Neonatal Duodenal Obstruction: A 15-Year Experience


  • Kamal Nain Rattan PGIMS, Rohtak, Haryana, India 124001
  • Jasbir Singh PGIMS, Rohtak, Haryana, India 124001
  • Poonam Dalal PGIMS, Rohatk, Haryana, India 124001



Duodenal atresia, Annular pancreas, Duodenal obstruction, Malrotation, Neonate


Background: Congenital duodenal obstruction is one of the commonest causes of neonatal intestinal obstruction. We are presenting our 15-year experience by analyzing clinical spectrum and outcome in neonates with duodenal obstruction admitted at our center.

Material and Methods: The hospital records of all neonates admitted with duodenal obstruction from June 2000 to June 2015 were reviewed. The patient records were analyzed for antenatal diagnosis, age, sex, clinical presentation, diagnosis, associated anomalies, surgical procedures performed; postoperative morbidity and mortality. We excluded from our study malrotation of gut associated with congenital diaphragmatic hernia and abdominal wall defects.

Results: A total of 81 patients were admitted, out of which 56 were males and 25 were females. Polyhydramnios was detected in 24 (30%) pregnancies. Average birth weight was 2.1±1.0Kg and average gestational age was 38 (SD±1) weeks with 17 (21%) preterm neonates. Presenting features were vomiting in 81(100%) which was bilious in 81% and non bilious in 19%, epigastric fullness in 56 (69%) and dehydration in 18 (22%) and failure to thrive in 16 (19%). Most common cause of obstruction was duodenal atresia in 38 (46.9%), followed by malrotation of gut in 33 (40.7%), and annular pancreas in 4 cases. Depending upon site of location, infra-ampullary obstruction was the most common in 64 (79%), supra-ampullary in 9 (7.4%) and ampullary 8 neonates. Both duodenal atresia and malrotation of gut was present in 4 cases. X-ray abdomen was most commonly used investigation to confirm the diagnosis. All cases were managed surgically by open laparotomy. Eleven (13.5%) patients died due to sepsis and associated congenital anomalies.

Conclusion: Congenital duodenal obstruction most commonly presents in early neonatal period with features of upper GIT obstruction like vomiting and epigastrium fullness as in our series. Early antenatal diagnosis and surgical interventions hold the key in achieving good outcome. Associated congenital anomalies, prematurity, sepsis and delayed presentation are the main risk factors for post-operative mortality and morbidity.


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Author Biographies

Kamal Nain Rattan, PGIMS, Rohtak, Haryana, India 124001

Senior Professor and Head, Department of Pediatric Surgery, PGIMS, Rohtak, Haryana India 124001

Jasbir Singh, PGIMS, Rohtak, Haryana, India 124001

Senior Resident, Department of Pediatrics, PGIMS Rohtak, Haryana, India 124001

Poonam Dalal, PGIMS, Rohatk, Haryana, India 124001

Associate Professor, Department of Pediatrics, PGIMS, Rohtak, Haryana, India 124001




How to Cite

Rattan KN, Singh J, Dalal P. Neonatal Duodenal Obstruction: A 15-Year Experience. J Neonatal Surg [Internet]. 2016Apr.2 [cited 2022Jan.22];5(2):13. Available from:

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