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Evolution and triggers of defibrillator shocks in patients with arrhythmogenic right ventricular cardiomyopathy
Nadine Molitor1, Daniel Hofer2, Tolga Çimen2
1Cardiology, Department of Cardiology, University Heart Center, University Hospital Zurich, Zurich, Switzerland nadine.molitor@usz.ch ardan.saguner@usz.ch.
Insights
The long-term risk of appropriate implantable cardioverter-defibrillator (ICD) shocks remains high for arrhythmogenic right ventricular cardiomyopathy (ARVC) patients. Physical activity, inflammation, and hypokalemia are common, reversible triggers for these shocks.
Area of Science:
- Cardiology
- Electrophysiology
- Genetics
Background:
- Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a genetic heart disease associated with ventricular arrhythmias and sudden cardiac death.
- Implantable cardioverter-defibrillators (ICDs) are crucial for preventing sudden cardiac death in ARVC patients.
- Understanding the patterns and triggers of appropriate ICD shocks is vital for managing ARVC patients.
Purpose of the Study:
- To assess the cumulative burden and evolution of appropriate ICD shocks in ARVC patients.
- To identify potential triggers of appropriate ICD shocks during long-term follow-up.
- To inform strategies for reducing and refining arrhythmic risk in ARVC.
Main Methods:
- Retrospective cohort study of 53 ARVC patients from the Swiss ARVC Registry.
- Analysis of patient records, including device interrogations and tracings, for long-term follow-up.
- Identification of appropriate ICD shock episodes and potential triggers.
Main Results:
- A high long-term risk of appropriate ICD shocks was observed in 54.7% of patients over a median follow-up of 7.9 years.
- Shock episodes predominantly occurred during daytime without seasonal preference.
- Reversible triggers, including physical activity, inflammation, and hypokalemia, were identified in 78.9% of shock episodes.
Conclusions:
- The long-term risk of appropriate ICD shocks in ARVC patients remains significant.
- Ventricular arrhythmias and subsequent shocks in ARVC patients often occur during the day.
- Recognizing and managing reversible triggers like physical activity, inflammation, and hypokalemia is key to optimizing ICD therapy in ARVC.
Introduction:
Implantable cardioverter-defibrillators (ICDs) can prevent sudden cardiac death due to ventricular arrhythmias in patients with arrhythmogenic right ventricular cardiomyopathy (ARVC). The aim of our study was to assess the cumulative burden, evolution and potential triggers of appropriate ICD shocks during long-term follow-up, which may help to reduce and further refine individual arrhythmic risk in this challenging disease.
Methods:
This retrospective cohort study included 53 patients with definite ARVC according to the 2010 Task Force Criteria from the multicentre Swiss ARVC Registry with an implanted ICD for primary or secondary prevention. Follow-up was conducted by assessing all available patient records from patient visits, hospitalisations, blood samples, genetic analysis, as well as device interrogation and tracings.
Results:
Fifty-three patients (male 71.7%, mean age 43±2.2 years, genotype positive 58.5%) were analysed during a median follow-up of 7.9 (IQR 10) years. In 29 (54.7%) patients, 177 appropriate ICD shocks associated with 71 shock episodes occurred. Median time to first appropriate ICD shock was 2.8 (IQR 3.6) years. Long-term risk of shocks remained high throughout long-term follow-up. Shock episodes occurred mainly during daytime (91.5%, n=65) and without seasonal preference. We identified potentially reversible triggers in 56 of 71 (78.9%) appropriate shock episodes, the main triggers representing physical activity, inflammation and hypokalaemia.
Conclusion:
The long-term risk of appropriate ICD shocks in patients with ARVC remains high during long-term follow-up. Ventricular arrhythmias occur more often during daytime, without seasonal preference. Reversible triggers are frequent with the most common triggers for appropriate ICD shocks being physical activity, inflammation and hypokalaemia in this patient population.
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