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Intensive care unit-acquired neuromyopathy and corticosteroids in survivors of persistent ARDS
Authors:Catherine L. Hough  Kenneth P. Steinberg  B. Taylor Thompson  Gordon D. Rubenfeld  Leonard D. Hudson
Affiliation:(1) Department of Medicine and The NHLBI ARDS Network, University of Washington, 325 Ninth Avenue, Mailstop 359762, Seattle, WA 98104, USA;(2) Department of Medicine and The NHLBI ARDS Network, Massachusetts General Hospital, Boston, MA, USA;(3) Department of Medicine, University of Toronto, Toronto, ON, Canada
Abstract:Objectives  To determine the incidence and outcomes of intensive care unit-acquired neuromyopathy and to investigate the role of methylprednisolone in survivors of persistent acute lung injury. Design  Secondary analysis of completed randomized placebo-controlled trial. Setting  Twenty-five hospitals in the NHLBI ARDS Network. Patients and participants  Patients enrolled in the ARDS Network study of methylprednisolone versus placebo for persistent ARDS who survived 60 days or to hospital discharge. Measurements and results  One hundred and twenty-eight study patients survived 60 days. Forty-three (34%) of these patients had evidence by chart review of ICU-acquired neuromyopathy, which was associated with prolonged mechanical ventilation, return to mechanical ventilation, and delayed return to home after critical illness. Treatment with methylprednisolone was not significantly associated with an increase in risk of neuromyopathy (OR 1.5; 95% CI 0.7–3.2). Conclusions  ICU-acquired-neuromyopathy is common among survivors of persistent ARDS and is associated with poorer clinical outcomes. We did not find a significant association between methylprednisolone treatment and neuromyopathy. Limitations of this study preclude definitive conclusions about the causal relationship between corticosteroids and ICU-acquired neuromuscular dysfunction. This article is discussed in the editorial available at: doi:.
Keywords:Acute lung injury  Acute respiratory distress syndrome  Critical illness  Glucocorticoids/therapeutic use  Paresis  Critical illness polyneuropathy
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