Complete Information on Esophageal Atresia

                                                                                         

Esophageal atresia is a condition in which a part of the oesophagus misses. Esophageal atresia is often associated another congenital anomalies, anomalies most generally cardiac. The disorder is a congenital defect, that the means it occurs before birth. There are several types of atresy oesophagienne. Esophageal atresia with the dent tracheoesophageal occurs in one from 3.000 to 5.000 births. This condition is frequently complicated by the saliva of breathing and secretions of infant in the lungs, causing pneumonia, obstruction, and probably dead. The disorder is usually detected little time after the birth when the food is tested.

Symptoms of esophageal atresia include bluish colouring with the skin with food tested, coughing, bâillonant, and obstructing with the food tested of food, radoter and poor. More one 30% people affected by this condition will also have another anomalies, such as disorders of heart or other digestive disorders of area. Roughly 50 % of children supported with the atresy oesophagienne have other associated problems which can be present. The atresy oesophagienne is considered a surgical urgency. Surgery to repair the oesophagus should be made quickly after the baby is stabilized so that the lungs are not damaged and the baby can be Fédéral.

Before the surgery, the baby is not fed by mouth. The care is taken to prevent the baby of secretions of breathing in the lungs. Mucus and saliva also without interruption will be removed by the intermediary of a catheter until the re-establishment occurred. When the surgery is carried out, the oesophagus is replugged and, if neccessary, is separated from the trachea. The therapy of oxygen is employed like necessary to maintain the saturation normal of oxygen. If one suspect the oral ea or TEF, all food are stopped and of the intravenous fluids are started.

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