent.
A formal identifier that is used to identify this concept map when it is represented in other formats, or referenced in a specification, model, design or an instance.
Additional identifier for the concept map
An identifier for the target resource. This is used when there is no way to reference the other resource directly, either because the entity it represents is not available through a FHIR server, or because there is no way for the author of the resource to convert a known identifier to an actual location. There is no requirement that a Reference.identifier point to something that is actually exposed as a FHIR instance, but it SHALL point to a business concept that would be expected to be exposed as a FHIR instance, and that instance would need to be of a FHIR resource type allowed by the reference.
Logical reference, when literal reference is not known
The entity (e.g. person, organization, clinical information system, or device) which was the source of the communication.
A reference to a value set containing a list of codes representing permitted answers for a "choice" or "open-choice" question.
Indicates the level of authority/intentionality associated with the care plan and where the care plan fits into the workflow chain.
Indicates another resource whose existence justifies permitting or not permitting this action.
Describes the type of outcome from the adverse event.
resolved | recovering | ongoing | resolvedWithSequelae | fatal | unknown
Identifies the change (or lack of change) at the point when the status of the goal is assessed.
What result was achieved regarding the goal?
usual | official | temp | secondary | old (If known)
Descriptive topics related to the content of the measure. Topics provide a high-level categorization grouping types of measures that can be useful for filtering and searching.
The category of the measure, such as Education, Treatment, Assessment, etc.
Contact details for a human to contact about the subscription. The primary use of this for system administrator troubleshooting.
Contact details for source (e.g. troubleshooting)
The numeric identifier of this series in the study.
How the party participates in the offer.
A material substance originating from a biological entity intended to be transplanted or infused into another (possibly the same) biological entity.
Text, attachment(s), or resource(s) that was communicated to the recipient.
A list of profiles (references to [StructureDefinition] resources) that this resource claims to conform to. The URL is a reference to [StructureDefinition.url].
Profiles this resource claims to conform to
The patient, location, group, organization, or practitioner etc. this is about record this flag is associated with.
The expected type of the target of the reference. If both Reference.type and Reference.reference are populated and Reference.reference is a FHIR URL, both SHALL be consistent. The type is the Canonical URL of Resource Definition that is the type this reference refers to. References are URLs that are relative to http://hl7.org/fhir/StructureDefinition/ e.g. "Patient" is a reference to http://hl7.org/fhir/StructureDefinition/Patient. Absolute URLs are only allowed for logical models (and can only be used in references in logical models, not resources).
Type the reference refers to (e.g. "Patient")
The identifier that is used to identify this version of the activity definition when it is referenced in a specification, model, design or instance. This is an arbitrary value managed by the activity definition author and is not expected to be globally unique. For example, it might be a timestamp (e.g. yyyymmdd) if a managed version is not available. There is also no expectation that versions can be placed in a lexicographical sequence. To provide a version consistent with the Decision Support Service specification, use the format Major.Minor.Revision (e.g. 1.0.0). For more information on versioning knowledge assets, refer to the Decision Support Service specification. Note that a version is required for non-experimental active assets.
Business version of the activity definition
When a measure includes multiple stratifiers, there will be a stratifier group for each stratifier defined by the measure.
The date on which the related person was born.
Address(es) of the practitioner that are not role specific (typically home address). Work addresses are not typically entered in this property as they are usually role dependent.
Address(es) of the practitioner that are not role specific (typically home address)
Insurance plans, coverage extensions, pre-authorizations and/or pre-determinations that may be needed for delivering the requested service.
Identifiers assigned to this event performer or other systems.
This element refers to a List of subject level MeasureReport resources, one for each subject in this population in this stratum.
Totals for amounts submitted, co-pays, benefits payable etc.
The person who created the explanation of benefit.
Defines observation requirements for the action to be performed, such as body weight or surface area.
What observations are required to perform this action
The trigger element defines when the event occurs.
The date (and optionally time) when the implementation guide was published. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the implementation guide changes.
Specific category assigned to the medication (e.g. anti-infective, anti-hypertensive, antibiotic, etc).
Specific category assigned to the medication
The identifier that is used to identify this version of the value set when it is referenced in a specification, model, design or instance. This is an arbitrary value managed by the value set author and is not expected to be globally unique. For example, it might be a timestamp (e.g. yyyymmdd) if a managed version is not available. There is also no expectation that versions can be placed in a lexicographical sequence.
A contact detail (e.g. a telephone number or an email address) by which the party may be contacted.
Contact details (telephone, email, etc.) for a contact
The name of the parameter used to allow access to the value of the parameter in evaluation contexts.
Reference range of possible or expected values.
Parties that may or should contribute or have contributed information to the adverse event, which can consist of one or more activities. Such information includes information leading to the decision to perform the activity and how to perform the activity (e.g. consultant), information that the activity itself seeks to reveal (e.g. informant of clinical history), or information about what activity was performed (e.g. informant witness).
Who was involved in the adverse event or the potential adverse event
An absolute URI that is the base structure from which this type is derived, either by specialization or constraint.
Definition that this type is constrained/specialized from
Business identifiers that are specific to this role.
The resource that identifies the actor. To identify actors by type, use group to identify a set of actors by some property they share (e.g. 'admitting officers').
Resource for the actor (or group, by role)
Identifies the source system, application, or software that produced the document manifest.
The location where the encounter takes place.
The content was developed with a focus and intent of supporting the contexts that are listed. These terms may be used to assist with indexing and searching for appropriate value set instances.
When the event definition was approved by publisher
The amount that is being ordered of the indicated item.
The requested amount of the item indicated
The timeframe during which the guarantor accepts responsibility for the account.
Instruct the server not to perform the create if a specified resource already exists. For further information, see the API documentation for ["Conditional Create"](http.html#ccreate). This is just the query portion of the URL - what follows the "?" (not including the "?").
Height of the image in pixels (photo/video).
The content was developed with a focus and intent of supporting the contexts that are listed. These terms may be used to assist with indexing and searching for appropriate search parameter instances.
Specifies a maximum number of results that are required (uses the _count search parameter).
Identity (code or path) or the element/item/ValueSet/text that the map depends on / refers to.
Sub-category for the Contract that distinguishes the kinds of systems that would be interested in the Contract within the context of the Contract's scope.
A packaging item, as a contained for medicine, possibly with other packaging items within.
Financial instrument by which payment information for health care.
A boolean-valued expression that is evaluated in the context of the container of the trigger definition and returns whether or not the trigger fires.
Whether the event triggers (boolean expression)
Captures the reason for the current state of the ClinicalImpression.
Specific text or code for finding or diagnosis, which may include ruled-out or resolved conditions.
A legal or geographic region in which the capability statement is intended to be used.
Intended jurisdiction for capability statement (if applicable)
Related artifacts for a knowledge resource
May be used to represent additional information that is not part of the basic definition of the element. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension.
Additional content defined by implementations
A natural language name identifying the questionnaire. This name should be usable as an identifier for the module by machine processing applications such as code generation.
Name for this questionnaire (computer friendly)
The date/time that the resource was modified on the server.
A set of profiles that all resources covered by this implementation guide must conform to.
The encounter that is the context in which this list was created.
The kind of structure being represented by the body structure at `BodyStructure.location`. This can define both normal and abnormal morphologies.
The financial cost center permits the tracking of charge attribution.
Organization that has ownership of the (potential, future) revenue
Server adds CORS headers when responding to requests - this enables Javascript applications to use the server.
Adds CORS Headers (http://enable-cors.org/)
Structural unit composed of a nucleic acid molecule which controls its own replication through the interaction of specific proteins at one or more origins of replication ([SO:0000340](http://www.sequenceontology.org/browser/current_svn/term/SO:0000340)).
A Person, Location, HealthcareService, or Device that is participating in the appointment.
Person, Location, HealthcareService, or Device
A reference from one resource to another.
Related identifiers or resources associated with the DocumentManifest.
Indicates a meaning for the group. This can be as simple as a unique identifier, or it can establish meaning in a broader context by drawing from a terminology, allowing groups to be correlated across measures.
The MessageDefinition that is the basis for the contents of this resource.
Reason for the dtatus of the Device availability.
online | paused | standby | offline | not-ready | transduc-discon | hw-discon | off
A copyright statement relating to the charge item definition and/or its contents. Copyright statements are generally legal restrictions on the use and publishing of the charge item definition.
The period during which the plan definition content was or is planned to be in active use.
When the plan definition is expected to be used
Human readable text describing the package.
The HealthcareService is not available during this period of time due to the provided reason.
Where applicable, the weight can be specified using a numerical value and its unit of measurement The unit of measurement shall be specified in accordance with ISO 11240 and the resulting terminology The symbol and the symbol identifier shall be used.
Who or what initiated the action and has responsibility for its activation.
Supporting evidence / manifestations that are the basis of the Condition's verification status, such as evidence that confirmed or refuted the condition.
The formal definition of the concept. The code system resource does not make formal definitions required, because of the prevalence of legacy systems. However, they are highly recommended, as without them there is no formal meaning associated with the concept.
Documentation for this instance of data.
The individual for whom the evaluation is being done.
Identifies the patient or group whose intended care is handled by the team.
Date of an accident which these services are addressing.
Specifies clinical/business/etc. metadata that can be used to retrieve, index and/or categorize an artifact. This metadata can either be specific to the applicable population (e.g., age category, DRG) or the specific context of care (e.g., venue, care setting, provider of care).
Describes the context of use for a conformance or knowledge resource
The EventDefinition resource provides a reusable description of when a particular event can occur.
The time period and frequency at which the enteral formula should be delivered to the patient.
The profile of the required data, specified as the uri of the profile definition.
A url for the artifact that can be followed to access the actual content.
The desired performer for doing the requested service. For example, the surgeon, dermatopathologist, endoscopist, etc.
Associated or related medications. For example, if the medication is a branded product (e.g. Crestor), this is the Therapeutic Moeity (e.g. Rosuvastatin) or if this is a generic medication (e.g. Rosuvastatin), this would link to a branded product (e.g. Crestor).
A medication resource that is associated with this medication
The date when the medication statement was asserted by the information source.
The actual data of the attachment - a sequence of bytes, base64 encoded.
The provider or software application that performed the assessment.
The Participating Organization provides/performs the role(s) defined by the code to the Primary Organization (e.g. providing services or is a member of).
Organization that provides/performs the role (e.g. providing services or is a member of)
The detailed description of a substance, typically at a level beyond what is used for prescribing.
The Questionnaire that defines and organizes the questions for which answers are being provided.
An expression that returns true or false, indicating whether the condition is satisfied. When using FHIRPath expressions, the %context evironment variable must be replaced at runtime with the ChargeItem resource to which this definition is applied.
This component contains the house number, apartment number, street name, street direction, P.O. Box number, delivery hints, and similar address information.
Street name, number, direction & P.O. Box etc.
Encounter during which the condition was first asserted.
Encounter or episode when condition first asserted
Contact details for an organization or a particular human that is responsible for the device.
Details for human/organization for support
The path by which the vaccine product is taken into the body.
Code indicating: Submitted, Co-Pay, deductible, eligible, benefit, tax, etc.
Adjudication category such as submitted, co-pay, eligible, benefit, etc.
Canonical URL for a GraphDefinition. If a URL is provided, it is the canonical URL for a [GraphDefinition] that it controls what resources are to be added to the bundle when building the document. The GraphDefinition can also specify profiles that apply to the various resources.
General specifications for this substance, including how it is related to other substances.
The value and associated unit of the low bound (inclusive) of the reference range.
Low bound of reference range, if relevant
The current state of the ChargeItemDefinition.
Dose form as manufactured and before any transformation into the pharmaceutical product.
A short, descriptive, user-friendly title for the event definition.
Name for this event definition (human friendly)
Indicates an action that has been taken or is committed to reduce or eliminate the likelihood of the risk identified by the detected issue from manifesting. Can also reflect an observation of known mitigating factors that may reduce/eliminate the need for any action.
Identification of the underlying physiological mechanism for the reaction risk.
allergy | intolerance - Underlying mechanism (if known)
Free text dosage can be used for cases where the dosage administered is too complex to code. When coded dosage is present, the free text dosage may still be present for display to humans. The dosage instructions should reflect the dosage of the medication that was administered.
The upper limit of detection of the measured points. This is needed if any of the data points have the value "U" (higher than detection limit).
The unique identifier assigned to the substance representing the moiety based on the ISO 11238 substance controlled vocabulary.
A suite of updated or additional Coverages from the Insurer.
Describes the severity of the adverse event, in relation to the subject. Contrast to AdverseEvent.serious - a severe rash might not be serious, but a mild heart problem is.
The event after which the goal should begin being pursued.
Indicates another resource whose existence justifies this communication.
Coded indication of the cause for the event - indicates a reason for the occurrence of the event that is a focus of this message.
A legal or geographic region in which the event definition is intended to be used.
Intended jurisdiction for event definition (if applicable)
Id of the read in this external repository.
The policy(s) which constitute this insurance coverage.
Who performed the medication administration and what they did
Factor overriding the factor determined by the rules associated with the code.
Extra information about the withdrawal period.
Describes a comparison of an immunization event against published recommendations to determine if the administration is "valid" in relation to those recommendations.
The period that the member was in the group, if known.
Measurements and simple assertions made about a patient, device or other subject.
The status of this naming system. Enables tracking the life-cycle of the content.
When the accident occurred see information codes see information codes
An order, proposal or plan fulfilled in whole or in part by this Communication.
Search parameters that are supported for searching all resources for implementations to support and/or make use of - either references to ones defined in the specification, or additional ones defined for/by the implementation.
Search parameters for searching all resources
The name of the organization or individual that published the code system.
Manufacturer of the item (Note that this should be named "manufacturer" but it currently causes technical issues).
This list of codes represents the main clinical acts, such as a colonoscopy or an appendectomy, being documented. In some cases, the event is inherent in the type code, such as a "History and Physical Report" in which the procedure being documented is necessarily a "History and Physical" act.
A copyright statement relating to the value set and/or its contents. Copyright statements are generally legal restrictions on the use and publishing of the value set.
A sample value for this element demonstrating the type of information that would typically be found in the element.
The TestScript.ruleset id value this assert will evaluate.
The location(s) at which this practitioner provides care.
A code representing the patient or other source's judgment about the state of the medication used that this statement is about. Generally this will be active or completed.
active | completed | entered-in-error | intended | stopped | on-hold | unknown | not-taken
A set of information summarized from a list of other resources.
The URL pointing to a FHIR-defined protocol, guideline, orderset or other definition that is adhered to in whole or in part by this Communication.
A URI that defines where the expression is found.
The date/time that the bundle was assembled - i.e. when the resources were placed in the bundle.
Identifies who is responsible for the information in this section, not necessarily who typed it in.
Will generally be set to show that the administration has been completed. For some long running administrations such as infusions, it is possible for an administration to be started but not completed or it may be paused while some other process is under way.
in-progress | not-done | on-hold | completed | entered-in-error | stopped | unknown
The fhirpath location(s) within the resource that was validated.
