Oesophageal atresia (EA) is a congenital abnormality of the oesophagus that is caused by
incomplete embryonic compartmentalization of the foregut. EA commonly occurs with a …

Introduction Improvements in care of patients with esophageal atresia (EA) and
tracheoesophageal fistula (TEF) have shifted the focus from mortality to morbidity and quality …

Abstract Background/Purpose Esophageal atresia/tracheoesophageal fistula (EA/TEF) is a
rare congenital anomaly lacking contemporary data detailing patient demographics …

Background Esophageal atresia (EA) and tracheoesophageal fistula (TEF) represent major
therapeutic challenges, frequently associated with serious morbidities following surgical …

Esophageal atresia (EA) and tracheoesophageal fistula (TEF) require emergency surgery in
the neonatal period to prevent aspiration and respiratory compromise. Surgery was once …

Introduction Many aspects of the management of esophageal atresia (EA) and
tracheoesophageal fistula (TEF) are controversial and the evidence for decision making is …

Recent developments in paediatric gastrointestinal surgery have focused on minimally
invasive surgery, the accumulation of high-quality clinical evidence, and scientific research …

Oesophageal atresia–tracheoesophageal fistula (EA-TEF) is a common congenital digestive
disease. Patients with EA-TEF face gastrointestinal, surgical, respiratory, otolaryngological …

Introduction Evidence supporting best practice for long-gap esophageal atresia is limited.
The European Reference Network for Rare Inherited Congenital Anomalies (ERNICA) …

The management of long-gap esophageal atresia remains challenging with limited
consensus on the definition, evaluation, and surgical approach to treatment. Efforts to …