Duodenal atresia
Revision as of 11:47, 7 February 2016 by Rossdonaldson1 (talk | contribs) (→Differential Diagnosis)
Background
- During weeks 6 and 7 of gestation, the GI tract becomes occluded then recanalizes during weeks 8 to 10
- Duodenal atresia is thought to result from failure of recanalization
Clinical Features
- Often presents with gastric distension and vomiting
- Often associated with other malformations such as biliary atresia or gallbladder agenesis
- May also be associated with cardiac, renal, or vertebral abnormalities
- About a quarter of patients born with duodenal atresia have Downs syndrome
Differential Diagnosis
- Malrotation with volvulus
- Hirschsprung disease
- Meconium ileus
- Intestinal atresia
Pediatric Abdominal Pain
0–3 Months Old
- Emergent
- Nonemergent
3 mo–3 y old
- Emergent
- Nonemergent
3 y old–adolescence
- Emergent
- Nonemergent
Diagnosis
- Presentation is very early in the postnatal period
- History
- Often includes history of abdominal distention and vomiting
- Obtain hx of whether vomiting is bilious or nonbilious and if vomiting follows feeds
- Physical Exam
- Dry mucus membranes, poor skin turgor, and sunken fontanelle
- Document signs of other congenital anomalies
- The abdomen is often markedly distended with visible or palpable loops of bowel.
- Examine perineum and assess for patency of the anus
Management
- Imaging
- AP, lateral, and cross table XR should be obtained on all infants with concern for obstruction
- Classic double bubble sign due to dilation of the stomach and proximal duodenum
- Absent distal gas
- Treatment
- NPO
- NG tube to suction
- Correct fluid and electrolyte abnormalities
- Ampicillin and gentamicin (to prevent post-op infection)
- Surgery
Disposition
- Admission
References
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