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Diagnosis and management of patients with inherited arrhythmia syndromes in Europe: results of the European Heart Rhythm Association Survey
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2014 (English)In: Europace, ISSN 1099-5129, E-ISSN 1532-2092, Vol. 16, no 4, 600-603 p.Article in journal (Refereed) Published
Abstract [en]

Inherited arrhythmia disorders associated with structurally normal heart (i.e. long and short QT syndrome, Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia, early repolarization syndrome, idiopathic ventricular fibrillation) cause 10 of 1.1 million sudden deaths in Europe and the USA. The purpose of this European Heart Rhythm Association (EHRA) electrophysiology wire survey was to assess the European clinical practice adopted for the diagnosis and management of these disorders. The survey was based on an electronic questionnaire sent out to the EHRA Research Network centres. Responses were received from 50 centres in 23 countries. The results of the survey show that inherited arrhythmia syndromes have a relatively low burden and are diagnosed and managed in accordance with the current guidelines. However, more than 50 of centres do not participate in any existing registry underlining the need for establishing a pan-European registry of these disorders.

Place, publisher, year, edition, pages
2014. Vol. 16, no 4, 600-603 p.
Keyword [en]
Inherited arrhythmia syndrome, Sudden death, Ventricular arrhythmia, Ion channelopathy, Genetic testing, EHRA survey, EP wire
National Category
Cardiac and Cardiovascular Systems
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URN: urn:nbn:se:uu:diva-225076DOI: 10.1093/europace/euu074ISI: 000334915000026OAI: oai:DiVA.org:uu-225076DiVA: diva2:727227
Available from: 2014-06-19 Created: 2014-05-27 Last updated: 2017-12-05Bibliographically approved

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Blomstrom-Lundqvist, Carina

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