From skeletal muscle weakness to functional outcomes following critical illness: a translational biology perspective

被引:67
作者
Batt, Jane [1 ,2 ,3 ]
Herridge, Margaret S. [2 ,3 ,4 ]
dos Santos, Claudia C. [1 ,2 ,3 ]
机构
[1] St Michaels Hosp, Keenan Res Ctr Biomed Sci, Toronto, ON M5B 1W8, Canada
[2] Univ Toronto, Interdept Div Crit Care Med, Toronto, ON, Canada
[3] Univ Toronto, Dept Med, Toronto, ON, Canada
[4] Univ Hlth Network, Toronto Gen Res Inst, Toronto, ON, Canada
关键词
critical care; UNIT-ACQUIRED WEAKNESS; MITOCHONDRIAL DYSFUNCTION; ILL PATIENTS; PROTEASOME INHIBITOR; GENE-EXPRESSION; RAT MODEL; AUTOPHAGY; PROTEIN; METABOLISM; DIAPHRAGM;
D O I
10.1136/thoraxjnl-2016-208312
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
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.
引用
收藏
页码:1091 / 1098
页数:8
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