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A Case of Brugada Syndrome… or Something Else? Behind Type 1 Brugada Pattern. [PDF]

open access: yesClin Case Rep
ABSTRACT Although Brugada syndrome has traditionally been considered a primary electrical disease, accumulating evidence supports the presence of subtle structural abnormalities, particularly involving the right ventricular outflow tract. Nevertheless, the identification of overt myocardial scar and biventricular arrhythmogenic substrate should prompt ...
Scarà A   +3 more
europepmc   +2 more sources

Clinical presentation and electrocardiographic features of Brugada syndrome in Iraq [PDF]

open access: yesThe Medical Journal of Basrah University, 2021
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
doaj   +1 more source

Brugada pattern in adolescent with acute myocarditis due to SARS‐CoV‐2

open access: yesJournal of the American College of Emergency Physicians Open, 2022
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

The Unmasking Effect: Propofol-Induced Brugada Pattern in a Critically Ill Patient

open access: yesCase Reports in Cardiology, 2022
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

Model of nursing care for patients with Brugada syndrome according to the international ICNP®

open access: yesJournal of Education, Health and Sport, 2019
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   +3 more sources

Brugada syndrome in a 4-year-old child with Lemierre syndrome—A case report

open access: yesJournal of the Saudi Heart Association, 2018
Brugada syndrome is a rare arrhythmogenic disease with characteristic electrocardiogram (ECG) findings. Fever represents an important triggering factor.
Sami Alanazi   +3 more
doaj   +1 more source

Atrial electrical abnormality in patients with Brugada syndrome assessed by signal-averaged electrocardiography

open access: yesIndian Heart Journal, 2017
Background: Ventricular fibrillation and atrial fibrillation are well-known arrhythmias in patients with Brugada syndrome. This study evaluated the characteristics of the atrial arrhythmogenic substrate using the signal-averaged electrogram (SAECG) in ...
Yasutsugu Nagamoto   +12 more
doaj   +1 more source

Anesthesia in patients with Brugada syndrome: two case reports

open access: yesJournal of Medical Case Reports, 2023
Background Brugada syndrome is a rare disease. It causes sudden cardiac arrest, which is a serious life-threatening event. Sudden cardiac death mostly results from coronary artery disease.
Che-Hao Hsu, Shin-Hong Lin, Li-Yen Chang
doaj   +1 more source

Reversible Brugada like electrocardiographic pattern in COVID-19 infection

open access: yesSaudi Journal for Health Sciences, 2021
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
doaj   +1 more source

Speckle tracking echocardiography data in Brugada syndrome patients

open access: yesData in Brief, 2019
Brugada syndrome is characterized by typical electrocardiogram changes and a high risk for sudden cardiac death (Priori et al., 2013). In addition to the well known electrical substrate, morphological and functional alterations appeared to be present in ...
Esther Scheirlynck   +9 more
doaj   +1 more source

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