Hartz R S, Fisher E B, Finkelmeier B, DeBoer A, Sanders J H, Moran J M, Michaelis L L
J Thorac Cardiovasc Surg. 1986 Jun;91(6):910-7.
A total of 589 porcine bioprostheses were implanted in 509 patients from January, 1976, through December, 1983. Of the valves implanted, 390 were Hancock and 199 were Carpentier-Edwards. A total of 1,633 patient-years was accrued, with a mean follow-up of 38 months per patient. Two hundred eight patients had aortic valve replacement, 209 had mitral valve replacement, and 79 had multiple valve replacements, of which 46 were aortic and mitral replacements. The mortality for isolated aortic valve replacement was 5.8%; for isolated mitral replacement, 8.6%, and for all patients, 10.9%. Late mortality was 3.9% per patient-year. The actuarial survival rate at 5 years was 79% for aortic, 68% for mitral, and 76% for aortic-mitral valve replacement. There were 12 thromboembolic events (0.73% per patient-year). Two episodes occurred in patients with an aortic bioprosthesis, nine in patients with a porcine mitral valve, and one in a patient with mitral and tricuspid bioprosthetic valves. The probability of remaining free of thromboembolism at 5 years was 99% for the group having aortic valve replacement, 93% for those having mitral replacement, and 100% for the group having aortic-mitral valve replacements. Thirteen episodes of endocarditis occurred (0.8% per patient-year). Seven of the 13 patients died as a direct result of endocarditis. The probability of remaining free of prosthetic endocarditis at 5 years was 97% for the aortic valve replacement group, 95% for the mitral group, and 97% for the aortic-mitral group. There were 20 instances of xenograft failure (1.2% per patient-year). The probability of remaining free of valve failure at 5 years was 96% for the aortic valve replacement group, 93% for the mitral group, and 93% for the aortic-mitral replacement group. Primary tissue failure of a prosthesis occurred in seven patients, all with Hancock valves (0.43% per patient-year). As yet there has been no primary tissue failure of the Carpentier-Edwards prosthesis. There also appears to be a lower incidence of thromboembolism (Edwards, 0.3% per patient-year; Hancock, 0.8% per patient-year) and endocarditis (Edwards, 0.6% per patient-year; Hancock, 1.0% per patient-year). The low incidence of complications with the porcine bioprosthetic valve, especially the Carpentier-Edwards, encourages us to recommend its continued use, especially in situations in which anticoagulation is contraindicated.
1976年1月至1983年12月期间,共509例患者植入了589个猪生物瓣膜。植入的瓣膜中,390个是Hancock瓣,199个是Carpentier-Edwards瓣。累计患者随访时间共1633人年,平均每位患者随访38个月。208例患者接受了主动脉瓣置换,209例接受了二尖瓣置换,79例接受了多瓣膜置换,其中46例为主动脉瓣和二尖瓣置换。单纯主动脉瓣置换的死亡率为5.8%;单纯二尖瓣置换的死亡率为8.6%,所有患者的死亡率为10.9%。晚期死亡率为每年3.9%。主动脉瓣置换术后5年的精算生存率为79%,二尖瓣置换为68%,主动脉瓣-二尖瓣置换为76%。发生了12次血栓栓塞事件(每年0.73%)。2次发生在植入主动脉生物瓣膜的患者中,9次发生在植入猪二尖瓣的患者中,1次发生在植入二尖瓣和三尖瓣生物瓣膜的患者中。主动脉瓣置换组5年无血栓栓塞的概率为99%,二尖瓣置换组为93%,主动脉瓣-二尖瓣置换组为100%。发生了13次心内膜炎事件(每年0.8%)。13例患者中有7例直接死于心内膜炎。主动脉瓣置换组5年无人工瓣膜心内膜炎的概率为97%,二尖瓣组为95%,主动脉瓣-二尖瓣组为97%。发生了20例异种移植物失败(每年1.2%)。主动脉瓣置换组5年无瓣膜失败的概率为96%,二尖瓣组为93%,主动脉瓣-二尖瓣置换组为93%。7例患者发生了假体原发性组织衰竭,均为Hancock瓣(每年0.43%)。Carpentier-Edwards假体尚未发生原发性组织衰竭。血栓栓塞(Edwards瓣每年0.3%;Hancock瓣每年0.8%)和心内膜炎(Edwards瓣每年0.6%;Hancock瓣每年1.0%)的发生率似乎也较低。猪生物瓣膜并发症发生率低,尤其是Carpentier-Edwards瓣,这促使我们建议继续使用,特别是在抗凝治疗禁忌的情况下。