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Updated: May 28, 2026

Unilateral Lung Volume Analysis Using Micro-CT for Enhanced Assessment of Pulmonary Fibrosis in Preclinical Models
Published on: June 20, 2025
Idiopathic pulmonary fibrosis: treatment update
Oisin J O'Connell1, Marcus P Kennedy, Michael T Henry
1Department of Respiratory Medicine, Cork University Hospital, Wilton, Cork, Ireland.
Abstract:
Idiopathic pulmonary fibrosis (IPF) is the most common of the idiopathic interstitial pneumonias. Despite multiple recent clinical trials, there is no strong evidence supporting a survival advantage for any agent in the management of patients with IPF. The limited effectiveness of current treatment regimes has led to a search for novel therapies including antifibrotic strategies. This article reviews the evidence supporting the treatments currently used in the management of IPF.
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