Management of esophageal atresia has merged from correction of the anomaly to the
complete spectrum of management of esophageal atresia and all its sequelae. It is the …

Esophageal atresia (EA) with or without trachea-esophageal fistula is relatively common
congenital malformation with most patients living into adulthood. As a result, care of the adult …

Esophageal atresia (EA) with or without tracheoesophageal fistula (TEF) is the most
common congenital anomaly of the esophagus. The improvement of survival observed over …

Esophageal atresia is among the most common congenital digestive malformations,
affecting 1 in 3,000 newborn babies at birth. Since the first successful primary repair of …

The evaluation and management of an infant with esophageal atresia (EA) and
tracheoesophageal fistula (TEF) are one of the most challenging but rewarding scenarios in …

Esophageal atresia (EA) is frequently diagnosed after birth in infants with feeding
intolerance and increased oral secretions. Patients with EA commonly have other …

Esophageal atresia and tracheoesophageal fistula are often-concomitant pathologies that
primarily afflict neonates. The complications of these anomalies may lead to increased …

Objective: To study the clinical profile of the cases of esophageal atresia (EA) and/or
tracheoesophageal fistula (TEF) and various factors affecting the surgical and early …

Although most patients with esophageal atresia (EA) and tracheo-esophageal fistula (TEF)
may benefit from “standard” management, which is deferred emergency surgery, some may …

Background The perioperative management of esophageal atresia/tracheo‐esophageal
fistula by open or thoracoscopic approach can be complicated by metabolic derangements …