Klotz Stefan, Stypmann Joerg, Welp Henryk, Schmid Christof, Drees Gabriele, Rukosujew Andreas, Scheld Hans H
Department of Thoracic and Cardiovascular Surgery, University Hospital Muenster, Muenster, Germany.
Ann Thorac Surg. 2006 Nov;82(5):1774-8. doi: 10.1016/j.athoracsur.2006.05.079.
Left ventricular assist devices (LVADs) with continuous flow properties are increasingly used to bridge heart failure patients to cardiac transplantation. Advantages in comparison with the pulsatile LVADs are smaller size, better endurance, and lower thromboembolic events. However, whether these new pumps have similar pre- and posttransplant outcomes is not clear.
Fifty patients with a continuous flow device (Micromed DeBakey, Houston, TX or InCor BerlinHeart, Berlin, Germany) were compared with an age-, disease-, and LVAD duration-matched control group (n = 80) supported with a pulsatile device (Novacor, WorldHeart, Oakland, CA or HeartMate, Thoratec Corp, Pleasanton, CA).
Age (44.3 +/- 13.4 vs 46.1 +/- 11.1 years), disease (idiopathic dilated cardiomyopathy, 58% vs 65%), and LVAD duration (138 +/- 131 vs 128 +/- 106 days) were comparable in both groups. Successful bridging to transplantation was similar with continuous flow in comparison with pulsatile device support (52% vs 56%, p = not significant [NS]). Thirty-day mortality after cardiac transplantation in patients with continuous flow LVAD support was 21.7% vs 22.2% with pulsatile LVADs (p = NS). Reasons for death were similar among the different LVAD groups. Long-term survival was similar in both LVAD groups compared with patients without previous LVAD support. Interestingly, severe rejections were significantly more frequent in patients with a continuous flow LVAD (p < 0.001).
The new generation of cardiac assist devices with continuous flow pattern has a similar rate of pre- and posttransplant mortality in comparison with pulsatile LVADs. However, the rate and severity of posttransplant rejection was significantly higher in the group with continuous flow devices. Further studies are warranted to explain the higher rate of severe rejections.
具有连续血流特性的左心室辅助装置(LVAD)越来越多地用于将心力衰竭患者过渡到心脏移植。与搏动性LVAD相比,其优点是尺寸更小、耐久性更好且血栓栓塞事件更少。然而,这些新型泵在移植前后的结果是否相似尚不清楚。
将50例使用连续血流装置(Micromed DeBakey,得克萨斯州休斯顿或InCor BerlinHeart,德国柏林)的患者与年龄、疾病和LVAD使用时长相匹配的对照组(n = 80)进行比较,对照组使用搏动性装置(Novacor,WorldHeart,加利福尼亚州奥克兰或HeartMate,Thoratec公司,加利福尼亚州普莱森顿)。
两组患者的年龄(44.3±13.4岁对46.1±11.1岁)、疾病(特发性扩张型心肌病,58%对65%)和LVAD使用时长(138±131天对128±106天)相当。与搏动性装置支持相比,连续血流装置成功过渡到移植的比例相似(52%对56%,p =无显著差异[NS])。接受连续血流LVAD支持的患者心脏移植后30天死亡率为21.7%,搏动性LVAD患者为22.2%(p = NS)。不同LVAD组的死亡原因相似。与未使用过LVAD支持的患者相比,两组LVAD患者的长期生存率相似。有趣的是,连续血流LVAD患者发生严重排斥反应的频率明显更高(p < 0.001)。
与搏动性LVAD相比,新一代具有连续血流模式的心脏辅助装置在移植前后的死亡率相似。然而,连续血流装置组移植后排斥反应的发生率和严重程度明显更高。有必要进行进一步研究以解释严重排斥反应发生率较高的原因。