PSCD

Establishing the role of Purkinje fibres in the development of arrhythmias for the prevention of Sudden Cardiac Death: Insights from a combined in vivo and ex vivo study

 Coordinatore UNIVERSITE DE BORDEAUX 

 Organization address address: PLACE PEY BERLAND 35
city: BORDEAUX
postcode: 33000

contact info
Titolo: Ms.
Nome: Véronique
Cognome: Debord-Lazaro
Email: send email
Telefono: 335547000000
Fax: 33557571557

 Nazionalità Coordinatore France [FR]
 Totale costo 193˙594 €
 EC contributo 193˙594 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2011-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2012
 Periodo (anno-mese-giorno) 2012-11-01   -   2014-10-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITE DE BORDEAUX

 Organization address address: PLACE PEY BERLAND 35
city: BORDEAUX
postcode: 33000

contact info
Titolo: Ms.
Nome: Véronique
Cognome: Debord-Lazaro
Email: send email
Telefono: 335547000000
Fax: 33557571557

FR (BORDEAUX) coordinator 193˙594.80
2    UNIVERSITE VICTOR SEGALEN BORDEAUX II

 Organization address address: RUE LEO SAIGNAT 146
city: BORDEAUX CEDEX
postcode: 33076

contact info
Titolo: Prof.
Nome: Michel
Cognome: Haissaguerre
Email: send email
Telefono: 33557656471
Fax: 33557656509

FR (BORDEAUX CEDEX) participant 0.00

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

ventricular    model    treatment    roles    vf    vivo    death    electrical    ex    optical    sources    cardiac    sudden    arrhythmias    disease    arrhythmogenesis    infarction    organisation    ablation    mechanisms    fibres    techniques    myocardial    electrophysiological    purkinje    therapies    scd   

 Obiettivo del progetto (Objective)

'Sudden cardiac death (SCD) following ventricular fibrillation (VF) is a major cause of mortality in the industrialised world. VF is characterised by chaotic electrical activity in the ventricles leading to severe cardiac dysfunction. Thus far, the underlying mechanisms for the initiation and maintenance of VF are not fully understood. Recent clinical developments in the treatment of VF by the Host’s laboratory have discovered distinct electrical activity associated with a specialised cell-type, Purkinje fibres, which were found to precede the spontaneous beats that manifest VF. Targeted radiofrequency (RF) ablation of these sources has markedly improved treatment and the rates of recurrence of arrhythmias in patients suffering from idiopathic VF. There is also growing evidence that the Purkinje system may be involved in arrhythmogenesis in cardiac pathologies such as myocardial infarction. Therefore, this proposal aims to utilise in vivo electrophysiological techniques in combination with a newly developed ex vivo optical imaging technique on a large animal model (sheep) to determine the roles of Purkinje fibres in the development of life-threatening arrhythmias with a focus on improving the effectiveness of ablation therapies. Furthermore, this approach shall be applied to further investigate a cardiac disease model that is at significant risk of arrhythmogenesis, myocardial infarction. The proposed aims shall be carried out in vivo using MRI and epicardial and endocardial electrophysiological recordings. This will be followed by optical mapping of ex vivo coronary-perfused ventricular preparations providing insight into the 3D organisation of electrical activity. These techniques will provide the appropriate tools for determining the precise location of arrhythmogenic sources, the organisation of arrhythmias and the roles of Purkinje fibres. Successful completion of these research goals will have an important impact on future therapies for sudden cardiac death.'

Introduzione (Teaser)

Sudden cardiac death (SCD) due to cardiovascular disease is the number one killer globally. EU-funded researchers worked on understanding the mechanisms leading to SCDs.

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