Iron toxicity: Difference between revisions

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==Differential Diagnosis==


==Diagnosis==
==Diagnosis==
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If unable to obtain a serum iron level a glucose > 150 mg/dL and leukocyte count above 15000 is 100% specific and 50% sensitive in predicint=g levels > 300mcg/mL<ref>Lacouture PG et al. Emergency assessment of severity in iron overdose by clinical and laboratory methods. J Pediatr 1981; 99:89-91.</ref>
If unable to obtain a serum iron level a glucose > 150 mg/dL and leukocyte count above 15000 is 100% specific and 50% sensitive in predicint=g levels > 300mcg/mL<ref>Lacouture PG et al. Emergency assessment of severity in iron overdose by clinical and laboratory methods. J Pediatr 1981; 99:89-91.</ref>
==Management==
==Management==
===Observation x 6 hrs===
===Observation x 6 hrs===

Revision as of 14:24, 25 August 2015

Background

  • Toxicity determined by mg/kg of elemental iron
  • Total amount of elemental iron ingested can calculated by multiplying the estimated number of tablets by the percentages of iron in the tablet preparation
  • Clinical severity is based approximated by elemental dose per kilograms:[1]
Mild: 10-20mg/kg
Moderate 20-60mg/kg
Severe >60mg/kg
  • Absence of GI symptoms w/in 6hr of ingestion excludes significant iron ingestion
  • Significant iron toxicity can result in a severe lactic acidosis from hypopefusion due to volume loss, vasodilation and negative inotropin effects.

Elemental Iron Percentages

Elemental Iron Percentages

Iron Preparation % of Elemental Iron
Ferrous Fumarate 33%
Ferrous Sulfate 20%
Ferrous Gluconate 12%
Ferric pyrophosphate 30%
Ferroglycine sulfate 16%
Ferrous carbonate (anhydrous) 38%

Pathophysiology

  • Direct caustic injury to gastric mucosa[2]
    • Causing vomitting, diarrhea, abdominal pain, and bleeding
  • Impaired cellular metabolism
    • Inhibiting the electron transport chain causes lactic acidosis
    • Direct hepatic, CNS, and cardiac toxicity
    • Cell membrane injury from lipid peroxidation[3]
  • Increased capillary permeability
    • Hypotension
    • Venodilation
  • Portal vein iron delivery to liver
    • Hepatotoxicity
  • Thrombin formation inhibition
    • Coagulopathy - direct effect on vitamin K clotting factors

Clinical Features

Iron Toxicity Stages
Stage Clinical Effect Time Frame
Stage 1 GI irritation: n/v, abd pain, diarrhea 30-60 mins
Stage 2: latent reduced GI symptoms 6-24 hours
Stage 3: shock and metabolic acidosis metabolic acidosis, lactic acidosis, dehydration, coags, renal failure 6-72 hours
Stage 4: hepatotox hepatic failure 12-96 hours
Stage 5: bowel obstruction GI bowel scarring/healing 2-8 weeks

Differential Diagnosis

Diagnosis

Work-Up

  • CBC
  • Chemistry
    • Anion gap metabolic acidosis
    • Hyperglycemia
  • Coags
  • LFTs
  • Iron levels
  • UA
    • Used to follow efficacy of Fe chelation (urine changes from rusty color to clear)
  • Type and Screen
  • In ambiguous cases consider abd xray as most Fe tabs are radioopague

Serum Iron Concentration

Serum Iron concentration can guide treatment but are not absolute in predicting or excluding toxicity: Peak serum iron level:

  • <300 mcg/dL: nontoxic or mild
  • 300-500 mcg/dL: Significant GI symptoms and potential for systemic toxicity
  • >500 mcg/dL: Moderate to severe systemic toxicity
  • >1000 mcg/dL: severe systemic toxicity and increased morbidity

If unable to obtain a serum iron level a glucose > 150 mg/dL and leukocyte count above 15000 is 100% specific and 50% sensitive in predicint=g levels > 300mcg/mL[4]

Management

Observation x 6 hrs

  • Patients with asymptomatic ingestion of <20mg/kg only require observation x 6hr
  • Volume resuscitation

GI decontamination

  • Consider only for large overdose with visible pills in the stomach on x-ray
  • Whole-bowel irrigation (polyethylene glycol) will promote increased gastric emptying and avoid large bezoar formation[5]

Polyethylene glycol dosing

Can be given orally or by NG tube

  • 20-40 mL/kg/hr in young children
  • 2L/hr in adults

Continue irrigation until the rectal effluent is clear

Deferoxamine

Deferoxamine chelates iron and creates a water-soluble compound ferrioxamine that is renally excreted and can be dialyzed.[1]

Indications

  • Systemic toxicity and iron level > 350 mcg/dL
  • Metabolic acidosis
  • Progressive symptoms
  • Serum iron level >500 mcg/dL

Dosing

  • 1000mg IV; start at 5mg/kg/hr, increase up to 15mg/kg/hr as tolerated for up to 24hrs
  • Subsequent doses are 500mg increments guided by clinical status of pt / urine color
  • Recommended amount during first 24hr is 360mg/kg not to exceed 6g.

Adverse effects

Contraindications

  • Renal failure patients not on hemodialysis

Hemodialysis

  • Not effective in removing iron due to large volumes of distribution
  • Dialysis can removes deferoxamine-iron complex in renal failure patients

Exchange Transfusion

  • Minimal evidence but has been described in larger overdoses[7]

Orogastric lavage

  • Does not remove large numbers of pills and may have serious adverse events

Activated charcoal

  • Does not bind iron

Disposition

  • Discharge after 6hr obs for asymptomatic (or only vomited 1-2x) AND ingestion <20mg/kg
  • Admit to ICU if deferoxamine required
  • Psychiatric evaluation if intentional ingestion

See Also

Toxidromes

References

  1. 1.0 1.1 Robotham JL, Lietman PS: Acute iron poisoning. A review. Am J Dis Child 1980; 134:875-879.
  2. Robotham JL, Lietman PS. Acute iron poisoning. A review. Am J Dis Child 1980; 134:875-879.
  3. Aisen P et al. Iron toxicosis. Int Rev Exp Pathol 1990. 31:1-46.
  4. Lacouture PG et al. Emergency assessment of severity in iron overdose by clinical and laboratory methods. J Pediatr 1981; 99:89-91.
  5. Position paper: Whole bowel irrigation. J Toxicol Clin Toxicol 2004; 42:843-854.
  6. Mazzoleni G. et al. Yersinia enterocolitica infection with ileal perforation associated with iron overload and deferoxamine therapy. Dig Dis Sci 1991; 36:1154-1160.
  7. Movassaghi N. et al. Comparison of exchange transfusion and deferoxamine in the treatment of acute iron poisoning. J Pediatr 1969; 75:604-608.