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Real world initiation of newly funded empagliflozin and dulaglutide under special authority for patients with type 2 diabetes in New Zealand
被引:0
|作者:
Chepulis, Lynne
[1
]
Rodrigues, Mark
[1
]
Gan, Han
[2
]
Keenan, Rawiri
[1
]
Kenealy, Tim
[3
]
Murphy, Rinki
[3
,4
]
Te Karu, Leanne
[3
]
Scott-Jones, Jo
[5
]
Clark, Penny
[6
]
Moffitt, Allan
[7
]
Mustafa, Sara
[1
]
Lawrenson, Ross
[1
]
Paul, Ryan
[1
,8
]
机构:
[1] Univ Waikato, Waikato Med Res Ctr, Private Bag 3105, Hamilton, New Zealand
[2] Univ Waikato, Sch Comp & Math Sci, Hamilton, New Zealand
[3] Univ Auckland, Fac Med & Hlth Sci, Auckland, New Zealand
[4] Hlth New Zealand Te Whatu Ora Te Toka Tumai, Auckland, New Zealand
[5] Midlands Hlth Network, Hamilton, New Zealand
[6] Northcare Med Ctr, Hamilton, New Zealand
[7] ProCare Hlth Ltd, Auckland, New Zealand
[8] Hlth New Zealand Te Whatu Ora Waikato, Hamilton, New Zealand
关键词:
SGLT2i;
GLP1RA;
Type;
2;
diabetes;
Health system access;
ACCESS;
MAORI;
ETHNICITY;
MORTALITY;
PACIFIC;
D O I:
10.1186/s12913-025-12601-3
中图分类号:
R19 [保健组织与事业(卫生事业管理)];
学科分类号:
摘要:
Background Type 2 diabetes (T2D) is sub-optimally managed for many in Aotearoa New Zealand, and disproportionately affects Maori and Pacific peoples. In February 2021, SGLT2i/GLP1RA agents were funded for use for the first time with prioritisation for Maori, 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 Maori (50.8%) and Pacific (48.8%) patients (vs. 36<middle dot>2-40<middle dot>7% of other ethnic groups; P < 0.001), but was comparable in those with and without CVRD (47<middle dot>1% vs. 48<middle dot>9%; P = 0.2). Prescribing was highest in practices with higher doctor/patient numbers, low-cost fees, Maori 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 Maori and Pacific patients with T2D in NZ, but work is required to improve prescribing for patients with CVRD.
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