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Michowitz, Yoav
Milman, Anat Andorin, Antoine Sarquella Brugada, Geòrgia Gonzalez Corcia, M. Cecilia Gourraud, Jean Baptiste Conte, Giulio Sacher, Frederic Juang, Jimmy J.M. Kim, Sung Hwan Leshem, Eran Mabo, Philippe Postema, Pieter G. Hochstadt, Aviram Wijeyeratne, Yanushi D. Denjoy, Isabelle Giustetto, Carla Mizusawa, Yuka Huang, Zhengrong Jespersen, Camilla H. Maeda, Shingo Takahashi, Yoshihide Kamakura, Tsukasa Aiba, Takeshi Arbelo, Elena Mazzanti, Andrea Allocca, Giuseppe Brugada, Ramon Casado-Arroyo, Ruben Champagne, Jean Priori, Silvia G. Veltmann, Christian Delise, Pietro Corrado, Domenico Brugada Terradellas, Josep Kusano, Kengo F. Hirao, Kenzo Calo, Leonardo Takagi, Masahiko Tfelt-Hansen, Jacob Yan, Gan Xin Gaita, Fiorenzo Leenhardt, Antoine Behr, Elijah R. Wilde, Arthur A.M. Nam, Gi Byoung Brugada Terradellas, Pedro Probst, Vincent Belhassen, Bernard |
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2019 April 16 | |
El tÃtol de la versió preprint d’aquest article és, Arrhythmic "Events in the Young with Brugada Syndrome: Characterization, Management and Risk Factors for Recurrence" Background: Information on young patients with Brugada syndrome (BrS) and arrhythmic events (AEs) is limited. Objectives: The purpose of this study was to describe their characteristics and management as well as risk factors for AE recurrence. Methods: A total of 57 patients (age ≤20 years), all with BrS and AEs, were divided into pediatric (age ≤12 years; n = 26) and adolescents (age 13 to 20 years; n = 31). Results: Patients’ median age at time of first AE was 14 years, with a majority of males (74%), Caucasians (70%), and probands (79%) who presented as aborted cardiac arrest (84%). A significant proportion of patients (28%) exhibited fever-related AE. Family history of sudden cardiac death (SCD), prior syncope, spontaneous type 1 Brugada electrocardiogram (ECG), inducible ventricular fibrillation at electrophysiological study, and SCN5A mutations were present in 26%, 49%, 65%, 28%, and 58% of patients, respectively. The pediatric group differed from the adolescents, with a greater proportion of females, Caucasians, fever-related AEs, and spontaneous type-1 ECG. During follow-up, 68% of pediatric and 64% of adolescents had recurrent AE, with median time of 9.9 and 27.0 months, respectively. Approximately one-third of recurrent AEs occurred on quinidine therapy, and among the pediatric group, 60% of recurrent AEs were fever-related. Risk factors for recurrent AE included sinus node dysfunction, atrial arrhythmias, intraventricular conduction delay, or large S-wave on ECG lead I in the pediatric group and the presence of SCN5A mutation among adolescents. Conclusions: Young BrS patients with AE represent a very arrhythmogenic group. Current management after first arrhythmia episode is associated with high recurrence rate. Alternative therapies, besides defibrillator implantation, should be considered |
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application/pdf | |
http://hdl.handle.net/10256/18112 | |
eng | |
Elsevier | |
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.jacc.2019.01.048 info:eu-repo/semantics/altIdentifier/issn/0735-1097 |
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Tots els drets reservats | |
Brugada, SÃndrome de
Brugada syndrome Quinidina Quinidine |
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Characterization and Management of Arrhythmic Events in Young Patients With Brugada Syndrome | |
info:eu-repo/semantics/article | |
DUGiDocs |