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  1. FHIR Specification Feedback
  2. FHIR-11061

A Consent Directive must name both the grantor and the grantee(s) or it is not a Consent Directive. - 2016-09 core #80

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    • Icon: Change Request Change Request
    • Resolution: Persuasive with Modification
    • Icon: Medium Medium
    • FHIR Core (FHIR)
    • DSTU2
    • Community-Based Care and Privacy
    • Consent
    • 6.4.4
    • Hide

      Persuasive with Mod – Change as recommended

      Change Consent.consentor to Consent.consentingParty

      Change Definition: 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.

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      Persuasive with Mod – Change as recommended Change Consent.consentor to Consent.consentingParty Change Definition: 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.
    • Kathleen Connor/John Moehrke: 4-0-0
    • Correction
    • Non-substantive
    • DSTU2

    Description

      Existing Wording: Consent.consentor Definition The patient/consumer that is responsible for agreeing to the consent represented by this resource. This is the person (usually) that agreed to the policy, along with the exceptions, e.g. the person who takes responsibility for the agreement. In the signature this corresponds to the role "Consent Signature".

      Proposed Wording: Consent.consentingParty or Consent.signer Definition: 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.

      Comment:

      A patient/consumer is not the only consenting party to a Consent Directive, even if the grantee has "pre-signed" by issuing an offer of a Consent Directive to the patient/consumer. Without including both, even if the grantee by implication, this is not a Consent Directive. The patient/consumer is not the only party "that agreed to the policy, along with the exceptions, e.g. the person who takes responsibility for the agreement." The grantee is responsible for agreeing AND for complying with the Consent Directive policies.

      The CBCC WG, as far as I recall, explicitly did not agree to this lopsided definition.

      Summary:

      A Consent Directive must name both the grantor and the grantee(s) or it is not a Consent Directive.

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            Unassigned Unassigned
            k.connor Kathleen Connor
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              Updated:
              Resolved: