Long-QT Syndrome After Age 40

Previous studies that assessed the risk of life-threatening cardiac events in patients with congenital long-QT syndrome (LQTS) have focused mainly on the first 4 decades of life, whereas the clinical course of this inherited cardiac disorder in the older population has not been studied. The risk of...

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Veröffentlicht in:	Circulation (New York, N.Y.) N.Y.), 2008-04, Vol.117 (17), p.2192-2201
Hauptverfasser:	GOLDENBERG, Ilan, MOSS, Arthur J, BENHORIN, Jesaia, KAUFMAN, Elizabeth S, LOCATI, Emanuela H, NAPOLITANO, Carlo, PRIORI, Silvia G, MING QI, SCHWARTZ, Peter J, TOWBIN, Jeffrey A, VINCENT, G. Michael, LI ZHANG, BRADLEY, James, POLONSKY, Slava, PETERSON, Derick R, MCNITT, Scott, ZAREBA, Wojciech, ANDREWS, Mark L, ROBINSON, Jennifer L, ACKERMAN, Michael J
Format:	Artikel
Sprache:	eng
Schlagworte:	Adrenergic beta-Antagonists - therapeutic use Adult Age Distribution Aged Biological and medical sciences Blood and lymphatic vessels Cardiology. Vascular system Death, Sudden, Cardiac - epidemiology Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous Electrocardiography Female Genotype Humans Kaplan-Meier Estimate Long QT Syndrome - diagnostic imaging Long QT Syndrome - drug therapy Long QT Syndrome - genetics Long QT Syndrome - mortality Male Medical sciences Middle Aged Multivariate Analysis Pacemaker, Artificial Phenotype Registries Risk Factors Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis Ultrasonography
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