A Real-World Prognosis in Idiopathic Pulmonary Fibrosis: A Special Reference to the Role of Antifibrotic Agents for the Elderly

Background: Idiopathic pulmonary fibrosis (IPF) is the most common and severe form of idiopathic interstitial pneumonia, and its prevalence increases with age. In the era of pre-antifibrotic agents, the median survival time of Japanese patients with IPF is 35 months, with a 5-year survival rate in w...

Descripción completa

Detalles Bibliográficos
Autores principales: Honda, Kojiro, Saraya, Takeshi, Ishii, Haruyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10219256/
https://www.ncbi.nlm.nih.gov/pubmed/37240670
http://dx.doi.org/10.3390/jcm12103564

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10219256/
https://www.ncbi.nlm.nih.gov/pubmed/37240670
http://dx.doi.org/10.3390/jcm12103564

Ejemplares similares