Prognosis and Follow-Up of Idiopathic Pulmonary Fibrosis

Idiopathic pulmonary fibrosis (IPF), a devastating progressive interstitial lung disease (ILD) with no known cause, is the most common and deadly of the idiopathic interstitial pneumonias. With a median survival of 3–5 years following diagnosis, IPF is characterized by a progressive decline in lung...

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Bibliographic Details
Published in:Med Sci (Basel)
Main Authors: Fernández Fabrellas, Estrella, Peris Sánchez, Ricardo, Sabater Abad, Cristina, Juan Samper, Gustavo
Format: Artigo
Language:Inglês
Published: MDPI 2018
Subjects:
Review
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC6024649/
https://ncbi.nlm.nih.gov/pubmed/29904028
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/medsci6020051
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