ABYSS Trial: Stopping Beta-Blockers Post-Heart Attack Increases Cardiovascular Risks Without Quality of Life Benefits

August 31, 2024
ABYSS Trial: Stopping Beta-Blockers Post-Heart Attack Increases Cardiovascular Risks Without Quality of Life Benefits
  • The ABYSS trial, presented at the ESC Congress 2024, found that interrupting beta-blocker treatment in patients with a history of myocardial infarction (MI) did not demonstrate cardiovascular safety compared to continuing the medication.

  • In this trial, 3,698 patients were randomly assigned to either continue or interrupt their beta-blocker therapy, with a follow-up period of at least one year.

  • All participants had a left ventricular ejection fraction of at least 40% and had not experienced any cardiovascular events in the previous six months.

  • The primary outcome, which included death, non-fatal MI, non-fatal stroke, or hospitalization for cardiovascular reasons, occurred in 23.8% of the interruption group compared to 21.1% in the continuation group.

  • This resulted in a risk difference of 2.8 percentage points and a hazard ratio of 1.16, indicating that non-inferiority was not achieved.

  • Patients who stopped taking beta-blockers had higher rates of cardiovascular hospitalization, with 18.9% in the interruption group versus 16.6% in the continuation group.

  • Death rates were similar between the two groups, at 4.1% in the interruption group and 4.0% in the continuation group, with myocardial infarction rates also comparable.

  • Discontinuation of beta-blockers was associated with increases in blood pressure and heart rate after six months, suggesting negative cardiovascular effects.

  • Contrary to expectations, there was no improvement in quality of life for patients who interrupted beta-blockers, as measured by the European Quality of Life-5 Dimensions questionnaire.

  • Professor Johanne Silvain, the trial's lead investigator, emphasized that the findings do not support the interruption of chronic beta-blocker treatment in post-MI patients.

  • Further trials are ongoing to provide additional data on the safety and efficacy of discontinuing beta-blocker therapy in this patient population.

  • These findings challenge existing guidelines that suggest beta-blockers can be safely discontinued after one year in certain patient populations.

Summary based on 3 sources


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Sources


Setbacks After Stopping Beta-Blockers

Medscape • Aug 31, 2024

Setbacks After Stopping Beta-Blockers

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