Closing Keynote
summary
Summarizes actions and specific asks: establishes a patient advocacy work group at HL7 and proposes adding a short patient rationale to every specification, reports a conference gender split of about 80/20, and warns that many consumer apps are unsafe. Notes lack of a legal right to free patient records in one country, tells a care failure that leaves a patient avoiding clinicians, cites delays from diagnosis to chemo taking six months versus one day with coordinated services, and urges adoption of the FHIR safety checklist.
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chapters (8)
- 0:00Welcome and thanks
- 1:32Keynote speakers and community
- 3:22Diversity in healthcare IT
- 6:08Patient access to records
- 9:26Patient advocacy work group
- 11:23Patient data safety debate
- 13:54Information blocking and care delays
- 16:23Closing remarks and gratitude
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