Intensive-care-unit-acquired muscle weakness

被引:0
作者
Deem, Steven
机构
[1] Univ Washington, Harborview Med Ctr, Dept Anesthesiol, Seattle, WA 98104 USA
[2] Univ Washington, Harborview Med Ctr, Dept Med, Seattle, WA 98104 USA
关键词
neuromuscular; weakness; polyneuropathy; myopathy; polyneuromyopathy; intensive care; inflammation; mechanical ventilation; insulin; critical illness;
D O I
暂无
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Neuromuscular abnormalities culminating in skeletal-muscle weakness occur very commonly in critically ill patients. Intensive-care-unit (ICU) acquired neuromuscular abnormalities are typically divided into 2 discrete classes: polyneuropathy and myopathy. However, it is likely that these 2 entities commonly coexist, with myopathy being the most common cause of weakness. Major risk factors for ICU-acquired neuromuscular abnormalities include sepsis, corticosteroid administration, and hyperglycemia, with other associated factors including neuromuscular blockade and increasing severity of illness. The pathogenesis of these disorders is not well defined, but probably involves inflammatory injury of nerve and/or muscle that is potentiated by functional denervation and corticosteroids. ICU-acquired neuromuscular abnormalities are associated with multiple adverse outcomes, including higher mortality, prolonged duration of mechanical ventilation, and increased length of stay. The only intervention proven to reduce the incidence of ICU-acquired neuromuscular abnormalities is intensive insulin therapy. Additional research is necessary to better delineate the causes and pathogenesis of these disorders and to identify potential preventive and therapeutic strategies. In addition, consensus guidelines for its classification and diagnosis are needed.
引用
收藏
页码:1042 / 1052
页数:11
相关论文
共 115 条
[81]   Loss of electrical excitability in an animal model of acute quadriplegic myopathy [J].
Rich, MM ;
Pinter, MJ ;
Kraner, SD ;
Barchi, RL .
ANNALS OF NEUROLOGY, 1998, 43 (02) :171-179
[82]   Muscle is electrically inexcitable in acute quadriplegic myopathy [J].
Rich, MM ;
Teener, JW ;
Raps, EC ;
Schotland, DL ;
Bird, SJ .
NEUROLOGY, 1996, 46 (03) :731-736
[83]   ATRACURIUM AND PROLONGED MUSCLE WEAKNESS [J].
ROSENBERG, SG .
ANESTHESIA AND ANALGESIA, 1994, 79 (06) :1211-1211
[84]   Economic impact of prolonged motor weakness complicating neuromuscular blockade in the intensive care unit [J].
Rudis, MI ;
Guslits, BJ ;
Peterson, EL ;
Hathaway, SJ ;
Angus, E ;
Beis, S ;
Zarowitz, BJ .
CRITICAL CARE MEDICINE, 1996, 24 (10) :1749-1756
[85]   Quadriplegic areflexic ICU illness: Selective thick filament loss and normal nerve histology [J].
Sander, HW ;
Golden, M ;
Danon, MJ .
MUSCLE & NERVE, 2002, 26 (04) :499-505
[86]   PERSISTENT PARALYSIS IN CRITICALLY ILL PATIENTS AFTER LONG-TERM ADMINISTRATION OF VECURONIUM [J].
SEGREDO, V ;
CALDWELL, JE ;
MATTHAY, MA ;
SHARMA, ML ;
GRUENKE, LD ;
MILLER, RD .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 327 (08) :524-528
[87]   RISK-FACTORS FOR HYDROCORTISONE MYOPATHY IN ACUTE SEVERE ASTHMA [J].
SHEE, CD .
RESPIRATORY MEDICINE, 1990, 84 (03) :229-233
[88]   ACUTE MYOPATHY WITH SELECTIVE LYSIS OF MYOSIN-FILAMENTS [J].
SHER, JH ;
SHAFIQ, SA ;
SCHUTTA, HS .
NEUROLOGY, 1979, 29 (01) :100-106
[89]   NEUROMUSCULAR CAUSES OF PROLONGED VENTILATOR DEPENDENCY [J].
SPITZER, AR ;
GIANCARLO, T ;
MAHER, L ;
AWERBUCH, G ;
BOWLES, A .
MUSCLE & NERVE, 1992, 15 (06) :682-686
[90]   Effect of insulin on human skeletal muscle mitochondrial ATP production, protein synthesis, and mRNA transcripts [J].
Stump, CS ;
Short, KR ;
Bigelow, ML ;
Schimke, JM ;
Nair, KS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (13) :7996-8001