An indicator of the intended usage for the supplemental data element. Supplemental data indicates the data is additional information requested to augment the measure information. Risk adjustment factor indicates the data is additional information used to calculate risk adjustment factors when applying a risk model to the measure calculation.
supplemental-data | risk-adjustment-factor
registered | available | cancelled | entered-in-error | unknown
The members of the team who provided the overall service as well as their role and whether responsible and qualifications.
Start position of the window on the reference sequence. If the coordinate system is either 0-based or 1-based, then start position is inclusive.
Start position of the window on the reference sequence
Contraindication for the medicinal product.
Identifier of the material presented to the patient.
Educational material document identifier
preparation | in-progress | not-done | suspended | aborted | completed | entered-in-error | unknown
The providers who are authorized for the services rendered to the patient.
The physical type of the container of the medicine.
The type of measure report. This may be an individual report, which provides the score for the measure for an individual member of the population; a subject-listing, which returns the list of members that meet the various criteria in the measure; a summary report, which returns a population count for each of the criteria in the measure; or a data-collection, which enables the MeasureReport to be used to exchange the data-of-interest for a quality measure.
individual | subject-list | summary | data-collection
Information about the specific installation that this terminology capability statement relates to.
The minimum volume to be conditioned in the container.
A simple summary of a planned activity suitable for a general care plan system (e.g. form driven) that doesn't know about specific resources such as procedure etc.
The request takes the place of the referenced completed or terminated request(s).
The value of the measured amount. The value includes an implicit precision in the presentation of the value.
Numerical value (with implicit precision)
Specified minimum cardinality for the element. This is optional; if present, it acts an implicit check on the input content.
The criteria for the supplemental data. This is typically the name of a valid expression defined within a referenced library, but it may also be a path to a specific data element. The criteria defines the data to be returned for this element.
Expression describing additional data to be reported
An interaction between a patient and healthcare provider(s) for the purpose of providing healthcare service(s) or assessing the health status of a patient.
Contact details that are specific to the role/location/service.
The date when a suspended the marketing or the marketing authorization of the product is anticipated to be restored.
Code specifying the type of source where event originated.
The type of source where event originated
Name of the location as used by humans. Does not need to be unique.
A natural language name identifying the library. This name should be usable as an identifier for the module by machine processing applications such as code generation.
Name for this library (computer friendly)
The encounter or episode of care that establishes the context for this event.
Encounter / Episode associated with event
Reference to the profile to be used for validation.
A code specifying which characteristic of the medicine is being described (for example, colour, shape, imprint).
Code specifying the type of characteristic of medication
The temperature interval for this set of handling instructions.
An expression that specifies the criteria for the population, typically the name of an expression in a library.
The criteria that defines this population
A formal identifier that is used to identify this message definition when it is represented in other formats, or referenced in a specification, model, design or an instance.
Primary key for the message definition on a given server
Organization that issued/manages the identifier.
Organization that issued id (may be just text)
This resource provides the insurance enrollment details to the insurer regarding a specified coverage.
The amount or quantity to provide as part of the first dispense.
Reference identifier of reference sequence submitted to NCBI. It must match the type in the Sequence.type field. For example, the prefix, “NG_” identifies reference sequence for genes, “NM_” for messenger RNA transcripts, and “NP_” for amino acid sequences.
The human readable description of this stratifier criteria.
The human readable description of this stratifier
Level of assurance that this link is associated with the target resource.
The name of the organization or individual that published the implementation guide.
The desired performer for doing the diagnostic testing.
External identifier - FHIR will generate its own internal identifiers (probably URLs) which do not need to be explicitly managed by the resource. The identifier here is one that would be used by another non-FHIR system - for example an automated medication pump would provide a record each time it operated; an administration while the patient was off the ward might be made with a different system and entered after the event. This identifier is particularly important when these records require updates.
An absolute URI that is used to identify this capability statement when it is referenced in a specification, model, design or an instance; also called its canonical identifier. This SHOULD be globally unique and SHOULD be a literal address at which at which an authoritative instance of this capability statement is (or will be) published. This URL can be the target of a canonical reference. It SHALL remain the same when the capability statement is stored on different servers.
Canonical identifier for this capability statement, represented as a URI (globally unique)
Organization that regulates and issues the qualification.
The payment status, typically paid: payment sent, cleared: payment received.
Whether payment has been sent or cleared
A text note which also contains information about who made the statement and when.
Reference to a canonical URL of another CapabilityStatement that this software implements. This capability statement is a published API description that corresponds to a business service. The server may actually implement a subset of the capability statement it claims to implement, so the capability statement must specify the full capability details.
Canonical URL of another capability statement this implements
Additional narrative about the propensity for the Adverse Reaction, not captured in other fields.
Additional text not captured in other fields
The referral requirements to have access/coverage for this benefit.
A unique identifier assigned to this immunization evaluation record.
Whether this schedule record is in active use or should not be used (such as was entered in error).
Indicates the specific details for the dispense or medication supply part of a medication request (also known as a Medication Prescription or Medication Order). Note that this information is not always sent with the order. There may be in some settings (e.g. hospitals) institutional or system support for completing the dispense details in the pharmacy department.
Who or what the document is about. The document can be about a person, (patient or healthcare practitioner), a device (e.g. a machine) or even a group of subjects (such as a document about a herd of farm animals, or a set of patients that share a common exposure).
Indicates the "level" of actionability associated with the Task, i.e. i+R[9]Cs this a proposed task, a planned task, an actionable task, etc.
unknown | proposal | plan | order | original-order | reflex-order | filler-order | instance-order | option
A type of resource exposed via the restful interface.
If present, indicates that the duration is a range - so to perform the action between [duration] and [durationMax] time length.
named-event | periodic | data-changed | data-added | data-modified | data-removed | data-accessed | data-access-ended
A short, descriptive, user-friendly title for this Contract definition, derivative, or instance in any legal state.t giving additional information about its content.
One or more teardown operations to perform
A digital identity certificate associated with the proxy entity submitting attested information on behalf of the attestation source.
The identifier that is used to identify this version of the example scenario when it is referenced in a specification, model, design or instance. This is an arbitrary value managed by the example scenario author and is not expected to be globally unique. For example, it might be a timestamp (e.g. yyyymmdd) if a managed version is not available. There is also no expectation that versions can be placed in a lexicographical sequence.
Business version of the example scenario
A natural language name identifying the message definition. This name should be usable as an identifier for the module by machine processing applications such as code generation.
Name for this message definition (computer friendly)
Number of digits after decimal separator when the results of this observation are of type Quantity.
Decimal precision of observation quantitative results
A code that indicates how the server supports conditional delete.
not-supported | single | multiple - how conditional delete is supported
The name of an anchor available on the page.
This allows documentation of any distinct behaviors about how the search parameter is used. For example, text matching algorithms.
Reference to another product, e.g. for linking authorised to investigational product.
An organization that is responsible for the provision and ongoing maintenance of the device.
A Boolean value to indicate that this activity definition is authored for testing purposes (or education/evaluation/marketing) and is not intended to be used for genuine usage.
Describes the type of involvement (e.g. transcriptionist, creator etc.). If the invoice has been created automatically, the Participant may be a billing engine or another kind of device.
Type of involevent in creation of this Invoice
Time when specimen was received for processing or testing.
The time when specimen was received for processing
Details about this request that were not represented at all or sufficiently in one of the attributes provided in a class. These may include for example a comment, an instruction, or a note associated with the statement.
Binds to a value set if this element is coded (code, Coding, CodeableConcept, Quantity), or the data types (string, uri).
Indicates the organization, department, etc. with responsibility for the account.
The set of normal coded results for the observation.
Value set of normal coded values for the observation
The patient who either received or did not receive the immunization.
Distinguishes the type of involvement of the performer in the medication administration.
The type of relationship to the related artifact.
documentation | justification | citation | predecessor | successor | derived-from | depends-on | composed-of
A short name or tag for the benefit, for example MED01, or DENT2.
Information about the [ValueSet/$validate-code](valueset-operation-validate-code.html) operation.
May be used to represent additional information that is not part of the basic definition of the resource, and that modifies the understanding of the element that contains it. Usually modifier elements provide negation or qualification. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer is allowed to define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension. Applications processing a resource are required to check for modifier extensions. Modifier extensions SHALL NOT change the meaning of any elements on Resource or DomainResource (including cannot change the meaning of modifierExtension itself).
Benefits and Authorization requirements by Category or Service
Identifies the original context in which this particular care plan was created.
Specifies if regulation allows for changes in the medication when dispensing.
A flag to indicate that the server allows or needs to allow the client to create new identities on the server (that is, the client PUTs to a location where there is no existing resource). Allowing this operation means that the server allows the client to create new identities on the server.
The age at which this reference range is applicable. This is a neonatal age (e.g. number of weeks at term) if the meaning says so.
Indicates the anotomic location on the subject's body where the device was used ( i.e. the target).
In case of Invoice cancellation a reason must be given (entered in error, superseded by corrected invoice etc.).
A [simple subset of FHIRPath](fhirpath.html#simple) limited to element names, repetition indicators and the default child access that identifies one of the elements in the resource that caused this issue to be raised.
Identifier(s) by which this encounter is known.
Key terms to aid in searching for or filtering the study.
The amount calculated for this component.
Monetary amount associated with this component
The total amount for the Invoice may be calculated as the sum of the line items with surcharges/deductions that apply in certain conditions. The priceComponent element can be used to offer transparency to the recipient of the Invoice of how the total price was calculated.
Additional textual instructions for the conservation or transport of the specimen.
General notes about the care plan not covered elsewhere.
Additional comments about the risk assessment.
Indicates when the request group was created.
The content was developed with a focus and intent of supporting the contexts that are listed. These terms may be used to assist with indexing and searching for appropriate implementation guide instances.
A short, descriptive, user-friendly title for the test script.
Name for this test script (human friendly)
E.g. Treatment, dietary, behavioral, etc.
A reference to the request that is fulfilled by this risk assessment.
Which method is used to get sequence quality.
Indicates whether this operation can be invoked on a particular instance of one of the given types.
Type of Invoice depending on domain, realm an usage (eg. internal/external, dental, preliminary).
A list of references from the Insurer to which these services pertain.
Pre-Authorization/Determination Reference
Provides a reason why the expected value in the element Observation.component.value[x] is missing.
Further description of the service as it would be presented to a consumer while searching.
Description of service as presented to a consumer while searching
Identifies who's expected to be involved in the activity.
An OperationOutcome containing hints and warnings produced as part of processing this entry in a batch or transaction.
OperationOutcome with hints and warnings (for batch/transaction)
Whether this is an operation or a named query.
The geographic region in which a health insurance product's benefits apply.
Details of the type of the media - usually, how it was acquired (what type of device). If images sourced from a DICOM system, are wrapped in a Media resource, then this is the modality.
The type of acquisition equipment/process
Property value as a code, e.g., NTP4 (synced to NTP).
The type of individual that is desired or required to perform or not perform the action.
The interval during which the managing organization assumes the defined responsibility.
Interval during responsibility is assumed
The quantity of substance in the unit of presentation, or in the volume (or mass) of the single pharmaceutical product or manufactured item.
Reason the appointment has been scheduled to take place, as specified using information from another resource. When the patient arrives and the encounter begins it may be used as the admission diagnosis. The indication will typically be a Condition (with other resources referenced in the evidence.detail), or a Procedure.
Reason the appointment is to takes place (resource)
Document identifier as assigned by the source of the document. This identifier is specific to this version of the document. This unique identifier may be used elsewhere to identify this version of the document.
The reason (purpose of use), specific to this agent, that was used during the event being recorded.
The minimal content derived from the basal information source at a specific stage in its lifecycle.
Content derived from the basal information
Business identifiers assigned to this clinical impression by the performer or other systems which remain constant as the resource is updated and propagates from server to server.
An absolute URI that is used to identify this value set when it is referenced in a specification, model, design or an instance; also called its canonical identifier. This SHOULD be globally unique and SHOULD be a literal address at which at which an authoritative instance of this value set is (or will be) published. This URL can be the target of a canonical reference. It SHALL remain the same when the value set is stored on different servers.
Canonical identifier for this value set, represented as a URI (globally unique)
Multiple results allowed for this kind of observation.
Visiting or postal addresses for the contact.
An identifier that is unique within the Questionnaire allowing linkage to the equivalent item in a QuestionnaireResponse resource.
The country in which the marketing authorisation has been granted shall be specified It should be specified using the ISO 3166 ‑ 1 alpha-2 code elements.
Characterizes how quickly the planned or in progress communication must be addressed. Includes concepts such as stat, urgent, routine.
When the plan definition was last reviewed
A participant in the test execution, either the execution engine, a client, or a server.
Indicates the current state of the care team.
proposed | active | suspended | inactive | entered-in-error
A text summary of the investigations and the diagnosis.
Id of the variantset in this external repository. The server will understand how to use this id to call for more info about variantsets in external repository.
Id of the variantset that used to call for variantset in repository
Free text or additional instructions or information pertaining to the oral diet.
Instructions or additional information about the oral diet
The value of the high bound of the reference range. The high bound of the reference range endpoint is inclusive of the value (e.g. reference range is >=5 - <=9). If the high bound is omitted, it is assumed to be meaningless (e.g. reference range is >= 2.3).
Notes about the past or intended usage of this identifier.
The individual, location, or organization that is reporting the data.
Indicates the medication order that is being dispensed against.
Medication order that authorizes the dispense
The type of the risk assessment performed.
A pharmaceutical product described in terms of its composition and dose form.
The identifier that is used to identify this version of the terminology capabilities when it is referenced in a specification, model, design or instance. This is an arbitrary value managed by the terminology capabilities author and is not expected to be globally unique. For example, it might be a timestamp (e.g. yyyymmdd) if a managed version is not available. There is also no expectation that versions can be placed in a lexicographical sequence.
Business version of the terminology capabilities
Other resources that pertain to this communication request and to which this communication request should be associated.
Resources that pertain to this communication request
Whether structure this definition describes is abstract or not - that is, whether the structure is not intended to be instantiated. For Resources and Data types, abstract types will never be exchanged between systems.
An absolute URI that is used to identify this implementation guide when it is referenced in a specification, model, design or an instance; also called its canonical identifier. This SHOULD be globally unique and SHOULD be a literal address at which at which an authoritative instance of this implementation guide is (or will be) published. This URL can be the target of a canonical reference. It SHALL remain the same when the implementation guide is stored on different servers.
Canonical identifier for this implementation guide, represented as a URI (globally unique)
Explanatory notes and implementation guidance about the data element, including notes about how to use the data properly, exceptions to proper use, etc. (Note: The text you are reading is specified in ElementDefinition.comment).
The third-tier service adjudications for submitted services.
Whether the organization's record is still in active use.
The base quantity that a measured value of zero represents. In addition, this provides the units of the entire measurement series.
Including possibly Data Carrier Identifier.
Indication of whether this ingredient affects the therapeutic action of the drug.
A shared identifier common to all requests that were authorized more or less simultaneously by a single author, representing the identifier of the requisition, prescription or similar form.
Expressions that describe applicability criteria for the priceComponent.
