Drug Guide

Generic Name

Potassium Citrate

Brand Names Urocit-K

Classification

Therapeutic: Electrolyte Supplement, Urinary Alkalinizer

Pharmacological: Potassium Salt of Citrate

FDA Approved Indications

  • Prevention and treatment of kidney stones (urolithiasis) caused by or associated with hypocitraturia
  • Metabolic acidosis (off-label use)

Mechanism of Action

Potassium citrate acts as a urinary alkalinizer by increasing urinary pH and citrate levels, which can bind calcium and reduce calcium stone formation. It also replenishes potassium in cases of deficiency.

Dosage and Administration

Adult: Typically, 15 to 30 mEq of potassium citrate two to four times daily, adjusted according to patient response and serum potassium levels.

Pediatric: Dosing varies based on age and weight; usually, 0.3 to 0.5 mEq/kg per dose, given 2-4 times daily, with close monitoring.

Geriatric: Use with caution; monitor serum potassium and renal function due to risk of hyperkalemia and renal impairment.

Renal Impairment: Adjust dose; use with caution as impaired renal function increases risk of hyperkalemia.

Hepatic Impairment: No specific adjustment required.

Pharmacokinetics

Absorption: Rapidly absorbed from the gastrointestinal tract.

Distribution: Distributed widely in total body water, predominantly in the extracellular fluid.

Metabolism: Not metabolized; excreted unchanged.

Excretion: Excreted by the kidneys. Kidney function affects elimination.

Half Life: Variable; approximately 1-3 hours, depending on urinary pH and renal function.

Contraindications

  • Hyperkalemia
  • Renal impairment or urinary tract obstructions
  • Signs of adrenal insufficiency

Precautions

  • Regular monitoring of serum potassium and renal function recommended; caution in patients with cardiac disease, adrenal insufficiency, or conditions predisposing to hyperkalemia. Use during pregnancy and lactation should be under medical supervision.

Adverse Reactions - Common

  • Hyperkalemia (Less common but serious if unmonitored)
  • Gastrointestinal discomfort (nausea, diarrhea) (Common)

Adverse Reactions - Serious

  • Arrhythmias due to hyperkalemia (Rare)
  • Metabolic disturbances (hypernatremia, hypokalemia if imbalance occurs) (Rare)

Drug-Drug Interactions

  • Potassium-sparing diuretics, ACE inhibitors, ARBs increase risk of hyperkalemia.
  • NSAIDs may impair renal function and potassium excretion.

Drug-Food Interactions

N/A

Drug-Herb Interactions

N/A

Nursing Implications

Assessment: Monitor serum electrolytes, renal function, and cardiac status.

Diagnoses:

  • Risk for electrolyte imbalance
  • Risk for cardiac arrhythmias

Implementation: Administer with food if gastrointestinal upset occurs; ensure adequate hydration; monitor for signs of hyperkalemia.

Evaluation: Serum potassium levels within acceptable range; patient's symptoms and cardiac rhythm remain stable.

Patient/Family Teaching

  • Take medication exactly as prescribed.
  • Report symptoms of hyperkalemia such as muscle weakness, irregular heartbeat, or numbness.
  • Maintain hydration and dietary potassium intake as advised.
  • Avoid excessive use of potassium-containing salt substitutes.

Special Considerations

Black Box Warnings:

  • Risk of severe hyperkalemia, which can be life-threatening.

Genetic Factors: N/A

Lab Test Interference: May elevate serum bicarbonate and potassium levels, affecting blood chemistry results.

Overdose Management

Signs/Symptoms: Hyperkalemia: muscle weakness, paresthesia, arrhythmia.

Treatment: Discontinue potassium source, administer calcium gluconate for cardiac stabilization, use sodium bicarbonate, glucose and insulin, or dialysis in severe cases.

Storage and Handling

Storage: Store at room temperature, away from moisture and heat.

Stability: Stable under recommended storage conditions.

This guide is for educational purposes only and is not intended for clinical use.