Negation Requirements

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Project Information

Scope Statement

Scope: Provide a set of classified requirements for the representation of negated clinical data, which standards developers can use to confirm coverage of requirements, demonstrate recommended patterns, and identify out-of-specification patterns.

Need: The ways current interoperability standards handle negation, or propose to do so,

  • are inconsistent & may not support transformations among different standards
  • may not support representation requirements
  • may not support computation requirements

Having a consistently articulated set of clinical requirements will allow standards designers to confirm support for these requirements and to provide clear guidance on recommended and prohibited patterns.

Meeting Information

Plan

  1. Planning:
  2. Collect content representation requirements (examples) - Done
  3. Classify content representation examples - Done
  4. Collect consumption requirements - in process
    1. UI
    2. Query
    3. CDS
  5. Classify consumption requirements
  6. Collect transform requirements
    1. CDA, FHIR in process
    2. V2, RIM, CIMI, ANF, DL pending
  7. Revise outline
  8. Draft guidelines
    1. concurrent
  9. Draft document
  10. Revise document

Issues/Hot Topics

  1. TermInfo currently responding to FHIR request regarding PC requirement for "no known allergies" in Allergy resource.
  2. CIMI on threshold of addressing a pattern for absent findings, other 'negation' topics.
    1. Pattern follows SCT: evaluations of observables may have negative results; Assertions may have 'absent' context values

Project Documents


Categorization

[[Category:Active_Projects]]