Perkins Gavin D, McAuley Daniel F, Richter Alex, Thickett David R, Gao Fang
Consultant, Intensive Care Unit, Birmingham Heartlands Hospital, Birmingham, UK.
Crit Care. 2004 Feb;8(1):25-32. doi: 10.1186/cc2417. Epub 2003 Dec 23.
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 beta2-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 beta2-agonists as a specific pharmacological intervention in patients with ARDS.
急性呼吸窘迫综合征(ARDS)是一组严重的临床、放射学和病理学体征,其特征为气体交换功能衰竭和难治性低氧血症。尽管经过了近30年的研究,但尚未证实有任何特异性药物疗法能有效调控导致该病的病理生理过程。多项体外及体内动物或人体研究提示β2受体激动剂在ARDS治疗中可能发挥作用。这些药物已显示可减少肺内中性粒细胞的扣押和活化、加速肺泡液体清除、增强表面活性物质分泌,并调节炎症和凝血级联反应。它们在临床实践中也被广泛应用,且危重症患者对其耐受性良好。本综述探讨了支持β2受体激动剂作为ARDS患者特异性药物干预措施的证据。