Long-QT Syndrome After Age 40
Author(s) -
Ilan Goldenberg,
Arthur J. Moss,
James Bradley,
Slava Polonsky,
Derick R. Peterson,
Scott McNitt,
Wojciech Zaręba,
Mark Andrews,
Jennifer L. Robinson,
Michael J. Ackerman,
Jesaia Benhorin,
Elizabeth S. Kaufman,
Emanuela H. Locati,
Carlo Napolitano,
Silvia G. Priori,
Ming Qi,
Peter J. Schwartz,
Jeffrey A. Towbin,
G. Michael Vincent,
Li Zhang
Publication year - 2008
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.107.729368
Subject(s) - medicine , hazard ratio , long qt syndrome , qt interval , sudden cardiac death , cardiology , population , confidence interval , pediatrics , environmental health
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.
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