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Tuesday, September 16, 2025

Aluminum Toxicity


Aluminum Toxicity – Treatment Overview

Introduction
Aluminum toxicity is a clinical condition caused by excess accumulation of aluminum in the body, most often in patients with chronic kidney disease (CKD) exposed to aluminum-containing phosphate binders, contaminated dialysate, or parenteral nutrition. It can also occur with excessive occupational exposure. Clinical features include:

  • Skeletal: Osteomalacia, bone pain, fractures.

  • Neurological: Encephalopathy, speech disorders, seizures, dementia-like symptoms.

  • Hematological: Microcytic anemia resistant to iron therapy.

Management involves removal of the source of aluminum exposure, chelation therapy, and supportive care.


Treatment Options and Doses

1. Elimination of Aluminum Exposure

  • Stop aluminum-containing medications (e.g., aluminum hydroxide antacids, phosphate binders).

  • Use non-aluminum phosphate binders (e.g., sevelamer, lanthanum, calcium carbonate).

  • Ensure dialysis fluid is free of aluminum contamination.


2. Chelation Therapy

  • Deferoxamine (DFO) – the primary chelating agent.

    • Dose: 5 mg/kg IV once weekly (infused slowly over 1–2 hours after dialysis in hemodialysis patients).

    • Mechanism: Binds aluminum to form aluminoxamine, which is excreted by the kidneys or removed by dialysis.

    • Used in symptomatic patients or those with elevated serum aluminum levels.


3. Dialysis Support

  • Adequate and high-flux hemodialysis to enhance aluminum clearance, especially after deferoxamine infusion.


4. Symptomatic and Supportive Management

  • Bone disease: Vitamin D supplementation (e.g., calcitriol), phosphate control, fracture management.

  • Neurological complications: Seizure control (e.g., levetiracetam, valproate) if required.

  • Anemia: Erythropoietin-stimulating agents (ESAs) may improve response after reducing aluminum load.


Monitoring

  • Serum aluminum levels: Elevated if >60 µg/L; toxic if >200 µg/L.

  • Bone biopsy: May be considered in cases of suspected aluminum-related osteomalacia.

  • Clinical monitoring: Neurological status, bone health, hemoglobin response to ESA therapy.




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