1. Experiences of the HIV Cascade of Care Among Indigenous Peoples: A Systematic Review.
- Author
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Jongbloed K, Pooyak S, Sharma R, Mackie J, Pearce ME, Laliberte N, Demerais L, Lester RT, Schechter MT, Loppie C, and Spittal PM
- Subjects
- Australia epidemiology, Canada epidemiology, Delivery of Health Care organization & administration, HIV Infections psychology, Humans, Indians, North American ethnology, Medication Adherence psychology, New Zealand epidemiology, Social Stigma, Social Support, United States epidemiology, Continuity of Patient Care, Cultural Competency, HIV Infections drug therapy, HIV Infections ethnology, Health Services Accessibility, Healthcare Disparities ethnology, Indians, North American psychology, Medication Adherence ethnology, Retention in Care
- Abstract
Indigenous leaders remain concerned that systemic oppression and culturally unsafe care impede Indigenous peoples living with HIV from accessing health services that make up the HIV cascade of care. We conducted a systematic review to assess the evidence related to experiences of the HIV care cascade among Indigenous peoples in Australia, Canada, New Zealand, and United States. We identified 93 qualitative and quantitative articles published between 1996 and 2017 reporting primary data on cascade outcomes disaggregated by Indigenous identity. Twelve involved data from Australia, 52 from Canada, 3 from New Zealand and 26 from United States. The majority dealt with HIV testing/diagnosis (50). Relatively few addressed post-diagnosis experiences: linkage (14); retention (20); treatment initiation (21); adherence (23); and viral suppression (24). With the HIV cascade of care increasingly the focus of global, national, and local HIV agendas, it is critical that culturally-safe care for Indigenous peoples is available at all stages.
- Published
- 2019
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