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ABSTRACT: Introduction
Idiopathic pulmonary fibrosis (IPF) has high morbidity and mortality with limited treatment options. Goal-oriented management approaches, such as the "treatable traits" concept, have yet to be implemented in IPF. This study aims to identify specific treatment goals in IPF for potential interventions by analysing outcomes from two national registries.Methods
We used data from the INSIGHTS-IPF registry, comprising 1232 IPF patients, enrolled from 2014 to 2020 as derivation cohort. Baseline and 6-month follow-up data were examined to assess clinical progression and predict 1-year mortality. Variables included forced vital capacity (FVC), diffusing capacity of the lung for carbon monoxide (D LCO), 6-min walk distance (6MWD), body mass index (BMI)
SUBMITTER: Behr J
PROVIDER: S-EPMC12813680 | biostudies-literature | 2026 Jan
REPOSITORIES: biostudies-literature