Conditions under which the priceComponent is applicable
Where applicable, the image can be provided The format of the image attachment shall be specified by regional implementations.
A richer description of the benefit, for example 'DENT2 covers 100% of basic, 50% of major but exclused Ortho, Implants and Costmetic services'.
Description of the benefit or services covered
A boolean flag indicating whether a prior authorization or pre-authorization is required prior to actual service delivery.
How the resource reference is interpreted when testing consent restrictions.
instance | related | dependents | authoredby
Represents a defined collection of entities that may be discussed or acted upon collectively but which are not expected to act collectively, and are not formally or legally recognized; i.e. a collection of entities that isn't an Organization.
A copyright statement relating to the message definition and/or its contents. Copyright statements are generally legal restrictions on the use and publishing of the message definition.
String of characters used to identify a name or a resource
The category of claim, e.g, oral, pharmacy, vision, institutional, professional.
The status of the subscription, which marks the server state for managing the subscription.
The status of this terminology capabilities. Enables tracking the life-cycle of the content.
A free text natural language description of the event definition from a consumer's perspective.
Natural language description of the event definition
A reference to an application-usable description of the identity that is represented by the signature.
Usage pattern including the number of times that the device may be used.
A container for slots of time that may be available for booking appointments.
A resource that includes narrative, extensions, and contained resources.
The list of Resources that consist of the parts of this manifest.
Sequence in which the items appear on the invoice.
Dental, Vision, Medical, Pharmacy, Rehab etc.
A code that defines the specific type of packaging that the medication can be found in (e.g. blister sleeve, tube, bottle).
A code that defines the specific type of packaging that the medication can be found in
The identifier that is used to identify this version of the operation definition when it is referenced in a specification, model, design or instance. This is an arbitrary value managed by the operation definition author and is not expected to be globally unique. For example, it might be a timestamp (e.g. yyyymmdd) if a managed version is not available. There is also no expectation that versions can be placed in a lexicographical sequence.
Business version of the operation definition
Defines the kind of structure that this definition is describing.
primitive-type | complex-type | resource | logical
The mime-type to use for RESTful operation in the 'Content-Type' header.
Mime type of the request payload contents, with charset etc.
A legal or geographic region in which the graph definition is intended to be used.
Intended jurisdiction for graph definition (if applicable)
A property defines an additional slot through which additional information can be provided about a concept.
A formal identifier that is used to identify this test script when it is represented in other formats, or referenced in a specification, model, design or an instance.
Additional identifier for the test script
A relative reference to a DNA strand based on gene orientation. The strand that contains the open reading frame of the gene is the "sense" strand, and the opposite complementary strand is the "antisense" strand.
Describes the medication dosage information details e.g. dose, rate, site, route, etc.
Time period when the contact point was/is in use.
An explanatory or alternate title for the activity definition giving additional information about its content.
Subordinate title of the activity definition
A name associated with the contact person.
Identifier associated with the package/container (usually a label affixed directly).
The date and time that this version of the report was made available to providers, typically after the report was reviewed and verified.
A friendly name that this endpoint can be referred to with.
A name that this endpoint can be identified by
Used for examplefor Out of Formulary, or any specifics.
Additional characteristics of the catalog entry
Comments made about the invoice by the issuer, subject or other participants.
A short, descriptive, user-friendly title for the value set.
Name for this value set (human friendly)
A reference to a Library resource containing any formal logic used by the activity definition.
Financial instrument which may be used to reimburse or pay for health care products and services.
Indicates how quickly the Task should be addressed with respect to other requests.
A link to a resource representing the person or set of individuals to whom the medication will be given.
An allele is one of a set of coexisting sequence variants of a gene ([SO:0001023](http://www.sequenceontology.org/browser/current_svn/term/SO:0001023)). Nucleotide(s)/amino acids from start position of sequence to stop position of sequence on the positive (+) strand of the observed sequence. When the sequence type is DNA, it should be the sequence on the positive (+) strand. This will lay in the range between variant.start and variant.end.
The method for sequencing, for example, chip information.
The order, proposal or plan that is fulfilled in whole or in part by this QuestionnaireResponse. For example, a ServiceRequest seeking an intake assessment or a decision support recommendation to assess for post-partum depression.
Request fulfilled by this QuestionnaireResponse
Where this search parameter is originally defined. If a derivedFrom is provided, then the details in the search parameter must be consistent with the definition from which it is defined. i.e. the parameter should have the same meaning, and (usually) the functionality should be a proper subset of the underlying search parameter.
Original definition for the search parameter
A list of alternate names that the organization is known as, or was known as in the past.
Captures the reason for the current state of the CommunicationRequest.
Identifiers associated with the image - these may include identifiers for the image itself, identifiers for the context of its collection (e.g. series ids) and context ids such as accession numbers or other workflow identifiers.
Which server these requirements apply to.
The type of value that a search parameter may contain, and how the content is interpreted.
The version of the FHIR specification on which this capability statement is based.
A textual explanation of the detected issue.
An error code,from a specified code system, which details why the eligibility check could not be performed.
A token parameter that refers to a search parameter defined on the specified type of the DataRequirement, and which searches on elements of type code, Coding, or CodeableConcept.
Named context for field, if desired, and a field is specified.
The operator type defines the conditional behavior of the assert. If not defined, the default is equals.
equals | notEquals | in | notIn | greaterThan | lessThan | empty | notEmpty | contains | notContains | eval
The triggering data of the event (if this is a data trigger).
The absolute geographic location of the Location, expressed using the WGS84 datum (This is the same co-ordinate system used in KML).
The value for this stratum, expressed as a CodeableConcept. When defining stratifiers on complex values, the value must be rendered such that the value for each stratum within the stratifier is unique.
The number of members of the population.
The maximum dose per day (maximum dose quantity to be administered in any one 24-h period) that can be administered as per the protocol referenced in the clinical trial authorisation.
Specifies an event that may occur multiple times. Timing schedules are used to record when things are planned, expected or requested to occur. The most common usage is in dosage instructions for medications. They are also used when planning care of various kinds, and may be used for reporting the schedule to which past regular activities were carried out.
A timing schedule that specifies an event that may occur multiple times
Indicates the authority who published the protocol (e.g. ACIP).
This property may convey specifics about the practice setting where the content was created, often reflecting the clinical specialty.
Additional details about where the content was created (e.g. clinical specialty)
Dynamic values that will be evaluated to produce values for elements of the resulting resource. For example, if the dosage of a medication must be computed based on the patient's weight, a dynamic value would be used to specify an expression that calculated the weight, and the path on the request resource that would contain the result.
A detailed description of how the activity definition is used from a clinical perspective.
Describes the clinical usage of the activity definition
Whether the search syntax is supported,.
The status of this compartment definition. Enables tracking the life-cycle of the content.
Indicates specific responsibility of an individual within the care team, such as "Primary care physician", "Trained social worker counselor", "Caregiver", etc.
Indicates a country, state or other region where the study is taking place.
Date the educational material was published.
Explanation of why this graph definition is needed and why it has been designed as it has.
A short, descriptive, user-friendly title for the structure map.
Name for this structure map (human friendly)
The populations that make up the stratum, one for each type of population appropriate to the measure.
A copyright statement relating to the terminology capabilities and/or its contents. Copyright statements are generally legal restrictions on the use and publishing of the terminology capabilities.
The target entity impacted by or of interest to parties to the agreement.
The start and end time of the encounter.
The entity (e.g. person, organization, clinical information system, device, group, or care team) which is the intended target of the communication.
The name of the arm in the study the subject is expected to follow as part of this study.
A record of a specific investigation that was undertaken.
preparation | in-progress | not-done | suspended | aborted | completed | entered-in-error
Indicates that a medication product is to be or has been dispensed for a named person/patient. This includes a description of the medication product (supply) provided and the instructions for administering the medication. The medication dispense is the result of a pharmacy system responding to a medication order.
A specification of the profile that describes the solution's overall support for the resource, including any constraints on cardinality, bindings, lengths or other limitations. See further discussion in [Using Profiles](profiling.html#profile-uses).
Base System profile for all uses of resource
Describes the unit that an observed value determined for this metric will have. For example: Percent, Seconds, etc.
A name or code (or both) briefly describing what the task involves.
Type of Contract Provision such as specific requirements, purposes for actions, obligations, prohibitions, e.g. life time maximum benefit.
Business identifier which may be used by other parties to reference or identify the prescription.
Reference to the resource (containing the contents of the resource needed for operations).
Whether this person's record is in active use.
The suspected agent causing the adverse event
When the target was validated against the primary source.
Indicates the current state of this consent.
draft | proposed | active | rejected | inactive | entered-in-error
The identifier that is used to identify this version of the measure when it is referenced in a specification, model, design or instance. This is an arbitrary value managed by the measure author and is not expected to be globally unique. For example, it might be a timestamp (e.g. yyyymmdd) if a managed version is not available. There is also no expectation that versions can be placed in a lexicographical sequence. To provide a version consistent with the Decision Support Service specification, use the format Major.Minor.Revision (e.g. 1.0.0). For more information on versioning knowledge assets, refer to the Decision Support Service specification. Note that a version is required for non-experimental active artifacts.
Concepts representing classification of patient encounter such as ambulatory (outpatient), inpatient, emergency, home health or others due to local variations.
Details for all kinds of technology mediated contact points for a person or organization, including telephone, email, etc.
Details of a Technology mediated contact point (phone, fax, email, etc.)
An identifier of the document encoding, structure, and template that the document conforms to beyond the base format indicated in the mimeType.
The content was developed with a focus and intent of supporting the contexts that are listed. These terms may be used to assist with indexing and searching for appropriate capability statement instances.
An abstract server representing a destination or receiver in a message exchange
The date (and possibly time) when the family member history was recorded or last updated.
When history was recorded or last updated
Patient's nominated primary care provider
This resource provides payment details and claim references supporting a bulk payment.
Substance identifier for each non-natural or radioisotope.
The protocol (set of recommendations) being followed by the provider who administered the dose.
The description and/or reference of the event(s) being documented. For example, this could be used to document such a colonoscopy or an appendectomy.
Identifies the routing target to send acknowledgements to.
A digital signature on the target Reference(s). The signer should match a Provenance.agent. The purpose of the signature is indicated.
Captures the reason for the current status.
A reference to a resource that this risk assessment is part of, such as a Procedure.
Whether the request is a proposal, plan, an original order or a reflex order.
A code that classifies the procedure for searching, sorting and display purposes (e.g. "Surgical Procedure").
End position of the window on the reference sequence. If the coordinate system is 0-based then end is is exclusive and does not include the last position. If the coordinate system is 1-base, then end is inclusive and includes the last position.
End position of the window on the reference sequence
Role type of agent assigned roles in this Contract.
A substance can be composed of other substances.
The quantity of the device present in the packaging of a medicinal product.
The closing time of day. Note: If the AllDay flag is set, then this time is ignored.
Closing time of day (ignored if allDay = true)
Information about security implementation from an interface perspective - what a client needs to know.
For version-less code systems, there should be a single version with no identifier.
Business identifiers assigned to this goal by the performer or other systems which remain constant as the resource is updated and propagates from server to server.
Image or images used to identify a location.
Identifies the organization or group who is responsible for ongoing maintenance of and access to the document.
Organization which maintains the document
Provides extra information about the medication statement that is not conveyed by the other attributes.
An absolute URI which is the code system from which the selected codes come from.
Relationships that this composition has with other compositions or documents that already exist.
Relationships to other compositions/documents
An identifier for the type of network access point that originated the audit event.
A financial tool for tracking value accrued for a particular purpose. In the healthcare field, used to track charges for a patient, cost centers, etc.
Why this entry is in the result set - whether it's included as a match or because of an _include requirement, or to convey information or warning information about the search process.
match | include | outcome - why this is in the result set
A formal name for the event. This may be an absolute URI that identifies the event formally (e.g. from a trigger registry), or a simple relative URI that identifies the event in a local context.
A procedure or observation that this questionnaire was performed as part of the execution of. For example, the surgery a checklist was executed as part of.
The base resource type(s) that this search parameter can be used against.
The resource type(s) this search parameter applies to
Indicates the relative path of an additional non-page, non-image file that is part of the IG - e.g. zip, jar and similar files that could be the target of a hyperlink in a derived IG.
Parameter that controlled the expansion process
Optional subject identifying the individual or individuals the report is for.
The patient or group of individuals assessed as part of this record.
The language which can be used to communicate with the patient about his or her health
If true, this entry is included in the expansion for navigational purposes, and the user cannot select the code directly as a proper value.
A code that classifies the general type of observation being made.
Account which is supposed to be balanced with this Invoice.
An alternate organizational reference to the case or file to which this particular claim pertains - e.g. Property/Casualy insurer claim # or Workers Compensation case # .
The owner of an asset has the residual control rights over the asset: the right to decide all usages of the asset in any way not inconsistent with a prior contract, custom, or law (Hart, 1995, p. 30).
Specific amount of the drug in the packaged product. For example, when specifying a product that has the same strength (For example, Insulin glargine 100 unit per mL solution for injection), this attribute provides additional clarification of the package amount (For example, 3 mL, 10mL, etc).
The name of the organization or individual that published the compartment definition.
When the questionnaire was last reviewed
Indicates the source data considered as part of the assessment (for example, FamilyHistory, Observations, Procedures, Conditions, etc.).
Condition or observation that supports why the medication was administered.
Extra details about the service that can't be placed in the other fields.
The version of the standard that is used to operate and communicate.
A code that identifies the charge, like a billing code.
Guidance specific to the implementation of this operation, such as limitations on the kind of transactions allowed, or information about system wide search is implemented.
An absolute URI that is used to identify this plan definition when it is referenced in a specification, model, design or an instance; also called its canonical identifier. This SHOULD be globally unique and SHOULD be a literal address at which at which an authoritative instance of this plan definition is (or will be) published. This URL can be the target of a canonical reference. It SHALL remain the same when the plan definition is stored on different servers.
Canonical identifier for this plan definition, represented as a URI (globally unique)
The name of the organization or individual that published the test script.
The type of message to be sent such as alert, notification, reminder, instruction, etc.
A set of key words or terms from external terminologies that may be used to assist with indexing and searching of templates nby describing the use of this structure definition, or the content it describes.
Set of definitional characteristics for a kind of observation or measurement produced or consumed by an orderable health care service.
Costs associated with the coverage provided by the product.
Indicates the timestamp when the user session was first created.
Indicates how quickly the {{title}} should be addressed with respect to other requests.
Adverse Reaction Events linked to exposure to substance
Related identifiers or resources associated with the DocumentReference.
Indicates the maximum length in characters that is permitted to be present in conformant instances and which is expected to be supported by conformant consumers that support the element.
A code specifying the state of the procedure. Generally this will be in-progress or completed state.
The query parameters for a query-type entities.
The status of this plan definition. Enables tracking the life-cycle of the content.
Whether the Medicinal Product is subject to special measures for regulatory reasons.
Stereochemistry shall be captured as described in 4.7.1.
The individual or organization that published the Contract precursor content.
Role that this diagnosis has within the encounter (e.g. admission, billing, discharge …).
