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Pirfenidone and Nintedanib in idiopathic pulmonary fibrosis: Real-life experience in an Italian referral centre

Background: Idiopathic pulmonary fibrosis has a median survival time after diagnosis of 2–5 years. The main goal of treating IPF is to stabilize or reduce the rate of disease progression. Nintedanib and Pirfenidone have been a breakthrough in the management of IPF. Here we evaluated the effectivenes...

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Bibliographische Detailangaben
Hauptverfasser: E. Bargagli, C. Piccioli, E. Rosi, E. Torricelli, L. Turi, E. Piccioli, M. Pistolesi, K. Ferrari, L. Voltolini
Format: Artigo
Sprache:Inglês
Veröffentlicht: Elsevier España 2019-05-01
Schriftenreihe:Pulmonology
Online Zugang:http://www.sciencedirect.com/science/article/pii/S2531043718300990
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