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主动脉缩窄合并心内缺损时的非体外循环中线修复:单阶段矫正的另一种方法。

Off-pump midline repair of coarctation of aorta when associated with intracardiac defects: an alternate approach for single-stage correction.

作者信息

Dutta Nilanjan, Ghosh Rajarshi, Awasthy Neeraj, Girotra Sumir, Radhakrishnan Sitaraman, Shrivastava Savitri, Iyer Parvathi Unninayar, Iyer Krishna Subramony

机构信息

Division of Pediatric and Congenital Heart Sciences, Fortis Escorts Heart Institute, New Delhi, India.

Division of Pediatric and Congenital Heart Sciences, Fortis Escorts Heart Institute, New Delhi, India

出版信息

Eur J Cardiothorac Surg. 2016 Dec;50(6):1089-1095. doi: 10.1093/ejcts/ezw260. Epub 2016 Jul 26.

Abstract

OBJECTIVES

Strategies for the optimal surgical management of coarctation of aorta with associated intracardiac defects continue to be debated upon. We describe a previously unreported surgical technique for the management of this combination of defects and present our early results.

METHODS

Thirty-one patients (median age: 73 days and median weight: 3.9 kg) underwent repair of coarctation of aorta with associated cardiac defects, in a single-stage, through a midline sternotomy. Twenty-eight patients had associated distal arch hypoplasia and 1 had a type I interruption. The coarctation and when necessary, the distal arch, was repaired prior to the institution of cardiopulmonary bypass. Cardiopulmonary bypass was subsequently instituted for the repair of the associated intracardiac defects.

RESULTS

All patients had successful repair of coarctation and distal arch hypoplasia without the need for rescue cardiopulmonary bypass. In addition, 29 patients had closure of one or more ventricular septal defects, 3 patients had an arterial switch procedure and 1 had repair of double outlet right ventricle. Repair of supramitral ring and subaortic membrane was performed in another 3 patients. One patient underwent concomitant mitral valve repair. There was one in-hospital mortality (3.22%) due to fulminant sepsis. The median follow-up was 29.5 months (range: 1-58 months). There was no late mortality. Two patients required balloon dilatation for recurrent coarctation. Overall event-free survival rate was 88.5% at both 2 and 3 years of follow-up after surgery. However, intervention-free survival at 2 and 3 years of follow-up was 91.7% among the survivors.

CONCLUSION

Repair of coarctation and distal arch hypoplasia or type I arch interruption is feasible prior to the institution of cardiopulmonary bypass without the use of hypothermic circulatory arrest or regional cerebral perfusion, with acceptable and reproducible results.

摘要

目的

对于合并心内缺损的主动脉缩窄的最佳手术治疗策略仍存在争议。我们描述一种此前未报道的用于治疗这种联合缺损的手术技术,并展示我们的早期结果。

方法

31例患者(中位年龄:73天,中位体重:3.9千克)通过正中胸骨切开术,一期修复合并心脏缺损的主动脉缩窄。28例患者合并远端主动脉弓发育不全,1例为I型主动脉弓中断。在建立体外循环之前,先修复主动脉缩窄,必要时修复远端主动脉弓。随后建立体外循环以修复合并的心内缺损。

结果

所有患者均成功修复主动脉缩窄和远端主动脉弓发育不全,无需挽救性体外循环。此外,29例患者关闭了一个或多个室间隔缺损,3例患者接受了动脉调转术,1例患者修复了右心室双出口。另外3例患者进行了二尖瓣上环形结构和主动脉瓣下隔膜修复。1例患者同时进行了二尖瓣修复。1例患者因暴发性脓毒症在院内死亡(3.22%)。中位随访时间为29.5个月(范围:1 - 58个月)。无晚期死亡。2例患者因复发性主动脉缩窄需要球囊扩张。术后2年和3年随访时,总体无事件生存率为88.5%。然而,在幸存者中,2年和3年随访时无需干预的生存率为91.7%。

结论

在建立体外循环之前,不使用低温循环停搏或局部脑灌注修复主动脉缩窄和远端主动脉弓发育不全或I型主动脉弓中断是可行的,结果可接受且具有可重复性。

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