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一种用于估计交叉研究中交互偏差的简单方法。

A simple method for the estimation of interaction bias in crossover studies.

作者信息

Cleophas T J

机构信息

Department of Medicine, Merwede Hospital Sliedrecht-Dordrecht, The Netherlands.

出版信息

J Clin Pharmacol. 1990 Nov;30(11):1036-40. doi: 10.1002/j.1552-4604.1990.tb03591.x.

Abstract

The crossover trial is considered the most powerful means of determining the efficacy of new drugs. However this study design is frequently invalidated by treatment-by-period interaction. If, for example, the effect of the first treatment period carries on into the next one, then it influences the response to the latter period (carryover effect). A second problem is that there are no reliable statistical methods to test for this potential bias. This article takes issue with these problems and gives an alternative method for the detection of interaction simply by looking at the data. In a crossover without interaction the second period should be a true reflection of the first. If, however, the data of a treatment are better in the second period than in the first, a carryover effect is probable. If worse, a rebound phenomenon or a negative carryover effect is likely. If both treatments are better or worse, a time effect or some other external influence might be present. The authors illustrate this simple method by a summary of a few selected trials that have been published recently. This method enables not only the detection of interaction but also the differentiation between different types of interactions. Therefore, investigators are advised to use it in order to make sure that there are no unexpected problems.

摘要

交叉试验被认为是确定新药疗效的最有效方法。然而,这种研究设计常常因治疗周期交互作用而失效。例如,如果第一个治疗周期的效果延续到下一个周期,那么它就会影响对后一个周期的反应(遗留效应)。第二个问题是,没有可靠的统计方法来检验这种潜在偏差。本文针对这些问题提出看法,并给出了一种仅通过查看数据来检测交互作用的替代方法。在无交互作用的交叉试验中,第二个周期应是第一个周期的真实反映。然而,如果一种治疗的数据在第二个周期比第一个周期更好,那么可能存在遗留效应。如果更差,则可能出现反弹现象或负遗留效应。如果两种治疗都更好或更差,可能存在时间效应或其他外部影响。作者通过总结最近发表的一些选定试验来说明这种简单方法。这种方法不仅能够检测交互作用,还能区分不同类型的交互作用。因此,建议研究人员使用它,以确保不存在意外问题。

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