Kayexalate (Sodium Polystyrene Sulfonate) for Hyperkalemia Treatment
Kayexalate (sodium polystyrene sulfonate) is indicated for the treatment of hyperkalemia with a standard dose of 15-60g daily, but should not be used as emergency treatment for life-threatening hyperkalemia due to its delayed onset of action. 1
Dosage and Administration
- Oral administration: 15-60g daily, typically given as 15g (four level teaspoons) 1-4 times daily 1
- Rectal administration: 30-50g every six hours 1
- Must be administered at least 3 hours before or 3 hours after other oral medications to prevent drug interactions 2
- Should be prepared fresh and used within 24 hours 2
Mechanism of Action
Sodium polystyrene sulfonate is a cation-exchange resin that works primarily in the distal colon by binding potassium ions in exchange for sodium ions. Each 15g dose contains approximately 1500mg of sodium 2.
Clinical Efficacy
- Reduces serum potassium by approximately 1.04 mEq/L compared to placebo when given as 30g daily for 7 days 2
- Has a delayed onset of action, making it unsuitable for emergency treatment of severe hyperkalemia 1
Position in Hyperkalemia Management Algorithm
For hyperkalemia management, treatment should follow this stepwise approach based on severity:
Severe hyperkalemia (>6.5 mEq/L or with ECG changes):
- Stabilize myocardial cell membrane: Calcium chloride 10% (5-10mL IV) or calcium gluconate 10% (15-30mL IV) over 2-5 minutes 3
- Shift potassium into cells:
- Insulin + glucose: 10U regular insulin with 25g glucose IV over 15-30 minutes
- Nebulized albuterol: 10-20mg over 15 minutes
- Sodium bicarbonate: 50 mEq IV over 5 minutes (if metabolic acidosis present)
- Promote potassium excretion:
- Diuresis: furosemide 40-80mg IV
- Dialysis (most effective for emergency treatment)
- Kayexalate: 15-50g with sorbitol PO or PR 3
Moderate hyperkalemia (5.0-6.5 mEq/L):
Important Warnings and Precautions
- Not for emergency use: Should not be used as emergency treatment for life-threatening hyperkalemia due to delayed onset 1
- Serious adverse events: Associated with intestinal necrosis and other serious gastrointestinal events 2, 4
- Mortality risk: Reports indicate a 20.7% mortality rate in patients experiencing GI adverse events 4
- Contraindications:
- Hypersensitivity to polystyrene sulfonate resins
- Obstructive bowel disease
- Neonates with reduced gut motility 1
Monitoring Requirements
- Measure serum potassium within 1 week of starting treatment
- Monitor more frequently in patients with CKD, heart failure, or diabetes
- Also monitor serum sodium, calcium, and magnesium due to nonselective binding properties 2
- Watch for signs of fluid overload in sodium-sensitive patients 1
Alternative Considerations
- For patients with severe hypertension and hyperkalemia, consider calcium polystyrene sulfonate where available (non-sodium containing alternative) 3
- Newer potassium binders (patiromer or sodium zirconium cyclosilicate) may have better safety profiles for chronic management 3, 2
Common Pitfalls to Avoid
- Concomitant sorbitol: Increases risk of intestinal necrosis 4
- Sodium overload: Each 15g dose contains approximately 1500mg of sodium, which can worsen fluid status in heart failure or hypertensive patients 2
- Drug interactions: Failure to separate administration from other medications by at least 3 hours 1
- Inadequate monitoring: Not checking electrolytes after initiation of therapy 2
By following this structured approach to hyperkalemia management with sodium polystyrene sulfonate, clinicians can effectively reduce potassium levels while minimizing risks associated with this medication.