Abstract

BackgroundTo summarise the evidentiary basis related to causes of inequities in chronic kidney disease among Indigenous Peoples.MethodsWe conducted a Kaupapa Māori meta-synthesis evaluating the epidemiology of chronic kidney diseases in Indigenous Peoples. Systematic searching of MEDLINE, Google Scholar, OVID Nursing, CENTRAL and Embase was conducted to 31 December 2019. Eligible studies were quantitative analyses (case series, case-control, cross-sectional or cohort study) including the following Indigenous Peoples: Māori, Aboriginal and Torres Strait Islander, Métis, First Nations Peoples of Canada, First Nations Peoples of the United States of America, Native Hawaiian and Indigenous Peoples of Taiwan. In the first cycle of coding, a descriptive synthesis of the study research aims, methods and outcomes was used to categorise findings inductively based on similarity in meaning using the David R Williams framework headings and subheadings. In the second cycle of analysis, the numbers of studies contributing to each category were summarised by frequency analysis.Completeness of reporting related to health research involving Indigenous Peoples was evaluated using the CONSIDER checklist.ResultsFour thousand three hundred seventy-two unique study reports were screened and 180 studies proved eligible. The key finding was that epidemiological investigators most frequently reported biological processes of chronic kidney disease, particularly type 2 diabetes and cardiovascular disease as the principal causes of inequities in the burden of chronic kidney disease for colonised Indigenous Peoples. Social and basic causes of unequal health including the influences of economic, political and legal structures on chronic kidney disease burden were infrequently reported or absent in existing literature.ConclusionsIn this systematic review with meta-synthesis, a Kaupapa Māori methodology and the David R Williams framework was used to evaluate reported causes of health differences in chronic kidney disease in Indigenous Peoples. Current epidemiological practice is focussed on biological processes and surface causes of inequity, with limited reporting of the basic and social causes of disparities such as racism, economic and political/legal structures and socioeconomic status as sources of inequities.

Highlights

  • To summarise the evidentiary basis related to causes of inequities in chronic kidney disease among Indigenous Peoples

  • While a substantial literature exists to evaluate the determinants of unequal health outcomes of Indigenous Peoples and minority populations, inequities have often been explained via individual “biological risk factors”, as opposed to identifying structural and systemic perpetrators of health inequities, including racism and coloniality [6,7,8]

  • There is a commonality of experience between Indigenous Peoples globally, and that is the ongoing impact of colonisation on health outcomes

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Summary

Introduction

To summarise the evidentiary basis related to causes of inequities in chronic kidney disease among Indigenous Peoples. Indigenous Peoples continue to experience health inequities in the incidence and outcomes of non-communicable diseases, including chronic kidney disease [2,3,4]. While a substantial literature exists to evaluate the determinants of unequal health outcomes of Indigenous Peoples and minority populations, inequities have often been explained via individual “biological risk factors”, as opposed to identifying structural and systemic perpetrators of health inequities, including racism and coloniality [6,7,8]. Indigeneity has been used in research as a biological risk factor to explain health inequities associated with non-communicable diseases including chronic kidney disease [11]. Understanding the relationship between power, colonisation, and loss of resources and the impact that these factors have on Indigenous health is a field of health research that can provide a more rigorous exploration of Indigenous health inequities to inform practice and policy [12,13,14]

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