Linked data and inclusion health: Harmonised international data linkage to identify determinants of health inequalities

A recent article in The Lancet establishing the principles of inclusion health, highlighted substantial gaps in our understanding of the drivers of health inequalities in socially excluded groups such as people with a history of incarceration, people who experience homelessness, sex workers, people...

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Main Authors: Jesse Young, Rohan Borschmann, Ximena Camacho, Josh Knight, Fiona Kouyoumdjian, Naveed Janjua, June Atkinson, Stuart Kinner
Format: Article
Language:English
Published: Swansea University 2018-08-01
Series:International Journal of Population Data Science
Online Access:https://ijpds.org/article/view/597
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spelling doaj-ec10ea70e48445cd981e305f2c7edb702020-11-25T02:49:38ZengSwansea UniversityInternational Journal of Population Data Science2399-49082018-08-013410.23889/ijpds.v3i4.597Linked data and inclusion health: Harmonised international data linkage to identify determinants of health inequalitiesJesse Young0Rohan Borschmann1Ximena Camacho2Josh Knight3Fiona Kouyoumdjian4Naveed Janjua5June Atkinson6Stuart Kinner7The University of MelbourneMurdoch Children's Research InstituteThe University of MelbourneThe University of MelbourneMcMaster UniversityBritish Columbia Centre for Disease ControlUniversity of OtagoMurdoch Children's Research Institute A recent article in The Lancet establishing the principles of inclusion health, highlighted substantial gaps in our understanding of the drivers of health inequalities in socially excluded groups such as people with a history of incarceration, people who experience homelessness, sex workers, people with mental illness, and people who inject drugs1. Cross-sectoral data linkage of electronic health records with services working with socially excluded groups was one of the key recommendations of this article. The magnitude of health disparities observed in people that experience social exclusion necessitates an international public health response and addressing the determinants of social exclusion has been identified as a key component of closing the gap of Indigenous disadvantage2. This symposium will establish data linkage as a key component of the inclusion health and will complement the efforts of the Pan American Health Oranization's (PAHO) Commission on Equity and Health Inequalities in the Americas. Traditional survey methodology is costly and often results in studies that are highly parochial in nature. Due to difficulties recruiting and retaining marginalized groups, these studies are commonly forced to adopt methodological concessions, often selecting the most convenient participants (i.e., selection bias) or incurring increased rates of loss-to-follow-up (i.e., attrition bias). Conversely, global studies aimed at modelling the burden of disease are often not sufficiently nuanced to answer specific inferential research questions. Data-linkage has the potential to overcome these common biases and limitations. Thus, harmonised international data-linkage studies are an important component of the inclusion health response to identify the determinants of health inequalities in socially excluded groups and inform the global inclusion health agenda. This symposium will bring together facilitators from three countries with extensive experience conducting data linkage studies that generate evidence on health and social inequality in socially excluded groups. Using a current multinational study as an example, barriers to international data-linkage studies, methodological solutions, and distributed approaches to generating international comparative evidence will be presented. Innovative examples of cross-sectoral approaches to linkage with social service, correctional and national survey data will be discussed. The development of a novel framework for identifying social exclusion exposures and determinants of health inequalities typically not captured in administrative health data will also be discussed. The session will conclude with a discussion aimed at forming the foundation of an international data linkage project to address these current gaps identified in the inclusion health series and best practice for translation to policy and practice to address health disparities in socially excluded groups. References • Aldridge et al. Morbidity and mortality in homeless individuals, prisoners, sex workers, and individuals with substance use disorders in high-income countries: a systematic review and meta-analysis. The Lancet. 2017;391(10117):241-250. https://doi.org/10.1016/S0140-6736(17)31869-X • Greenwood M et al. Challenges in health equity for Indigenous peoples in Canada. The Lancet. 2018;Epub ahead of print. https://doi.org/10.1016/S0140-6736(18)30177-6 https://ijpds.org/article/view/597
collection DOAJ
language English
format Article
sources DOAJ
