The Choosing Wisely campaign and shared decision-making with Māori
Choosing Wisely seeks to prevent harm by reducing the number of unnecessary tests, treatments and procedures, and by promoting shared decision-making. This article, published in the New Zealand Medical Journal, scopes perspectives of Māori patients/consumers and Māori health practitioners around Choosing Wisely and explores shared decision-making between Māori and their medical practitioners.
The whitewashing of contracts: Unpacking the discourse within Māori health provider contracts in Aotearoa/New Zealand
Māori health providers emerged in Aotearoa/New Zealand in the 1980s as a mechanism to achieve self-determination for Māori communities. However, the contracts funding Māori health providers limit expressions of self-determination and fail to reflect Te Tiriti O Waitangi, the founding treaty of Aotearoa/New Zealand. Significant health reforms are proposed in Aotearoa/New Zealand, including the creation of a Māori Health Authority that will commission services from Māori health providers. This paper, published in Health & Social Care in the Community, aims to critique the government contracts provided to Māori health providers in the light of the health reforms.
The needs of Pacific families affected by age-related cognitive impairment in New Zealand: interviews with providers from health-care organisations
Pacific populations in New Zealand are aging, but little is known in the health-care environment about their experiences with cognitive impairment. The aim of this study, published in the Journal of Primary Health Care, was to explore the needs of Pacific peoples affected by age-related cognitive decline from the perspectives of health-care providers.
Strengthening public health contracting: findings of a follow-up nationwide survey from Aotearoa
In 2010 and 2015 nationwide surveys monitored government management of public health providers. These surveys found evidence of inconsistent management which disadvantaged Māori providers, consistent with institutional racism. In Dec 2019 to March 2020 a follow-up nationwide telephone survey was completed. Public health units, primary health organisations, Māori health providers and non-governmental organisations with public health contracts responded. This paper, published in Kōtuitui, focuses on the findings about contracts, and relationships.
"We Need a System that's Not Designed to Fail Māori": Experiences of Racism Related to Kidney Transplantation in Aotearoa New Zealand
Reported experiences of racism in Aotearoa New Zealand are consistently associated with negative measures of health, self-rated health, life satisfaction, and reduced access to high-quality healthcare with subsequent poor health outcomes. In this paper, published in the Journal of Racial and Ethnic Health Disparities, the authors report on perceptions and experiences of prejudice and racism by Indigenous Māori with kidney disease and their family members and donors who took part in a wider study about experiences of kidney transplantation.
'It absolutely needs to move out of that structure': Māori with bipolar disorder identify structural barriers and propose solutions to reform the New Zealand mental health system
This paper, published in Ethnicity & Health, synthesises critique from Māori patients with Bipolar Disorder and their whānau to identify barriers and propose changes to improve the structure and function of the New Zealand mental health system.