cardio:hf:eplerenone
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Eplerenone
Eplerenone is a selective Mineralocorticoid Receptor Antagonist (MRA).
It blocks aldosterone at the collecting duct and reduces cardiac remodeling.
Used in:
- Post–myocardial infarction with LV dysfunction
- Resistant Hypertension
Mechanism of Action
Eplerenone selectively antagonizes the mineralocorticoid (aldosterone) receptor.
Aldosterone normally:
- ↑ ENaC expression
- ↑ Sodium reabsorption
- ↑ Potassium secretion
- Promotes myocardial fibrosis and remodeling
Blocking aldosterone results in:
- ↓ Sodium reabsorption
- ↑ Potassium retention
- ↓ Ventricular remodeling
- ↓ Fibrosis
The mortality benefit is due to neurohormonal modulation — not diuresis alone.
Renal Effects
Site:
- Collecting duct
Effects:
- Mild natriuresis
- ↑ Potassium retention
Diuretic strength:
- Weak compared to Loop Diuretics
Clinical Use
HFrEF:
- Mortality reduction
- Added to:
Post-MI LV Dysfunction:
- Reduces mortality
- Reduces sudden cardiac death
Resistant Hypertension:
- Alternative to Spironolactone
Mortality Data
EPHESUS Trial:
- Reduced mortality post-MI with LV dysfunction
EMPHASIS-HF Trial:
- Reduced mortality in mild HFrEF
Benefit driven by:
- Reduced remodeling
- Reduced arrhythmogenic fibrosis
Adverse Effects
Electrolytes:
- Hyperkalemia
- Mild hyponatremia
Compared to Spironolactone:
- Less gynecomastia
- Fewer endocrine effects
- More selective receptor profile
Contraindications
Avoid in:
- Severe renal impairment
- Baseline hyperkalemia
- Concomitant strong CYP3A4 inhibitors
Use caution when combined with:
Monitor:
- Potassium
- Renal function
Eplerenone vs Spironolactone
- Less selective
- Causes gynecomastia
- More commonly used
Eplerenone:
- More selective MRA
- Fewer endocrine side effects
- Preferred post-MI
Clinical Pearls
- Selective MRA
- Reduces mortality in HFrEF
- Reduces mortality post-MI
- Causes hyperkalemia
- Less gynecomastia than spironolactone
- Neurohormonal benefit > diuretic effect
Related
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