Key result
Empagliflozin cuts first heart failure hospitalization ~23% vs. placebo after acute myocardial infarction.
Why the study?
The effect of empagliflozin on first and recurrent heart failure events after acute myocardial infarction was unknown despite prior evidence of benefit in other populations.
Does empagliflozin reduce the risk of heart failure hospitalizations in patients with acute myocardial infarction complicated by left ventricular dysfunction or congestion?
RCT (n=6,522)
Double-blind
randomized
Does empagliflozin reduce the risk of heart failure hospitalizations in patients with acute myocardial infarction complicated by left ventricular dysfunction or congestion?
Empagliflozin reduces the risk of first and recurrent heart failure hospitalizations in patients with acute myocardial infarction complicated by left ventricular dysfunction or congestion.
Supports early empagliflozin initiation within 14 days post-MI; extends SGLT2-inhibitor benefits to the acute infarct setting.
BACKGROUND: Empagliflozin reduces the risk of heart failure (HF) events in patients with type 2 diabetes at high cardiovascular risk, chronic kidney disease, or prevalent HF irrespective of ejection fraction. Whereas the EMPACT-MI trial (Effect of Empagliflozin on Hospitalization for Heart Failure and Mortality in Patients With Acute Myocardial Infarction) showed that empagliflozin does not reduce the risk of the composite of hospitalization for HF and all-cause death, the effect of empagliflozin on first and recurrent HF events after myocardial infarction is unknown. METHODS: EMPACT-MI was a double-blind, randomized, placebo-controlled, event-driven trial that randomized 6522 patients hospitalized for acute myocardial infarction at risk for HF on the basis of newly developed left ventricular ejection fraction of <45% or signs or symptoms of congestion to receive empagliflozin 10 mg daily or placebo within 14 days of admission. In prespecified secondary analyses, treatment groups were analyzed for HF outcomes. RESULTS: Over a median follow-up of 17.9 months, the risk for first HF hospitalization and total HF hospitalizations was significantly lower in the empagliflozin compared with the placebo group (118 [3.6%] versus 153 [4.7%] patients with events; hazard ratio, 0.77 [95% CI, 0.60, 0.98]; P =0.031, for first HF hospitalization; 148 versus 207 events; rate ratio, 0.67 [95% CI, 0.51, 0.89]; P =0.006, for total HF hospitalizations). Subgroup analysis showed consistency of empagliflozin benefit across clinically relevant patient subgroups for first and total HF hospitalizations. The need for new use of diuretics, renin-angiotensin modulators, or mineralocorticoid receptor antagonists after discharge was less in patients randomized to empagliflozin versus placebo (all P <0.05). CONCLUSIONS: Empagliflozin reduced the risk of HF in patients with left ventricular dysfunction or congestion after acute myocardial infarction. REGISTRATION: URL: https://www.clinicaltrials.gov ; Unique identifier: NCT04509674.
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Hernandez et al. (2024) conducted an RCT in Acute myocardial infarction at risk for heart failure (n=6,522). Empagliflozin vs. Placebo was evaluated on First heart failure hospitalization (HR 0.77, 95% CI 0.60, 0.98, p=0.031). Empagliflozin reduced the risk of first heart failure hospitalization compared with placebo (3.6% vs 4.7%; HR 0.77; 95% CI 0.60-0.98; P=0.031) in patients after acute myocardial infarction.
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