[体外循环条件下1岁儿童先天性心脏缺陷合并肺动脉高压的手术治疗]。

Grudnaia khirurgiia (Moscow, Russia) Pub Date : 1989-05-01
V V Aleksi-Meskhishvili, A S Sharykin, S A Popov, A P Nikoliuk
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引用次数: 0

摘要

在1983年至1987年期间,对204名年龄在25天至12个月(体重3至10公斤)的先天性心脏病和肺动脉高压患儿进行了手术。173例患者行室间隔缺损手术治疗(总死亡率6.9%),9例患者采用Senning法矫正了合并室间隔缺损的大血管转位(死亡率11%),14例患者完全消除了肺静脉异常引流(死亡率28.6%)。在主动脉-肺瘘、主动脉和肺动脉起源于右心室和共同心室的矫正术中,没有发生致命的结果。在所有患者中,除4例(2例继发性肺动脉高压,另外2例原发性肺动脉高压)外,肺动脉压力显著降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Surgical treatment of congenital heart defects with pulmonary hypertension in children during their 1st year of life under the conditions of extracorporeal circulation].

In the period between 1983 and 1987 operations were carried out on 204 children aged from 25 days to 12 months (body weight of 3 to 10 kg) for congenital heart diseases and pulmonary hypertension. Surgery for ventricular septal defect was undertaken on 173 patients (total mortality 6.9%), transposition of the major vessels with concurrent ventricular septal defect was corrected by Senning's method in 9 patients (mortality 11%), total anomalous pulmonary vein drainage was relieved in 14 patients (mortality 28.6%). No fatal outcomes occurred in correction of an aorto-pulmonary fistula, origin of the aorta and pulmonary artery from the right ventricle, and a common ventricle. In all patients, with the exception of 4 (2 with secondary and another 2 with primary pulmonary hypertension), pressure in the pulmonary artery reduced significantly.

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