The date (and optionally time) when the event definition was published. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the event definition changes.
A Boolean value to indicate that this message definition is authored for testing purposes (or education/evaluation/marketing) and is not intended to be used for genuine usage.
Information about security of implementation
Details of the official nature of this name.
An encounter that provides additional information about the healthcare context in which this request is made.
The encounter associated with this nutrition order
When the activity definition was approved by publisher
A summary of the events of interest that have occurred, such as when the administration was verified.
A list of events of interest in the lifecycle
RiskAssessment expressing likely outcome.
Whether or not to implicitly create the fixture during setup. If true, the fixture is automatically created on each server being tested during setup, therefore no create operation is required for this fixture in the TestScript.setup section.
Whether or not to implicitly create the fixture during setup
Indicates what happened as a result of this condition. If the condition resulted in death, deceased date is captured on the relation.
Unique id for the element within a resource (for internal references). This may be any string value that does not contain spaces.
The patient whose sequencing results are described by this resource.
The path by which the pharmaceutical product is taken into or makes contact with the body.
The organization responsible for the management of the instance and oversight of the data on the server at the specified URL.
The date (and optionally time) when the code system was published. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the code system changes.
Describes the intended use of this particular set of codes.
proposal | plan | original-order | encoded | reflex-order
Identifies the resource instances that are members of the group.
The human-readable barcode string. Can correspond to the UDI pattern in devices.
The identifier that is used to identify this version of the test script when it is referenced in a specification, model, design or instance. This is an arbitrary value managed by the test script author and is not expected to be globally unique. For example, it might be a timestamp (e.g. yyyymmdd) if a managed version is not available. There is also no expectation that versions can be placed in a lexicographical sequence.
Identifies the expected level of importance associated with reaching/sustaining the defined goal.
A representation of the meaning of the code in the system, following the rules of the system.
Comments on the availability to describe any extended information. Such as custom constraints on the slots that may be associated.
Prior communication that this communication is in response to.
Specifies the order applied to the items in the section entries.
An explanatory or alternate title for the library giving additional information about its content.
Mode of this document declaration - whether an application is a producer or consumer.
The person who entered the order on behalf of another individual for example in the case of a verbal or a telephone order.
Codes to indicate the target population this reference range applies to.
The date the occurrence of the immunization was first captured in the record - potentially significantly after the occurrence of the event.
When the immunization was first captured in the subject's record
A code or name that describes this diagnostic report.
Identifier for the organization that is used to identify the organization across multiple disparate systems.
Identifies this organization across multiple systems
An operation applied to the product, for manufacturing or adminsitrative purpose.
The device that was manipulated (changed) during the procedure.
A description of the status of the adjudication or processing.
A specific set of Roles/Locations/specialties/services that a practitioner may perform at an organization for a period of time.
The supporting materials are applicable for all detail intens, product/servce categories and specific billing codes.
A free text natural language description of the search parameter from a consumer's perspective. and how it used.
Natural language description of the search parameter
The usual time that a specimen of this kind is retained after the ordered tests are completed, for the purpose of additional testing.
A concept that may be defined by a formal reference to a terminology or ontology or may be provided by text.
Concept - reference to a terminology or just text
The period of time during which this relationship is or was active. If there are no dates defined, then the interval is unknown.
Period of time that this relationship is considered valid
A legal or geographic region in which the charge item definition is intended to be used.
Intended jurisdiction for charge item definition (if applicable)
Identifies the person who picked up the medication. This will usually be a patient or their caregiver, but some cases exist where it can be a healthcare professional.
A detailed description, from a clinical perspective, of how the measure is used.
Describes the clinical usage of the measure
A code that is used to identify the property. The code is used internally (in CodeSystem.concept.property.code) and also externally, such as in property filters.
Identifies the property on the concepts, and when referred to in operations
A record of the last error that occurred when the server processed a notification.
Additional guidance for the measure including how it can be used in a clinical context, and the intent of the measure.
The beginning of the time period in which the marketing authorization is in the specific status shall be specified A complete date consisting of day, month and year shall be specified using the ISO 8601 date format.
A description of the steps that might be taken to reduce the identified risk(s).
If the evaluation could not be completed due to lack of information, or additional information would potentially result in a more accurate response, this element will a description of the data required in order to proceed with the evaluation. A subsequent request to the service should include this data.
Period during which the qualification is valid.
False positives, i.e. the number of sites in the Query Call Set for which there is no path through the Truth Call Set that is consistent with this site. Sites with correct variant but incorrect genotype are counted here.
Text that describes the entity in more detail.
Identifies what "kind" of plan this is to support differentiation between multiple co-existing plans; e.g. "Home health", "psychiatric", "asthma", "disease management", "wellness plan", etc.
The period during which the participatingOrganization is affiliated with the primary organization.
The status of this activity definition. Enables tracking the life-cycle of the content.
A description of the kind of resource the activity definition is representing. For example, a MedicationRequest, a ServiceRequest, or a CommunicationRequest. Typically, but not always, this is a Request resource.
What to do when there is no mapping for the source concept. "Unmapped" does not include codes that are unamatched, and the unmapped element is ignored in a code is specified to have equivalence = unmatched.
Links to Provenance records for past versions of this resource or fulfilling request or event resources that identify key state transitions or updates that are likely to be relevant to a user looking at the current version of the resource.
A shared identifier common to all requests that were authorized more or less simultaneously by a single author, representing the identifier of the requisition or prescription.
Describes the clinical encounter or type of care this documentation is associated with.
The time period and frequency at which the supplement(s) should be given. The supplement should be given for the combination of all schedules if more than one schedule is present.
A record of a healthcare consumer’s choices, which permits or denies identified recipient(s) or recipient role(s) to perform one or more actions within a given policy context, for specific purposes and periods of time.
A legal or geographic region in which the test script is intended to be used.
Intended jurisdiction for test script (if applicable)
The target resource that represents a measurement from which this observation value is derived. For example, a calculated anion gap or a fetal measurement based on an ultrasound image.
Related measurements the observation is made from
Unique identifier for this supply request.
A natural language name identifying the search parameter. This name should be usable as an identifier for the module by machine processing applications such as code generation.
Name for this search parameter (computer friendly)
The URL pointing to a *FHIR*-defined protocol, guideline, orderset or other definition that is adhered to in whole or in part by this Task.
Indicates whether the record for the group is available for use or is merely being retained for historical purposes.
Whether this group's record is in active use
Whether or not the test execution will require the given capabilities of the server in order for this test script to execute.
Explanation of why this activity definition is needed and why it has been designed as it has.
How a resource is related to the compartment
If true, indicates that the age value specified is an estimated value.
A natural language name identifying the implementation guide. This name should be usable as an identifier for the module by machine processing applications such as code generation.
Name for this implementation guide (computer friendly)
Didactic or other informational resources associated with the goal that provide further supporting information about the goal. Information resources can include inline text commentary and links to web resources.
A legal or geographic region in which the code system is intended to be used.
Intended jurisdiction for code system (if applicable)
The party who benefits from the insurance coverage; the patient when services are provided.
The type of coverage: social program, medical plan, accident coverage (workers compensation, auto), group health or payment by an individual or organization.
Type of coverage such as medical or accident
A comment about the image. Typically, this is used to provide an explanation for why the image is included, or to draw the viewer's attention to important features.
Comment about the image (e.g. explanation)
A contact detail for the practitioner, e.g. a telephone number or an email address.
A contact detail for the practitioner (that apply to all roles)
The kind(s) of organization that this is.
Criterion for rejection of the specimen in its container by the laboratory.
The device used to generate the observation data.
Explanation of why this value set is needed and why it has been designed as it has.
If true, indicates that the described activity is one that must NOT be engaged in when following the plan. If false, or missing, indicates that the described activity is one that should be engaged in when following the plan.
Detailed and structured anatomical location information. Multiple locations are allowed - e.g. multiple punch biopsies of a lesion.
Permanent link to the MessageDefinition for this message.
This property allows a non condition-specific note to the made about the related person. Ideally, the note would be in the condition property, but this is not always possible.
Any manipulation of product post-collection.
A categorization for the type of document referenced - helps for indexing and searching. This may be implied by or derived from the code specified in the DocumentReference.type.
A master file for to the medicinal product (e.g. Pharmacovigilance System Master File).
Contains business-specific nuances of the business state.
One or more codes that represent the summary conclusion (interpretation/impression) of the diagnostic report.
Codes for the clinical conclusion of test results
Other maps used by this map (canonical URLs).
A possible alternate material for the packaging.
A formal identifier that is used to identify this measure when it is represented in other formats, or referenced in a specification, model, design or an instance.
A reply to an appointment request for a patient and/or practitioner(s), such as a confirmation or rejection.
This observation is a group observation (e.g. a battery, a panel of tests, a set of vital sign measurements) that includes the target as a member of the group.
Related resource that belongs to the Observation group
active | inactive | entered-in-error | unknown
The period of time that the health insurance product is available.
The clinician performing the assessment.
Gold standard sequence used for comparing against.
A specialized legal clause or condition based on overarching contract type.
Contract Term Type specific classification
Identifies the maximum number of resources of this type that must be pointed to by a message in order for it to be valid against this MessageDefinition.
A larger event of which this particular Observation is a component or step. For example, an observation as part of a procedure.
The patient that the item is associated with (implanted in, given to).
Links to the FHIR specification that describes this interaction and the resources involved in more detail.
The order of applicability of this coverage relative to other coverages which are currently in force. Note, there may be gaps in the numbering and this does not imply primary, secondary etc. as the specific positioning of coverages depends upon the episode of care.
preliminary | final | appended | amended | entered-in-error
Comments that apply to the overall list.
Indicates whether the event succeeded or failed.
Identification of the facility/location where the medication was shipped to, as part of the dispense event.
The status of this event definition. Enables tracking the life-cycle of the content.
When the measure was approved by publisher
Identifier of this Invoice, often used for reference in corresponcence about this invoice or for tracking of payments.
The referral resource which lists the date, practitioner, reason and other supporting information.
This modifier is used to convey order-specific modifiers about the type of food that should be given. These can be derived from patient allergies, intolerances, or preferences such as Halal, Vegan or Kosher. This modifier applies to the entire nutrition order inclusive of the oral diet, nutritional supplements and enteral formula feedings.
Order-specific modifier about the type of food that should be given
A list of all the series.modality values that are actual acquisition modalities, i.e. those in the DICOM Context Group 29 (value set OID 1.2.840.10008.6.1.19).
All series modality if actual acquisition modalities
Provides a summary of relevant clinical guidelines or other clinical recommendations supporting the measure.
The principal physical location where the this task is performed.
A number appearing on the outer packaging of a specific batch.
Indicates a Condition, Observation, AllergyIntolerance, or QuestionnaireResponse that justifies this family member history event.
True if this item is marked as deleted in the list.
If this item is actually marked as deleted
A short, descriptive, user-friendly title for the operation definition.
Name for this operation definition (human friendly)
Specific specialty of the participatingOrganization in the context of the role.
A formal computable definition of a graph of resources - that is, a coherent set of resources that form a graph by following references. The Graph Definition resource defines a set and makes rules about the set.
If this is the default version for this code system.
The anatomical location where the related service has been applied.
Task that this particular task is part of.
The set of accounts that may be used for billing for this Encounter.
Distinguishes the type of involvement of the performer in the series.
The service request this appointment is allocated to assess (e.g. incoming referral or procedure request).
The service request this appointment is allocated to assess
When the document manifest was created for submission to the server (not necessarily the same thing as the actual resource last modified time, since it may be modified, replicated, etc.).
Specifies contact information for a person or organization.
Information about the message that this message is a response to. Only present if this message is a response.
Used in supporting related concepts, e.g. NDC to RxNorm.
Any additional identifier(s) for the catalog item, in the same granularity or concept
The identifier that is used to identify this version of the code system when it is referenced in a specification, model, design or instance. This is an arbitrary value managed by the code system author and is not expected to be globally unique. For example, it might be a timestamp (e.g. yyyymmdd) if a managed version is not available. There is also no expectation that versions can be placed in a lexicographical sequence. This is used in [Coding](datatypes.html#Coding).version.
Business version of the code system (Coding.version)
The CoverageEligibilityRequest provides patient and insurance coverage information to an insurer for them to respond, in the form of an CoverageEligibilityResponse, with information regarding whether the stated coverage is valid and in-force and optionally to provide the insurance details of the policy.
If the list is empty, why the list is empty.
Over what time-period is fulfillment sought.
A series of measurements taken by a device, with upper and lower limits. There may be more than one dimension in the data.
A series of measurements taken by a device
The practitioner who is responsible for the action specified in this request.
The identifier that is used to identify this version of the questionnaire when it is referenced in a specification, model, design or instance. This is an arbitrary value managed by the questionnaire author and is not expected to be globally unique. For example, it might be a timestamp (e.g. yyyymmdd) if a managed version is not available. There is also no expectation that versions can be placed in a lexicographical sequence.
This code defines the purpose of the list - why it was created.
The date and time when the device was manufactured.
True positives, from the perspective of the query data, i.e. the number of sites in the Query Call Set for which there are paths through the Truth Call Set that are consistent with all of the alleles at this site, and for which there is an accurate genotype call for the event.
True positives from the perspective of the query data
The source or owner that assigns the price to the medication.
The source or owner for the price information
A reference to the entity that is a member of the group. Must be consistent with Group.type.
A copyright statement relating to the library and/or its contents. Copyright statements are generally legal restrictions on the use and publishing of the library.
Comments about this mapping, including version notes, issues, scope limitations, and other important notes for usage.
Versions, Issues, Scope limitations etc.
Telecommunications form for contact point - what communications system is required to make use of the contact.
phone | fax | email | pager | url | sms | other
Indicates that specific elements of the type are referenced by the knowledge module and must be supported by the consumer in order to obtain an effective evaluation. This does not mean that a value is required for this element, only that the consuming system must understand the element and be able to provide values for it if they are available. The value of mustSupport SHALL be a FHIRPath resolveable on the type of the DataRequirement. The path SHALL consist only of identifiers, constant indexers, and .resolve() (see the [Simple FHIRPath Profile](fhirpath.html#simple) for full details).
Indicates specific structure elements that are referenced by the knowledge module
If code comparison is case sensitive when codes within this system are compared to each other.
Business identifiers assigned to this care plan by the performer or other systems which remain constant as the resource is updated and propagates from server to server.
The Library resource is a general-purpose container for knowledge asset definitions. It can be used to describe and expose existing knowledge assets such as logic libraries and information model descriptions, as well as to describe a collection of knowledge assets.
How the type relates to the baseDefinition.
specialization | constraint - How relates to base definition
The number of times to repeat the action within the specified period. If frequencyMax is present, this element indicates the lower bound of the allowed range of the frequency.
A detailed description of a device, typically as part of a regulated medicinal product. It is not intended to replace the Device resource, which covers use of device instances.
Ways that the service accepts referrals, if this is not provided then it is implied that no referral is required.
The list of diagnosis relevant to this episode of care.
The device used in administering the medication to the patient. For example, a particular infusion pump.
