Duration of atrial fibrillation persistence: Implications for recurrence risk after catheter ablation and efficacy of

Yasuharu Matsunaga-Lee1, Koichi Inoue2, Nobuaki Tanaka3

  • 1Division of Cardiology, Osaka Rosai Hospital, Sakai, Japan.

Heart Rhythm
|February 2, 2024
PubMed

Insights

For patients with long-standing atrial fibrillation (AF) undergoing catheter ablation, AF persistence longer than 2.4 years is linked to higher recurrence. The PVI-plus strategy may be superior for these cases.

Area of Science:

  • Cardiology
  • Electrophysiology
  • Medical Devices

Background:

  • Catheter ablation is a common treatment for atrial fibrillation (AF).
  • Optimal ablation strategies and duration of AF persistence predicting outcomes in long-standing AF (LsAF) remain unclear.

Purpose of the Study:

  • To assess the impact of AF duration on outcomes after catheter ablation.
  • To determine the optimal cutoff duration of AF persistence for predicting outcomes in LsAF.

Main Methods:

  • Analysis of data from the EARNEST-PVI trial.
  • Comparison of pulmonary vein isolation (PVI) alone versus PVI-plus strategies.
  • Evaluation of arrhythmia-free survival in patients with persistent AF (PerAF) and LsAF, stratified by AF duration.

Main Results:

  • The optimal cutoff for AF persistence was 2.4 years.
  • LsAF between 1-2.4 years showed outcomes comparable to PerAF.
  • LsAF >2.4 years demonstrated a significantly higher recurrence risk (HR 2.22) compared to PerAF.
  • In LsAF >2.4 years, PVI-plus was superior to PVI-alone (HR 0.36).

Conclusions:

  • AF duration exceeding 2.4 years is associated with poorer outcomes after catheter ablation.
  • The PVI-plus strategy may offer improved efficacy for LsAF >2.4 years.
  • Further research may refine ablation strategies based on AF persistence duration.
Abstract

Related Concept Videos

Disturbances in Heart Rhythm01:28

Disturbances in Heart Rhythm

Arrhythmia or dysrhythmia refers to an abnormal heart rhythm caused by a defect in the heart's conduction system. It can cause the heart to beat irregularly, too quickly, or too slowly, leading to symptoms like chest pain, shortness of breath, and fainting. Factors such as stress, caffeine, alcohol, nicotine, cocaine, certain drugs, congenital defects, diseases, and electrolyte abnormalities can trigger arrhythmias.
Arrhythmias are categorized by their speed, rhythm, and origin. A slow...
957
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...
746
Antiarrhythmic Drugs: Class III Agents as Potassium Channel Blockers01:12

Antiarrhythmic Drugs: Class III Agents as Potassium Channel Blockers

Class III antiarrhythmic drugs are a group of medications that can prolong action potentials in the heart. They achieve this by blocking potassium channels or enhancing inward currents from sodium channels. However, these drugs have a unique property of "reverse use-dependence," which is most pronounced at slower heart rates and can lead to torsades de pointes—a specific type of arrhythmia. However, it is essential to note that excessive QT interval prolongation—a measure of...
999