Abstract
Background. Long QT syndrome (LQTS) is a congenital disorder accompanied by a high incidence of sudden cardiac death. β-Adrenergic blockade is the therapy of choice, and it is successful in 75-80% of patients. For those in whom cardiac events (syncope or cardiac arrest) are not prevented by β-blockade, experimental studies suggest that left cardiac sympathetic denervation (LCSD) may be useful. Methods and Results. We identified 85 LQTS patients worldwide who underwent LCSD, and we provide here the first large-scale evaluation of its efficacy. The time interval between the first cardiac event and LCSD and the follow-up period after LCSD were similar (5.6±6.1 versus 5.9±5.7 years). The mean age of the patients at surgery was 20±13 years. LCSD was followed by highly significant (p
Original language | English |
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Pages (from-to) | 503-511 |
Number of pages | 9 |
Journal | Circulation |
Volume | 84 |
Issue number | 2 |
Publication status | Published - 1991 |
Keywords
- QT interval
- Sudden cardiac death
- Sympathetic nervous system
ASJC Scopus subject areas
- Physiology
- Cardiology and Cardiovascular Medicine