Type 2 & other diabetes

Adherence to GLP ‐1 receptor agonists and SGLT2 inhibitors by out‐of‐pocket spending among Medicare beneficiaries with diabetes

Diabetes Obes MetabPublished Longitudinal survey cohort study

Authors' conclusion

OOP costs for GLP-1RAs and SGLT2i are substantial, potentially posing a particular burden for low-income Medicare beneficiaries. Policy changes may reduce this burden, although adherence improvements appear limited to beneficiaries using SGLT2i.

Study context

Population
Medicare beneficiaries with diabetes using GLP-1RAs or SGLT2i in year one; low-income = income below 200% of the Federal Poverty Level
Participants
97 vs 73
Exposure
Baseline cumulative out-of-pocket (OOP) drug expenses and year-two adherence
  • GLP-1RAn = 97
  • SGLT2in = 73
Outcome
Association between baseline cumulative OOP drug expenses and adherence (proportion of days covered, PDC)
Follow-up
Year two
Methodological detailssurvey-weighted generalized Poisson regression, Medicare Current Beneficiary Survey 2016-2021
  • Survey-weighted generalized Poisson regression
  • Medicare Current Beneficiary Survey 2016-2021

Main finding

As reported in the abstract

SGLT2i: higher OOP costs (mean $204; $0-$2649) associated with lower adherence, adjusted adherence ratio per $100 increase
0.959 (95% CI: 0.932-0.987)

Observational data: associations, not effects.

Further findings

Dual Medicare-Medicaid coverage and adherence

Dual coverage associated with increased adherence, adjusted adherence ratio
1.580 (95% CI: 1.061-2.352)

High-income GLP-1RA users

Higher OOP expenditures associated with increased adherence in the highest income range

Original publication

Adherence to GLP ‐1 receptor agonists and SGLT2 inhibitors by out‐of‐pocket spending among Medicare beneficiaries with diabetes. Diabetes Obes Metab. Published 16 July 2025. doi:10.1111/dom.16619

Composed by AI from the published abstract and checked against it. How Briefs are made →

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.