Commutability of reference materials in clinical chemistry.

C Franzini
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Abstract

The term commutability applied to reference materials denotes the ability of the material to show interassay changes comparable to those observed in the measurement of the same analyte in human serum. In this study commutability was studied by first establishing the relationship between the results obtained on patient serum samples with two independent methods for a given analyte. Then, the calibration or control material was assayed with the same pair of methods, and its interassay bias was statistically compared with that shown by patient sera. The results obtained in 27 experiments showed that the frequencies of noncommutability in the measurement of some nonenzymic organic components, enzymes, and inorganic ions were, respectively, 25/83, 44/99, and 32/61. The impact of noncommutability of the materials on the results of external quality assessment schemes (EQAS), matrix interferences, and the behavior of particular components are considered. The conclusion drawn is that each material should be tested for commutability before it is used as a reference material.

临床化学中标准物质的交换性。
可交换性一词适用于标准物质,是指该物质显示出与在人血清中测量相同分析物时观察到的测定间变化相当的能力。在这项研究中,可交换性是通过首先建立两种独立方法对给定分析物在患者血清样品上获得的结果之间的关系来研究的。然后,用相同的方法对校准或对照物质进行检测,并将其与患者血清显示的检测间偏差进行统计学比较。27次实验结果表明,非酶有机组分、酶和无机离子的非交换频率分别为25/83、44/99和32/61。考虑了材料的非交换性对外部质量评估方案(EQAS)结果、矩阵干扰和特定组分行为的影响。得出的结论是,每种材料在用作参考材料之前都应进行可交换性测试。
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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