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Performance evaluation of the Sysmex? XE-2100D automated hematology analyzer

机译:Sysmex的性能评估? XE-2100D全自动血液分析仪

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Introduction: The Sysmex® XE-2100D is a multiparameter hematology analyzer designed for hematology testing in samples with ethylenediamine tetraacetic acid (EDTA). Objectives: Considering the importance of this hematology analyzer for clinical and laboratory practice, the objective of this study was to evaluate its analytical performance, comparing the obtained results with quality specifications described in literature. Material and method: In the evaluation of analytical performance, according to recommendations of the document H26-A2 of the Clinical and Laboratory Standards Institute (CLSI), intra-run imprecision, inter-run imprecision, linearity, carryover, autosampler evaluation, clinical sensitivity of the atypical lymphocytes flag (n = 400 samples) were included, as well as the comparison between automated and manual leukocyte differential count (n = 400 samples), based on an adaptation of the document H20-A2 of CLSI. Results: Repeatability, reproducibility, linearity and carryover were satisfactory according to the manufacturer's specifications. The clinical sensitivity of the atypical lymphocytes flag showed efficiency, sensitivity and specificity of 92.5%, 65.2% and 94.1% respectively. The correlation coefficients between the automated and manual differential counts of neutrophils, lymphocytes, monocytes, eosinophils and basophils were 0.991, 0.99, 0.872, 0.974 and 0.557, respectively. Conclusions: The results were in accordance with quality specifications described in literature, indicating reliability in Sysmex® XE-2100D. This fact ensures certainty to both laboratory professionals and medical staff. We conclude that the Sysmex® XE-2100D showed excellent analytical performance, and is useful to provide reliable hematology data.
机译:简介:Sysmex®XE-2100D是一款多参数血液学分析仪,设计用于使用乙二胺四乙酸(EDTA)对样品进行血液学测试。目的:考虑到这种血液分析仪在临床和实验室实践中的重要性,本研究的目的是评估其分析性能,将获得的结果与文献中描述的质量规格进行比较。材料和方法:在分析性能评估中,根据临床和实验室标准协会(CLSI)文件H26-A2的建议,批内不精密度,批间不精密度,线性,残留,自动进样器评估,临床敏感性根据CLSI的H20-A2文件的修改,其中包括非典型淋巴细胞标志的数量(n = 400个样本),以及自动和手动白细胞差异计数之间的比较(n = 400个样本)。结果:根据制造商的规范,重复性,再现性,线性和残留均令人满意。非典型淋巴细胞标志物的临床敏感性分别为92.5%,65.2%和94.1%。中性粒细胞,淋巴细胞,单核细胞,嗜酸性粒细胞和嗜碱性粒细胞的自动和手动差分计数之间的相关系数分别为0.991、0.99、0.872、0.974和0.557。结论:结果符合文献中所述的质量规格,表明Sysmex®XE-2100D的可靠性。这一事实确保了实验室专业人员和医务人员的确定性。我们得出的结论是,Sysmex®XE-2100D具有出色的分析性能,可用于提供可靠的血液学数据。

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