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增强型与常规能量给予试验(TARGET)的统计分析计划

Statistical analysis plan for the Augmented versus Routine Approach to Giving Energy Trial (TARGET).

出版信息

Crit Care Resusc. 2018 Mar;20(1):15-21.

PMID:29458317
Abstract

BACKGROUND

The Augmented versus Routine Approach to Giving Energy Trial (TARGET) is a 4000-patient randomised, double-blind controlled trial designed to evaluate whether enteral delivery of recommended energy goals using a 1.5 kcal/mL enteral nutrition formulation improves clinical outcomes, compared with a 1 kcal/mL enteral nutrition formulation delivered at the same goal rate, in critically ill patients receiving invasive mechanical ventilation.

OBJECTIVE

In keeping with best practice, and in accordance with other trials conducted by the investigators, a pre-specified statistical analysis plan has been described and made public before completion of patient recruitment and data collection into the TARGET trial.

METHODS

Our statistical analysis plan was designed by the TARGET chief investigators and statisticians and approved by the TARGET Management Committee. We reviewed the data collected as specified in the trial protocol and collected in the case report form. We present information pertaining to data collection, pre-specified subgroups, processes of care and trial outcomes. Primary and secondary outcomes are defined and methods for assessing functional outcomes (secondary outcomes) are described.

RESULTS

We have developed a statistical analysis plan that includes our methods for presenting the trial profile, baseline characteristics, processes of care, outcomes and adverse events. Seven pre-specified subgroups and our methods for statistical comparisons between groups are described.

CONCLUSION

We have developed a pre-specified statistical analysis plan for TARGET. To minimise analytical bias, this plan has been developed and made available to the public domain before completing recruitment and data collection.

摘要

背景

强化能量供给与常规能量供给对比试验(TARGET)是一项纳入4000例患者的随机双盲对照试验,旨在评估对于接受有创机械通气的重症患者,使用1.5千卡/毫升的肠内营养制剂按照推荐能量目标进行肠内营养供给,与使用1千卡/毫升的肠内营养制剂以相同目标速率供给相比,是否能改善临床结局。

目的

按照最佳实践,并根据研究人员进行的其他试验,在TARGET试验完成患者招募和数据收集之前,已制定并公布了一份预先指定的统计分析计划。

方法

我们的统计分析计划由TARGET首席研究员和统计学家设计,并经TARGET管理委员会批准。我们审查了试验方案中规定并在病例报告表中收集的数据。我们展示了与数据收集、预先指定的亚组、护理过程和试验结局相关的信息。定义了主要和次要结局,并描述了评估功能结局(次要结局)的方法。

结果

我们制定了一项统计分析计划,其中包括我们展示试验概况、基线特征、护理过程、结局和不良事件的方法。描述了七个预先指定的亚组以及我们进行组间统计比较的方法。

结论

我们为TARGET制定了一项预先指定的统计分析计划。为了尽量减少分析偏倚,该计划在完成招募和数据收集之前已制定并向公众公开。

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Crit Care Resusc. 2018 Mar;20(1):15-21.
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