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EPHESUS Post-MI Eplerenone Response Score

  • Age (years)
  • Left Ventricular Ejection Fraction (LVEF %, use integer or decimal)
  • Diabetes mellitus
  • Clinical signs/symptoms of heart failure at enrollment (e.g., rales, pulmonary congestion, peripheral edema)
  • Days since index MI (integer)
  • Serum creatinine (mg/dL)
  • Serum potassium (mEq/L)
  • EPHESUS Post-MI Eplerenone Response Score: explanation and clinical context
    This tool implements two things: (1) an objective eligibility check based on the original EPHESUS trial inclusion criteria — specifically enrollment 3–14 days after acute myocardial infarction (MI) with left ventricular ejection fraction (LVEF) ≤40% and either signs/symptoms of heart failure or diabetes — and (2) an exploratory, unvalidated response index that weights several clinical features commonly associated with higher event risk and with observed subgroup/biomarker responses in post-hoc EPHESUS analyses. The original EPHESUS randomized trial demonstrated that initiation of eplerenone (25 mg daily, titrated) in appropriately eligible post-MI patients produced roughly a 15% relative reduction in all-cause mortality compared with placebo. This calculator does not attempt to produce a validated individual absolute mortality estimate; rather, it (A) confirms whether a patient matches the trial population and (B) provides an exploratory point index to help clinicians identify patients whose baseline characteristics resemble higher-risk subgroups that have been associated with larger absolute event rates in published analyses. Use this tool as an adjunct to clinical judgment; decisions about starting mineralocorticoid receptor antagonists should include assessment of renal function, potassium, concomitant therapies (ACEi/ARB), blood pressure, and monitoring capability.

    Reference:
    Pitt B, et al. Eplerenone, a Selective Aldosterone Blocker, in Patients with (post-MI) Heart Failure — EPHESUS (primary trial report). NEJM 2003. Additional EPHESUS analyses and biomarker substudies (mortality timing, PIIINP predictors, timing of initiation) inform subgroup insights and monitoring recommendations. See: Pitt et al. NEJM 2003; Pitt et al. 2005 EPHESUS 30-day analysis; Stienen et al. (biomarker substudy) for predictors of biochemical response.