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The Brugada Syndrome: From Bench To Bedside

Charles Antzelevitch (Editor), Pedro Brugada (Associate Editor), Joseph Brugada (Associate Editor), Ramon Brugada (Associate Editor)
ISBN: 978-1-4051-2778-3
248 pages
January 2005, Wiley-Blackwell
The Brugada Syndrome: From Bench To Bedside (1405127783) cover image

Description

Until recently, the cellular basis for sudden death, the Brugada Syndrome, has largely remained an unknown to modern arrhythmologists and cardiologists, particularly in the absence of any structural heart disease. Detailed observations of age-groups, especially the young, families and populations where sudden death frequently occurs, and improved understanding of its contributory factors and mechanisms are, however, showing the way forward.

This addition to the Clinical Approaches to Tachyarrhythmias (CATA) Series, written by the investigators who discovered and probed the Brugada Syndrome, discusses the history, etiology, pathology and clinical manifestations of sudden death. From diagnosis, prognosis, to therapeutic approaches using the latest in cathater ablation techniques, electrophysiological surgery, and genetic appraisal, the work is a testimony to the author's investigation. Using clinical cases in Thailand and Laos, they further unravel the syndrome's molecular mechanisms, studying related syndromes, such as the long-QT syndrome, infant death, and arryhthmogenic right ventricular cardiomyopathy.

By being informed of the electrophysiological abnormalities that contribute to familial and genetic diseases, physicians, cardiologists and all those who care for patients with cardiac arrhythmias will be better able to identify and treat patients in whom the Brugada Syndrome may strike next.

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Table of Contents

Contributors.

Preface.

Dedication.

1 Brugada Syndrome: Overview.

2 History of the Brugada Syndrome.

3 Biophysical Analysis of Mutant Sodium Channels in Brugada Syndrome.

4 Molecular Genetics of the Brugada Syndrome.

5 Cellular Mechanisms Underlying the Brugada Syndrome.

6 Brugada Syndrome: Diagnostic Criteria.

7 Value of 12 Lead ECG and Derived Methodologies in the Diagnosis of Brugada Disease.

8 Brugada Syndrome: Relationship to Other Arrhythmogenic Syndromes.

9 ST Segment Elevation and Sudden Death in the Athlete.

10 Brugada Syndrome Genetics. Genetic Screening- Role in Diagnosis.

11 Genotype-Phenotype Relationship in Brugada Syndrome.

12 Gender Differences in Brugada Syndrome.

13 Predisposing Factors.

14 Acquired Forms of Brugada Syndrome.

15 Brugada Syndrome and supraventricular tacharrhythmias.

16 Prognosis in Individuals with the Brugada Syndrome.

17 Treatment of the Brugada Syndrome with the Implantable Cardioverter Defibrillator.

18 Pharmacologic Approach to Therapy of the Brugada Syndrome: Quinidine as an Alterative to ICD Therapy?.

19 Potential for Ablation Therapy in Patients with the Brugada Syndrome.

Index

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Author Information

Charles Antzelevitch, PhD, is Executive Director/Director of Research; Gordon K. Moe Scholar; Professor of Pharmacology at the Masonic Medical Research Laboratory; Utica, New York.

Pedro Brugada, MD, PhD, is Professor of Cardiology at the Cardiovascular Center OLV Hospital in Aalst, Belgium.

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The Wiley Advantage

Brugada Syndrome (the cellular basis for sudden death) has until now remained largely unknown and under-diagnosed

A short and expert text in the CATA Series written by the investigators who discovered the syndrome

Covers the history, etiology, pathology and clinical manifestations of sudden death

A case-based guide to diagnosis, prognosis and therapeutic strategy to aid early recognition and treatment

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