Changes in management of idiopathic pulmonary fibrosis: impact on disease severity and mortality

Background Idiopathic pulmonary fibrosis (IPF) is a serious interstitial lung disease (ILD) with a median survival of 3-5 years. The aim of the present study was to evaluate disease severity and survival in patients diagnosed with IPF in the era of antifibrotic therapies compared with an earlier IPF...

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Bibliographic Details
Main Authors: Charlotte Hyldgaard, Janne Møller, Elisabeth Bendstrup
Format: Article
Language:English
Published: Taylor & Francis Group 2020-01-01
Series:European Clinical Respiratory Journal
Subjects:
Online Access:http://dx.doi.org/10.1080/20018525.2020.1807682