HIV care and support services and the treatment outcomes of newcomers living with HIV in Manitoba

dc.contributor.authorMaritim, Charity
dc.contributor.examiningcommitteeBruce, Sharon (Community Health Sciences) Restall, Gayle (Occupational Therapy)en_US
dc.contributor.supervisorBecker, Marissa (Community Health Sciences)en_US
dc.date.accessioned2019-09-05T12:19:20Z
dc.date.available2019-09-05T12:19:20Z
dc.date.issued2019-08-10en_US
dc.date.submitted2019-08-14T15:14:28Zen
dc.date.submitted2019-09-04T20:45:28Zen
dc.degree.disciplineCommunity Health Sciencesen_US
dc.degree.levelMaster of Science (M.Sc.)en_US
dc.description.abstractBACKGROUND: Despite the over-representation of immigrants and refugees (newcomers) in the HIV epidemic in Canada, there is limited research on their HIV care needs and treatment outcomes. This study addressed this knowledge gap by describing how newcomers are linked into HIV care in Manitoba, challenges faced when accessing care and their treatment outcomes. METHODS: An environmental scan was performed to collect data from literature sources and from semi-structured interviews with key informants who provide services to newcomers. The scan data were examined using qualitative content analysis. Clinical data from 1986 to 2017 were obtained from a cohort of people who receive care from the Manitoba HIV Program. Retrospective cohort analysis of secondary data was completed to compare differences in socio-demographic and clinical characteristics and treatment outcomes between newcomers, Indigenous and Canadian-born non-Indigenous persons in HIV care. RESULTS: Newcomers are linked to the Manitoba HIV Program through pathways that involve the Surveillance Unit at Manitoba Health, Seniors and Active Living, Regional Health Authorities’ Public Health Departments, Settlement Coordinators and physicians. Effective linkage and engagement in care may be limited by language barriers, stigma, distrust of medical systems, trauma, financial insecurity and lack of holistic support. By the end of 2017, there were 86 newcomers, 259 Indigenous and 356 Canadian-born non-Indigenous persons enrolled in the cohort. Newcomers in the cohort were younger, with a mean age of 43 years compared to the Indigenous group (45 years) and Canadian-born non-Indigenous group (52 years) (p<0.05). Newcomers were more likely to be female (45%) compared to Indigenous (42%) and Canadian-born non-Indigenous (13%) cohort participants (p<0.05). A higher proportion of newcomers self-reported their HIV risk exposure as heterosexual contact (80%) compared to the Indigenous group (53%) and Canadian-born non-Indigenous group (30%). A higher proportion of newcomers were also diagnosed with tuberculosis (TB) within 6 months of entry into care (21%), compared to 6% of Indigenous and 0.6% of Canadian-born non-Indigenous persons. By the end of 2017, newcomers and Canadian-born non-Indigenous persons achieved viral load suppression (<200 copies/ml) at a similar proportion (93%), different from 82% of Indigenous participants who had a suppressed viral load (p<0.05). CONCLUSIONS: Newcomers achieved a viral suppression rate of over 90%. However, they still experience various challenges when accessing HIV care and require holistic support beyond antiretrovirals alone. Tuberculosis also continues to be a common co-infection among newcomers living with HIV highlighting the importance of TB screening, early access to treatment and prevention with treatment of latent TB.en_US
dc.description.noteOctober 2019en_US
dc.identifier.urihttp://hdl.handle.net/1993/34161
dc.language.isoengen_US
dc.rightsopen accessen_US
dc.subjectManitobaen_US
dc.subjectHIVen_US
dc.subjectImmigrants and Refugeesen_US
dc.subjectEnvironmental Scanen_US
dc.subjectHIV treatment outcomesen_US
dc.subjectHIV care servicesen_US
dc.titleHIV care and support services and the treatment outcomes of newcomers living with HIV in Manitobaen_US
dc.typemaster thesisen_US
local.subject.manitobayesen_US
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