Key result
Māori ethnicity linked to ~71% higher odds of repeat HbA1c testing after elevated results.
Why the study?
Rates of cardiometabolic blood screening, elevated results, and clinical follow-up actions needed to be estimated and compared between Māori and non-Māori mental health service users with psychosis in Canterbury, Aotearoa New Zealand.
Are there differences in cardiometabolic screening rates, elevated results, and follow-up actions between Māori and non-Māori patients with psychosis?
Cohort (n=3,840)
Are there differences in cardiometabolic screening rates, elevated results, and follow-up actions between Māori and non-Māori patients with psychosis?
Odds Ratio: 1.71 (95% CI 1.16–2.5)
Absolute Event Rate: 51.9% vs 38.8%
There are significant gaps in guideline-directed cardiometabolic screening for patients with psychosis, with Māori patients experiencing higher rates of elevated cardiometabolic risk markers despite being younger.
May support targeted follow-up for Māori after elevated HbA1c; leaves open whether screening disparities persist or affect outcomes in psychosis.
Objective: Estimate and compare rates of cardiometabolic blood screening, elevated results and clinical follow-up actions for Māori and non-Māori mental health service users with psychosis in Canterbury, Aotearoa New Zealand. Methods: A retrospective cohort study ( N = 3840) with dynamic entry was conducted with people aged 18–64 years with a psychosis diagnosis in Canterbury Specialist Mental Health Service (1 August 2012 to 31 December 2019). Linked administrative data captured lipid and HbA1c screening within 1 year of study entry, elevated results (triglycerides > 2.2 mmol/L; total cholesterol:high-density lipoprotein cholesterol > 5; HbA1c > 40 mmol/mol) from individual study entry to 31 December 2023, and clinical actions (repeat test; statin/metformin dispensing) within 1 year following an elevated result. Results: 887/3840 (23%) of Canterbury Specialist Mental Health Service users with psychosis were Māori. First-year screening rates were modest (31–44%), similar by ethnicity and broadly higher among clozapine/olanzapine users. Māori had higher odds of both elevated lipids and HbA1c. About one-third of elevated results were followed up with re-testing within 1 year. Rates of follow-up testing and medication dispensing were broadly similar for Māori and non-Māori, except Māori were more likely to receive repeat HbA1c testing after an elevated result (odds ratio = 1.71 [1.16, 2.50]). Conclusions: Findings highlight large gaps in cardiometabolic screening and follow-up actions among Māori and non-Māori Specialist Mental Health Service users with psychosis. Māori presented with psychosis 4 years younger, had significantly higher rates of elevated cardiometabolic risk markers and were more likely to receive HbA1c re-testing following an elevated result.
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Monk et al. (2026) conducted a cohort in Psychosis (n=3,840). Māori ethnicity vs. Non-Māori ethnicity was evaluated on Repeat HbA1c testing within 1 year following an elevated result (OR 1.71, 95% CI 1.16, 2.50). Māori with psychosis were significantly more likely to receive repeat HbA1c testing within 1 year following an elevated result compared to non-Māori (OR 1.71).
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