Salameh Aida, Dhein Stefan
Clinic for Pediatric Cardiology, Heart Centre University of Leipzig Leipzig, Germany.
Rudolf-Boehm-Institute for Pharmacology and Toxicology, University of Leipzig Leipzig, Germany.
Front Pharmacol. 2015 Dec 22;6:296. doi: 10.3389/fphar.2015.00296. eCollection 2015.
Surgical correction of congenital cardiac malformations or aortocoronary bypass surgery in many cases implies the use of cardiopulmonary-bypass (CPB). However, a possible negative impact of CPB on internal organs such as brain, kidney, lung and liver cannot be neglected. In general, CPB initiates a systemic inflammatory response (SIRS) which is presumably caused by contact of blood components with the surface of CPB tubing. Moreover, during CPB the heart typically undergoes a period of cold ischemia, and the other peripheral organs a global low flow hypoperfusion. As a result, a plethora of pro-inflammatory mediators and cytokines is released activating different biochemical pathways, which finally may result in the occurrence of microthrombosis, microemboli, in depletion of coagulation factors and haemorrhagic diathesis besides typical ischemia-reperfusion injuries. In our review we will focus on possible pharmacological interventions in patients to decrease negative effects of CPB and to improve post-operative outcome with regard to heart and other organs like brain, kidney, or lung.
在许多情况下,先天性心脏畸形的外科矫正或主动脉冠状动脉搭桥手术都需要使用体外循环(CPB)。然而,CPB对诸如脑、肾、肺和肝脏等内部器官可能产生的负面影响不容忽视。一般来说,CPB会引发全身炎症反应(SIRS),这可能是由血液成分与CPB管道表面接触引起的。此外,在CPB期间,心脏通常会经历一段冷缺血期,而其他外周器官则会出现全身性低流量灌注不足。结果,大量促炎介质和细胞因子被释放,激活不同的生化途径,最终除了典型的缺血再灌注损伤外,还可能导致微血栓形成、微栓塞、凝血因子耗竭和出血素质的发生。在我们的综述中,我们将重点关注针对患者的可能的药物干预措施,以减少CPB的负面影响,并改善心脏以及脑、肾或肺等其他器官的术后结果。