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Analytical performance, reference values and decision limits. A need to differentiate between reference intervals and decision limits and to define analytical quality specifications

机译:分析性能,参考值和决策极限。需要区分参考区间和决策极限并定义分析质量规格

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With the increasing use of decision limits (action limits, cutoff points) specified for a number of analytical components in diagnosis and for action in critical situations, formulated in national or international recommendations, the traditional interpretation of reference intervals has been uncertain, and sometimes the two concepts are being mixed up by incorporating risk calculations in the reference intervals. There is, therefore, a need to clarify the two concepts and to keep them definitely separated. Reference intervals are the 95% limits for the descriptions of the distributions of the values of analytical components measured on reference samples from reference individuals. Decision limits are based on guidelines from national and international expert groups defining specific concentrations of certain components as limits for decision about diagnosis or well-defined specific actions. Analytical quality specifications for reference intervals have been defined for bias since the 1990s, but in the re ommendations specified in the clinical guidelines analytical quality specifications are only scarcely defined. The demands for negligible biases are, however, even more essential for decision limits, as the choice is no longer left to the clinician, but emerge directly from the concentration. Even a small bias will change the number of diseased individuals, so the demands for negligible biases are obvious. A view over the analytical quality as published gives a variable picture of bias for many components, but with many examples of considerable bias which must be critical - yet no specifications have been stipulated until now.
机译:在国家或国际建议中,随着越来越多地使用针对诊断中的许多分析成分和危急情况下采取的措施所规定的决策极限(作用极限,临界点),对参考区间的传统解释已变得不确定,有时通过将风险计算合并到参考区间中,两个概念被混淆了。因此,有必要澄清两个概念并使它们明确分开。参考区间是描述参考个体的参考样品上测得的分析成分值分布的95%极限。决定极限是基于国家和国际专家组的指导原则,将某些成分的特定浓度定义为诊断或明确定义的特定动作的决定极限。自1990年代以来,已经定义了参考区间的分析质量规范以用于偏差,但是在临床指南中指定的建议中,几乎没有定义分析质量规范。但是,对于偏倚可以忽略不计的要求对于决策限制甚至更为重要,因为这种选择不再留给临床医生,而是直接从集中注意力中浮现出来。即使很小的偏见也会改变患病个体的数量,因此对可忽略的偏见的需求显而易见。对已发表的分析质量的看法给出了许多成分的偏差的可变图,但有许多示例说明了相当大的偏差,这是至关重要的,但到目前为止尚未规定任何规格。

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