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The impact of right-sided aortic arch on surgical outcomes in esophageal atresia: A systematic review

In brief

Right-sided aortic arch occurs in about 5% of esophageal atresia infants and most receive right-side repair

A systematic review of 107 newborns with both EA/TEF and a right-sided aortic arch found the arch in 5.2% of 1,640 EA cases. Surgeons used a right-thoracic approach in the majority of operations, yet mortality ranged from 17% to 63% and postoperative complications were common, prompting consideration of left-side approaches for complex vascular anatomy.

Journal
Journal of pediatric surgery (Q1)
Published
11 September 2026
Study design
Systematic review of cohort studies
Evidence level
Level 2, Moderate (CEBM 2a)
Authors
Elif Yüksel, Bekir Erdeve, Sinem Aydöner, Gonca Gerçel, Özlem Boybeyi, Ece Arslan, et al.
PMID
42727760
DOI
10.1016/j.jpedsurg.2026.163466

Why clinicians should know about it

  • Picked for Neonatology (top studies of the week, 13 September 2026): Systematic review of EA/TEF surgical outcomes

Abstract

OBJECTIVE: The management of esophageal atresia and tracheoesophageal fistula (EA/TEF) in the presence of a right-sided aortic arch (RAA) remains a significant surgical challenge. This systematic review aims to analyze the diagnostic trends, surgical approaches, and clinical outcomes for EA/TEF patients with an associated RAA. METHODS: A comprehensive and systematic literature search was performed across major electronic databases, including PubMed, MEDLINE and Embase and systematic review was conducted in accordance with PRISMA guidelines, evaluating studies published between January 2000 and January 2026. The research protocol, detailing the predefined methodology, search strategy, and inclusion criteria, was prospectively registered on the PROSPERO (CRD420261339983) platform prior to the initiation of data extraction. Eligible studies included clinical trials, observational studies, and case series (n≥5) reporting on the incidence, surgical strategies (thoracotomy side/thoracoscopy), and postoperative complications in neonates diagnosed with both EA/TEF and a RAA. RESULTS: A total of nine studies were included in this systematic review. In eight studies consecutively evaluating all patients with EA/TEF (n=1640), the prevalence of a RAA was determined to be 5.2% (86/1640). With the inclusion of one specific case series (n=21) that exclusively reported on patients with concurrent EA and RAA, the clinical characteristics, surgical approaches, and survival outcomes of a total of 107 patients with RAA were analyzed in this review. Preoperative echocardiography (ECHO) correctly identified arch laterality in 10% to 80% of cases across the included studies, with detection rates improving to over 70% in series from the last decade. A right-sided approach (thoracotomy or thoracoscopy) was the most common surgical strategy, used in 62.5% to 100% of cases, while intraoperative conversion to the contralateral side was rare. Associated congenital heart disease was highly prevalent, ranging from 42% to 90%. Overall mortality ranged from 16.6% to 62.5% across studies, primarily driven by complex cardiac anomalies and severe tracheal impingement from vascular rings. Postoperative morbidity included anastomotic leaks (0% to 42.8%), strictures (14.3% to 53%), and chylothorax (0% to 25%). CONCLUSION: While right-sided repair is technically feasible for most surgeons due to anatomical familiarity, it might be associated with increased long-term morbidity. Preoperative identification of RAA and associated vascular rings is crucial for surgical planning. A personalized approach, considering a left thoracotomy or thoracoscopy in complex vascular cases, may be considered to optimize outcomes and reduce ischemic complications. Due to the rarity of concurrent EA/TEF and RAA, alongside the heterogeneity of available data, a formal meta-analysis could not be performed.

Abstract as published, via PubMed.

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For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.