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Estimation of the Risk Difference Under a Noncompliance Randomized Clinical Trial with Missing Outcomes

机译:不合规随机临床试验中缺失结果的风险差异估计

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摘要

In a randomized clinical trial (RCT), we often come across the situations in which there are patients who do not comply with their assigned treatments or whose outcomes are missing due to their refusal or loss to follow-up. Because noncompliance and missing outcomes do not generally occur completely at random, analyzing data as treated or excluding patients with missing outcomes from our analysis can produce a biased estimate of a treatment effect. In this paper, we consider estimation of the risk difference (RD) in the presence of both noncompliance and missing outcomes under a RCT. On the basis of a constant risk additive model proposed elsewhere, we derive the maximum likelihood estimator (MLE) and develop three asymptotic interval estimators in closed form for the RD when we have outcome missing at random. We apply Monte Carlo simulation to evaluate and compare the performance of these estimators in a variety of situations. We note that all interval estimators developed here can perform well with respect to the coverage probability in all the situations considered here. We find that the interval estimator using tanh - 1(x) transformation is generally more precise than the other two estimators with respect to the average length. Finally, we use the data taken from a randomized trial studying the association between flu vaccine and the risk of flu-related hospitalization to illustrate the practical use of these interval estimators.
机译:在随机临床试验(RCT)中,我们经常遇到这样的情况:有些患者不遵守指定的治疗方法,或者由于拒绝治疗或失去随访而导致其结局丢失。由于不合规和遗漏结果通常不会完全随机发生,因此分析治疗数据或从我们的分析中排除遗漏结果的患者可能会产生治疗效果的偏倚估计。在本文中,我们考虑在RCT下既存在违规情况又缺少结果的情况下对风险差异(RD)的估计。在其他地方提出的恒定风险累加模型的基础上,我们推导出最大似然估计量(MLE),并在结果随机丢失时针对RD开发三个渐近区间估计量的闭合形式。我们应用蒙特卡洛模拟来评估和比较这些估算器在各种情况下的性能。我们注意到,在这里考虑的所有情况下,此处开发的所有间隔估计器在覆盖概率方面都可以表现良好。我们发现,就平均长度而言,使用tanh-1(x)变换的间隔估计器通常比其他两个估计器更为精确。最后,我们使用一项研究流感疫苗与流感相关住院风险之间关系的随机试验数据,来说明这些间隔估计量的实际应用。

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