Role of implantable cardioverter defibrillator therapy in patients with long QT syndrome

Long QT syndrome (LQTS) is one of several primary electrical disorders or hereditary arrhythmia syndromes along with the short QT syndrome, Brugada syndrome, and catecholaminergic polymorphic ventricular tachycardia. Since its initial recognition in 1957 by Jervell and Lange-Nielsen ( Am Heart J. 19...

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Veröffentlicht in:The American heart journal 2007-04, Vol.153 (4), p.53-58
Hauptverfasser: Daubert, James P., MD, Zareba, Wojciech, MD, PhD, Rosero, Spencer Z., MD, Budzikowski, Adam, MD, PhD, Robinson, Jennifer L., MS, Moss, Arthur J., MD
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container_end_page 58
container_issue 4
container_start_page 53
container_title The American heart journal
container_volume 153
creator Daubert, James P., MD
Zareba, Wojciech, MD, PhD
Rosero, Spencer Z., MD
Budzikowski, Adam, MD, PhD
Robinson, Jennifer L., MS
Moss, Arthur J., MD
description Long QT syndrome (LQTS) is one of several primary electrical disorders or hereditary arrhythmia syndromes along with the short QT syndrome, Brugada syndrome, and catecholaminergic polymorphic ventricular tachycardia. Since its initial recognition in 1957 by Jervell and Lange-Nielsen ( Am Heart J. 1957;54:59-68), LQTS has been intimately associated with risk for sudden cardiac death. The implantable defibrillator was developed by Morowski et al ( N Engl J Med. 1980;303:322-4) as a treatment to prevent sudden cardiac death. Consequently, implanted cardioverter-defibrillator therapy deserves serious consideration as an important therapy for LQTS.
doi_str_mv 10.1016/j.ahj.2007.01.025
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source MEDLINE; Elsevier ScienceDirect Journals
subjects Cardiac arrhythmia
Cardiovascular
Defibrillators, Implantable - adverse effects
Heart attacks
Humans
Long QT Syndrome - drug therapy
Long QT Syndrome - therapy
Mortality
Mutation
title Role of implantable cardioverter defibrillator therapy in patients with long QT syndrome
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