Literature DB >> 28770718

Short QT Syndromes.

Fiorenzo Gaita1, Carla Giustetto1, Andrea Mazzanti1.   

Abstract

The short QT syndrome is a recently described genetic arrhythmogenic disorder, characterized by abnormally short QT intervals and a high incidence of sudden death and atrial fibrillation. Clinical manifestations may also be present in infants; a family history of cardiac sudden death is often present. Gain-of-function mutations in 3 genes encoding potassium channels and loss-of-function mutations in 2 genes encoding the cardiac L-type calcium channel have been identified. Today, the first choice therapy is implantable cardioverter-defibrillator implantation; however, pharmacologic treatment with hydroquinidine, which prolongs QT and reduces the inducibility of ventricular arrhythmias, may be proposed for children and probably for elderly asymptomatic patients.
Copyright © 2010 Elsevier Inc. All rights reserved.

Entities:  

Year:  2010        PMID: 28770718     DOI: 10.1016/j.ccep.2010.09.004

Source DB:  PubMed          Journal:  Card Electrophysiol Clin        ISSN: 1877-9182


  1 in total

1.  Short QT syndrome in infancy. Therapeutic drug monitoring of hydroquinidine in a newborn infant.

Authors:  Elisa Pirro; Silvia De Francia; Elena Banaudi; Chiara Riggi; Francesca De Martino; Francesca M Piccione; Carla Giustetto; Silvia Racca; Gabriella Agnoletti; Francesco Di Carlo
Journal:  Br J Clin Pharmacol       Date:  2011-12       Impact factor: 4.335

  1 in total

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