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

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

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

Background Esophageal atresia (EA) is a rare congenital anomaly characterized by a
discontinuity of the esophagus. Following surgical repair, survival rates have improved …

Purpose: to review recent literature concerning long-term health issues and transitional care
in esophageal atresia (EA) patients. PubMed, Scopus, Embase and Web of Science …

Aim Despite advances of outcomes of esophageal atresia (EA), knowledge on patients'
health-related quality of life (HRQoL) is sparse. Due to the heterogeneity of EA, larger …

Abstract Background In 10–15% of children with esophageal atresia (EA) delayed
reconstruction of esophageal atresia (DREA) is necessary due to long-gap EA and/or …

Patients born with esophageal atresia (EA) require advanced reconstructive surgery and risk
long-term digestive and respiratory morbidity. We describe the state of current literature on …

Objectives: Esophageal atresia (EA) is a rare malformation characterized of discontinuity of
the esophagus, concurrent with or without a tracheoesophageal fistula (TEF). We report the …

Introduction Early-life medical and surgical interventions in babies born preterm and/or with
surgical conditions influence later life health and educational outcomes. Obtaining long-term …