calcium acetate

Brand: PhosLo, Eliphos

Prototype: sevelamer
Drug Class: phosphate binder
Drug Family: electrolyte agent
Subclass: calcium-based phosphate binder
Organ Systems: renal

Mechanism of Action

Dissociates in the GI tract to release calcium ions that bind dietary phosphate to form insoluble calcium phosphate complexes; these complexes are not absorbed and are excreted in feces, reducing phosphate absorption and lowering serum phosphate in patients with chronic kidney disease.

dietary phosphate (GI lumen)

Indications

  • hyperphosphatemia in end-stage renal disease (dialysis patients)

Contraindications

  • hypercalcemia
  • hypersensitivity to calcium salts
  • renal calculi (calcium-based)

Adverse Effects

Common

  • hypercalcemia
  • nausea
  • constipation
  • pruritus

Serious

  • vascular calcification (from hypercalcemia)
  • adynamic bone disease
  • milk-alkali syndrome

Pharmacokinetics (ADME)

Absorption approximately 40% of calcium absorbed systemically when taken with meals; phosphate binding occurs in GI lumen
Distribution calcium distributes widely; major component of bone
Metabolism not applicable for phosphate-binding function
Excretion unabsorbed calcium-phosphate complexes excreted in feces
Half-life N/A
Onset phosphate lowering within 1 week of consistent use
Peak N/A
Duration effect depends on consistent administration with meals
Protein Binding N/A
Vd N/A

Drug Interactions

Drug / Agent Mechanism Severity
fluoroquinolones and tetracyclines calcium chelates these antibiotics, reducing their absorption; separate by at least 2 hours moderate
levothyroxine calcium reduces thyroid hormone absorption; separate by 4 hours moderate
iron supplements calcium decreases iron absorption; separate by 2 hours moderate
digoxin hypercalcemia potentiates digoxin toxicity major

Nursing Considerations

  1. Administer with each meal (not before or after) to maximize phosphate binding in the GI lumen; the dose must be individualized based on the serum phosphate level and dietary phosphate intake.
  2. Monitor serum calcium, phosphate, and intact PTH regularly; if serum calcium exceeds 10.5 mg/dL, reduce dose or switch to a non-calcium-based binder to prevent vascular calcification.
  3. Counsel dialysis patients about the risk of hypercalcemia from calcium-based binders, particularly when also receiving calcitriol or other vitamin D analogs that increase calcium absorption.
  4. Educate patients to take other oral medications at least 2 hours before or after calcium acetate to prevent chelation-based absorption interactions, particularly fluoroquinolones and levothyroxine.

Clinical Pearls

  • Calcium acetate contains twice the elemental calcium per gram as calcium carbonate but is less soluble at higher pH values — in the alkaline environment of the small intestine, calcium acetate may be more effective at phosphate binding than calcium carbonate.
  • Guidelines (KDIGO) recommend limiting calcium-based phosphate binders due to concerns about positive calcium balance and vascular calcification; non-calcium binders (sevelamer, lanthanum) are preferred when hypercalcemia is present or calcium load is a concern.

Safety Profile

Pregnancy generally-safe
Lactation safe
Renal Adjustment Not required
Hepatic Adjustment Not required
TDM Not required

Concordance Terms

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