Difference between revisions of "Negation Requirements"

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==Plan==
 
==Plan==
* Collect content requirements (examples) - in process
+
# Complete collection of content requirements (examples) - in process
* Classify content examples - in process
+
# Classify content examples - in process
* Collect consumption requirements - in process
+
# Collect consumption requirements - in process
** UI
+
## UI
** Query  
+
## Query  
** CDS  
+
## CDS  
* Classify consumption requirements -   
+
# Classify consumption requirements -   
* Collect compatibility requirements
+
# Collect compatibility requirements
** V2, RIM, FHIR, CIMI, DL
+
## V2, RIM, FHIR, CIMI, DL
* Identify other requirements
+
# Identify other requirements
* Draft guidelines
+
# Draft guidelines
** Review requirements & guidelines with design teams
+
## Review requirements & guidelines with design teams
* Draft document
+
# Draft document
* Revise document
+
# Revise document
  
 
==Issues/Hot Topics==
 
==Issues/Hot Topics==

Revision as of 14:56, 21 June 2017


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Remember

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. Complete collection of content requirements (examples) - in process
  2. Classify content examples - in process
  3. Collect consumption requirements - in process
    1. UI
    2. Query
    3. CDS
  4. Classify consumption requirements -
  5. Collect compatibility requirements
    1. V2, RIM, FHIR, CIMI, DL
  6. Identify other requirements
  7. Draft guidelines
    1. Review requirements & guidelines with design teams
  8. Draft document
  9. 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]]