ISTH Congress Abstracts

Official abstracts site for the ISTH Congress

MENU 
  • Home
  • Congress Archive
    • ISTH 2022 Congress
    • ISTH 2021 Congress
    • ISTH 2020 Congress
  • Resources
  • Search

Evaluation of EQA Material on Lumira Dx Point of Care Platform: UK NEQAS for Blood Coagulation Study

L. Brown, D. Kitchen, I. Jennings, S. Kitchen, A. Lowe, S. Munroe - Peart, I. Walker

UK National External Quality Assessment Scheme, Blood Coagulation, Sheffield, United Kingdom

Abstract Number: PB0597

Meeting: ISTH 2020 Congress

Theme: Diagnostics and OMICs » Laboratory Diagnostics

Background: The Lumira Dx is a point of care platform which uses cartridge based technology for INR testing in patients on VKA therapy.

Aims: To determine the suitability of UK National External Quality Assessment Scheme for Blood Coagulation (NEQAS BC) lyophilised plasma samples for use with Lumira Dx and to explore the possibility of establishing an external quality assessment (EQA) programme for this platform.

Methods: UK NEQAS BC conducted a study to determine suitability of NEQAS BC lyophilised plasma samples for Lumira Dx. After a series of testing using samples previously used in POC INR EQA programme a suitable diluent with an optimum time for sample reconstitution, calcium chloride concentration and volume was established. Precision was evaluated via repeated testing of an EQA sample previously used in POC INR programmes on three Lumira Dx platforms. This was followed by testing samples with increasing INR values previously used in POC INR programmes. Obtained results were compared to the POC INR sample specific medians established previously.

Results: A reasonable precision with CV% range 2.7 – 5.4 was observed across three platforms after repeated testing of a sample previously used in POC INR EQA programme (mean INR 3.0). The results of testing samples with increasing INR values previously used in POC INR EQA programmes are shown in the table. Obtained results on Lumira Dx were comparable to the sample specific medians established previously in POC INR programmes across three platforms.

Conclusions: In summary, Lumira Dx has demonstrated good precision (all < 10%) while testing NEQAS BC POC INR samples across three platforms. The study has demonstrated the suitability of NEQAS BC lyophilised plasma samples for testing on Lumira Dx. NEQAS BC can provide an EQA POC INR programme for this platform.

Sample POC EQA programme median INRs Platform 1 Platform 2 Platform 3
XS19:04 1.6 (n = 3703) 1.8 2 1.9
XS19:05 1.9 ( n =3754) 2.1 2.1 2.1
XS19:03 2.1 (n = 3698) 2.3 2.6 2.4
XS18:07 2.7 ( n= 3899) 2.9 3.1 2.9
XS19:06 3 (n = 3635) 3.4 3.5 3.1
XS18:01 5.7 (n = 3762) 6.4 6.4 5.6

[Results of testing previously used samples in UK NEQAS POC INR programmes on Lumira Dx]

To cite this abstract in AMA style:

Brown L, Kitchen D, Jennings I, Kitchen S, Lowe A, Munroe - Peart S, Walker I. Evaluation of EQA Material on Lumira Dx Point of Care Platform: UK NEQAS for Blood Coagulation Study [abstract]. Res Pract Thromb Haemost. 2020; 4 (Suppl 1). https://abstracts.isth.org/abstract/evaluation-of-eqa-material-on-lumira-dx-point-of-care-platform-uk-neqas-for-blood-coagulation-study/. Accessed September 29, 2023.

« Back to ISTH 2020 Congress

ISTH Congress Abstracts - https://abstracts.isth.org/abstract/evaluation-of-eqa-material-on-lumira-dx-point-of-care-platform-uk-neqas-for-blood-coagulation-study/

Simple Search

Supported By:

Takeda logo

ISTH 2022 Congress site

Visit the official web site for the ISTH 2022 Virtual Congress ยป

  • Help & Support
  • About Us
  • Cookies & Privacy
  • Wiley Job Network
  • Terms & Conditions
  • Advertisers & Agents
Copyright © 2023 John Wiley & Sons, Inc. All Rights Reserved.
Wiley