Abstract:

Intestinal atresia is a rare congenital malformation that requires surgical intervention. Aim of this study, the results of this experience and share our clinic for the treatment of severe congenital anomalies. To this end, the treatment in our clinic between July 2006 and July 2011 and followedup 75 patients with intestinal atresia were examined. These patients, gender, ekanomalileri, antenatal surveillance, pre-operative follow-up, operation procedure, and complications were evaluated for postoperative follow-up. 33 of these patients 44% were male and 42 56% were female. Most of the cases 60% had no antenatal diagnosis. The average birth weight of 2520 g. 900-4100 g . Average of 118 hours in our clinic arrival times 5 hours-40 days . Admission, the patients 50% percent with sepsis. Most of these infants 66% had additional anomalies. The patients were operated on as soon as appropriate. After surgery, patients were followed up for the baby in intensive care, and experienced personnel. Early diagnosis is very important. Patients should be operated as soon as appropriate. Instead of applying a standard surgical and follow-up, the patient should apply the most appropriate initiatives. Complications, and appropriate intervention should be determined before proceeding

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