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白塞病所致主动脉瓣关闭不全:11年手术经验

Aortic regurgitation caused by Behçet's disease: surgical experience during an 11-year period.

作者信息

Ma Wei-Guo, Zheng Jun, Zhu Jun-Ming, Liu Yong-Min, Li Ming, Sun Li-Zhong

机构信息

Department of Cardiovascular Surgery, Fu Wai Hospital and Cardiovascular Institute, Chinese Academy of Medical Sciences, Beijing, China.

出版信息

J Card Surg. 2012 Jan;27(1):39-44. doi: 10.1111/j.1540-8191.2011.01392.x.

Abstract

BACKGROUND AND AIM OF THE STUDY

Aortic regurgitation (AR) caused by Behçet's disease is a rare clinical condition and surgical experience is limited. Many patients undergoing simple aortic valve replacement (AVR) required a second or third operation as a result of prosthetic valve dehiscence. We analyze our experience with surgical management for AR in Behçet's disease during an 11-year period.

METHODS

From April 1997 through December 2008, 10 male patients (mean age, 38.4 ± 6.9 years) with AR caused by Behçet's disease underwent surgical treatment. The primary procedures were AVR in seven cases and aortic root replacement in three (two Bentall, one Cabrol). The duration of follow-up was 5.3 ± 3.6 years.

RESULTS

In the seven patients with simple AVR, valve dehiscence occurred in six after an interval of 2.9 ± 1.7 months, necessitating 11 reoperations (four redo AVRs, one redo redo-AVR, four aortic root replacements, and two heart transplants) with one early death. In aortic root replacement patients, two Bentall patients survived and required no reintervention, and the Cabrol patient died from electromechanical uncoupling one year postoperatively. Of the seven survivors, the definite procedure was aortic root replacement in four cases, heart transplantation in two, and AVR in one.

CONCLUSIONS

The rate of valve dehiscence was high after isolated AVR in patients with AR caused by Behçet's disease. At the first operation, aortic root replacement should be the procedure of choice, preferably with a homograft. Heart transplantation might be a feasible alternative to aortic root replacement in selected patients.

摘要

研究背景与目的

白塞病所致主动脉瓣关闭不全(AR)是一种罕见的临床病症,手术经验有限。许多接受单纯主动脉瓣置换术(AVR)的患者因人工瓣膜裂开而需要进行二次或三次手术。我们分析了11年间白塞病所致AR的外科治疗经验。

方法

1997年4月至2008年12月,10例(平均年龄38.4±6.9岁)白塞病所致AR的男性患者接受了手术治疗。主要手术方式为7例行AVR,3例行主动脉根部置换术(2例Bentall手术,1例Cabrol手术)。随访时间为5.3±3.6年。

结果

在7例单纯AVR患者中,6例在2.9±1.7个月后发生瓣膜裂开,需要进行11次再次手术(4次再次AVR、1次再次再次AVR、4次主动脉根部置换术和2次心脏移植),1例早期死亡。在主动脉根部置换术患者中,2例Bentall手术患者存活且无需再次干预,Cabrol手术患者术后1年死于电机械分离。7例幸存者中,4例行主动脉根部置换术,2例行心脏移植,1例行AVR。

结论

白塞病所致AR患者单纯AVR术后瓣膜裂开发生率较高。初次手术时,应首选主动脉根部置换术,最好使用同种异体移植物。对于部分患者,心脏移植可能是主动脉根部置换术的可行替代方案。

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