使用谷氨酰胺减少热损伤的随机试验(RE-ENERGIZE 试验):临床试验方案。

Scars, burns & healing Pub Date : 2017-12-12 eCollection Date: 2017-01-01 DOI:10.1177/2059513117745241
Daren K Heyland, Paul Wischmeyer, Marc G Jeschke, Lucy Wibbenmeyer, Alexis F Turgeon, Henry T Stelfox, Andrew G Day, Dominique Garrel
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引用次数: 0

摘要

背景:烧伤是全球范围内的一个重大公共卫生问题。与其他任何损伤相比,与严重烧伤相关的炎症和分解代谢会加剧营养缺乏,导致免疫功能受损,增加感染、器官功能障碍和死亡的风险。因此,在过去的几十年中,许多试验评估了不同营养策略对严重烧伤的影响。谷氨酰胺尤其值得关注,因为它似乎对重症患者的一些关键应激反应途径至关重要。本手稿的目的是提供在 2700 名严重烧伤患者中进行肠内补充谷氨酰胺大型临床试验的理由和方案:我们提出了一项多中心、双盲、务实、随机的临床试验,涉及全球 80 个三级重症监护病房(ICU)烧伤中心。我们的目标是招募有中度或高度死亡风险的深度二度和/或三度烧伤患者。我们将排除筛查前入院时间超过 72 小时的患者以及患有晚期肝病和肾病的患者。研究干预包括肠内谷氨酰胺 0.5 克/千克/天与等热量麦芽糊精对照组的肠内给药。主要结果是六个月的死亡率。主要次要结果包括:6个月后出院存活时间、重症监护室和医院死亡率、住院时间和与健康相关的生活质量:这项研究将是国际上首次对谷氨酰胺在烧伤患者中的作用进行研究的大型多中心试验。无论结果是否定还是肯定,这项试验的结果都将为全球烧伤护理的临床实践提供参考。Clinicaltrials.gov ID #NCT00985205。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A RandomizEd trial of ENtERal Glutamine to minimIZE thermal injury (The RE-ENERGIZE Trial): a clinical trial protocol.

A RandomizEd trial of ENtERal Glutamine to minimIZE thermal injury (The RE-ENERGIZE Trial): a clinical trial protocol.

A RandomizEd trial of ENtERal Glutamine to minimIZE thermal injury (The RE-ENERGIZE Trial): a clinical trial protocol.

A RandomizEd trial of ENtERal Glutamine to minimIZE thermal injury (The RE-ENERGIZE Trial): a clinical trial protocol.

Background: Burn injury represents a significant public health problem worldwide. More than in any other injury, the inflammation and catabolism associated with severe burns can exacerbate nutrient deficiencies resulting in impaired immune function and increased risk of developing infection, organ dysfunction and death. Consequently, over the last few decades numerous trials have evaluated the impact of different nutritional strategies in severe burn injury. Glutamine is of particular interest, as it appears vital for a number of key stress-response pathways in serious illness. The purpose of the current manuscript is to provide the rationale and protocol for a large clinical trial of supplemental enteral glutamine in 2700 severe burn-injured patients.

Methods: We propose a multicentre, double-blind, pragmatic, randomized, clinical trial involving 80 tertiary intensive care unit (ICU) burn centres worldwide. We aim to enrol patients with deep second- and/or third-degree burns at moderate or high risk for death. We will exclude patients admitted > 72 h before screening and patients with advanced liver and kidney disease. The study intervention consists of enteral glutamine 0.5 g/kg/day vs. isocaloric maltodextran control delivered enterally. Primary outcome will be six-month mortality. Key secondary outcomes include time to discharge alive from hospital, ICU and hospital mortality, length of stay and health-related quality of life at six months.

Significance: This study will be the first large international multicentre trial examining the effects of glutamine in burn patients. Negative or positive, the results of this trial will inform the clinical practice of burns care worldwide.Clinicaltrials.gov ID #NCT00985205.

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