This page is part of the FHIR Specification (v4.3.0: R4B - STU). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions . Page versions: R4B R4 R3
Community Based Collaborative Care Work Group | Maturity Level: N/A | Standards Status: Informative |
Raw XML (canonical form + also see XML Format Specification)
Definition for Code SystemConsentCategoryCodes
<?xml version="1.0" encoding="UTF-8"?> <CodeSystem xmlns="http://hl7.org/fhir"> <id value="consent-category"/> <meta> <lastUpdated value="2022-05-28T12:47:40.239+10:00"/> <profile value="http://hl7.org/fhir/StructureDefinition/shareablecodesystem"/> </meta> <text> <status value="generated"/> <div xmlns="http://www.w3.org/1999/xhtml"> <p> This code system http://terminology.hl7.org/CodeSystem/consentcategorycodes defines the following codes:</p> <table class="codes"> <tr> <td style="white-space:nowrap"> <b> Code</b> </td> <td> <b> Display</b> </td> <td> <b> Definition</b> </td> </tr> <tr> <td style="white-space:nowrap">acd <a name="consent-category-acd"> </a> </td> <td> Advance Directive</td> <td> Any instructions, written or given verbally by a patient to a health care provider in anticipation of potential need for medical treatment. [2005 Honor My Wishes]</td> </tr> <tr> <td style="white-space:nowrap">dnr <a name="consent-category-dnr"> </a> </td> <td> Do Not Resuscitate</td> <td> A legal document, signed by both the patient and their provider, stating a desire not to have CPR initiated in case of a cardiac event. Note: This form was replaced in 2003 with the Physician Orders for Life-Sustaining Treatment [POLST].</td> </tr> <tr> <td style="white-space:nowrap">emrgonly <a name="consent-category-emrgonly"> </a> </td> <td> Emergency Only</td> <td> Opt-in to disclosure of health information for emergency only consent directive. Comment: This general consent directive specifically limits disclosure of health information for purpose of emergency treatment. Additional parameters may further limit the disclosure to specific users, roles, duration, types of information, and impose uses obligations. [ActConsentDirective (2.16.840.1.113883.1.11.20425)]</td> </tr> <tr> <td style="white-space:nowrap">hcd <a name="consent-category-hcd"> </a> </td> <td> Health Care Directive</td> <td> Patient's document telling patient's health care provider what the patient wants or does not want if the patient is diagnosed as being terminally ill and in a persistent vegetative state or in a permanently unconscious condition.[2005 Honor My Wishes]</td> </tr> <tr> <td style="white-space:nowrap">npp <a name="consent-category-npp"> </a> </td> <td> Notice of Privacy Practices</td> <td> Acknowledgement of custodian notice of privacy practices. Usage Notes: This type of consent directive acknowledges a custodian's notice of privacy practices including its permitted collection, access, use and disclosure of health information to users and for purposes of use specified. [ActConsentDirective (2.16.840.1.113883.1.11.20425)]</td> </tr> <tr> <td style="white-space:nowrap">polst <a name="consent-category-polst"> </a> </td> <td> POLST</td> <td> The Physician Order for Life-Sustaining Treatment form records a person's health care wishes for end of life emergency treatment and translates them into an order by the physician. It must be reviewed and signed by both the patient and the physician, Advanced Registered Nurse Practitioner or Physician Assistant. [2005 Honor My Wishes] Comment: Opt-in Consent Directive with restrictions.</td> </tr> <tr> <td style="white-space:nowrap">research <a name="consent-category-research"> </a> </td> <td> Research Information Access</td> <td> Consent to have healthcare information in an electronic health record accessed for research purposes. [VALUE SET: ActConsentType (2.16.840.1.113883.1.11.19897)]</td> </tr> <tr> <td style="white-space:nowrap">rsdid <a name="consent-category-rsdid"> </a> </td> <td> De-identified Information Access</td> <td> Consent to have de-identified healthcare information in an electronic health record that is accessed for research purposes, but without consent to re-identify the information under any circumstance. [VALUE SET: ActConsentType (2.16.840.1.113883.1.11.19897)</td> </tr> <tr> <td style="white-space:nowrap">rsreid <a name="consent-category-rsreid"> </a> </td> <td> Re-identifiable Information Access</td> <td> Consent to have de-identified healthcare information in an electronic health record that is accessed for research purposes re-identified under specific circumstances outlined in the consent. [VALUE SET: ActConsentType (2.16.840.1.113883.1.11.19897)]</td> </tr> </table> </div> </text> <extension url="http://hl7.org/fhir/StructureDefinition/structuredefinition-wg"> <valueCode value="cbcc"/> </extension> <url value="http://terminology.hl7.org/CodeSystem/consentcategorycodes"/> <identifier> <system value="urn:ietf:rfc:3986"/> <value value="urn:oid:2.16.840.1.113883.4.642.1.1226"/> </identifier> <version value="4.3.0"/> <name value="ConsentCategoryCodes"/> <title value="Consent Category Codes"/> <status value="draft"/> <experimental value="false"/> <description value="FHIR Specific Example codes for Consent Category"/> <caseSensitive value="true"/> <hierarchyMeaning value="is-a"/> <content value="complete"/> <concept> <code value="acd"/> <display value="Advance Directive"/> <definition value="Any instructions, written or given verbally by a patient to a health care provider in anticipation of potential need for medical treatment. [2005 Honor My Wishes]"/> </concept> <concept> <code value="dnr"/> <display value="Do Not Resuscitate"/> <definition value="A legal document, signed by both the patient and their provider, stating a desire not to have CPR initiated in case of a cardiac event. Note: This form was replaced in 2003 with the Physician Orders for Life-Sustaining Treatment [POLST]."/> </concept> <concept> <code value="emrgonly"/> <display value="Emergency Only"/> <definition value="Opt-in to disclosure of health information for emergency only consent directive. Comment: This general consent directive specifically limits disclosure of health information for purpose of emergency treatment. Additional parameters may further limit the disclosure to specific users, roles, duration, types of information, and impose uses obligations. [ActConsentDirective (2.16.840.1.113883.1.11.20425)]"/> </concept> <concept> <code value="hcd"/> <display value="Health Care Directive"/> <definition value="Patient's document telling patient's health care provider what the patient wants or does not want if the patient is diagnosed as being terminally ill and in a persistent vegetative state or in a permanently unconscious condition.[2005 Honor My Wishes]"/> </concept> <concept> <code value="npp"/> <display value="Notice of Privacy Practices"/> <definition value="Acknowledgement of custodian notice of privacy practices. Usage Notes: This type of consent directive acknowledges a custodian's notice of privacy practices including its permitted collection, access, use and disclosure of health information to users and for purposes of use specified. [ActConsentDirective (2.16.840.1.113883.1.11.20425)]"/> </concept> <concept> <code value="polst"/> <display value="POLST"/> <definition value="The Physician Order for Life-Sustaining Treatment form records a person's health care wishes for end of life emergency treatment and translates them into an order by the physician. It must be reviewed and signed by both the patient and the physician, Advanced Registered Nurse Practitioner or Physician Assistant. [2005 Honor My Wishes] Comment: Opt-in Consent Directive with restrictions."/> </concept> <concept> <code value="research"/> <display value="Research Information Access"/> <definition value="Consent to have healthcare information in an electronic health record accessed for research purposes. [VALUE SET: ActConsentType (2.16.840.1.113883.1.11.19897)]"/> </concept> <concept> <code value="rsdid"/> <display value="De-identified Information Access"/> <definition value="Consent to have de-identified healthcare information in an electronic health record that is accessed for research purposes, but without consent to re-identify the information under any circumstance. [VALUE SET: ActConsentType (2.16.840.1.113883.1.11.19897)"/> </concept> <concept> <code value="rsreid"/> <display value="Re-identifiable Information Access"/> <definition value="Consent to have de-identified healthcare information in an electronic health record that is accessed for research purposes re-identified under specific circumstances outlined in the consent. [VALUE SET: ActConsentType (2.16.840.1.113883.1.11.19897)]"/> </concept> </CodeSystem>
Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.