RareWays is a research directory. It helps you understand the science. It is not medical advice. Always discuss your care options with your healthcare team.
Coverage: 2020-01-01 onwards, with up to 300 results per query from PubMed and Europe PMC and separate limits on other sources. This is a selected index, not a complete literature search.
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Oesophageal Atresia: Research Summary
Printed from RareWays (rareways.org)
For general awareness only. Not medical advice. Discuss all care options with your healthcare team.
5 Most Recent Research Articles
- 1.
Developmental vulnerability in infants and toddlers following esophageal atresia repair: A parent-reported functional assessment using WIDEA-FS.
Coronado Juliana et al., Early human development (11 October 2026)
https://pubmed.ncbi.nlm.nih.gov/42887094/
- 2.
Perioperative monitoring in oesophageal atresia and congenital diaphragmatic hernia patients - exploring the impact of diagnosis on neurocardiovascular coupling.
de Munck Sophie et al., Journal of clinical monitoring and computing (8 October 2026)
https://pubmed.ncbi.nlm.nih.gov/42848109/
- 3.
[Analysis of clinical characteristics and diagnostic value of bronchoscopy in children with congenital esophageal atresia and tracheoesophageal fistula].
Zhang L H et al., Zhonghua er ke za zhi = Chinese journal of pediatrics (2 October 2026)
https://pubmed.ncbi.nlm.nih.gov/42742020/
- 4.
Anti-reflux medication after esophageal atresia repair: a retrospective study from a tertiary center in Saudi Arabia
Areej Mohammed Alzamil et al., Annals of Middle Eastern Medicine (1 October 2026)
https://doi.org/10.24911/amem.15-3099
- 5.
Tracheomalacia and Tracheoesophageal Fistula.
von Allmen Douglas et al., Otolaryngologic clinics of North America (1 October 2026)
https://pubmed.ncbi.nlm.nih.gov/42128761/
Source: RareWays research directory. Data from PubMed, Europe PMC, OpenAlex, ClinicalTrials.gov.
Always verify information with your healthcare team before making any decisions about your care.
Oesophageal Atresia
Oesophageal atresia is a rare birth condition in which the oesophagus, the tube that carries food to the stomach, does not form properly and is closed off. It often occurs with an abnormal connection to the windpipe, called a tracheo-oesophageal fistula. It is usually found soon after birth and treated with surgery. Some children need ongoing care for swallowing, breathing or reflux.
This overview is general information, not an individual medical assessment. Research is selected automatically and may include mismatches. How we select and explain research.
Most Recent Research
OBJECTIVE: To characterize early adaptive and functional neurodevelopment after esophageal atresia (EA) repair using the Warner Initial Developmental Evaluation of Adaptive and Functional Skills (WIDEA-FS) compared with healthy controls. STUDY DESIGN: WIDEA-FS assessments were obtained from preterm (n = 18) and term-born (n = 19) children following repair of short-gap (n = 23) or long-gap EA (n = 14), with or without tracheoesophageal fistula, and from healthy term-born controls (n = 19), between 11 and 40 months of age. Total and domain scores (self-care, mobility, communication, social cognition) were compared using general linear modeling and age-stratified analyses according to gestational age (term-born vs. preterm) and surgical subtype (shot-gap vs. long-gap EA). Functional vulnerability was classified using published WIDEA-FS reference criteria and compared with clinician-documented developmental concerns. Early intervention utilization was also characterized in the patient cohort. RESULTS: Total and domain-specific scores increased significantly with age across all groups (p < 0.001). Children following EA repair demonstrated lower total and self-care scores than healthy controls, irrespective of gestational age or surgical subtype (p < 0.05). No group differences emerged for mobility, communication, or social cognition scores. Classification using published WIDEA-FS reference criteria identified a subset of children with communication and social-cognitive vulnerabilities, with communication-related vulnerability observed exclusively among children with EA. WIDEA-FS scoring demonstrated moderate concordance with clinician-documented concerns (sensitivity 75%, specificity 77%, negative predictive value 97%). The majority of children with EA (86%) received early intervention services, most commonly physical and feeding therapy. CONCLUSION: Overall, children demonstrated age-appropriate adaptive functioning after EA repair. However, a subset exhibited domain-specific functional vulnerabilities, particularly in communication and social cognition. The high utilization of early intervention services likely contributed to favorable functional outcomes, potentially underestimating the underlying developmental vulnerability in this population. These findings support continued neurodevelopmental surveillance and highlight the potential utility of parent-reported measures for early identification of children who may benefit from targeted developmental interventions.
Common Questions
What is Oesophageal Atresia?
Oesophageal atresia is a rare birth condition in which the oesophagus, the tube that carries food to the stomach, does not form properly and is closed off. It often occurs with an abnormal connection to the windpipe, called a tracheo-oesophageal fistula. It is usually found soon after birth and treated with surgery. Some children need ongoing care for swallowing, breathing or reflux.
How many clinical trials are available for Oesophageal Atresia?
RareWays currently indexes 17 clinical trials for Oesophageal Atresia, of which 2 are actively recruiting. These counts cover indexed trials across countries, not just your country. An Australian site does not necessarily mean that site is recruiting. Check locations, eligibility and current availability with the study team.
Where does the research data for Oesophageal Atresia come from?
RareWays aggregates research from PubMed, Europe PMC, OpenAlex, and ClinicalTrials.gov. Data is refreshed automatically every day. All articles and trials link directly to their original sources.
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