نتایج جستجو برای: brugada syndrome
تعداد نتایج: 622336 فیلتر نتایج به سال:
Follow-up FromChildhood to Adulthood of IndividualsWith Family History of Brugada Syndrome andNormal Electrocardiograms Brugada syndrome is an inherited primary arrhythmia syndromecharacterizedbycoved-typeST-segmentelevation inthe rightprecordial leadswithout structuralheartdiseaseand isassociatedwith increased riskof suddendeath.1 The syndrome is geneticallyandclinicallyheterogeneousandcanpres...
BACKGROUND Provocative testing with sodium channel blockers is advocated for the evaluation of unexplained cardiac arrest (UCA) with the primary purpose of unmasking the typical ECG features of Brugada syndrome. The Cardiac Arrest Survivors with Preserved Ejection Fraction Registry (CASPER) systematically assesses subjects with UCA or a family history of sudden death (FHSD). OBJECTIVE The pur...
The Brugada syndrome accounts for approximately 20% of cases of sudden cardiac death in patients with structurally normal hearts (1–3). The syndrome is characterized by an ST-segment elevation in right precordial leads (V1 to V3) unrelated to ischemia, electrolyte disturbances or obvious structural heart disease, and is sometimes accompanied by a right bundle branch block (RBBB) morphology of t...
Brugada Syndrome is a genetic cardiac disease characterized by electrocardiogram changes consisting of an incomplete right bundle branch block, and ST-segment elevations in right precordial leads V1-V3. These patients are at high risk for developing spontaneous arrhythmias that can be fatal. Many factors during general anesthesia, such as medications, temperature changes, and heart rate variati...
Brugada syndrome, first described over 20 years ago, is characterized by a typical electrocardiographic pattern with coved-type ST-segment elevation in the right precordial leads and a high risk of sudden death in otherwise healthy young adults. The electrocardiographic pattern is sometimes intermittent, and fever is a possible trigger. The authors present the case of a 68-year-old woman who ca...
Since its description in 1992, Brugada Syndrome has become the second cause of death among young adults in some countries1. The Brugada syndrome is an autosomal dominant disease with incomplete penetrance, which may cause syncope and sudden cardiac death in young individuals with a normal heart. It is characterized by an electrocardiographic (ECG) pattern of complete or incomplete right bundle ...
Brugada syndrome is a rare cardiac arrhythmia characterized by electrocardiographic right bundle branch block and persistent ST-segment elevation in the right precordial leads. It is associated with ventricular fibrillation and a high risk for sudden cardiac death, predominantly in younger males with structurally normal hearts. Patients can remain asymptomatic, and electrocardiographic patterns...
BACKGROUND Mutations in the cardiac sodium channel, SCN5A, have been associated with one type of long-QT syndrome, with isolated cardiac conduction defects and Brugada syndrome. The sodium channelopathies exhibit marked variation in clinical phenotypes. The mechanisms underlying the phenotypical diversity, however, remain unknown. Exonic SCN5A mutations can be detected in 20% of Brugada syndrom...
Brugada syndrome is characterized by an electrocardiograph pattern of right bundle-branch block and has an increased risk for cardiac arrest due to malignant arrhythmia. We describe the successful anesthetic management for electroconvulsive therapy in a patient with Brugada electrocardiograph pattern. Patients with Brugada ECG pattern are not recommended to use neostigmine which augments ST ele...
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