Pulmonary acceleration time to optimize the timing of lung transplant in cystic fibrosis

Pulmonary hypertension (PH) may affect survival in cystic fibrosis (CF) and can be assessed on echocardiographic measurement of the pulmonary acceleration time (PAT). The study aimed at evaluating PAT as a tool to optimize timing of lung transplant in CF patients. Prospective multicenter longitudina...

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Detalles Bibliográficos
Autores principales: Damy, Thibaud, Burgel, Pierre-Régis, Pepin, Jean-Louis, Boelle, Pierre-Yves, Cracowski, Claire, Murris-Espin, Marlène, Nove-Josserand, Raphaele, Stremler, Nathalie, Simon, Tabassome, Adnot, Serge, Fauroux, Brigitte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342752/
https://www.ncbi.nlm.nih.gov/pubmed/22558523
http://dx.doi.org/10.4103/2045-8932.94838

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342752/
https://www.ncbi.nlm.nih.gov/pubmed/22558523
http://dx.doi.org/10.4103/2045-8932.94838

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