Esophageal Atresia: From worry to wisdom–Parental information needs and considerations on etiology, care, and parental support
Esophageal atresia (EA) is one of the most common congenital gastrointestinal anomalies, posing complex challenges across diagnosis, treatment, and long-term care. This narrative review addresses four key domains: etiology and diagnosis; surgical repair techniques; feeding challenges; and parental stress and support. It outlines current evidence and clinical considerations relevant to families, clinical staff, and researchers. By highlighting informational gaps and long-term concerns, the review supports improved communication, care planning, and research direction for optimizing outcomes in children with EA.
Authors
- Emily Whitesel (ORCID: https://orcid.org/0009-0001-9119-1329)
- Dusica Bajic (ORCID: https://orcid.org/0000-0002-3943-2105)
- J. Rodriguez Coronado
- Benjamin Zendejas (ORCID: https://orcid.org/0000-0002-1231-5283)
- R. D. G. Leslie (ORCID: https://orcid.org/0000-0003-0505-4000)
- Katherine Merritt Doucet
Institutions
- Tufts University (US)
- Boston Children's Hospital (US)
- Harvard University (US)
- Lemuel Shattuck Hospital (US)
Publication Details
- Journal
- Global Pediatrics
- Published
- 2025-10-18
- DOI
- https://doi.org/10.1016/j.gpeds.2025.100299
- Primary Topic
- Esophageal and GI Pathology
- Type
- article
- Field-Weighted Citation Impact
- 0.00