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使用西班牙 EQAS 数据研究不同浓度血液学参数的分析性能。

Study of the analytical performance at different concentrations of hematological parameters using Spanish EQAS data.

机构信息

Hematology External Quality Assessment Laboratory, Biomedical Diagnostic Center, Hospital Clinic of Barcelona, Barcelona, Spain.

CORE Laboratory, Biomedical Diagnostic Center, Hospital Clinic of Barcelona, Barcelona, Spain, Phone: +34 932272175.

出版信息

Clin Chem Lab Med. 2019 Nov 26;57(12):1980-1987. doi: 10.1515/cclm-2019-0108.

Abstract

Background External quality assessment programs are one of the currently available tools to evaluate the analytical performance of clinical laboratories, where the measurement error (ME) obtained can be compared with quality specifications to evaluate possible deviations. The objective of this work was to analyze the ME behavior over the analytical range to assess the need to establish concentration-dependent specifications. Methods A total of 389,000 results from 585 laboratories and 2628 analyzers were collected from the Spanish external quality assessment schemes (EQAS) in hematology during the years 2015-2016. The parameters evaluated included white blood cells, red blood cells, hemoglobin, hematocrit, mean corpuscular volume, mean corpuscular hemoglobin, mean corpuscular hemoglobin concentration, platelets, prothrombin time, activated partial thromboplastin time, neutrophils, lymphocytes, monocytes, eosinophils, basophils, reticulocytes, hemoglobin A2, antithrombin, factor VIII, protein C and von Willebrand factor. The 90th percentile of ME was calculated for every concentration evaluated of each parameter. Results We found a significant variation in the analytical performance of leukocytes, platelets, neutrophils, lymphocytes, monocytes, eosinophils, basophils, prothrombin time, reticulocytes, hemoglobin A2, antithrombin and protein C. Furthermore, this ME variation may not allow complying with the same biological variability requirements within the whole analytical range studied. Conclusions Our work shows the importance of implementing concentration-dependent specifications which can help laboratories to use proper criteria for quality specifications selection and for a better external quality control results evaluation.

摘要

背景

外部质量评估计划是评估临床实验室分析性能的现有工具之一,其中获得的测量误差(ME)可以与质量规范进行比较,以评估可能的偏差。本工作的目的是分析分析范围内的 ME 行为,以评估是否需要建立浓度依赖性规范。

方法

共收集了 2015-2016 年西班牙血液学外部质量评估计划(EQAS)中 585 个实验室和 2628 个分析仪的 389,000 个结果。评估的参数包括白细胞、红细胞、血红蛋白、血细胞比容、平均红细胞体积、平均红细胞血红蛋白、平均红细胞血红蛋白浓度、血小板、凝血酶原时间、活化部分凝血活酶时间、中性粒细胞、淋巴细胞、单核细胞、嗜酸性粒细胞、嗜碱性粒细胞、网织红细胞、血红蛋白 A2、抗凝血酶、VIII 因子、蛋白 C 和血管性血友病因子。计算了每个参数每个浓度的 ME 的第 90 个百分位数。

结果

我们发现白细胞、血小板、中性粒细胞、淋巴细胞、单核细胞、嗜酸性粒细胞、嗜碱性粒细胞、凝血酶原时间、网织红细胞、血红蛋白 A2、抗凝血酶和蛋白 C 的分析性能存在显著差异。此外,这种 ME 变化可能不允许在整个研究分析范围内遵守相同的生物学变异性要求。

结论

我们的工作表明实施浓度依赖性规范的重要性,这可以帮助实验室选择适当的质量规范标准,并更好地评估外部质量控制结果。

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