The Management of Post Analytical Correction Factors.

Q1 Biochemistry, Genetics and Molecular Biology
Clinical Biochemist Reviews Pub Date : 2017-04-01
Roger Barton, Mark Mackay, Graham Rd Jones, Tony Badrick
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引用次数: 0

Abstract

Clinical laboratories may systematically apply factors to assay results after analysis, but before reporting, in order to facilitate comparison of data from different methods. This may be done to align with other patient results, reference intervals or clinical decision points. These factors, which we term Post Analytical Correction Factors (PACF), may be applied to all types of results derived from the method, i.e. quality control (QC) and external quality assurance (EQA), as well as the patient results. As the principal use of PACF is comparing patient results, it is important that the laboratory use commutable materials (i.e. patient samples) and a formal process to establish, apply and manage PACF. We report on preliminary guidelines for PACF from a recent workshop.

分析后校正因子的管理。
临床实验室可能会在分析之后,但在报告之前,系统地对分析结果应用因子,以便于比较不同方法的数据。这可能是为了与其他患者结果、参考区间或临床决策点保持一致。这些因素,我们称之为分析后校正因素(PACF),可以应用于该方法得出的所有类型的结果,即质量控制(QC)和外部质量保证(EQA),以及患者结果。由于PACF的主要用途是比较患者的结果,因此实验室必须使用可交换的材料(即患者样本)和正式的流程来建立、应用和管理PACF。我们在最近的一次研讨会上报告PACF的初步指导方针。
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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来源期刊
Clinical Biochemist Reviews
Clinical Biochemist Reviews Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
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