EDPAH

Mechanisms of Exertional Dyspnea in Patients with Idiopathic Pulmonary Arterial Hypertension

 Coordinatore UNIVERSITE PIERRE ET MARIE CURIE - PARIS 6 

 Organization address address: Place Jussieu 4
city: PARIS
postcode: 75252

contact info
Titolo: Ms.
Nome: Ella
Cognome: Bouquet
Email: send email
Telefono: 33144279777
Fax: 33144277484

 Nazionalità Coordinatore France [FR]
 Totale costo 50˙000 €
 EC contributo 50˙000 €
 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-2010-RG
 Funding Scheme MC-IRG
 Anno di inizio 2010
 Periodo (anno-mese-giorno) 2010-11-01   -   2012-10-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITE PIERRE ET MARIE CURIE - PARIS 6

 Organization address address: Place Jussieu 4
city: PARIS
postcode: 75252

contact info
Titolo: Ms.
Nome: Ella
Cognome: Bouquet
Email: send email
Telefono: 33144279777
Fax: 33144277484

FR (PARIS) coordinator 50˙000.00

Mappa


 Word cloud

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

dyspnea    respiratory    hypertension    pulmonary    mechanics    muscle    arterial    patients    exercise    symptom    function   

 Obiettivo del progetto (Objective)

'Activity-related dyspnea appears to be the earliest and dominant symptom limiting exercise in the majority of patients afflicted by pulmonary arterial hypertension. This symptom progresses relentlessly with time leading invariably to avoidance of activity with consequent skeletal muscle deconditioning and poor perceived quality of life. Unfortunately, effective management of this disabling symptom awaits a better understanding of its underlying physiology. A growing body of evidence have highlighted that patients with pulmonary arterial hypertension may present with respiratory muscle weakness and abnormal lung function/respiratory mechanics. Despite these findings, to date little is known about the potential contribution of abnormalities in respiratory mechanics and ventilatory muscle function to dyspnea causation during physical exercise in patients with pulmonary arterial hypertension. This is, therefore, the main focus of the present study, with the aim of identifying potential unexplored physiological mechanisms that can be targeted for therapeutic manipulation.'

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