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[75例规则型与不规则型完全性房室通道的外科治疗]

[Surgical treatment of complete atrioventricular canals, regular and irregular forms, in 75 patients].

作者信息

Lacour-Gayet F, Planché C, Langlois J, Bruniaux J, Gentile M, Chambran P, Losay J, Binet J P

出版信息

Arch Mal Coeur Vaiss. 1986 May;79(5):708-16.

PMID:3092771
Abstract

The cases of 75 consecutive patients operated for complete atrioventricular canal between 1/1/1978 and 1/1/1985 at Marie-Lannelongue Hospital were reviewed. The age ranged from 1.5 months to 16 years. Forty-nine per cent of patients were operated in the first year of life in the period 1982-1984. Seventy-eight per cent of patients were operated before one year of age. Certain anatomical characteristics enable regular and irregular forms of the condition to be distinguished. Regular forms are characterised by the association of a defect of the inter atrio-ventricular septum, of a common atrioventricular orifice and of ventricles of equal volume without other associated malformations. Irregular forms include the parachute mitral valve, the double mitral orifice, deficient mitral valvular tissue, ventricular hypoplasia, subaortic stenosis, abnormal right ventricular muscular bands, associated cardiac malformations and pulmonary obstructive vascular disease. Surgery comprises repair of the ventricular septal defect and the ostium primum with two separate patches, respecting the anterior and posterior valves and partial or complete closure of the cleft valve. The hospital mortality rate was 33 p. cent. It was 16 p. cent in regular forms and 58 p. cent in irregular forms (p less than 0.01). The hospital mortality of patients operated before 1 year of age with the regular form of the malformation was 22 p. cent. Six children were reoperated secondarily with 2 deaths. Four pacemakers were implanted for complete atrioventricular block. The secondary mortality was 10 p. cent. Thirty-nine patients were followed up for an average of 28 months (range 3 months to 5.5 years).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

回顾了1978年1月1日至1985年1月1日期间在玛丽 - 拉讷隆格医院接受完全性房室通道手术的75例连续患者的病例。年龄范围从1.5个月至16岁。49%的患者在1982 - 1984年期间于出生后第一年接受手术。78%的患者在1岁前接受手术。某些解剖学特征可区分该病症的规则和不规则形式。规则形式的特征为房室间隔缺损、共同房室口以及等容积心室的联合,且无其他相关畸形。不规则形式包括降落伞样二尖瓣、双二尖瓣口、二尖瓣组织缺损、心室发育不全、主动脉瓣下狭窄、异常右心室肌束、相关心脏畸形和肺阻塞性血管疾病。手术包括用两个单独的补片修复室间隔缺损和原发孔,保留前后瓣膜并部分或完全关闭裂开的瓣膜。医院死亡率为33%。规则形式的死亡率为16%,不规则形式为58%(P<0.01)。畸形为规则形式且在1岁前接受手术的患者医院死亡率为22%。6名儿童接受了二次手术,2例死亡。4例因完全性房室传导阻滞植入了起搏器。二次死亡率为10%。39例患者接受了平均28个月(范围3个月至5.5年)的随访。(摘要截断于250字)

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