HL7 FHIR Consent Directive Project

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HL7 FHIR Consent Directive Project

New Weekly Meeting Logistics

Fridays 12:00 - 1:30 PM Eastern Time

• Phone: +1 770-657-9270, Participant Code: 994563
• Web meeting Info: https://global.gotomeeting.com/join/520841173

Call Agenda, Attendance, and Call Notes

• FHIR Consent February 5, 2016
• FHIR Consent January 29, 2015
• FHIR Consent December 30, 2015
• FHIR Consent December 23, 2015 is Cancelled
• FHIR Consent December 16, 2015
• FHIR Consent December 9, 2015
• FHIR Consent IG - December 4, 2015
• December 2, 2015
• November 18, 2015
• November 11, 2015
• November 4, 2015
• October 28, 2015

Purpose

To track the progress of the HL7 FHIR Consent Directive Project. Prior to 10/27/2015, some of this content was kept on the [HL7 Patient Friendly Language Consent Directive Project] page.

FHIR Consent Directive Artifacts

• FHIR Consent Directive Use Cases
• FHIR Consent Directive Library
• Consent Directive Examples
• FHIR Consent Directive Value Sets
• FHIR Consent Directive DSTU 1 Artifacts

Work breakdown

Work on the existing path, thus deferring resolution of "Consent as a Resource" vs "Consent as a Profile on Contract". It is best to get progress, and this difference is holding progress. Once we make more progress we can resolve and adjust.

• Start effort on developing this effort as an Implementation Guide (IG)
• Have many profiles within the IG
  • Simple acknowledgement without deviations... Equivalent to BPPC
    • Opt-In, Opt-Out, Opt-Out-fully, etc
  • Consent with explicitly authorized individuals
    • organization or individual or service delivery location
  • Consent with explicitly identified types of objects to exclude
    • By clinical type of data
    • By repository holding that data
  • Consent with explicitly identified objects to exclude
    • Consent with explicitly identified object and any other object related to that object (order number --> all results)(e.g. accession number)
  • Consents with explicitly identified author to include/exclude
  • Defining combination of terms within a single policy
  • Defining combination of terms when they are individual policies (opt-out + opt-in-for-Bob != opt-in-for-Bob + opt-out)
• Explain how Consent is related to a Questionnaire presented to a patient
• Produce a set of Consent logical Principles
  • e.g. when writing rules, you are only adding things into scope
• Explain how CDA-ConsentDirective can inform FHIR Consent.
•  ???