This page is part of the FHIR Specification (v5.0.0-ballot: FHIR R5 Ballot Preview). 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: R5 R4B R4 R3
Community Based Collaborative Care Work Group | Maturity Level: N/A | Standards Status: Informative | Compartments: Patient |
Raw XML (canonical form + also see XML Format Specification)
Withhold or withdraw consent for disclosure of records related to specific domain (e.g. DI, LAB, etc.) (id = "consent-example-notThis")
<?xml version="1.0" encoding="UTF-8"?> <Consent xmlns="http://hl7.org/fhir"> <id value="consent-example-notThis"/> <text> <status value="generated"/> <div xmlns="http://www.w3.org/1999/xhtml"> <p> The following scenario is based on existing jurisdictional policy and are realized in existing systems in Canada. The default policy is one of implied consent for the provision of care, so these scenarios all deal with withdrawal or withholding consent for that purpose. Withhold or withdraw consent for disclosure of a specific record (e.g. Lab Order/Result) </p> <p> Patient "Donal D DUCK"'s Primary Care Provider, Dr. Philip Primary, has ordered a set of lab test which Adam wishes to keep as private as possible. At the sample collection facility, he indicates that he would like withhold consent to disclose the order and all results associated with that specific order from all other providers </p> </div> </text> <status value="active"/> <category> <coding> <system value="http://loinc.org"/> <code value="59284-0"/> </coding> </category> <subject> <reference value="Patient/f001"/> <display value="P. van de Heuvel"/> </subject> <dateTime value="2018-12-28"/> <controller> <reference value="Organization/f001"/> </controller> <sourceAttachment> <title value="The terms of the consent in lawyer speak."/> <!-- likely use url pointer to common text --> </sourceAttachment> <regulatoryBasis> <coding> <system value="http://terminology.hl7.org/CodeSystem/v3-ActCode"/> <code value="INFA"/> </coding> </regulatoryBasis> <provision> <!-- this is opt-in - e.g. everything approved unless otherwise stated --> <type value="permit"/> <provision> <type value="deny"/> <data> <meaning value="related"/> <reference> <reference value="MedicationRequest/medrx0305"/> </reference> </data> </provision> </provision> </Consent>
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.