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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

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