View source for 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 [[http://wiki.hl7.org/index.php?title=HL7_Patient_Friendly_Consent_Directive_Project HL7 Patient Friendly Language Consent Directive Project]] page.

==[[FHIR Consent Directive Implemenation Guide]]==

==[[Current Open FHIR CPs]]==

==FHIR Consent Directive Artifacts==
*[[FHIR Consent Directive Use Cases]]
*[[FHIR Consent Directive Library]]
*[[Consent Directive Examples]]
*[[FHIR Consent Directive Value Sets]]
*[http://gforge.hl7.org/gf/project/cbcc/docman/Patient%20Friendly%20Security%20and%20Privacy%20Natural%20Language%20for%20Consent%20Directives/FHIR%20Contract%20Resource%20for%20CD/ FHIR Consent Directive DSTU 1 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.
* ???