Professional Documents
Culture Documents
Esophageal Atresia
Esophageal Atresia
Esophageal atresia (EA) with distal tracheo-esophageal fistula (TEF) is the most common
congenital anomaly of the esophagus, followed by EA without TEF also known as pure
esophageal atresia and pure TEF.
Development - The trachea and esophagus begin as a ventral diverticulum of the foregut
during the third intrauterine week of life. A proliferation of endodermal cells appears on
the lateral aspect of this growing diverticulum. These cell masses will divide the foregut
into trachea and esophageal tubes.
Newbors- EA causes
excessive salivation,
choking,
coughing,
regurgitation with first feed
inability to pass a feeding tube into the stomach.
Correct dehydration,
acid-base disturbances,
respiratory distress
Repair
thoracotomy,
closure of TEF
primary anastomosis.
Prognosis depends on –
birth weight,
severity of pulmonary dysfuntion,
presence of major congenital cardiac disease.
most common complications after surgery: are in order of frequency: stricture, leakage
and recurrent TEF.