Special considerations for heart transplantation in congenital heart disease. The Paediatric Heart Transplant Group.

The Journal of heart transplantation Pub Date : 1990-11-01
A H Menkis, F N McKenzie, R J Novick, W J Kostuk, P W Pflugfelder, M Goldbach, H Rosenberg
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Abstract

Congenital heart disease as an indication for heart transplantation accounts for a small number of the total heart transplant experience--less than 3% in most centers. We have performed heart transplantation in eight such patients, accounting for 4% of our total experience. All these patients had specific anatomic anomalies relevant to transplantation. None had morbidity directly related to their anatomic defect and subsequent transplant. Six of the eight had undergone no prior palliative or corrective repairs. One child had a left Blalock-Taussig shunt, and one had bilateral Glenn shunts and a Fontan repair. Technical considerations for orthotopic heart transplantation are described for transposition of the great arteries, left superior vena cava with and without bridging innominate vein, common atrium, presence of Blalock-Taussig shunt, bilateral Glenn shunts, and Fontan repair. Anatomic congenital heart disease is becoming a more frequent indication in heart transplantation. Heart transplantation in the presence of structural congenital heart disease may be technically challenging. Nevertheless, transplantation offers an effective therapeutic alternative for patients with end-stage congestive heart failure and congenital heart disease.

先天性心脏病心脏移植的特殊考虑。儿科心脏移植组。
先天性心脏病作为心脏移植的指征只占心脏移植总经验的一小部分——在大多数中心不到3%。我们已经为8例这样的患者做了心脏移植手术,占我们总经验的4%。所有患者均有与移植相关的特殊解剖异常。没有一例与解剖缺陷和随后的移植直接相关的发病率。8名患者中有6名之前没有接受过姑息治疗或纠正性修复。一个孩子有左blallock - taussig分流,一个有双侧Glenn分流和Fontan修复。本文描述了原位心脏移植的技术考虑,包括大动脉转位、左上腔静脉有或没有桥接无名静脉、普通心房、存在blallock - taussig分流、双侧Glenn分流和Fontan修复。解剖性先天性心脏病正成为心脏移植中更常见的指征。存在结构性先天性心脏病的心脏移植可能在技术上具有挑战性。然而,移植为终末期充血性心力衰竭和先天性心脏病患者提供了一种有效的治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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