Arrhythmia & Electrophysiology Review · 2016 · 34 citations · 60 references
MedicineCardiologyCardiovascular GeneticsClinical CardiologyPreventive CardiologyCardiac Risk AssessmentCardiovascular DiseaseHypertrophic Cardiomyopathy GeneticsImplantable Cardioverter-defibrillator CareSudden Cardiac Death PreventionArrhythmogenic Risk StratificationImplantable Cardioverter DefibrillatorsSudden Cardiac Death Risk AssessmentSudden Death PreventionSudden Death Risk Assessment
Hypertrophic cardiomyopathy (HCM) is a common and heterogeneous disorder that increases an individual's risk of sudden cardiac death (SCD). This review article discusses the relevant factors that are involved in the challenge of preventing SCD in patients with HCM. The epidemiology of SCD in patients is reviewed as well as the structural and genetic basis behind ventricular arrhythmias in HCM. The primary prevention of SCD with implantable cardioverter-defibrillator (ICD) therapy is the cornerstone of modern treatment for individuals at high risk of SCD. The focus here is on the current and emerging predictors of SCD as well as risk stratification recommendations from both North American and European guidelines. Issues related to ICD implantation, such as programming, complications and inappropriate therapies, are discussed. The emerging role of the fully subcutaneous ICD and the data regarding its implantation are reviewed.
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Prevalence of Hypertrophic Cardiomyopathy in a General Population of Young Adults
Barry J. Maron, Julius M. Gardin, John M. Flack et al. · Circulation · 1995 · 2.3K citations · Full text