Key result
Aldosterone antagonists show no 2-year mortality benefit post-MI with low EF, but increase hyperkalemia risk.
Why the study?
Does aldosterone antagonist therapy reduce mortality in older post-myocardial infarction patients with reduced ejection fraction in routine clinical practice?
Cohort (n=12,080)
Yes
Does aldosterone antagonist therapy reduce mortality in older post-myocardial infarction patients with reduced ejection fraction in routine clinical practice?
Hazard Ratio: 0.99 (95% CI 0.88–1.13)
Absolute Event Rate: 38.7% vs 37.7%
In older patients with reduced EF after acute MI, routine use of aldosterone antagonists was not associated with reduced mortality overall, highlighting potential discrepancies between real-world effectiveness and clinical trial efficacy.
Questions real-world mortality benefit of aldosterone antagonists in older post-MI patients with low EF; leaves open translation of trial efficacy to routine care.
BACKGROUND: While aldosterone antagonists have proven benefit among post-myocardial infarction (MI) patients with low ejection fraction (EF), how this treatment is used among older MI patients in routine practice is not well described. METHODS AND RESULTS: Using ACTION Registry-GWTG linked to Medicare data, we examined 12 080 MI patients ≥65 years with EF ≤40% who were indicated for aldosterone antagonist therapy per current guidelines and without documented contraindications. Of these, 11% (n=1310) were prescribed aldosterone antagonists at discharge. Notably, 10% of patients prescribed an aldosterone antagonist were eligible for, but not concurrently treated with, an angiotensin-converting enzyme inhibitor/angiotensin receptor blocker. Spironolactone was the predominantly prescribed aldosterone antagonist. At 2-year follow-up, aldosterone antagonist use was not associated with lower mortality (unadjusted 39% versus 38%; HR 0.99, 95% CI 0.88-1.33 using inverse probability-weighted propensity adjustment) except in symptomatic HF patients (HR 0.84, 95% CI 0.72-0.99, Pinteraction=0.009). Risks of hyperkalemia were low at 30 days, but significantly higher among patients prescribed aldosterone antagonists (unadjusted 2.3% versus 1.5%; adjusted HR 2.04, 95% CI 1.16-3.60), as was 2-year risk of acute renal failure (unadjusted 6.7% versus 4.8%; adjusted HR 1.39, 95% CI 1.01-1.92) compared with patients not prescribed aldosterone antagonists. CONCLUSIONS: Aldosterone antagonist use among eligible older MI patients in routine clinical practice was not associated with lower mortality except in patients with HF symptoms, but was associated with increased risks of hyperkalemia and acute renal failure. These results underscore the importance of close post-discharge monitoring of this patient population.
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Wang et al. (2016) conducted a cohort in Post-myocardial infarction with reduced ejection fraction (n=12,080). Aldosterone antagonist vs. Not prescribed aldosterone antagonist was evaluated on Death within 2 years post-discharge (HR 0.99, 95% CI 0.88-1.13). Aldosterone antagonist prescription at discharge was not associated with lower 2-year mortality in older post-MI patients with low ejection fraction (HR 0.99), but increased the risk of hyperkalemia.
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