Difference between revisions of "C-CDA Scorecard Rubric Update"
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==New Rubrics to review== | ==New Rubrics to review== |
Revision as of 16:14, 30 May 2018
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- SDWG page
Contents
Project Summary
The following process has been established and approved by SDWG: the C-CDA R2.1 Rubric Process, it is used to identify and evaluate potential best practice tests (rubrics) that could be added to the C-CDA scoring tools. The current rubric is being utilized by the ONC C-CDA Scorecard. Please review the process and use this page to propose new rubrics.
Meeting Time / Info
Wednesday's from 11 am - 12 pm EST
Next meeting is 6/6/18
https://meetingserver.hhs.gov/orion/join?siteurl=meetingserver
UPDATE TELECON
New Rubrics to review
Rubrics to be pushed to SDWG
1. Check whether there is an encounter in the Encounter section (not a null flavor)
2. Check whether the encompassing encounter is present in all encounter based documents ie Discharge Summary, Referral Note, etc. (do not ding if using CCD/Care Plan)
3. Check if the Encounter date/time and ID in the header is present in one of the EncounterActivity entries in the Encounter section of the body.
4. Patient Birth Sex must always be present in every C-CDA document
a. This should be recorded as part of the SocialHistory/BirthSexObservation template
5. If a note activity is present, it must include a link to an Encounter in the encounters section or encompassing encounter
6. Allergy Observation entry must have a reaction. Require a nullFlavor if not known.
7. If there’s a goal you must be able to tell what health concern(s) the goal is related to (Care Plan Document Template specific rubric for now, but will throw a warning for CCD, Referral Note and Discharge Summary - may ding for all document templates in the future)
8. If there’s an intervention you must be able to tell what goal(s) the intervention is related to (Care Plan Document Template specific rubric for now, but will throw a warning for CCD, Referral Note and Discharge Summary - may ding for all document templates in the future)
9. Author entry must include at least a timestamp with information of the last modified date and be present within the Problems entry, which could be at the concern or observation level.
10. Author entry must include at least a timestamp with information of the last modified date and be present within the Medication Activity entry.
11. Author entry must include at least a timestamp with information of the last modified date and be present within the Allergies entry, which could be at the concern or observation level.
12. The narrative name of the Allergy medication should represent the concept meaning of the code in the entry
13. The narrative name of the Immunization should represent the concept meaning of the code in the entry
14. The narrative name of the drug should represent the concept meaning of the code in the entry
15. The machine readable doseQuantity should agree with the narrative sig
16. The Substance administration/effectiveTime @xsi:type = pivl should agree with the narrative sig
17. The Substance administration/effectiveTime @institution specified should agree with the narrative sig
18. The substance administration/route code should agree with the narrative sig
19. The substance administration/route code should reconcile with the medication consumable
20. The substance administration status code should not conflict with the medication status observation
21. When Medication status is active the high time should be in the future relative to the document generation date
22. The narrative name of the Problem should represent the meaning of the code in the Problem Observation value
23. BMI should match height and weight
24. There should be a document level identifier that specifies the document type
25. Allergies should be structured in UNII, NDF-RT, SNOMED or RxNorm
26. The problem observation value should not be set to the problem observation code (problem type value set)
27. If the observation range in the reference range with a value of PQ should not use string
28. Vital signs and results should use a LOINC Code
29. Vital sign and results units should be UCUM conformant
30. Procedures should be structured in CPT, ICD-9, ICD-10, SNOMED, HCPCS or LOINC (will update current rubric to include all of these)