Generated Narrative: StructureDefinition ext-R5-DeviceDefinition.guideline Name Flags Card. Type Description & Constraints Extension 0..1 Extension(4.0.1) R5: Information aimed at providing directions for the usage of this model of device (new) #xD; Slices for extension 0..* Extension Extension Slice: Unordered, Open by value:url #xD; extension:useContext 0..* Extension R5: The circumstances that form the setting for using the device (new) #xD; url 1..1 uri "useContext" #xD; value[x] 0..1 UsageContext The circumstances that form the setting for using the device #xD; extension:usageInstruction 0..1 Extension R5: Detailed written and visual directions for the user on how to use the device (new) #xD; url 1..1 uri "usageInstruction" #xD; value[x] 0..1 markdown Detailed written and visual directions for the user on how to use the device #xD; extension:relatedArtifact 0..* Extension R5: A source of information or reference for this guideline (new) #xD; url 1..1 uri "relatedArtifact" #xD; value[x] 0..1 RelatedArtifact A source of information or reference for this guideline #xD; extension:indication 0..* Extension R5: A clinical condition for which the device was designed to be used (new) #xD; url 1..1 uri "indication" #xD; value[x] 0..1 CodeableConcept A clinical condition for which the device was designed to be used #xD; extension:contraindication 0..* Extension R5: A specific situation when a device should not be used because it may cause harm (new) #xD; url 1..1 uri "contraindication" #xD; value[x] 0..1 CodeableConcept A specific situation when a device should not be used because it may cause harm #xD; extension:warning 0..* Extension R5: Specific hazard alert information that a user needs to know before using the device (new) #xD; url 1..1 uri "warning" #xD; value[x] 0..1 CodeableConcept Specific hazard alert information that a user needs to know before using the device #xD; extension:intendedUse 0..1 Extension R5: A description of the general purpose or medical use of the device or its function (new) #xD; url 1..1 uri "intendedUse" #xD; value[x] 0..1 string A description of the general purpose or medical use of the device or its function #xD; url 1..1 uri "http://hl7.org/fhir/5.0/StructureDefinition/extension-DeviceDefinition.guideline" #xD; value[x] 0..0 Value of extension #xD; Documentation for this format
R5: Information aimed at providing directions for the usage of this model of device (new)
R5: `DeviceDefinition.guideline` (new:BackboneElement)
This extension is part of the cross-version definitions generated to enable use of the element `DeviceDefinition.guideline` as defined in FHIR R5 in FHIR R4. The source element is defined as: `DeviceDefinition.guideline` 0..1 `BackboneElement` Across FHIR versions, the element set has been mapped as: * R5: `DeviceDefinition.guideline` 0..1 `BackboneElement` Following are the generation technical comments: Element `DeviceDefinition.guideline` has a context of DeviceDefinition based on following the parent source element upwards and mapping to `DeviceDefinition`. Element `DeviceDefinition.guideline` has no mapping targets in FHIR R4. Typically, this is because the element has been added (is a new element).
Element `DeviceDefinition.guideline` has a context of DeviceDefinition based on following the parent source element upwards and mapping to `DeviceDefinition`. Element `DeviceDefinition.guideline` has no mapping targets in FHIR R4. Typically, this is because the element has been added (is a new element). For more structured data, a ClinicalUseDefinition that points to the DeviceDefinition can be used.
All FHIR elements must have a @value or children
hasValue() or (children().count() > id.count())
Must have either extensions or value[x], not both
exists(f:extension)!=exists(f:*[starts-with(local-name(.), 'value')])
Unique id for the element within a resource (for internal references). This may be any string value that does not contain spaces.
Extensions are always sliced by (at least) url
exists(f:extension)!=exists(f:*[starts-with(local-name(.), "value")])
R5: The circumstances that form the setting for using the device (new)
R5: `DeviceDefinition.guideline.useContext` (new:UsageContext)
Element `DeviceDefinition.guideline.useContext` is part of an existing definition because parent element `DeviceDefinition.guideline` requires a cross-version extension. Element `DeviceDefinition.guideline.useContext` has a context of DeviceDefinition based on following the parent source element upwards and mapping to `DeviceDefinition`. Element `DeviceDefinition.guideline.useContext` has no mapping targets in FHIR R4. Typically, this is because the element has been added (is a new element).
Additional content defined by implementations
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.
There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.
Source of the definition for the extension code - a logical name or a URL.
The definition may point directly to a computable or human-readable definition of the extensibility codes, or it may be a logical URI as declared in some other specification. The definition SHALL be a URI for the Structure Definition defining the extension.
The circumstances that form the setting for using the device
The circumstances that form the setting for using the device.
R5: Detailed written and visual directions for the user on how to use the device (new)
R5: `DeviceDefinition.guideline.usageInstruction` (new:markdown)
Element `DeviceDefinition.guideline.usageInstruction` is part of an existing definition because parent element `DeviceDefinition.guideline` requires a cross-version extension. Element `DeviceDefinition.guideline.usageInstruction` has a context of DeviceDefinition based on following the parent source element upwards and mapping to `DeviceDefinition`. Element `DeviceDefinition.guideline.usageInstruction` has no mapping targets in FHIR R4. Typically, this is because the element has been added (is a new element).
