Hauora Māori – Māori health: a right to equal outcomes in primary care
Author:
Sheridan Nicolette1, Jansen Rawiri McKree2, Harwood Matire3, Love Tom4, Kenealy Timothy3, Aguirre-Duarte Nelson5, Arroll Bruce3, Atmore Carol6, Carryer Jenny1, CNZM Peter Crampton7, Dowell Anthony7, Fishman Tana, Gauld Robin7, Hoare Karen1, Jackson Gary8, Kerse Ngaire3, Lampshire Debra3, McBain Lynn7, MacRae Jayden9, Mills Jane10, Øvretveit John11, Percival Teuila8, Perera Roshan12, Roland Martin13, Ryan Debbie14, Schmidt-Busby Jacqueline5, Stokes Tim7, Stubbe Maria7, Watt Daniel4
Affiliation:
1. Massey University 2. Te Aka Whai Ora – Māori Health Authority 3. University of Auckland 4. Sapere Research Group 5. Comprehensive Care 6. WellSouth Primary Health Network 7. University of Otago 8. Te Whatu Ora - Health New Zealand Counties Manukau 9. Datacraft Analytics 10. La Trobe University 11. Karolinska Institutet 12. Health Hawkes Bay - Te Oranga o Te Matau-a-Māui 13. University of Cambridge 14. Pacific Perspectives
Abstract
Abstract
Background
For more than a century, Māori have experienced poorer health than non-Māori. In 2019 an independent Tribunal found the Government had breached Te Tiriti o Waitangi by “failing to design and administer the current primary health care system to actively address persistent Māori health inequities”. Many Māori (44%) have unmet need for primary care. Seven models of primary care were identified, including Māori-owned practices. We hypothesised patient health outcomes for Māori would differ between models of care.
Methods
Cross-sectional primary care data were analysed at 30 September 2018. National datasets were linked to practices at patient level, to measure associations between practice characteristics and patient health outcomes. Primary outcomes: polypharmacy (≥55 years), HbA1c testing, child immunisations, ambulatory sensitive hospitalisations (0-14, 45-64 years) and emergency department attendances. Regressions include only Māori patients, across all models of care.
Results
660,752 Māori patients were enrolled in 924 practices with 124,854 in 65 Māori-owned practices.
Māori practices had: no significant association with HbA1c testing, ambulatory sensitive hospitalisations or ED attendance, and a significant association with lower polypharmacy (3.7% points) and lower childhood immunisations (13.4% points).
Māori practices had higher rates of cervical smear and cardiovascular risk assessment, lower rates of HbA1c tests, and more nurse (46%) and doctor (8%) time (FTE) with patients.
The average Māori practice had 52% Māori patients compared to 12% across all practices. Māori practices enrolled a higher percentage of children and young people, five times more patients in high deprivation areas, and patients with more multimorbidity.
More Māori patients lived rurally (21.5% vs 15%), with a greater distance to the nearest ED. Māori patients were more likely to be dispensed antibiotics or tramadol.
Conclusions
Māori practices are an expression of autonomy in the face of enduring health system failure. Apart from lower immunisation rates, health outcomes were not different from other models of care, despite patients having higher health risk profiles. Across all models, primary care need was unmet for many Māori, despite increased clinical input. Funding must support under-resourced Māori practices and ensure accountability for the health outcomes of Māori patients in all models of general practice.
Publisher
Research Square Platform LLC
Reference34 articles.
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