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2025-03-18 LIDR Meeting Notes

2025-03-18 LIDR Meeting Notes

Date

Mar 18, 2025

Attendees

 Name

Organization

 Name

Organization

Hung Luu

Children’s

Riki Merrick

Vernetzt, APHL

Andrea Pitkus

UW

Xavier Gansel

Biomerieux

Pam Banning

3M - Solventum

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

Russ Ott

FDA

Akila Namasivayam

FDA

Desiree Mustaquim

CDC

Carmen Pugh

long term lab professional

Christina Gallegos

APHL

John Spinosa

Lantana

Matthew Dietz

FDA

Logistics

  • Consider connectathon for LIDR - Dan will take a look - no update

  • LIDR White Paper under SC review until Feb 21 (Still no further action)

    • Reviewing the last comments:

      • Result Values:

        • Updated that organisms should come from SNOMED CT organism hierarchy - the detail that for some the differentiation may not be good enough to do that and discussion around whether or not to use finding hierarchy terms to represent these situations instead of listing multiple organisms is too detailed for this paper

        • sometimes folks may send NCBI TaxIDs - applies mostly for sequencing, some may not yet have SCT codes, in other cases folks are just used to it - for LIDR we won’t be able to list all possible answers for sequencing test, so may not apply here (but for instance data)

        • Updated specimen source to specimen type modifier

        • Updated the first instance of Resultable LOINC to orderable LOINC (updated the 24 Urine to have an analyte)

        • created separate bullet for second instance of resultable LOINC and added examples

        • answered cutoff question

        • will need to review Figure 6 and Figure 8 and related texts to ensure they are both in good locations/ needed

        • discussed the need for supporting different versions of the same code system

    • OPEN ACTIONS:

      • Review again for making sure it doesn’t look like LOINC is a bad standard - we don't want to perpetuate inocrrect information - it is not a LOINC issue, it is trying to highlight the issue with modeling lab tests and how folks apply LOINC @Stan Huff

      • Review Figure 6 and associated text against Figure 8 and associtated text and combine / adjust as needed @riki.merrick

      • Add in Refernece to AUTO 16 and provide the mapping between LIDR entries and instance data @Russell Ott to check for his verion of the mapping file

      • Review the LIVD/LIDR requirements section to ensure we have the proper vendor view @Xavier Gansel and @Ed Heierman

  • In looking at FHIR US Core

    • there is guidance to use the system from LOINC to identify the specimen, which does not work for all of the labtests

    • lab tests are defined by the lab and not the physician that is used in the EHR-s builds

    • Need to make sure folksunderstand the need to support the speicmen resource in FHIR to properly define the specimen for many tests

Reviewing minutes from the last call - Action Item Follow up

  • Pull out the definitions from LIVD for test kit and equipment and put here: SHIELD Glossary

    • Review operational definition of “equivalence”

      • Will look for a CLSI defintion

      • also check IFCC definition

Next call

Monday 4/1/2025 9:05 - 9:55 AM ET

Adjourned

9:52 AM ET

Chat

Andrea Pitkus 9:24 AM
NCBI - WWW Error Blocked Diagnostic

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