2016
DOI: 10.1016/j.ijcard.2016.05.018
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Surveillance after cardiac arrest in patients with Brugada syndrome without an implantable defibrillator: An alarm effect of the previous syncope

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Cited by 10 publications
(9 citation statements)
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“…Many studies have shown that syncope was an independent predictor of risk, and provided sufficient evidence (Brugada et al, 2004 ; Priori et al, 2012 ; Calvo et al, 2016 ). The presence of symptoms in patients was significantly associated with arrhythmic events (23 vs. 3.8%, P < 0.00001) in our analysis.…”
Section: Discussionmentioning
confidence: 99%
“…Many studies have shown that syncope was an independent predictor of risk, and provided sufficient evidence (Brugada et al, 2004 ; Priori et al, 2012 ; Calvo et al, 2016 ). The presence of symptoms in patients was significantly associated with arrhythmic events (23 vs. 3.8%, P < 0.00001) in our analysis.…”
Section: Discussionmentioning
confidence: 99%
“…BrS patients who suffered from previous syncope were more likely to exhibit EPS inducibility (Priori et al, 2013). Many studies provided sufficient evidence, showing that syncope was an independent predictor of risk (Brugada et al, 2004; Priori et al, 2012; Calvo et al, 2016).…”
Section: Discussionmentioning
confidence: 99%
“…This should include alerting the patient to the relevance of syncope as an alarm symptom that must be followed by immediate admission to an accident and emergency department for acute evaluation. [2]…”
Section: Syncope and Sudden Cardiac Arrestmentioning
confidence: 99%
“…Despite the wide spectrum of clinical manifestations, young and apparently healthy individuals are the most frequently affected by this devastating event. [1,2] During the last 20 years, the genetic basis of Brugada syndrome has been extensively investigated, leading to major changes in gene encoding of the alpha-subunit of the Nav1.5 ( SCN5A , driving the fast depolarising sodium current), the gene most frequently associated with functional abnormalities underlying arrhythmogenicity. However, testing identifies genetic disorders in only 20–30% of the patients analysed, indicating a big gap in knowledge and understanding of the genetic aetiology of the syndrome.…”
mentioning
confidence: 99%