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Bench-to-bedside review:: β2-agonists and the acute respiratory distress syndrome

Journal

CRITICAL CARE
Volume 8, Issue 1, Pages 25-32

Publisher

BMC
DOI: 10.1186/cc2417

Keywords

acute lung injury; acute respiratory distress syndrome; alveolar epithelium; beta(2)-agonists; pharmacotherapy

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The acute respiratory distress syndrome (ARDS) is a devastating constellation of clinical, radiological and pathological signs characterized by failure of gas exchange and refractory hypoxia. Despite nearly 30 years of research, no specific pharmacological therapy has yet proven to be efficacious in manipulating the pathophysiological processes that underlie this condition. Several in vitro and in vivo animal or human studies suggest a potential role for beta(2)-agonists in the treatment of ARDS. These agents have been shown to reduce pulmonary neutrophil sequestration and activation, accelerate alveolar fluid clearance, enhance surfactant secretion, and modulate the inflammatory and coagulation cascades. They are also used widely in clinical practice and are well tolerated in critically ill patients. The present review examines the evidence supporting a role for beta(2)-agonists as a specific pharmacological intervention in patients with ARDS.

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