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首页> 外文期刊>Clinical Biochemistry >Analytical performance and workflow evaluation of the Roche E170 modular immunoassay analyzer in a pediatric setting.
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Analytical performance and workflow evaluation of the Roche E170 modular immunoassay analyzer in a pediatric setting.

机译:Roche E170模块化免疫分析仪在儿科环境中的分析性能和工作流程评估。

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OBJECTIVES: To evaluate the analytical performance of the Roche E170 modular analytics immunoassay analyzer and assess its impact on workflow efficiency and ability to consolidate workstations in a pediatric setting. DESIGN AND METHODS: Analytical performance of eleven common immunoassays was assessed. Total imprecision was determined using Roche PreciControl Universal controls, Bio-Rad Lyphochek Immuno Plus, Anemia controls, and a human serum pool. Method comparison was performed with approximately 100 patient specimens. High dose hook effect, sample carryover, and results comparison between the two measuring channels were evaluated. For the workflow study, the time required for sample and reagent handling, instrument preparation, and hands-on time were assessed. RESULTS: Correlation coefficients with existing methods ranged from 0.941 to 0.999. Biases of -19% to 70% were observed. Total imprecision ranged from 1.1 to 7.6%. No sample carryovers were encountered. Results from both measuring channels were comparable. CONCLUSION: E170 is suitable for use in a pediatric setting. The analytical performance is acceptable and gives equivalent results to our existing systems. The precision is comparable and acceptable. Some improvement in efficiency, workflow, cost saving, and consolidation of workstations is possible. Significant workflow improvements can only be realized when integrated with the chemistry modules.
机译:目的:评估罗氏E170模块化分析免疫分析仪的分析性能,并评估其对工作流程效率的影响以及在儿科环境中整合工作站的能力。设计与方法:评估了11种常见免疫测定的分析性能。使用Roche PreciControl Universal对照,Bio-Rad Lyphochek Immuno Plus,贫血对照和人血清库确定总不精确度。方法比较是对大约100个患者标本进行的。评估了高剂量的钩效应,样品残留以及两个测量通道之间的结果比较。对于工作流程研究,评估了样品和试剂处理,仪器准备以及动手时间所需的时间。结果:现有方法的相关系数在0.941至0.999之间。观察到-19%至70%的偏差。总不精确度在1.1到7.6%之间。没有遇到样品残留。两个测量通道的结果均具有可比性。结论:E170适用于小儿科环境。分析性能是可以接受的,并且可以与我们现有的系统得出等效的结果。精度是可比较的并且可以接受。在效率,工作流程,成本节省和工作站合并方面可能会有所改善。只有与化学模块集成在一起,才能实现工作流程的显着改善。

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