Detailed written and visual directions for the user on how to use the device
Detailed written and visual directions for the user on how to use the device.
R5: A source of information or reference for this guideline (new)
R5: `DeviceDefinition.guideline.relatedArtifact` (new:RelatedArtifact)
Element `DeviceDefinition.guideline.relatedArtifact` is part of an existing definition because parent element `DeviceDefinition.guideline` requires a cross-version extension. Element `DeviceDefinition.guideline.relatedArtifact` has a context of DeviceDefinition based on following the parent source element upwards and mapping to `DeviceDefinition`. Element `DeviceDefinition.guideline.relatedArtifact` has no mapping targets in FHIR R4. Typically, this is because the element has been added (is a new element).
A source of information or reference for this guideline
A source of information or reference for this guideline.
R5: A clinical condition for which the device was designed to be used (new)
R5: `DeviceDefinition.guideline.indication` (new:CodeableConcept)
Element `DeviceDefinition.guideline.indication` is part of an existing definition because parent element `DeviceDefinition.guideline` requires a cross-version extension. Element `DeviceDefinition.guideline.indication` has a context of DeviceDefinition based on following the parent source element upwards and mapping to `DeviceDefinition`. Element `DeviceDefinition.guideline.indication` has no mapping targets in FHIR R4. Typically, this is because the element has been added (is a new element). A ClinicalUseDefinition that points to the DeviceDefinition can be used if more structured data is needed.
Element `DeviceDefinition.guideline.indication` is part of an existing definition because parent element `DeviceDefinition.guideline` requires a cross-version extension. Element `DeviceDefinition.guideline.indication` has a context of DeviceDefinition based on following the parent source element upwards and mapping to `DeviceDefinition`. Element `DeviceDefinition.guideline.indication` has no mapping targets in FHIR R4. Typically, this is because the element has been added (is a new element).
A clinical condition for which the device was designed to be used
A clinical condition for which the device was designed to be used.
A ClinicalUseDefinition that points to the DeviceDefinition can be used if more structured data is needed.
R5: A specific situation when a device should not be used because it may cause harm (new)
R5: `DeviceDefinition.guideline.contraindication` (new:CodeableConcept)
Element `DeviceDefinition.guideline.contraindication` is part of an existing definition because parent element `DeviceDefinition.guideline` requires a cross-version extension. Element `DeviceDefinition.guideline.contraindication` has a context of DeviceDefinition based on following the parent source element upwards and mapping to `DeviceDefinition`. Element `DeviceDefinition.guideline.contraindication` has no mapping targets in FHIR R4. Typically, this is because the element has been added (is a new element). A ClinicalUseDefinition that points to the DeviceDefinition can be used if more structured data is needed.
Element `DeviceDefinition.guideline.contraindication` is part of an existing definition because parent element `DeviceDefinition.guideline` requires a cross-version extension. Element `DeviceDefinition.guideline.contraindication` has a context of DeviceDefinition based on following the parent source element upwards and mapping to `DeviceDefinition`. Element `DeviceDefinition.guideline.contraindication` has no mapping targets in FHIR R4. Typically, this is because the element has been added (is a new element).
A specific situation when a device should not be used because it may cause harm
A specific situation when a device should not be used because it may cause harm.
R5: Specific hazard alert information that a user needs to know before using the device (new)
R5: `DeviceDefinition.guideline.warning` (new:CodeableConcept)
Element `DeviceDefinition.guideline.warning` is part of an existing definition because parent element `DeviceDefinition.guideline` requires a cross-version extension. Element `DeviceDefinition.guideline.warning` has a context of DeviceDefinition based on following the parent source element upwards and mapping to `DeviceDefinition`. Element `DeviceDefinition.guideline.warning` has no mapping targets in FHIR R4. Typically, this is because the element has been added (is a new element). A ClinicalUseDefinition that points to the DeviceDefinition can be used if more structured data is needed.
Element `DeviceDefinition.guideline.warning` is part of an existing definition because parent element `DeviceDefinition.guideline` requires a cross-version extension. Element `DeviceDefinition.guideline.warning` has a context of DeviceDefinition based on following the parent source element upwards and mapping to `DeviceDefinition`. Element `DeviceDefinition.guideline.warning` has no mapping targets in FHIR R4. Typically, this is because the element has been added (is a new element).
Specific hazard alert information that a user needs to know before using the device
Specific hazard alert information that a user needs to know before using the device.
R5: A description of the general purpose or medical use of the device or its function (new)
R5: `DeviceDefinition.guideline.intendedUse` (new:string)
Element `DeviceDefinition.guideline.intendedUse` is part of an existing definition because parent element `DeviceDefinition.guideline` requires a cross-version extension. Element `DeviceDefinition.guideline.intendedUse` has a context of DeviceDefinition based on following the parent source element upwards and mapping to `DeviceDefinition`. Element `DeviceDefinition.guideline.intendedUse` has no mapping targets in FHIR R4. Typically, this is because the element has been added (is a new element).
A description of the general purpose or medical use of the device or its function
A description of the general purpose or medical use of the device or its function.
Value of extension - must be one of a constrained set of the data types (see [Extensibility](http://hl7.org/fhir/R4/extensibility.html) for a list).