de Perrot Marc, Liu Mingyao, Waddell Thomas K, Keshavjee Shaf
Toronto Lung Transplant Program, Toronto General Hospital, University Health Network, University of Toronto, Toronto, Ontario, Canada.
Am J Respir Crit Care Med. 2003 Feb 15;167(4):490-511. doi: 10.1164/rccm.200207-670SO.
Ischemia-reperfusion-induced lung injury is characterized by nonspecific alveolar damage, lung edema, and hypoxemia occurring within 72 hours after lung transplantation. The most severe form may lead to primary graft failure and remains a significant cause of morbidity and mortality after lung transplantation. Over the past decade, better understanding of the mechanisms of ischemia-reperfusion injury, improvements in the technique of lung preservation, and the development of a new preservation solution specifically for the lung have been associated with a reduction in the incidence of primary graft failure from approximately 30 to 15% or less. Several strategies have also been introduced into clinical practice for the prevention and treatment of ischemia-reperfusion-induced lung injury with various degrees of success. However, only three randomized, double-blinded, placebo-controlled trials on ischemia-reperfusion-induced lung injury have been reported in the literature. In the future, the development of new agents and their application in prospective clinical trials are to be expected to prevent the occurrence of this potentially devastating complication and to further improve the success of lung transplantation.
缺血再灌注诱导的肺损伤的特征是在肺移植后72小时内出现非特异性肺泡损伤、肺水肿和低氧血症。最严重的形式可能导致原发性移植肺功能衰竭,并且仍然是肺移植后发病和死亡的重要原因。在过去十年中,对缺血再灌注损伤机制的更好理解、肺保存技术的改进以及专门针对肺的新型保存液的开发,已使原发性移植肺功能衰竭的发生率从约30%降至15%或更低。还引入了几种策略用于临床实践中预防和治疗缺血再灌注诱导的肺损伤,并取得了不同程度的成功。然而,文献中仅报道了三项关于缺血再灌注诱导的肺损伤的随机、双盲、安慰剂对照试验。未来,有望开发新药物并将其应用于前瞻性临床试验,以预防这种潜在的毁灭性并发症的发生,并进一步提高肺移植的成功率。