Suppr超能文献

两种比例之比置信区间计算方法的回顾与评价以及非劣效性临床试验的考量

Review and evaluation of methods for computing confidence intervals for the ratio of two proportions and considerations for non-inferiority clinical trials.

作者信息

Dann Rebekkah S, Koch Gary G

机构信息

Department of Biostatistics, University of North Carolina, Chapel Hill, North Carolina 27599, USA.

出版信息

J Biopharm Stat. 2005;15(1):85-107. doi: 10.1081/bip-200040844.

Abstract

This article reviews several methods for forming confidence intervals for a risk ratio of two independent binomial proportions (which are both less than 0.50) and evaluates their statistical performance. These methods include use of a Taylor Series expansion to estimate variance, solutions to a quadratic equation, and maximum likelihood methods. In addition, for improvement of the properties of the methods based on large sample approximations, situations where either binomial count was less than or equal to 3 were managed conservatively by having an exact confidence interval for the odds ratio become the confidence interval for its risk ratio counterpart. Methods were initially evaluated by computing confidence limits for certain cases. Second, simulations were used to identify the better methods for controlling the Type I error rate while maintaining power. Last, relationships between methods were evaluated by calculating the percent of disagreement in the decision made regarding non inferiority. Methods in the group using a Taylor Series expansion in variance estimation perform similarly to the Pearson method preferred in the literature. In addition, the group of methods using a Taylor Series expansion are most easily computed. Applications of these findings are discussed for ratios that arise in randomized clinical trials that are conducted to show noninferiority of a new medical product to a reference control. Consideration is given as well to sample size calculations for noninferiority clinical trials.

摘要

本文回顾了几种为两个独立二项比例(均小于0.50)的风险比构建置信区间的方法,并评估了它们的统计性能。这些方法包括使用泰勒级数展开来估计方差、二次方程的求解方法以及最大似然法。此外,为了改进基于大样本近似方法的性质,对于二项计数小于或等于3的情况,通过将优势比的精确置信区间作为其风险比对应物的置信区间来进行保守处理。方法最初通过计算某些情况下的置信限进行评估。其次,使用模拟来确定在保持检验效能的同时控制I型错误率的更好方法。最后,通过计算在非劣效性决策中不一致的百分比来评估方法之间的关系。在方差估计中使用泰勒级数展开的方法组的性能与文献中首选的皮尔逊方法相似。此外,使用泰勒级数展开的方法组计算起来最容易。讨论了这些发现在为显示新医疗产品相对于对照参考的非劣效性而进行的随机临床试验中出现的比例方面的应用。同时也考虑了非劣效性临床试验的样本量计算。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验