World Journal of Pediatrics

, Volume 10, Issue 3, pp 238–244 | Cite as

Congenital duodenal obstruction in neonates: a decade’s experience from one center

  • Qing-Jiang Chen
  • Zhi-Gang Gao
  • Jin-Fa Tou
  • Yun-Zhong Qian
  • Min-Ju Li
  • Qi-Xing Xiong
  • Qiang Shu
Original Article



Congenital duodenal obstruction (CDO) is one of the most common anomalies in newborns, and accounting for nearly half of all cases of neonatal intestinal obstruction. This study aimed to review our single-center experience in managing congenital duodenal obstruction while evaluate the outcomes.


We conducted a retrospective analysis of the records of all neonates dianogsed with congenital duodenal obstruction admitted to our center between January 2003 and December 2012. We analyzed demographic criteria, clinical manifestations, associated anomalies, radiologic findings, surgical methods, postoperative complications, and final outcomes.


The study comprised 287 newborns (193 boys and 94 girls). Birth weight ranged from 950 g to 4850 g. Fifty-three patients were born prematurely between 28 and 36 weeks’ gestation. Malrotation was diagnosed in 174 patients, annular pancreas in 66, duodenal web in 55, duodenal atresia or stenosis in 9, preduodenal portal vein in 2, and congenital band compression in 1. Twenty patients had various combinations of these conditions. Presenting symptoms included bilious vomiting, dehydration, and weight loss. X-rays of the upper abdomen demonstrated the presence of a typical double-bubble sign or air-fluid levels in 68.64% of patients, and confirmatory upper and/or lower gastrointestinal contrast studies were obtained in 64.11%. Multiple associated abnormalities were observed in 50.52% of the patients. Various surgical approaches were used, including Ladd’s procedure, duodenoplasty, duodenoduodenostomy, duodenojejunostomy, or a combination of these. Seventeen patients died postoperatively and 14 required re-operation.


Congenital duodenal obstruction is a complex entity with various etiologies and often includes multiple concomitant disorders. Timely diagnosis and aggressive surgery are key to improving prognosis. Care should be taken to address all of the causes of duodenal obstruction and/or associated alimentary tract anomalies during surgery.

Key words

congenital duodenal obstruction neonate 


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Copyright information

© Children's Hospital, Zhejiang University School of Medicine and Springer-Verlag Berlin Heidelberg 2014

Authors and Affiliations

  • Qing-Jiang Chen
    • 1
  • Zhi-Gang Gao
    • 1
  • Jin-Fa Tou
    • 1
  • Yun-Zhong Qian
    • 1
  • Min-Ju Li
    • 1
  • Qi-Xing Xiong
    • 1
  • Qiang Shu
    • 2
    • 3
  1. 1.Department of Pediatric General Surgery, Children’s HospitalZhejiang University Shool of MedicineHangzhouChina
  2. 2.Department of Pediatric Thoracic Surgery, Children’s HospitalZhejiang University Shool of MedicineHangzhouChina
  3. 3.Department of Pediatric Thoracic Surgery, Children’s HospitalZhejiang University Shool of MedicineHangzhouChina

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