학술논문

Acute respiratory distress syndrome.
Document Type
article
Source
Nature reviews. Disease primers. 5(1)
Subject
Humans
Respiratory Distress Syndrome
Adult
Carbon Dioxide
Angiopoietin-2
von Willebrand Factor
Cadherins
Interleukin-8
Vasodilator Agents
Antigens
CD
Glucocorticoids
Radiography
Respiration
Artificial
High-Frequency Ventilation
Positive-Pressure Respiration
Quality of Life
Ventilator-Induced Lung Injury
Biomarkers
Antigens
CD
Respiration
Artificial
Respiratory Distress Syndrome
Adult
Clinical Sciences
Language
Abstract
The acute respiratory distress syndrome (ARDS) is a common cause of respiratory failure in critically ill patients and is defined by the acute onset of noncardiogenic pulmonary oedema, hypoxaemia and the need for mechanical ventilation. ARDS occurs most often in the setting of pneumonia, sepsis, aspiration of gastric contents or severe trauma and is present in ~10% of all patients in intensive care units worldwide. Despite some improvements, mortality remains high at 30-40% in most studies. Pathological specimens from patients with ARDS frequently reveal diffuse alveolar damage, and laboratory studies have demonstrated both alveolar epithelial and lung endothelial injury, resulting in accumulation of protein-rich inflammatory oedematous fluid in the alveolar space. Diagnosis is based on consensus syndromic criteria, with modifications for under-resourced settings and in paediatric patients. Treatment focuses on lung-protective ventilation; no specific pharmacotherapies have been identified. Long-term outcomes of patients with ARDS are increasingly recognized as important research targets, as many patients survive ARDS only to have ongoing functional and/or psychological sequelae. Future directions include efforts to facilitate earlier recognition of ARDS, identifying responsive subsets of patients and ongoing efforts to understand fundamental mechanisms of lung injury to design specific treatments.