Contraindications for Aldactone (Spironolactone)
Aldactone (spironolactone) is absolutely contraindicated in patients with hyperkalemia, Addison's disease, and those taking eplerenone concurrently. 1
Absolute Contraindications
- Hyperkalemia (serum potassium >5.0 mEq/L) 2, 1
- Addison's disease 1
- Concurrent use of eplerenone (another aldosterone antagonist) 1
- Severe renal dysfunction:
- Serum creatinine >2.5 mg/dL in men
- Serum creatinine >2.0 mg/dL in women
- eGFR <30 mL/min/1.73 m² 2
Relative Contraindications and Caution Required
Medication Combinations with High Risk
- Concomitant use of potassium supplements 2
- Concomitant use of other potassium-sparing diuretics 2
- Combined use of ACE inhibitors AND ARBs with spironolactone (triple therapy) 2
- High-dose ACE inhibitors (e.g., captopril ≥75 mg daily; enalapril or lisinopril ≥10 mg daily) 2
- Potent CYP3A4 inhibitors 2
- NSAIDs and COX-2 inhibitors (increase risk of hyperkalemia and renal dysfunction) 2
High-Risk Patient Populations
- Elderly patients (particularly those >75 years) 3, 4
- Diabetes mellitus 2, 3
- Liver disorders 2
- Patients at risk for dehydration 3
- Worsening heart failure 3
- Patients with LVEF <20% (require extra monitoring) 4
Monitoring Requirements
Before Initiation
- Check renal function and serum electrolytes 2
- Ensure serum potassium <5.0 mEq/L 2
- Ensure serum creatinine ≤2.5 mg/dL in men or ≤2.0 mg/dL in women 2
- Ensure eGFR >30 mL/min/1.73 m² 2
After Initiation
- Recheck renal function and serum electrolytes at:
- More frequent monitoring for high-risk patients 4
Management of Complications
Hyperkalemia
- If K⁺ rises to >5.5 mmol/L: Halve dose (e.g., to 25 mg on alternate days) 2
- If K⁺ rises to ≥6.0 mmol/L: Stop spironolactone immediately 2, 3
Worsening Renal Function
- If creatinine rises to >220 μmol/L (2.5 mg/dL): Halve dose 2
- If creatinine rises to >310 μmol/L (3.5 mg/dL): Stop spironolactone immediately 2
Other Side Effects
Practical Prescribing Points
- Starting dose should be 12.5-25 mg daily 2
- For patients with concerns about hyperkalemia or marginal renal function (eGFR 30-49 mL/min/1.73 m²), consider every-other-day dosing 2
- Discontinue potassium supplementation when starting spironolactone 2, 4
- Daily doses exceeding 25 mg significantly increase hyperkalemia risk 3, 6
- Monitor body weight changes closely as they may indicate fluid status changes 4
Common Pitfalls to Avoid
- Failing to discontinue potassium supplements when initiating spironolactone
- Not monitoring renal function and electrolytes frequently enough in high-risk patients
- Using doses >25 mg daily in elderly patients or those with compromised renal function
- Combining with ACE inhibitors and ARBs simultaneously
- Not recognizing early signs of hyperkalemia or renal dysfunction
The risk-benefit ratio of spironolactone must be carefully considered, particularly in elderly patients and those with multiple comorbidities, as real-world studies show significantly higher rates of hyperkalemia and renal dysfunction than reported in clinical trials 4.