Using three external quality assurance schemes to achieve equivalent international normalized ratio results in primary and secondary healthcare

Author:

Stavelin Anne1,Rønneseth Eva1,Gidske Gro12,Solsvik Anne Elisabeth1,Sandberg Sverre12

Affiliation:

1. The Norwegian Organization for Quality Improvement of Laboratory Examinations (Noklus), Haraldsplass Deaconess Hospital , Bergen , Norway

2. Department of Global Public Health and Primary Care , University of Bergen , Bergen , Norway

Abstract

Abstract Objectives Accurate prothrombin time international normalized ratio (INR) results are essential for safe anticoagulation treatment. Patients are treated both in primary and secondary healthcare, therefore equivalence of INR results from point-of-care (POC) and hospital measurement procedures (MPs) are important. It is not possible to evaluate this equivalence in traditional external quality assessment (EQA). The aim of this paper is to describe a special quality assurance system consisting of three different EQA schemes to monitor the harmonization of INR results in Norway. Methods The EQA scheme for hospital laboratories uses commutable control materials and evaluates participant performance and the equivalence of hospital MPs. The EQA scheme for primary healthcare laboratories uses non-commutable control materials and evaluates participant performance. A third EQA scheme for selected primary healthcare laboratories uses native patient split samples and evaluates the equivalence between POC and hospital MPs. Results The relationship between the three EQA schemes is presented. The split sample EQA scheme provides a link between the hospital scheme and the scheme for primary healthcare. Results from 2017 to 2022 are presented for all three schemes. When aberrant EQA results occur Noklus takes actions to be able to have a sustainable equivalence between INR results. Conclusions All three EQA schemes are important for monitoring the harmonization of INR results in Norway. This quality assurance system, including help and guidance of the participants, will reduce the risk of harm to patients due to non-equivalence of results from different MPs.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

Reference30 articles.

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2. Perry, DJ, Fitzmaurice, DA, Kitchen, S, Mackie, IJ, Mallett, S. Point-of-care testing in haemostasis. Br J Haematol 2010;150:501–14. https://doi.org/10.1111/j.1365-2141.2010.08223.x.

3. Poller, L. International normalized ratios (INR): the first 20 years. J Thromb Haemostasis 2004;2:849–60. https://doi.org/10.1111/j.1538-7836.2004.00775.x.

4. WHO. Expert committee on biological standardization – guidelines for thromboplastins and plasma used to control oral anticoagulant therapy with vitamin K antagonists. Geneva: World Health Organization; 2013, Techical Report Series No 979, 62nd Report.

5. CLSI. Procedures for validation of INR and local calibration of PT/INR systems; approved guideline. Wayne, Pennsylvania, USA: Clinical and Laboratory Standards Institute; 2005, CLSI document H54-A.

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