Iron Poisoning

Descriptive text is not available for this imageBASICS

DESCRIPTION

  • Iron toxicity depends on the amount of elemental iron ingested, although tolerable and lethal concentrations can vary between people.
  • Doses of elemental iron:
    • <20 mg/kg are generally not symptomatic.
    • 20 to 60 mg/kg are variably symptomatic.
    • >60 mg/kg are severely toxic and potentially fatal.
  • In 2020, a 14-month-old child died due to iron toxicity after ingestion of ferrous sulfate tablets with a reported level of >2,000 mcg/dL.

EPIDEMIOLOGY

  • Pediatric iron exposures are decreasing, likely due to increased awareness and public health efforts; however, iron exposures can be toxic, and poisoning fatalities continue to occur.
  • Iron ingestions can be divided into unintentional exposures (generally in younger children) and intentional exposures (more common in adolescents).
  • Incidence: >9,000 iron exposures per year in children <6 years old in the United States (2020)
  • Many factors contribute to the incidence of iron ingestion:
    • Adult multivitamins contain more iron than children’s chewable vitamins.
    • Prenatal vitamins contain the highest amount of elemental iron per tablet—up to 100 mg.
    • Vitamins and iron tablets can be colorful and resemble candy, making them appealing to young children.
    • Caregivers often fail to appreciate the danger of overdose from vitamins with iron and pure iron preparations.
  • Overall exposures and deaths from iron toxicity have downtrended in the pediatric age range.

RISK FACTORS

  • Birth of a sibling: up to 1 year after birth, due to increased availability of prenatal vitamins
  • Age: Among unintentional ingestion, almost all serious mortality and morbidity are in children <5 years of age with ingestion of adult iron formulations.

GENERAL PREVENTION

  • Parental education: Keep all medications and vitamins away and out of reach, in child-resistant packaging.
  • In 1997, federal regulations required unit-dose packaging (blister packs) for all iron preparations with >30 mg of elemental iron per dose.
  • The U.S. Food and Drug Administration (FDA) removed regulations in 2003, although many manufacturers voluntarily continue this type of packaging.

PATHOPHYSIOLOGY

  • Iron directly damages cells, interfering with aerobic respiration.
  • The primary systems affected by iron are the gastrointestinal (GI) tract, including the liver, and the cardiovascular system.
  • There are five stages of iron poisoning:
    • Stage I (GI phase)
      • Occurs up to 6 hours postingestion
      • Characterized by GI mucosal injury, leading to abdominal pain, vomiting, diarrhea, and GI bleeding (hematemesis or hematochezia)
      • Metabolic acidosis may be present, and death may be caused by capillary leakage and hypovolemic shock.
    • Stage II (latent)
      • 6 to 24 hours after ingestion
      • Relative stability and temporary resolution of GI symptoms
      • Although there may be improvement of symptoms, there is continued cellular toxicity and metabolic acidosis.
    • Stage III (shock)
      • 12 to 24 hours after ingestion (can occur earlier with high-dose ingestions)
      • Systemic symptoms: hemodynamic instability, shock, metabolic acidosis
      • Coagulopathy is common and worsens GI bleeding (can occur even without hepatotoxicity).
      • Vasodilation can lead to hypovolemia, and myocardial injury can lead to cardiogenic shock.
    • Stage IV (hepatotoxicity)
      • Within 48 hours after ingestion
      • May result in liver failure
    • Stage V (late)
      • 2 to 8 weeks postingestion
      • Gastric injury may result in strictures, leading to vomiting and potentially gastric outlet obstruction.
  • Not all patients will present with every stage, and timing of each stage can vary between patients.

There's more to see -- the rest of this topic is available only to subscribers.