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

Steven Allen, Romeo Ignacio, Richard A. Falcone, Maria H. Alonso, Rebeccah L. Brown, Victor F. Garcia, Thomas H. Inge, Frederick C. Ryckman, Brad W. Warner, Richard G. Azizkhan, Gregory M. Tiao

Research output: Contribution to journalArticle

33 Citations (Scopus)

Abstract

During repair of an 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.

Original languageEnglish (US)
Pages (from-to)479-483
Number of pages5
JournalJournal of Pediatric Surgery
Volume41
Issue number3
DOIs
StatePublished - Jan 1 2006

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Thoracic Aorta
Patient Rights
Esophageal atresia with or without tracheoesophageal fistula
Birth Weight
Gestational Age
Blood Vessels
Decision Making

All Science Journal Classification (ASJC) codes

  • Surgery
  • Pediatrics, Perinatology, and Child Health

Cite this

Allen, Steven ; Ignacio, Romeo ; Falcone, Richard A. ; Alonso, Maria H. ; Brown, Rebeccah L. ; Garcia, Victor F. ; Inge, Thomas H. ; Ryckman, Frederick C. ; Warner, Brad W. ; Azizkhan, Richard G. ; Tiao, Gregory M. / The effect of a right-sided aortic arch on outcome in children with esophageal atresia and tracheoesophageal fistula. In: Journal of Pediatric Surgery. 2006 ; Vol. 41, No. 3. pp. 479-483.
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abstract = "During repair of an 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.",
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Allen, S, Ignacio, R, Falcone, RA, Alonso, MH, Brown, RL, Garcia, VF, Inge, TH, Ryckman, FC, Warner, BW, Azizkhan, RG & Tiao, GM 2006, 'The effect of a right-sided aortic arch on outcome in children with esophageal atresia and tracheoesophageal fistula', Journal of Pediatric Surgery, vol. 41, no. 3, pp. 479-483. https://doi.org/10.1016/j.jpedsurg.2005.10.051

The effect of a right-sided aortic arch on outcome in children with esophageal atresia and tracheoesophageal fistula. / Allen, Steven; Ignacio, Romeo; Falcone, Richard A.; Alonso, Maria H.; Brown, Rebeccah L.; Garcia, Victor F.; Inge, Thomas H.; Ryckman, Frederick C.; Warner, Brad W.; Azizkhan, Richard G.; Tiao, Gregory M.

In: Journal of Pediatric Surgery, Vol. 41, No. 3, 01.01.2006, p. 479-483.

Research output: Contribution to journalArticle

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T1 - The effect of a right-sided aortic arch on outcome in children with esophageal atresia and tracheoesophageal fistula

AU - Allen, Steven

AU - Ignacio, Romeo

AU - Falcone, Richard A.

AU - Alonso, Maria H.

AU - Brown, Rebeccah L.

AU - Garcia, Victor F.

AU - Inge, Thomas H.

AU - Ryckman, Frederick C.

AU - Warner, Brad W.

AU - Azizkhan, Richard G.

AU - Tiao, Gregory M.

PY - 2006/1/1

Y1 - 2006/1/1

N2 - During repair of an 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.

AB - During repair of an 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.

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