Protocol and Statistical Analysis Plan for the Mode of Ventilation During Critical Illness (MODE) Trial

Kevin P. Seitz MD , Bradley D. Lloyd RRT-ACCS , Li Wang MS , Matthew S. Shotwell PhD , Edward T. Qian MD , Roger K. Richardson RRT-ACCS, JM , Jeffery C. Rooks RRT, MMHC , Vanessa Hennings-Williams RRT-ACCS, MBA , Claire E. Sandoval RRT-ACCS , Whitney D. Richardson RRT , Tracy Morgan RRT , Amber N. Thompson RRT-ACCS , Pamela G. Hastings RRT-ACCS , Terry P. Ring RRT-ACCS, MBA , Joanna L. Stollings PharmD , Erica M. Talbot MD , David J. Krasinski MD , Bailey Decoursey MD , Kevin W. Gibbs MD , Wesley H. Self MD, MPH , Jonathan D. Casey MD
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Abstract

Background

For every critically ill adult receiving invasive mechanical ventilation, clinicians must select a mode of ventilation. The mode of ventilation determines whether the ventilator directly controls the tidal volume or the inspiratory pressure. Newer hybrid modes allow clinicians to set a target tidal volume; the ventilator controls and adjusts the inspiratory pressure. A strategy of low tidal volumes and low plateau pressure improves outcomes, but the optimal mode to achieve these targets is not known.

Research Question

Can a cluster-randomized trial design be used to assess whether the mode of mandatory ventilation affects the number of days alive and free of invasive mechanical ventilation among critically ill adults?

Study Design and Methods

The Mode of Ventilation During Critical Illness (MODE) trial is a cluster-randomized, multiple-crossover pilot trial being conducted in the medical ICU at an academic center. The MODE trial compares the use of volume control, pressure control, and adaptive pressure control. The study ICU is assigned to a single-ventilator mode (volume control vs pressure control vs adaptive pressure control) for continuous mandatory ventilation during each 1-month study block. The assigned mode switches every month in a randomly generated sequence. The primary outcome is ventilator-free days to study day 28, defined as the number of days alive and free of invasive mechanical ventilation from the final receipt of mechanical ventilation to 28 days after enrollment. Enrollment began November 1, 2022, and will end on July 31, 2023.

Results

This manuscript describes the protocol and statistical analysis plan for the MODE trial of ventilator modes comparing volume control, pressure control, and adaptive pressure control.

Interpretation

Prespecifying the full statistical analysis plan prior to completion of enrollment increases rigor, reproducibility, and transparency of the trial results.

Clinical Trial Registration

The trial was registered with clinicaltrials.gov on October 3, 2022, before initiation of patient enrollment on November 1, 2022 (ClinicalTrials.gov identifier: NCT05563779).

危重病人通气模式(MODE)试验方案和统计分析计划
背景对于每一位接受有创机械通气的重症成人,临床医生都必须选择一种通气模式。通气模式决定了呼吸机是直接控制潮气量还是吸气压力。较新的混合模式允许临床医生设定目标潮气量;呼吸机控制并调节吸气压力。研究问题能否采用分组随机试验设计来评估强制通气模式是否会影响成人重症患者的存活天数和无创机械通气天数? 研究设计和方法重症期间通气模式(MODE)试验是一项分组随机、多重交叉试验,目前正在一家学术中心的内科 ICU 进行。MODE 试验比较了容量控制、压力控制和自适应压力控制的使用。在每个为期 1 个月的研究区块中,研究重症监护室会被分配到一种单一通气模式(容量控制 vs 压力控制 vs 自适应压力控制)进行持续强制通气。所分配的模式每月随机切换一次。主要结果是到研究第 28 天时无呼吸机天数,即从最后接受机械通气到入组 28 天时无侵入性机械通气的存活天数。入组时间从 2022 年 11 月 1 日开始,将于 2023 年 7 月 31 日结束。结果本手稿介绍了比较容量控制、压力控制和自适应压力控制的 MODE 呼吸机模式试验的方案和统计分析计划。临床试验注册该试验于2022年10月3日在clinicaltrials.gov注册,之后于2022年11月1日开始招募患者(ClinicalTrials.gov标识符:NCT05563779)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CHEST critical care
CHEST critical care Critical Care and Intensive Care Medicine, Pulmonary and Respiratory Medicine
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