Antifibrotic therapy reduces mortality and acute exacerbation in idiopathic pulmonary fibrosis: Chest
Antifibrotic treatment appears to reduce the risk of all-cause mortality and acute exacerbation in idiopathic pulmonary fibrosis, according to recently published study results in Chest journal.
(IPF) is a progressive fibrosing interstitial lung disease associated with significant morbidity and mortality. Nintedanib and pirfenidone are two antifibrotic medications currently approved for slowing the rate of lung function decline in IPF, but information on treatment effect on mortality and risk of acute exacerbation (AE) remains limited or unknown.
With this limited background, researchers undertook the study to evaluate whether antifibrotic treatment decrease risk of mortality and AE. The study was designed as a comprehensive search of several databases, including Ovid MEDLINE(R), Ovid Embase, Ovid Cochrane Central Register of Controlled Trials, Ovid Cochrane Database of Systematic Reviews, and Scopus, was conducted. Studies were included if they were original articles comparing mortality or AE events in IPF patients with and without antifibrotic treatment.
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