利用集成嵌套拉普拉斯近似法设计贝叶斯自适应临床试验,以评估急性呼吸衰竭的新型机械通气策略。

IF 2 3区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Contemporary clinical trials Pub Date : 2024-05-10 DOI:10.1016/j.cct.2024.107560
Reyhaneh Hosseini , Ziming Chen , Ewan Goligher , Eddy Fan , Niall D. Ferguson , Michael O. Harhay , Sarina Sahetya , Martin Urner , Christopher J. Yarnell , Anna Heath
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引用次数: 0

摘要

背景:自适应试验通常需要通过模拟来确定设计参数值、证明误差率并确定样本量。我们设计了一项贝叶斯自适应试验,通过模拟来比较急性低氧血症呼吸衰竭患者的通气策略。分析的复杂性通常需要计算昂贵的马尔可夫链蒙特卡洛方法,但使用集成嵌套拉普拉斯近似(INLA)算法提供快速、近似的贝叶斯推断,克服了模拟的这一障碍:我们模拟了两臂贝叶斯自适应试验,试验采用均等随机化,将参与者分为两种疾病严重程度状态。分析采用比例几率模型,并使用 INLA 进行拟合。根据预先规定的优效或无效的后验概率阈值停止试验,每个状态分别停止试验。我们计算了 64 种方案的 I 型误差和功率,这些方案在开始适应性分析前改变了概率阈值和初始最小样本量。为了确定最佳设计,我们进一步评估了类型I误差低于5%、功率高于80%且平均样本量可行的两种设计:结果:随着初始样本量和无效阈值的增加,功率普遍提高。所选设计的初始招募人数为 500 人,优效阈值为 0.9925,无效阈值为 0.95。该设计保持了较高的功率,并有可能在超过可行样本量之前得出结论:我们设计了一项贝叶斯自适应试验,利用 INLA 算法评估新的通气策略,通过模拟有效地评估了各种设计。
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Designing a Bayesian adaptive clinical trial to evaluate novel mechanical ventilation strategies in acute respiratory failure using integrated nested Laplace approximations

Background

Adaptive trials usually require simulations to determine values for design parameters, demonstrate error rates, and establish the sample size. We designed a Bayesian adaptive trial comparing ventilation strategies for patients with acute hypoxemic respiratory failure using simulations. The complexity of the analysis would usually require computationally expensive Markov Chain Monte Carlo methods but this barrier to simulation was overcome using the Integrated Nested Laplace Approximations (INLA) algorithm to provide fast, approximate Bayesian inference.

Methods

We simulated two-arm Bayesian adaptive trials with equal randomization that stratified participants into two disease severity states. The analysis used a proportional odds model, fit using INLA. Trials were stopped based on pre-specified posterior probability thresholds for superiority or futility, separately for each state. We calculated the type I error and power across 64 scenarios that varied the probability thresholds and the initial minimum sample size before commencing adaptive analyses. Two designs that maintained a type I error below 5%, a power above 80%, and a feasible mean sample size were evaluated further to determine the optimal design.

Results

Power generally increased as the initial sample size and the futility threshold increased. The chosen design had an initial recruitment of 500 and a superiority threshold of 0.9925, and futility threshold of 0.95. It maintained high power and was likely to reach a conclusion before exceeding a feasible sample size.

Conclusions

We designed a Bayesian adaptive trial to evaluate novel strategies for ventilation using the INLA algorithm to efficiently evaluate a wide range of designs through simulation.

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来源期刊
CiteScore
3.70
自引率
4.50%
发文量
281
审稿时长
44 days
期刊介绍: Contemporary Clinical Trials is an international peer reviewed journal that publishes manuscripts pertaining to all aspects of clinical trials, including, but not limited to, design, conduct, analysis, regulation and ethics. Manuscripts submitted should appeal to a readership drawn from disciplines including medicine, biostatistics, epidemiology, computer science, management science, behavioural science, pharmaceutical science, and bioethics. Full-length papers and short communications not exceeding 1,500 words, as well as systemic reviews of clinical trials and methodologies will be published. Perspectives/commentaries on current issues and the impact of clinical trials on the practice of medicine and health policy are also welcome.
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