Sensitive data federation analysis model in population health
Reusing Real World Observations (RWO) and health data for research, health innovation and policy is key to better health in general, pandemic preparedness and imminent cost savings. However, the generally accepted notion that ‘citizens should be in control of the reuse of their personal data’ remains a paper mantra unless we design and implement a user friendly, trusted and sustainable environment that allows the realisation of that ambition. Performing GDPR compliant research will be entirely dependent on solving the trusted data federation challenge.
We seek projects and initiatives working on population health data, clinical data, and genetic data to participate in this Case Study. Sign-up here.
Significance of the Case Study
This Case Study will explore how innovative technology can change the current methods in care and improve the crucial influence of healthy citizens and patients in an advanced globally interoperable health data system. The resulting technology will be relevant for future initiatives that need to reuse sensitive data of individuals. The current limited or non-existent level of reuse of critical data on infection, viral spread and post-vaccination as well as long term effects related to COVID-19 will severely hamper preparedness for future SARS-CoV-2 related problems, including the emergence of new variants. Reuse of sensitive RWO is of much wider use than just for COVID-19. Hence this Case Study aims to greatly contribute to the generic abilities of the global society to tackle future health issues.
Research challenges and requirements for GOSC
Better use of data and evidence based personalised medicine could potentially save society hundreds of billions of Euros each year. Successful and reusable components of a system enabling this societal health benefit and cost saving can be reused. Many public organisations and private companies have indicated keen interest in a GDPR compliant access to a real world, citizen and patient controlled system that can help them to learn from the data. The Case Study will adhere to joint principles of open protocols and standards, around which multiple vendor solutions can be operational to create a distributed, safe and scalable environment. Reuse can be for any purpose for which consent of the citizen is pre-recorded in the system, and can range from improved care outcome studies, to outbreak management, to vaccine follow up to drug rationalisation and virtual clinical trials or post marketing surveillance by the pharmaceutical industry.
Engagement with the GOSC Initiative
Controlled and globally distributed access to sensitive data is a very important issue for social and health sciences, particularly when topics with global dimensions. The Case Study will seek to demonstrate how to make better steps to make available those parts of the data which can be made shared. Commonly agreed FAIR implementation profiles will be created and FAIR data points established in various ‘GOSC’ regions. The feasibility for distributed analytics over datasets held in various regions will then be explored and demonstrated. Community accepted standards will be used throughout and only if needed new choices and challenges in terms of standards and technology will be addressed.
- A FAIR-based system with optimal scaling potential and no vendor lock in, entirely based on FAIR Digital Objects.
- Fully distributed and GDPR compliant analytics and learning with full respect for and actual involvement of the citizen.
- FAIR Data Points in a number of locations, with synthetic (and if possible real world data) to demonstrate cross-regional-OSC re-use of sensitive data for analytical purposes.
Initial Contacts and Participants/Invitees
Simon Hodson, CODATA
Hana Pergl, CODATA
Barend Mons, CODATA, GO FAIR and LUMC
Erik Schultes, GO FAIR
LIU Lei, University of Fudan
Additional participants are invited: sign-up here, if interested to join the Case Study.