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Targeted full energy and protein delivery in critically ill patients: a study protocol for a pilot randomised control trial (FEED Trial)

机译:危重患者的目标全能量和蛋白质输送:一项随机对照试验试验的研究方案(FEED试验)

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Current guidelines for the provision of protein for critically ill patients are based on incomplete evidence, due to limited data from randomised controlled trials. The present pilot randomised controlled trial is part of a program of work to expand knowledge about the clinical effects of protein delivery to critically ill patients. The primary aim of this pilot study is to determine whether an enteral feeding protocol using a volume target, with additional protein supplementation, delivers a greater amount of protein and energy to mechanically ventilated critically ill patients than a standard nutrition protocol. The secondary aims are to evaluate the potential?effects of this feeding strategy on muscle mass and other patient-centred outcomes.MethodsThis prospective, single-centred, pilot, randomised control trial will include 60 participants who are mechanically ventilated and can be enterally fed. Following informed consent, the participants receiving enteral nutrition in the intensive care unit (ICU) will be allocated using a randomisation algorithm in a 1:1 ratio to the intervention (high-protein daily volume-based feeding protocol, providing 25?kcal/kg and 1.5?g/kg protein) or standard care (hourly rate-based feeding protocol providing 25?kcal/kg and 1?g/kg protein). The co-primary outcomes are the average daily protein and energy delivered to the end of day 15 following randomisation. The secondary outcomes include change in quadriceps muscle layer thickness (QMLT) from baseline (prior to randomisation) to ICU discharge and other nutritional and patient-centred outcomes.DiscussionThis trial aims to examine whether a volume-based feeding protocol with supplemental protein increases protein and energy delivery. The potential effect of such increases on muscle mass loss will be explored. These outcomes will assist in formulating larger randomised control trials to assess mortality and morbidity.Trial registrationAustralian New Zealand Clinical Trials Registry (ANZCTR),?ACTRN: 12615000876594 UTN: U1111-1172-8563.
机译:由于来自随机对照试验的数据有限,目前为重症患者提供蛋白质的指南基于不完整的证据。本试验的随机对照试验是一项工作计划的一部分,旨在扩大有关向危重病人提供蛋白质的临床效果的知识。这项初步研究的主要目的是确定采用容积靶标和附加蛋白质补充剂的肠内喂养方案是否比标准营养方案为机械通气危重患者提供更多量的蛋白质和能量。次要目的是评估这种进食策略对肌肉质量和其他以患者为中心的结局的潜在影响。方法该前瞻性,单中心,先导,随机对照试验将包括60名机械通气且可以肠内喂养的参与者。获得知情同意后,将使用随机算法以1:1的比例将接受重症监护病房(ICU)肠内营养的参与者分配给干预措施(高蛋白日剂量为基础的喂养方案,提供25?kcal / kg和1.5?g / kg蛋白质)或标准护理(基于每小时速率的喂养方案,提供25?kcal / kg和1?g / kg蛋白质)。共同主要结果是随机分组后第15天结束时传递的平均每日蛋白质和能量。次要结果包括股四头肌肌层厚度(QMLT)从基线(随机化之前)到ICU排出的变化以及其他营养和以患者为中心的结果。讨论该试验旨在研究以体积为基础的补充蛋白质喂养方案是否会增加蛋白质和能量输送。将探讨这种增加对肌肉质量损失的潜在影响。这些结果将有助于制定更大的随机对照试验以评估死亡率和发病率。试验注册澳大利亚新西兰临床试验注册中心(ANZCTR),ACTRN:12615000876594 UTN:U1111-1172-8563。

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