Intestinal Obstruction

Descriptive text is not available for this imageBASICS

DESCRIPTION

  • Intestinal obstruction is a blockage that keeps liquids, food, and other contents from passing through the small and large intestine.
    • May be partial or complete, constant or intermittent, mechanical or nonmechanical (functional)
    • May arise from intrinsic abnormalities (duodenal or intestinal atresia, duplication) or intraluminal (e.g., meconium ileus, meconium plug syndrome)
    • May arise from extrinsic factors (e.g., adhesions, bands, volvulus, or incarcerated hernia)
    • May also be caused by dysmotility of the gastrointestinal (GI) tract (i.e., hypomotility or paralysis of the intestine) secondary to a developmental disorder of the neuro enteric system (Hirschsprung disease) or more diffused neuromotor dysmotility (intestinal pseudoobstruction)
    • Most commonly involves the small bowel
  • If untreated, obstruction can lead to intestinal ischemia and becomes a life-threatening situation.

EPIDEMIOLOGY

  • Intestinal obstruction occurs in approximately 1 in 2,000 births.
  • Intestinal obstruction accounts for >15% admissions for abdominal pain from the emergency department.

ETIOLOGY

May be congenital (e.g., atresia, duplication, malrotation), acquired (e.g., neoplastic, inflammatory), or iatrogenic (e.g., adhesions, radiation stricture); etiology varies by age:

  • Neonates
    • Intestinal atresia (most common cause in neonates)
    • Obstructive meconium disorders (associated or not with cystic fibrosis)
      • Meconium ileus
      • Meconium plug syndrome
      • Meconium peritonitis
    • Duodenal atresia (high prevalence associated with Down syndrome)
    • Annular pancreas
    • Anorectal malformation/imperforate anus
    • Malrotation
    • Hirschsprung disease (Down syndrome)/small left colon (diabetic mothers)
  • Infants
    • Pyloric stenosis (age: 1 to 2 months)
    • Intussusception (age: 2 months to 3 years)
    • Postoperative adhesions
    • Incarcerated inguinal hernia
    • Hirschsprung disease
    • Duplications
    • Meckel diverticulum
  • Older children
    • Postoperative or postinfectious intestinal adhesions (e.g., perforated appendicitis)
    • Inflammatory bowel disease (IBD)
    • Malrotation with or without midgut volvulus
    • Annular pancreas
    • Meckel diverticulum
    • Superior mesenteric artery syndrome
    • Corrosive injury
    • Foreign body ingestion
    • Juvenile polyposis and related syndromes
    • Distal intestinal obstruction syndrome (cystic fibrosis)
    • Roundworm (Ascaris lumbricoides)
    • Gastric and intestinal bezoars
    • Colonic volvulus secondary to aerophagia and constipation (more common in neurodevelopmentally impaired)
    • Cancer-related intestinal obstruction and radiotherapy-induced adhesions

PATHOPHYSIOLOGY

  • Pathophysiology depends on the mechanism of the obstruction.
  • Mechanical obstruction
    • Intestinal dilation proximal to site of obstruction as the bowel fills with intestinal contents and air secondary to bacterial overgrowth proximal to the obstruction
    • Buildup of intestinal contents results in further distention, nausea, and vomiting.
    • Internal and external losses result in hypovolemia, oliguria, and azotemia.
    • Bacteria proliferate in the small bowel and its contents can become feculent.
    • “Closed loop” obstruction occurs when contents cannot get in or out of an intestinal segment.
  • Ischemic obstruction
    • Occurs secondary to occlusion of intestinal blood supply
    • Causes
      • Twisting/kink of feeding blood vessels like in volvulus
      • Increased intramural pressure in the setting of bowel distention can result in decreased perfusion to the affected area.
      • Both occur in incarcerated hernia.
    • With progression, gangrene, peritonitis, and perforation may occur.
    • Damage to the normal gut barrier may enable bacteria, bacterial toxins, and inflammatory mediators to enter the circulation, causing sepsis.
  • Functional obstruction (paralytic ileus)
    • Failure of intestinal motor function without mechanical obstruction
      • Congenital disorders like Hirschsprung disease and intestinal pseudoobstruction
      • Postoperative ileus
      • Other causes: infection (pneumonia, gastroenteritis, urinary tract infection, peritonitis, systemic sepsis), drugs (e.g., opiates, loperamide, vincristine), metabolic abnormalities (hypokalemia, hypomagnesemia, uremia, myxedema, and diabetic ketoacidosis)
      • Maternal substance abuse during pregnancy

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