IF 4.2 4区 医学 Q1 ANESTHESIOLOGY
WooJin Jung, Kwan Lee, Hyung-Hwan Kim, Chiyeon Lim
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引用次数: 0

摘要

方差分析(ANCOVA)是一种统计方法,通过考虑协变量或固定效应等因素来评估组间的平均差异,常用于评估临床试验中的疗效终点。在进行方差分析时,所有治疗组的回归模型斜率应相同,组别与协变量之间不存在交互作用。因此,在进行分析之前,必须检验带有交互作用的完整方差分析模型的显著性。如果完整模型中的交互作用具有统计学意义,则应使用包含交互作用的模型;否则,应使用不包含交互作用的简化模型进行方差分析。如果方差分析模型不显著,则不适合采用这种分析方法,可考虑采用多变量分析或个别回归线估算。如果通过方差分析检验了组间均值的差异,则应计算并检验调整后均值(最小二乘均值)的置信区间。由于结果可能会因方差分析模型中使用的协变量而改变,因此在进行分析前应预先确定协变量。如果在临床试验开始后必须定义新的协变量,则应在统计分析计划中明确说明。这被视为重大修正;因此,必须在临床试验结束前重新定义协变量,并在临床研究报告中加以说明。此外,还必须提供一份明确的报告,说明重新定义协变量是否会影响样本量或决策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
How to construct analysis of covariance in clinical trials : ANCOVA with one covariate in a completely randomized design structure.

Analysis of covariance (ANCOVA) is a statistical method used to assess mean differences between groups by considering factors such as covariates or fixed effects and is often used to assess efficacy endpoints in clinical trials. When performing ANCOVA, the slope of the regression model should be the same for all treatment groups, with no interaction between the group and the covariate. Therefore, before analysis, the significance of the full ANCOVA model with interactions must be tested. If the interaction in the full model is statistically significant, the model that includes the interaction should be used; otherwise, ANCOVA using a reduced model without the interaction should be performed. If the ANCOVA model is not significant, this analysis method is not appropriate and a multivariate analysis or individual regression line estimation can be considered. If the difference in means between the groups is tested by ANCOVA, the confidence interval for the adjusted mean (least-squares mean) should be calculated and tested. Because the results may change depending on the covariates used in the ANCOVA model, the covariates should be predefined before performing the analysis. If a new covariate must be defined after a clinical trial is initiated, it should be specified in the statistical analysis plan. This is considered a major amendment; thus, the covariates must be redefined before clinical trial completion and must be described in the clinical study report. A clear report describing whether the redefinition of the covariates affected the sample size or decision-making is also necessary.

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来源期刊
CiteScore
6.20
自引率
6.90%
发文量
84
审稿时长
16 weeks
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