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Effect of Empagliflozin on Heart Failure Outcomes after Acute Myocardial Infarction: Insights from the EMPACT-MI Trial
Hernandez, A.F. ✉
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Udell, J.A.
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Jones, W.S.
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Anker, S.D.
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Petrie, M.C.
;
Harrington, J.
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Mattheus, M.
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Seide, S.
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Zwiener, I.
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Amir, O.
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Bahit, M.C.
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Bauersachs, J.
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Bayes-Genis, A.
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Chen, Y.
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Chopra, V.K.
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Figtree, G.A.
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Ge, J.
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Goodman, S.G.
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Gotcheva, N.
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Goto, S.
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Gasior, T.
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Jamal, W.
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Januzzi, J.L.
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Jeong, M.H.
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Lopatin, Y.
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Lopes, R.D.
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Merkely, B. [Merkely, Béla Péter (Kardiológia), szerző] Városmajori Szív- és Érgyógyászati Klinika (SE / AOK / K); Kardiológia Központ - Kardiológiai Tanszék (SE / AOK / K); Sportorvostan Tanszék (SE / AOK / K); Repülõ- és Űrorvostani Tanszék (SE / AOK / K)
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Parikh, P.B.
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Parkhomenko, A.
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Ponikowski, P.
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Rossello, X.
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Schou, M.
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Simic, D.
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Steg, P.G.
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Szachniewicz, J.
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Van, Der Meer P.
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Vinereanu, D.
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Zieroth, S.
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Brueckmann, M.
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Sumin, M.
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Bhatt, D.L.
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Butler, J.
Angol nyelvű Sokszerzős vagy csoportos szerzőségű szakcikk (Folyóiratcikk) Tudományos
Megjelent:
CIRCULATION 0009-7322 1524-4539
149
(21)
pp. 1627-1638
2024
SJR Scopus - Cardiology and Cardiovascular Medicine: D1
Azonosítók
MTMT: 35051000
DOI:
10.1161/CIRCULATIONAHA.124.069217
WoS:
001290801600001
Scopus:
85192082139
PubMed:
38581389
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. © 2024 The Authors.
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2025-04-03 16:34
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