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
a surgical procedure performed to correct congenital defects of the esophagus (the muscular tube that connects the mouth to the stomach) and the trachea
The medical term for this condition is esophageal atresia. It is a congenital condition where the esophagus does not connect to the stomach. This condition requires surgical intervention to repair the connection between the esophagus and stomach.
The frequency of esophageal atresia is estimated to be around 1 in 2,500 to 1 in 4,000 live births. It is a rare congenital condition where the esophagus does not develop properly, leading to a gap that prevents food and liquids from reaching the stomach.
Esophageal atresia is typically caused by the abnormal development of the fetus during pregnancy, leading to the esophagus not forming properly in the womb. Genetic factors or certain environmental influences may also play a role in its development.
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 two most common congenital esophageal abnormalities are esophageal atresia (EA) and tracheoesophageal fistula (TEF).
EA/TEF is reported to occur in about 1: 4500 births
An x-ray procedure known as esophagography is usually performed at two months, six months, and one year of age to monitor the digestive function as the child grows
About 10% of children with EA have what is called the VATER syndrome
Congenital lack of the connection between esophagus and stomach; food cannot enter the stomach
The main treatment for biliary atresia is a surgical procedure called the Kasai procedure, which involves connecting the liver directly to the small intestine to allow bile to flow. If the Kasai procedure is not successful or if complications arise, a liver transplant may be needed. In addition, some medications and nutritional support may be required to manage symptoms and support liver function.