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在以立体视锐度为结果的随机临床试验中使用早期失败标准时的偏倚风险。

Risk of Bias When Using Early Failure Criteria in Randomized Clinical Trials With Stereoacuity Outcomes.

作者信息

Panjwani Meet, Holmes Jonathan M

机构信息

Department of Ophthalmology and Vision Science, University of Arizona - Tucson, Tucson, AZ, USA.

出版信息

Transl Vis Sci Technol. 2024 Dec 2;13(12):1. doi: 10.1167/tvst.13.12.1.

Abstract

PURPOSE

The purpose of this study was to explore the effects of early failure criteria for participants in randomized clinical trials (RCTs) on overall trial conclusions.

METHOD

We simulated 10,000 hypothetical RCTs with 2 treatments, 1 linear improvement and 1 with increasing rate of improvement and 6 follow-up visits. Each RCT had 400 participants, with the same baseline stereoacuity distribution. We incorporated random test-retest noise for every visit, and scores were rounded to the nearest observable score. Early failure was defined as worsening of two or more levels. We compared mean outcome stereoacuity between treatment groups, with and without the failure rule, using the two-sample t-test and the proportion of erroneous RCTs (significantly different mean outcome values, where truth is known to be no different). Sensitivity analyses were performed to explore the influence of sample size, baseline distribution of stereoacuity, overall magnitude of mean improvement, magnitude of change for the failure rule, and distribution of noise.

RESULTS

A greater proportion of 10,000 simulated RCTs had an erroneous mean difference in outcome with the early failure rule than without (5.49%, 95% confidence interval [CI] = 5.05% to 5.94% vs. 0, 0%, 95% CI = 0% to 0.000001%, difference 5.49%, P < 0.0001). Sensitivity analysis revealed that increased sample size and wider distribution of noise had the greatest influence on increasing proportions of erroneous RCT conclusions.

CONCLUSIONS

Study designs incorporating participant-level early failure rules increase the risk of erroneous RCT conclusions and should be avoided.

TRANSLATIONAL RELEVANCE

We provide data informing the design of future clinical trials. Earlier failure rules at the participant level should be avoided.

摘要

目的

本研究旨在探讨随机临床试验(RCT)中参与者早期失败标准对试验总体结论的影响。

方法

我们模拟了10000项假设的RCT,涉及两种治疗方法,一种是线性改善,另一种是改善率递增,并有6次随访。每项RCT有400名参与者,具有相同的基线立体视敏度分布。每次随访都纳入了随机重测噪声,分数四舍五入到最接近的可观察分数。早期失败定义为恶化两个或更多等级。我们使用两样本t检验比较了有和没有失败规则的治疗组之间的平均结局立体视敏度,以及错误RCT的比例(平均结局值有显著差异,而实际情况已知无差异)。进行敏感性分析以探讨样本量、立体视敏度的基线分布、平均改善的总体幅度、失败规则的变化幅度以及噪声分布的影响。

结果

在10000项模拟的RCT中,有早期失败规则的试验得出错误平均差异结局的比例高于没有该规则的试验(5.49%,95%置信区间[CI]=5.05%至5.94%,而无规则时为0,0%,95%CI=0%至0.000001%,差异为5.49%,P<0.0001)。敏感性分析表明,样本量增加和噪声分布更宽对错误RCT结论比例增加的影响最大。

结论

纳入参与者水平早期失败规则的研究设计会增加RCT得出错误结论的风险,应予以避免。

转化相关性

我们提供的数据可为未来临床试验的设计提供参考。应避免在参与者水平采用更早的失败规则。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa55/11614026/2d0b683f17a6/tvst-13-12-1-f001.jpg

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