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电解质测量的性能通过真实度验证方案进行评估。

Performance of electrolyte measurements assessed by a trueness verification program.

出版信息

Clin Chem Lab Med. 2016 Aug 1;54(8):1319-27. doi: 10.1515/cclm-2015-1110.

DOI:10.1515/cclm-2015-1110
PMID:27010777
Abstract

BACKGROUND

In this study, we analyzed frozen sera with known commutabilities for standardization of serum electrolyte measurements in China.

METHODS

Fresh frozen sera were sent to 187 clinical laboratories in China for measurement of four electrolytes (sodium, potassium, calcium, and magnesium). Target values were assigned by two reference laboratories. Precision (CV), trueness (bias), and accuracy [total error (TEa)] were used to evaluate measurement performance, and the tolerance limit derived from the biological variation was used as the evaluation criterion.

RESULTS

About half of the laboratories used a homogeneous system (same manufacturer for instrument, reagent and calibrator) for calcium and magnesium measurement, and more than 80% of laboratories used a homogeneous system for sodium and potassium measurement. More laboratories met the tolerance limit of imprecision (coefficient of variation [CVa]) than the tolerance limits of trueness (biasa) and TEa. For sodium, calcium, and magnesium, the minimal performance criterion derived from biological variation was used, and the pass rates for total error were approximately equal to the bias (<50%). For potassium, the pass rates for CV and TE were more than 90%. Compared with the non homogeneous system, the homogeneous system was superior for all three quality specifications.

CONCLUSIONS

The use of commutable proficiency testing/external quality assessment (PT/EQA) samples with values assigned by reference methods can monitor performance and provide reliable data for improving the performance of laboratory electrolyte measurement. The homogeneous systems were superior to the non homogeneous systems, whereas accuracy of assigned values of calibrators and assay stability remained challenges.

摘要

背景

本研究分析了已知可互换性的冷冻血清,旨在为中国血清电解质测量的标准化提供依据。

方法

新鲜冷冻血清被送往中国的 187 家临床实验室,用于测量四种电解质(钠、钾、钙和镁)。靶值由两个参考实验室分配。使用精密度(CV)、准确度(偏倚)和准确度[总误差(TEa)]来评估测量性能,并用生物学变异衍生的容忍限作为评估标准。

结果

约一半的实验室使用同种系统(仪器、试剂和校准品来自同一制造商)测量钙和镁,超过 80%的实验室使用同种系统测量钠和钾。更多的实验室符合不精密度(变异系数[CVa])的容忍限,而符合准确度(偏倚)和 TEa 的容忍限的实验室较少。对于钠、钙和镁,使用生物学变异衍生的最小性能标准,总误差的通过率接近偏倚(<50%)。对于钾,CV 和 TE 的通过率均超过 90%。与非同种系统相比,同种系统在所有三个质量规范方面都具有优势。

结论

使用赋值参考方法的可互换能力验证/外部质量评估(PT/EQA)样本可以监测性能,并为改善实验室电解质测量性能提供可靠数据。同种系统优于非同种系统,而校准品赋值的准确性和分析稳定性仍然是挑战。

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