Li H H, Jeffrey R R, Davidson K G, Seifert D, Körfer R, Grunkemeier G L
Providence Health System, Portland, Oregon, USA.
J Heart Valve Dis. 1998 Nov;7(6):647-54.
The Ultracor heart valve is a recent entry in the evolution of the tilting disc valve. This report summarizes the experience with the Ultracor valve from three European centers.
Between 1990 and 1996, 446 patients received 499 Ultracor heart valve prostheses in 450 procedures, including 225 (50.0%) aortic, 172 (38.2%) mitral and 49 (10.9%) double valve replacements. An additional four (1.0%) patients had mitral valve replacement (MVR) added to a previous aortic valve replacement (AVR) and were considered double valve replacement (DVR) patients. The total follow up was 751 patient-years (pt-yr) for AVR (mean 3.4), 440 pt-yr for MVR (mean 2.6) and 125 pt-yr for DVR (mean 2.4). Nine patients (one AVR, eight MVR) were lost to follow up, which was 98% complete.
The actuarial survival rate, including operative mortality rate, at five years was 90% for AVR, 77% for MVR and 82% for DVR. The linearized complication rates (%/year) for AVR, MVR and DVR were: 2.1, 4.0 and 4.0 for late mortality; 0.1, 3.0 and 0.8 for thromboembolism; 0, 0.2 and 0 for thrombosis; 2.0, 1.6 and 1.6 for anticoagulant-related hemorrhage (ACH); 0.3, 0.5 and 1.6 for prosthetic valve endocarditis (PVE); and 0.5, 0.9 and 3.2 for reoperation, respectively. The actuarial rates of freedom from complications at five years were: thromboembolism, 99% for AVR and 88% for MVR; thrombosis, 100% for AVR and 99% for MVR; ACH, 91% for AVR and 94% for MVR; PVE, 99% for AVR and 97% for MVR; reoperation, 98% for AVR and 98% for MVR. No structural failure was observed.
Seven years' experience showed the Ultracor heart valve prosthesis to be comparable with other currently used mechanical heart valves. Continued evaluation of this prosthesis is warranted in order to obtain a more extended clinical follow up.
Ultracor心脏瓣膜是倾斜盘式瓣膜发展历程中的新成员。本报告总结了欧洲三个中心使用Ultracor瓣膜的经验。
1990年至1996年间,446例患者在450例手术中接受了499个Ultracor心脏瓣膜假体,其中包括225例(50.0%)主动脉瓣置换术、172例(38.2%)二尖瓣置换术和49例(10.9%)双瓣膜置换术。另外4例(1.0%)患者在先前的主动脉瓣置换术基础上增加了二尖瓣置换术,被视为双瓣膜置换术患者。主动脉瓣置换术的总随访时间为751患者年(pt-yr)(平均3.4年),二尖瓣置换术为440 pt-yr(平均2.6年),双瓣膜置换术为125 pt-yr(平均2.4年)。9例患者(1例主动脉瓣置换术、8例二尖瓣置换术)失访,随访完成率为98%。
包括手术死亡率在内的五年精算生存率,主动脉瓣置换术为90%,二尖瓣置换术为77%,双瓣膜置换术为82%。主动脉瓣置换术、二尖瓣置换术和双瓣膜置换术的线性化并发症发生率(%/年)分别为:晚期死亡率2.1、4.0和4.0;血栓栓塞0.1、3.0和0.8;血栓形成0、0.2和0;抗凝相关出血(ACH)2.0、1.6和1.6;人工瓣膜心内膜炎(PVE)0.3、0.5和1.6;再次手术0.5、0.9和3.2。五年无并发症的精算率分别为:血栓栓塞方面,主动脉瓣置换术为99%,二尖瓣置换术为88%;血栓形成方面,主动脉瓣置换术为100%,二尖瓣置换术为99%;ACH方面,主动脉瓣置换术为91%,二尖瓣置换术为94%;PVE方面,主动脉瓣置换术为99%,二尖瓣置换术为97%;再次手术方面,主动脉瓣置换术为98%,二尖瓣置换术为98%。未观察到结构故障。
七年的经验表明,Ultracor心脏瓣膜假体与目前使用的其他机械心脏瓣膜相当。有必要对该假体进行持续评估,以获得更长期的临床随访结果。