Elimination of fatal arrhythmias through ablation of triggering premature ventricular contraction in type 3 long QT syndrome

Z Cheng, P Gao, K Cheng, T Chen… - Annals of …, 2012 - Wiley Online Library
Congenital long QT syndrome (LQTS) is the most common inherited arrhythmia, fatal
arrhythmias are the main causes of sudden death, and often induced by the premature …

[HTML][HTML] Successful radiofrequency catheter ablation of a premature ventricular contraction triggering ventricular fibrillation in a patient with short QT syndrome

Y Morimoto, A Watanabe, H Morita, N Nishii… - HeartRhythm Case …, 2019 - Elsevier
Short QT syndrome (SQTS) is a very rare inherited arrhythmic disease that is associated with
sudden cardiac death (SCD) caused by ventricular tachyarrhythmias. Gussak and …

Delayed paced ventricular activation in the long QT syndrome is associated with ventricular fibrillation

RC Saumarez, M Pytkowski, M Sterlinski, RNW Hauer… - Heart Rhythm, 2006 - Elsevier
BACKGROUND: LQTS may cause sudden cardiac death (SCD), but the mechanisms linking
gene mutations to ventricular fibrillation (VF) are unclear. OBJECTIVE: To determine …

Analyses of triggers for recurrent cardiac events in 38 patients with symptomatic long QT syndrome

K Li, F She, J Yang, YW Liu, R He, Y Xie… - Zhonghua xin xue …, 2021 - europepmc.org
Objective: To evaluate the main triggers of recurrent cardiac events in patients with
symptomatic congenital long QT syndrome (cLQTS). Methods: In this retrospective case …

[PDF][PDF] Long QT-syndrome with torsades de pointes managed considering financial constraints faced by the patient

R Patel, S Aggarwal, PSS Athwal, S Randhawa… - Cureus, 2021 - cureus.com
Long QT syndrome (LQTS) is a rare arrhythmogenic condition characterized by abnormally
long QT intervals on an electrocardiogram. The prevalence varies between 1 in 3000 and 1 …

Classification and mechanism of Torsade de Pointes initiation in patients with congenital long QT syndrome

T Noda, W Shimizu, K Satomi, K Suyama… - European heart …, 2004 - academic.oup.com
Aims To examine the initiating mode of Torsade de Pointes (TdP) in patients with congenital
long QT syndrome (LQTS). Methods and results We evaluated 111 episodes of TdP …

A rare cause of 2: 1 AV block: long QT syndrome

C Patel, S Narayanaswamy… - Journal of …, 2008 - academia.edu
A 6-year-old female with congenital long QT syndrome (LQTS) presented to the hospital with
recurrent syncope. She had frequent episodes of Torsade de pointes (TdP) that occurred at …

[PDF][PDF] Catheter ablation of ventricular fibrillation storm in a long QT syndrome genotype carrier with normal QT interval

J Yap, VH Tan, LF Hsu, R Liew - Singapore Med J, 2013 - smj.org.sg
Patients with long QT syndrome can sometimes present with a ventricular fibrillation (VF)
storm. Catheter ablation of culprit premature ventricular complexes responsible for the …

[HTML][HTML] Mode of onset of torsade de pointes in congenital long QT syndrome

S Viskin, SR Alla, HV Barron, K Heller, L Saxon… - Journal of the American …, 1996 - Elsevier
OBJECTIVES.: We sought to describe the mode of onset of spontaneous torsade de pointes
in the congenital long QT syndrome. BACKGROUND.: Contemporary classifications of the …

“Atrial torsades de pointes” in the long QT syndrome

SP Seslar, SM Shepard, CI Berul - Journal of interventional cardiac …, 2009 - Springer
A 16 year-old asymptomatic male was diagnosed with long QT syndrome (LQTS) at age 7
due to family history and an abnormal electrocardiogram. Genetic testing confirmed the …