author Jesse Young
Rohan Borschmann
Ximena Camacho
Josh Knight
Fiona Kouyoumdjian
Naveed Janjua
June Atkinson
Stuart Kinner
spellingShingle Jesse Young
Rohan Borschmann
Ximena Camacho
Josh Knight
Fiona Kouyoumdjian
Naveed Janjua
June Atkinson
Stuart Kinner
Linked data and inclusion health: Harmonised international data linkage to identify determinants of health inequalities
International Journal of Population Data Science
author_facet Jesse Young
Rohan Borschmann
Ximena Camacho
Josh Knight
Fiona Kouyoumdjian
Naveed Janjua
June Atkinson
Stuart Kinner
author_sort Jesse Young
title Linked data and inclusion health: Harmonised international data linkage to identify determinants of health inequalities
title_short Linked data and inclusion health: Harmonised international data linkage to identify determinants of health inequalities
title_full Linked data and inclusion health: Harmonised international data linkage to identify determinants of health inequalities
title_fullStr Linked data and inclusion health: Harmonised international data linkage to identify determinants of health inequalities
title_full_unstemmed Linked data and inclusion health: Harmonised international data linkage to identify determinants of health inequalities
title_sort linked data and inclusion health: harmonised international data linkage to identify determinants of health inequalities
publisher Swansea University
series International Journal of Population Data Science
issn 2399-4908
publishDate 2018-08-01
description A recent article in The Lancet establishing the principles of inclusion health, highlighted substantial gaps in our understanding of the drivers of health inequalities in socially excluded groups such as people with a history of incarceration, people who experience homelessness, sex workers, people with mental illness, and people who inject drugs1. Cross-sectoral data linkage of electronic health records with services working with socially excluded groups was one of the key recommendations of this article. The magnitude of health disparities observed in people that experience social exclusion necessitates an international public health response and addressing the determinants of social exclusion has been identified as a key component of closing the gap of Indigenous disadvantage2. This symposium will establish data linkage as a key component of the inclusion health and will complement the efforts of the Pan American Health Oranization's (PAHO) Commission on Equity and Health Inequalities in the Americas. Traditional survey methodology is costly and often results in studies that are highly parochial in nature. Due to difficulties recruiting and retaining marginalized groups, these studies are commonly forced to adopt methodological concessions, often selecting the most convenient participants (i.e., selection bias) or incurring increased rates of loss-to-follow-up (i.e., attrition bias). Conversely, global studies aimed at modelling the burden of disease are often not sufficiently nuanced to answer specific inferential research questions. Data-linkage has the potential to overcome these common biases and limitations. Thus, harmonised international data-linkage studies are an important component of the inclusion health response to identify the determinants of health inequalities in socially excluded groups and inform the global inclusion health agenda. This symposium will bring together facilitators from three countries with extensive experience conducting data linkage studies that generate evidence on health and social inequality in socially excluded groups. Using a current multinational study as an example, barriers to international data-linkage studies, methodological solutions, and distributed approaches to generating international comparative evidence will be presented. Innovative examples of cross-sectoral approaches to linkage with social service, correctional and national survey data will be discussed. The development of a novel framework for identifying social exclusion exposures and determinants of health inequalities typically not captured in administrative health data will also be discussed. The session will conclude with a discussion aimed at forming the foundation of an international data linkage project to address these current gaps identified in the inclusion health series and best practice for translation to policy and practice to address health disparities in socially excluded groups. References • Aldridge et al. Morbidity and mortality in homeless individuals, prisoners, sex workers, and individuals with substance use disorders in high-income countries: a systematic review and meta-analysis. The Lancet. 2017;391(10117):241-250. https://doi.org/10.1016/S0140-6736(17)31869-X • Greenwood M et al. Challenges in health equity for Indigenous peoples in Canada. The Lancet. 2018;Epub ahead of print. https://doi.org/10.1016/S0140-6736(18)30177-6
url https://ijpds.org/article/view/597
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