Abstract
Hypertrophic cardiomyopathy (HCM) accounts for an estimated third of all sudden cardiac deaths (SCD) in young athletes secondary to lethal ventricular arrhythmias. Current guidelines restrict patients with HCM from participating in competitive sports because the risk for SCD is increased during intense physical exertion. Both atrial and ventricular arrhythmias occur in HCM. The most common documented arrhythmia in patients with HCM is atrial fibrillation. Ventricular arrhythmias in patients with HCM may present as sudden cardiac death. Primary prevention indications for ICDs in patients with HCM should be individualized with careful family screening of family members as arrhythmias may be the first clinical manifestation of the disease. This review article discusses the features of atrial and ventricular arrhythmias in HCM and their management. In addition, the review discusses the risk factors for sudden cardiac death, the role of alternative strategies in HCM like dual chamber pacing and the arrhythmias that occur after septal myectomy.
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Nair, K., Cameron, D., Moravsky, G., Butany, J. (2014). Arrhythmias and Hypertrophic Cardiomyopathy. In: Kibos, A., Knight, B., Essebag, V., Fishberger, S., Slevin, M., Țintoiu, I. (eds) Cardiac Arrhythmias. Springer, London. https://doi.org/10.1007/978-1-4471-5316-0_19
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