Direct Switch from Spironolactone to Eplerenone
You can switch directly from spironolactone to eplerenone without a washout period, using a 2:1 dose conversion ratio (50 mg eplerenone = 25 mg spironolactone), with mandatory electrolyte and renal function monitoring at 1 and 4 weeks post-switch. 1
Conversion Protocol
Dose Equivalence
- Use a 2:1 conversion ratio: 50 mg eplerenone daily equals 25 mg spironolactone daily 1
- If the patient is on spironolactone 25 mg daily, switch to eplerenone 50 mg daily 1
- If on spironolactone 50 mg daily, switch to eplerenone 100 mg daily 1
- No washout period is required between stopping spironolactone and starting eplerenone 1
Pre-Switch Assessment
Before making the switch, verify the following parameters are acceptable 2:
- Serum potassium ≤5.0 mmol/L (do not switch if >5.0 mmol/L) 1
- Serum creatinine <220 μmol/L (2.5 mg/dL) 2
- eGFR >30 mL/min/1.73 m² (avoid both agents if <30) 1
For patients with eGFR 30-49 mL/min/1.73 m², reduce the starting eplerenone dose to 25 mg daily or every other day 1
Mandatory Monitoring Schedule
The European Society of Cardiology provides explicit monitoring requirements that apply to both drugs 2:
- Check electrolytes and renal function at 1 week post-switch 2
- Recheck at 4 weeks post-switch 2
- Continue monitoring at 1,2,3, and 6 months after achieving stable dose 2
- Then monitor every 6 months thereafter 2
Managing Hyperkalemia After Switch
Both drugs carry similar hyperkalemia risk, though clinical trials showed comparable rates between spironolactone and eplerenone 3:
- If potassium rises to >5.5 mmol/L: Halve the eplerenone dose (e.g., 50 mg to 25 mg, or 25 mg every other day) 2
- If potassium rises to >6.0 mmol/L: Stop eplerenone immediately and monitor closely; specific treatment may be needed 2
Clinical Context for Idiopathic Hyperaldosteronism
In a prospective randomized trial specifically comparing these agents in IHA patients, direct switching was performed successfully 3:
- Two patients developed gynecomastia on spironolactone 400 mg and were switched directly to eplerenone 150 mg daily at week 16 3
- The switch resulted in resolution of gynecomastia while maintaining blood pressure control 3
- Both drugs normalized serum potassium (>3.5 mmol/L) in all IHA patients within 4 weeks 3
- Mild hyperkalemia occurred in 2/17 patients on spironolactone and 3/17 on eplerenone, demonstrating similar risk profiles 3
Key Advantages of Eplerenone
The primary indication for switching from spironolactone to eplerenone is gynecomastia or breast discomfort in men, which occurs in approximately 10% of male patients on spironolactone but is infrequent with eplerenone 2:
- Eplerenone is more selective for the mineralocorticoid receptor, avoiding sex hormone receptor effects 4, 5
- In IHA specifically, eplerenone demonstrated equivalent blood pressure control to spironolactone 3
- Systolic blood pressure decreased more rapidly with eplerenone in the IHA trial 3
Critical Pitfalls to Avoid
- Do not discontinue potassium supplements abruptly without checking baseline potassium first - both drugs are potassium-sparing 1
- Do not combine with both ACE inhibitor AND ARB - this dramatically increases hyperkalemia risk 2
- Do not switch if baseline potassium is already >5.0 mmol/L - address hyperkalemia first 1
- Do not assume eplerenone eliminates hyperkalemia risk - the rates are similar between drugs 3, 6