Results of the multicenter evaluation of the CEDIA Phenobarbital assay.

G Klein, W Collinsworth, A Courbe, O Diez, I Domke, E Hänseler, P Haux, R Kattermann, A Knoke, P Lehmann
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Abstract

The CEDIA Phenobarbital assay has been evaluated in twelve clinical laboratories in Europe and U.S.A. on Boehringer Mannheim/Hitachi analysis systems. The evaluation focused on the analysis of imprecision and accuracy. Within-run and between-day coefficients of variations of the new assay were comparable to those of established routine methods. As demonstrated in an interlaboratory survey study with controls and human sera, results obtained in different laboratories showed a good agreement. The CEDIA Phenobarbital assay measured very accurately, as particularly confirmed by comparison with HPLC. It can be recommended as a reliable and practicable test for monitoring of phenobarbital on Boehringer Mannheim/Hitachi analyzers used in routine clinical chemistry.

CEDIA苯巴比妥测定的多中心评价结果。
CEDIA苯巴比妥测定法已在欧洲和美国的12个临床实验室在勃林格曼海姆/日立分析系统上进行了评估。评价的重点是不精密度和准确度的分析。新测定法的运行内和日间变异系数与常规方法相当。一项针对对照和人血清的实验室间调查研究表明,在不同实验室获得的结果显示出良好的一致性。CEDIA苯巴比妥测定法测量非常准确,特别是与HPLC比较证实。在常规临床化学中使用的勃林格曼海姆/日立分析仪上,它可以作为一种可靠和实用的监测苯巴比妥的测试。
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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