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实验室间在血浆抗癫痫药物浓度测定方面的变异性。

Interlaboratory variability in determination of plasma antiepileptic drug concentrations.

作者信息

Pippenger C E, Penry J K, White B G, Daly D D, Buddington R

出版信息

Arch Neurol. 1976 May;33(5):351-5. doi: 10.1001/archneur.1976.00500050037007.

Abstract

The usefulness of plasma antiepileptic drug concentrations in treatment of epilepsy has been established, and many laboratories provide this service. A "blind" survey utilizing pooled patient plasma samples was conducted among 197 laboratories in the United States and Canada to establish the interlaboratory reproducibility. Three "patient specimens" containing different amounts of phenobarbital, phenytoin (diphenylhydantoin), primidone, and ethosuximide were employed; 112 laboratories reported results within five weeks. The average cost for analyzing four drugs in a single sample was $43.27. Half of the laboratories reported results outside +/- 1 standard deviation of the mean of five reference laboratories. Wide interlaboratory variability must be considered by the practicing physician. Until certified antiepileptic drug standards in a biologic matrix are available from the National Bureau of Standards, a volunteer quality control program among laboratories is needed.

摘要

血浆抗癫痫药物浓度在癫痫治疗中的作用已得到证实,许多实验室都提供这项检测服务。在美国和加拿大的197家实验室中,利用汇集的患者血浆样本进行了一项“盲法”调查,以确定实验室间的重现性。使用了三份含有不同含量苯巴比妥、苯妥英(二苯乙内酰脲)、扑米酮和乙琥胺的“患者标本”;112家实验室在五周内报告了结果。分析单个样本中四种药物的平均成本为43.27美元。一半的实验室报告的结果超出了五个参考实验室均值的±1个标准差范围。临床医生必须考虑到实验室间存在的较大差异。在国家标准局提供生物基质中的认证抗癫痫药物标准之前,需要在各实验室之间开展一个自愿性质的质量控制项目。

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