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Evolution of treatments for patients with acute lung injury

机译:急性肺损伤患者治疗方法的演变

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Acute lung injury(ALI)and acute respiratory distress syndrome(ARDS)are acute life-threatening forms of hypoxemic respiratory failure.ALI/ARDS patients require intensive care with prolonged mechanical ventilation.Despite advances in our understanding of the pathophysiology of ALI/ARDS,mortality rates remain > 30% and survivors suffer significant decrements in their quality of life.The evolving understanding of ALI/ARDS and the complex interactions involved in ALI/ARDS open the door for many potential targets for treatment.The condition is characterised by an acute inflammatory state that leads to increased capillary permeability and accumulation of proteina-ceous pulmonary oedema.The changes that occur as a result of this inflammation clinically manifest themselves as hypoxemia,infiltrates on chest radiograph and reduced lung compliance.Many years have been dedicated to analysing the complexities involved in ALI/ARDS in order to improve current and future possibilities for treatment,with the aim of improving patient outcomes.Although some therapies have demonstrated benefits of improved oxygenation,such as surfactant and nitric oxide,these benefits have not translated into reductions in the duration of mechanical ventilation or mortality.Inflammatory mediator-targeted therapies were promising early on;however,larger trials have found therapies such as cytokine modulation,platelet-activating factor inhibition and neutrophil elastase inhibitors to be ineffective in the treatment of ALI/ARDS.Preclinical studies with beta_2-agonists and granulo-cyte macrophage colony-stimulating factor have shown promise for restoring alveolar capillary barrier integrity or reducing pulmonary oedema,and further studies are being conducted to test for true clinical benefit.Despite previous therapeutic failures,newer surfactant formulations have shown promise,particularly in patients with direct forms of lung injury,and are currently in Phase III trials.Anticoagulant therapy with activated protein C has been shown to improve survival in sepsis,the most common risk factor for the development of ALI/ARDS,and is now being studied in ALI/ARDS.Until new data emerge,the focus must remain on supportive care,including optimised mechanical ventilation,nutritional support,manipulation of fluid balance and prevention of intervening medical complications.
机译:急性肺损伤(ALI)和急性呼吸窘迫综合征(ARDS)是危及生命的低氧血症性呼吸衰竭形式。ALI/ ARDS患者需要长期机械通气的重症监护。尽管我们对ALI / ARDS的病理生理学有了进一步的了解,死亡率仍然保持在30%以上,幸存者的生活质量明显下降。对ALI / ARDS的不断发展的理解以及ALI / ARDS涉及的复杂相互作用为许多潜在的治疗目标打开了大门。炎症状态导致毛细血管通透性增加和蛋白性肺水肿积聚。这种炎症引起的变化在临床上表现为低氧血症,在胸部X线片上浸润并降低了肺顺应性。多年以来一直致力于分析ALI / ARDS涉及的复杂性,以改善当前和未来的治疗可能性为了改善患者的预后,尽管一些疗法已证明改善氧合的益处,例如表面活性剂和一氧化氮,但这些益处并没有转化为减少机械通气时间或死亡率的降低。针对炎症介质的疗法有望在早期得到应用。 ;但是,更大的试验发现细胞因子调节,血小板活化因子抑制和中性粒细胞弹性蛋白酶抑制剂等疗法对ALI / ARDS无效。β_2激动剂和粒细胞巨噬细胞集落刺激因子的临床前研究表明有望恢复肺泡毛细血管屏障的完整性或减少肺水肿,并且正在进行进一步的研究以测试其真正的临床益处。尽管以前的治疗失败,但更新的表面活性剂制剂已显示出希望,特别是在直接形式的肺损伤患者中,目前在III期临床试验中蛋白C已被证明可以改善败血症的生存,败血症是ALI / ARDS发生的最常见风险因素,目前正在ALI / ARDS中进行研究。在出现新数据之前,重点必须放在支持治疗上,包括优化机械通风,营养支持,控制体液平衡和预防医疗并发症。

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