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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:


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:


Clinical Use

HFrEF:

Post-MI LV Dysfunction:

  • Reduces mortality
  • Reduces sudden cardiac death

Resistant Hypertension:


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

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

cardio/hf/eplerenone.1770946168.txt.gz · Last modified: by andrew2393cns