PDex profiles base Device resource and not US Core Implantable Device Profile

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    • Type: Comment
    • Resolution: Considered - No action required
    • Priority: Medium
    • US Core (FHIR)
    • 3.1.1
    • Cross-Group Projects
    • US Core Implantable Device Profile
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      Floyd Eisenberg made changes - 2020-12-03 06:37

      Resolution Description Approve variance from US Core Approve variance from US Core
       
       
       
      CGP Voted on variance approval: Drew Torres/Eric Haas: 9-0-0
           
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      Floyd Eisenberg  made changes - 2020-12-03 06:37 Resolution Description Approve variance from US Core Approve variance from US Core       CGP Voted on variance approval: Drew Torres/Eric Haas: 9-0-0      

      The Us Core 3.1.1. Profile for implantable devices is too restrictive in its scope (implantable devices) for use by Payer in reporting devices (not just implantables) to members or other payers as part of the CMS Interoperability Final Rule and to providers (as part of the scope of PDex).  We have created a profile on the base Device resource that follows the US Core profile as closely as possible.  We request an exception regarding the use of US Core Profiles for this specific use case.

       

            Assignee:
            Unassigned
            Reporter:
            Robert Dieterle
            Watchers:
            3 Start watching this issue

              Created:
              Updated:
              Resolved: