Objective The authors study reviewed patients who underwent operations
for omphalocele and gastroschisis to determine survival, morbidity, a
nd long-term quality of life. Method Clinical follow-up of 94 patients
cared for with omphalocele and gastroschisis during a 10- to 20-year
period after birth. Result Eighty-three patients survived initial trea
tment. Sixty-one had long-term follow-up. Mean follow-up in the group
was 14.2 years. Survival was favorable in the absence of lethal or co-
existing major congenital anomalies. Nineteen patients required 31 reo
perations, most for abdominal wall hernias and the sequelae of intesti
nal atresia. Current quality of life was described as favorable (good)
in 80% of patients. Conclusions Survival rate in patients with abdomi
nal wall defects is favorable and deaths occur substantially in patien
ts with co-existing lethal, or multiple, congenital anomalies. Reopera
tive surgery is necessary principally in those patients who have postc
losure abdominal wall hernias, and in those with bower atresia at birt
h. Reoperations are not likely to be necessary after school age. Quali
ty of life in survivors is patient-perceived as entirely satisfactory.