Rose E A, Gelijns A C, Moskowitz A J, Heitjan D F, Stevenson L W, Dembitsky W, Long J W, Ascheim D D, Tierney A R, Levitan R G, Watson J T, Meier P, Ronan N S, Shapiro P A, Lazar R M, Miller L W, Gupta L, Frazier O H, Desvigne-Nickens P, Oz M C, Poirier V L
College of Physicians and Surgeons, Columbia University, New York, NY, USA.
N Engl J Med. 2001 Nov 15;345(20):1435-43. doi: 10.1056/NEJMoa012175.
Implantable left ventricular assist devices have benefited patients with end-stage heart failure as a bridge to cardiac transplantation, but their long-term use for the purpose of enhancing survival and the quality of life has not been evaluated.
We randomly assigned 129 patients with end-stage heart failure who were ineligible for cardiac transplantation to receive a left ventricular assist device (68 patients) or optimal medical management (61). All patients had symptoms of New York Heart Association class IV heart failure.
Kaplan-Meier survival analysis showed a reduction of 48 percent in the risk of death from any cause in the group that received left ventricular assist devices as compared with the medical-therapy group (relative risk, 0.52; 95 percent confidence interval, 0.34 to 0.78; P=0.001). The rates of survival at one year were 52 percent in the device group and 25 percent in the medical-therapy group (P=0.002), and the rates at two years were 23 percent and 8 percent (P=0.09), respectively. The frequency of serious adverse events in the device group was 2.35 (95 percent confidence interval, 1.86 to 2.95) times that in the medical-therapy group, with a predominance of infection, bleeding, and malfunction of the device. The quality of life was significantly improved at one year in the device group.
The use of a left ventricular assist device in patients with advanced heart failure resulted in a clinically meaningful survival benefit and an improved quality of life. A left ventricular assist device is an acceptable alternative therapy in selected patients who are not candidates for cardiac transplantation.
植入式左心室辅助装置已使终末期心力衰竭患者受益,作为心脏移植的桥梁,但尚未评估其用于提高生存率和生活质量的长期效果。
我们将129例不符合心脏移植条件的终末期心力衰竭患者随机分为两组,一组接受左心室辅助装置治疗(68例),另一组接受最佳药物治疗(61例)。所有患者均有纽约心脏协会IV级心力衰竭症状。
Kaplan-Meier生存分析显示,与药物治疗组相比,接受左心室辅助装置治疗的组任何原因导致的死亡风险降低了48%(相对风险为0.52;95%置信区间为0.34至0.78;P=0.001)。装置组一年生存率为52%,药物治疗组为25%(P=0.002),两年生存率分别为23%和8%(P=0.09)。装置组严重不良事件的发生频率是药物治疗组的2.35倍(95%置信区间为1.86至2.95),主要为感染、出血和装置故障。装置组患者一年时生活质量显著改善。
在晚期心力衰竭患者中使用左心室辅助装置可带来具有临床意义的生存获益和生活质量改善。左心室辅助装置是不适于心脏移植的特定患者可接受的替代治疗方法。