The care needs of patients with idiopathic pulmonary fibrosis and their carers (CaNoPy): results of a qualitative study

BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is a chronic, fibrotic interstitial lung disease of unknown origin. It has a median survival of three years but a wide range in survival rate which is difficult to predict at the time of diagnosis. Specialist guidance promotes a patient centred approac...

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Detalles Bibliográficos
Autores principales: Sampson, Cathy, Gill, Ben Hope, Harrison, Nicholas Kim, Nelson, Annmarie, Byrne, Anthony
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4670492/
https://www.ncbi.nlm.nih.gov/pubmed/26637194
http://dx.doi.org/10.1186/s12890-015-0145-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4670492/
https://www.ncbi.nlm.nih.gov/pubmed/26637194
http://dx.doi.org/10.1186/s12890-015-0145-5

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