Advances in VT ablation for arrhythmogenic cardiomyopathy: evidence, mapping and ablation strategies, and predictive
Mohamed Abdelazeem1,2, Amir Abdelghany3,4, Mohamed Sharief5
1UMass Chan-Baystate Medical Centre, Springfield, MA, USA. mohamed.abdelazeem@baystatehealth.org.
Insights
Catheter ablation for ventricular tachycardia (VT) in arrhythmogenic cardiomyopathy (ACM) is complex. While it reduces VT burden, recurrence rates are high, especially in younger patients with extensive scarring.
Area of Science:
- Cardiology
- Genetics
- Electrophysiology
Background:
- Arrhythmogenic cardiomyopathy (ACM) presents diverse phenotypes (ARVC, ALVC, ABVC) linked to genetic mutations.
- Fibrosis is the primary substrate for ventricular tachycardia (VT) in ACM.
- VT ablation in ACM is challenging due to disease complexity and substrate variability.
Purpose of the Study:
- To critically review the role and efficacy of VT catheter ablation in arrhythmogenic cardiomyopathy.
- To assess current evidence, mapping/ablation techniques, and outcomes for VT ablation in ACM patients.
Main Methods:
- Review of current literature on VT ablation in arrhythmogenic cardiomyopathy.
- Analysis of mapping and ablation strategies, including endocardial-epicardial approaches.
- Evaluation of outcomes and predictors of success in VT ablation for ACM.
Main Results:
- Catheter ablation, especially combined approaches, can reduce VT burden in ACM.
- High recurrence rates of VT are observed, particularly in younger patients and those with extensive myocardial scarring.
- Predictors of ablation success require further elucidation in this complex patient group.
Conclusions:
- VT ablation is a valuable tool in managing arrhythmogenic cardiomyopathy but is limited by high recurrence rates.
- Further research is needed to optimize ablation strategies and improve long-term outcomes for ACM patients.
- Personalized risk stratification and tailored ablation techniques are crucial for successful VT management in ACM.
Abstract:
Catheter ablation of ventricular tachycardia (VT) in arrhythmogenic cardiomyopathy (ACM) is a crucial yet challenging procedure, given the evolving disease definitions, diverse subtypes, genetic variability, complexities in risk stratification, and the intricate substrate distribution characteristic of this condition. Initially described as a right ventricular cardiomyopathy (ARVC), ACM now encompasses left-dominant (ALVC) and biventricular (ABVC) phenotypes, driven by desmosomal (e.g., DSP, PKP2) and non-desmosomal (e.g., FLNC, LMNA) mutations, with fibrosis as the primary arrhythmic substrate. Catheter ablation, particularly combined endocardial-epicardial approaches, reduces VT burden but faces high recurrence rates in younger patients and those with extensive scarring. In this review, we critically assess the role of VT ablation in ACM, current evidence, available techniques for mapping and ablation, outcomes and predictors of success of the ablation procedure in this patient group.
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