Coexistent Brugada Syndrome and Wolff-Parkinson-White Syndrome: What is the Optimal Management? [PDF]
Coexistent Brugada syndrome and Wolff-Parkinson-White (WPW) syndrome is rare, and as such poses management challenges. The overlap of symptoms attributable to each condition, the timing of ventricular stimulation after accessory pathway ablation and the ...
Abhishek Jaiswal, MBBS+2 more
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Fever Unmasked Brugada Syndrome in Pediatric Patient: A Case Report [PDF]
Introduction: Brugada syndrome is an arrhythmogenic disorder that is a known cause of sudden cardiac death. It is characterized by a pattern of ST segment elevation in the precordial leads on an electrocardiogram (EKG) due to a sodium channelopathy. Case
Orhay Mirzapolos+2 more
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Model of nursing care for patients with Brugada syndrome according to the international ICNP® [PDF]
Introduction Brugada syndrome is a rare disease involving genetic disorders of heart rhythm. The disease was discovered in 1992 by the Brugada brothers, Spanish cardiologists.
Aleksandra Stosiek+3 more
doaj +5 more sources
Long-term of epicardial radiofrequency ablation and benefit for recurrent ventricular arrhythmia in Brugada syndrome: A systematic review and meta-analysis. [PDF]
Epicardial radiofrequency ablation significantly reduces recurrent ventricular arrhythmias and ICD shocks in Brugada syndrome, with excellent long‐term safety and no reported mortality. Epicardial ablation is an effective strategy for sustained rhythm stabilization. Abstract Background Brugada syndrome (BrS) is a rare cardiac channelopathy linked to an
Adji AS+7 more
europepmc +2 more sources
Distinct functional defect of three novel Brugada syndrome related cardiac sodium channel mutations [PDF]
The Brugada syndrome is characterized by ST segment elevation in the right precodial leads V1-V3 on surface ECG accompanied by episodes of ventricular fibrillation causing syncope or even sudden death.
Juang Jyh-Ming+8 more
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Risk stratification of elderly patients with Brugada syndrome: Results from a large Japanese cohort of idiopathic ventricular fibrillation. [PDF]
This study suggests that asymptomatic elderly patients with Brugada syndrome may be at a very low risk of developing life‐threatening arrhythmias. Abstract Background Brugada syndrome (BrS) is an inherited cardiac channelopathy associated with a high risk of sudden cardiac death (SCD) due to ventricular fibrillation (VF).
Shinohara T+10 more
europepmc +2 more sources
Clinical presentation and electrocardiographic features of Brugada syndrome in Iraq [PDF]
Background: Brugada syndrome is a clinical entity composed of twelve leads electrocardiographic changes of coved or saddle shaped ST-segment elevation in V1 and V2 with serious ventricular arrhythmias which may cause sudden cardiac death. Objectives: The
AMAR AL-HAMDI
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The Unmasking Effect: Propofol-Induced Brugada Pattern in a Critically Ill Patient
Brugada syndrome is a known cause of dysrhythmias and sudden cardiac death. It is linked to mutations in myocardial sodium channel leading to hyperexcitable cardiac myocytes.
Esiemoghie Akhigbe+4 more
doaj +1 more source
Brugada pattern in adolescent with acute myocarditis due to SARS‐CoV‐2
Brugada syndrome is a genetic disorder characterized by abnormal findings on electrocardiogram (ECG) that can precipitate ventricular tachyarrhythmias and sudden cardiac death.
David Bergamo, Courtney Nelson
doaj +1 more source
Reversible Brugada like electrocardiographic pattern in COVID-19 infection
Brugada syndrome, a rare genetic disease increases the risk of arrhythmias and sudden cardiac death. Various trigger factors has been associated with Brugada syndrome. Arrhythmias have been reported in COVID 19. We report a patient with transient Brugada
Kamal Kant Jena+5 more
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