ISSN 1178-6191

Maori Health Review

Making Education Easy Issue 121 – 2026

Maori Health Review

New Zealand paediatric respiratory stock-take survey

Authors: McNamara DG et al.

Summary: A survey of health practitioners across New Zealand has highlighted inadequate staffing and provision of services for paediatric respiratory care. Responses (n =23) were obtained from 17 hospitals, of which only three (located in main centres) employed respiratory- and sleep-specialist senior medical officers. Paediatricians with an interest in respiratory care were evenly distributed, with low numbers reported in the Northern region, Wellington and Canterbury. Senior nurse staffing was generally consistent across the country, except in the Northern region. However, allied health staffing was inconsistent, with many districts in the Te Manawa Taki region reporting little or no respiratory physiotherapy staff. More than half of all districts across the country had limited or no access to videofluoroscopic swallow studies, as well as poor access to chest computed tomography scanning under general anaesthesia.

Comment: Respiratory conditions are leading causes for hospitalisations and time off school for tamariki Māori, and so these results are concerning. With the move to more localised health service decision making, such as workforce development and coordination, I hope we see improvements as soon as possible.

Reference: N Z Med J. 2026;139(1632):114-119.

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Research Review publications are intended for New Zealand health professionals.

The co-creation of eating and wellbeing guidelines with rangatahi (young people) in Aotearoa New Zealand

Authors: Railton R et al.

Summary: Rangatahi Māori have successfully co-created a set of eating and wellbeing guidelines for New Zealand young people, known as the Manaora Rangatahi Guidelines. Wānanga were held at a marae in Hawke’s Bay, with feedback presentations at four local secondary schools. A total of 17 rangatahi worked alongside Māori and non-Māori experts to create 10 eating and 10 wellbeing guideline messages, and 94 students provided feedback via surveys. The guidelines addressed contemporary issues such as sustainable eating, ultra-processed foods, social dimensions of eating and physical activity, screen time and cyberbullying. Respect, rights and responsibilities were emphasised. Several of the guideline messages incorporated the concepts of mauri (life force).

Reference: Public Health Nutr. 2026;29(1):e87.

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Rangatahi youth-led dissemination campaign for co-created eating and wellbeing guidelines

Authors: Christison L et al.

Summary: Rangatahi Māori have successfully co-created a low-cost digital media campaign to disseminate the Manaora Rangatahi Guidelines, using peer to-peer messaging and videos. Rangatahi (n = 17) co-developed a dissemination plan, filmed video clips for each of the 20 guideline messages, and supported the 20-week digital media campaign. Video clips were professionally developed with support from three Māori influencers and a video production company. Two videos, each covering one eating and one wellbeing guideline message, were released every fortnight over 20 weeks. The campaign achieved >1.48 million impressions and >19,000 engagement actions on Instagram and TikTok. Paid promotion strategies boosted the number of impressions generated. The estimated total cost of the campaign was NZD 125,000.

Comment: I love these two studies because rangatahi were not treated as participants but as genuine partners. The success of the social media campaign – with almost 1.5 million impressions – shows that Indigenous youth-led approaches are successful – we just need to trust them to lead it.

Reference: JMIR Form Res. 2026;10:e71833

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Maori Health Review

Gastric cancer survival (in)equity from 2002 to 2021: examining demographic and clinical characteristics among Māori and non-Māori

Authors: Satherley N et al.

Summary: While gastric cancer mortality risk is still higher for Māori compared with non Māori, this disparity has reduced in recent years, according to a registry study. Records for 1452 Māori and 6402 non-Māori diagnosed with gastric cancer were obtained from the New Zealand Cancer Registry, and linked with mortality data from Statistics New Zealand. Ethnic inequity in gastric cancer mortality was apparent over the period 2002 to 2017, but was smaller in more recent periods, particularly 1-year age-standardised mortality. The mortality difference for Māori compared with non-Māori was most pronounced for those aged 45-64 years.

Reference: N Z Med J. 2026;139(1632):44-70.

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Journey towards piloting Helicobacter pylori screen-and-treat to address health inequities in Aotearoa New Zealand

Authors: Teng A et al.

Summary: A paper reviewing H. pylori infection, sequelae and testing in New Zealand has suggested there is an urgent need to introduce a Māori-led, screen-and-treat pilot for the infection. The prevalence of H. pylori is higher in Māori and Pacific peoples compared with Europeans, but they are less likely to be tested for the infection. They are also more likely to be hospitalised for peptic ulcer and to develop gastric cancer than Europeans.

Comment: Getting H. pylori testing and treatment right is so important for Māori and Pacific peoples who have higher rates of both H. pylori infection and associated gastric cancer. International research now shows that H. pylori is the single greatest modifiable risk factor for gastric cancer and may carry a greater population-level risk than inherited stomach cancer gene syndromes. Together, these papers demonstrate that inequities in testing, access to treatment, and early intervention are not just issues of infection management, but major contributors to preventable cancer inequities, reinforcing the importance of Māori-led approaches.

Reference: Helicobacter. 2026;31(2):e70123.

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Participant experiences of the Knee Care for Arthritis through Pharmacy Service (KneeCAPS)

Authors: Darlow B et al.

