Determining major adverse cardiovascular event risk of beta-blocker discontinuation after acute coronary syndromes

Nicolas Johner1,2, Baris Gencer1,3,4

  • 1Cardiology Division, Geneva University Hospitals, Geneva, Switzerland.

Insights

Routine beta-blocker use after acute coronary syndromes (ACS) may be unnecessary for patients with preserved ejection fraction (≥50%). Individualized treatment decisions are recommended, weighing risks and benefits of deprescribing beta-blockers.

Area of Science:

  • Cardiology
  • Clinical Pharmacology
  • Evidence-Based Medicine

Background:

  • Beta-blockers historically reduced mortality post-acute coronary syndromes (ACS) before reperfusion therapies.
  • Contemporary ACS management with early reperfusion and secondary prevention has shifted the benefit-risk profile of beta-blockers.
  • The role of beta-blockers in ACS patients with preserved left ventricular ejection fraction (LVEF) is increasingly questioned.

Purpose of the Study:

  • To review contemporary evidence on beta-blocker efficacy in ACS patients with preserved LVEF.
  • To evaluate implications for different LVEF categories, ACS subtypes, and treatment durations.
  • To provide expert opinion on individualizing beta-blocker therapy post-ACS.

Main Methods:

  • Systematic review of PubMed database (inception to January 2025).
  • Analysis of recent randomized trials (REDUCE-AMI, ABYSS) and contemporary observational data.
  • Assessment of factors influencing beta-blocker prescription and discontinuation.

Main Results:

  • Sufficient evidence suggests abandoning routine beta-blocker prescription for post-ACS patients with LVEF ≥50%.
  • Individualized decision-making is crucial, balancing cardiovascular event risk against deprescribing benefits.
  • Factors like adverse effects, polypharmacy, and long-term stability favor discontinuation.

Conclusions:

  • Routine beta-blocker use is not recommended for post-ACS patients with LVEF ≥50%.
  • Personalized treatment strategies should consider patient-specific factors, LVEF, and tolerance.
  • Beta-blockers remain indicated for specific conditions like LVEF ≤40%, arrhythmias, angina, and refractory hypertension.
Abstract

Related Concept Videos

Heart Failure Drugs: β-Blockers01:22

Heart Failure Drugs: β-Blockers

β-adrenergic antagonists, commonly known as β-blockers, block the effects of sympathetic neurotransmitters such as noradrenaline (NA) and adrenaline (ADR). They have several beneficial effects in heart failure treatment. They reduce heart rate, the force of contraction, and cardiac muscle relaxation. They also slow the atrial-ventricular conduction rate and raise the threshold for arrhythmias. The concentration of β-blockers determines their effects on bronchodilation,...
446
Adrenergic Antagonists: Pharmacological Actions of β-Receptor Blockers01:27

Adrenergic Antagonists: Pharmacological Actions of β-Receptor Blockers

β-receptor blockers significantly impact the cardiovascular system by counteracting catecholamine-induced sympathetic responses. These medications decrease heart rate, contractility, and cardiac output, potentially leading to cardiac depression, life-threatening bradycardia, and death. Therapeutically, β-blockers function as mild antihypertensives and are utilized in treating angina pectoris and cardiac arrhythmias. However, nonselective β-blockers inhibit β2-receptors in...
1.0K
Adrenergic Antagonists: Chemistry and Classification of β-Receptor Blockers01:25

Adrenergic Antagonists: Chemistry and Classification of β-Receptor Blockers

β-adrenergic antagonists, or β-blockers, modulate the sympathetic nervous system by targeting β-adrenoceptors and inhibiting catecholamine-mediated sympathetic responses. β-blockers differ in their adrenoceptor subtype affinity, lipophilicity, and α-blocking capabilities. The history of β-blocker development began with the prototype, dichloroisoprenaline, which exhibited partial agonist activity. As a result, propranolol was developed as a pure antagonist but...
798
Antihypertensive Drugs: Types of β-Blockers01:28

Antihypertensive Drugs: Types of β-Blockers

β receptors are classified into three subclasses: β1, β2, and β3. β1 receptors are primarily located in the heart and kidneys. When they get activated, they increase heart rate, contractility, and renin release. This process enhances blood pressure and aids in stress management. In contrast, β2 receptors are situated mainly in the lungs, blood vessels, and skeletal muscles. Upon activation, they trigger smooth muscle relaxation, causing bronchodilation and...
914
Antiarrhythmic Drugs: Class II Agents as β-Adrenergic Blockers01:24

Antiarrhythmic Drugs: Class II Agents as β-Adrenergic Blockers

Adrenergic stimulation generally impacts cardiac rate and rhythm. Specifically, stimulation of the β-adrenoceptors triggers an increase in intracellular calcium ion influx and pacemaker currents, which may cause arrhythmias. Catecholamines like adrenaline also demonstrate β2-adrenoceptor-mediated hypokalemia, impacting cardiac action potential and disrupting the normal cardiac rhythm. Class II antiarrhythmic drugs are β-adrenoceptor antagonists or β-blockers, which...
913
Acute Coronary Syndrome III: Diagnostic Studies01:30

Acute Coronary Syndrome III: Diagnostic Studies

Diagnosing acute coronary syndrome or ACS begins with a thorough patient history. Notable symptoms include central, crushing chest pain radiating to the left arm, neck, jaw, or back, along with shortness of breath, sweating (diaphoresis), nausea, vomiting, dizziness, and palpitations.It is crucial to note any history of cardiac illnesses and assess risk factors, including age, gender, smoking, hypertension, diabetes, hyperlipidemia, and a sedentary lifestyle.During physical examination, vital...
26