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针对已姑息至单心室修复的复杂先天性心脏缺陷进行双心室修复。

Two-ventricle repair for complex congenital heart defects palliated towards single-ventricle repair.

作者信息

Kottayil Brijesh P, Sunil Gopalraj S, Kappanayil Mahesh, Mohanty Sweta Harish, Francis Edwin, Vaidyanathan Balu, Balachandran Rakhi, Nair Suresh G, Kumar Raman Krishna

机构信息

Department of Cardiovascular and Thoracic Surgery, Amrita Institute of Medical Sciences and Research Centre, Kochi, Kerala, India.

出版信息

Interact Cardiovasc Thorac Surg. 2014 Mar;18(3):266-71. doi: 10.1093/icvts/ivt495. Epub 2013 Dec 5.

Abstract

OBJECTIVES

Complex congenital heart defects that present earlier in life are sometimes channelled towards single-ventricle repair, because of anatomical or logistic challenges involved in two-ventricle correction. Given the long-term functional and survival advantage, we have been consciously exploring the feasibility of a biventricular repair in these patients when they present later for Fontan completion.

METHODS

Since June 2009, 71 patients were referred for staged completion of the Fontan procedure. Following detailed evaluation that included three-dimensional echocardiography and magnetic resonance imaging, 10 patients (Group 1-median age 6 years) were identified and later underwent complex biventricular repair with takedown of Glenn shunt, while completion of extracardiac Fontan repair was done in 61 patients (Group 2-median age 7 years).

RESULTS

Two-ventricle repair was accomplished in all the 10 Group 1 patients. One patient developed complete heart block requiring permanent pacemaker insertion. Late patch dehiscence occurred in another (awaiting repair). At a median follow-up of 15 months, there was no mortality among the Group 1 patients and all except for 1 patient were symptom free. There were 2 early deaths (3.3%) in the Group 2 patients.

CONCLUSIONS

Two-ventricular repair, although surgically challenging, should be considered in all patients with two functional ventricles who come for Fontan completion. Comprehensive preoperative imaging and meticulous planning helps in identifying suitable candidates.

摘要

目的

由于双心室矫正存在解剖或后勤方面的挑战,一些在生命早期出现的复杂先天性心脏缺陷有时会采用单心室修复。鉴于双心室修复具有长期功能和生存优势,我们一直在有意识地探索这些患者在后期进行Fontan手术完成时进行双心室修复的可行性。

方法

自2009年6月以来,71例患者被转诊分期完成Fontan手术。经过包括三维超声心动图和磁共振成像在内的详细评估,确定了10例患者(第1组,中位年龄6岁),随后对其进行了复杂的双心室修复,拆除了Glenn分流,而61例患者(第2组,中位年龄7岁)完成了心外Fontan修复。

结果

第1组的所有10例患者均完成了双心室修复。1例患者发生完全性心脏传导阻滞,需要植入永久性起搏器。另1例出现晚期补片裂开(等待修复)。在中位随访15个月时,第1组患者无死亡,除1例患者外均无症状。第2组患者有2例早期死亡(3.3%)。

结论

对于所有前来完成Fontan手术的具有两个功能心室的患者,尽管双心室修复在手术上具有挑战性,但仍应予以考虑。全面的术前影像学检查和细致的规划有助于确定合适的候选者。

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