November 1, 2002European Heart Journal
Proposed Diagnostic Criteria for the Brugada Syndrome
Population
Patients with Brugada syndrome
Design
Guideline
Authors
Discussion
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Implication
Requires family screening post-sudden death and male-focused syncope evaluation; reinforces consensus diagnostic criteria for this inherited arrhythmia.
Structured PICO
P
Population
Patients with Brugada syndrome
This document proposes diagnostic criteria for Brugada syndrome, highlighting its epidemiological and clinical presentation characteristics.
Cite This Study
Arthur A.M. Wilde (2002) conducted a review in Brugada syndrome. Brugada syndrome is a familial disease with an incidence of 5-66 per 10,000, characterized by an 8:1 male predominance and arrhythmic events at an average age of 40 years.