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The Sysmex XN‐L (XN‐350) hematology analyzer offers a compact solution for laboratories in niche diagnostics

INTRODUCTION: In 2015, Sysmex launched a new series of hematology analyzers (XN‐L Series) designed to fulfill the needs of niche laboratories in areas such as pediatrics, dialysis, neurology, and oncology while providing a compact solution. In this study, we evaluate the whole blood and body fluid m...

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Autores principales: Khartabil, Tania A., de Frankrijker, Magda M., de Rijke, Yolanda B., Russcher, Henk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7891428/
https://www.ncbi.nlm.nih.gov/pubmed/32949451
http://dx.doi.org/10.1111/ijlh.13339
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author Khartabil, Tania A.
de Frankrijker, Magda M.
de Rijke, Yolanda B.
Russcher, Henk
author_facet Khartabil, Tania A.
de Frankrijker, Magda M.
de Rijke, Yolanda B.
Russcher, Henk
author_sort Khartabil, Tania A.
collection PubMed
description INTRODUCTION: In 2015, Sysmex launched a new series of hematology analyzers (XN‐L Series) designed to fulfill the needs of niche laboratories in areas such as pediatrics, dialysis, neurology, and oncology while providing a compact solution. In this study, we evaluate the whole blood and body fluid modes of one of these analyzers, the XN‐350. METHODS: A total of 300 residual EDTA samples were measured on the XN‐350 in whole blood mode and the XN‐1000 to evaluate method comparison, flagging sensitivity, repeatability, reproducibility, linearity, carryover, and stability. In addition, 191 samples were obtained and processed in body fluid mode which included, cerebrospinal fluid (CSF), continuous ambulatory peritoneal dialysis (CAPD), ascites, synovial, and pleural fluid to perform method comparison, repeatability, reproducibility, linearity, limit of quantitation, and carryover studies. RESULTS: Strong agreement was shown between the XN‐350 and XN‐1000 for both whole blood and body fluid modes in results and flagging. Linearity results in both modes on the XN‐350 showed a high R (2) value (>.99). For WBC, RBC, HGB, and PLT, the carryover results were well within the predetermined criteria of ≤0.5% for whole blood and ≤0.3% for CSF. Repeatability and reproducibility were acceptable for both modes, and there were no significant deviations present in stability for whole blood. In addition, there was high agreement in all body fluid types evaluated. CONCLUSION: The performance of the XN‐350 is comparable to the XN‐1000 in both whole blood and body fluid modes, making it a reliable alternative to larger analyzers for smaller, niche laboratories.
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spelling pubmed-78914282021-03-02 The Sysmex XN‐L (XN‐350) hematology analyzer offers a compact solution for laboratories in niche diagnostics Khartabil, Tania A. de Frankrijker, Magda M. de Rijke, Yolanda B. Russcher, Henk Int J Lab Hematol ORIGINAL ARTICLES INTRODUCTION: In 2015, Sysmex launched a new series of hematology analyzers (XN‐L Series) designed to fulfill the needs of niche laboratories in areas such as pediatrics, dialysis, neurology, and oncology while providing a compact solution. In this study, we evaluate the whole blood and body fluid modes of one of these analyzers, the XN‐350. METHODS: A total of 300 residual EDTA samples were measured on the XN‐350 in whole blood mode and the XN‐1000 to evaluate method comparison, flagging sensitivity, repeatability, reproducibility, linearity, carryover, and stability. In addition, 191 samples were obtained and processed in body fluid mode which included, cerebrospinal fluid (CSF), continuous ambulatory peritoneal dialysis (CAPD), ascites, synovial, and pleural fluid to perform method comparison, repeatability, reproducibility, linearity, limit of quantitation, and carryover studies. RESULTS: Strong agreement was shown between the XN‐350 and XN‐1000 for both whole blood and body fluid modes in results and flagging. Linearity results in both modes on the XN‐350 showed a high R (2) value (>.99). For WBC, RBC, HGB, and PLT, the carryover results were well within the predetermined criteria of ≤0.5% for whole blood and ≤0.3% for CSF. Repeatability and reproducibility were acceptable for both modes, and there were no significant deviations present in stability for whole blood. In addition, there was high agreement in all body fluid types evaluated. CONCLUSION: The performance of the XN‐350 is comparable to the XN‐1000 in both whole blood and body fluid modes, making it a reliable alternative to larger analyzers for smaller, niche laboratories. John Wiley and Sons Inc. 2020-09-19 2021-02 /pmc/articles/PMC7891428/ /pubmed/32949451 http://dx.doi.org/10.1111/ijlh.13339 Text en © 2020 The Authors. International Journal of Laboratory Hematology published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle ORIGINAL ARTICLES
Khartabil, Tania A.
de Frankrijker, Magda M.
de Rijke, Yolanda B.
Russcher, Henk
The Sysmex XN‐L (XN‐350) hematology analyzer offers a compact solution for laboratories in niche diagnostics
title The Sysmex XN‐L (XN‐350) hematology analyzer offers a compact solution for laboratories in niche diagnostics
title_full The Sysmex XN‐L (XN‐350) hematology analyzer offers a compact solution for laboratories in niche diagnostics
title_fullStr The Sysmex XN‐L (XN‐350) hematology analyzer offers a compact solution for laboratories in niche diagnostics
title_full_unstemmed The Sysmex XN‐L (XN‐350) hematology analyzer offers a compact solution for laboratories in niche diagnostics
title_short The Sysmex XN‐L (XN‐350) hematology analyzer offers a compact solution for laboratories in niche diagnostics
title_sort sysmex xn‐l (xn‐350) hematology analyzer offers a compact solution for laboratories in niche diagnostics
topic ORIGINAL ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7891428/
https://www.ncbi.nlm.nih.gov/pubmed/32949451
http://dx.doi.org/10.1111/ijlh.13339
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