A natural language name identifying the concept map. This name should be usable as an identifier for the module by machine processing applications such as code generation.
Name for this concept map (computer friendly)
organ | tissue | fluid | cells | biologicalAgent
Details of a Health Insurance product/plan provided by an organization.
Number of Series in the Study. This value given may be larger than the number of series elements this Resource contains due to resource availability, security, or other factors. This element should be present if any series elements are present.
Whether a substitution was performed on the dispense
If true, indicates that this slice definition is constraining a slice definition with the same name in an inherited profile. If false, the slice is not overriding any slice in an inherited profile. If missing, the slice might or might not be overriding a slice in an inherited profile, depending on the sliceName.
If this slice definition constrains an inherited slice definition (or not)
A code to indicate the Professional Service or Product supplied (eg. CTP, HCPCS,USCLS,ICD10, NCPDP,DIN,ACHI,CCI).
Additional details and instructions about the how the services are to be delivered. For example, and order for a urinary catheter may have an order detail for an external or indwelling catheter, or an order for a bandage may require additional instructions specifying how the bandage should be applied.
The results of the calculation, one for each population group in the measure.
A reference to a Library resource containing the formal logic used by the measure.
Invidual data point representing the GQ (genotype quality) score threshold.
List of locations where the patient has been
Further information supporting this charge.
A legal or geographic region in which the measure is intended to be used.
Intended jurisdiction for measure (if applicable)
An integer indicating the number of times, in addition to the original dispense, (aka refills or repeats) that the patient can receive the prescribed medication. Usage Notes: This integer does not include the original order dispense. This means that if an order indicates dispense 30 tablets plus "3 repeats", then the order can be dispensed a total of 4 times and the patient can receive a total of 120 tablets. A prescriber may explicitly say that zero refills are permitted after the initial dispense.
The organization or lab that should be responsible for this result.
Who should be responsible for test result
Indicates the type of dispensing event that is performed. Examples include: Trial Fill, Completion of Trial, Partial Fill, Emergency Fill, Samples, etc.
The workflow status of the nutrition order/request.
proposed | draft | planned | requested | active | on-hold | completed | cancelled | entered-in-error
A richer description of the benefit, for example 'DENT2 covers 100% of basic, 50% of major but excludes Ortho, Implants and Cosmetic services'.
A homogeneous material with a definite composition.
The assigned lot number of a batch of the specified product.
When the document reference was created.
When this document reference was created
Logical source location within the healthcare enterprise network. For example, a hospital or other provider location within a multi-entity provider group.
Logical source location within the enterprise
The preferred location(s) where the procedure should actually happen in coded or free text form. E.g. at home or nursing day care center.
The content was developed with a focus and intent of supporting the contexts that are listed. These terms may be used to assist with indexing and searching for appropriate measure instances.
The location header created by processing this operation, populated if the operation returns a location.
The location (if the operation returns a location)
The maximum number of times this element is permitted to appear in the instance.
Specifies the particular kind of composition (e.g. History and Physical, Discharge Summary, Progress Note). This usually equates to the purpose of making the composition.
This element defines the specific type of event that occurred or that was prevented from occurring.
Type of the event itself in relation to the subject
Specific parameters for the ordered item. For example, the size of the indicated item.
The date the immunization recommendation(s) were created.
A categorization for the type of the composition - helps for indexing and searching. This may be implied by or derived from the code specified in the Composition Type.
Captures the reason for the current state of the MedicationStatement.
The principal physical location where the dispense was performed.
Whether inactive codes - codes that are not approved for current use - are in the value set. If inactive = true, inactive codes are to be included in the expansion, if inactive = false, the inactive codes will not be included in the expansion. If absent, the behavior is determined by the implementation, or by the applicable $expand parameters (but generally, inactive codes would be expected to be included).
Whether inactive codes are in the value set
The date and time that this nutrition order was requested.
Date and time the nutrition order was requested
Parties financially responsible for the account.
organization | patient | practitioner | relatedperson.
Indicates the reason the immunization event was not performed.
The technical endpoints providing access to services operated for the health insurance product.
Identifier for the supply delivery event that is used to identify it across multiple disparate systems.
The individual or set of individuals receiving the goods and services billed in this invoice.
Power adjustment for multifocal lenses measured in dioptres (0.25 units).
A FHIRPath expression that returns a set of elements for the search parameter.
FHIRPath expression that extracts the values
Stratum results, one for each unique value in the stratifier
The patient or group that is the focus of this communication request.
The quantity of the device present in the packaging (e.g. the number of devices present in a pack, or the number of devices in the same package of the medicinal product).
Who attested the composition in the specified way.
Reference of resource for which payment is being made.
The source of the data when the report of the immunization event is not based on information from the person who administered the vaccine.
Indicates the source of a secondarily reported record
True if the dispenser dispensed a different drug or product from what was prescribed.
Whether a substitution was or was not performed on the dispense
A formal identifier that is used to identify this event definition when it is represented in other formats, or referenced in a specification, model, design or an instance.
Additional identifier for the event definition
A time during the day, with no date specified
Identifies the period time over which the supplied product is expected to be used, or the length of time the dispense is expected to last.
The dates the subject began and ended their participation in the study.
Ability of the primary source to push updates/alerts (yes; no; undetermined).
The URL pointing to an externally maintained protocol, guideline, orderset or other definition that is adhered to in whole or in part by this FamilyMemberHistory.
A symbol in syntax defined by the system. The symbol may be a predefined code or an expression in a syntax defined by the coding system (e.g. post-coordination).
If the compositional grammar defined by the code system is supported.
Provides a complete explanation of the meaning of the data element for human readability. For the case of elements derived from existing elements (e.g. constraints), the definition SHALL be consistent with the base definition, but convey the meaning of the element in the particular context of use of the resource. (Note: The text you are reading is specified in ElementDefinition.definition).
Full formal definition as narrative text
The organization which is the target of the request.
Party which is the target of the request
Any other notes and comments about the procedure.
Additional information about the procedure
This special resource type is used to represent an operation request and response (operations.html). It has no other use, and there is no RESTful endpoint associated with it.
Whether the client must identify the map.
Describes the intended objective(s) of carrying out the care plan.
Organization where the role is available (primary organization/has members).
Organization where the role is available
Provides guidance on the use of the namespace, including the handling of formatting characters, use of upper vs. lower case, etc.
The resource ChargeItem describes the provision of healthcare provider products for a certain patient, therefore referring not only to the product, but containing in addition details of the provision, like date, time, amounts and participating organizations and persons. Main Usage of the ChargeItem is to enable the billing process and internal cost allocation.
Who read the study and interpreted the images or other content.
ChargeItems can be grouped to larger ChargeItems covering the whole set.
Specific parameters for the ordered item. For example, the prism value for lenses.
The record of the person or animal who is involved in the study.
The manufacturer or establishment associated with the process.
Identifies portions of the patient's record that specifically influenced the formation of the plan. These might include comorbidities, recent procedures, limitations, recent assessments, etc.
If there is a photo/symbol associated with this HealthcareService, it may be included here to facilitate quick identification of the service in a list.
Facilitates quick identification of the service
Specification of the participation type the user plays when performing the event.
A short, descriptive, user-friendly title for the library.
Indicates another resource whose existence justifies this request.
The canonical URI of an additional ConceptMap resource instance to use for mapping if this ConceptMap resource contains no matching mapping for the source concept.
Canonical URI for an additional ConceptMap to use for mapping if the source concept is unmapped
An expression that specifies the criteria for the stratifier. This is typically the name of an expression defined within a referenced library, but it may also be a path to a stratifier element.
This resource allows for the definition of various types of plans as a sharable, consumable, and executable artifact. The resource is general enough to support the description of a broad range of clinical artifacts such as clinical decision support rules, order sets and protocols.
Physical form of the location, e.g. building, room, vehicle, road.
An absolute URI that is used to identify this code system when it is referenced in a specification, model, design or an instance; also called its canonical identifier. This SHOULD be globally unique and SHOULD be a literal address at which at which an authoritative instance of this code system is (or will be) published. This URL can be the target of a canonical reference. It SHALL remain the same when the code system is stored on different servers. This is used in [Coding](datatypes.html#Coding).system.
Canonical identifier for this code system, represented as a URI (globally unique) (Coding.system)
The practitioner or organization who performed the action.
Individual or organization who was performing
The name of the organization or individual that published the event definition.
The name of the organization that is responsible for issuing identifiers or codes for this namespace and ensuring their non-collision.
The period during which the event definition content was or is planned to be in active use.
When the event definition is expected to be used
Individual or device responsible for the issue being raised. For example, a decision support application or a pharmacist conducting a medication review.
The provider or device that identified the issue
Indicates the patient status with respect to the path to immunity for the target disease.
A description of the property- why it is defined, and how its value might be used.
Why the property is defined, and/or what it conveys
Indicates the current status of the evaluation of the vaccination administration event.
A human language representation of the concept as seen/selected/uttered by the user who entered the data and/or which represents the intended meaning of the user.
Plain text representation of the concept
A natural language name identifying the value set. This name should be usable as an identifier for the module by machine processing applications such as code generation.
Name for this value set (computer friendly)
The URL pointing to a FHIR-defined protocol, guideline, orderset or other definition that is adhered to in whole or in part by this FamilyMemberHistory.
The name of this element definition slice, when slicing is working. The name must be a token with no dots or spaces. This is a unique name referring to a specific set of constraints applied to this element, used to provide a name to different slices of the same element.
Name for this particular element (in a set of slices)
A name associated with the organization.
The low limit. The boundary is inclusive.
The type of relationship that this composition has with anther composition or document.
The specific procedure that is performed. Use text if the exact nature of the procedure cannot be coded (e.g. "Laparoscopic Appendectomy").
The date (and optionally time) when the operation definition was published. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the operation definition changes.
A formal identifier that is used to identify this code system when it is represented in other formats, or referenced in a specification, model, design or an instance. (business identifier).
Additional identifier for the code system
The kind of facility where the patient was seen.
Indicates the intended dispensing Organization specified by the prescriber.
An approximate time period during the day, potentially linked to an event of daily living that indicates when the action should occur.
An absolute URI that identifies the target system that the concepts will be mapped to.
Target system that the concepts are to be mapped to
Indicates when the plan did (or is intended to) come into effect and end.
The encounter during which the procedure was performed.
Encounter or episode associated with the procedure
False negatives, i.e. the number of sites in the Truth Call Set for which there is no path through the Query Call Set that is consistent with all of the alleles at this site, or sites for which there is an inaccurate genotype call for the event. Sites with correct variant but incorrect genotype are counted here.
Descriptive information, usage information or implantation information that is not captured in an existing element.
Explanation of why this terminology capabilities is needed and why it has been designed as it has.
Why this terminology capabilities is defined
The identifier that is used to identify this version of the library when it is referenced in a specification, model, design or instance. This is an arbitrary value managed by the library author and is not expected to be globally unique. For example, it might be a timestamp (e.g. yyyymmdd) if a managed version is not available. There is also no expectation that versions can be placed in a lexicographical sequence. To provide a version consistent with the Decision Support Service specification, use the format Major.Minor.Revision (e.g. 1.0.0). For more information on versioning knowledge assets, refer to the Decision Support Service specification. Note that a version is required for non-experimental active artifacts.
Organization on behalf of which the contact is acting or for which the contact is working.
Organization that is associated with the contact
Specified type for the element. This works as a condition on the mapping - use for polymorphic elements.
Rule only applies if source has this type
A formal identifier that is used to identify this charge item definition when it is represented in other formats, or referenced in a specification, model, design or an instance.
Additional identifier for the charge item definition
The codes for the code filter. If values are given, the filter will return only those data items for which the code-valued attribute specified by the path has a value that is one of the specified codes. If codes are specified in addition to a value set, the filter returns items matching a code in the value set or one of the specified codes.
This flag is used to signify that the code system does not commit to concept permanence across versions. If true, a version must be specified when referencing this code system.
The overall status of the Appointment. Each of the participants has their own participation status which indicates their involvement in the process, however this status indicates the shared status.
proposed | pending | booked | arrived | fulfilled | cancelled | noshow | entered-in-error | checked-in
A URI that is a reference to a canonical URI on a FHIR resource
Vaccine that was administered or was to be administered.
The identifier that is used to identify this version of the implementation guide when it is referenced in a specification, model, design or instance. This is an arbitrary value managed by the implementation guide author and is not expected to be globally unique. For example, it might be a timestamp (e.g. yyyymmdd) if a managed version is not available. There is also no expectation that versions can be placed in a lexicographical sequence.
Business version of the implementation guide
The structural representation as text string in a format e.g. InChI, SMILES, MOLFILE, CDX.
Oral nutritional products given in order to add further nutritional value to the patient's diet.
The MeasureReport resource contains the results of the calculation of a measure; and optionally a reference to the resources involved in that calculation.
Indicates the number of times the requested action should occur.
The URL pointing to an externally-defined charge item definition that is adhered to in whole or in part by this definition.
Underlying externally-defined charge item definition
Whether the server can return nested value sets.
Service is not available (seasonally or for a public holiday) from this date.
Additional notes or commentary about the communication by the sender, receiver or other interested parties.
The amount of medication that has been dispensed. Includes unit of measure.
Describes the reason for the guidance response in coded or textual form.
Provides a description of the circumstances in which this response should be used (as opposed to one of the alternative responses).
Describes the intention of how one or more practitioners intend to deliver care for a particular patient, group or community for a period of time, possibly limited to care for a specific condition or set of conditions.
The reason that can be presented to the user as to why this time is not available.
Reason presented to the user explaining why time not available
The relative base, or reference lens edge, for the prism.
Business identifier associated with the detected issue record.
The set of accounts that may be used for billing for this EpisodeOfCare.
Indicates the duration of time over which repetitions are to occur; e.g. to express "3 times per day", 3 would be the frequency and "1 day" would be the period. If periodMax is present, this element indicates the lower bound of the allowed range of the period length.
The version identifier for the software covered by this statement.
The meaning of the population group as defined in the measure definition.
The name of the imaging view e.g. Lateral or Antero-posterior (AP).
Imaging view, e.g. Lateral or Antero-posterior
The version of the code system which was used when choosing this code. Note that a well-maintained code system does not need the version reported, because the meaning of codes is consistent across versions. However this cannot consistently be assured, and when the meaning is not guaranteed to be consistent, the version SHOULD be exchanged.
A series of data points which are decimal values separated by a single space (character u20). The special values "E" (error), "L" (below detection limit) and "U" (above detection limit) can also be used in place of a decimal value.
Decimal values with spaces, or "E" | "U" | "L"
Precusory content structure and use, i.e., a boilerplate, template, application for a contract such as an insurance policy or benefits under a program, e.g., workers compensation.
The reason the risk assessment was performed.
Altitude. The value domain and the interpretation are the same as for the text of the altitude element in KML (see notes below).
A code (or set of codes) that identify this substance.
Policy or plan the activity was defined by. Typically, a single activity may have multiple applicable policy documents, such as patient consent, guarantor funding, etc.
Policy or plan the activity was defined by
Comments made about the request by the requester, sender, recipient, subject or other participants.
