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随机临床试验成本效益数据的统计分析。

Statistical analysis of cost-effectiveness data from randomized clinical trials.

机构信息

SickKids Research Institute, Population Health Sciences, 555 University Avenue, Toronto, Ontario M5G 1X8, Canada.

出版信息

Expert Rev Pharmacoecon Outcomes Res. 2006 Jun;6(3):337-46. doi: 10.1586/14737167.6.3.337.

Abstract

Since the mid-1990s, motivated by the availability of patient-level cost data in randomized clinical trials, there has been rapid development in the statistical methods for analyzing cost-effectiveness data. Initial efforts concentrated on inference about the incremental cost-effectiveness ratio (ICER), but due to difficulties associated with ratio statistics, interest has settled more recently on incremental net benefit (INB). Regardless of the approach, five parameters need to be estimated: the between-treatment arm differences in mean effectiveness and mean cost, and the corresponding variances and covariance. With the estimates of these parameters, the analyst can plot the cost-effectiveness acceptability curve and estimate the ICER and the INB, and calculate confidence limits for both. A review of these methods is given. The particular statistical procedure used for estimating the five parameters depends on whether or not censoring is present; whether or not covariates are adjusted for; whether or not random effects, such as country, are adjusted for; and the assumptions regarding the distribution for cost. A review of the statistical procedures, particular to each combination of these conditions, is given, where they exist.

摘要

自 20 世纪 90 年代中期以来,由于随机临床试验中患者水平成本数据的可用性,用于分析成本效益数据的统计方法得到了快速发展。最初的工作集中在增量成本效益比(ICER)的推断上,但由于比率统计的困难,最近人们的兴趣更多地集中在增量净效益(INB)上。无论采用哪种方法,都需要估计五个参数:治疗组间平均效果和平均成本的差异,以及相应的方差和协方差。通过这些参数的估计,分析人员可以绘制成本效益可接受性曲线,并估计 ICER 和 INB,并计算两者的置信限。本文对这些方法进行了回顾。用于估计五个参数的特定统计程序取决于是否存在删失;是否调整了协变量;是否调整了国家等随机效应;以及对成本分布的假设。本文还对特定于这些条件组合的统计程序进行了回顾,如果存在这些条件的话。

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