Lifetime medical costs attributable to sickle cell disease among nonelderly individuals with commercial insurance.
Ontology highlight
ABSTRACT: Sickle cell disease (SCD) is a severe monogenic disease associated with high morbidity, mortality, and a disproportionate burden on Black and Hispanic communities. Our objective was to estimate the total healthcare costs and out-of-pocket (OOP) costs attributable to SCD among commercially insured individuals over their nonelderly lifetimes (0 to 64 years of age). We constructed a retrospective cohort of individuals with diagnosed SCD using Truven Health Marketscan commercial claims data from 2007 through 2018, compared with matched control subjects from the Medical Expenditure Panel Survey. We estimated Kaplan-Meier sample average costs using previously reported survival curves for SCD and control subjects. Individuals with SCD (20 891) and control subjects (33 588) were included in our an
SUBMITTER: Johnson KM
PROVIDER: S-EPMC9898623 | biostudies-literature | 2023 Feb
REPOSITORIES: biostudies-literature
ACCESS DATA