Duodenal atresia

Revision as of 23:17, 4 November 2018 by Kxl328 (talk | contribs) (Clinical Features)

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
  • 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

Clinical Features

Presentation is very early in the postnatal period

History

  • Abdominal distention and bilious emesis within first 24 hours of birth

Physical Exam

  • Dry mucus membranes, poor skin turgor, and sunken fontanelle
  • Signs of other congenital anomalies
  • The abdomen is often markedly distended with visible or palpable loops of bowel
  • NG tube aspirate >20 mL
  • Examine perineum and assess for patency of the anus

Differential Diagnosis

  • Malrotation with volvulus
  • Hirschsprung disease
  • Meconium ileus
  • Intestinal atresia

Nausea and vomiting (newborn)

Newborn '
Obstructive intestinal anomalies
Neurologic
Renal
Infectious
Metabolic/endocrine
Miscellaneous

Evaluation

  • 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

Management

  • NPO
  • NG tube to suction
  • Correct fluid and electrolyte abnormalities
  • Ampicillin and gentamicin (to prevent post-op infection)
  • Surgery

Disposition

  • Admission

References