Can a patient with idiopathic hyperaldosteronism (IH) taking spironolactone (aldactone) be switched directly to eplerenone (inspra) without stopping spironolactone for a few days?

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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

References

Guideline

Conversion of Eplerenone to Spironolactone

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Primary aldosteronism - treatment options.

Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society, 2003

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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