Brugada Syndrome: Current Practices in Diagnosis, Prognosis, and Treatment

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Brugada Syndrome: Current Practices in Diagnosis, Prognosis, and Treatment

Introduction Brugada syndrome (BrS) is a hereditable syndrome, first reported in 1992, characterized by right bundle branch block and an uncommon form of ST-T wave elevation in the V1 and V2 leads. It is associated with risk of sudden cardiac death (SCD) arising from of polymorphic ventricular tachyarrhythmias [1,2]. The manifestations of BrS vary widely, from asymptomatic individuals to those ...

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Diagnosis of Brugada Syndrome

Implantable cardioverter defibrillator (ICD) is considered to be the main therapy for prevention of sudden cardiac death in patients with Brugada syndrome (BrS). However, there have been several reports suggesting a higher prevalence of complications, such as inappropriate shocks, lead failure, and device infection compared with the incidence of lethal ventricular arrhythmia. BrS is mainly diag...

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Worrisome thoughts about the diagnosis and treatment of patients with Brugada waves and the Brugada syndrome.

The Brugadas have made a significant contribution to medicine. Their discovery of a new clinical syndrome and ECG abnormalities has created a great deal of interest and has opened Pandora's box. Here, we discuss some worrisome thoughts about the condition. We stress the need for improved diagnostic criteria and treatment because it is not always possible to perform coronary arteriography, elect...

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Clinical aspects and prognosis of Brugada syndrome in children.

BACKGROUND Brugada syndrome is an arrhythmogenic disease characterized by an ECG pattern of ST-segment elevation in the right precordial leads and augmented risk of sudden cardiac death. Little is known about the clinical presentation and prognosis of this disease in children. METHODS AND RESULTS Thirty children affected by Brugada syndrome who were <16 years of age (mean, 8+/-4 years) were i...

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ژورنال

عنوان ژورنال: International Cardiovascular Forum Journal

سال: 2017

ISSN: 2409-3424,2410-2636

DOI: 10.17987/icfj.v9i0.407