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无人工管道的肺动脉流出道重建。

Reconstruction of the pulmonary outflow tract without prosthetic conduit.

作者信息

Lecompte Y, Neveux J Y, Leca F, Zannini L, Tu T V, Duboys Y, Jarreau M M

出版信息

J Thorac Cardiovasc Surg. 1982 Nov;84(5):727-33.

PMID:7132411
Abstract

New techniques of correction of complex congenital anomalies, avoiding the use of prosthetic conduits, are presented. In transposition of the great arteries (TGA) with ventricular septal defect (VSD) and pulmonary stenosis, the technique comprised the resection of infundibular septum, the suturing of an intraventricular baffle directing blood from the left ventricle to the aorta, and the reconstruction of the pulmonary outflow tract by direct implantation of the posterior rim of the pulmonary arterial trunk on the right ventricle, completed by an anterior patch. In most cases, the pulmonary bifurcation was translated anterior to the ascending aorta. This technique was feasible even in infants and in patients with a small VSD. Thirteen patients, from 3 months to 8 years of age, were treated by this technique, with four deaths, one residual VSD (reoperated), and eight good results (4 to 16 months). A similar repair was used in three cases of double-outlet right ventricle (DORV) with subpulmonic VSD and pulmonary stenosis or pulmonary artery banding, with two operative deaths and one good result. The same technique of pulmonary outflow tract reconstruction was used in four cases of truncus arteriosus. Two deaths were attributed to severe pulmonary regurgitation, a complication which should be prevented in future cases by a reliable method of inserting a valve in the pulmonary outflow tract. In pulmonary atresia with VSD and absent pulmonary trunk, the continuity between the right ventricle and the pulmonary branches was established via an arterial tube resected from the ascending aorta. This technique was successfully used in one child with extremely small pulmonary branches. These preliminary results led us to conclude that many complex congenital cardiac anomalies can be effectively treated without a prosthetic conduit.

摘要

本文介绍了复杂先天性畸形矫治的新技术,避免使用人工管道。在伴有室间隔缺损(VSD)和肺动脉狭窄的大动脉转位(TGA)中,该技术包括切除漏斗间隔,缝合将左心室血液导向主动脉的室内挡板,以及通过将肺动脉干后缘直接植入右心室并在前部补片完成来重建肺流出道。在大多数情况下,肺分叉移至升主动脉前方。即使在婴儿和小VSD患者中,该技术也是可行的。13例年龄从3个月至8岁的患者接受了该技术治疗,4例死亡,1例残余VSD(再次手术),8例效果良好(4至16个月)。在3例伴有肺动脉下VSD和肺动脉狭窄或肺动脉束带的右心室双出口(DORV)病例中采用了类似的修复方法,2例手术死亡,1例效果良好。在4例动脉干畸形病例中使用了相同的肺流出道重建技术。2例死亡归因于严重的肺反流,未来病例中应通过在肺流出道插入瓣膜的可靠方法来预防这种并发症。在伴有VSD和肺动脉干缺如的肺动脉闭锁中,通过从升主动脉切除的动脉导管建立右心室与肺分支之间的连续性。该技术成功应用于1例肺分支极小的儿童。这些初步结果使我们得出结论,许多复杂先天性心脏畸形无需人工管道即可得到有效治疗。

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