2024-11-04 LIDR Meeting Notes

Date

Nov 4, 2024

Attendees

 Name

Organization

 Name

Organization

Hung Luu

Children’s

Riki Merrick

Vernetzt, APHL

Andrea Pitkus

UW

Pam Banning

3M - Solventum

Xavier Gansel

Biomerieux

Amy McCormick

Epic

Dan Rutz

Epic

Rob Rae

CAP

Rob Hausam

Hausam Consulting

Sandy Jones

CDC

Stan Huff

Graphite

Ed Heierman

Abbott / IICC

Andrew Quinn

 

Laurent Lardin

Biomerieux

Anthony Killeen

UMN

Craig Collom

 

Marti Velezis

 Sonrisa / FDA

Walter Sujansky

FDA

Susan Downer

JMC

Ralf Herzog

Roche

Cornelia Felder

Roche

Daniel Golson

JMC

Andrea Prada

JMC

Maria Sagat

 CAP

Raja Cholan

FDA

Russ Ott

FDA

Akila Namasivayam

FDA

Desiree Mustaquim

CDC

Carmen Pugh

CDC

Christina Gallegos

APHL

John Spinosa

Lantana

Matthew Dietz

FDA

Agenda and Notes

Topic

Notes

Topic

Notes

Call Schedule

send OOO via chat or email

Next week is Veterans Day (and AMIA), so no call

 LIDR White Paper Review

Reviewing the comments on the LIDR White Paper = LIDR White Paper

  • Diagram feedback follow up:

    • LIVD entries has split rows - Russ found some examples and will collate for the next call

    • Beautified version of the diagram is being worked on - for next call

  • Roadmap section:

    • Do we need to reiterate here who will be using LIDR?

      • IVD vendors

      • EHR-S/LIS (and need to decide whose coding trumps, if discordant)

      • Labs

    • Identify scope as 501k and EUA approved tests for now (no LDT, US focused)

    • Have LIVD format from Biomerieux, Roche, Abbott available

      • could use this as proof of concept content - share in FHIR format

      • It took Biomerieux 6 years to create all their content - at first created a tool to make content creation easier, took a while to cover the backlog, still need for maintenance, but much faster just to assign codes for new tests now

      • need to recruit more vendors

      • could ask larger reference labs to review content we have and fill in gaps form vednors they are using, but who are not participating (could reference labs include their instrumentation information in their catalogs? - they share it with partners they are interfacing with, but keeping it in the catlogs would be a BIG maintenance ask

Open To Dos:

  • 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?)

  • Andrea to write up her sentences as per comments

Reviewing minutes from the last call - Action Item Follow up

ACTION ITEMS

All review the updated roadmap section and teh how to get inolved section and add feedback as comments on the page

Next call

Monday 11/18/2024 9:05 - 9:55 AM ET

Adjourned

9:53 AM ET