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ABSTRACT: Background
Idiopathic pulmonary fibrosis (IPF) is a rare life-threating interstitial lung disease (ILD). This study characterizes demographics, health care utilization, and comorbidities among elderly IPF patients and estimates prevalence and incidence rates for selected outcomes.Methods
Cohort study using a large US health insurance database (Optum's Medicare Advantage plan).Inclusion criteria
≥ 1 diagnosis code for IPF (2008 - 2014), age ≥65 years, no diagnosis of IPF or other ILD in prior 12 months. Demographics, health care utilization, comorbidities and incidence rates for various outcomes were estimated. Follow-up continued until the earliest of: health plan disenrollment, death, a claim for another known cause of ILD, or end of the study period.Results
SUBMITTER: Mortimer K
PROVIDER: S-EPMC6327584 | biostudies-literature | 2019 Jan
REPOSITORIES: biostudies-literature