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The characteristics and potential origin of the proximal left anterior fascicle premature ventricular complexes.

Authors:
Songwen Chen Yong Wei Genqing Zhou Xiaofeng Lu Shaowen Liu

Heart Rhythm 2022 Jun 18. Epub 2022 Jun 18.

Department of Cardiology, Shanghai General Hospital, Shanghai Jiao Tong University, School of Medicine, China. Electronic address:

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http://dx.doi.org/10.1016/j.hrthm.2022.05.040DOI Listing
June 2022

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Successful radiofrequency catheter ablation of idiopathic premature ventricular complexes originating from the outflow tract improves heart failure-related quality of life.

Authors:
Olcay Özveren Ferit Onur Mutluer Ahmet Tutuncu Erhan Tenekecioglu Selcuk Kanat Tolga Aksu

J Interv Card Electrophysiol 2022 Jun 22. Epub 2022 Jun 22.

Department of Cardiology, Yeditepe University Hospital, Hastahane Sok. No: 4, 34752, Istanbul, Turkey.

Background: To investigate the effect of successful RFCA in patients with idiopathic outflow tract PVCs (OT-PVC) on left heart functions, neurohormonal activation, functional status, and heart failure-related quality of life (HFQoL), with an integrated approach.

Methods: Patients with frequent OT-PVCs, determined by 12-lead surface ECG who underwent radiofrequency catheter ablation (RFCA) with an acute success, were prospectivelly enrolled. Left heart functions were evaluated with the use of transthoracic echocardiography, neurohormonal activation with N-terminal Pro-brain natriuretic peptide (BNP), functional class with New York Heart Association (NYHA) and 6-min walking distance (6MWD), and HFQoL with Minnesota Living with Heart Failure Questionnaire (MLHFQ), at baseline and at 6 months. Read More

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June 2022
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The characteristics and potential origin of the proximal left anterior fascicle premature ventricular complexes.

Authors:
Songwen Chen Yong Wei Genqing Zhou Xiaofeng Lu Shaowen Liu

Heart Rhythm 2022 Jun 18. Epub 2022 Jun 18.

Department of Cardiology, Shanghai General Hospital, Shanghai Jiao Tong University, School of Medicine, China. Electronic address:

View Article and Full-Text PDF
June 2022
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Initiation of ventricular arrhythmia in the acquired long QT syndrome.

Authors:
C Alexander M J Bishop R J Gilchrist B A MRes F L Burton G L Smith R C Myles

Cardiovasc Res 2022 Jun 21. Epub 2022 Jun 21.

Institute of Cardiovascular & Medical Sciences, University of Glasgow, Glasgow, UK.

Aims: Long QT syndrome (LQTS) carries a risk of life-threatening polymorphic ventricular tachycardia (Torsades de Pointes, TdP) and is a major cause of premature sudden cardiac death. TdP is induced by R-on-T premature ventricular complexes (PVCs), thought to be generated by cellular early-afterdepolarisations (EADs). However, EADs in tissue require cellular synchronisation, and their role in TdP induction remains unclear. Read More

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June 2022
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Author's Reply-The characteristics and potential origin of the proximal left anterior fascicle premature ventricular complexes.

Authors:
Jinlin Zhang

Heart Rhythm 2022 Jun 17. Epub 2022 Jun 17.

Department of Cardiology, Wuhan Asian Heart Hospital, Wuhan, China.

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June 2022
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Prognostic factors in hypertrophic cardiomyopathy in children: An MRI based study.

Authors:
Lamia Ait Ali Chiara Marrone Duarte Saraiva Martins Diala Khraiche Pierluigi Festa Nicola Martini Giuseppe Santoro Giancarlo Todiere Elena Panaioli Damien Bonnet Nathalie Boddaert Giovanni Donato Aquaro Francesca Raimondi

Int J Cardiol 2022 Jun 16. Epub 2022 Jun 16.

MD, Unité médico-chirurgicale de cardiologie congénitale et pédiatrique, centre de référence des maladies cardiaques congénitales complexes - M3C, Hôpital universitaire Necker-Enfants Malades, Université de Paris, France and Azienda Ospedaliero Universitaria Meyer, Florence, Italy. Electronic address:

Background: Clinical and prognostic role of cardiac magnetic resonance (CMR) in adult population with hypertrophic cardiomyopathy (HCM) have been largely assessed. We sought to investigate the role of CMR for predicting cardiovascular events in children with HCM.

Methods: CMR was performed in 116 patients with HCM (37 sarcomeric mutations, 31 other mutations, mean age 10. Read More

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June 2022
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