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Idiopathic Pulmonary Fibrosis: Best Practice in Monitoring and Managing a Relentless Fibrotic Disease

Journal article
Authors W. A. Wuyts
M. Wijsenbeek
B. Bondue
D. Bouros
P. Bresser
C. R. Cordeiro
O. Hilberg
Jesper Magnusson
E. D. Manali
A. Morais
S. Papiris
S. Shaker
M. Veltkamp
E. Bendstrup
Published in Respiration
Volume 99
Issue 1
Pages 73-82
ISSN 0025-7931
Publication year 2020
Published at Institute of Medicine, Department of Internal Medicine and Clinical Nutrition
Pages 73-82
Language en
Keywords Nintedanib, Pirfenidone, Interstitial lung disease, Therapeutics, Treatment, Mortality, forced vital capacity, quality-of-life, clinical-practice, acute, exacerbation, lung-transplant, antacid therapy, home spirometry, palliative care, position paper, survival, Respiratory System
Subject categories Clinical Medicine


Idiopathic pulmonary fibrosis (IPF) is a fibrosing interstitial lung disease that is, by definition

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