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Beta-blocker interruption effects on blood pressure and heart rate after myocardial infarction: the AβYSS trial
Niki Procopi1, Michel Zeitouni1, Mathieu Kerneis1
1Sorbonne Université, Hôpital Pitié-Salpêtrière (AP-HP), ACTION Study Group, INSERM UMRS 1166, Institut de Cardiologie, 83 blvd de l'Hôpital, 75013 Paris, France.
Insights
Stopping beta-blocker therapy after myocardial infarction increases blood pressure and heart rate. This interruption poses risks, particularly for patients with a history of hypertension.
Area of Science:
- Cardiology
- Clinical Trials
- Pharmacology
Background:
- Beta-blockers are standard treatment post-myocardial infarction (MI).
- The AβYSS trial investigated the impact of beta-blocker interruption versus continuation after MI.
Purpose of the Study:
- To evaluate the effects of beta-blocker interruption on blood pressure (BP) and heart rate (HR) post-MI.
- To assess the impact of beta-blocker interruption on cardiovascular outcomes, especially in patients with hypertension.
Main Methods:
- A randomized trial (AβYSS) involving 3698 patients post-MI.
- Linear mixed-effects models analyzed changes in BP and HR over a median 3.0-year follow-up.
- Cox proportional hazards models assessed outcomes in subgroups based on hypertension history.
Main Results:
- Beta-blocker interruption significantly increased systolic BP (+3.7 mmHg), diastolic BP (+3.3 mmHg), and HR (+10 bpm) at 6 months, persisting throughout follow-up.
- These effects were observed in both hypertensive and non-hypertensive patients.
- Hypertensive patients experienced a higher risk of primary events (death, MI, stroke, cardiovascular hospitalization) and a marked increase in primary endpoint risk with beta-blocker interruption.
Conclusions:
- Interruption of beta-blocker treatment after MI causes sustained increases in BP and HR.
- Beta-blocker withdrawal may have adverse effects on cardiovascular outcomes, particularly in patients with a history of hypertension.
Background And Aims:
This study aims to report the effects of β-blocker interruption on blood pressure (BP) and heart rate (HR) in the AβYSS trial where patients were randomized to interruption or continuation of β-blocker treatment after a myocardial infarction (MI).
Methods:
Changes in HR and BP from baseline to post-randomization are reported using linear mixed repeated model, in the 3698 patients of the AβYSS trial with a median follow-up of 3.0 years. Additionally, changes in HR and BP and the impact on the primary endpoint (death, MI, stroke, hospitalization for cardiovascular reason) in the pre-specified subgroups of patients with or without history of hypertension were assessed using linear mixed repeated and adjusted Cox proportional hazards model, respectively.
Results:
β-blocker interruption was associated with significant increase {least square mean difference [95% confidence interval (CI)]} in systolic BP [+3.7 (2.6, 4.8) mmHg, P < .001], diastolic BP [+3.3 (2.6, 4.0) mmHg, P < .001], and resting HR [+10 [9, 11) b.p.m., P < .001] at 6 months that persisted over the duration of follow-up despite an increase in antihypertensive drugs in the β-blocker interruption group. The effects were observed in both hypertensive (43% of the population) and non-hypertensive patients. Hypertensive patients were at higher risk of events (25.8% vs. 19.2%) as compared with patients without hypertension (adjusted hazard ratio 1.18, 95% CI 1.01-1.36, P = .03). Patients with hypertension had a particularly marked increase in the primary endpoint (risk difference 5.02%, 0.72%-9.32%, P = .014) when randomized to β-blocker interruption.
Conclusions:
Interruption of β-blocker treatment after an uncomplicated MI led to a sustained increase in BP and HR, with potentially deleterious effects on outcomes, especially in patients with history of hypertension.
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