Analysis of clinical characteristics, risk factors and complications associated with Brugada Syndrome: An integrative review

Resumen

Brugada Syndrome is a channelopathy resulting from genetic alterations that influence the regulation of sodium channels in the heart muscle, leading, consequently, to arrhythmias, detected by means of an electrocardiogram with ST-segment elevation, given the variably asymptomatic condition of young people with hereditary development of the disease. The diagnosis, when evidenced through clinical manifestations, occurs through syncope or cardiac arrest. Data were analyzed through an integrative literature review and sampling data didactically represented in weighted base articles. Based on digital researches platforms such as PUBMED, SCIELO, SCOPUS and BVS, it is possible, through inclusion and eligibility criteria, to understand the findings and comparatively understand symptoms, clinical conditions, family members and treatment before the target audience.

DOI:https://doi.org/10.56238/sevened2024.005-014