Applying sigma metrics to assess quality control processes in the transfusion transmissible infection screening laboratory of a blood center.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2024
Historique:
received: 10 06 2024
accepted: 06 10 2024
medline: 25 10 2024
pubmed: 25 10 2024
entrez: 24 10 2024
Statut: epublish

Résumé

In the field of healthcare, quality and efficiency are of paramount importance to ensure the provision of safe and reliable diagnostic services. Blood screening laboratories play a critical role in detecting and preventing the spread of infectious diseases, ensuring the safety of blood transfusions, and supporting medical diagnoses. To enhance the quality of processes in such laboratories, the Six Sigma methodology has gained significant recognition for its ability to systematically identify and minimize variations, thereby improving overall efficiency and reducing errors. This retrospective study aims to explore the application of Six Sigma metrics in the context of blood screening laboratories, providing an in-depth analysis of its implementation, benefits, and challenges. The performance of three serology assays, i.e., anti-HCV, HIV Ag/Ab combo, and HBsAg, using internal quality control (IQC) daily data extracted from six Alinity i instruments (Abbott GmbH, Germany), from February to April 2023, was evaluated. Mean, standard deviation (SD), and coefficient of variation (CV%) was calculated for positive controls. Bias was calculated using peer group data. Sigma metrics were calculated using allowable total error (TEa %) based on difference between the observed mean of the positive control and the s/co cut-off of assay. The observed CV% for positive controls was ≤10%. The TEa% ranged from 66% to 79% for the analytes using the observed mean. All the assays showed Six Sigma performance (σ>6) with and without bias. The study observed that the serology assays showed very high sigma values (σ>6) and thus, simplified statistical quality control (SQC) design based on Westgard Sigma rules could be implemented without compromising blood safety.

Identifiants

pubmed: 39446744
doi: 10.1371/journal.pone.0312422
pii: PONE-D-24-21310
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0312422

Informations de copyright

Copyright: © 2024 Bhatnagar et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

Sten Westgard is an employee of Westgard QC who is consulting partner for broad range of IVD companies. Sonu Bhatnagar is an Abbott employee and company shareholder. This does not alter our adherence to PLOS ONE policies on sharing data and materials. Rest of the authors have no conflict of interest to declare.

Auteurs

Sonu Bhatnagar (S)

Transfusion Medicine, Abbott Laboratories, Singapore, Singapore.

Sten Westgard (S)

Westgard QC, Inc., Madison, WI, United States of America.

Nguyen Thi Thanh Dung (NTT)

National Institute of Hematology and Blood Transfusion, National Blood Center, Ha Noi, Vietnam.

Tran Ngoc Que (TN)

National Institute of Hematology and Blood Transfusion, National Blood Center, Ha Noi, Vietnam.

Bach Quoc Khanh (BQ)

National Institute of Hematology and Blood Transfusion, National Blood Center, Ha Noi, Vietnam.

Nguyen Ha Thanh (NH)

National Institute of Hematology and Blood Transfusion, National Blood Center, Ha Noi, Vietnam.

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