Beta-Blockers after Myocardial Infarction and Preserved Ejection Fraction
- PMID: 38587241
- DOI: 10.1056/NEJMoa2401479
Beta-Blockers after Myocardial Infarction and Preserved Ejection Fraction
Abstract
Background: Most trials that have shown a benefit of beta-blocker treatment after myocardial infarction included patients with large myocardial infarctions and were conducted in an era before modern biomarker-based diagnosis of myocardial infarction and treatment with percutaneous coronary intervention, antithrombotic agents, high-intensity statins, and renin-angiotensin-aldosterone system antagonists.
Methods: In a parallel-group, open-label trial performed at 45 centers in Sweden, Estonia, and New Zealand, we randomly assigned patients with an acute myocardial infarction who had undergone coronary angiography and had a left ventricular ejection fraction of at least 50% to receive either long-term treatment with a beta-blocker (metoprolol or bisoprolol) or no beta-blocker treatment. The primary end point was a composite of death from any cause or new myocardial infarction.
Results: From September 2017 through May 2023, a total of 5020 patients were enrolled (95.4% of whom were from Sweden). The median follow-up was 3.5 years (interquartile range, 2.2 to 4.7). A primary end-point event occurred in 199 of 2508 patients (7.9%) in the beta-blocker group and in 208 of 2512 patients (8.3%) in the no-beta-blocker group (hazard ratio, 0.96; 95% confidence interval, 0.79 to 1.16; P = 0.64). Beta-blocker treatment did not appear to lead to a lower cumulative incidence of the secondary end points (death from any cause, 3.9% in the beta-blocker group and 4.1% in the no-beta-blocker group; death from cardiovascular causes, 1.5% and 1.3%, respectively; myocardial infarction, 4.5% and 4.7%; hospitalization for atrial fibrillation, 1.1% and 1.4%; and hospitalization for heart failure, 0.8% and 0.9%). With regard to safety end points, hospitalization for bradycardia, second- or third-degree atrioventricular block, hypotension, syncope, or implantation of a pacemaker occurred in 3.4% of the patients in the beta-blocker group and in 3.2% of those in the no-beta-blocker group; hospitalization for asthma or chronic obstructive pulmonary disease in 0.6% and 0.6%, respectively; and hospitalization for stroke in 1.4% and 1.8%.
Conclusions: Among patients with acute myocardial infarction who underwent early coronary angiography and had a preserved left ventricular ejection fraction (≥50%), long-term beta-blocker treatment did not lead to a lower risk of the composite primary end point of death from any cause or new myocardial infarction than no beta-blocker use. (Funded by the Swedish Research Council and others; REDUCE-AMI ClinicalTrials.gov number, NCT03278509.).
Copyright © 2024 Massachusetts Medical Society.
Comment in
-
No benefit of β-blockers after myocardial infarction with preserved ejection fraction.Nat Rev Cardiol. 2024 Jun;21(6):354. doi: 10.1038/s41569-024-01030-0. Nat Rev Cardiol. 2024. PMID: 38649758 No abstract available.
-
Beta-Blockers after Myocardial Infarction and Preserved Ejection Fraction.N Engl J Med. 2024 Jul 4;391(1):94. doi: 10.1056/NEJMc2406095. N Engl J Med. 2024. PMID: 38959488 No abstract available.
-
Beta-Blockers after Myocardial Infarction and Preserved Ejection Fraction.N Engl J Med. 2024 Jul 4;391(1):94-95. doi: 10.1056/NEJMc2406095. N Engl J Med. 2024. PMID: 38959489 No abstract available.
-
Beta-Blockers after Myocardial Infarction and Preserved Ejection Fraction. Reply.N Engl J Med. 2024 Jul 4;391(1):95. doi: 10.1056/NEJMc2406095. N Engl J Med. 2024. PMID: 38959490 No abstract available.
Similar articles
-
Design and rationale of randomized evaluation of decreased usage of beta-blockers after acute myocardial infarction (REDUCE-AMI).Eur Heart J Cardiovasc Pharmacother. 2023 Feb 2;9(2):192-197. doi: 10.1093/ehjcvp/pvac070. Eur Heart J Cardiovasc Pharmacother. 2023. PMID: 36513329 Free PMC article. Clinical Trial.
-
Beta-Blocker Interruption or Continuation after Myocardial Infarction.N Engl J Med. 2024 Oct 10;391(14):1277-1286. doi: 10.1056/NEJMoa2404204. Epub 2024 Aug 30. N Engl J Med. 2024. PMID: 39213187 Clinical Trial.
-
Design and rationale of the Danish trial of beta-blocker treatment after myocardial infarction without reduced ejection fraction: study protocol for a randomized controlled trial.Trials. 2020 May 23;21(1):415. doi: 10.1186/s13063-020-4214-6. Trials. 2020. PMID: 32446298 Free PMC article.
-
Early intravenous beta-blockers in patients undergoing primary percutaneous coronary intervention for ST-segment elevation myocardial infarction: A patient-pooled meta-analysis of randomized clinical trials.Eur Heart J Acute Cardiovasc Care. 2020 Aug;9(5):469-477. doi: 10.1177/2048872619830609. Epub 2019 Feb 14. Eur Heart J Acute Cardiovasc Care. 2020. PMID: 30759994 Free PMC article. Review.
-
Does Oral Beta-Blocker Therapy Improve Long-Term Survival in ST-Segment Elevation Myocardial Infarction With Preserved Systolic Function? A Meta-Analysis.J Cardiovasc Pharmacol Ther. 2016 May;21(3):280-5. doi: 10.1177/1074248415608011. Epub 2015 Sep 29. J Cardiovasc Pharmacol Ther. 2016. PMID: 26424094 Review.
Cited by
-
Real-world research on beta-blocker usage trends in China and safety exploration based on the FDA Adverse Event Reporting System (FAERS).BMC Pharmacol Toxicol. 2024 Nov 14;25(1):86. doi: 10.1186/s40360-024-00815-w. BMC Pharmacol Toxicol. 2024. PMID: 39543745 Free PMC article.
-
β-blockers after MI: does ABYSS confirm REDUCEd use after all?Nat Rev Cardiol. 2024 Oct 9. doi: 10.1038/s41569-024-01093-z. Online ahead of print. Nat Rev Cardiol. 2024. PMID: 39384949 No abstract available.
-
Two-year clinical outcome of patients with mildly reduced ejection fraction after acute myocardial infarction: insights from the prospective KAMIR-NIH Registry.Front Cardiovasc Med. 2024 Sep 20;11:1458740. doi: 10.3389/fcvm.2024.1458740. eCollection 2024. Front Cardiovasc Med. 2024. PMID: 39371398 Free PMC article.
-
Allopurinol versus Trimetazidine as Antianginal: A Randomized Clinical Trial.Arq Bras Cardiol. 2024 Aug;121(8):e20240500. doi: 10.36660/abc.20240500. Arq Bras Cardiol. 2024. PMID: 39292120 Free PMC article. Clinical Trial. English, Portuguese. No abstract available.
-
Association between Inflammation and New-Onset Atrial Fibrillation in Acute Coronary Syndromes.J Clin Med. 2024 Aug 27;13(17):5088. doi: 10.3390/jcm13175088. J Clin Med. 2024. PMID: 39274304 Free PMC article. Review.
Publication types
MeSH terms
Substances
Associated data
Grants and funding
LinkOut - more resources
Full Text Sources
Medical