{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,30]],"date-time":"2026-10-30T15:43:09Z","timestamp":1793374989186,"version":"4.5.0"},"reference-count":13,"publisher":"American Academy of Pediatrics (AAP)","issue":"5","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2022,5,1]]},"abstract":"<jats:p>Intestinal atresia is a form of congenital bowel obstruction that requires operative repair in the early neonatal period. Duodenal atresia and jejunoileal (JI) atresia are appropriately seen as distinct entities. Both can be suspected with fetal imaging, which can assist with prenatal counseling of families. Duodenal atresia is more commonly associated with comorbidities, whereas JI atresia is more often an isolated finding. Surgical repair is essential and is typically well tolerated. Although it may take time to achieve intestinal function postoperatively, these infants are usually able to tolerate full feeds after resolution of the ileus. Excellent short- and long-term outcomes for isolated duodenal atresia and JI atresia are expected.<\/jats:p>","DOI":"10.1542\/pir.2021-005177","type":"journal-article","created":{"date-parts":[[2022,5,1]],"date-time":"2022-05-01T03:08:01Z","timestamp":1651374481000},"page":"266-274","source":"Crossref","is-referenced-by-count":20,"title":["Intestinal Atresias"],"prefix":"10.1542","volume":"43","author":[{"given":"Barrie S.","family":"Rich","sequence":"first","affiliation":[{"name":"Division of Pediatric Surgery, Cohen Children\u2019s Medical Center, Zucker School of Medicine at Hofstra\/Northwell, New Hyde Park, NY"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Eran","family":"Bornstein","sequence":"additional","affiliation":[{"name":"Division of Maternal Fetal Medicine, Lenox Hill Hospital, New York, NY"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Stephen E.","family":"Dolgin","sequence":"additional","affiliation":[{"name":"Division of Pediatric Surgery, Cohen Children\u2019s Medical Center, Zucker School of Medicine at Hofstra\/Northwell, New Hyde Park, NY"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"417","published-online":{"date-parts":[[2022,5,1]]},"reference":[{"issue":"8","key":"2022050103075697400_B1","doi-asserted-by":"crossref","first-page":"727","DOI":"10.1007\/s00383-009-2406-y","article-title":"Duodenal atresia: associated anomalies, prenatal diagnosis and outcome","volume":"25","author":"Choudhry","year":"2009","journal-title":"Pediatr Surg Int"},{"issue":"2","key":"2022050103075697400_B2","doi-asserted-by":"crossref","first-page":"93","DOI":"10.1055\/s-2008-1038478","article-title":"Congenital duodenal obstruction in children: a decade\u2019s experience","volume":"18","author":"Mustafawi","year":"2008","journal-title":"Eur J Pediatr Surg"},{"issue":"7","key":"2022050103075697400_B3","doi-asserted-by":"crossref","first-page":"1467","DOI":"10.1016\/j.jpedsurg.2010.02.049","article-title":"Influence of Down\u2019s syndrome on management and outcome of patients with congenital intrinsic duodenal obstruction","volume":"45","author":"Niramis","year":"2010","journal-title":"J Pediatr Surg"},{"issue":"6","key":"2022050103075697400_B4","doi-asserted-by":"crossref","first-page":"867","DOI":"10.1016\/j.jpedsurg.2004.02.025","article-title":"Duodenal atresia and stenosis: long-term follow-up over 30 years","volume":"39","author":"Escobar","year":"2004","journal-title":"J Pediatr Surg"},{"issue":"9","key":"2022050103075697400_B5","doi-asserted-by":"crossref","first-page":"773","DOI":"10.1089\/lap.2010.0173","article-title":"Should we be concerned about jejunoileal atresia during repair of duodenal atresia?","volume":"20","author":"St Peter","year":"2010","journal-title":"J Laparoendosc Adv Surg Tech A"},{"issue":"9","key":"2022050103075697400_B6","doi-asserted-by":"crossref","first-page":"1669","DOI":"10.1016\/j.jpedsurg.2017.11.045","article-title":"Perinatal hemorrhage from ulceration of the umbilical cord: a potentially catastrophic association with duodenal and jejunal obstruction","volume":"53","author":"Aronowitz","year":"2018","journal-title":"J Pediatr Surg"},{"issue":"11","key":"2022050103075697400_B7","doi-asserted-by":"crossref","first-page":"2145","DOI":"10.1016\/j.jpedsurg.2018.04.039","article-title":"Neonatal echocardiogram in duodenal obstruction is unnecessary after normal fetal cardiac imaging","volume":"53","author":"Stephens","year":"2018","journal-title":"J Pediatr Surg"},{"issue":"12","key":"2022050103075697400_B8","doi-asserted-by":"crossref","first-page":"1952","DOI":"10.1016\/j.jpedsurg.2017.08.046","article-title":"Is selective echocardiography in duodenal atresia the future standard of care?","volume":"52","author":"Khan","year":"2017","journal-title":"J Pediatr Surg"},{"issue":"5","key":"2022050103075697400_B9","doi-asserted-by":"crossref","first-page":"523","DOI":"10.1002\/uog.14651","article-title":"Accuracy of prenatal ultrasound in detecting jejunal and ileal atresia: systematic review and meta-analysis","volume":"45","author":"Virgone","year":"2015","journal-title":"Ultrasound Obstet Gynecol"},{"issue":"6899","key":"2022050103075697400_B10","doi-asserted-by":"crossref","first-page":"1065","DOI":"10.1016\/S0140-6736(55)92852-X","article-title":"Congenital intestinal atresia; 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