评估 Sysmex XQ-320 三部分差值血液分析仪及其标记功能。

IF 2.6 4区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY Journal of Clinical Laboratory Analysis Pub Date : 2024-02-23 DOI:10.1002/jcla.25017
Christine Coutaz, Adrien Mamin, Konstantinos Mintzas
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引用次数: 0

摘要

背景:三部分差分法(3PD)血液分析仪是一种快速、易用、经济的获取病人生理信息的重要方法。在这项研究中,我们评估了新型三部分差值分析仪 Sysmex XQ-320,研究了它与其前身(Sysmex XP-300)和五部分差值分析仪 Sysmex XN-9000 的可比性,并探索了它的标记潜力:方法:使用新鲜血液和质控材料对重复性、实验室内精密度、日间精密度、迁移性和线性进行了分析性能研究。以 XN-9000 为金标准,在 493 份样本中对 XQ-320 和 XP-300 进行了方法比较:结果:在分析性能研究中,XQ-320 优于制造商的技术指标,除了 MXD 在实验室内和使用 1 级质控材料时的日间精确度。在 20 个可报告参数中,XQ-320 与 XN-9000 的相关值大多大于 0.94(MXD# 0.891、MXD% 0.898 和 MCHC 0.849)。与 XP-300 相比,白细胞减少范围内的 WBC(偏差 -0.038 对 -0.097)和 PLT(偏差 2.568 对 -7.877,截距 3.880 对 -8.845)有所改善。XQ-320 和 XP-300 在白细胞直方图异常分布标志方面的一致性为 91.9%,在 PLT 标志方面的一致性为 95.3%。在 XN-9000 标记的样本中,XQ-320 上观察到中性粒细胞增加和混合细胞减少的模式:结论:XQ-320 显示出卓越的分析性能,与 XN-9000 的相关性非常好甚至极佳,比 XP-300 更胜一筹。标记与参数模式相结合可识别出更多疑似异常样品,因此 XQ-320 是使用 3PD 分析仪的实验室的绝佳解决方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Evaluation of the Sysmex XQ-320 three-part differential haematology analyser and its flagging capabilities

Background

Three-part differential (3PD) haematology analysers offer a quick, easy-to-use and economical way to acquire important information about a patient's physiology. In this study, we evaluated a new 3PD analyser, the Sysmex XQ-320, investigated its comparability with its predecessor (Sysmex XP-300) and the five-part differential analyser Sysmex XN-9000, and explored its flagging potential.

Methods

Analytical performance studies were conducted for repeatability, within-laboratory precision, between-day precision, carry-over and linearity with fresh blood and QC material. Method comparison was performed in 493 samples comparing XQ-320 with XP-300, using the XN-9000 as the gold standard.

Results

The XQ-320 excelled manufacturer's specifications in the analytical performance studies, except for MXD in within-laboratory and between-day precisions using the QC material level 1. The XQ-320 showed correlation values greater than 0.94 with XN-9000 for the majority of the 20 reportable parameters (MXD# 0.891, MXD% 0.898 and MCHC 0.849). Improvements over the XP-300 were observed in WBC in the leucocytopenic range (bias −0.038 vs. −0.097) and PLT (bias 2.568 vs. −7.877, intercept 3.880 vs. −8.845). Concordance between XQ-320 and XP-300 was 91.9% for the WBC histogram abnormal distribution flag and 95.3% for the PLT flag. Patterns of increased neutrophils and decreased mixed cells on the XQ-320 were observed in samples that raised a flag on XN-9000.

Conclusion

The XQ-320 showed excellent analytical performance, and very good to excellent correlation with XN-9000 with improvements over XP-300. Flagging combined with parameter patterns identified additional suspected abnormal samples, thus making the XQ-320 an excellent solution for laboratories utilising 3PD analysers.

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来源期刊
Journal of Clinical Laboratory Analysis
Journal of Clinical Laboratory Analysis 医学-医学实验技术
CiteScore
5.60
自引率
7.40%
发文量
584
审稿时长
6-12 weeks
期刊介绍: Journal of Clinical Laboratory Analysis publishes original articles on newly developing modes of technology and laboratory assays, with emphasis on their application in current and future clinical laboratory testing. This includes reports from the following fields: immunochemistry and toxicology, hematology and hematopathology, immunopathology, molecular diagnostics, microbiology, genetic testing, immunohematology, and clinical chemistry.
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