Polymorphic Ventricular Tachycardia/Ventricular Fibrillation and Sudden Cardiac Death in the Normal Heart.
Identifieur interne : 001941 ( Main/Exploration ); précédent : 001940; suivant : 001942Polymorphic Ventricular Tachycardia/Ventricular Fibrillation and Sudden Cardiac Death in the Normal Heart.
Auteurs : Ashok J. Shah [Australie] ; Meleze Hocini [France] ; Arnaud Denis [France] ; Nicolas Derval [France] ; Frederic Sacher [France] ; Pierre Jais [France] ; Michel Haissaguerre [France]Source :
- Cardiac electrophysiology clinics [ 1877-9190 ] ; 2016.
Descripteurs français
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English descriptors
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Abstract
Primary electrical diseases manifest with polymorphic ventricular tachycardia (PMVT) and ventricular fibrillation (VF) and along with idiopathic VF contribute to about 10% of sudden cardiac deaths (SCDs) overall. These disorders include long QT syndrome, Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia, short QT syndrome, and early repolarization syndrome. This article reviews the clinical electrophysiological management of PMVT/VF in a structurally normal heart affected with these disorders.
DOI: 10.1016/j.ccep.2016.04.007
PubMed: 27521091
Affiliations:
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Shah</name><affiliation wicri:level="1"><nlm:affiliation>Cardio Vascular Services, South Consulting Suites, Peel Health Campus, 110 Lakes Road, Mandurah, Western Australia 6210, Australia. 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Electronic address: michel.haissaguerre@chu-bordeaux.fr.</nlm:affiliation><country xml:lang="fr">France</country><wicri:regionArea>Department of Electrophysiology and Cardiac Pacing, Hôpital Cardiologique du Haut Lévêque, Avenue de Magellan, Pessac Cedex 33604</wicri:regionArea><wicri:noRegion>33604</wicri:noRegion><wicri:noRegion>33604</wicri:noRegion></affiliation></author></analytic><series><title level="j">Cardiac electrophysiology clinics</title><idno type="eISSN">1877-9190</idno><imprint><date when="2016" type="published">2016</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adolescent</term><term>Catheter Ablation</term><term>Death, Sudden, Cardiac</term><term>Female</term><term>Humans</term><term>Male</term><term>Middle Aged</term><term>Tachycardia, Ventricular</term><term>Ventricular Fibrillation</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Ablation par cathéter</term><term>Adolescent</term><term>Adulte d'âge moyen</term><term>Femelle</term><term>Fibrillation ventriculaire</term><term>Humains</term><term>Mort subite cardiaque</term><term>Mâle</term><term>Tachycardie ventriculaire</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adolescent</term><term>Catheter Ablation</term><term>Death, Sudden, Cardiac</term><term>Female</term><term>Humans</term><term>Male</term><term>Middle Aged</term><term>Tachycardia, Ventricular</term><term>Ventricular Fibrillation</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Ablation par cathéter</term><term>Adolescent</term><term>Adulte d'âge moyen</term><term>Femelle</term><term>Fibrillation ventriculaire</term><term>Humains</term><term>Mort subite cardiaque</term><term>Mâle</term><term>Tachycardie ventriculaire</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Primary electrical diseases manifest with polymorphic ventricular tachycardia (PMVT) and ventricular fibrillation (VF) and along with idiopathic VF contribute to about 10% of sudden cardiac deaths (SCDs) overall. These disorders include long QT syndrome, Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia, short QT syndrome, and early repolarization syndrome. This article reviews the clinical electrophysiological management of PMVT/VF in a structurally normal heart affected with these disorders.</div></front></TEI><affiliations><list><country><li>Australie</li><li>France</li></country></list><tree><country name="Australie"><noRegion><name sortKey="Shah, Ashok J" sort="Shah, Ashok J" uniqKey="Shah A" first="Ashok J" last="Shah">Ashok J. Shah</name></noRegion></country><country name="France"><noRegion><name sortKey="Hocini, Meleze" sort="Hocini, Meleze" uniqKey="Hocini M" first="Meleze" last="Hocini">Meleze Hocini</name></noRegion><name sortKey="Denis, Arnaud" sort="Denis, Arnaud" uniqKey="Denis A" first="Arnaud" last="Denis">Arnaud Denis</name><name sortKey="Derval, Nicolas" sort="Derval, Nicolas" uniqKey="Derval N" first="Nicolas" last="Derval">Nicolas Derval</name><name sortKey="Haissaguerre, Michel" sort="Haissaguerre, Michel" uniqKey="Haissaguerre M" first="Michel" last="Haissaguerre">Michel Haissaguerre</name><name sortKey="Jais, Pierre" sort="Jais, Pierre" uniqKey="Jais P" first="Pierre" last="Jais">Pierre Jais</name><name sortKey="Sacher, Frederic" sort="Sacher, Frederic" uniqKey="Sacher F" first="Frederic" last="Sacher">Frederic Sacher</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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