Definition

  • Disorder of young infants
  • Caused by hypertrophy of the pylorus,
  • Can progress to near-complete obstruction of the gastric outlet
  • Leading to forceful vomiting.

Incidence

  • 1.5-4 per 1000 live births in Caucasians
  • Lower incidence in African and Asian children
  • 85% occurs in males
  • 20% of those affected have a family history of pyloric stenosis
  • Usually occurs between 10 days and 11 weeks old
  • Rare to be before or after that

Pathophysiology

  • Not a congenital abnormality
  • Develops after birth
  • Hypertrophy of the pylorus
    • In the circular muscular layer and mucosa
  • No cause yet found

Presentation

  • Non-bilious vomiting at 2-8 weeks of age,
    • peak between 3-5 weeks
  • Initially vomiting may not be frequent or forceful
    • Eventually progresses to projectile vomiting
  • Examination findings:
    • May be dehydrated
    • Hungry
    • Visible peristalsis in the upper abdomen (gastric contraction)
    • Palpation of pylorus in the epigastrium (the “olive”)

Diagnosis

  • Bloods
    • Often has hypochloraemia, hyponatremia and hypokalaemia
    • Metabloic alkalosis
  • Ultrasound scan
  • Barium swallow if USS not available

Management

  • Rehydration - correction of hypochloraemia and other electrolyte abnormalities prior to surgery
  • Surgery - Ramstedt operation
    • Pyloromyotomy
    • May be done open or laparoscopic
    • Pyloric muscle is split longitudinally down to the mucosa
    • Normal oral feeds can be commenced 24 hours post op