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Estimation of inter-laboratory reference change values from external quality assessment data

INTRODUCTION: It is common for patients to switch between several healthcare providers. In this context, the long-term follow-up of medical conditions based on laboratory test results obtained from different laboratories is a challenge. The measurement uncertainty in an inter-laboratory context shou...

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Autores principales: Paal, Michael, Habler, Katharina, Vogeser, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Croatian Society of Medical Biochemistry and Laboratory Medicine 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8340502/
https://www.ncbi.nlm.nih.gov/pubmed/34393596
http://dx.doi.org/10.11613/BM.2021.030902
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author Paal, Michael
Habler, Katharina
Vogeser, Michael
author_facet Paal, Michael
Habler, Katharina
Vogeser, Michael
author_sort Paal, Michael
collection PubMed
description INTRODUCTION: It is common for patients to switch between several healthcare providers. In this context, the long-term follow-up of medical conditions based on laboratory test results obtained from different laboratories is a challenge. The measurement uncertainty in an inter-laboratory context should also be considered in data mining research based on routine results from randomly selected laboratories. As a proof-of-concept study, we aimed at estimating the inter-laboratory reference change value (IL-RCV) for exemplary analytes from publicly available data on external quality assessment (EQA) and biological variation. MATERIALS AND METHODS: External quality assessment data of the Reference Institute for Bioanalytics (RfB, Bonn, Germany) for serum creatinine, calcium, aldosterone, PSA, and of whole blood HbA1c from campaigns sent out in 2019 were analysed. The median CVs of all EQA participants were calculated based on 8 samples from 4 EQA campaigns per analyte. Using intra-individual biological variation data from the EFLM database, positive and negative IL-RCV were estimated with a formula based on log transformation under the assumption that the analytes under examination have a skewed distribution. RESULTS: We estimated IL-RCVs for all exemplary analytes, ranging from 13.3% to 203% for the positive IL-RCV and - 11.8% to - 67.0% for the negative IL-RCV (serum calcium - serum aldosterone), respectively. CONCLUSION: External quality assessment data together with data on the biological variation – both freely available – allow the estimation of inter-laboratory RCVs. These differ substantially between different analytes and can help to assess the boundaries of interoperability in laboratory medicine.
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spelling pubmed-83405022021-08-12 Estimation of inter-laboratory reference change values from external quality assessment data Paal, Michael Habler, Katharina Vogeser, Michael Biochem Med (Zagreb) Short Communications INTRODUCTION: It is common for patients to switch between several healthcare providers. In this context, the long-term follow-up of medical conditions based on laboratory test results obtained from different laboratories is a challenge. The measurement uncertainty in an inter-laboratory context should also be considered in data mining research based on routine results from randomly selected laboratories. As a proof-of-concept study, we aimed at estimating the inter-laboratory reference change value (IL-RCV) for exemplary analytes from publicly available data on external quality assessment (EQA) and biological variation. MATERIALS AND METHODS: External quality assessment data of the Reference Institute for Bioanalytics (RfB, Bonn, Germany) for serum creatinine, calcium, aldosterone, PSA, and of whole blood HbA1c from campaigns sent out in 2019 were analysed. The median CVs of all EQA participants were calculated based on 8 samples from 4 EQA campaigns per analyte. Using intra-individual biological variation data from the EFLM database, positive and negative IL-RCV were estimated with a formula based on log transformation under the assumption that the analytes under examination have a skewed distribution. RESULTS: We estimated IL-RCVs for all exemplary analytes, ranging from 13.3% to 203% for the positive IL-RCV and - 11.8% to - 67.0% for the negative IL-RCV (serum calcium - serum aldosterone), respectively. CONCLUSION: External quality assessment data together with data on the biological variation – both freely available – allow the estimation of inter-laboratory RCVs. These differ substantially between different analytes and can help to assess the boundaries of interoperability in laboratory medicine. Croatian Society of Medical Biochemistry and Laboratory Medicine 2021-08-05 2021-10-15 /pmc/articles/PMC8340502/ /pubmed/34393596 http://dx.doi.org/10.11613/BM.2021.030902 Text en Croatian Society of Medical Biochemistry and Laboratory Medicine. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communications
Paal, Michael
Habler, Katharina
Vogeser, Michael
Estimation of inter-laboratory reference change values from external quality assessment data
title Estimation of inter-laboratory reference change values from external quality assessment data
title_full Estimation of inter-laboratory reference change values from external quality assessment data
title_fullStr Estimation of inter-laboratory reference change values from external quality assessment data
title_full_unstemmed Estimation of inter-laboratory reference change values from external quality assessment data
title_short Estimation of inter-laboratory reference change values from external quality assessment data
title_sort estimation of inter-laboratory reference change values from external quality assessment data
topic Short Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8340502/
https://www.ncbi.nlm.nih.gov/pubmed/34393596
http://dx.doi.org/10.11613/BM.2021.030902
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