Sudden death in hypertrophic cardiomyopathy. Assessment of patients at high risk.
نویسندگان
چکیده
T he incidence of sudden death in hypertrophic cardiomyopathy is 2-4% a year in adults and 4-6% a year in children and adolescents.1 These data have been generated from referral cardiac centers and may reflect a bias to the more severe patients.2 The identification and management of patients with hypertrophic cardiomyopathy who are at increased risk of sudden death remains a major problem, particularly in younger patients.
منابع مشابه
Apical Hypertrophic Cardiomyopathy in a Case with Chest Pain and Family History of Sudden Cardiac Death: A Case Report
Hypertrophic cardiomyopathy (HCM) is the most common genetic cardiovascular disease, which is caused by a multitude of mutations in genes encoding proteins of the cardiac sarcomere (1). Apical hypertrophic cardiomyopathy (AHCM) is an uncommon type of HCM. The sudden cardiac death is less likely to occur in the patients inflicted with AHCM (2). Herein, we presented the case of a 29-year-old man ...
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INTRODUCTION Background: The actual prognosis of hypertrophic cardiomyopathy, a disorder previously thought of to be notorious for an increased risk of untimely death is poorly defined. Objective: The present study describes the findings of patients with Hypertrophic Cardiomyopathy followed for more than nineteen years in a large clinic population. Materials and Methods: A clinic population of ...
متن کاملRisk stratification and prevention of sudden death in hypertrophic cardiomyopathy.
Sudden unexpected death, often occurring in young, asymptomatic patients, is the most devastating facet of the natural history of hypertrophic cardiomyopathy, and appears to be the consequence of primary ventricular tachyarrhythmias arising in an electrically unstable myocardial substrate characterized by disorganized cellular architecture, ischemia, cell death, and replacement scarring. Althou...
متن کاملRefining the characterization of residual function in hypertrophic cardiomyopathy through remote segment 4D strain analysis
Background Quantitative assessment of late gadolinium enhancement (LGE) by cardiovascular magnetic resonance imaging (CMR) has been associated with an increased risk of sudden cardiac death (SCD) in patients with hypertrophic cardiomyopathy (HCM). However, patients with lesser degrees of LGE may still remain at high risk of adverse cardiac events due to the diffuse pathophysiology of HCM. Non-i...
متن کامل[Myocardial fibrosis in patients with hypertrophic cardiomyopathy and high risk for sudden death].
BACKGROUND The stratification of risk for sudden death in hypertrophic cardiomyopathy (HCM) continues to be a true challenge due to the great heterogeneity of this disease's presentation, as most individuals remain asymptomatic during their entire lives and others present sudden death as first symptom. Recent studies have suggested that myocardial fibrosis may represent an important substrate f...
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عنوان ژورنال:
- Circulation
دوره 80 5 شماره
صفحات -
تاریخ انتشار 1989