Summary: The experiences of individuals involved in the community pharmacist-led KneeCAPS trial were captured in a cross-sectional, qualitative study. After screening for knee osteoarthritis, intervention arm participants were offered explanations, support with goal setting and referral for exercise, dietary support, and/or medication review. A total of 23 intervention arm participants (11 Māori, 12 non-Māori) were interviewed after completing the trial. Two main themes were identified: 1) perceptions of value in receiving goal orientated, empowering and collaborative care that led to sustained behaviour changes, with Māori participants also reporting holistic and culturally responsive care; and 2) unclear processes or missed opportunities in service delivery, unmet expectations, and disruptions in care due to complexities outside of KneeCAPS.

Comment: Great to finally include research about osteoarthritis and Māori here! Also love that the study moves beyond documenting the inequities to exploring Māori-led solutions.

Reference: Osteoarthr Cartil Open. 2026;8(2):100759.

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Declining incidence of atrial fibrillation associated ischemic stroke in Auckland, New Zealand

Authors: Mahawish KM et al.

Summary: An analysis of Auckland Regional Community Stroke study data found that although the incidence of atrial fibrillation-associated ischaemic stroke decreased for the year ended August 2021 compared with the year ended February 2012, persistent ethnic inequities remained. The overall crude incidence decreased from 49.0 to 32.7 per 100,000 population across the two time periods. When incidence was analysed by ethnicity, temporal reductions were evident for Europeans, but not for Māori or Pacific peoples. Dispensing of oral anticoagulants increased over the two time periods in all ethnic groups.

Comment: An important reminder that a ‘one size fits all’ solution in health can widen disparities. As the authors note, to achieve equity we need interventions for those with the greatest disease burden so that they experience the greatest gains.

Reference: J Am Heart Assoc. 2026;15(5):e045260.

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Maori Health Review

Uptake and early outcomes of a meal replacement intervention in an ethnically diverse adult population living with obesity and significant comorbidity

Authors: Shand J et al.

Summary: A meal replacement intervention delivered in a specialist service achieved clinically meaningful weight loss and improved metabolic and psychological outcomes in a predominantly Māori and Pacific population of adults with obesity and significant comorbidities. Participants (n = 128) had been declined bariatric surgery, were young adults with type 2 diabetes, or had been deferred from a corneal transplant because of their weight. Participants received a 12-week, meal replacement low energy diet, with adjunctive obesity medications available under pre-specified criteria. At baseline, mean body weight was 145.0 kg, body mass index was 49.9 kg/m2, and 73% of participants were receiving treatment for type 2 diabetes (mean glycosylated haemoglobin [HbA1c] 67.6 mmol/mol). Overall, 72% of participants completed the intervention, and achieved a mean weight loss of 10.9 kg. Among those with diabetes, 67% completed the intervention, with 33% achieving an HbA1c <50 mmol/mol on no diabetes medication. Mean psychological and quality of life scores improved.

Comment: Great to see another resource for weight loss in our kete – along with Green prescriptions, new medicines (and hopefully some of them funded in the next 12 months) and surgery. I understand work is being undertaken to help whānau choose the best option for them, based on both clinical and life factors. Watch this space!

Reference: Diabetes Obes Metab. 2026;28(5):3924-3932.

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Foetal movement information and maternal concerns in the third trimester

Authors: Bradford BF et al.

Summary: Foetal movement worries are common for women in the third trimester of pregnancy in New Zealand, but Māori and Pacific women are less likely to seek advice when concerned than European women, according to a survey of 1640 women with singleton pregnancies. Of the surveyed population, 63.5% were European, 16.2% were Māori and 7.3% were Pacific peoples. Median gestation time was 31 weeks, 55.9% were nulliparous, and 83.3% had been concerned about foetal movement. Adjusted odds ratios for seeking advice when concerned were 0.69 (95% CI 0.51%-0.93%; p = 0.02) for Māori and 0.58 (95% CI 0.38%-0.88%; p = 0.01) for Pacific compared with European women. Advice seeking was also less likely when a doctor was the main maternity provider compared with a midwife (adjusted odds ratio 0.59; 95% CI 0.39%-0.92%, p = 0.02), and in those who received fewer compared with the recommended number of antenatal visits (adjusted odd ratio 0.55; 95% CI 0.34%-0.88%; p = 0.01).

Comment: The finding that Māori and Pacific wāhine were less likely to seek advice should be interpreted within the context of longstanding barriers to good antenatal care for them. The fact that advice seeking was more likely with a midwife highlights the importance of a good relationship, trust and continuity – all things we can implement to improve stillbirth outcomes.

Reference: Aust N Z J Obstet Gynaecol. 2026;66(2):e70122.

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The use of blood biomarkers in lung cancer screening in Aotearoa New Zealand: a cross-sectional survey of Māori perspectives and preferences

Authors: Colhoun S et al.

Summary: A cross-sectional survey of Māori found that participants generally supported using blood samples in lung cancer screening, but there were some regional differences. Survey participants were potential lung cancer “screenees” and their whānau from Te Tai Tokerau and Tāmaki Makaurau. Overall, most participants (83.7% screenees; 81.4% whānau) were at least “comfortable” donating blood, although participants from Te Tai Tokerau were less comfortable than those from Tāmaki Makaurau. Clear information about blood use, protecting the health of future generations, and being able to consent to specific uses were identified as key priorities for using blood samples in lung cancer screening.

Comment: From Te Tai Tokerau myself, I was both fascinated and unfortunately not surprised with the regional differences described here – they reflect longstanding issues in access, trust and negative experiences with the health system in Te Norta. However, peoples’ rights to the best healthcare and outcomes, particularly given higher lung cancer rates and deaths, mean that further work to address these issues is necessary.

Reference: N Z Med J. 2026;139(1633):76-92.

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