Comments made about communication request
Distinguishes the type of involvement of the performer in the procedure. For example, surgeon, anaethetist, endoscopist.
Where applicable, the shape can be specified An appropriate controlled vocabulary shall be used The term and the term identifier shall be used.
Requirements for delivery and special handling of this kind of conditioned specimen.
The person or animal or group receiving the medication.
The location(s) where this healthcare service may be provided.
Location(s) where service may be provided
Extra information about the medication administration that is not conveyed by the other attributes.
The time at which the expansion was produced by the expanding system.
Indicates the sites on the subject's body where the procedure should be performed (I.e. the target sites).
A Map of relationships between 2 structures that can be used to transform data.
Human-friendly description of the resource instance.
Indicates who was responsible for creating the resource instance.
A legal or geographic region in which the concept map is intended to be used.
Intended jurisdiction for concept map (if applicable)
The organization the device or practitioner was acting on behalf of.
Organization the device or practitioner was acting for
A free text natural language description of the compartment definition from a consumer's perspective.
Natural language description of the compartment definition
Comments made about the term action made by the requester, performer, subject or other participants.
A field that should be used to capture parameters that were used in the measurement of a property.
Indicates whether this identifier is the "preferred" identifier of this type.
Is this the id that should be used for this type
Extra information about the immunization that is not conveyed by the other attributes.
A plan, proposal or order that is fulfilled in whole or in part by this request.
When the plan definition was approved by publisher
Healthcare services provided through the role.
Time aspect of specimen collection (duration or offset).
Messages resulting from the evaluation of the artifact or artifacts. As part of evaluating the request, the engine may produce informational or warning messages. These messages will be provided by this element.
Messages resulting from the evaluation of the artifact or artifacts
A code that classifies the clinical discipline, department or diagnostic service that created the report (e.g. cardiology, biochemistry, hematology, MRI). This is used for searching, sorting and display purposes.
An e-mail, phone, website or other contact point to use to resolve issues with message communications.
What to do when there is no mapping for the source concept
The overall type of event, intended for search and filtering purposes.
product-problem | product-quality | product-use-error | wrong-dose | incorrect-prescribing-information | wrong-technique | wrong-route-of-administration | wrong-rate | wrong-duration | wrong-time | expired-drug | medical-device-use-error | problem-different-manufacturer | unsafe-physical-environment
Code to indicate the nature of the payment, adjustment, funds advance, etc.
A length - a value with a unit that is a physical distance.
Identifier assigned by the dispensing facility - this is an identifier assigned outside FHIR.
The literature, knowledge-base or similar reference that describes the propensity for the detected issue identified.
Indicates who or what is being asked to perform (or not perform) the ction.
Actor that wil execute (or not) the action
The URL pointing to an externally maintained definition that is adhered to in whole or in part by this Contract.
This resource provides: the claim details; adjudication details from the processing of a Claim; and optionally account balance information, for informing the subscriber of the benefits provided.
Definition of the role the participatingOrganization plays in the association.
Definition of the role the participatingOrganization plays
Identifier for a substance upon which a defining property depends.
The identifier assigned by the lab when accessioning specimen(s). This is not necessarily the same as the specimen identifier, depending on local lab procedures.
Prospective warnings of potential issues when providing care to the patient.
The patient or group present at the encounter.
Describes the intended objective(s) for a patient, group or organization care, for example, weight loss, restoring an activity of daily living, obtaining herd immunity via immunization, meeting a process improvement objective, etc.
Documentation about the system's messaging capabilities for this endpoint not otherwise documented by the capability statement. For example, the process for becoming an authorized messaging exchange partner.
Name of the input parameter to the $expand operation; may be a server-assigned name for additional default or other server-supplied parameters used to control the expansion process.
Name as assigned by the client or server
Time period during which the coverage is in force. A missing start date indicates the start date isn't known, a missing end date means the coverage is continuing to be in force.
An explanatory or alternate title for the event definition giving additional information about its content.
Subordinate title of the event definition
Information about a person that is involved in the care for a patient, but who is not the target of healthcare, nor has a formal responsibility in the care process.
The drug concentration measured at certain discrete points in time.
The product or brand name of the nutritional supplement such as "Acme Protein Shake".
Product or brand name of the nutritional supplement
A code that classifies the general type of substance. This is used for searching, sorting and display purposes.
The code system defines a compositional (post-coordination) grammar.
If code system defines a compositional grammar
The encounter or episode of care that establishes the context for this MedicationStatement.
Encounter / Episode associated with MedicationStatement
Individual organization or Device currently responsible for task execution.
A digital identity certificate associated with the attestation source.
Identifies the type of vision correction product which is required for the patient.
There SHALL be a code if there is a value and it SHALL be an expression of currency. If system is present, it SHALL be ISO 4217 (system = "urn:iso:std:iso:4217" - currency).
An amount of money. With regard to precision, see [Decimal Precision](datatypes.html#precision)
An area where general notes can be placed about this specific condition.
The source of the information about the allergy that is recorded.
Source of the information about the allergy
The encounter or episode at which the request is initiated.
Plain text narrative that identifies the resource in addition to the resource reference.
The type of the object that was involved in this audit event.
The insurer which is responsible for the explanation of benefit.
An error code, from a specified code system, which details why the claim could not be adjudicated.
If a locked date is defined, then the Content Logical Definition must be evaluated using the current version as of the locked date for referenced code system(s) and value set instances where ValueSet.compose.include.version is not defined.
Fixed date for references with no specified version (transitive)
Coded expression for the type of tissue for which the withdrawal period applues, e.g. meat, milk.
A copyright statement relating to the test script and/or its contents. Copyright statements are generally legal restrictions on the use and publishing of the test script.
The flag allows the system constructing the list to indicate the role and significance of the item in the list.
Status/Workflow information about this item
Actual or potential/avoided event causing unintended physical injury resulting from or contributed to by medical care, a research study or other healthcare setting factors that requires additional monitoring, treatment, or hospitalization, or that results in death.
The code specifying the level of confidentiality of the Composition.
The encounter where the assessment was performed.
The reason or the indication for ordering or not ordering the medication.
Reason or indication for ordering or not ordering the medication
The time for the server to turn the subscription off.
When to automatically delete the subscription
The organization performing the service.
Organization requesting the charged service
The contact for the health insurance product for a certain purpose.
Special processing that should be applied to the container for this kind of specimen.
A copyright statement relating to Contract precursor content. Copyright statements are generally legal restrictions on the use and publishing of the Contract precursor content.
Describes the type of the issue. The system that creates an OperationOutcome SHALL choose the most applicable code from the IssueType value set, and may additional provide its own code for the error in the details element.
Whether the product is currently available.
The targeted disease for the recommendation.
An integer with a value that is not negative (e.g. >= 0)
The container holding the specimen. The recursive nature of containers; i.e. blood in tube in tray in rack is not addressed here.
The identifier that is used to identify this version of the concept map when it is referenced in a specification, model, design or instance. This is an arbitrary value managed by the concept map author and is not expected to be globally unique. For example, it might be a timestamp (e.g. yyyymmdd) if a managed version is not available. There is also no expectation that versions can be placed in a lexicographical sequence.
The result if validation fails (fatal; warning; record only; none).
Category of the medication or product (e.g. branded product, therapeutic moeity, generic product, innovator product, etc).
External specification that the content is mapped to
A code that classifies the general type of observation.
A legal or geographic region in which the plan definition is intended to be used.
Intended jurisdiction for plan definition (if applicable)
Any other notes and comments made about the service request. For example, internal billing notes.
A structure definition used by this map. The structure definition may describe instances that are converted, or the instances that are produced.
Reference to a specific published clinical protocol that was followed during this assessment, and/or that provides evidence in support of the diagnosis.
The actual condition specified. Could be a coded condition (like MI or Diabetes) or a less specific string like 'cancer' depending on how much is known about the condition and the capabilities of the creating system.
Typically date of issue is different from the beginning of the validity. This can be used to see when an item was last updated.
A profile on the document Bundle that constrains which resources are present, and their contents.
Constraint on the resources used in the document
The time the dispensed product was provided to the patient or their representative.
Business identifier for the marketing authorization, as assigned by a regulator.
The FHIRPath expression to evaluate against the fixture body. When variables are defined, only one of either expression, headerField or path must be specified.
The FHIRPath expression against the fixture body
The type this structure describes. If the derivation kind is 'specialization' then this is the master definition for a type, and there is always one of these (a data type, an extension, a resource, including abstract ones). Otherwise the structure definition is a constraint on the stated type (and in this case, the type cannot be an abstract type). References are URLs that are relative to http://hl7.org/fhir/StructureDefinition e.g. "string" is a reference to http://hl7.org/fhir/StructureDefinition/string. Absolute URLs are only allowed in logical models.
Type defined or constrained by this structure
The details of a healthcare service available at a location.
The frequency with which the target must be validated (none; initial; periodic).
A expression that is evaluated in a specified context and returns a value. The context of use of the expression must specify the context in which the expression is evaluated, and how the result of the expression is used.
An expression that can be used to generate a value
The information needed by an IG publisher tool to publish the whole implementation guide.
Free text formula administration, feeding instructions or additional instructions or information.
Formula feeding instructions expressed as text
The date (and optionally time) when the measure was published. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the measure changes.
If the ingredient is a known or suspected allergen.
Will be used to grab the HTTP header field value from the headers that sourceId is pointing to.
The content was developed with a focus and intent of supporting the contexts that are listed. These terms may be used to assist with indexing and searching for appropriate structure map instances.
Only perform the operation if the last updated date matches. See the API documentation for ["Conditional Read"](http.html#cread).
A link to a resource representing the person to whom the vision products will be supplied.
A code that identifies a particular service (i.e., procedure, diagnostic investigation, or panel of investigations) that have been requested.
Associated or related medication information
The name of the organization or individual that published the structure definition.
The algorithm, process or mechanism used to evaluate the risk.
A single component of the device version.
This list of codes represents the main clinical acts, such as a colonoscopy or an appendectomy, being documented. In some cases, the event is inherent in the typeCode, such as a "History and Physical Report" in which the procedure being documented is necessarily a "History and Physical" act.
Code(s) that apply to the event being documented
The procedure that trigger the dispense.
Types with only a value and no additional elements as children
A larger event of which this particular procedure is a component or step.
The device, practitioner, etc. who entered the charge item.
A natural language name identifying the event definition. This name should be usable as an identifier for the module by machine processing applications such as code generation.
Name for this event definition (computer friendly)
The type of FHIR resource at which instances of this graph start.
Type of resource at which the graph starts
Indicates whether or not the patient prefers this language (over other languages he masters up a certain level).
Information about a user's current session.
The status history permits the encounter resource to contain the status history without needing to read through the historical versions of the resource, or even have the server store them.
The condition that is the focus of the study. For example, In a study to examine risk factors for Lupus, might have as an inclusion criterion "healthy volunteer", but the target condition code would be a Lupus SNOMED code.
An absolute URI that is used to identify this structure definition when it is referenced in a specification, model, design or an instance; also called its canonical identifier. This SHOULD be globally unique and SHOULD be a literal address at which at which an authoritative instance of this structure definition is (or will be) published. This URL can be the target of a canonical reference. It SHALL remain the same when the structure definition is stored on different servers.
Canonical identifier for this structure definition, represented as a URI (globally unique)
An encounter or episode of care that provides additional information about the healthcare context in which this request is made.
Encounter or Episode during which request was created
The encounter or episode of care that establishes the context for this AdverseEvent.
Encounter or episode of care that establishes the context for this AdverseEvent
Identifies whether this portion of the statement is describing the ability to initiate or receive restful operations.
Identifies the actual instance of what caused the adverse event. May be a substance, medication, medication administration, medication statement or a device.
Refers to the specific entity that caused the adverse event
Whether the server supports paging on expansion.
Identity (code or path) or the element/item being mapped.
A formally or informally recognized grouping of people, principals, organizations, or jurisdictions formed for the purpose of achieving some form of collective action such as the promulgation, administration and enforcement of contracts and policies.
Authority under which this Contract has standing
Structural Variant Inner End. If the coordinate system is 0-based then end is is exclusive and does not include the last position. If the coordinate system is 1-base, then end is inclusive and includes the last position.
The units of time for the duration, in UCUM units.
The date (and optionally time) when the capability statement was published. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the capability statement changes.
A description of a triggering event. Triggering events can be named events, data events, or periodic, as determined by the type element.
Defines an expected trigger for a module
The device identifier (DI) is a mandatory, fixed portion of a UDI that identifies the labeler and the specific version or model of a device.
The date-valued attribute of the filter. The specified path SHALL be a FHIRPath resolveable on the specified type of the DataRequirement, and SHALL consist only of identifiers, constant indexers, and .resolve(). The path is allowed to contain qualifiers (.) to traverse sub-elements, as well as indexers ([x]) to traverse multiple-cardinality sub-elements (see the [Simple FHIRPath Profile](fhirpath.html#simple) for full details). Note that the index must be an integer constant. The path must resolve to an element of type date, dateTime, Period, Schedule, or Timing.
Designates which child elements are used to discriminate between the slices when processing an instance. If one or more discriminators are provided, the value of the child elements in the instance data SHALL completely distinguish which slice the element in the resource matches based on the allowed values for those elements in each of the slices.
Element values that are used to distinguish the slices
The reference to the definition for the device.
A string to represent reference sequence
The food type(s) (e.g. meats, all foods) that the texture modification applies to. This could be all foods types.
Concepts that are used to identify an entity that is ingested for nutritional purposes
Abstract name given to a destination server in this test script. The name is provided as a number starting at 1.
The index of the abstract destination server starting at 1
Explanation of why this test script is needed and why it has been designed as it has.
The capacity (volume or other measure) of this kind of container.
The practitioner or organization that is responsible for the report's conclusions and interpretations.
Individual who is making the condition statement.
Indicates when the specific member or organization did (or is intended to) come into effect and end.
Categorization of study arm, e.g. experimental, active comparator, placebo comparater.
Information about the search process that lead to the creation of this entry.
A label for human use intended to distinguish like teams. E.g. the "red" vs. "green" trauma teams.
Name of the team, such as crisis assessment team
A photo, video, or audio recording acquired or used in healthcare. The actual content may be inline or provided by direct reference.
The human-readable title to display for the package of resources when rendering the implementation guide.
Date and optionally time the procedure was performed .
The period of time that the specified participant participated in the encounter. These can overlap or be sub-sets of the overall encounter's period.
Period of time during the encounter that the participant participated
Identifies when the resource was first created.
Indicates the source of the vaccine actually administered. This may be different than the patient eligibility (e.g. the patient may be eligible for a publically purchased vaccine but due to inventory issues, vaccine purchased with private funds was actually administered).
A free text natural language description of the variable and its purpose.
Natural language description of the variable
Codes or comments regarding information or actions assciated with the pre-authorization.
Codes or text of materials to be submitted
Type of coverage (Medical; Dental; Mental Health; Substance Abuse; Vision; Drug; Short Term; Long Term Care; Hospice; Home Health).
The status of this message definition. Enables tracking the life-cycle of the content.
