Speckle tracking echocardiography data in Brugada syndrome patients.

Brugada syndrome Inducible Mechanical dispersion Speckle tracking echocardiography Spontaneous type 1 Strain

Journal

Data in brief
ISSN: 2352-3409
Titre abrégé: Data Brief
Pays: Netherlands
ID NLM: 101654995

Informations de publication

Date de publication:
Aug 2019
Historique:
received: 29 06 2019
revised: 18 07 2019
accepted: 22 07 2019
entrez: 28 8 2019
pubmed: 28 8 2019
medline: 28 8 2019
Statut: epublish

Résumé

Brugada syndrome is characterized by typical electrocardiogram changes and a high risk for sudden cardiac death (Priori et al., 2013). In addition to the well known electrical substrate, morphological and functional alterations appeared to be present in a subset of the Brugada syndrome patients (Catalano et al., 2009). Echocardiographic speckle tracking enables us to detect subtle contraction alterations (Smiseth et al.,2016). We performed transthoracic echocardiography with speckle tracking analysis in 82 healthy controls and 175 Brugada syndrome patients. Main findings are presented and discussed in the article "Contraction alterations in Brugada syndrome; association with life-threatening ventricular arrhythmias" (Scheirlynck et al., 2019). This related Data article contains segmental longitudinal strain values for RV and LV, and the comparison of echocardiographic parameters between Brugada syndrome patients with spontaneous and drug-induced type 1 pattern and between patients with and without ventricular arrhythmia inducibility during electrophysiological study.

Identifiants

pubmed: 31453301
doi: 10.1016/j.dib.2019.104330
pii: S2352-3409(19)30684-5
pii: 104330
pmc: PMC6700482
doi:

Types de publication

Journal Article

Langues

eng

Pagination

104330

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Auteurs

Esther Scheirlynck (E)

Department of Cardiology, Centrum voor Hart- en Vaatziekten, Universitair Ziekenhuis Brussel, Brussels, Belgium.
Life Sciences and Medicine, Vrije Universiteit Brussel, Brussels, Belgium.

Sophie Van Malderen (S)

Life Sciences and Medicine, Vrije Universiteit Brussel, Brussels, Belgium.

Andreea Motoc (A)

Department of Cardiology, Centrum voor Hart- en Vaatziekten, Universitair Ziekenhuis Brussel, Brussels, Belgium.
Life Sciences and Medicine, Vrije Universiteit Brussel, Brussels, Belgium.

Øyvind H Lie (ØH)

Department of Cardiology, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Center for Cardiological Innovation, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Institute for Clinical Medicine, University of Oslo, Oslo, Norway.

Carlo de Asmundis (C)

Department of Cardiology, Centrum voor Hart- en Vaatziekten, Universitair Ziekenhuis Brussel, Brussels, Belgium.

Juan Sieira (J)

Department of Cardiology, Centrum voor Hart- en Vaatziekten, Universitair Ziekenhuis Brussel, Brussels, Belgium.

Gian-Battista Chierchia (GB)

Department of Cardiology, Centrum voor Hart- en Vaatziekten, Universitair Ziekenhuis Brussel, Brussels, Belgium.

Pedro Brugada (P)

Department of Cardiology, Centrum voor Hart- en Vaatziekten, Universitair Ziekenhuis Brussel, Brussels, Belgium.

Bernard Cosyns (B)

Department of Cardiology, Centrum voor Hart- en Vaatziekten, Universitair Ziekenhuis Brussel, Brussels, Belgium.
Life Sciences and Medicine, Vrije Universiteit Brussel, Brussels, Belgium.

Steven Droogmans (S)

Department of Cardiology, Centrum voor Hart- en Vaatziekten, Universitair Ziekenhuis Brussel, Brussels, Belgium.
Life Sciences and Medicine, Vrije Universiteit Brussel, Brussels, Belgium.

Classifications MeSH