Stroke and Embolic Events in Hypertrophic Cardiomyopathy
نویسندگان
چکیده
Hypertrophic cardiomyopathy (HCM) is one of the most common genetic cardiac disorders, with markedly heterogeneous clinical manifestations and natural history. Although stroke and systemic embolic events are known to occur as complications of HCM, few data are available on the occurrence and profile of these events in this patient population. In a previous study, stroke and systemic embolic events showed an incidence of 0.8% per year, and these ominous and profound complications were more common in patients with atrial fibrillation (AF). Anticoagulation has proved effective in reducing the incidence of these events in patients with HCM and AF. Also, current guidelines state that anticoagulation is indicated in patients with HCM with paroxysmal, persistent, or chronic AF, regardless of known embolic risk factors such as those covered by the congestive heart failure, hypertension, age=75 years, diabetes mellitus, stroke score. Given the often paroxysmal and asymptomatic nature of AF, however, its diagnosis is sometimes difficult in real-world clinical practice. It is therefore possible that a subclinical, asymptomatic (silent) paroxysmal episode or a first paroxysmal episode of AF in patients without previously documented AF may lead to stroke and peripheral embolization. The epidemiology of these events in patients without documented AF is an important clinical issue. This is especially true for patients at high risk of embolization, such as those with HCM, although the connection remains unclear. The aim of this study was to investigate the frequency and clinical features of patients with HCM with stroke and systemic embolic events in a tertiary referral cohort in Japan and to clarify the epidemiology and risk factors of these events in patients with HCM without previously documented AF.
منابع مشابه
High risk of systemic embolism in hypertrophic cardiomyopathy.
Six of 66 patients with hypertrophic cardiomyopathy had an embolic event during an average observation period of 3.73 years. Five of these had probable cerebral embolism, while 1 patient had a femoral artery embolism. The calculated incidence of systemic embolism was 2.4% per patient year. All embolic events occurred in the patients with atrial fibrillation. In comparison to patients without sy...
متن کاملCombined measurements of cardiac troponin I and brain natriuretic peptide are useful for predicting adverse outcomes in hypertrophic cardiomyopathy.
BACKGROUND Although serum cardiac troponin I (cTnI) and plasma brain natriuretic peptide (BNP) have become clinically important tools as diagnostic and prognostic markers for ischemic heart disease and heart failure, the usefulness of these biomarkers for risk stratification of hypertrophic cardiomyopathy (HCM) is not clear. METHODS AND RESULTS We studied 167 patients with HCM, and cTnI and B...
متن کاملCardiac abnormalities in ischemic cerebrovascular disease studied by two-dimensional echocardiography.
In the study of cardiac abnormalities responsible for the development of cerebral embolism two-dimensional echocardiography was performed on 350 patients with ischemic cerebrovascular disease. The results were compared with those obtained from 350 controls without any history of stroke. Atrial fibrillation was detected on ECG in 115 cases (33%) of the patients and in 35 cases (10%) of the contr...
متن کاملDIFFUSE CORONARY ARTERIAL ECTASIA WITH HYPERTROPHIC CARDIOMYOPATHY
A 40 year old male, a known case of hypertrophic cardiomyopathy, was admitted for catheterization. At catheterization and angiography, septum was hypertrophied to about 5cm and diffuse coronary artery aneurysm was revealed. We found no previous report of coronary artery aneurysm in hypertrophic cardiomyopathy.
متن کاملApical 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 ...
متن کامل