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同时植入圣犹达医疗公司的主动脉和二尖瓣假体。

Simultaneous implantation of St. Jude Medical aortic and mitral prostheses.

作者信息

Armenti F, Stephenson L W, Edmunds L H

机构信息

Department of Surgery, Hospital of the University of Pennsylvania, Philadelphia 19104.

出版信息

J Thorac Cardiovasc Surg. 1987 Nov;94(5):733-9.

PMID:3669701
Abstract

Since January 1980, 92 consecutive patients received St. Jude Medical aortic and mitral prostheses simultaneously. Mean age was 57.6 years (standard deviation 12.4); 14 were 70 years or older. Twenty-three had a previous cardiac operation and 22 had additional procedures performed at the time of double valve replacement. Before the operation 62% of the patients were in New York Heart Association functional class III and 29% were in class IV or required emergency operation. There were six (6.5%) deaths within 30 days. None of the hospital deaths were valve related; all occurred in patients who had additional risk concerns. Follow-up is 100% complete and ranges from 2 to 80 months, totaling 242 patient-years (mean 33.8 months). All except four hospital survivors reached class I or II and 40 patients (47%) remain asymptomatic. The actuarial survival rates are 82% at 1 year, 70% at 3 years, and 60% at 5 years. Causes of late death include heart failure (10), sudden, unexplained death (five), reoperation for coronary artery disease (one), noncardiac (four), and valve related (five). The linearized rate of fatal valve-related events is 2.1% pt-yr. A total of 22 valve-related complications (including five fatal) occurred is 18 patients, for a linearized rate or incidence of 9.1%/pt-yr. Eleven thromboembolic episodes (rate 4.6%/pt-yr) occurred in nine patients; three of these (1.2%/pt-yr) were fatal. Thromboembolic and bleeding complications represented 64% of all valve-related complications. Four patients had six episodes of prosthetic valve endocarditis (incidence 2.5%/pt-yr), of which one (incidence 0.4%/pt-yr) was fatal. Paravalvular leak contributed to the fifth valve-related death. At 5 years, 83% of patients were free of thromboembolic complications; 94% were free of anticoagulant-related hemorrhage; and 71% were free of all valve-related complications. There are few comparable data for patients who have had simultaneous replacement of aortic and mitral valves with other mechanical prostheses. The total incidence of valve-related complications for patients with bioprostheses ranges between 3.9%/pt-yr and 10.4%/pt-yr and is similar to the 9.1%/pt-yr observed in the present series. The type of valve-related complication (thromboemboli and bleeding versus valve deterioration) is the principal difference between St. Jude Medical and bioprosthetic valves in patients who require simultaneous replacement of aortic and mitral valves.

摘要

自1980年1月以来,92例连续患者同时接受了圣犹达医疗公司的主动脉瓣和二尖瓣人工瓣膜置换术。平均年龄为57.6岁(标准差12.4);14例患者年龄在70岁及以上。23例患者曾接受过心脏手术,22例患者在进行双瓣置换时还接受了其他手术。术前,62%的患者处于纽约心脏协会心功能Ⅲ级,29%的患者处于Ⅳ级或需要急诊手术。30天内有6例(6.5%)死亡。所有医院死亡病例均与瓣膜无关;均发生在有其他风险因素的患者中。随访率为100%,随访时间为2至80个月,总计242患者年(平均33.8个月)。除4例住院幸存者外,所有患者的心功能均达到Ⅰ级或Ⅱ级,40例患者(47%)仍无症状。1年、3年和5年的精算生存率分别为82%、70%和60%。晚期死亡原因包括心力衰竭(10例)、不明原因猝死(5例)、冠状动脉疾病再次手术(1例)、非心脏原因(4例)和瓣膜相关原因(5例)。致命性瓣膜相关事件的线性化发生率为2.1%/患者年。18例患者共发生22例瓣膜相关并发症(包括5例致命并发症),线性化发生率为9.1%/患者年。9例患者发生11次血栓栓塞事件(发生率4.6%/患者年);其中3例(发生率1.2%/患者年)为致命性事件。血栓栓塞和出血并发症占所有瓣膜相关并发症的64%。4例患者发生6次人工瓣膜心内膜炎(发生率2.5%/患者年),其中1例(发生率0.4%/患者年)为致命性事件。瓣周漏导致了第5例瓣膜相关死亡。5年时,83%的患者无血栓栓塞并发症;94%的患者无抗凝相关出血;71%的患者无所有瓣膜相关并发症。对于同时置换主动脉瓣和二尖瓣的其他机械瓣膜患者,可比数据较少。生物瓣膜患者瓣膜相关并发症的总发生率在3.9%/患者年至10.4%/患者年之间,与本系列观察到的9.1%/患者年相似。在需要同时置换主动脉瓣和二尖瓣的患者中,瓣膜相关并发症的类型(血栓栓塞和出血与瓣膜退变)是圣犹达医疗公司瓣膜与生物瓣膜之间的主要差异。

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