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Difference between revisions of "HL7 FHIR Consent Directive Project"

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==Call Agenda, Attendance, and Call Notes==
 
==Call Agenda, Attendance, and Call Notes==
  
 +
* [[FHIR Consent November 4, 2016]]
 
* FHIR Consent August 3, 2016 - CANCELLED
 
* FHIR Consent August 3, 2016 - CANCELLED
 
* FHIR Consent July 27, 2016 - CANCELLED
 
* FHIR Consent July 27, 2016 - CANCELLED

Revision as of 20:04, 4 November 2016

Back to CBCC Wiki: Meetings

This work is authorized under project 1130 HL7 Patient Friendly Consent Directive Project

HL7 FHIR Consent Directive Project

New Weekly Meeting Logistics

Wednesday 3:00-4:30 PM Eastern Time

Call Agenda, Attendance, and Call Notes

NOTE: No meetings from May 6 - May 20. Calls resume on May 27

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.

working space

FHIR Consent Directive Implementation Guide

Current Open FHIR CPs

FHIR Consent Directive Artifacts

Consent Directive Examples

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.
  •  ???
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