Treatment Of Esophageal Atresia

Who Has Esophageal Atresia?

Newborn baby spit she won't swallow and can't eat. Attempts to place a probe where the probe stands still thick when seen from the mouth. In films does not exceed the lower of the esophagus and remains at the top of the probe or bending is seen. Babies diagnosed with esophageal atresia and the upper esophageal aspirated and placed at the end of the tooth into the pouch as the baby is deposited at the term. Otherwise secretions through the trachea and lungs can lead to problems. Nutrition in esophageal atresia without fistula type with only cough and cyanosis may be seen. In these patients, the diagnosis can be put on later.


Is It Necessary Esophageal Atresia Surgery?

Surgery the baby to survive is essential. According to the esophagus alone, the scales type, type of surgery and the timing will be different. Short of surgery, the type of the fistula in most spaced retrieval condition that prevents the baby's (unless you have inflammation of the lungs, severe cardiac anomalies, very small prematurelik) is 1-2 days old will be operated on and stabilized. The long-range fistulsuz type of nutrition provided here by placing a hose feeding into the stomach. The upper esophageal pouch with a probe that is placed into the saliva is absorbed. Thus, dilation of the esophagus are expected.


How Is The Esophageal Atresia Surgery Performed?

Preferably from the right side of the chest cavity is entered. Lower and upper esophageal areas. After leaving Thrace Thrace to the opening portion of the esophagus is repaired. Then the esophageal ends are sewn together. Long-range for people who despite the wait, you may not be able to sew end to end. In this case the mind can be done to the esophagus from the stomach or bowel.

Who Has Esophageal Atresia?

Who Has Esophageal Atresia?

The esophagus is a food borrowing stretching from mouth to mussel. In the esophageal atresis, a part of the food boron has not formed. This occurs when the baby is in the mother's womb and during the development of the food pipe and the breathing tube. More than 90% have a connection between the food pipe and the trachea (fistula). Most of these fistulas are in the lower part of the food borne which is connected to the stomach. This fistula causes air to pass from the pit to the stomach and intestines. It is seen in 2000-3000 births. Additional diseases and chromosomal anomalies can be seen in 60-70% of cases. (V = vertabra), A = anal atresia, C = cardiac, TE = tracheoesophageal, R = renal, L = limb (arm-leg) anomalies.


Can Diagnosis Be Available With Mother?

Ultrasonography is not visible or small, the appearance of the upper esophageal pouch and the excess of amniotic fluid brings to mind first the esophageal atresia. Sometimes, however, the stomach may not be visible even in normal fetuses. If the stomach is not swallowed for any other reason, the stomach may appear small. In contrast, the appearance of stomach and amount of amniotic fluid may be normal in fistulas between trachea and lower esophagus. Babies with esophageal atresia should, of course, be delivered in a center with a Pediatric Surgeon.


How To Understand The Esophageal Atresis?

The newborn can not swallow the baby spit and can not feed. When attempting to place a thick probe in the mouth, it can be seen that the probe has not advanced. It is also seen in the film that the sword is held or curled on the upper part of the food tube which is not passed down. The infants who are diagnosed with esophageal atresia are placed in the upper esophageal pouch and the saliva is aspirated for a while and the baby head is laid down as above. Otherwise, secretions may pass through the pus and lead to lung problems. Nonspecific fistulae without esophageal atresia may result in nausea and coughing and morulae. Diagnosis may be delayed in these patients.