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Measurements of neonatal bilirubin and albumin concentrations: a need for improvement and quality control

Accurate and precise bilirubin and albumin measurements are essential for proper management of jaundiced neonates. Data hereon are lacking for Dutch laboratories. We aimed to determine variability of measurements of bilirubin and albumin concentrations typical for (preterm) neonates. Aqueous, human...

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Autores principales: van Imhoff, Deirdre E., Dijk, Peter H., Weykamp, Cas W., Cobbaert, Christa M., Hulzebos, Christian V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3139054/
https://www.ncbi.nlm.nih.gov/pubmed/21213112
http://dx.doi.org/10.1007/s00431-010-1383-4
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author van Imhoff, Deirdre E.
Dijk, Peter H.
Weykamp, Cas W.
Cobbaert, Christa M.
Hulzebos, Christian V.
author_facet van Imhoff, Deirdre E.
Dijk, Peter H.
Weykamp, Cas W.
Cobbaert, Christa M.
Hulzebos, Christian V.
author_sort van Imhoff, Deirdre E.
collection PubMed
description Accurate and precise bilirubin and albumin measurements are essential for proper management of jaundiced neonates. Data hereon are lacking for Dutch laboratories. We aimed to determine variability of measurements of bilirubin and albumin concentrations typical for (preterm) neonates. Aqueous, human serum albumin-based samples with different concentrations of bilirubin (100, 200, 300, 400, and 500 μmol/L) and albumin (0, 10, 15, 20, 25, and 30 g/L) were sent to laboratories of all Dutch neonatal intensive care units (n = 10). Bilirubin and albumin recoveries of the specimens were measured using locally available routine analytical methods. The mean, standard deviation, and coefficients of variations (CV) were calculated per sample. Bilirubin concentrations were underestimated in the absence of albumin (maximal CV 26.0%). When the albumin concentration was 10 or 20 g/L, the bilirubin concentrations of the samples were overestimated (maximal CV 14.1% and 9.2%, respectively). Variability increased with higher weighed-in bilirubin concentrations. Measured albumin levels were ~10% lower than albumin levels of manufactured samples. Bilirubin concentration did not influence albumin measurements. The maximal CV was 6.8%. In conclusion, interlaboratory variability of bilirubin and albumin measurements is high. Recalibration and introduction of a specific quality assessment scheme for neonatal samples is recommended to ensure exchangeability of bilirubin and albumin measurements among laboratories and to control the observed large variability.
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spelling pubmed-31390542011-08-26 Measurements of neonatal bilirubin and albumin concentrations: a need for improvement and quality control van Imhoff, Deirdre E. Dijk, Peter H. Weykamp, Cas W. Cobbaert, Christa M. Hulzebos, Christian V. Eur J Pediatr Original Paper Accurate and precise bilirubin and albumin measurements are essential for proper management of jaundiced neonates. Data hereon are lacking for Dutch laboratories. We aimed to determine variability of measurements of bilirubin and albumin concentrations typical for (preterm) neonates. Aqueous, human serum albumin-based samples with different concentrations of bilirubin (100, 200, 300, 400, and 500 μmol/L) and albumin (0, 10, 15, 20, 25, and 30 g/L) were sent to laboratories of all Dutch neonatal intensive care units (n = 10). Bilirubin and albumin recoveries of the specimens were measured using locally available routine analytical methods. The mean, standard deviation, and coefficients of variations (CV) were calculated per sample. Bilirubin concentrations were underestimated in the absence of albumin (maximal CV 26.0%). When the albumin concentration was 10 or 20 g/L, the bilirubin concentrations of the samples were overestimated (maximal CV 14.1% and 9.2%, respectively). Variability increased with higher weighed-in bilirubin concentrations. Measured albumin levels were ~10% lower than albumin levels of manufactured samples. Bilirubin concentration did not influence albumin measurements. The maximal CV was 6.8%. In conclusion, interlaboratory variability of bilirubin and albumin measurements is high. Recalibration and introduction of a specific quality assessment scheme for neonatal samples is recommended to ensure exchangeability of bilirubin and albumin measurements among laboratories and to control the observed large variability. Springer-Verlag 2011-01-07 2011 /pmc/articles/PMC3139054/ /pubmed/21213112 http://dx.doi.org/10.1007/s00431-010-1383-4 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Paper
van Imhoff, Deirdre E.
Dijk, Peter H.
Weykamp, Cas W.
Cobbaert, Christa M.
Hulzebos, Christian V.
Measurements of neonatal bilirubin and albumin concentrations: a need for improvement and quality control
title Measurements of neonatal bilirubin and albumin concentrations: a need for improvement and quality control
title_full Measurements of neonatal bilirubin and albumin concentrations: a need for improvement and quality control
title_fullStr Measurements of neonatal bilirubin and albumin concentrations: a need for improvement and quality control
title_full_unstemmed Measurements of neonatal bilirubin and albumin concentrations: a need for improvement and quality control
title_short Measurements of neonatal bilirubin and albumin concentrations: a need for improvement and quality control
title_sort measurements of neonatal bilirubin and albumin concentrations: a need for improvement and quality control
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3139054/
https://www.ncbi.nlm.nih.gov/pubmed/21213112
http://dx.doi.org/10.1007/s00431-010-1383-4
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