Implementing a streamlined data access governance process for the release of routinely collected electronic health record data for research

ObjectivesIn Australia, there are no standardised processes for the release of Electronic Health Record (EHR) data for research. We describe our streamlined ethics and data access governance framework for the release of EHR data for research. ApproachIn consultation with our academic and health service partner organisations and with reference to national and international standards, we developed a process to safely and efficiently release EHR data for research. The Five Safes Framework guided our processes ensuring: safe people; safe projects; safe settings; safe data; and safe outputs. Piloting of processes has commenced. ResultsStreamlined data access and release processes acceptable to all stakeholders were implemented using an online system. Independent researcher and consumer review of an Expression of Interest, followed by ethics review/approval from the health service research office ensures projects are methodologically and ethically sound. Completion of a detailed technical assessment form, implementation of a signed data use agreement and release of de-identified data to a secure e-research environment promotes safe data and settings. Constraints around publication are enforced via pre-publication review ensuring safe outputs. Nine projects are in process using our system with an average of 4 days for EOI review and 6 days for TAF review. ConclusionWe have established a streamlined data access pathway to minimise duplication of effort and allow timely and secure access to EHR research data. We have built in efficiencies and promoted a cultural shift for clinicians who have previously not had data access processes governed in this way.

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Publication Details

Journal
International Journal for Population Data Science
Published
2024-09-10
DOI
https://doi.org/10.23889/ijpds.v9i5.2809
Primary Topic
Ethics in Clinical Research
Type
article
Field-Weighted Citation Impact
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article

Implementing a streamlined data access governance process for the release of routinely collected electronic health record data for research

Emily Belle Parker, Nadine E. Andrew, Tanya Ravipati, Richard Beare et al.
International Journal for Population Data Science
Ethics in Clinical Research
article

Implementing a streamlined data access governance process for the release of routinely collected electronic health record data for research

Emily Belle Parker, Nadine E. Andrew, Tanya Ravipati, Richard Beare, Velandai Srikanth, Naude Kim, Lee-Anne Clavarino
article en

Abstract

ObjectivesIn Australia, there are no standardised processes for the release of Electronic Health Record (EHR) data for research. We describe our streamlined ethics and data access governance framework for the release of EHR data for research. ApproachIn consultation with our academic and health service partner organisations and with reference to national and international standards, we developed a process to safely and efficiently release EHR data for research. The Five Safes Framework guided our processes ensuring: safe people; safe projects; safe settings; safe data; and safe outputs. Piloting of processes has commenced. ResultsStreamlined data access and release processes acceptable to all stakeholders were implemented using an online system. Independent researcher and consumer review of an Expression of Interest, followed by ethics review/approval from the health service research office ensures projects are methodologically and ethically sound. Completion of a detailed technical assessment form, implementation of a signed data use agreement and release of de-identified data to a secure e-research environment promotes safe data and settings. Constraints around publication are enforced via pre-publication review ensuring safe outputs. Nine projects are in process using our system with an average of 4 days for EOI review and 6 days for TAF review. ConclusionWe have established a streamlined data access pathway to minimise duplication of effort and allow timely and secure access to EHR research data. We have built in efficiencies and promoted a cultural shift for clinicians who have previously not had data access processes governed in this way.

International Journal for Population Data ScienceVol. 9(5)
Peninsula Research (US), Peninsula Health (AU)
Openalex Percentile: Top 77%
Ethics in Clinical Research
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