Matches in SemOpenAlex for { <https://semopenalex.org/work/W2117029947> ?p ?o ?g. }
- W2117029947 abstract "In the absence of structural heart disease, sudden cardiac death is frequently caused by inherited arrhythmia syndromes, such as long QT syndrome, Brugada syndrome and catecholaminergic polymorphic ventricular tachycardia. Managing these conditions often requires a combination of lifestyle modification, pharmacotherapy and less frequently, invasive therapy. Over the past decade, patient management has been greatly enhanced by tailored pharmacotherapy as a result of a deeper appreciation for arrhythmia mechanisms and supportive evidence from multicenter cohort studies. This article reviews current knowledge regarding drug therapy for inherited arrhythmias. Anti-arrhythmic mechanisms and available clinical evidence are highlighted while maintaining a practical perspective on patient management." @default.
- W2117029947 created "2016-06-24" @default.
- W2117029947 creator A5003758535 @default.
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- W2117029947 creator A5064311226 @default.
- W2117029947 creator A5068211518 @default.
- W2117029947 creator A5076908160 @default.
- W2117029947 date "2015-05-20" @default.
- W2117029947 modified "2023-10-11" @default.
- W2117029947 title "Pharmacotherapy for inherited arrhythmia syndromes: mechanistic basis, clinical trial evidence and practical application" @default.
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