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房室通道缺损中双孔二尖瓣的外科治疗。25例患者的经验。

Surgical treatment of double-orifice mitral valve in atrioventricular canal defects. Experience in 25 patients.

作者信息

Lee C N, Danielson G K, Schaff H V, Puga F J, Mair D D

出版信息

J Thorac Cardiovasc Surg. 1985 Nov;90(5):700-5.

PMID:4058042
Abstract

Double-orifice mitral valve is an uncommon but surgically important condition. The experience in 25 cases of double-orifice mitral valve associated with atrioventricular canal defects was reviewed. This constituted 4.3% of the 581 cases of atrioventricular canal defects operated upon between 1961 and July, 1984. The combined mitral orifice area ranged from 85% to 91% of normal in those patients whose valves were sized intraoperatively. Ten associated cardiac defects were repaired in six patients. Of 23 patients having cleft mitral valve, 21 had partial closure of the cleft. There was one operative death (4.0%), which occurred early in the series in a patient in whom the tissue bridge was severed and massive mitral regurgitation resulted. In the remaining 24 patients the tissue bridge was left intact, and all survived operation. No patient had clinically significant mitral stenosis during a follow-up of 1 to 14 years (mean 4.9 years). Two patients (8%) developed progressive mitral regurgitation and required mitral valve replacement 3 and 11 years postoperatively. One of these patients died and a second death occurred suddenly 2 years following operation. All survivors are in Functional Class I or II. The noncleft orifice of a double-orifice mitral valve usually is competent and rarely requires closure. The cleft, because it constitutes a type of parachute (single papillary muscle) valve, should be closed partially so as to relieve valve incompetence without causing undue stenosis. The incidence of late development of mitral regurgitation is similar to that of atrioventricular canal without double-orifice mitral valve. Repair of atrioventricular canal associated with double-orifice mitral valve can be achieved with a low operative mortality and excellent late results.

摘要

双孔二尖瓣是一种不常见但在外科手术中很重要的病症。回顾了25例双孔二尖瓣合并房室通道缺损的病例。这占1961年至1984年7月间接受手术治疗的581例房室通道缺损病例的4.3%。术中测量瓣膜大小的患者,其二尖瓣联合瓣口面积为正常的85%至91%。6例患者修复了10处相关心脏缺损。23例有二尖瓣裂缺的患者中,21例裂缺部分闭合。有1例手术死亡(4.0%),发生在该系列早期,是一名组织桥被切断并导致大量二尖瓣反流的患者。其余24例患者的组织桥保持完整,均存活。在1至14年(平均4.9年)的随访中,没有患者出现具有临床意义的二尖瓣狭窄。2例患者(8%)出现进行性二尖瓣反流,术后3年和11年需要进行二尖瓣置换。其中1例患者死亡,另1例在术后2年突然死亡。所有存活者心功能均为Ⅰ级或Ⅱ级。双孔二尖瓣的非裂缺瓣口通常功能正常,很少需要闭合。由于二尖瓣裂缺构成一种降落伞(单乳头肌)瓣膜类型,应部分闭合以减轻瓣膜关闭不全,而不引起过度狭窄。二尖瓣反流晚期发生率与无双孔二尖瓣的房室通道相似。双孔二尖瓣合并房室通道的修复手术死亡率低,远期效果良好。

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