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Hemolytic specimens in complete blood cell count: Red cell parameters could be revised by plasma free hemoglobin

INTRODUCTION: Hemolysis is the main cause of unqualified clinical samples. In this study, we established a method for detecting and evaluating hemolysis in whole blood test. We used a mathematical formula for correcting the influence of hemolysis on complete blood cell count (CBC) so as to avoid re‐...

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Autores principales: Peng, Zhaoyang, Xiang, Wenqing, Zhou, Jianming, Cao, Jiajia, Li, Zhe, Gao, Hui, Zhang, Junfeng, Shen, Hongqiang
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/PMC7307363/
https://www.ncbi.nlm.nih.gov/pubmed/31968147
http://dx.doi.org/10.1002/jcla.23218
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author Peng, Zhaoyang
Xiang, Wenqing
Zhou, Jianming
Cao, Jiajia
Li, Zhe
Gao, Hui
Zhang, Junfeng
Shen, Hongqiang
author_facet Peng, Zhaoyang
Xiang, Wenqing
Zhou, Jianming
Cao, Jiajia
Li, Zhe
Gao, Hui
Zhang, Junfeng
Shen, Hongqiang
author_sort Peng, Zhaoyang
collection PubMed
description INTRODUCTION: Hemolysis is the main cause of unqualified clinical samples. In this study, we established a method for detecting and evaluating hemolysis in whole blood test. We used a mathematical formula for correcting the influence of hemolysis on complete blood cell count (CBC) so as to avoid re‐venipuncture and obtain more accurate parameters of red blood cell detection, reduce the burden of patients, and improve the efficiency of diagnosis and treatment. METHODS: Hemolytic samples were selected and then corrected using the new formula. Plasma free hemoglobin (fHB) was used as the criterion to determine the degree of hemolysis; the uncertainty of measurement is acceptable as the limit value of deviation between the measured value and the revised value. Hemolysis simulation analysis in vitro and continuous monitoring of clinical patients were used to verify the correction effect. RESULTS: A total of 83 clinical samples with hemolysis were collected and analyzed; fHB 1.4 g/L was selected as the unacceptable value for clinical hemolysis detection. In hemolytic samples, the red blood cell parameters corrected by formula are significantly different from those uncorrected and had a good consistency with those before hemolysis. CONCLUSION: The results show that the hemolysis phenomenon of CBC has a significant impact on routine blood testing. By using the new formula, the influence of hemolysis on erythrocyte and related parameters can be quickly and easily corrected, thus avoiding venipuncture again for re‐examination, reducing diagnostic errors, and saving medical resources.
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spelling pubmed-73073632020-06-23 Hemolytic specimens in complete blood cell count: Red cell parameters could be revised by plasma free hemoglobin Peng, Zhaoyang Xiang, Wenqing Zhou, Jianming Cao, Jiajia Li, Zhe Gao, Hui Zhang, Junfeng Shen, Hongqiang J Clin Lab Anal Research Articles INTRODUCTION: Hemolysis is the main cause of unqualified clinical samples. In this study, we established a method for detecting and evaluating hemolysis in whole blood test. We used a mathematical formula for correcting the influence of hemolysis on complete blood cell count (CBC) so as to avoid re‐venipuncture and obtain more accurate parameters of red blood cell detection, reduce the burden of patients, and improve the efficiency of diagnosis and treatment. METHODS: Hemolytic samples were selected and then corrected using the new formula. Plasma free hemoglobin (fHB) was used as the criterion to determine the degree of hemolysis; the uncertainty of measurement is acceptable as the limit value of deviation between the measured value and the revised value. Hemolysis simulation analysis in vitro and continuous monitoring of clinical patients were used to verify the correction effect. RESULTS: A total of 83 clinical samples with hemolysis were collected and analyzed; fHB 1.4 g/L was selected as the unacceptable value for clinical hemolysis detection. In hemolytic samples, the red blood cell parameters corrected by formula are significantly different from those uncorrected and had a good consistency with those before hemolysis. CONCLUSION: The results show that the hemolysis phenomenon of CBC has a significant impact on routine blood testing. By using the new formula, the influence of hemolysis on erythrocyte and related parameters can be quickly and easily corrected, thus avoiding venipuncture again for re‐examination, reducing diagnostic errors, and saving medical resources. John Wiley and Sons Inc. 2020-01-22 /pmc/articles/PMC7307363/ /pubmed/31968147 http://dx.doi.org/10.1002/jcla.23218 Text en © 2020 The Authors. Journal of Clinical Laboratory Analysis Published by Wiley Periodicals, Inc. 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 Research Articles
Peng, Zhaoyang
Xiang, Wenqing
Zhou, Jianming
Cao, Jiajia
Li, Zhe
Gao, Hui
Zhang, Junfeng
Shen, Hongqiang
Hemolytic specimens in complete blood cell count: Red cell parameters could be revised by plasma free hemoglobin
title Hemolytic specimens in complete blood cell count: Red cell parameters could be revised by plasma free hemoglobin
title_full Hemolytic specimens in complete blood cell count: Red cell parameters could be revised by plasma free hemoglobin
title_fullStr Hemolytic specimens in complete blood cell count: Red cell parameters could be revised by plasma free hemoglobin
title_full_unstemmed Hemolytic specimens in complete blood cell count: Red cell parameters could be revised by plasma free hemoglobin
title_short Hemolytic specimens in complete blood cell count: Red cell parameters could be revised by plasma free hemoglobin
title_sort hemolytic specimens in complete blood cell count: red cell parameters could be revised by plasma free hemoglobin
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7307363/
https://www.ncbi.nlm.nih.gov/pubmed/31968147
http://dx.doi.org/10.1002/jcla.23218
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