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Article

[How i treat a patient with idiopathic pulmonary fibrosis].

Revue medicale de Liege - 1 Sept 2017

Guiot J, Duysinx B, Bonhomme O, Louis R, Corhay J-L

Abstract excerpt

Idiopathic pulmonary fibrosis (IPF) is a rare disorder of unknown origin, which is associated with a high mortality and whose incidence has been increasing for several years. Nowadays there are two anti-fibrotic therapies (pirfenidone - nintedanib) known to reduce significantly the decline in respiratory function tests of patients suffering from this condition. The only curative therapeutic option remains the...

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PMID: 28892311

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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