Safety-enhanced design (MU3))
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Revision as of 08:30, 17 January 2022 by Bradymiller (talk | contribs) (→Criteria that need to be tested)
Overview
- Working with Columbia HIT
Criteria that are testing
- a1: Computerized provider order entry (CPOE) – medications
- a2: CPOE – laboratory
- a5: Demographics
- a9: Clinical decision support
- a14: Implantable device list
Research
- Actual rule:
- Example reports:
Usability demos
- Plan 3 duplicate demos that will contain 1 patient (Ed Smith) with one lab option (PSA) and with ICD10 code set installed. Demos can be easily reset after the test is complete. Demos will have private credentials (ie. public will not be able to access them).
Usability testing instruction sets
Task 1: Enter and modify demographics.
- Enter in Gender Identity and Sexual Orientation
- Change DOB (will change it to a date that will trigger the colonoscopy cdr rule)
- (a5: Demographics)
- (a9: Clinical decision support)
Task 2: Enter in medication order.
- Order Lipitor (via prescription).
- (a1: Computerized provider order entry (CPOE) – medications)
Task 3: Order a lab.
- Order PSA
- (a2: CPOE – laboratory)
Task 4: Add a implantable device.
- Add UDI (01)10050428383077(11)141231(17)150707(10)A213B1(21)1234
- (a14: Implantable device list)