Type 2 & other diabetes

Low uptake and disparities in therapeutic inertia of cardiorenal protective diabetes medications for patients with type 2 diabetes and above-target hemoglobin A1c

BMJ Open Diabetes Res CarePublished Retrospective cohort study

Authors' conclusion

Despite compelling indications, initiation of SGLT2i and GLP-1RA remained low overall and was significantly lower among Black and Hispanic patients, underscoring therapeutic inertia as a modifiable barrier to optimal diabetes care.

Study context

Population
Patients with T2D and above-target HbA1c with clinical indications for SGLT2i or GLP-1 RA, not currently using them, no contraindications; 56% White, 37% Black, 3% Hispanic, 2% Asian, 2% other
Participants
10,345 patients30,740 encounters
Exposure
New SGLT2i or GLP-1 RA prescribing by race and ethnicity
Outcome
Therapeutic inertia: lack of new prescription orders for SGLT2i or GLP-1 RA
Methodological detailselectronic health record data 2018-2022, log-link Poisson generalized estimating equation models
  • Electronic health record data 2018-2022
  • Log-link Poisson generalized estimating equation models

Main finding

As reported in the abstract

New prescribing rate · 2018-2022

New SGLT2i prescribing increased over time but remained low

0.9%-4.3%

New GLP-1 RA prescribing increased over time but remained low

1.2%-5.2%

Observational data: associations, not effects.

Further findings

OutcomeRR (95% CI)
New SGLT2i prescription by race and ethnicityBlackvs WhiteAdjusted for sociodemographic, clinical and service factors0.59 (0.42–0.82)
New GLP-1 RA prescription by race and ethnicityBlackvs WhiteAdjusted for sociodemographic, clinical and service factors0.62 (0.49–0.79)
New GLP-1 RA prescription by race and ethnicityHispanicvs WhiteAdjusted0.48 (0.25–0.92)

Original publication

Low uptake and disparities in therapeutic inertia of cardiorenal protective diabetes medications for patients with type 2 diabetes and above-target hemoglobin A1c. BMJ Open Diabetes Res Care. Published 22 April 2026. doi:10.1136/bmjdrc-2025-005546

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