The effect of a right-sided aortic arch on outcome in children with esophageal atresia and tracheoesophageal fistula

被引:29
作者
Allen, SR [1 ]
Ignacio, R [1 ]
Falcone, RA [1 ]
Alonso, MH [1 ]
Brown, RL [1 ]
Garcia, VF [1 ]
Inge, TH [1 ]
Ryckman, FC [1 ]
Warner, BW [1 ]
Azizkhan, RG [1 ]
Tiao, GM [1 ]
机构
[1] Childrens Hosp, Med Ctr, Div Pediat & Thorac Surg, Cincinnati, OH 45229 USA
关键词
esophageal atresia; tracheoesophageal fistula; right-sided aortic arch;
D O I
10.1016/j.jpedsurg.2005.10.051
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
During repair of in esophageal atresia with tracheoesophageal fistula (EA/TEF), a right-sided aortic arch (RAA) presents a technical challenge. We reviewed our experience with EA/TEF focusing on the impact of RAA. Methods: A retrospective review of patients with EA/TEF at Our institution from 1990 to 2004 was performed. Of 61 patients, 53 had a left aortic arch (LAA) and 8 had RAA. Results: The mean gestational age and birth weight were similar between patients with LAA and RAA. There were more vascular rings in patients with RAA than with LAA (37.5% vs 3.8%. P = .009). A preoperative echocardiogram correctly identified the location of the arch in all with LAA but only 62.5% of those with RAA. Operative complications occurred in 25% of patients with RAA and 11% of patients with LAA. Conclusions: Management of a child with RAA and EA/TEF is technically challenging. Preoperative identification of the great vessel anomalies may impact operative decision making. Therefore, careful diagnostic evaluation of a patient with an aortic arch that cannot be easily defined by ECHO should be considered before definitive repair. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:479 / 483
页数:5
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