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FHIR Consent Directive Implemenation Guide
Revision as of 15:04, 13 February 2016 by JohnMoehrke (talk | contribs)
Back to HL7 FHIR Consent Directive Project
You can get to current Privacy Consent Directive IG in the continuous build directly: http://hl7-fhir.github.io/pcd/pcd.html
This page is used to develop new content before committing it to the Current build.
- Do NOT write more than is necessary for our reader to understand how to use
- Rely on prior works to explain basics
- Less is More
Draft Privacy Consent Directive IG
Introduction (Glen)
- Need to have consent be informed consent
- Relationship with Contract - why is a consent a contract? (Kathleen)
- Relationship with the resources it uses - Patient, Document, AuditEvent, Provenance
- Relationship with Resources it controls -
- Use of Questionnaire for UX with patient
Abstract Data Model (Kathleen)
- What needs to be recorded
- Types of Consent
- Basic - TPO
- Exception vs Inclusion
- Research (Beth)
- Patient Centric
- Jurisdiction Models (David) -- look to Goldstein paper
- Implied
- Explicit
- Chinese?
- Cross-Organization vs Within-an-Organization
Abstract Interaction Model (John)
- Actors
- Involved in capturing consent
- Involved in enforcing consent
- Affected transparently
- Transactions
- Create, Read, Update, Delete -- Replace
- Request access decision
Related Work (John, Kathleen)
- Consent Receipt
- Use of AuditEvent - disclosure
- Relationship to OAuth scopes
- Relationship to UMA -- HEART
- IHE BPPC and APPC
- HL7 CDA Privacy Consent Directive IG
- HL7 Patient Frendly Consent
- HL7 HCS
- ONC Patient Choice (David)
Examples
- USA Realm examples (Kathleen)
- Canada Examples (Pat, Ken)
- European Examples (Alex, Tarik)
- Research Examples (Rob, Kathleen)
Other Draft Materials
FHIR Consent Directive in Trust Framework
Discussed in Mike Davis' FHIR Contract Design Considerations