Abstract
Background: Left cardiac sympathetic denervation (LCSD) was reported to be effective in patients with intractable ryanodine receptor mutation-associated catecholaminergic polymorphic ventricular tachycardia (CPVT). Objectives: To report our experience with LCSD in calsequestrin (CASQ2) mutation-associated CPVT. Methods: LCSD was performed in three patients with CASQ2 mutation-associated CPVT with symptoms and exerciseinduced ventricular arrhythmia despite high dose beta-blocker. Results: None of them experienced symptoms or exerciseinduced ventricular arrhythmia after LCSD. However, all had recurrence of symptoms and/or exercise-induced ventricular arrhythmia after 6 months (6–18 months). Conclusions: LCSD conferred short-term suppression but less than optimal long-term suppression of exercise-induced ventricular arrhythmia among CASQ2-associated CPVT patients.
Original language | English |
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Pages (from-to) | 538-540 |
Number of pages | 3 |
Journal | Israel Medical Association Journal |
Volume | 17 |
Issue number | 9 |
State | Published - Sep 2015 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2015, Israel Medical Association. All rights reserved.
Keywords
- Calsequestrin (CASQ2)
- Catecholaminergic polymorphic ventricular tachycardia (CPVT)
- Left cardiac sympathetic denervation (LCSD)