One-stage total repair of aortic arch anomaly using regional perfusion

被引:16
作者
Lim, Hong-Gook
Kim, Woong-Han
Jang, Woo-Sung
Lim, Cheong
Kwak, Jae Gun
Lee, Cheul
Hwang, Seong Wook
Lee, Chang-Ha
机构
[1] Seoul Natl Univ, Coll Med, Childrens Hosp, Dept Thorac & Cardiovasc Surg,Clin Res Inst, Seoul 110744, South Korea
[2] Sejong Gen Hosp, Sejong Heart Inst, Dept Thorac & Cardiovasc Surg, Puchon, South Korea
关键词
CHD; great vessel anomalies; aortic arch; coarctation; CPB; circulatory arrest; neurocognitive deficits;
D O I
10.1016/j.ejcts.2006.10.035
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Primary repair of aortic arch obstructions and associated cardiac anomalies is a surgical challenge in neonates and infants. Deep hypothermic circulatory arrest prolongs myocardial ischemia and might induce cerebra( and myocardial dysfunction. Methods: From March 2000 to December 2005, 69 neonates or infants with aortic arch anomaly underwent one-stage biventricular repair with continuous cerebral perfusion in the presence of a nonworking beating heart using the dual perfusion technique on the innominate artery and aortic root. Preoperative diagnoses of arch anomaly comprised aortic coarctation (n = 54) or an interrupted aortic arch (n = 15). Combined anomalies were ventricular septal defect (n = 52), anomalous origin of the right pulmonary artery from ascending aorta in = 3), hypoptastic left heart syndrome (n = 2), truncus arteriosus (n = 2), atrioventricular septal defect (n = 2), double outlet right ventricle (n = 1), total anomalous pulmonary venous return (n 1), partial anomalous pulmonary venous return (n = 1), and aortic stenosis (n = 1). Results: The mean regional perfusion time was 27.8 +/- 9.8 min. There was no operative mortality. Postoperative tow cardiac output was present in four patients (5.8%). A neurologic complication was noted in one patient (1.5%) who developed transient chorea, but recovered completely. During 32.8 +/- 17.5 months of follow-up, one late death (1.5%) occurred. There was neither reoperation associated with arch anomaly nor recoarctation except in one patient. One patient developed left main bronchial compression necessitating aortopexy. Conclusions: One-stage total arch repair using our regional perfusion technique is an excellent method that may minimize neurologic and myocardial complications without mortality. Our surgical strategy for arch anomaly has a low rate of residual and recurrent coarctation when performed in neonates and infants. (c) 2007 European Association for Cardio-Thoracic Surgery. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:242 / 248
页数:7
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