Calcium disodium EDTA

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Administration

  • Type: Chelating agent
  • Dosage Forms: injection (200 mg/mL)
  • Routes of Administration: IV (preferred), IM (with procaine to reduce pain)
  • Common Trade Names: Calcium Disodium Versenate, CaNa2EDTA

Adult Dosing

Lead poisoning (symptomatic or BLL >70 mcg/dL)

  • 1000-1500 mg/m²/day IV as continuous infusion or divided q6-12h
  • Maximum: 3 g/day (or 50 mg/kg/day if using weight-based dosing)
  • Duration: 5 days; may repeat after 2-4 day drug-free interval if needed
  • For lead encephalopathy: use in combination with dimercaprol (BAL); start BAL 4 hours before CaNa2EDTA

IM dosing (if IV not available)

  • Same dose; mix with 1% procaine to reduce injection pain

Pediatric Dosing

Lead poisoning (BLL ≥45 mcg/dL or symptomatic)

  • 1000-1500 mg/m²/day IV as continuous infusion or divided q6-12h
  • Maximum: 50 mg/kg/day
  • Duration: 5 days; may repeat after 2-4 day drug-free interval
  • For lead encephalopathy: always use with dimercaprol (BAL); start BAL 4 hours before CaNa2EDTA

Special Populations

Pregnancy Rating

  • B

Lactation risk

  • Unknown; use caution

Renal Dosing

  • Adult: Contraindicated in anuria; reduce dose in renal impairment; monitor renal function closely
  • Pediatric: Same as adult

Hepatic Dosing

  • Adult: No specific adjustment
  • Pediatric: No specific adjustment

Contraindications

  • Allergy to class/drug
  • Anuria or severe renal disease
  • Hepatorenal syndrome
  • Active hepatitis

Adverse Reactions

Serious

  • Nephrotoxicity (renal tubular necrosis — dose-dependent; monitor BUN/Cr daily)
  • Severe hypocalcemia (if disodium EDTA used instead — ensure CALCIUM disodium EDTA is used)
  • Cardiac arrhythmias (from electrolyte shifts)
  • Bone marrow suppression

Common

  • Nausea, vomiting
  • Injection site pain (IM)
  • Fever, chills
  • Fatigue, malaise
  • Transient hypotension
  • Zinc depletion (with prolonged courses)

Pharmacology

  • Half-life: 20-60 minutes (IV)
  • Metabolism: Not metabolized
  • Excretion: Renal (>95% excreted as chelate complex within 24 hours)

Mechanism of Action

  • Forms stable, water-soluble chelate complex with divalent and trivalent metals (especially lead)
  • Chelate complex is excreted renally, reducing body lead burden
  • Does not cross the blood-brain barrier significantly (which is why BAL is used concurrently for encephalopathy)

Comments

  • CRITICAL: Ensure CALCIUM disodium EDTA (CaNa2EDTA) is used — NOT disodium EDTA (Na2EDTA), which causes fatal hypocalcemia
  • For lead encephalopathy, always start dimercaprol (BAL) 4 hours before CaNa2EDTA to prevent redistribution of lead into the brain
  • Monitor serum BUN, creatinine, electrolytes, CBC, and urinalysis daily during treatment
  • Adequate hydration is essential but avoid overhydration in encephalopathic patients (risk of cerebral edema)
  • A "provocation test" (single dose followed by urine lead measurement) is no longer recommended
  • Consider succimer (DMSA) as oral alternative for BLL 45-69 mcg/dL without encephalopathy

Indications by Condition

The following table is automatically generated from disease/condition pages across WikEM.


See Also

References

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