Keenan Research Center for Biomedical Science, St Michael's Hospital, Toronto, Ontario, Canada
Interdepartmental Division of Critical Care Medicine and Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
Thorax. 2019 Nov;74(11):1091-1098. doi: 10.1136/thoraxjnl-2016-208312. Epub 2019 Aug 20.
Intensive care unit acquired weakness (ICUAW) is now a well-known entity complicating critical illness. It increases mortality and in the critical illness survivor it is associated with physical disability, substantially increased health resource utilisation and healthcare costs. Skeletal muscle wasting is a key driver of ICUAW and physical functional outcomes in both the short and long term. To date, there is no intervention that can universally and consistently prevent muscle loss during critical illness, or enhance its recovery following intensive care unit discharge, to improve physical function. Clinical trials of early mobilisation or exercise training, or enhanced nutritional support have generated inconsistent results and we have no effective pharmacological interventions. This review will delineate our current understanding of the mechanisms underpinning the development and persistence of skeletal muscle loss and dysfunction in the critically ill individual, highlighting recent discoveries and clinical observations, and utilisation of this knowledge in the development of novel therapeutics.
重症加强治疗病房获得性衰弱(ICUAW)是目前一种众所周知的危重病并发症。它增加了死亡率,在危重病幸存者中,它与身体残疾、健康资源利用和医疗保健成本显著增加有关。骨骼肌减少是 ICUAW 和短期及长期身体功能结果的关键驱动因素。迄今为止,尚无一种干预措施能够在危重病期间普遍而一致地预防肌肉损失,或在重症监护病房出院后促进其恢复,以改善身体功能。早期活动或运动训练或强化营养支持的临床试验结果不一致,我们也没有有效的药物干预措施。本综述将阐述我们目前对导致危重病个体骨骼肌丢失和功能障碍发展和持续的机制的理解,重点介绍最近的发现和临床观察,并将这些知识应用于新型治疗药物的开发。