Expanding opportunities in health data: Enhancing research by facilitating linkage of Ontario’s population-level health administrative data with data from patient support programs (PSPs)

ObjectivesPatient Support Programs (PSPs) provide real-world evidence on short-term outcomes and drug adherence for specialty care. These data are collected directly from patients by pharmaceutical companies. Data linkage is facilitated by a publicly-funded health research institute which houses population-based, individual-level health administrative data for 14 million Ontario residents in Canada since 1992. Linkage provides a more comprehensive and transparent view of patients’ pathways and care. ApproachIndustry-funded research conducted through the data & analytic service must align with the institute’s mission, vision and values, and demonstrate a clear public benefit. For transparency, and to support broader public benefit and research access, final deliverables and analytic plans are posted on the institute’s website. Privacy impact assessments are conducted to ensure ethics approvals, consent and data sharing agreements are established, prior to data importation. To safeguard privacy, designated data covenantors encrypt and link the PSP data with in-house data holdings. Analyses are performed by senior analytic staff, providing researchers with summary-level reports. ResultsSince 2016, the institute has worked with organizations to link data for research, including PSP data on thousands of patients, enabling crucial insight into treatment patterns, drug adherence, costs and long-term outcomes. ConclusionLinkage of privately-owned PSP data with administrative health data at the institute, provides opportunities to identify gaps in care and improve quality of research. Data challenges around bias, transparency, completeness, and comprehensiveness are minimized. ImplicationsResults provide decision-makers and healthcare professionals with a trusted and comprehensive understanding of patient care pathways to improve health outcomes.

Authors

Publication Details

Journal
International Journal for Population Data Science
Published
2024-09-10
DOI
https://doi.org/10.23889/ijpds.v9i5.2814
Primary Topic
Primary Care and Health Outcomes
Type
article
Field-Weighted Citation Impact
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article

Expanding opportunities in health data: Enhancing research by facilitating linkage of Ontario’s population-level health administrative data with data from patient support programs (PSPs)

Jacob Etches, Lisa Ishiguro, Luke Mondor, Keresa Arnold et al.
International Journal for Population Data Science
Primary Care and Health Outcomes
article

Expanding opportunities in health data: Enhancing research by facilitating linkage of Ontario’s population-level health administrative data with data from patient support programs (PSPs)

Jacob Etches, Lisa Ishiguro, Luke Mondor, Keresa Arnold, Minnie Ho, Dina Skvirisky, Jeruby Retnakanthan, Saskin Saskin, Charles Victor
article en

Abstract

ObjectivesPatient Support Programs (PSPs) provide real-world evidence on short-term outcomes and drug adherence for specialty care. These data are collected directly from patients by pharmaceutical companies. Data linkage is facilitated by a publicly-funded health research institute which houses population-based, individual-level health administrative data for 14 million Ontario residents in Canada since 1992. Linkage provides a more comprehensive and transparent view of patients’ pathways and care. ApproachIndustry-funded research conducted through the data & analytic service must align with the institute’s mission, vision and values, and demonstrate a clear public benefit. For transparency, and to support broader public benefit and research access, final deliverables and analytic plans are posted on the institute’s website. Privacy impact assessments are conducted to ensure ethics approvals, consent and data sharing agreements are established, prior to data importation. To safeguard privacy, designated data covenantors encrypt and link the PSP data with in-house data holdings. Analyses are performed by senior analytic staff, providing researchers with summary-level reports. ResultsSince 2016, the institute has worked with organizations to link data for research, including PSP data on thousands of patients, enabling crucial insight into treatment patterns, drug adherence, costs and long-term outcomes. ConclusionLinkage of privately-owned PSP data with administrative health data at the institute, provides opportunities to identify gaps in care and improve quality of research. Data challenges around bias, transparency, completeness, and comprehensiveness are minimized. ImplicationsResults provide decision-makers and healthcare professionals with a trusted and comprehensive understanding of patient care pathways to improve health outcomes.

International Journal for Population Data ScienceVol. 9(5)
Openalex Percentile: Top 74%
Primary Care and Health Outcomes
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