McCarthy P M, Portner P M, Tobler H G, Starnes V A, Ramasamy N, Oyer P E
Department of Cardiovascular Surgery, Stanford University, Calif.
J Thorac Cardiovasc Surg. 1991 Oct;102(4):578-86; discussion 586-7.
At Stanford University, a Novacor left ventricular assist system (Baxter Healthcare Corporation, Novacor Division, Oakland, Calif.) was placed as a bridge to heart transplantation in 13 patients. During the hospitalization preceding device implantation, all patients were receiving inotropic support for biventricular failure, 11 had pulmonary edema, 6 had life-threatening ventricular arrhythmias, 5 had liver dysfunction with coagulopathy, and 2 had renal failure necessitating artificial support. The mean cardiac index before implantation of the Novacor system was 1.5. All survivors with the Novacor device had a dramatic increase in cardiac output (mean cardiac index = 3.1). One patient with cardiac allograft rejection died during implantation of the left ventricular assist system. Two patients died of pulmonary sepsis and multiorgan failure after the device was implanted. All patients who had the Novacor device implanted for more than 7 days were able to walk and ride stationary bicycles while awaiting transplantation. Ten patients (77%) underwent successful heart transplantation after a mean of 18 days' support with the Novacor device. One patient died of presumed sepsis 2 days after transplantation. Nine patients (90%) are alive 4 months to 6 years after transplantation. In the overall United States experience, 68 patients (as of May 1990) have had a Novacor left ventricular assist device implanted. Five were still being supported, 39 had received a transplant (62%), and 35 patients (90%) survived the transplant hospitalization (1 died later). No instances of device failure have occurred. Overall, the Novacor assist system provided effective bridging to transplantation, with posttransplant survival similar to results after routine transplantation. Modifications and improvements based on this clinical experience have been made in the areas of patient selection, techniques of operative placement, postoperative management, and design of the assist system. Isolated left heart support with a fully implantable left ventricular assist system will be offered as an alternative to heart transplantation for selected patients by 1992.
在斯坦福大学,13例患者植入了诺瓦科尔左心室辅助系统(百特医疗保健公司,诺瓦科尔分部,加利福尼亚州奥克兰)作为心脏移植的过渡手段。在装置植入前的住院期间,所有患者均因双心室衰竭接受了正性肌力支持,11例有肺水肿,6例有危及生命的室性心律失常,5例有肝功能障碍合并凝血病,2例有肾衰竭需要人工支持。诺瓦科尔系统植入前的平均心脏指数为1.5。所有植入诺瓦科尔装置的幸存者心输出量均显著增加(平均心脏指数 = 3.1)。1例心脏移植排斥患者在左心室辅助系统植入期间死亡。2例患者在装置植入后死于肺部感染和多器官衰竭。所有植入诺瓦科尔装置超过7天的患者在等待移植期间都能够行走和骑健身自行车。10例患者(77%)在接受诺瓦科尔装置平均18天的支持后成功进行了心脏移植。1例患者在移植后2天死于疑似感染。9例患者(90%)在移植后4个月至6年存活。在美国的总体经验中,截至1990年5月,有68例患者植入了诺瓦科尔左心室辅助装置。5例仍在接受支持,39例接受了移植(62%),35例患者(90%)在移植住院期间存活(1例后来死亡)。未发生装置故障。总体而言,诺瓦科尔辅助系统为移植提供了有效的过渡手段,移植后的生存率与常规移植结果相似。基于这一临床经验,在患者选择、手术植入技术、术后管理和辅助系统设计等方面进行了改进。到1992年,将为选定的患者提供完全可植入的左心室辅助系统进行孤立性左心支持,作为心脏移植的替代方案。