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Related Experiment Video

Updated: Mar 31, 2026

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Discontinuation of Beta-Blocker Therapy after Myocardial Infarction.

Ki Hong Choi1, Danbee Kang2, Weon Kim3

  • 1Heart Vascular Stroke Institute, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.

The New England Journal of Medicine
|March 30, 2026
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Summary

Discontinuing long-term beta-blocker therapy after myocardial infarction is safe for stable patients without heart failure. This approach is noninferior to continuing therapy for major adverse cardiovascular events.

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Area of Science:

  • Cardiology
  • Clinical Trials
  • Pharmacotherapy

Background:

  • The necessity of long-term beta-blocker (BB) therapy post-myocardial infarction (MI) is uncertain in patients without left ventricular systolic dysfunction or heart failure, especially with modern reperfusion and secondary prevention strategies.
  • Contemporary management of MI has evolved, prompting re-evaluation of established treatment protocols.

Purpose of the Study:

  • To determine if discontinuing beta-blocker therapy beyond one year post-myocardial infarction is noninferior to continuing it in stable patients without heart failure.
  • To assess the composite outcome of all-cause death, recurrent MI, or heart failure hospitalization.

Main Methods:

  • An open-label, randomized, noninferiority trial involving 2540 stable patients post-MI with LVEF ≥40% and no heart failure, who had received BB therapy for at least 1 year.
  • Patients were randomized 1:1 to either discontinue or continue beta-blocker therapy.
  • The primary endpoint was a composite of death, recurrent MI, or heart failure hospitalization, with a noninferiority margin set at HR 1.4.

Main Results:

  • A total of 2540 patients were randomized; 1246 to discontinuation and 1294 to continuation.
  • At a median follow-up of 3.1 years, the 4-year event rate was 7.2% in the discontinuation group and 9.0% in the continuation group (HR 0.80; 95% CI 0.57-1.13).
  • The study met its noninferiority endpoint (P=0.001), with similar rates of serious adverse events in both groups.

Conclusions:

  • Discontinuation of beta-blocker therapy beyond one year post-myocardial infarction is noninferior to continuation in stable patients without heart failure.
  • This finding supports a potential de-escalation of long-term beta-blocker therapy in select post-MI patients.
  • The study provides crucial evidence for optimizing pharmacotherapy in cardiovascular secondary prevention.