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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 |
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creator | Yu, T C 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. |
doi_str_mv | 10.12809/hkmj154653 |
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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”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2786269055/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2786269055?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25752,27923,27924,37011,44589,74897</link.rule.ids></links><search><creatorcontrib>Yu, T C</creatorcontrib><creatorcontrib>Anthony PY Liu</creatorcontrib><creatorcontrib>Lun, K S</creatorcontrib><creatorcontrib>Chung, Brian HY</creatorcontrib><creatorcontrib>Yung, T C</creatorcontrib><title>Clinical and genetic profile of catecholaminergic polymorphic ventricular tachycardia in Hong Kong Chinese children Local experience in Hong Kong</title><title>Hong Kong medical journal = Xianggang yi xue za zhi</title><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.</description><subject>Anticonvulsants</subject><subject>Beta blockers</subject><subject>Cardiac arrhythmia</subject><subject>Catecholamines</subject><subject>Denervation</subject><subject>Electrocardiography</subject><subject>Epilepsy</subject><subject>Fainting</subject><subject>Fitness equipment</subject><subject>Heart rate</subject><subject>Hospitals</subject><subject>Laboratories</subject><subject>Medical treatment</subject><subject>Mortality</subject><subject>Mutation</subject><subject>Patients</subject><issn>1024-2708</issn><issn>2226-8707</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNqNTstKxTAUDKJgfaz8gQOuq2nuTR_rolzQpftLSE-b1PSkJql4P8M_tgU37tzMDMwMM4zdFfyhEDVvHs37NBZyX8rdGcuEEGVeV7w6Z1nBxT4XFa8v2VWMI-eilg3P2HfrLFmtHCjqYEDCZDXMwffWIfgetEqojXdqsoRh2EzvTpMPs1n1J1IKVi9OBUhKm5NWobMKLMHB0wAvG7RmrUYEbazrAhK8-m0Qv2YMFknjn_gNu-iVi3j7y9fs_vnprT3k66mPBWM6jn4JtFpHUdWlKBsu5e5_qR891l19</recordid><startdate>20160801</startdate><enddate>20160801</enddate><creator>Yu, T C</creator><creator>Anthony PY Liu</creator><creator>Lun, K S</creator><creator>Chung, Brian HY</creator><creator>Yung, T C</creator><general>Hong Kong Academy of Medicine</general><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BVBZV</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20160801</creationdate><title>Clinical and genetic profile of catecholaminergic polymorphic ventricular tachycardia in Hong Kong Chinese children Local experience in Hong Kong</title><author>Yu, T C ; Anthony PY Liu ; Lun, K S ; Chung, Brian HY ; Yung, T C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_27862690553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>chi ; eng</language><creationdate>2016</creationdate><topic>Anticonvulsants</topic><topic>Beta blockers</topic><topic>Cardiac arrhythmia</topic><topic>Catecholamines</topic><topic>Denervation</topic><topic>Electrocardiography</topic><topic>Epilepsy</topic><topic>Fainting</topic><topic>Fitness equipment</topic><topic>Heart rate</topic><topic>Hospitals</topic><topic>Laboratories</topic><topic>Medical treatment</topic><topic>Mortality</topic><topic>Mutation</topic><topic>Patients</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yu, T C</creatorcontrib><creatorcontrib>Anthony PY Liu</creatorcontrib><creatorcontrib>Lun, K S</creatorcontrib><creatorcontrib>Chung, Brian HY</creatorcontrib><creatorcontrib>Yung, T C</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>East & South Asia Database</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Hong Kong medical journal = Xianggang yi xue za zhi</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yu, T C</au><au>Anthony PY Liu</au><au>Lun, K S</au><au>Chung, Brian HY</au><au>Yung, T C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical and genetic profile of catecholaminergic polymorphic ventricular tachycardia in Hong Kong Chinese children Local experience in Hong Kong</atitle><jtitle>Hong Kong medical journal = Xianggang yi xue za zhi</jtitle><date>2016-08-01</date><risdate>2016</risdate><volume>22</volume><issue>4</issue><spage>314</spage><pages>314-</pages><issn>1024-2708</issn><eissn>2226-8707</eissn><abstract>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.</abstract><cop>Hong Kong</cop><pub>Hong Kong Academy of Medicine</pub><doi>10.12809/hkmj154653</doi><oa>free_for_read</oa></addata></record> |
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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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