Why the study?
What is the long-term clinical course and what are the risk factors for sudden cardiac death in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy?
Population
313 patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy, mean age 44.8 +/- 16.5 years…
Design
Cohort
Follow-up
8.5 years
Authors
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Low mortality in ARVD/C supports conservative monitoring; LV dysfunction association with SCD is hypothesis-generating and needs prospective validation.
What is the long-term clinical course and what are the risk factors for sudden cardiac death in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy?
In patients with ARVD/C, the clinical course is characterized by recurrent malignant ventricular arrhythmias in symptomatic cases, with left ventricular dysfunction serving as a key risk factor for sudden cardiac death.
Stefan Peters (2007) studied this question.
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