Baseline characteristics and survival of patients of idiopathic pulmonary fibrosis: a longitudinal analysis of the Swedish IPF Registry.
Jing GaoDimitrios KalafatisLisa CarlsonIda H A PesonenChuan-Xing LiÅsa WheelockJesper M MagnussonC Magnus SköldPublished in: Respiratory research (2021)
Disease severity, phenotypes, and anti-fibrotic treatment are closely associated with the outcome in IPF, with treated patients surviving longer. Phenotypes may contribute to predicting outcomes of patients with IPF and suggest the patients' need for special management, whereas single or composite variables have some limitations as disease predictors.