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Date

Attendees

 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

Agenda and Notes

Topic

Notes

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

Pick up at Requirement #10:

  • 10+ UDI’s - when would that be the case?

    • create a system UDI that describes the process and combines all the components

    • UDI at component level for some

    • no need to support a speciif number

  • Delete “There should be a description of how UDIs are collected, stored, and transmitted.” - this is needed as educational material for implementation - if not here, where do we keep this information? - Make a parking lot item where should this live - maybe the Crossproduct ? Has to be adreesed for lab workflow etc

  • Remove “Need LIS functionality for easy use of UDIs to reduce manual labor, typos, and errors of hand entry, etc. This should include the use of barcodes for entry into databases (LIS, LIDR, etc.)” - this falls into the same implementaiton guidance / needs to make this happen in real world data

  • Is the intent to include UDI in all results going back to provider?

    • idea is that yes - we need to include it in the record as part of the test build

    • that is a lot of data and it will be hard to get that into the LIS for panel tests that can have multiple UDIs

    • assumption that no EHR-s and LIS can support this today - this is what we would like to see

    • the LIS and EHR-s cannot do anything with the information, when it gets too big

    • it would be best to have a single UDI to combine the compoents into the process - this should be coming from the vendors - in LIDR we should support the highest granularity - in the instance data this could/should be only using the combination UDI

  • #11

    • Reviewing the requirements - htey may be too speicfic to an implementation

    • if a vendor notifies the lab - is the lab expected to notifying ordering providers / PH

      • tis would be handled the same way as versioning - this would not be retroactive, correct in system and send out going forward

      • also hopefully vendors would notify LIDR and then LIDR can push this information out to all the labs

    • supporting onboarding of labs to use LIDR contnet

    • QA testing will include testing for use of this data - similar to proficiency testing

Start with 12.b on 9/9/2024

ACTION ITEMS

Please see the action items at top of this page - Next deliverable is White paper draft by end of this month!!!

Next call

No call 9/2/2024 - Happy Labor Day!

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

Adjourned

9:54 AM ET

Action items

  •  

Quick decisions not requiring context or tracking

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    Decisions requiring context or tracking

    For decisions that require more context (e.g., documentation of discussion, options considered) and/or tracking, use the decision template to capture more information.