Refractory Ventricular Tachycardia in a Long QT Syndrome Child Successfully Controlled by Left Cardiac Sympathetic Denervation
Author(s) -
Jih-Chin Chang,
Chung-Ping Hsu,
Betau Hwang,
Pi-Chang Lee,
C. J. Tsai,
MingChih Lin,
ShengLing Jan,
YunChing Fu
Publication year - 2012
Publication title -
pediatrics and neonatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.569
H-Index - 36
eISSN - 2212-1692
pISSN - 1875-9572
DOI - 10.1016/j.pedneo.2012.08.014
Subject(s) - medicine , cardiology , long qt syndrome , sympathetic denervation , refractory (planetary science) , ventricular tachycardia , sudden cardiac death , denervation , tachycardia , cardiac arrhythmia , complication , anesthesia , qt interval , physics , astrobiology , atrial fibrillation
Long QT syndrome 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. However, for those in whom refractory arrhythmia or cardiac events are not prevented by medication, the literature suggests that left cardiac sympathetic denervation may be useful. Here we present a girl 20 months of age with refractory ventricular tachycardia due to long QT syndrome successfully treated by left cardiac sympathetic denervation. There was no significant complication.
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