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Difference between revisions of "July 16, 2013 DS4P Joint Project"

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(Created page with " IG Front matter submitted by Richard Thoreson '' This Guide is about segmenting clinical records, so that personally identified information (PII) can be selectively shared. ...")
 
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=Data Segmentation for Privacy=
  
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[[Security| Meeting Information]]
  
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[[Security|Back to Security Main Page]]
  
IG Front matter submitted by Richard Thoreson
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[[HL7 DS4P CBCC-Security WG Joint Project|Back to HL7 DS4P Project Main Page]]
  
''  This Guide is about segmenting clinical records, so that personally identified information (PII) can be selectively shared.  It mainly specifies an interoperable, standards-based privacy policy document.  Policy execution is largely left up to EHRs, PHRs and HIE venders.  This specification conveys policy information that venders can import, export, and execute, without human hands.   
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==Attendees:==
  
  The following analysis also considers and illustrates how privacy policies can be incorporated as clinical records are shared for care coordination, quality and public health reporting, and research.  The idea is that patients are more likely to consent to sharing sensitive PII, and providers are more likely to share valuable business records, if both are given meaningful opportunities to select who can see and use what data, and for what purpose.  ''
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* [mailto: Wendy Baker]
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* [mailto:jc@securityrs.com Johnathan Coleman]
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* [mailto:kathleen_connor@comcast.net Kathleen Connor]
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* [mailto:Mike.davis@va.gov Mike Davis], Security Co-Chair
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* [mailto:duane.decouteau@gmail.com Duane DeCouteau]
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* [mailto:michael.dufel@jerichosysystems.com Mike Dufel]
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* [mailto:AJames@drc.com Adrianne James]
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* [mailto:Brian.Handspicker@its.ny.gov Brian Handspicker]
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* [mailto:Adrianne.James@drc.com Adrianne James]
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* [mailto:Holly.Miller@va.gov Holly Miller]
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* [mailto:Harry.Rhodes@AHIMA.org Harry Rhodes]
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* [mailto:david.staggs@jerichosystems.com David Staggs]
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* [mailto:Richard.Thoreson@samhsa.hhs.gov Richard Thoreson], CBCC Co-Chair
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[[Security|Back to Security Main Page]]
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==Agenda:==
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# Roll Call, Agenda, Meeting Minutes
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# Implementation Guide Update
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# Notification of Intent to Ballot Security and Ontology
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==DRAFT Minutes==
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IG Front matter submitted by Richard Thoreson via e-mail:
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''  This Guide is about segmenting clinical records, so that personally identified information (PII) can be selectively shared.  It mainly specifies an interoperable, standards-based privacy policy document.  Policy execution is largely left up to EHRs, PHRs and HIE venders.  This specification conveys policy information that venders can import, export, and execute, without human hands.''
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''  The following analysis also considers and illustrates how privacy policies can be incorporated as clinical records are shared for care coordination, quality and public health reporting, and research.  The idea is that patients are more likely to consent to sharing sensitive PII, and providers are more likely to share valuable business records, if both are given meaningful opportunities to select who can see and use what data, and for what purpose.  ''

Revision as of 19:59, 16 July 2013

Data Segmentation for Privacy

Meeting Information

Back to Security Main Page

Back to HL7 DS4P Project Main Page

Attendees:


Back to Security Main Page

Agenda:

  1. Roll Call, Agenda, Meeting Minutes
  2. Implementation Guide Update
  3. Notification of Intent to Ballot Security and Ontology

DRAFT Minutes

IG Front matter submitted by Richard Thoreson via e-mail:

This Guide is about segmenting clinical records, so that personally identified information (PII) can be selectively shared. It mainly specifies an interoperable, standards-based privacy policy document. Policy execution is largely left up to EHRs, PHRs and HIE venders. This specification conveys policy information that venders can import, export, and execute, without human hands.

The following analysis also considers and illustrates how privacy policies can be incorporated as clinical records are shared for care coordination, quality and public health reporting, and research. The idea is that patients are more likely to consent to sharing sensitive PII, and providers are more likely to share valuable business records, if both are given meaningful opportunities to select who can see and use what data, and for what purpose.