Difference between revisions of "Negation Requirements"

From HL7Wiki
Jump to navigation Jump to search
Line 28: Line 28:
 
==Plan==
 
==Plan==
 
# Planning:  
 
# Planning:  
## choose meeting times for Fall 17
+
# Collect content representation requirements (examples) - Done
## plan tasks, roles.
+
# Classify content representation examples - Done
# Complete collection of content requirements (examples) - Done
 
# 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 transform requirements
## V2, RIM, FHIR, CIMI, DL
+
## CDA, FHIR in process
# Identify other requirements
+
## V2, RIM, CIMI, ANF, DL pending
# Create [[Negation project ballot outline | outline]]
+
# Revise [[Negation project ballot outline | outline]]
 
# Draft guidelines
 
# Draft guidelines
## Review requirements & guidelines with design teams
+
## concurrent
 
# Draft document   
 
# Draft document   
 
# Revise document
 
# Revise document

Revision as of 16:58, 8 August 2018


Return to Patient Care

Return to Vocabulary


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]]