Jakob Stephan M
Department of Intensive Care Medicine, University Hospital, Bern, Switzerland.
Crit Care. 2002 Aug;6(4):306-12. doi: 10.1186/cc1515. Epub 2002 Apr 8.
Inadequate splanchnic perfusion is associated with increased morbidity and mortality, particularly if liver dysfunction coexists. Heart failure, increased intra-abdominal pressure, haemodialysis and the presence of obstructive sleep apnoea are among the multiple clinical conditions that are associated with impaired splanchnic perfusion in critically ill patients. Total liver blood flow is believed to be relatively protected when gut blood flow decreases, because hepatic arterial flow increases when portal venous flow decreases (the hepatic arterial buffer response [HABR]). However, there is evidence that the HABR is diminished or even abolished during endotoxaemia and when gut blood flow becomes very low. Unfortunately, no drugs are yet available that increase total hepato-splanchnic blood flow selectively and to a clinically relevant extent. The present review discusses old and new concepts of splanchnic vasoregulation from both experimental and clinical viewpoints. Recently published trials in this field are discussed.
内脏灌注不足与发病率和死亡率增加相关,尤其是在并存肝功能不全的情况下。心力衰竭、腹腔内压力升高、血液透析以及阻塞性睡眠呼吸暂停的存在是与危重症患者内脏灌注受损相关的多种临床情况。当肠道血流量减少时,总肝血流量被认为受到相对保护,因为门静脉血流量减少时肝动脉血流量增加(肝动脉缓冲反应 [HABR])。然而,有证据表明,在内毒素血症期间以及肠道血流量变得非常低时,HABR会减弱甚至消失。不幸的是,目前尚无药物能够选择性地增加总肝内脏血流量并达到临床相关程度。本综述从实验和临床角度讨论了内脏血管调节的新旧概念。还讨论了该领域最近发表的试验。