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
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Sprache:eng
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Zusammenfassung: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 aborted cardiac arrest or death from age 41 though 75 years was assessed in 2759 subjects from the International LQTS Registry, categorized into electrocardiographically affected (corrected QT interval [QTc] > or = 470 ms), borderline (QTc 440 to 469 ms), and unaffected (QTc < 440 ms) subgroups. The affected versus unaffected adjusted hazard ratio for aborted cardiac arrest or death was 2.65 (P
ISSN:0009-7322
1524-4539
DOI:10.1161/CIRCULATIONAHA.107.729368