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Reviewing minutes from the last call - Action Item Follow up | |
Call Schedule | send OOO via chat or email |
LIDR White Paper Review | Reviewing the comments on the LIDR White Paper = LIDR White Paper Need to check reference style and pick one Reviewed comments on introduction - Still need to check for best place to talk about CLSI AUTO-16/IHE LAW (question: has anyone implemented in the US in production?) Review updated LIDR content creation diagram: What kind f content would come from FDA? CLIA setting, at home use etc maybe additional elements from the package insert once test is approved and that information is public Need to make sure the linkage for any feedback / additionally submitted content is properly linked to the correct LIDR entry
Does distribution include naming convention? different labs may create different names for the same test would the unqiue LIDR row ID help with that? don't want to get hung up on single id again - labs need to report based on the LIDR fingerprint (all the correctly coded data like LOINC, SCT, proper specimen infomration, unit sof measure, UDI
Note that this diagram does not include the details of distribution - we left this here to make clear that content doesn’t just go into LIDR, but also comes back out - but there is feedback ability - hence the double-arrows What if a lab decides to report slightly different from how the maunufacturer prefers - example Flu A/B test or HIV 1/2 test - manufacturer has single nominal results vs lab sets these up as 2 individual tests with ordinal test - both are valid and the latter is often used to ensure that display for provider is not changed in a way that information could get lost LIDR administrator can make those updates Who is the LIDR administrator - needs to be impartial Ideally SHIELD community administers LIDR In Figure 7 there is “Labs' conformance to LIDR' - what happens if the update is not in LIDR?
How does feedback from the labs to vendor work? Diagram ready to beautify - Russ will ask Peyton and team to do
Roadmap for LIDR - how do we make LIDR a reality? Riki just drafted - ideally should become an actual tool, but that will need funding and assurance of impartial administation may not move forward on just goodwill Xavier might be able to help with the FHIR pilot of LIVD
Other notes:
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ACTION ITEMS | All read the roadmap and the how to get invovled Review on 11/04 then send to Steering Committee for review and vote 11/05 or the next |
Next call | Monday 11/04/2024 9:05 - 9:55 AM ET |
Adjourned | 9:55 AM ET |