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Updated: Jun 11, 2025

Catheter Ablation in Combination With Left Atrial Appendage Closure for Atrial Fibrillation
Published on: February 26, 2013
Hybrid versus catheter ablation for Hypertrophic CardioMyopathy with Atrial Fibrillation (HCM-AF): study protocol for
Yajie Tang1,2, Le Li1,3, Sipeng Chen4
1State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.
Insights
This study compares hybrid ablation to catheter ablation for atrial fibrillation (AF) in hypertrophic cardiomyopathy (HCM) patients. It assesses rhythm control effectiveness to improve outcomes in this specific patient group.
Area of Science:
- Cardiology
- Electrophysiology
- Clinical Trials
Background:
- Atrial fibrillation (AF) is a significant predictor of adverse events in hypertrophic cardiomyopathy (HCM) patients.
- Catheter ablation (CA) is less effective for maintaining sinus rhythm in HCM patients with AF compared to the general population.
- Hybrid ablation offers a potentially more effective approach, but comparative data in HCM is lacking.
Purpose of the Study:
- To compare the rhythm control effectiveness of hybrid ablation versus catheter ablation (CA) in non-obstructive hypertrophic cardiomyopathy (non-oHCM) patients with AF.
- To evaluate the efficacy of these procedures in maintaining sinus rhythm and reducing AF relapse.
- To assess the impact on mortality, stroke, heart failure, and quality of life.
Main Methods:
- A prospective, multicentre, randomized trial with blinded outcome assessment.
- Sixty-six non-oHCM patients with non-paroxysmal AF randomized 1:1 to hybrid ablation or CA.
- Primary endpoint: freedom from atrial tachycardia >30s at 12 months without antiarrhythmic drugs; secondary endpoints include mortality, stroke, rehospitalization, and quality of life.
Main Results:
- This section is not yet available as the study is ongoing.
- The study is designed to provide definitive comparative data on rhythm control strategies.
- Results will be disseminated following trial completion.
Conclusions:
- This trial will provide crucial evidence on the comparative effectiveness of hybrid versus catheter ablation for AF in non-oHCM patients.
- Findings are expected to guide treatment strategies for this challenging patient population.
- The study aims to optimize rhythm control and improve long-term outcomes in HCM patients with AF.
Introduction:
Atrial fibrillation (AF) is an independent predictor of adverse outcomes in patients with hypertrophic cardiomyopathy (HCM). Although catheter ablation is highly recommended for general AF populations, it is less effective in maintaining sinus rhythm in patients with HCM associated with AF. Hybrid ablation, combining a cosmetic approach with a lower rate of AF relapse, lacks comparative studies to verify its efficacy against CA in HCM. This study aims to assess the rhythm control effectiveness of hybrid versus CA in non-obstructive HCM (non-oHCM) patients with AF.
Methods/Analysis:
This prospective, multicentre, randomised trial involves a blinded assessment of outcomes in non-oHCM patients with non-paroxysmal AF. Sixty-six candidates from three centres will be randomised 1:1 to either hybrid or CA, including isthmus addressed lesion sets. Participants will be stratified by left atrial (LA) size (LA diameter ≤50 mm or >50 mm). Follow-ups at the 3rd, 6th and 12th months will evaluate the primary endpoint of freedom from documented atrial tachycardia lasting over 30 s within 12 months post-procedure without antiarrhythmic drugs, along with secondary endpoints of all-cause mortality, cardiovascular-related mortality, cerebral stroke, peripheral vascular embolism, heart failure-related rehospitalisation, all-cause rehospitalisation and quality of life assessments.
Ethics And Disseminationapproval:
The central ethics committee at Fuwai Hospital has approved the Hypertrophic CardioMyopathy with Atrial Fibrillation trial (approval number: 2022-1736). Results will be disseminated through publications in peer-reviewed journals and presentations at conferences.
Trial Registration Number:
NCT05610215.
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