reactions to anesthesia or medications; bleeding or clot formation; narrowing of the repaired organs; nerve injury; fluid imbalances; and collapsed lung (pneumothorax).
Esophageal atresia occurs in approximately 1 in 4,000 live births.
The cause of esophageal atresia, like that of most birth defects, is unknown.
he fistula will first be closed off, creating a separate airway. Then the blind esophageal pouch will be opened and connected to the other portion of the esophagus
infants who have no complications, such as heart or lung problems or other types of intestinal malformations, can usually have esophageal surgery within the first 24 hours of life
a surgical procedure performed to correct congenital defects of the esophagus (the muscular tube that connects the mouth to the stomach) and the trachea
Esophageal Atresia
Surgery to correct esophageal atresia is usually successful. Post-operative complications may include difficulty swallowing, since the esophagus may not contract efficiently, and gastrointestinal reflux, in which the acidic.
The operation will be delayed for low birth weight infants or those with complicated malformations, usually until their nutritional status can be improved
The two most common congenital esophageal abnormalities are esophageal atresia (EA) and tracheoesophageal fistula (TEF).
Congenital Esophageal Atresia
EA/TEF is reported to occur in about 1: 4500 births
Congenital lack of the connection between esophagus and stomach; food cannot enter the stomach