Badrick Tony, Loh Tze Ping
RCPA Quality Assurance Programs, St Leonards, Sydney, Australia.
National University Hospital, Singapore.
Clin Biochem. 2023 Apr;114:39-42. doi: 10.1016/j.clinbiochem.2023.01.011. Epub 2023 Feb 1.
Effective Quality Control remains one of the pillars of Clinical Biochemistry. An understanding of the possible analytical errors that may occur, how to detect them efficiently and how to prevent them from causing patient harm are critical components of a Quality System. For some time, there have been questions about the theoretical basis of the models used to describe and detect analytical error. The current theory recognises two types of error, systematic and random and a system based on sampling the analytical process using a synthetic material to detect these errors. However, there are at least two other errors that are present. One is related to the QC material and the other, irregular errors. In this Opinion Piece, some of the underlying assumptions of Quality Control systems are described and analysed.
有效的质量控制仍然是临床生物化学的支柱之一。了解可能发生的分析误差、如何有效地检测它们以及如何防止它们对患者造成伤害是质量体系的关键组成部分。一段时间以来,人们对用于描述和检测分析误差的模型的理论基础存在疑问。当前的理论认识到两种类型的误差,即系统误差和随机误差,以及一种基于使用合成材料对分析过程进行采样以检测这些误差的系统。然而,至少还存在另外两种误差。一种与质量控制材料有关,另一种是不规则误差。在这篇观点文章中,对质量控制系统的一些基本假设进行了描述和分析。