The cultural safety of reports of research on primary healthcare use by Indigenous Peoples: a systematic review

Abstract

Abstract Introduction The use of primary healthcare is associated with better chronic disease outcomes for Indigenous Peoples. Community-driven and owned health research data in understanding PHC use enablers provide opportunities to enhance PHC use within communities. Therefore, may reduce chronic disease burden. Methods Medline, CINAHL and Embase were all systematically searched from 1st January 2002 to 4th April 2023. Papers were included if they were original studies, published in English and included data (quantitative, qualitative and/or mixed methods) on primary healthcare use for chronic disease (chronic kidney disease, cardiovascular disease and/or diabetes mellitus) by Indigenous Peoples from Western colonial countries. Study screening and data extraction were undertaken independently by two authors, at least one of whom was Indigenous. The baseline characteristics of the papers were analyzed using descriptive statistics. Aspects of cultural safety of the research papers were assessed using two quality appraisal tools: the CONSIDER tool and the CREATE tool (subset analysis). This systematic review was conducted in accordance with the Assessing the Methodological Quality of Systematic Reviews (AMSTAR) tool. Results We identified 35 papers from Australia, New Zealand, Canada, and the United States. Most papers were quantitative (n = 21) and included data on 42438 people. Cultural safety across the included papers varied significantly with gaps in adequate reporting of research partnerships, provision of clear collective consent from participants and Indigenous research governance throughout the research process, particularly in dissemination. The majority of the papers (94%, 33/35) stated that research aims emerged from communities or empirical evidence. We also found that 71.4% (25/35) papers also reported of using strengths-based approaches by considering the impacts of colonization on reduced primary healthcare access. Conclusion Research on Indigenous PHC use must be changed to privilege Indigenous voices throughout the research process including dissemination, provide further engagement opportunities for the community and include sufficient detail on partnership agreements between Indigenous and non-Indigenous researchers.