HIV Among Indigenous peoples: A Review of the Literature on HIV-Related Behaviour Since the Beginning of the Epidemic
- PMID: 25731659
- PMCID: PMC4551545
- DOI: 10.1007/s10461-015-1023-0
HIV Among Indigenous peoples: A Review of the Literature on HIV-Related Behaviour Since the Beginning of the Epidemic
Abstract
From the early days of the HIV epidemic, Indigenous peoples were identified as a population group that experiences social and economic determinants-including colonialism and racism-that increase exposure to HIV. There are now substantial disparities in HIV rates between Indigenous and non-Indigenous peoples in some countries. We conducted a comprehensive literature review to assess the evidence on HIV-related behaviors and determinants in four countries-Australia, Canada, New Zealand and the United States-in which Indigenous peoples share important features of colonization and marginalization. We identified 107 articles over more than 20 years. The review highlights the determinants of HIV-related behaviors including domestic violence, stigma and discrimination, and injecting drug use. Many of the factors associated with HIV risk also contribute to mistrust of health services, which in turn contributes to poor HIV and health outcomes among Indigenous peoples.
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References
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- Te Puni Kokiri. Mate ketoketo/Arai kore. A report about HIV/AIDS and Māori. Wellington, New Zealand: Te Puni Kokiri, 1994.
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- Public Health Agency of Canada . HIV/AIDS Epi updates. Ottawa: Health Canada; 2010.
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- Minority Rights Group International . State of the world’s minorities and Indigenous peoples 2013: focus on health. London: Minority Rights Group; 2013.
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- Reading CL, Wien F. Health inequalities and social determinants of Aboriginal peoples’ health. Prince George: National Collaborating Centre for Aboriginal Health; 2009.
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