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Disparities in Use of Novel Diabetes Medications by Insurance: A Nationally Representative Cohort Study

Background Minority racial and ethnic populations have the highest prevalence of type 2 diabetes mellitus but lower use of sodium-glucose co-transporter-2 inhibitors (SGLT2i) and glucagon-like peptide-1 receptor agonists (GLP1ra), novel medications that reduce morbidity and mortality. Observed dispa...

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Bibliographic Details
Published in:Journal of general internal medicine : JGIM 2024-11, Vol.39 (15), p.2987-2994
Main Authors: Bepo, Lurit, Nguyen, Oanh K., Makam, Anil N.
Format: Article
Language:English
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Summary:Background Minority racial and ethnic populations have the highest prevalence of type 2 diabetes mellitus but lower use of sodium-glucose co-transporter-2 inhibitors (SGLT2i) and glucagon-like peptide-1 receptor agonists (GLP1ra), novel medications that reduce morbidity and mortality. Observed disparities may be due to differences in insurance coverage, which have variable cost-sharing, prior authorization, and formulary restrictions that influence medication access. Objective To assess whether racial/ethnic differences in SGLT2i and GLP1ra use differ by payer. Design Cross-sectional analysis of 2018 and 2019 Medical Expenditure Panel Survey data. Participants Adults ≥ 18 years old with diabetes. Main Measures We defined insurance as private, Medicare, or Medicaid using ≥ 7 months of coverage in the calendar year. We defined race/ethnicity as White (non-Hispanic) vs non-White (including Hispanic). The primary outcome was use of ≥ 1 SGLT2i or GLP1ra medication. We used multivariable logistic regression to assess the interaction between payer and race/ethnicity adjusted for cardiovascular, socioeconomic, and healthcare access factors. Key Results We included 4997 adults, representing 24.8 million US adults annually with diabetes (mean age 63.6 years, 48.8% female, 38.8% non-White; 33.5% private insurance, 56.8% Medicare, 9.8% Medicaid). In our fully adjusted model, White individuals with private insurance had significantly more medication use versus non-White individuals (16.1% vs 8.3%, p  
ISSN:0884-8734
1525-1497
1525-1497
DOI:10.1007/s11606-024-08961-x