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Lung function trajectories in patients with idiopathic pulmonary fibrosis

Lung function trajectories in patients with idiopathic pulmonary fibrosis

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_7eec8ee325ea47e999553190ed708c3e

Lung function trajectories in patients with idiopathic pulmonary fibrosis

About this item

Full title

Lung function trajectories in patients with idiopathic pulmonary fibrosis

Publisher

London: BioMed Central Ltd

Journal title

Respiratory research, 2023-08, Vol.24 (1), p.1-209, Article 209

Language

English

Formats

Publication information

Publisher

London: BioMed Central Ltd

More information

Scope and Contents

Contents

Background Idiopathic pulmonary fibrosis (IPF) is a progressive fibrosing interstitial lung disease characterised by decline in lung function. We evaluated trajectories of forced vital capacity (FVC) and diffusing capacity (DLco) in a cohort of patients with IPF. Methods Patients with IPF that was diagnosed or confirmed at the enrolling centre in t...

Alternative Titles

Full title

Lung function trajectories in patients with idiopathic pulmonary fibrosis

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_7eec8ee325ea47e999553190ed708c3e

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_7eec8ee325ea47e999553190ed708c3e

Other Identifiers

ISSN

1465-993X,1465-9921

E-ISSN

1465-993X,1465-9921

DOI

10.1186/s12931-023-02503-5

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