Real world initiation of newly funded empagliflozin and dulaglutide under special authority for patients with type 2 diabetes in New Zealand.
BMC Health Serv Res · 2025
Last updated 2026-05-28In New Zealand, 46% of eligible patients with type 2 diabetes started taking SGLT2i/GLP1RA medications after they became funded in 2021, with higher initiation rates among Māori (50.8%) and Pacific (48.8%) patients compared to other groups (36.2–40.7%). Prescribing was similar for patients with and without cardiovascular or kidney disease (47.1% vs. 48.9%). Practices with more doctors per patient, lower fees, Māori health providers, and no after-hours access had the highest prescribing rates.
AI summary of the abstract below.
| Journal | BMC Health Serv Res, 2025 |
|---|---|
| Citations | 5 |
| Relative citation ratio | 2.38 |
| Molecules | dulaglutide |
| Conditions studied | Type 2 Diabetes |
Abstract
BACKGROUND: Type 2 diabetes (T2D) is sub-optimally managed for many in Aotearoa New Zealand, and disproportionately affects Māori and Pacific peoples. In February 2021, SGLT2i/GLP1RA agents were funded for use for the first time with prioritisation for Māori, Pacific and those with cardiovascular and/or renal disease or risk (CVRD). This study evaluates the impact of health system factors on initiation of SGLT2i/GLP1RA therapy.
METHODS: Primary care data was collected for patients with T2D aged 18-75 years from four primary care organisations (302 general practices) in the Auckland / Waikato region of New Zealand (Feb 2021 - July 2022). Initiation of SGLT2i/GLP1RA therapy was reviewed by patient (age, gender, ethnicity, CVRD status) and health system variables (funding, provider type, staffing, patient numbers, rurality, after-hours access). Logistic regression was used to estimate the odds ratio of a patient being dispensed SGLT2i/GLP1RA.
RESULTS: Of 57,743 patients with T2D, 22,331 were eligible for funded SGLT2i/GLP1RA access and 10,272 of those (46.0%) were prescribed. Initiation of therapy was highest in Māori (50.8%) and Pacific (48.8%) patients (vs. 36·2-40·7% of other ethnic groups; P < 0.001), but was comparable in those with and without CVRD (47·1% vs. 48·9%; P = 0.2). Prescribing was highest in practices with higher doctor/patient numbers, low-cost fees, Māori health providers and clinics without after-hours access.
CONCLUSION: Prioritised access for SGLT2i/GLP1RA appears to be associated with a reduced health equity gap for Māori and Pacific patients with T2D in NZ, but work is required to improve prescribing for patients with CVRD.
Verbatim abstract via PubMed 40140836 ↗
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