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Standardization in clinical enzymology: a challenge for the theory of metrological traceability.

机译:临床酶学的标准化:对计量溯源性理论的挑战。

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The goal of standardization for measurement of the catalytic concentration of enzymes is to achieve comparable results in human samples, independent of the reagent kits, instruments, and laboratory where the assay is performed. To pursue this objective, the IFCC has established reference systems for the most important clinical enzymes. These systems are based on the following requirements: a) reference methods, well described and evaluated extensively; b) suitable reference materials; and c) reference laboratories operating in a highly controlled manner. When these reference systems are used appropriately, the diagnostic industry can assign traceable values to commercial calibrators. Clinical laboratories that use procedures with validated calibrators to measure human specimens can now obtain values that are traceable to higher-order reference procedures. These reference systems constitute the structure of the traceability chain to which the routine methods can be linked via an appropriate calibration process, provided that they have a comparable specificity (i.e., they are measuring the same catalytic quantity).
机译:标准化酶催化浓度的测量目标是在人类样品中获得可比的结果,而与进行测定的试剂盒,仪器和实验室无关。为了实现这一目标,IFCC建立了最重要的临床酶参考系统。这些系统基于以下要求:a)参考方法,其详细描述和评估广泛; b)合适的参考资料; c)高度受控的参考实验室。当适当使用这些参考系统时,诊断行业可以为商业校准器分配可追溯值。现在,使用带有经过验证的校准器的程序来测量人体标本的临床实验室可以获取可追溯到高阶参考程序的值。这些参考系统构成了可追溯性链的结构,只要它们具有可比的特异性(即,它们测量的是相同的催化量),常规方法就可以通过适当的校准过程与之链接。

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