RT-150

14th International Congress
THE "NEW FRONTIERS"
OF ARRHYTHMIAS 2000

Jan. 29 - Feb. 5, 2000
Marilleva, Trento, Italy

RT-150

Acquired long QT syndrome

Yee Guan Yap, A. John Camm.
British Heart Foundation Research Fellow in Cardiology, Department of Cardiological Sciences, St. George’s Hospital Medical School, London, UK

Introduction

Prolonged QT interval on 12-lead electrocardiogram (ECG) has been known to cause a specific form of life-threatening polymorphic ventricular tachycardia, namely torsades de pointes. If persists, it can lead to ventricular fibrillation and sudden death. There are 2 major forms of Long QT syndrome (LQTS): the rare congenital form and the more common acquired form. While there are many causes of acquired LQTS, the identification of the genetic defects in congenital LQTS has helped in the understanding of the patho-mechanism of acquired LQTS, at least in drug-induced LQTS.
Many factors can cause QT prolongation and the appearance of prolonged QT interval has been shown to be a prognostic risk factor in many cardiac as well as non-cardiac conditions. Nevertheless, the commonest cause of acquired long QT syndrome is drug-induced, and this issue has been identified as a considerable public health problem. In this article, we will discuss acquired LQTS with particular emphasis on drug-induced LQTS.

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