Business identifiers assigned to this care team by the performer or other systems which remain constant as the resource is updated and propagates from server to server.
An endpoint (network accessible address) to which messages and/or replies are to be sent.
The URL pointing to an externally maintained protocol, guideline, orderset or other definition that is adhered to in whole or in part by this ServiceRequest.
Where applicable, the imprint can be specified as text.
How long this thing happens for when it happens. If durationMax is present, this element indicates the lower bound of the allowed range of the duration.
Direct container of specimen (tube/slide, etc.)
Upper limit on medication per administration.
Source of the definition for the extension code - a logical name or a URL.
A ValueSet resource instances specifies a set of codes drawn from one or more code systems, intended for use in a particular context. Value sets link between [CodeSystem] definitions and their use in [coded elements](terminologies.html).
The organization that is the custodian of the person record.
A physical entity which is the primary unit of operational and/or administrative interest in a study.
Additional validation information for the out parameters - a single profile that covers all the parameters. The profile is a constraint on the parameters resource.
Validation information for out parameters
Defines an affiliation/assotiation/relationship between 2 distinct oganizations, that is not a part-of relationship/sub-division relationship.
A reference to the actual resource from which the narrative in the section is derived.
A reference to data that supports this section
Specified per moiety according to the Hill system, i.e. first C, then H, then alphabetical. and each moiety separated by a dot.
A link to a resource representing an earlier order related order or prescription.
An order/prescription that is being replaced
A mime type that indicates the technical format of the signature. Important mime types are application/signature+xml for X ML DigSig, application/jose for JWS, and image/* for a graphical image of a signature, etc.
A definition of a FHIR structure. This resource is used to describe the underlying resources, data types defined in FHIR, and also for describing extensions and constraints on resources and data types.
An indication that the content of the record is based on information from the person who administered the vaccine. This reflects the context under which the data was originally recorded.
Indicates context the data was recorded in
An identifier for the network access point of the user device for the audit event.
Identifier for the network access point of the user device
Desired type of performer for doing the requested service.
When the questionnaire was approved by publisher
The content was developed with a focus and intent of supporting the contexts that are listed. These terms may be used to assist with indexing and searching for appropriate naming system instances.
Allows linking the DeviceUseStatement to the underlying Request, or to other information that supports or is used to derive the DeviceUseStatement.
Links to other relevant information, including pathology reports.
When this Consent was issued / created / indexed.
When this Consent was created or indexed
The quantity or amount of instances. For example if several units are being counted for inventory, this quantity can be more than one, provided they are not unique. Seriallized items are considered unique and as such would have a quantity max 1. This element is required and its presence asserts that the reource refers to a physical item.
Identifies the conditions/problems/concerns/diagnoses/etc. whose management and/or mitigation are handled by this plan.
A Boolean value to indicate that this terminology capabilities is authored for testing purposes (or education/evaluation/marketing) and is not intended to be used for genuine usage.
The human readable description of this population criteria.
If true remove all history excluding audit.
The person who administered the collection of the image.
Unique instance identifiers assigned to a device by the device or gateway software, manufacturers, other organizations or owners. For example: handle ID.
The practitioner who is billing and responsible for the claimed services rendered to the patient.
A selector of legal concerns for this Contract definition, derivative, or instance in any legal state.
home | work | temp | old | billing - purpose of this address
An absolute URI that is used to identify this terminology capabilities when it is referenced in a specification, model, design or an instance; also called its canonical identifier. This SHOULD be globally unique and SHOULD be a literal address at which at which an authoritative instance of this terminology capabilities is (or will be) published. This URL can be the target of a canonical reference. It SHALL remain the same when the terminology capabilities is stored on different servers.
Canonical identifier for this terminology capabilities, represented as a URI (globally unique)
The name of used to identify the parameter.
Name in Parameters.parameter.name or in URL
Where the specimen came from. This may be from patient(s),from a location (e.g., the source of an environmental sample), or a sampling of a substance or a device.
The person who answered the questions about the subject.
A total count of the desired number of repetitions across the duration of the entire timing specification. If countMax is present, this element indicates the lower bound of the allowed range of count values.
The date (and optionally time) when the example scenario was published. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the example scenario changes. (e.g. the 'content logical definition').
Condition for which the medicinal use applies.
Base definition for all elements in a resource.
Describes a measurement, calculation or setting capability of a medical device.
The security role that the user was acting under, that come from local codes defined by the access control security system (e.g. RBAC, ABAC) used in the local context.
Whether improvement in the measure is noted by an increase or decrease in the measure score.
The resource this Schedule resource is providing availability information for. These are usually expected to be one of HealthcareService, Location, Practitioner, PractitionerRole, Device, Patient or RelatedPerson.
E.g. HealthCareService, Location, Practitioner, etc.
The name of the actor as shown in the page.
The assigned number for the marketing authorization.
A free text natural language description of the measure from a consumer's perspective.
Natural language description of the measure
How this list was prepared - whether it is a working list that is suitable for being maintained on an ongoing basis, or if it represents a snapshot of a list of items from another source, or whether it is a prepared list where items may be marked as added, modified or deleted.
Whether the event actually happened, or just had the potential to. Note that this is independent of whether anyone was affected or harmed or how severely.
Security labels that protects the action.
An amount of economic utility in some recognized currency.
This attribute provides information on the status of the marketing of the medicinal product See ISO/TS 20443 for more information and examples.
Request for additional supporting or authorizing information, such as: documents, images or resources.
A copyright statement relating to the plan definition and/or its contents. Copyright statements are generally legal restrictions on the use and publishing of the plan definition.
A reference to an element that holds a coded value that corresponds to a code system property. The idea is that the information model carries an element somewhere that is labeled to correspond with a code system property.
Reference to property mapping depends on
The high limit. The boundary is inclusive.
Identifies the quantity expected to be supplied, administered or consumed by the subject.
The type of the required data, specified as the type name of a resource. For profiles, this value is set to the type of the base resource of the profile.
If present, indicates that the period is a range from [period] to [periodMax], allowing expressing concepts such as "do this once every 3-5 days.
A protocol, guideline, orderset, or other definition that was adhered to in whole or in part by this event.
Whether this related person record is in active use.
Whether this related person's record is in active use
Types of resource (if a resource is referenced).
Types of resource (if a resource reference)
Power adjustment for astigmatism measured in dioptres (0.25 units).
A short name assigned to the expression to allow for multiple reuse of the expression in the context where it is defined.
Short name assigned to expression for reuse
The party who has signed-up for or 'owns' the contractual relationship to the policy or to whom the benefit of the policy for services rendered to them or their family is due.
If one or more days of week is provided, then the action happens only on the specified day(s).
The results of running the series of required clean up steps
The visit or admission or other contact between patient and health care provider the immunization was performed as part of.
The group of specified substance, e.g. group 1 to 4.
A profile that reflects constraints for the focal resource (and potentially for related resources).
Profile that must be adhered to by focus
The type of classification for which an insurer-specific class tag or number and optional name is provided, for example may be used to identify a class of coverage or employer group, Policy, Plan.
The place where the device can be found.
Whether this organization affiliation record is in active use.
Receiver Operator Characteristic (ROC) Curve to give sensitivity/specificity tradeoff.
Receiver Operator Characteristic (ROC) Curve
Codes categorizing the type of study such as investigational vs. observational, type of blinding, type of randomization, safety vs. efficacy, etc.
Codes to indicate what part of the targeted reference population it applies to. For example, the normal or therapeutic range.
The URL pointing to a FHIR-defined protocol, guideline, orderset or other definition that is adhered to in whole or in part by this Procedure.
Whether this body site is in active use.
Information supporting the clinical impression.
Identifier for the TestScript assigned for external purposes outside the context of FHIR.
The maximum time interval of conservation of the specimen with these conditions.
Id for container. There may be multiple; a manufacturer's bar code, lab assigned identifier, etc. The container ID may differ from the specimen id in some circumstances.
Whether the cost applies to in-network or out-of-network providers (in-network; out-of-network; other).
A sub-expression that defines how to extract values for this component from the output of the main SearchParameter.expression.
Subexpression relative to main expression
The URL pointing to a FHIR-defined protocol, guideline, questionnaire or other definition that is adhered to in whole or in part by this CarePlan.
Type of cost (copay; individual cap; family cap; coinsurance; deductible).
The type of origin profile the test system supports.
A duration of time during which an organism (or a process) has existed.
Person who received the answers to the questions in the QuestionnaireResponse and recorded them in the system.
Person who received and recorded the answers
This element is depracated because it is XML specific. It is replaced by issue.expression, which is format independent, and simpler to parse. For resource issues, this will be a simple XPath limited to element names, repetition indicators and the default child access that identifies one of the elements in the resource that caused this issue to be raised. For HTTP errors, will be "http." + the parameter name.
Deprecated: Path of element(s) related to issue
The volume of formula to provide to the patient per the specified administration schedule.
A free text natural language description of the naming system from a consumer's perspective. Details about what the namespace identifies including scope, granularity, version labeling, etc.
Natural language description of the naming system
The organization that manages the consent, and the framework within which it is executed.
Links to Provenance records for past versions of this Contract definition, derivative, or instance, which identify key state transitions or updates that are likely to be relevant to a user looking at the current version of the Contract. The Provence.entity indicates the target that was changed in the update. http://build.fhir.org/provenance-definitions.html#Provenance.entity.
The instant of time at which the activity was recorded.
When the activity was recorded / updated
A legal or geographic region in which the questionnaire is intended to be used.
Intended jurisdiction for questionnaire (if applicable)
A record of a request for service such as diagnostic investigations, treatments, or operations to be performed.
Description of clinical condition indicating why the ImagingStudy was requested.
A high-level category for the plan definition that distinguishes the kinds of systems that would be interested in the plan definition.
order-set | clinical-protocol | eca-rule | workflow-definition
The date and time this version of the media was made available to providers, typically after having been reviewed.
A date or partial date (e.g. just year or year + month). There is no time zone. The format is a union of the schema types gYear, gYearMonth and date. Dates SHALL be valid dates.
A Boolean value to indicate that this structure definition is authored for testing purposes (or education/evaluation/marketing) and is not intended to be used for genuine usage.
Who is providing the attested information (owner; authorized representative; authorized intermediary; non-authorized source).
A detailed description of how the plan definition is used from a clinical perspective.
Describes the clinical usage of the plan
The resource instance being linked as part of the group.
The date the evaluation of the vaccine administration event was performed.
A code that identifies the kind of trait being asserted.
Details about the device statement that were not represented at all or sufficiently in one of the attributes provided in a class. These may include for example a comment, an instruction, or a note associated with the statement.
Addition details (comments, instructions)
Identifies two or more records (resource instances) that are referring to the same real-world "occurrence".
The URL pointing to a protocol, guideline, orderset, or other definition that is adhered to in whole or in part by this MedicationRequest.
Indicates whether or not substitution can or should be part of the dispense. In some cases substitution must happen, in other cases substitution must not happen. This block explains the prescriber's intent. If nothing is specified substitution may be done.
A natural language name identifying the structure definition. This name should be usable as an identifier for the module by machine processing applications such as code generation.
Name for this structure definition (computer friendly)
Reference to the resource (containing the contents of the ruleset needed for assertions).
The quantity of vaccine product that was administered.
The date (and optionally time) when the structure map was published. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the structure map changes.
A code that specifies this medication, or a textual description if no code is available. Usage note: This could be a standard medication code such as a code from RxNorm, SNOMED CT, IDMP etc. It could also be a national or local formulary code, optionally with translations to other code systems.
Type of Asset availability for use or ownership.
A formal identifier that is used to identify this plan definition when it is represented in other formats, or referenced in a specification, model, design or an instance.
Additional identifier for the plan definition
The kind of material that forms the specimen.
Kind of material that forms the specimen
Identifiers assigned to this order by the order sender or by the order receiver.
Who is responsible for publishing the recommendations
Who verified the instruction (Patient, Relative or other Authorized Person).
The primary process by which the target is validated (edit check; value set; primary source; multiple sources; standalone; in context).
Provides reason why the activity isn't yet started, is on hold, was cancelled, etc.
Demographics and other administrative information about an individual or animal receiving care or other health-related services.
Extra information about the dispense that could not be conveyed in the other attributes.
The identified conditions and other health record elements that are intended to be addressed by the goal.
An explanatory or alternate title for the measure giving additional information about its content.
This element identifies another resource that can be used as a proxy of the security sensitivity to use when deciding and enforcing access control rules for the Binary resource. Given that the Binary resource contains very few elements that can be used to determine the sensitivity of the data and relationships to individuals, the referenced resource stands in as a proxy equivalent for this purpose. This referenced resource may be related to the Binary (e.g. Media, DocumentReference), or may be some non-related Resource purely as a security proxy. E.g. to identify that the binary resource relates to a patient, and access should only be granted to applications that have access to the patient.
Identifies another resource to use as proxy when enforcing access control
Exceptions, special conditions and supporting information applicable for this service or product line.
The Measure resource provides the definition of a quality measure.
An assessment of the likely outcome(s) for a patient or other subject as well as the likelihood of each outcome.
A copyright statement relating to the questionnaire and/or its contents. Copyright statements are generally legal restrictions on the use and publishing of the questionnaire.
The network service providing access (e.g., query, view, or retrieval) for the study. See implementation notes for information about using DICOM endpoints. A study-level endpoint applies to each series in the study, unless overridden by a series-level endpoint with the same Endpoint.connectionType.
The type of relation to the related item: child, parent, packageContent, containerPackage, usedIn, uses, requires, etc.
has-input | has-output | uses | triggers | is-replaced-by
A Boolean value to indicate that this library is authored for testing purposes (or education/evaluation/marketing) and is not intended to be used for genuine usage.
A formal identifier that is used to identify this example scenario when it is represented in other formats, or referenced in a specification, model, design or an instance.
Additional identifier for the example scenario
Allows linking the MedicationStatement to the underlying MedicationRequest, or to other information that supports or is used to derive the MedicationStatement.
A short human readable summary of the series
Date of first marketing authorization for a company's new medicinal product in any country in the World.
A Boolean value to indicate that this value set is authored for testing purposes (or education/evaluation/marketing) and is not intended to be used for genuine usage.
Per the recommended DICOM mapping, this element is derived from the Study Description attribute (0008,1030). Observations or findings about the imaging study should be recorded in another resource, e.g. Observation, and not in this element.
Whether or not to implicitly delete the fixture during teardown. If true, the fixture is automatically deleted on each server being tested during teardown, therefore no delete operation is required for this fixture in the TestScript.teardown section.
Whether or not to implicitly delete the fixture during teardown
Specimen in container intended for testing by lab
The patient, or group of patients, location, or device this observation is about and into whose record the observation is placed. If the actual focus of the observation is different from the subject (or a sample of, part, or region of the subject), the `focus` element or the `code` itself specifies the actual focus of the observation.
Who and/or what the observation is about
A name/code for the group ("set") of investigations. Typically, this will be something like "signs", "symptoms", "clinical", "diagnostic", but the list is not constrained, and others such groups such as (exposure|family|travel|nutritional) history may be used.
