Literature DB >> 26112164

One little, too little: Counting Canada's indigenous people for improved health reporting.

Brenda Elias1, Karen Busby2, Pat Martens3.   

Abstract

The way state governments, worldwide, count or do not count Indigenous peoples has contributed to inconsistent reporting of Indigenous health statistics. To address unreliable reporting in Canada, we reviewed laws on Indian status and the development of a national Indian Registration System (IRS) to track Indian status and eligibility. With this information as a guide, we linked the IRS to the Manitoba provincial health registry systems and were able to identify individuals with Indian status for health reporting. To improve reporting, we identified individuals often missed in this type of linkage. For instance, we identified children and adult children who were eligible for Indian status but not yet registered. Equally as important, we identified individuals not eligible for Indian status but have Indian heritage and/or represent potential individual Indian status eligibility cases before the courts to right a historic form of identity sex discrimination that has made them invisible in Canadian society and health reporting. A familial kinship approach was used to identify Indian children and adult children typically missed when a strict legal entitlement criteria is used for data linkage. Our reflective socio-legal data linkage approach expanded the number of Indian peoples for health reporting purposes and demonstrated a feasible, inclusive way to report on the health of Indians in Canada.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Canada; Data linkage; Health administrative databases; Indian status; Indigenous; Indigenous rights

Mesh:

Year:  2015        PMID: 26112164     DOI: 10.1016/j.socscimed.2015.06.014

Source DB:  PubMed          Journal:  Soc Sci Med        ISSN: 0277-9536            Impact factor:   4.634


  6 in total

1.  Cancer incidence, mortality, and stage at diagnosis in First Nations living in Manitoba.

Authors:  K M Decker; E V Kliewer; A A Demers; K Fradette; N Biswanger; G Musto; B Elias; D Turner
Journal:  Curr Oncol       Date:  2016-08-12       Impact factor: 3.677

2.  Prevalence and Incidence of Rheumatoid Arthritis in Canadian First Nations and Non-First Nations People: A Population-Based Study.

Authors:  Carol A Hitchon; Sazzadul Khan; Brenda Elias; Lisa M Lix; Christine A Peschken
Journal:  J Clin Rheumatol       Date:  2020-08       Impact factor: 3.902

3.  Examining the Impact of First Nations Status on the Relationship Between Diabetes and Cancer.

Authors:  Kathleen M Decker; Pascal Lambert; Alain Demers; Erich V Kliewer; Grace Musto; Natalie Biswanger; Brenda Elias; Donna Turner
Journal:  Health Equity       Date:  2020-05-18

4.  Creating a Canadian Indigenous Research Network Against Cancer to Address Indigenous Cancer Disparities.

Authors:  Angeline Letendre; Gail Garvey; Alexandra King; Malcolm King; Reg Crowshoe; Lea Bill; Nadine R Caron; Brenda Elias
Journal:  JCO Glob Oncol       Date:  2020-02

Review 5.  Wellbeing of Indigenous Peoples in Canada, Aotearoa (New Zealand) and the United States: A Systematic Review.

Authors:  Alana Gall; Kate Anderson; Kirsten Howard; Abbey Diaz; Alexandra King; Esther Willing; Michele Connolly; Daniel Lindsay; Gail Garvey
Journal:  Int J Environ Res Public Health       Date:  2021-05-28       Impact factor: 3.390

6.  Defining a study population using enhanced reporting of Aboriginality and the effects on study outcomes.

Authors:  C McInerney; I Ibiebele; S Torvaldsen; J B Ford; J M Morris; M Nelson; D Randall
Journal:  Int J Popul Data Sci       Date:  2020-03-20
  6 in total

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