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# Calcium Acetate
## Overview
Calcium acetate is a phosphate binder used to reduce serum phosphorus levels in patients with hyperphosphatemia, typically associated with chronic kidney disease (CKD).
## Primary Indications
* Hyperphosphatemia in patients with end-stage renal disease (ESRD) on dialysis.
## Adult Dosing
* **Dosage:** Typically initiated at 2 tablets (667 mg elemental calcium per tablet) orally three times daily with meals.
* **Titration:** Dose is adjusted based on serum phosphorus levels. May be increased up to 4 tablets orally three times daily with meals.
* **Maximum Dose:** Not to exceed 12 tablets (4000 mg elemental calcium) per day.
## Pediatric Dosing
* Data is limited. Dosing should be individualized under specialist guidance. Some sources suggest 1.25 to 2.5 g/m²/day divided into 3-4 doses with meals, adjusted based on response.
## Dose Adjustments
* **Renal Impairment:** Dose should be carefully adjusted based on serum phosphorus and calcium levels.
## Contraindications
* Hypercalcemia.
* Hypersensitivity to calcium acetate.
* Ventricular fibrillation.
## Adverse Effects
* **Common:** Hypercalcemia (manifesting as nausea, vomiting, constipation, abdominal pain, anorexia, thirst, polyuria, confusion, lethargy, bone pain, kidney stones).
* **Less Common:** Cardiac arrhythmias.
## Key Drug Interactions
* **Tetracyclines and Fluoroquinolones:** Calcium acetate can decrease the absorption of these antibiotics. Administer at least 2 hours before or 6 hours after calcium acetate.
* **Digoxin:** Concurrent use with calcium acetate can increase the risk of digoxin toxicity due to hypercalcemia.
* **Thiazide Diuretics:** May increase the absorption of calcium and potentiate hypercalcemia.
* **Vitamin D Analogs:** May increase the risk of hypercalcemia.
## Monitoring
* Serum phosphorus levels (target typically < 5.5 mg/dL).
* Serum calcium levels (monitor for hypercalcemia).
* BUN and creatinine.
* Serum magnesium and alkaline phosphatase.
## Clinical Pearls
* Must be taken with meals to effectively bind dietary phosphorus.
* Monitor calcium-x-phosphate product to avoid extraskeletal calcification. Target typically < 55 mg²/dL².
* Consider dose reduction or discontinuation if hypercalcemia occurs.
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*Disclaimer: This information is intended for healthcare professionals. Always consult the most current prescribing information and relevant clinical guidelines before making treatment decisions.*