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Analytical Quality Requirements in Human Biomonitoring Programs: Trace Elements in Human Blood

Human biomonitoring (HBM) programs consist of several interrelated and equally important steps. Of these steps, the study design must answer a specific question: How many individuals must be recruited in order to define the spatial or temporal trends of exposure to environmental pollutants in a give...

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Autores principales: Snoj Tratnik, Janja, Mazej, Darja, Horvat, Milena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6651690/
https://www.ncbi.nlm.nih.gov/pubmed/31261622
http://dx.doi.org/10.3390/ijerph16132287
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author Snoj Tratnik, Janja
Mazej, Darja
Horvat, Milena
author_facet Snoj Tratnik, Janja
Mazej, Darja
Horvat, Milena
author_sort Snoj Tratnik, Janja
collection PubMed
description Human biomonitoring (HBM) programs consist of several interrelated and equally important steps. Of these steps, the study design must answer a specific question: How many individuals must be recruited in order to define the spatial or temporal trends of exposure to environmental pollutants in a given HBM study? Two components must be considered at this stage: the population variability of the expected exposure and the performance characteristics of the analytical methods used. The objective of the present study was to quantify the contribution to the required sample size arising from (i) measurement uncertainty and (ii) inter-laboratory measurement variability. For this purpose, the sample size was calculated using the measurement uncertainty of one laboratory, inter-laboratory comparison exercise data, and population variability for commonly studied metals (mercury, cadmium, and lead) in blood. Measurement uncertainty within one laboratory proved to have little influence on the sample size requirements, while the inter-laboratory variability of the three metals increased the requirements considerably, particularly in cases of low population variability. The multiple laboratories approach requires that laboratory variability be considered as early as the planning stage; a single-laboratory approach is thus a cost-effective compromise in HBM to reduce variability due to the participation of different laboratories.
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spelling pubmed-66516902019-08-08 Analytical Quality Requirements in Human Biomonitoring Programs: Trace Elements in Human Blood Snoj Tratnik, Janja Mazej, Darja Horvat, Milena Int J Environ Res Public Health Article Human biomonitoring (HBM) programs consist of several interrelated and equally important steps. Of these steps, the study design must answer a specific question: How many individuals must be recruited in order to define the spatial or temporal trends of exposure to environmental pollutants in a given HBM study? Two components must be considered at this stage: the population variability of the expected exposure and the performance characteristics of the analytical methods used. The objective of the present study was to quantify the contribution to the required sample size arising from (i) measurement uncertainty and (ii) inter-laboratory measurement variability. For this purpose, the sample size was calculated using the measurement uncertainty of one laboratory, inter-laboratory comparison exercise data, and population variability for commonly studied metals (mercury, cadmium, and lead) in blood. Measurement uncertainty within one laboratory proved to have little influence on the sample size requirements, while the inter-laboratory variability of the three metals increased the requirements considerably, particularly in cases of low population variability. The multiple laboratories approach requires that laboratory variability be considered as early as the planning stage; a single-laboratory approach is thus a cost-effective compromise in HBM to reduce variability due to the participation of different laboratories. MDPI 2019-06-28 2019-07 /pmc/articles/PMC6651690/ /pubmed/31261622 http://dx.doi.org/10.3390/ijerph16132287 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Snoj Tratnik, Janja
Mazej, Darja
Horvat, Milena
Analytical Quality Requirements in Human Biomonitoring Programs: Trace Elements in Human Blood
title Analytical Quality Requirements in Human Biomonitoring Programs: Trace Elements in Human Blood
title_full Analytical Quality Requirements in Human Biomonitoring Programs: Trace Elements in Human Blood
title_fullStr Analytical Quality Requirements in Human Biomonitoring Programs: Trace Elements in Human Blood
title_full_unstemmed Analytical Quality Requirements in Human Biomonitoring Programs: Trace Elements in Human Blood
title_short Analytical Quality Requirements in Human Biomonitoring Programs: Trace Elements in Human Blood
title_sort analytical quality requirements in human biomonitoring programs: trace elements in human blood
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6651690/
https://www.ncbi.nlm.nih.gov/pubmed/31261622
http://dx.doi.org/10.3390/ijerph16132287
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