Time to diagnosis of idiopathic pulmonary fibrosis in the IPF-PRO Registry

BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is a progressive disease with high mortality. Patient characteristics associated with diagnostic delays are not well described. METHODS: Subjects who had not been diagnosed with IPF prior to referral and received a new diagnosis of IPF at an enrolling...

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Detalles Bibliográficos
Autores principales: Snyder, Laurie D, Mosher, Christopher, Holtze, Colin H, Lancaster, Lisa H, Flaherty, Kevin R, Noth, Imre, Neely, Megan L, Hellkamp, Anne S, Bender, Shaun, Conoscenti, Craig S, de Andrade, Joao A, Whelan, Timothy PM
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Interstitial Lung Disease
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7337884/
https://www.ncbi.nlm.nih.gov/pubmed/32624493
http://dx.doi.org/10.1136/bmjresp-2020-000567

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7337884/
https://www.ncbi.nlm.nih.gov/pubmed/32624493
http://dx.doi.org/10.1136/bmjresp-2020-000567

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