Acquired Long QT Syndrome and Electrophysiology of Torsade de Pointes
- PMID: 31114687
- PMCID: PMC6528034
- DOI: 10.15420/aer.2019.8.3
Acquired Long QT Syndrome and Electrophysiology of Torsade de Pointes
Abstract
Congenital long QT syndrome (LQTS) has been the most investigated cardiac ion channelopathy. Although congenital LQTS remains the domain of cardiologists, cardiac electrophysiologists and specialised centres, the much more frequently acquired LQTS is the domain of physicians and other members of healthcare teams required to make therapeutic decisions. This paper reviews the electrophysiological mechanisms of acquired LQTS, its ECG characteristics, clinical presentation, and management. The paper concludes with a comprehensive review of the electrophysiological mechanisms of torsade de pointes.
Keywords: Long QT syndrome; electrophysiology; torsade de pointes.
Conflict of interest statement
Disclosure: The authors have no conflicts of interest to declare.
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