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房室通道缺损病例中二尖瓣双孔的手术修复。

Surgical repair of double-orifice of the mitral valve in cases with an atrioventricular canal defects.

作者信息

Ohta N, Sakamoto K, Kado M, Nagato H, Nishioka M, Fujimoto Y, Yokota M

机构信息

Department of Cardiovascular Surgery, Shizuoka Children's Hospital, Urushiyama, Shizuoka 420-8660, Japan.

出版信息

Jpn J Thorac Cardiovasc Surg. 2001 Nov;49(11):656-9. doi: 10.1007/BF02912474.

Abstract

OBJECTIVE

A Double-orifice in the mitral valve is an uncommon congenital cardiac lesion which occurs as an isolated anomaly or in association with other cardiac malformation. This report deals with our surgical experience of a double-orifice of the mitral valve in cases with an atrioventricular canal defect.

PATIENTS AND METHODS

From 1991 through 1999, ten patients were diagnosed to have a double-orifice of the mitral valve at Shizuoka Children's Hospital. Each patient had associated major cardiac malformations, among which atrioventricular canal defect underwent surgical management, with five of these undergoing complete correction with or without previous pulmonary artery banding. Of these 10, the five cases were enrolled in this study. Two of these had a complete type, and the other three had a partial type. The cleft in the left-sided atrioventricular valve was closed partially in four and left untouched in one. Bridging tissue, when present, was left intact. There was no regurgitation from any accessory orifice and no repair for an accessory orifice was needed.

RESULT

There was no late death and no replacement of the valve with prosthesis. During follow-up ranging from 1 to 4 years, none of the patients developed severe stenosis or progressive regurgitation in the left-sided atrioventricular valve.

CONCLUSION

Meticulous surgical management of a double-orifice in the mitral valve in association with atrioventricular canal defect an achieve an acceptable midterm result without developing severe dysfunction in the left-sided atrioventricular valve.

摘要

目的

二尖瓣双孔是一种罕见的先天性心脏病变,可作为孤立异常出现,也可与其他心脏畸形并存。本报告介绍了我们在房室管缺损病例中治疗二尖瓣双孔的手术经验。

患者与方法

1991年至1999年期间,静冈儿童医院诊断出10例二尖瓣双孔患者。每名患者均伴有严重心脏畸形,其中对房室管缺损进行了手术治疗,其中5例进行了完全矫正,部分患者术前进行了肺动脉环扎。在这10例患者中,5例纳入本研究。其中2例为完全型,另外3例为部分型。4例患者左侧房室瓣的瓣裂部分闭合,1例未处理。如有桥接组织,则保持完整。未发现任何副孔有反流,也无需对副孔进行修复。

结果

无晚期死亡病例,也未进行瓣膜置换。在1至4年的随访期间,所有患者左侧房室瓣均未出现严重狭窄或进行性反流。

结论

对合并房室管缺损的二尖瓣双孔进行细致的手术治疗,可获得可接受的中期结果,且左侧房室瓣不会出现严重功能障碍。

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