The management of duodenal atresia (DA) in two Scandinavian pediatric
centers is reported. A total of 67 infants with DA were retrospectivel
y analyzed. A high incidence of associated anomalies was present, incl
uding Down's syndrome in 40% and cardiac anomalies in 20% of the infan
ts. No immediate postoperative mortality was noted. The operative proc
edures were duodenoduodenostomy and duodenojejunostomy. Follow-up did
not disclose any frequent gastrointestinal disturbances or differences
in postoperative complications when the two procedures were compared.
The prognosis for these patients is thus determined exclusively by th
e presence of associated anomalies, especially Down's syndrome and car
diac malformations.