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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/51339
Title: Atrial fibrillation and risk of major arrhythmic events in Brugada syndrome: A meta-analysis
Authors: Jakrin Kewcharoen
Pattara Rattanawong
Chanavuth Kanitsoraphan
Raktham Mekritthikrai
Narut Prasitlumkum
Prapaipan Putthapiban
Poemlarp Mekraksakit
Robert J. Pattison
Wasawat Vutthikraivit
Texas Tech University Health Sciences Center at Lubbock
Faculty of Medicine, Ramathibodi Hospital, Mahidol University
University of Hawaii at Manoa
Einstein Medical Center
Keywords: Medicine
Issue Date: 1-Nov-2019
Citation: Annals of Noninvasive Electrocardiology. Vol.24, No.6 (2019)
Abstract: © 2019 Wiley Periodicals, Inc. Background: Brugada syndrome (BrS) is a common cause of sudden cardiac death (SCD). There is recent evidence that atrial fibrillation (AF) is associated with increased risk of SCD in general population. However, whether AF increases a risk of major arrhythmic events (MAE) in patients with BrS is still unclear. We performed a systematic review and meta-analysis to explore the effect of AF on MAE in BrS population. Methods: We searched the databases of MEDLINE and EMBASE from inception to March 2019. Included studies were published cohort studies reporting rates of MAE (ventricular fibrillation, sustained ventricular tachycardia, SCD, or sudden cardiac arrest) in BrS patients, with and without previous documented AF. Data from each study were combined using the random-effects model. Results: Six studies from 1,703 patients were included. There was a significant association between AF and an increased risk of MAE in patients with BrS (pooled OR = 2.37, 95% CI = 1.36–4.13, p-value =.002, I2 = 40.3%). Conclusions: Our meta-analysis demonstrated that AF is associated with an increased risk of MAE in patients with BrS.
URI: http://repository.li.mahidol.ac.th/dspace/handle/123456789/51339
metadata.dc.identifier.url: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85070326904&origin=inward
ISSN: 1542474X
1082720X
Appears in Collections:Scopus 2019

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