Unlocking First Nations health information through data linkage

Introduction The importance of Indigenous data sovereignty and Indigenous-led research processes is increasingly being recognized in Canada and internationally. For First Nations in Ontario, Canada, access to routinely-collected demographic and health systems data is critical to planning and meas...

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Main Authors: Jennifer Walker, Evelyn Pyper, Carmen R Jones, Saba Khan, Nelson Chong, Dan Legge, Michael J Schull, David Henry
Format: Article
Language:English
Published: Swansea University 2018-05-01
Series:International Journal of Population Data Science
Online Access:https://ijpds.org/article/view/450
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spelling doaj-47f5489befe941b5bd9ec165f74dbfee2020-11-24T23:32:11ZengSwansea UniversityInternational Journal of Population Data Science2399-49082018-05-013110.23889/ijpds.v3i1.450450Unlocking First Nations health information through data linkageJennifer WalkerEvelyn PyperCarmen R JonesSaba KhanNelson ChongDan LeggeMichael J SchullDavid HenryIntroduction The importance of Indigenous data sovereignty and Indigenous-led research processes is increasingly being recognized in Canada and internationally. For First Nations in Ontario, Canada, access to routinely-collected demographic and health systems data is critical to planning and measuring health status and outcomes in their populations. Linkage of this data with the Indian Register (IR), under First Nations data governance, has unlocked data for use by First Nations organizations and communities. Objectives To describe the linkage of the IR database to the Ontario Registered Persons Database (RPDB) within the context of Indigenous data sovereignty principles.  Methods Deterministic and probabilistic record linkage methods were used to link the IR to the RPDB. There is no established population of First Nations people living in Ontario with which we could establish a linkage rate. Accordingly, several approaches were taken to determine a denominator that would represent the total population of First Nations we would hope to link to the RPDB.  Results Overall, 201,678 individuals in the national IR database matched to Ontario health records by way of the RPDB, of which 98,562 were female and 103,116 were male. Of those First Nations individuals linked to the RPDB, 90.2% (n=181,915) lived in Ontario when they first registered with IR, or were affiliated with an Ontario First Nation Community. The proportion of registered First Nations people linking to the RPDB improved across time, from 62.8% in the 1960s to 94.5% in 2012. Conclusions This linkage of the IR and RPDB has resulted in the creation of the largest First Nations health research study cohort in Canada. The linked data are being used by First Nations communities to answer questions that ultimately promote wellbeing, effective policy, and healing.https://ijpds.org/article/view/450
collection DOAJ
language English
format Article
sources DOAJ
author Jennifer Walker
Evelyn Pyper
Carmen R Jones
Saba Khan
Nelson Chong
Dan Legge
Michael J Schull
David Henry
spellingShingle Jennifer Walker
Evelyn Pyper
Carmen R Jones
Saba Khan
Nelson Chong
Dan Legge
Michael J Schull
David Henry
Unlocking First Nations health information through data linkage
International Journal of Population Data Science
author_facet Jennifer Walker
Evelyn Pyper
Carmen R Jones
Saba Khan
Nelson Chong
Dan Legge
Michael J Schull
David Henry
author_sort Jennifer Walker
title Unlocking First Nations health information through data linkage
title_short Unlocking First Nations health information through data linkage
title_full Unlocking First Nations health information through data linkage
title_fullStr Unlocking First Nations health information through data linkage
title_full_unstemmed Unlocking First Nations health information through data linkage
title_sort unlocking first nations health information through data linkage
publisher Swansea University
series International Journal of Population Data Science
issn 2399-4908
publishDate 2018-05-01
description Introduction The importance of Indigenous data sovereignty and Indigenous-led research processes is increasingly being recognized in Canada and internationally. For First Nations in Ontario, Canada, access to routinely-collected demographic and health systems data is critical to planning and measuring health status and outcomes in their populations. Linkage of this data with the Indian Register (IR), under First Nations data governance, has unlocked data for use by First Nations organizations and communities. Objectives To describe the linkage of the IR database to the Ontario Registered Persons Database (RPDB) within the context of Indigenous data sovereignty principles.  Methods Deterministic and probabilistic record linkage methods were used to link the IR to the RPDB. There is no established population of First Nations people living in Ontario with which we could establish a linkage rate. Accordingly, several approaches were taken to determine a denominator that would represent the total population of First Nations we would hope to link to the RPDB.  Results Overall, 201,678 individuals in the national IR database matched to Ontario health records by way of the RPDB, of which 98,562 were female and 103,116 were male. Of those First Nations individuals linked to the RPDB, 90.2% (n=181,915) lived in Ontario when they first registered with IR, or were affiliated with an Ontario First Nation Community. The proportion of registered First Nations people linking to the RPDB improved across time, from 62.8% in the 1960s to 94.5% in 2012. Conclusions This linkage of the IR and RPDB has resulted in the creation of the largest First Nations health research study cohort in Canada. The linked data are being used by First Nations communities to answer questions that ultimately promote wellbeing, effective policy, and healing.
url https://ijpds.org/article/view/450
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