© 2003 by BMJ Publishing Group & British Cardiac Society
EDITORIAL
Contemporary considerations for risk stratification, sudden death and prevention in hypertrophic cardiomyopathy
Correspondence to:
Correspondence to:
Barry J Maron, MD, Minneapolis Heart Institute Foundation, 920 E 28th Street, Suite 60, Minneapolis, MN 55407, USA;
hcm.maron@mhif.org
For patients with hypertrophic cardiomyopathy, the likelihood of receiving primary prevention for sudden death with an ICD may depend in part on the country of residence
Keywords: sudden death; hypertrophic cardiomyopathy; risk stratification
| The first 150 words of the full text of this article appear below. |
Sudden death has been the most devastating, unpredictable and recognisable complication of hypertrophic cardiomyopathy (HCM), since the modern description of the disease by Teare over 40 years ago.1 HCM is now recognised as the most common cause of sudden cardiac death in young people, including trained athletes,2,3 although only a minority of all HCM patients are susceptible to the risk of sudden death (perhaps 1015%).4 Nevertheless, the identification of this patient subset has been a priority, and the subject of a considerable body of literature.310 Because of the power and availability of the implantable cardioverter-defibrillator (ICD) for both primary and secondary prevention of sudden death, and its recent application to HCM,9 it now more important than ever to identify those patients within this broad disease spectrum who are at high risk for a catastrophic event.
Defining reliable clinical markers for sudden death, and isolating the minority of HCM patients who
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