Management in hypertrophic cardiomyopathy is aimed at improving symptoms an
d exercise capacity and preventing complications. particularly sudden death
. The strategy for management of symptoms is to identify potentially import
ant mechanisms at which treatment can be targeted. Assessment is feasible w
ith non-invasive evaluation. All patients with hypertrophic cardiomyopathy
should undergo risk assessment for sudden death. regardless of their sympto
matic. morphological and haemodynamic status. Recent prospective studies ha
ve examined five risk markers: family history of sudden death (two or more
members aged < 45 years). unexplained syncope, non-sustained ventricular ta
chycardia on Hotter monitoring, abnormal exercise blood pressure response a
nd severe left ventricular hypertrophy (greater than or equal to3 cm). The
majority of patients had none of these risk factors and did not die suddenl
y. Annual sudden death rates were at least 2% among patients with two or mo
re of these risk markers. which warrants consideration of prophylactic trea
tment (amiodarone, implantable cardioverter-defibrillator) in such patients
. (C) 2001 The European Society of Cardiology.