La maladie de Parkinson en France (serveur d'exploration)

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Risk factors of adverse presentation as the first arrhythmia in Wolff-Parkinson-White syndrome.

Identifieur interne : 000A65 ( PubMed/Corpus ); précédent : 000A64; suivant : 000A66

Risk factors of adverse presentation as the first arrhythmia in Wolff-Parkinson-White syndrome.

Auteurs : Béatrice Brembilla-Perrot ; Clément Tatar ; Christine Suty-Selton

Source :

RBID : pubmed:20487358

English descriptors

Abstract

The aim of the study was the evaluation of the predictors of adverse presentation as first arrhythmia in Wolff-Parkinson-White syndrome; they usually affect young patients with septal or multiple accessory pathways (AP).

DOI: 10.1111/j.1540-8159.2010.02782.x
PubMed: 20487358

Links to Exploration step

pubmed:20487358

Le document en format XML

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<title xml:lang="en">Risk factors of adverse presentation as the first arrhythmia in Wolff-Parkinson-White syndrome.</title>
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<name sortKey="Brembilla Perrot, Beatrice" sort="Brembilla Perrot, Beatrice" uniqKey="Brembilla Perrot B" first="Béatrice" last="Brembilla-Perrot">Béatrice Brembilla-Perrot</name>
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<nlm:affiliation>Department of Cardiology, University Hospital of Brabois, Vandoeuvre, France. b.brembilla-perrot@chu-nancy.fr</nlm:affiliation>
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<name sortKey="Tatar, Clement" sort="Tatar, Clement" uniqKey="Tatar C" first="Clément" last="Tatar">Clément Tatar</name>
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<name sortKey="Suty Selton, Christine" sort="Suty Selton, Christine" uniqKey="Suty Selton C" first="Christine" last="Suty-Selton">Christine Suty-Selton</name>
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<title xml:lang="en">Risk factors of adverse presentation as the first arrhythmia in Wolff-Parkinson-White syndrome.</title>
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<name sortKey="Brembilla Perrot, Beatrice" sort="Brembilla Perrot, Beatrice" uniqKey="Brembilla Perrot B" first="Béatrice" last="Brembilla-Perrot">Béatrice Brembilla-Perrot</name>
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<term>Accessory Atrioventricular Bundle (diagnosis)</term>
<term>Accessory Atrioventricular Bundle (physiopathology)</term>
<term>Adolescent</term>
<term>Adult</term>
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Atrial Fibrillation (complications)</term>
<term>Atrial Fibrillation (diagnosis)</term>
<term>Atrial Fibrillation (epidemiology)</term>
<term>Child</term>
<term>Child, Preschool</term>
<term>Death, Sudden, Cardiac (etiology)</term>
<term>Death, Sudden, Cardiac (prevention & control)</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Retrospective Studies</term>
<term>Risk Factors</term>
<term>Syncope (diagnosis)</term>
<term>Syncope (physiopathology)</term>
<term>Tachycardia, Reciprocating (diagnosis)</term>
<term>Tachycardia, Reciprocating (physiopathology)</term>
<term>Wolff-Parkinson-White Syndrome (complications)</term>
<term>Wolff-Parkinson-White Syndrome (diagnosis)</term>
<term>Wolff-Parkinson-White Syndrome (epidemiology)</term>
<term>Young Adult</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en">
<term>Atrial Fibrillation</term>
<term>Wolff-Parkinson-White Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en">
<term>Accessory Atrioventricular Bundle</term>
<term>Atrial Fibrillation</term>
<term>Syncope</term>
<term>Tachycardia, Reciprocating</term>
<term>Wolff-Parkinson-White Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="epidemiology" xml:lang="en">
<term>Atrial Fibrillation</term>
<term>Wolff-Parkinson-White Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en">
<term>Death, Sudden, Cardiac</term>
</keywords>
<keywords scheme="MESH" qualifier="physiopathology" xml:lang="en">
<term>Accessory Atrioventricular Bundle</term>
<term>Syncope</term>
<term>Tachycardia, Reciprocating</term>
</keywords>
<keywords scheme="MESH" qualifier="prevention & control" xml:lang="en">
<term>Death, Sudden, Cardiac</term>
</keywords>
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<term>Adolescent</term>
<term>Adult</term>
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Child</term>
<term>Child, Preschool</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Retrospective Studies</term>
<term>Risk Factors</term>
<term>Young Adult</term>
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<div type="abstract" xml:lang="en">The aim of the study was the evaluation of the predictors of adverse presentation as first arrhythmia in Wolff-Parkinson-White syndrome; they usually affect young patients with septal or multiple accessory pathways (AP).</div>
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<Year>2010</Year>
<Month>11</Month>
<Day>05</Day>
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<DateCompleted>
<Year>2011</Year>
<Month>02</Month>
<Day>28</Day>
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<DateRevised>
<Year>2010</Year>
<Month>11</Month>
<Day>05</Day>
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<ISSN IssnType="Electronic">1540-8159</ISSN>
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<Volume>33</Volume>
<Issue>9</Issue>
<PubDate>
<Year>2010</Year>
<Month>Sep</Month>
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<Title>Pacing and clinical electrophysiology : PACE</Title>
<ISOAbbreviation>Pacing Clin Electrophysiol</ISOAbbreviation>
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<ArticleTitle>Risk factors of adverse presentation as the first arrhythmia in Wolff-Parkinson-White syndrome.</ArticleTitle>
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<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">The aim of the study was the evaluation of the predictors of adverse presentation as first arrhythmia in Wolff-Parkinson-White syndrome; they usually affect young patients with septal or multiple accessory pathways (AP).</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Our population comprised 645 patients with a preexcitation syndrome. Among them, adverse presentation (sudden death, hemodynamically not tolerated atrial fibrillation [AF]) occurred in 60 (9%) (group I). Their clinical and electrophysiological features were compared to group II patients, which consisted of 75 patients with syncope (IIa), 287 with reentrant tachycardia (RT) (IIb), 211 asymptomatic patients (IIc), and 12 with well-tolerated AF.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Sixteen group I patients had triggering factors. Group I patients were older (40 ± 18.5) than group II (34 ± 16) (P = 0.02). Male gender was as frequent in both groups (63%, 59%). Free wall left AP was more frequent in group I (65%) than in group II (37%) (P < 0.001), septal AP less frequent (27% vs 47%) (P = 0.004), multiple APs exceptional. RT was more frequent in group I (57%) than in group IIc (12%) (P < 0.001), less frequent than in group IIb (90.5%) (P < 0.001). AF was more frequent in group I (85%) than in group IIc (22%), or IIb (19%) (P < 0.001). Maximal rate through AP was higher in group I than in group II (P < 0.001).</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Adverse presentation in WPW may affect patients older than 35 years of both sexes, with a single free wall lateral AP. All could have been identified by an electrophysiological study.</AbstractText>
<CopyrightInformation>©2010, The Authors. Journal compilation ©2010 Wiley Periodicals, Inc.</CopyrightInformation>
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