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Difference between revisions of "HL7 FHIR Consent Directive Project"
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* FHIR Consent November 11, 2016 - CANCELLED | * FHIR Consent November 11, 2016 - CANCELLED | ||
* [[FHIR Consent November 4, 2016]] | * [[FHIR Consent November 4, 2016]] | ||
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==Purpose== | ==Purpose== | ||
Revision as of 19:43, 3 February 2017
This work is authorized under project 1130 HL7 Patient Friendly Consent Directive Project
HL7 FHIR Consent Directive Project
Contents
New Weekly Meeting Logistics
NEW Weekly meeting; Fridays 2:00 - 3:00 PM Eastern Time
- Phone: +1 770-657-9270, Participant Code: 994563
- Web meeting Info: https://global.gotomeeting.com/join/995119629
Call Agenda, Attendance, and Call Notes
- FHIR Consent Feb 24, 2017
- FHIR Consent Feb 17, 2017 - CANCELLED
- FHIR Consent Feb 10, 2017 - CANCELLED
- FHIR Consent Feb 3, 2017 FINAL CALL Prior to STU3
- FHIR Consent Jan 27, 2017
- FHIR Consent Jan 19, 2017 - CANCELLED
- FHIR Consent Jan 12, 2017 - CANCELLED
- FHIR Consent Jan 5, 2017
- FHIR Consent Dec 30, 2016 - CANCELLED
- FHIR Consent Dec 23, 2016 - CANCELLED
- FHIR Consent Dec 16, 2016
- FHIR Consent Dec 9, 2016
- FHIR Consent Dec 2, 2016
- FHIR Consent November 25, 2016 - CANCELLED
- FHIR Consent November 18, 2016
- FHIR Consent November 11, 2016 - CANCELLED
- FHIR Consent November 4, 2016
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
- None
FHIR Consent Directive Artefacts
- Current Information for Discussion
THese have been provided by Mike Davis, Kathleen Connor and John Moehrke as illustrations for possible reasons for and against having multiple Purpose of Use elements on the FHIR Consent Resource.
- Historical Documents
- FHIR Consent Directive DSTU 1 Artifacts
Consent Directive Examples
Work breakdown
Work on the existing path, then expand to review consent for more than disclosure. 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)
- Simple acknowledgement without deviations... Equivalent to BPPC
- 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.
