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Topic | Discussed? | Notes |
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Upcoming OOO | Yes |
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Previous Action Items | Yes |
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CDC and ONC meeting Update | Carmela is detailed from ONC to the new CDC Standards Devision supporting CDC comments on USCDI V5 draft specifically talking about specimen collection date/time, performed test date/time, lab received date/time and specimen collection method Lab related date/timestamps - vs specific triggers for collecting those, that are clincially important - specimen collection date/time is different from generic procedure time (since specimen collection, while techincally a procedure, is not specifically captured as such in HIT systems) specialization of generic elements - example medical record number vs patient identifier (in 2019 congress was having a discussion around a national unique patient identifier) test kit unique identifier (model = device level), lot number (may be harder than the device level id) and instance level identifier (serial number) = production identifier - these things are recorded in the lab, but not currently in the LIS = https://www.fda.gov/medical-devices/unique-device-identification-system-udi-system/udi-basics currently all FDA 510k devices have to have a device level identifier UDI - it would be great if you could just scan the test kit / reagent / instrument barcode when the lab gets the testkit/reagent/instrument | |
Specimen CMT - review of terms with questions |
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CALL ADJOURNED | 12:57 PM ET | |
Specimen CMT pilot implementers | No |
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Specimen CMT - Hosting Options | No |
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Specimen CMT - education | No |
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Specimen CMT - tracking implementation impact
| No |
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Specimen CMT - Compare to NHS Medical Terminology testing | No |
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LOINC to SNOMED CT mapping | No |
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Reporting Biomarkers to Cancer registries | No | National Program of Cancer Registries (NPCR) | CDC Sandy will put together a one-pager |
Future projects for this call after CMT | No |
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From Chat:
You 12:00 PM
2024-03-21 LabMCoP Meeting notesNotes
Rajesh Dash to Everyone 12:15 PM
Production Identifier
https://www.fda.gov/medical-devices/unique-device-identification-system-udi-system/udi-basics
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John Snyder (NLM) 12:33 PM
Groshong catheters are a type of central venous catheter, which are placed under direct fluoroscopic visualization in an angiography suite.
Recording:
Action items
Quick decisions not requiring context or tracking
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