Pharmacological Therapy for the Prevention and Treatment of Weakness After Critical Illness: A Systematic Review*

医学 梅德林 奇纳 重症监护医学 数据提取 随机对照试验 心理干预 弱点 肌肉无力 物理疗法 内科学 外科 精神科 政治学 法学
作者
Stephen J. Shepherd,Richard Newman,Stephen J. Brett,David Griffith
出处
期刊:Critical Care Medicine [Lippincott Williams & Wilkins]
卷期号:44 (6): 1198-1205 被引量:45
标识
DOI:10.1097/ccm.0000000000001652
摘要

Objectives: ICU-acquired weakness is a common complication of critical illness and can have significant effects upon functional status and quality of life. As part of preliminary work to inform the design of a randomized trial of a complex intervention to improve recovery from critical illness, we sought to identify pharmacological interventions that may play a role in this area. Data Sources: We systematically reviewed the published literature relating to pharmacological intervention for the treatment and prevention of ICU-acquired weakness. Study Selection: We searched MEDLINE, EMBASE, CINAHL+, Web of Science, and both U.S. and European trial registries up to July 2014 alongside reviews and reference lists from populations with no age or language restrictions. We included studies that reported a measure of muscle structure or physical function as an outcome measure. Data Extraction: We estimated pooled odds ratios and 95% CI using data extracted from published articles or where available, original data provided by the authors. Assessment of bias was performed using the Cochrane Collaboration’s risk of bias tool. Data Synthesis: Ten studies met the inclusion criteria. The current body of evidence does not support the use of any pharmacological agent in this setting, although maintaining euglycemia may reduce the prevalence of critical illness polyneuropathy. Conclusions: At present, no pharmacological intervention can be recommended to prevent or treat ICU-acquired weakness. Further research is required into this field to include more novel agents such as myostatin inhibitors. Challenges in the conduct of research in this area are highlighted.
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