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2025-02-13 Meeting notes

2025-02-13 Meeting notes

Date

Feb 13, 2025

Attendees

Present

Name

Organization

Present

Name

Organization

 

Nancy Cornish

CDC

 

Manjula Gama-Ralalage

CDC

X

Riki Merrick

APHL

X

Christina Gallegos

APHL

X

Amy Liu

Inductive Health / APHL

 -

Raj Dash

Duke / CAP

 

John Snyder

National Library of Medicine (SNOMED CT)

X

Andrea Pitkus

UW

X

Kathy Walsh

Labcorp

 -

Rob Hausam

Hausam Consulting

 

Pam Banning

 3M

 

Sandy Jones

CDC

 

 

Carmen Pugh

CDC

Discussion topics

Upcoming OOO

 

CSTE Presentation

Riki

  • CSTE ELR call presentation on wound cultures and Specimen CMT (modeled for ELR) by Nancy, Riki, and Manjula has been postponed (not March) to a TBD date later

European Lab related Vocab

Riki

European Lab Terminology group working on finalizing their list of containers and asking for review - they are still reviewing and I forwarded our comments

they are looking to get more feedback from larger groups, so we could provide more feedback

Filtered on those without LabMCoP comment and “not Yes” and reviewed stool, culture swabs - file at end of review with filters on:

Riki will send to Feijke for merging into their files

CALL ADJOURNED

 

11:32 AM ET

Specimen CMT - review of terms with questions

 Not discussed

 nothing new - Amy transcribing some prior decisions into data base currently

Previous Action Items

  Not discussed

Specimen CMT pilot implementers

  Not discussed

Specimen CMT - Hosting Options

  Not discussed

  • How can we publish the content in the dB?

  • How do we decide what format to share this in - get input from EHR-s and LIS vendors.

  • Write letter of mulitple stakeholders to request EHR-s and LIS vendors to implement

    • indicating that this is a patient safety issue, as incorrect Abx treatment will contribute to multi-drug resistance (use CTSI findings to provide background)

      • focus on blood, urine, wound cultures (get data from NHSN, too)

    • Nancy is talking to DHQP about the linkage with specimen collection

    • While we have HIT certification that is for the EHR-s there is currently no enforcement for implementation at the organizations

    • need C-suite buy-in

    • Professional organizations - like CAP and ACOS and AJCC get them to write the synoptic reports (better structuring of data) - for surgical aspects - similar to what CAP has done for Cancer (though they do not have the SCT codes included in the past - may be including SNOMED CT starting in 2025, but they are also using the SCT codes for observables) https://www.facs.org/for-medical-professionals/news-publications/news-and-articles/bulletin/2021/12/synoptic-reporting-for-cancer-surgery-current-requirements-and-future-state/: The four CoC accreditation standards that include synoptic operative reporting requirements apply to sentinel lymph node biopsy for breast cancer (Standard 5.3), axillary lymph node dissection for breast cancer (Standard 5.4), wide local excision for primary cutaneous melanoma (Standard 5.5), and colonic resection for colon cancer (Standard 5.6). These accreditation standards were developed from the evidence-based recommendations for cancer surgery detailed in the Operative Standards for Cancer Surgery manuals.7,8

    • try to get AMA support to get providers to adopt this

    • Reach out to IDSA, too

Specimen CMT - education

  Not discussed

  •  Need education for providers and IT folks that helps with set up of the EHR-S / LIS configuration

  • if we have a use case of how a patient is impacted on their journey through the healthcare system - CAP created a nice video that showed how patient care was affected by incorrect data https://infobeta.cap.org/shield/

Specimen CMT - tracking implementation impact

  • Setting baseline

  • Define metrics

  Not discussed

 

Specimen CMT - Compare to NHS Medical Terminology testing

  Not discussed

 Will get updated vocab at a later date

Future projects for this call after CMT

 Not discussed

  • In general the call is intended as a forum for ANY messaging related issues to work out.

  • In the past we have

    • reviewed containers re-vive that - and how does that interact with devices (UDI identification?)

    • review code systems around additives (HL70371 and SCT substance and product hierarchies)

    • started work on cross-mapping between HL7 method codes and SNOMED CT procedure / technique concepts

      • American College of Surgeons is working on procedure protocol and synoptic data elements / surgical synoptic reports - we could work with them together on that

    • Look at other HL7 tables that we would want to migrate SCT (i.e., Specimen Condition table, etc.)

Recording:

 Per APHL policy we are not currently allowed to record any meetings

From Chat:

  • Andrea Pitkus 11:05 AM
    I can only stay until half hour.
    also the LOINC release with LOINC-SCT Ontology is due this month

  • Kathy Walsh - Labcorp  to  Everyone 11:21 AM

    1. One or more clean LabCorp-approved stool collection kits (order LabCorp N° 03192) containing a 1-gallon can, absorbent sheet, Armlock O-ring, and a leakproof plastic bag

    2. Collect stool directly into can. Do not fill any can more than 2/3 full. Secure lid with pressure and firmly attach the O-ring. State collection time on the can label. Place the can and the absorbent sheet into the leakproof plastic bag and seal. Send the entire can, or if submitting aliquot, follow this procedure:

    3. Weigh specimen and collection container and subtract the weight of an empty container of same type (one-gallon can weight with lid: 360 g metal or 320 g plastic container). This is the “net weight” to be recorded on the test request form.

    4. Open the container and observe whether the contents are liquid. If liquid stool, secure the lid, mix, and submit an aliquot of the total collection. If solid stool, add deionized water (approximately 500 mL) to the specimen container and mix thoroughly to create a homogenous specimen. Submit a 5 to 25 mL aliquot of the total collection in an empty stool transport vial (LabCorp N° 59517) or screw-cap urine bottle (LabCorp N° 20648), sterile no additives.

    5. Record on both the container and the test request form the amount of water added to liquefy the stool or if no water was required.

     

Action items

Quick decisions not requiring context or tracking

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Decisions requiring context or tracking

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