Prolonged QT and cardiac arrest after heart transplantation: inherited or acquired?

J Electrocardiol. 2011 May-Jun;44(3):350-2. doi: 10.1016/j.jelectrocard.2010.12.001. Epub 2011 Jan 26.

Abstract

The long QT syndrome is an inherited arrhythmogenic disease characterized by prolongation of QT interval, syncope, and sudden cardiac death because of ventricular tachycardia, mainly in the form of Torsades de Pointes. We present an unusual case of prolonged QT interval and cardiac arrest caused by Torsades de Pointes in the early phase after orthotopic heart transplant.

Publication types

  • Case Reports

MeSH terms

  • Accidents, Traffic
  • Brain Injuries / complications
  • Brain Injuries / physiopathology
  • Defibrillators, Implantable
  • Electrocardiography / methods*
  • Heart Arrest / etiology*
  • Heart Arrest / physiopathology
  • Heart Arrest / prevention & control
  • Heart Transplantation / adverse effects*
  • Humans
  • Long QT Syndrome / etiology*
  • Long QT Syndrome / physiopathology
  • Long QT Syndrome / prevention & control
  • Male
  • Middle Aged