Screening for Pulmonary Hypertension in Interstitial Lung Disease: Preliminary Results from the PHINDER Study

The PHINDER trial is a real-time, collaborative study across many medical centers to improve non-invasive methods of screening for pulmonary hypertension, or PH (dangerously high blood pressure in the lungs), that affects patients with chronic lung scarring disease. The preliminary analysis took data from an initial group of 190 enrolled patients with interstitial lung disease,…

Effect of Antifibrotic Therapy on Survival in Patients With Idiopathic Pulmonary Fibrosis

Real-world studies have reported reduced mortality in patients with idiopathic pulmonary fibrosis (IPF) treated with antifibrotic therapy; however, the initiation or discontinuation of therapy during these studies may have introduced bias. This study investigated the effect of antifibrotic therapy on mortality and other outcomes in patients with IPF using causal inference methodology.