Warwick Clinical Trials Unit, University of Warwick, Coventry, UK.
Cancer Research UK Clinical Trials Unit, University of Birmingham, Birmingham, UK.
BMJ Open. 2019 Mar 7;9(3):e024256. doi: 10.1136/bmjopen-2018-024256.
The traditional approach of null hypothesis testing dominates the design and analysis of randomised controlled trials. This study aimed to demonstrate how a simple Bayesian analysis could have been used to analyse the Optimisation of Perioperative Cardiovascular Management to Improve Surgical Outcome (OPTIMISE) trial to obtain more clinically interpretable results.
DESIGN, SETTING, PARTICIPANTS AND INTERVENTIONS: The OPTIMISE trial was a pragmatic, multicentre, observer-blinded, randomised controlled trial of 734 high-risk patients undergoing major gastrointestinal surgery in 17 acute care hospitals in the UK. Patients were randomly allocated to a cardiac output-guided haemodynamic therapy algorithm for intravenous fluid and inotropic drug administration during and in the 6 hours following surgery (n=368) or to standard care (n=366). The primary outcome was a binary outcome consisting of a composite of predefined 30-day moderate or major complications and mortality.
We repeated the primary outcome analysis of the OPTIMISE trial using Bayesian statistical methods to calculate the probability that the intervention was superior, and the probability that a clinically relevant difference existed. We explored the impact of a flat prior and an evidence-based prior on our analyses.
Although OPTIMISE was not powered to detect a statistically significant difference between the treatment arms for the observed effect size (relative risk=0.84, 95% CI 0.70 to 1.01; p=0.07), by using Bayesian analyses we were able to demonstrate that there was a 96.9% (flat prior) to 99.5% (evidence-based prior) probability that the intervention was superior to the control.
The use of a Bayesian analytical approach provided a different interpretation of the findings of the OPTIMISE trial (compared with the original frequentist analysis), and suggested patient benefit from the intervention. Incorporation of information from previous studies provided further evidence of a benefit from the intervention. Bayesian analyses can produce results that are more easily interpretable and relevant to clinicians and policy-makers.
ISRCTN04386758; Post-results.
假设检验的传统方法主导了随机对照试验的设计和分析。本研究旨在展示如何使用简单的贝叶斯分析来分析优化围手术期心血管管理以改善手术结局(OPTIMISE)试验,以获得更具临床可解释性的结果。
设计、地点、参与者和干预措施: OPTIMISE 试验是一项在英国 17 家急性护理医院进行的、具有实用性、多中心、观察者盲法、随机对照试验,共纳入 734 例高危胃肠道手术患者。患者随机分配至心脏输出导向的血流动力学治疗算法,用于手术期间和术后 6 小时内的静脉输液和正性肌力药物治疗(n=368)或标准治疗(n=366)。主要结局是一个由 30 天内预定的中度或重度并发症和死亡率组成的复合结局。
我们使用贝叶斯统计方法重复了 OPTIMISE 试验的主要结局分析,以计算干预措施优越性的概率,以及存在临床相关差异的概率。我们探讨了平坦先验和基于证据的先验对我们分析的影响。
尽管 OPTIMISE 试验的观察到的效应大小(相对风险=0.84,95%CI 0.70 至 1.01;p=0.07)不足以检测治疗组之间的统计学差异,但通过使用贝叶斯分析,我们能够证明干预措施优于对照组的概率为 96.9%(平坦先验)至 99.5%(基于证据的先验)。
使用贝叶斯分析方法提供了对 OPTIMISE 试验结果的不同解释(与原始频率分析相比),并表明干预措施对患者有益。纳入来自先前研究的信息提供了干预措施获益的进一步证据。贝叶斯分析可以产生更易于解释且与临床医生和决策者相关的结果。
ISRCTN04386758;事后分析。