Long-term outcome in patients with Marfan syndrome: is aortic dissection the only cause of sudden death?
AT Yetman, RA Bornemeier, BW McCrindle - Journal of the American …, 2003 - jacc.org
AT Yetman, RA Bornemeier, BW McCrindle
Journal of the American College of Cardiology, 2003•jacc.orgObjectives: We sought to assess outcomes in a series of young patients with Marfan
syndrome and to define the prevalence of ventricular arrhythmias in this patient population.
Background: While sudden death is a well-recognized outcome in Marfan syndrome,
ventricular arrhythmias are not well described. Methods: Patients were followed with
echocardiography, electrocardiography, and ambulatory electrocardiography. The
prevalence and associated factors for ventricular dysrhythmias were defined. Results …
syndrome and to define the prevalence of ventricular arrhythmias in this patient population.
Background: While sudden death is a well-recognized outcome in Marfan syndrome,
ventricular arrhythmias are not well described. Methods: Patients were followed with
echocardiography, electrocardiography, and ambulatory electrocardiography. The
prevalence and associated factors for ventricular dysrhythmias were defined. Results …
Objectives
We sought to assess outcomes in a series of young patients with Marfan syndrome and to define the prevalence of ventricular arrhythmias in this patient population.
Background
While sudden death is a well-recognized outcome in Marfan syndrome, ventricular arrhythmias are not well described.
Methods
Patients were followed with echocardiography, electrocardiography, and ambulatory electrocardiography. The prevalence and associated factors for ventricular dysrhythmias were defined.
Results
Seventy patients with Marfan syndrome diagnosed at birth to 52 years were followed for a period of up to 24 years. All patients had cardiovascular involvement and were started on medical therapy. No patient died from aortic dissection, while 4% died from arrhythmias. Ventricular arrhythmias were present in 21% and were associated with increased left ventricular size, mitral valve prolapse, and abnormalities of repolarization.
Conclusions
Cardiac complications are rare in young patients with Marfan syndrome receiving medical therapy and close clinical follow-up. Sudden death still occurs, and appears more common in patients with a dilated left ventricle. Left ventricular dilation may predispose to alterations of repolarization and fatal ventricular arrhythmias.
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