4.6 Article

Qualitative evaluation of a mandatory health insurance 'wait period' in a publicly funded health system: understanding health inequities for newcomer im/migrant women

Journal

BMJ OPEN
Volume 11, Issue 8, Pages -

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/bmjopen-2020-047597

Keywords

qualitative research; reproductive medicine; public health; health policy

Funding

  1. Canadian Institutes of Health Research (CIHR) [PJT 165834]
  2. Vancouver Foundation [FOI19-2552]
  3. Michael Smith Foundation for Health Research
  4. Simon Fraser University [M003130]
  5. BC SUPPORT Unit (Fraser Centre) Graduate Student Fellowship
  6. Frederick Banting and Charles Best Canada Graduate Scholarship-Master's (CGS M)
  7. CIHR New Investigator Award
  8. U.S. National Institutes of Health

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The study evaluated the impact of a residency-based waiting period for health insurance coverage on im/migrant women's health and settlement experiences in British Columbia, Canada. The findings showed that the waiting period resulted in mistrust, internalized stigma, administrative burden, delays in care, and difficult choices between survival and healthcare. Community organizations provided support but could not address all gaps created by the policy.
Objectives To evaluate impacts of a residency-based waiting period for health insurance coverage on lived experiences of health and settlement for im/migrant women in British Columbia, Canada. Design The IRIS study is a mixed-methods, community-based, qualitative evaluation of recently arrived im/migrant women's access to sexual and reproductive care. In-depth, semistructured interviews were conducted by trained multilingual and multicultural interviewers with lived migration experience in the participant's preferred language. Setting Metro Vancouver, British Columbia, Canada from July 2018 to January 2020. Participants Data collected from community focus groups (four groups, n=29) of both service providers and im/migrant women was used. Following this, qualitative interviews with service providers (n=10) and im/migrant women (n=47) were conducted. Eligible participants self-identified as women; were aged 18-49 and had arrived in Canada from another country. Eligible providers were employed in the health, social or legal sectors working with im/migrant women. Results The wait period resulted in mistrust and internalised stigma for racialised im/migrant women, for whom the policy resulted in feeling 'undeserving' of care. Resulting administrative burden produced delays and unmet need for care, particularly related to sexual and reproductive healthcare and children's health. Unexpected costs meant difficult choices between survival and care. Negative health outcomes included the inability to family plan, difficulties during pregnancy, as well as hardships related not being able to seek help for sick children. Community-based organisations provided support in many areas but could not fill all gaps produced by this policy. Conclusions Findings highlight severe, yet commonly overlooked, health inequities produced by a mandatory health coverage wait period within a purportedly 'universal' healthcare system. Health system policies such as mandatory 'waiting periods' produce discriminatory and inequitable outcomes for im/migrant women. Policy reforms towards full 'healthcare for all' are urgently needed to affirm the health and human rights of all im/migrants.

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