Efficacy of Antifibrotic Therapy in Progressive Pulmonary Fibrosis
How effective are the antifibrotic agents nintedanib and pirfenidone for patients with idiopathic pulmonary fibrosis and non-IPF?
Idiopathic Pulmonary Fibrosis
Step Count Thresholds to Predict All-Cause Mortality in Idiopathic Pulmonary Fibrosis
Can a certain level of daily physical activity improve the prognosis for patients with idiopathic pulmonary fibrosis?
Do Antifibrotics Reduce Mortality, Exacerbations in Idiopathic Pulmonary Fibrosis?
A systematic review examined the effect of nintedanib and pirfenidone therapy on mortality and acute exacerbations in idiopathic pulmonary fibrosis.
Early Identification of Idiopathic Pulmonary Fibrosis From iUIP CT Patterns
How often does the CT pattern “indeterminate for usual interstitial pneumonia” indicate early IPF, and what influences progression to IPF?
Do Fine Crackles on Chest Auscultation Indicate Idiopathic Pulmonary Fibrosis?
Can fine crackles on chest auscultation be used for early diagnosis of idiopathic pulmonary fibrosis and other interstitial lung diseases?
How Effective is Pulmonary Rehabilitation for Idiopathic Pulmonary Fibrosis?
Pulmonary rehabilitation has proved effective for patients with COPD; is it similarly effective for patients with idiopathic pulmonary fibrosis?
Pulmonary Rehab for Interstitial Lung Disease and Idiopathic Pulmonary Fibrosis
A review of 21 studies evaluated the long-term outcomes associated with pulmonary rehabilitation for patients with pulmonary fibrosis, including ILD.
Implementation of Guidelines for Idiopathic Pulmonary Fibrosis Management
How effective are international guidelines for the management of idiopathic pulmonary fibrosis?
Cyclophosphamide Not Recommended for Acute Exacerbation of Pulmonary Fibrosis
A clinical trial disproved the notion that adding cyclophosphamide pulses to glucocorticoids was effective for acute exacerbation of IPF.
In Idiopathic Pulmonary Fibrosis, 4 Comorbidity Clusters May Reflect Phenotypes
Researchers in Denmark assessed the real-world prevalence of multimorbidity among adults with idiopathic pulmonary fibrosis.
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