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Evaluation of the analytical performance of the PC100 platelet counter

INTRODUCTION: Platelet count can be altered in various diseases and treatments and measuring it may provide better insight into the expected outcome. So far, quantification of platelet count is done within laboratory conditions by using established hematology analyzers, whereas a point-of-care devic...

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Autores principales: Nagy, Magdolna, Fazaeli, Sepanta, van Oerle, René, ten Cate, Hugo, Schemmann, Marcel, Sherry, John, Kelleher, Gillian, Spronk, Henri M. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8094460/
https://www.ncbi.nlm.nih.gov/pubmed/33947405
http://dx.doi.org/10.1186/s12959-021-00283-w
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author Nagy, Magdolna
Fazaeli, Sepanta
van Oerle, René
ten Cate, Hugo
Schemmann, Marcel
Sherry, John
Kelleher, Gillian
Spronk, Henri M. H.
author_facet Nagy, Magdolna
Fazaeli, Sepanta
van Oerle, René
ten Cate, Hugo
Schemmann, Marcel
Sherry, John
Kelleher, Gillian
Spronk, Henri M. H.
author_sort Nagy, Magdolna
collection PubMed
description INTRODUCTION: Platelet count can be altered in various diseases and treatments and measuring it may provide better insight into the expected outcome. So far, quantification of platelet count is done within laboratory conditions by using established hematology analyzers, whereas a point-of-care device could be used for this purpose outside of the clinical laboratories. AIM: Our aim was to assess the closeness of agreement between a newly developed point-of-care PC100 platelet counter and two reference methods (Sysmex® XP-300, Sysmex® XN-9000) in measuring platelet counts in whole blood and platelet-rich-plasma (PRP). METHOD: Whole blood was obtained from 119 individuals, of which 74 were used to prepare PRP samples. Whole blood platelet count was measured by the two reference methods and the PC100 platelet counter. PRP was prepared from the whole blood and platelet count was adjusted to the range of 250–3600 × 10(3)/μl and measured with the PC100 platelet counter and Sysmex® XP-300. RESULTS: A median difference of − 1.35% and − 2.98% occurred in whole blood platelet count between the PC100 platelet counter and the Sysmex® XP-300 and Sysmex® XN-9000, respectively. A strong linear correlation (r ≥ 0.98) was seen in both cases and regression equations indicated neither a constant nor a proportional bias between the methods. Direct comparison of the two reference methods revealed a median difference of − 1.15% and a strongly linear relationship (r = 0.99). Platelet count in PRP resulted in a median difference of 1.42% between the PC100 platelet counter and the reference method, Sysmex® XP-300. While the difference between two methods increased with concentration of platelets in PRP, a strong linear relationship remained throughout the whole measuring interval indicated by the high correlation coefficient (r = 0.99). Assessment of the predicted bias at predefined platelet counts showed that the bias in platelet counts falls within the acceptance criterion for both whole blood and PRP measurements. CONCLUSIONS: Our results show that the PC100 platelet counter can be used interchangeably with the reference methods for determining platelet counts.
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spelling pubmed-80944602021-05-04 Evaluation of the analytical performance of the PC100 platelet counter Nagy, Magdolna Fazaeli, Sepanta van Oerle, René ten Cate, Hugo Schemmann, Marcel Sherry, John Kelleher, Gillian Spronk, Henri M. H. Thromb J Research INTRODUCTION: Platelet count can be altered in various diseases and treatments and measuring it may provide better insight into the expected outcome. So far, quantification of platelet count is done within laboratory conditions by using established hematology analyzers, whereas a point-of-care device could be used for this purpose outside of the clinical laboratories. AIM: Our aim was to assess the closeness of agreement between a newly developed point-of-care PC100 platelet counter and two reference methods (Sysmex® XP-300, Sysmex® XN-9000) in measuring platelet counts in whole blood and platelet-rich-plasma (PRP). METHOD: Whole blood was obtained from 119 individuals, of which 74 were used to prepare PRP samples. Whole blood platelet count was measured by the two reference methods and the PC100 platelet counter. PRP was prepared from the whole blood and platelet count was adjusted to the range of 250–3600 × 10(3)/μl and measured with the PC100 platelet counter and Sysmex® XP-300. RESULTS: A median difference of − 1.35% and − 2.98% occurred in whole blood platelet count between the PC100 platelet counter and the Sysmex® XP-300 and Sysmex® XN-9000, respectively. A strong linear correlation (r ≥ 0.98) was seen in both cases and regression equations indicated neither a constant nor a proportional bias between the methods. Direct comparison of the two reference methods revealed a median difference of − 1.15% and a strongly linear relationship (r = 0.99). Platelet count in PRP resulted in a median difference of 1.42% between the PC100 platelet counter and the reference method, Sysmex® XP-300. While the difference between two methods increased with concentration of platelets in PRP, a strong linear relationship remained throughout the whole measuring interval indicated by the high correlation coefficient (r = 0.99). Assessment of the predicted bias at predefined platelet counts showed that the bias in platelet counts falls within the acceptance criterion for both whole blood and PRP measurements. CONCLUSIONS: Our results show that the PC100 platelet counter can be used interchangeably with the reference methods for determining platelet counts. BioMed Central 2021-05-04 /pmc/articles/PMC8094460/ /pubmed/33947405 http://dx.doi.org/10.1186/s12959-021-00283-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Nagy, Magdolna
Fazaeli, Sepanta
van Oerle, René
ten Cate, Hugo
Schemmann, Marcel
Sherry, John
Kelleher, Gillian
Spronk, Henri M. H.
Evaluation of the analytical performance of the PC100 platelet counter
title Evaluation of the analytical performance of the PC100 platelet counter
title_full Evaluation of the analytical performance of the PC100 platelet counter
title_fullStr Evaluation of the analytical performance of the PC100 platelet counter
title_full_unstemmed Evaluation of the analytical performance of the PC100 platelet counter
title_short Evaluation of the analytical performance of the PC100 platelet counter
title_sort evaluation of the analytical performance of the pc100 platelet counter
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8094460/
https://www.ncbi.nlm.nih.gov/pubmed/33947405
http://dx.doi.org/10.1186/s12959-021-00283-w
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