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Two Evaluation Budgets for the Measurement Uncertainty of Glucose in Clinical Chemistry

BACKGROUND: Measurement uncertainty characterizes the dispersion of the quantity values attributed to a measurand. Although this concept was introduced to medical laboratories some years ago, not all medical researchers are familiar with it. Therefore, the evaluation and expression of measurement un...

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Autores principales: Chen, Hui, Zhang, Ling, Bi, Xiaoyun, Deng, Xiaoling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Laboratory Medicine 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3129347/
https://www.ncbi.nlm.nih.gov/pubmed/21779190
http://dx.doi.org/10.3343/kjlm.2011.31.3.167
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author Chen, Hui
Zhang, Ling
Bi, Xiaoyun
Deng, Xiaoling
author_facet Chen, Hui
Zhang, Ling
Bi, Xiaoyun
Deng, Xiaoling
author_sort Chen, Hui
collection PubMed
description BACKGROUND: Measurement uncertainty characterizes the dispersion of the quantity values attributed to a measurand. Although this concept was introduced to medical laboratories some years ago, not all medical researchers are familiar with it. Therefore, the evaluation and expression of measurement uncertainty must be highlighted using a practical example. METHODS: In accordance with the procedure for evaluating and expressing uncertainty, provided by the Joint Committee for Guides in Metrology (JCGM), we used plasma glucose (Glu) as an example and defined it as the measurand. We then analyzed the main sources of uncertainty, evaluated each component of uncertainty, and calculated the combined uncertainty and expanded uncertainty with 2 budgets for single measurements and continuous monitoring, respectively. RESULTS: During the measurement of Glu, the main sources of uncertainty included imprecision, within-subject biological variance (BV(w)), calibrator uncertainty, and systematic bias. We evaluated the uncertainty of each component to be 1.26%, 1.91%, 5.70%, 0.42%, and -2.87% for within-run imprecision, between-day imprecision, BV(w), calibrator uncertainty, and systematic bias, respectively. For a single specimen, the expanded uncertainty was 7.38% or 6.1±0.45 mmol/L (κ=2); in continuous monitoring of Glu, the expanded uncertainty was 13.58% or 6.1±0.83 mmol/L (κ=2). CONCLUSIONS: We have demonstrated the overall procedure for evaluating and reporting uncertainty with 2 different budgets. The uncertainty is not only related to the medical laboratory in which the measurement is undertaken, but is also associated with the calibrator uncertainty and the biological variation of the subject. Therefore, it is helpful in explaining the accuracy of test results.
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spelling pubmed-31293472011-07-12 Two Evaluation Budgets for the Measurement Uncertainty of Glucose in Clinical Chemistry Chen, Hui Zhang, Ling Bi, Xiaoyun Deng, Xiaoling Korean J Lab Med Clinical Chemistry BACKGROUND: Measurement uncertainty characterizes the dispersion of the quantity values attributed to a measurand. Although this concept was introduced to medical laboratories some years ago, not all medical researchers are familiar with it. Therefore, the evaluation and expression of measurement uncertainty must be highlighted using a practical example. METHODS: In accordance with the procedure for evaluating and expressing uncertainty, provided by the Joint Committee for Guides in Metrology (JCGM), we used plasma glucose (Glu) as an example and defined it as the measurand. We then analyzed the main sources of uncertainty, evaluated each component of uncertainty, and calculated the combined uncertainty and expanded uncertainty with 2 budgets for single measurements and continuous monitoring, respectively. RESULTS: During the measurement of Glu, the main sources of uncertainty included imprecision, within-subject biological variance (BV(w)), calibrator uncertainty, and systematic bias. We evaluated the uncertainty of each component to be 1.26%, 1.91%, 5.70%, 0.42%, and -2.87% for within-run imprecision, between-day imprecision, BV(w), calibrator uncertainty, and systematic bias, respectively. For a single specimen, the expanded uncertainty was 7.38% or 6.1±0.45 mmol/L (κ=2); in continuous monitoring of Glu, the expanded uncertainty was 13.58% or 6.1±0.83 mmol/L (κ=2). CONCLUSIONS: We have demonstrated the overall procedure for evaluating and reporting uncertainty with 2 different budgets. The uncertainty is not only related to the medical laboratory in which the measurement is undertaken, but is also associated with the calibrator uncertainty and the biological variation of the subject. Therefore, it is helpful in explaining the accuracy of test results. The Korean Society for Laboratory Medicine 2011-07 2011-06-28 /pmc/articles/PMC3129347/ /pubmed/21779190 http://dx.doi.org/10.3343/kjlm.2011.31.3.167 Text en Copyright © 2011 The Korean Society for Laboratory Medicine http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Chemistry
Chen, Hui
Zhang, Ling
Bi, Xiaoyun
Deng, Xiaoling
Two Evaluation Budgets for the Measurement Uncertainty of Glucose in Clinical Chemistry
title Two Evaluation Budgets for the Measurement Uncertainty of Glucose in Clinical Chemistry
title_full Two Evaluation Budgets for the Measurement Uncertainty of Glucose in Clinical Chemistry
title_fullStr Two Evaluation Budgets for the Measurement Uncertainty of Glucose in Clinical Chemistry
title_full_unstemmed Two Evaluation Budgets for the Measurement Uncertainty of Glucose in Clinical Chemistry
title_short Two Evaluation Budgets for the Measurement Uncertainty of Glucose in Clinical Chemistry
title_sort two evaluation budgets for the measurement uncertainty of glucose in clinical chemistry
topic Clinical Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3129347/
https://www.ncbi.nlm.nih.gov/pubmed/21779190
http://dx.doi.org/10.3343/kjlm.2011.31.3.167
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