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杂交手术作为高危左心发育不良综合征及其变异患儿的一种外科姑息治疗方法。

Hybrid procedure as an alternative to surgical palliation of high-risk infants with hypoplastic left heart syndrome and its variants.

机构信息

Evelina Children's Hospital, Department of Congenital Heart Disease, Guy's & St Thomas' NHS Foundation Trust, London, United Kingdom.

出版信息

J Thorac Cardiovasc Surg. 2010 May;139(5):1211-5. doi: 10.1016/j.jtcvs.2009.11.037. Epub 2010 Feb 1.

Abstract

OBJECTIVES

Despite improvements in the surgical management of neonates with the hypoplastic left heart syndrome and its variants, there is a subset of children who have a high predicted mortality. We have analyzed and report our results with the hybrid approach in the management of these high-risk patients.

METHODS

Children identified by our selection criteria underwent the initial hybrid procedure performed in the catheterization laboratory. This consists of surgical banding of the branch pulmonary arteries and stenting of the arterial duct. This was followed 3 to 6 months later by the combined stage I and II Norwood operation or biventricular repair.

RESULTS

Between December 2005 and May 2008, 21 neonates were selected for the hybrid procedure, of whom 16 had typical hypoplastic left heart syndrome. The remaining 5 neonates had severe aortic stenosis with borderline left ventricular dimensions or poor left ventricular function at presentation. Four neonates had a virtually intact interatrial septum and required urgent intervention immediately after birth. There were 6 deaths as inpatients or up to 30 days after the procedure and 1 interstage death before the combined stage I and II operation. Thus far, of 12 babies who have undergone the next operation, 9 have had the combined stage I and II operation and 3 have had a biventricular repair. Two of these 12 babies have died after the combined stage I and II operation.

CONCLUSION

A hybrid approach may be a valuable alternative to the management of high-risk neonates with hypoplastic left heart syndrome and its variants.

摘要

目的

尽管左心发育不全综合征及其变异型新生儿的外科治疗已有改善,但仍有一部分儿童具有较高的死亡预测风险。我们分析并报告了采用杂交手术方法治疗这些高危患者的结果。

方法

符合我们选择标准的患儿在导管室进行初始杂交手术。该手术包括对肺动脉分支进行手术缩窄和动脉导管支架置入。3-6 个月后,再进行一期和二期 Norwood 手术或双心室修复。

结果

2005 年 12 月至 2008 年 5 月,21 名新生儿被选入杂交手术组,其中 16 名患有典型左心发育不全综合征。其余 5 名新生儿在就诊时存在严重的主动脉瓣狭窄、左心室尺寸临界或左心室功能不佳。4 名新生儿房间隔几乎完整,出生后立即需要紧急干预。共有 6 例住院期间或手术后 30 天内死亡,1 例在一期和二期手术前死亡。迄今为止,12 名接受下一次手术的婴儿中,9 名接受了一期和二期手术,3 名接受了双心室修复。这 12 名婴儿中有 2 名在一期和二期手术后死亡。

结论

杂交手术方法可能是治疗左心发育不全综合征及其变异型高危新生儿的一种有价值的替代方法。

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