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Clinical and genetic profile of catecholaminergic polymorphic ventricular tachycardia in Hong Kong Chinese children Local experience in Hong Kong

Objective: To report our experience in the management of catecholaminergic polymorphic ventricular tachycardia in Hong Kong Chinese children. Methods: This case series study was conducted in a tertiary paediatric cardiology centre in Hong Kong. All paediatric patients diagnosed at our centre with ca...

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Published in:Hong Kong medical journal = Xianggang yi xue za zhi 2016-08, Vol.22 (4), p.314
Main Authors: Yu, T C, Anthony PY Liu, Lun, K S, Chung, Brian HY, Yung, T C
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Language:chi ; eng
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Anthony PY Liu
Lun, K S
Chung, Brian HY
Yung, T C
description Objective: To report our experience in the management of catecholaminergic polymorphic ventricular tachycardia in Hong Kong Chinese children. Methods: This case series study was conducted in a tertiary paediatric cardiology centre in Hong Kong. All paediatric patients diagnosed at our centre with catecholaminergic polymorphic ventricular tachycardia from January 2008 to October 2014 were included. Results: Ten patients (five females and five males) were identified. The mean age at presentation and at diagnosis were 11.0 (standard deviation, 2.9) years and 12.5 (2.8) years, respectively. The mean delay time from first presentation to diagnosis was 1.5 (standard deviation, 1.3) years. They presented with recurrent syncope and six patients had a history of aborted cardiac arrest. Four patients were initially misdiagnosed to have epilepsy. Catecholaminergic polymorphic ventricular tachycardia was diagnosed by electrocardiogram at cardiac arrest (n=2), or provocation test, either by catecholamine infusion test (n=6) or exercise test (n=2). Mutations of the RyR2gene were confirmed in six patients. Nine patients were commenced on beta-blockers after diagnosis. Despite medications, three patients developed aborted or resuscitated cardiac arrest (n=2) and syncope (n=1). Left cardiac sympathetic denervation was performed in five patients and an implantable cardioverter defibrillator was implanted in another. There was no mortality during follow-up. Conclusions: Catecholaminergic polymorphic ventricular tachycardia should be considered in children who present with recurrent syncope during exercise or emotional stress. Despite beta-blocker treatment, recurrent ventricular arrhythmias occur and may result in cardiac arrest.
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Methods: This case series study was conducted in a tertiary paediatric cardiology centre in Hong Kong. All paediatric patients diagnosed at our centre with catecholaminergic polymorphic ventricular tachycardia from January 2008 to October 2014 were included. Results: Ten patients (five females and five males) were identified. The mean age at presentation and at diagnosis were 11.0 (standard deviation, 2.9) years and 12.5 (2.8) years, respectively. The mean delay time from first presentation to diagnosis was 1.5 (standard deviation, 1.3) years. They presented with recurrent syncope and six patients had a history of aborted cardiac arrest. Four patients were initially misdiagnosed to have epilepsy. Catecholaminergic polymorphic ventricular tachycardia was diagnosed by electrocardiogram at cardiac arrest (n=2), or provocation test, either by catecholamine infusion test (n=6) or exercise test (n=2). Mutations of the RyR2gene were confirmed in six patients. Nine patients were commenced on beta-blockers after diagnosis. Despite medications, three patients developed aborted or resuscitated cardiac arrest (n=2) and syncope (n=1). Left cardiac sympathetic denervation was performed in five patients and an implantable cardioverter defibrillator was implanted in another. There was no mortality during follow-up. Conclusions: Catecholaminergic polymorphic ventricular tachycardia should be considered in children who present with recurrent syncope during exercise or emotional stress. Despite beta-blocker treatment, recurrent ventricular arrhythmias occur and may result in cardiac arrest.</description><identifier>ISSN: 1024-2708</identifier><identifier>EISSN: 2226-8707</identifier><identifier>DOI: 10.12809/hkmj154653</identifier><language>chi ; eng</language><publisher>Hong Kong: Hong Kong Academy of Medicine</publisher><subject>Anticonvulsants ; Beta blockers ; Cardiac arrhythmia ; Catecholamines ; Denervation ; Electrocardiography ; Epilepsy ; Fainting ; Fitness equipment ; Heart rate ; Hospitals ; Laboratories ; Medical treatment ; Mortality ; Mutation ; Patients</subject><ispartof>Hong Kong medical journal = Xianggang yi xue za zhi, 2016-08, Vol.22 (4), p.314</ispartof><rights>2016. This work is published under https://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). 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Nine patients were commenced on beta-blockers after diagnosis. Despite medications, three patients developed aborted or resuscitated cardiac arrest (n=2) and syncope (n=1). Left cardiac sympathetic denervation was performed in five patients and an implantable cardioverter defibrillator was implanted in another. There was no mortality during follow-up. Conclusions: Catecholaminergic polymorphic ventricular tachycardia should be considered in children who present with recurrent syncope during exercise or emotional stress. 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subjects Anticonvulsants
Beta blockers
Cardiac arrhythmia
Catecholamines
Denervation
Electrocardiography
Epilepsy
Fainting
Fitness equipment
Heart rate
Hospitals
Laboratories
Medical treatment
Mortality
Mutation
Patients
title Clinical and genetic profile of catecholaminergic polymorphic ventricular tachycardia in Hong Kong Chinese children Local experience in Hong Kong
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