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临床化学分析中分析前变量不确定度预算模型。

A model for an uncertainty budget for preanalytical variables in clinical chemistry analyses.

作者信息

Rynning Marit, Wentzel-Larsen Tore, Bolann Bjørn J

机构信息

Laboratory of Clinical Biochemistry, Haukeland University Hospital, Helse Bergen HF, Bergen, Norway.

出版信息

Clin Chem. 2007 Jul;53(7):1343-8. doi: 10.1373/clinchem.2007.086371. Epub 2007 May 10.

Abstract

BACKGROUND

We sought a practical method to calculate preanalytical uncertainties. In clinical chemistry measurements, the combined preanalytical uncertainty is a function of the magnitude and probability distribution of the different uncertainty sources and the number of such sources.

METHODS

Results from an optimal practice for handling of the blood samples (termed the standard method) were compared with alternative methods that deviate from the standard method but are used in current practice. For categorically distributed uncertainty sources (e.g., use of different kinds of blood tubes), alternative treatments were modeled discretely using a known probability distribution for each alternative. For continuously distributed sources (e.g., clotting time), we assumed a rectangular distribution. We calculated the expectation, variance, and SD of differences between results from current practice and the standard method. We tabulated uncertainty budgets for the differences between current practice and the standard method for each uncertainty source. The expected individual biases and variances were summed to obtain the combined expected bias and variance.

RESULTS

The combined expected bias (SD) for glucose was -0.15 (0.130) mmol/L, with prolonged clotting time giving the greatest contribution. The combined expected bias (SD) for calcium was -0.011 (0.0182) mmol/L, for magnesium 0.006 (0.026) mmol/L, and for creatinine 0.5 (1.81) micromol/L.

CONCLUSION

By comparing a standard method for preanalytical sample handling to alternative methods used in current practice, and considering the distribution of alternative methods, our modeling approach allows the development of an uncertainty budget for preanalytical variables in clinical chemistry analyses.

摘要

背景

我们寻求一种计算分析前不确定度的实用方法。在临床化学测量中,分析前的综合不确定度是不同不确定度来源的大小、概率分布以及此类来源数量的函数。

方法

将处理血样的最佳实践方法(称为标准方法)的结果与偏离标准方法但在当前实践中使用的替代方法进行比较。对于分类分布的不确定度来源(例如,使用不同种类的采血管),使用每种替代方法的已知概率分布对替代处理进行离散建模。对于连续分布的来源(例如,凝血时间),我们假设为矩形分布。我们计算了当前实践结果与标准方法结果之间差异的期望值、方差和标准差。我们将每个不确定度来源的当前实践与标准方法之间差异的不确定度预算制成表格。将预期的个体偏差和方差相加,以获得综合预期偏差和方差。

结果

葡萄糖的综合预期偏差(标准差)为-0.15(0.130)mmol/L,凝血时间延长的贡献最大。钙的综合预期偏差(标准差)为-0.011(0.0182)mmol/L,镁为0.006(0.026)mmol/L,肌酐为0.5(1.81)μmol/L。

结论

通过将分析前样本处理的标准方法与当前实践中使用的替代方法进行比较,并考虑替代方法的分布,我们的建模方法允许为临床化学分析中的分析前变量制定不确定度预算。

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