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Dichotomizing partial compliance and increased participant burden in factorial designs: the performance of four noncompliance methods

机译:将部分合规性和增加的参与者负担二分为二:四种不合规方法的性能

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Background Noncompliance to treatment assignment is an inevitable occurrence in randomized clinical trials (RCTs). Intention to treat (ITT) is generally considered the best method for addressing noncompliance in RCTs. Alternatives to ITT exist, including per protocol (PP), as treated (AT), and instrumental variables (IV). These three methods define participant compliance dichotomously, but partial compliance is a common occurrence in RCTs. By defining a threshold, above which a participant is called a complier, PP, AT and IV can be used, but the resulting loss of information may affect their performance. Trials with factorial designs may experience higher rates of noncompliance due to the heavier burden that participants experience by being assigned to multiple experimental treatments. Methods Using simulations, we assessed the performance of ITT, PP, AT, and IV in both the partial compliance setting and in a 2-by-2 factorial design with increased participant burden for those randomized to both active treatments. Results The bias, mean squared error, and type I error rates of the IV method after dichotomizing partial compliance were heavily inflated. The performance of all four methods depended on the level of noncompliance present, with higher average noncompliance leading to poorer performance. PP and AT showed improved bias and power relative to ITT without inflating the type I error beyond acceptable limits. However, the PP and AT heavily inflated the type I error rates when participant compliance was affected by the participants’ general health. Conclusions There are consequences for dichotomizing compliance information to make it fit into well-known methods. The results suggest the need for a method of estimating treatment effects that can utilize partial compliance information.
机译:背景在随机临床试验(RCT)中,不可避免地发生了不符合治疗方案的情况。通常认为治疗意向(ITT)是解决RCT中不合规的最佳方法。存在ITT的替代方案,包括按方案(PP),经处理(AT)和工具变量(IV)。这三种方法一分为二地定义了参与者的依从性,但是部分依从性在RCT中很常见。通过定义一个阈值,可以将PP,AT和IV用作参与者,在该阈值之上称为参与者,但是所导致的信息丢失可能会影响其性能。析因设计的试验可能会出现更高的不合规率,这是由于参与者被分配了多种实验治疗方法所承受的重担。方法使用模拟方法,我们评估了ITT,PP,AT和IV在部分依从性设置和2×2因子设计中的表现,这些参与者随机分配给两种积极治疗的参与者负担增加。结果将部分依从性二等分后,IV方法的偏倚,均方误差和I型错误率被严重夸大。所有四种方法的性能都取决于存在的不合规程度,平均不合规性越高,性能越差。 PP和AT相对于ITT表现出更好的偏置和功率,而不会将I型错误夸大到可接受的范围内。但是,当参与者的服从性受到参与者总体健康的影响时,PP和AT会严重夸大I型错误率。结论将合规性信息二分法以使其适合众所周知的方法会有后果。结果表明需要一种可以利用部分依从性信息来估计治疗效果的方法。

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