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ABSTRACT: Introduction
Idiopathic pulmonary fibrosis (IPF) is the classic progressive fibrosing interstitial lung disease (ILD), but some patients with ILDs other than IPF also develop a progressive fibrosing phenotype (PF-ILD). Information on use and cost of healthcare resources in patients with PF-ILD is limited.Methods
We used USA-based medical insurance claims (2014-2016) to assess use and cost of healthcare resources in PF-ILD. Patients with at least two ILD claims and at least one pulmonologist visit were considered to have ILD. Pulmonologist visit frequency was used as a proxy to identify PF-ILD (at least four visits in 2016, or at least three more visits in 2016 vs. 2014).Results
Of 2517 patients with non-IPF ILD, 15% (n = 373) had PF-ILD. Mean annual medical costs as
SUBMITTER: Olson AL
PROVIDER: S-EPMC7467408 | biostudies-literature | 2020 Jul
REPOSITORIES: biostudies-literature