A free text natural language description of the terminology capabilities from a consumer's perspective. Typically, this is used when the capability statement describes a desired rather than an actual solution, for example as a formal expression of requirements as part of an RFP.
Natural language description of the terminology capabilities
accepted | declined | tentative | needs-action
Dental: basic, major, ortho; Vision exam, glasses, contacts; etc.
Indicates how quickly this SupplyRequest should be addressed with respect to other requests.
A legal or geographic region in which the search parameter is intended to be used.
Intended jurisdiction for search parameter (if applicable)
Identifies the start date and the expected (or actual, depending on status) end date for the study.
If the type is a reference to another resource, how the resource is or can be aggregated - is it a contained resource, or a reference, and if the context is a bundle, is it included in the bundle.
contained | referenced | bundled - how aggregated
A flag that indicates that the server supports conditional create.
A unique identifier for a dependent under the coverage.
The expiry or preparation date and time.
Indicates the authority who published the protocol (e.g. ACIP) that is being followed.
The time that the episode was in the specified status.
The date (and optionally time) when the naming system was published. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the naming system changes.
Allows a service to provide unique, business identifiers for the response.
Unique identifier for this copy of the Consent Statement.
Identifier for this record (external references)
Allow request for incomplete expansions?
Time period during which identifier is/was valid for use.
Time period when id is/was valid for use
Identifies additional names by which this element might also be known.
Any complications that occurred during the procedure, or in the immediate post-performance period. These are generally tracked separately from the notes, which will typically describe the procedure itself rather than any 'post procedure' issues.
Search parameters supported by implementation
The individual attesting to information.
The set of steps expected to be performed as part of the execution of the study.
Record details about an anatomical structure. This resource may be used when a coded concept does not provide the necessary detail needed for the use case.
Contact details to assist a user in learning more about or engaging with the study.
If a set of search matches, this is the total number of entries of type 'match' across all pages in the search. It does not include search.mode = 'include' or 'outcome' entries and it does not provide a count of the number of entries in the Bundle.
A natural language name identifying the test script. This name should be usable as an identifier for the module by machine processing applications such as code generation.
Name for this test script (computer friendly)
Unique, human-readable label for this arm of the study.
Whether the operation affects state = false (see [HTTP specification definition of idempotent](https://tools.ietf.org/html/rfc7231#section-4.2.2). Side effects such as producing audit trail entries do not count as 'changing state/content'.
Whether content is changed by the operation
The ChargeItemDefinition resource provides the properties that apply to the (billing) codes necessary to calculate costs and prices. The properties may differ largely depending on type and realm, therefore this resource gives only a rough structure and requires profiling for each type of billing code system.
Business identifier assigned to the risk assessment.
The name of the administrative area (county).
Name of the tester producing this report (Organization or individual).
Describes a set of data that must be provided in order to be able to successfully perform the computations defined by the library.
Type of program under which the medication is monitored.
If the list price or the rule based factor associated with the code is overridden, this attribute can capture a text to indicate the reason for this action.
Reason for overriding the list price/factor
Structural Variant Outer End. If the coordinate system is 0-based then end is is exclusive and does not include the last position. If the coordinate system is 1-base, then end is inclusive and includes the last position.
A copyright statement relating to the example scenario and/or its contents. Copyright statements are generally legal restrictions on the use and publishing of the example scenario.
A billed item may include goods or services provided in multiple encounters.
The name of the organization or individual that published the value set.
The vaccine preventable disease the dose is being administered against.
Vaccine preventatable disease being targetted
Another Location which this Location is physically part of.
Another Location this one is physically part of
If present, indicates that the count is a range - so to perform the action between [count] and [countMax] times.
Reference to the study the subject is participating in.
The current state of the health insurance product.
Text description about the reaction as a whole, including details of the manifestation if required.
The rules that the server should use to determine when to generate notifications for this subscription.
Information about a medication that is used to support knowledge.
Expresses what part of the target specification corresponds to this element.
To communicate any details or issues about the specimen or during the specimen collection. (for example: broken vial, sent with patient, frozen).
The practitioner that is the care manager/care coordinator for this patient.
Care manager/care coordinator for the patient
May be used to represent additional information that is not part of the basic definition of the resource. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension.
One or more specimens that the laboratory procedure will use.
High level categorization, e.g. polymer or nucleic acid.
A reference to the last assessment that was conducted on this patient. Assessments are often/usually ongoing in nature; a care provider (practitioner or team) will make new assessments on an ongoing basis as new data arises or the patient's conditions changes.
Any complications that occurred during the procedure, or in the immediate post-performance period.
A condition that is a result of the procedure
Where applicable, the width can be specified using a numerical value and its unit of measurement The unit of measurement shall be specified in accordance with ISO 11240 and the resulting terminology The symbol and the symbol identifier shall be used.
A resource reference indicating why this task needs to be performed.
The extent of the content of the code system (the concepts and codes it defines) are represented in this resource instance.
not-present | example | fragment | complete | supplement
The date and time beyond which this device is no longer valid or should not be used (if applicable).
Date and time of expiry of this device (if applicable)
A code or description indicating how the input is intended to be used as part of the task execution.
A canonical URL referencing a FHIR-defined protocol, guideline, orderset or other definition that is adhered to in whole or in part by this request.
The encounter or episode of care that establishes the context for this care team.
Encounter or episode associated with CareTeam
The distinct identification code required by §1271.290(c) for a human cell, tissue, or cellular and tissue-based product regulated as a device.
The distinct identification code for a biological product regulated as a device
An explanatory or alternate user-friendly title for this Contract definition, derivative, or instance in any legal state.t giving additional information about its content.
The date (and optionally time) when the graph definition was published. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the graph definition changes.
Business identifiers assigned to this adverse event by the performer or other systems which remain constant as the resource is updated and propagates from server to server.
One or more sets of investigations (signs, symptoms, etc.)
A Boolean value to indicate that this capability statement is authored for testing purposes (or education/evaluation/marketing) and is not intended to be used for genuine usage.
Who was responsible for asserting the observed value as "true".
Reason or justification for the use of the device.
Representation of the content produced in a DICOM imaging study. A study comprises a set of series, each of which includes a set of Service-Object Pair Instances (SOP Instances - images or other data) acquired or produced in a common context. A series is of only one modality (e.g. X-ray, CT, MR, ultrasound), but a study may have multiple series of different modalities.
A pointer to official web page, PDF or other rendering of the implementation guide.
Location of rendered implementation guide
Another group that this group adds rules to.
Full details of any issues found in the message.
Indicates a meaning for the supplemental data. This can be as simple as a unique identifier, or it can establish meaning in a broader context by drawing from a terminology, allowing supplemental data to be correlated across measures.
Marketing status of the medicinal product, in contrast to marketing authorizaton.
An identifier that applies to this person's qualification in this role.
An identifier for this qualification for the practitioner
When the substance is no longer valid to use. For some substances, a single arbitrary date is used for expiry.
A Capability Statement documents a set of capabilities (behaviors) of a FHIR Server that may be used as a statement of actual server functionality or a statement of required or desired server implementation.
The network address of the endpoint. For solutions that do not use network addresses for routing, it can be just an identifier.
Network address or identifier of the end-point
A period of time after authorization before generic product applicatiosn can be submitted.
The date (and optionally time) when the questionnaire was published. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the questionnaire changes.
Identifies when the current status. I.e. When initially created, when achieved, when cancelled, etc.
Upper limit on medication per lifetime of the patient.
Identifies the 'type' of resource - equivalent to the resource name for other resources.
The kind of change that happened to the device during the procedure.
The name of the organization or individual that published the graph definition.
Any restrictions on medication substitution
Patient or consumer-oriented instructions
The content was developed with a focus and intent of supporting the contexts that are listed. These terms may be used to assist with indexing and searching for appropriate example scenario instances.
A date, date-time or partial date (e.g. just year or year + month). If hours and minutes are specified, a time zone SHALL be populated. The format is a union of the schema types gYear, gYearMonth, date and dateTime. Seconds must be provided due to schema type constraints but may be zero-filled and may be ignored. Dates SHALL be valid dates.
The meaning of this stratifier, as defined in the measure definition.
Ideally this is an absolute URL that is used to identify the version-specific TestScript that was executed, matching the `TestScript.url`.
Reference to the version-specific TestScript that was executed to produce this TestReport
A free text natural language description of the value set from a consumer's perspective.
Natural language description of the value set
The relative path for primary page for this resource within the IG.
This records identifiers associated with this medication request that are defined by business processes and/or used to refer to it when a direct URL reference to the resource itself is not appropriate. For example a reimbursement system might issue its own id for each prescription that is created. This is particularly important where FHIR only provides part of an entire workflow process where records must be tracked through an entire system.
The person or organization that provided the information about the taking of this medication. Note: Use derivedFrom when a MedicationStatement is derived from other resources, e.g. Claim or MedicationRequest.
Person or organization that provided the information about the taking of this medication
Explanation of why this library is needed and why it has been designed as it has.
The date range of services associated with this account.
The type of container associated with the specimen (e.g. slide, aliquot, etc.).
Kind of container directly associated with specimen
Identifies the broad classification of the kind of resources the group includes.
person | animal | practitioner | device | medication | substance
The date that the attachment was first created.
Preparation of the patient for specimen collection.
Describes the type of the calibration method.
A reference to the actual resource from which data was derived.
The kind of dose or rate specified, for example, ordered or calculated.
The plan/proposal/order describing the proposed service in detail.
Molecular formula shall be captured as described in 4.7.3.
A coded entry to indicate how the data was entered.
A Boolean value to indicate that this event definition is authored for testing purposes (or education/evaluation/marketing) and is not intended to be used for genuine usage.
Provides the rationale that drove the inclusion of this particular activity as part of the plan or the reason why the activity was prohibited.
Why activity should be done or why activity was prohibited
A signature along with supporting context. The signature may be a digital signature that is cryptographic in nature, or some other signature acceptable to the domain. This other signature may be as simple as a graphical image representing a hand-written signature, or a signature ceremony Different signature approaches have different utilities.
A Signature - XML DigSig, JWS, Graphical image of signature, etc.
The URL pointing to an externally maintained protocol, guideline, orderset or other definition that is adhered to in whole or in part by this NutritionOrder.
Display text for an identifier for the group
Additional supporting documentation that explains the purpose of the group and the types of mappings within it.
Additional description/explanation for group
Identifies the time action was first taken against the task (start) and/or the time final action was taken against the task prior to marking it as completed (end).
A modifier supported for the search parameter.
missing | exact | contains | not | text | in | not-in | below | above | type | identifier | ofType
Indicates the order in which the dosage instructions should be applied or interpreted.
Indicator that the user is or is not the requestor, or initiator, for the event being audited.
Calculated sensitivity if the GQ score threshold was set to "score" field value.
A location where the data can be accessed.
Defines specimen requirements for the action to be performed, such as required specimens for a lab test.
What specimens are required to perform this action
Estimated or actual date the AdverseEvent began, in the opinion of the reporter.
Identifies what kind of team. This is to support differentiation between multiple co-existing teams, such as care plan team, episode of care team, longitudinal care team.
A number appearing on the immediate packaging (and not the outer packaging).
A natural language name identifying the plan definition. This name should be usable as an identifier for the module by machine processing applications such as code generation.
Name for this plan definition (computer friendly)
A free text natural language description of the activity definition from a consumer's perspective.
Natural language description of the activity definition
A free text description of the outcome of the event.
Explains how that element affects the interpretation of the resource or element that contains it.
Reason that this element is marked as a modifier
On whom or what the service is to be performed. This is usually a human patient, but can also be requested on animals, groups of humans or animals, devices such as dialysis machines, or even locations (typically for environmental scans).
The patient or group that was the focus of this communication.
Additional information supplied about each concept
A code that classifies whether the media is an image, video or audio recording or some other media category.
Classification of media as image, video, or audio
The organization that assigns the identifier algorithm.
Identifies the target end system in situations where the initial message transmission is to an intermediary system.
Particular delivery destination within the destination
Identifies who is the agent. Such as the author of the manifest, and adding documents to it.
Who and/or what had an agent participation
Specific type of encounter (e.g. e-mail consultation, surgical day-care, skilled nursing, rehabilitation).
Service types, codes and supporting information
The request this encounter satisfies (e.g. incoming referral or procedure request).
The ServiceRequest that initiated this encounter
The legal status of supply in a jurisdiction or region.
A string which has at least one character and no leading or trailing whitespace and where there is no whitespace other than single spaces in the contents
Composition information about the substance
Identifies a profile structure or implementation Guide that applies to the datatype this element refers to. If any profiles are specified, then the content must conform to at least one of them. The URL can be a local reference - to a contained StructureDefinition, or a reference to another StructureDefinition or Implementation Guide by a canonical URL. When an implementation guide is specified, the type SHALL conform to at least one profile defined in the implementation guide.
Profiles (StructureDefinition or IG) - one must apply
The number of false negatives if the GQ score threshold was set to "score" field value.
The date (and optionally time) when the library was published. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the library changes.
An item that this catalog entry is related to
Resource(s) that are the subject of the event
A list of operators that can be used with the filter.
Identifiers assigned to this research study by the sponsor or other systems.
The name of the organization or individual that published the message definition.
The use context of this name for example if there is a different name a drug active ingredient as opposed to a food colour additive.
Calculated fScore if the GQ score threshold was set to "score" field value.
candidate | eligible | follow-up | ineligible | not-registered | off-study | on-study | on-study-intervention | on-study-observation | pending-on-study | potential-candidate | screening | withdrawn
A reference from the Insurer to which these services pertain.
The action to be performed for collecting the specimen.
A search parameter that defines a named search item that can be used to search/filter on a resource.
A flag that indicates that the server supports conditional update.
The shelf-life and storage information for a medicinal product item or container can be described using this class.
Member of the team who provided the overall service.
Additional data or information such as resources, documents, images etc. including references to the data or the actual inclusion of the data.
Additional Data or supporting information
Procedure request to obtain this biologically derived product.
The URL pointing to an *externally* maintained protocol, guideline, orderset or other definition that is adhered to in whole or in part by this Task.
Describes a required data item for evaluation in terms of the type of data, and optional code or date-based filters of the data.
A persistent identifier for the bundle that won't change as a bundle is copied from server to server.
Represents when this particular CarePlan record was created in the system, which is often a system-generated date.
A product specific contact, person (in a role), or an organization.
The name of the individual or organization responsible for the contribution.
An image that can be displayed as a thumbnail of the person to enhance the identification of the individual.
The content was developed with a focus and intent of supporting the contexts that are listed. These terms may be used to assist with indexing and searching for appropriate library instances.
Ingredient role e.g. Active ingredient, excipient.
The contact details for the individual (if a name was provided) or the organization.
Contact details for individual or organization
A clinical condition, problem, diagnosis, or other event, situation, issue, or clinical concept that has risen to a level of concern.
A reference to supply which authenticates the process.
Access to on-line information about the device.
Status of funds reservation (For provider, for Patient, None).
The maximum treatment period during which an Investigational Medicinal Product can be administered as per the protocol referenced in the clinical trial authorisation.