Bollen Casper W, Uiterwaal Cuno S P M, van Vught Adrianus J, van der Tweel Ingeborg
Pediatric Intensive Care Unit , University Medical Center Utrecht, Utrecht, The Netherlands.
Epidemiology. 2006 Nov;17(6):644-9. doi: 10.1097/01.ede.0000239658.19288.22.
Clinical trials can be stopped early based on interim analyses or sequential analyses. In principle, sequential analyses can also be used to decide whether enough evidence has been gathered in completed trials to make further trials unnecessary. We demonstrate such an application through a retrospective analysis of clinical trials comparing ventilation methods for the treatment of preterm newborns.
We identified 5 recent trials that compared high-frequency ventilation with conventional mechanical ventilation in the treatment of preterm newborns. Death or chronic lung disease and chronic lung disease in survivors were the primary clinical outcomes of interest. We applied sequential meta-analyses to these 5 studies.
After including the first study of the last 5 trials in a sequential meta-analysis, the boundary of "no clinically relevant effect" was crossed for both outcomes (death or chronic lung disease). A sensitivity analysis using a reduction in the size of assumed clinically relevant effect showed the same findings after 2 trials.
Sequential meta-analyses showed that a lack of clinically relevant effect had been established after the first of the 5 trials. If such an analysis had been conducted after the first or second of these clinical trials, it might have led to changes in the study design of subsequent trials or even to a reassessment of the need for further trials.
临床试验可基于期中分析或序贯分析提前终止。原则上,序贯分析也可用于判定在已完成的试验中是否已收集到足够证据,从而无需开展进一步试验。我们通过对比较早产新生儿通气治疗方法的临床试验进行回顾性分析来展示这样一种应用。
我们确定了5项近期试验,这些试验比较了高频通气与传统机械通气在早产新生儿治疗中的效果。死亡或慢性肺病以及存活者中的慢性肺病是主要关注的临床结局。我们对这5项研究应用了序贯荟萃分析。
在序贯荟萃分析中纳入最后5项试验中的第一项研究后,两个结局(死亡或慢性肺病)均越过了“无临床相关效应”的界限。使用假定的临床相关效应大小缩减进行的敏感性分析在纳入2项试验后显示了相同结果。
序贯荟萃分析表明,在5项试验中的第一项试验后即已确定缺乏临床相关效应。如果在这些临床试验的第一项或第二项试验后进行这样的分析,可能会导致后续试验的研究设计发生变化,甚至重新评估是否需要进一步试验。