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Digital Health Compass: Empowering Citizens to Navigate their Health Journey

This panel discussion explores the need for a digital health compass to help citizens, patients, and caregivers navigate the complexities of healthcare. The discussion will cover topics such as co-production, standards, digital health literacy, and the importance of involving patients in decision-making. The panelists will share their insights on how to create a personal digital health compass and the role of different stakeholders in achieving this vision.

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Digital Health Compass: Empowering Citizens to Navigate their Health Journey

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  1. In Search of a Digital Health Compass My Data, My Decision, Our ePower

  2. Moderator: John Rayner Tell me and I forget, Show me and I may remember, Involve me and I’ll understand • Panelist’s introduction • How to co-produce – converge • Standards • Digital Health Literacy • Q&A – interaction with you all

  3. Knowledge is power. • Extensive investments in digital health technology – however low adoption of eHealthservicesand persistent health disparities call for multidisciplinary action. • Navigating for health online is challenging, and understanding culture, education, skills, costs, perceptions of power and role is essential. • Citizens engaged in self-care, patients coping with persistent, chronic disease or living with an implanted device, or informal carers helping an elderly relative, a child or neighbor with illness or declining health, need a digital health compass.

  4. Panelists Anne Moen Catherine Chronaki Ed Hammond Petra Wilson Christian Lovis Robert Stegwee

  5. Objectives • How do we like to engage with health issues ? • Citizens – patients, caregivers and providers • Convergence to create a personal digital health compass ? • Contributions – joint efforts by health care, informatics, policy, standards, and industry • Broad scope of Informatics in service for health

  6. Vision – a digital health compass • Increasingly complex health care environment • Person centered practices and partnerships • Self care between care episodes • Coordination of care • Knowledge representation and data sharing .

  7. Today’s situation Citizens, patients and caregivers do not use digital health services to meet their health and wellness needs for several (good) reasons Few models for partnerships and information sharing between citizens – professionals Little integration and interoperability of health data for collaboration purposes

  8. Co-creation  tomorrow’s care Health care Requirements & Experiences Digital literacy, eSkills Health & Digital Health Literacy Personal characteristics health & wellness

  9. Candidate dimensions Expert Empower Engage Equity Evaluate Enable Evolve Educate

  10. Moving forward • Information back to citizen • resources that make sense – relevant data • Engage – convenient – balance – targets • What really matters – • Human relationships – empathy – the people • Complex information environment • Data driven collaboration – selfcarebetween care

  11. Joint actions – Convergence Citizen – patient perspective Provided resources and citizen demand Standards Industry

  12. Why the Patient Needs a New Compass Scarcity - resources, HCPs, time Complexity - comorbidity, medication, environment Personalisation - retail, leisure, education Mobility - work, communication, money

  13. What the compass should provide to the Patient • Engage me in my own health and care • Access to relevant, timely and understandable information. Empower me to make decision & inform others - Ability to share information and interact on information

  14. What are the building blocks ? • Data • Add • Access • Share • Control • Trust • partners • System • Redress • Access • Reimbursement • Security • mobility • Standards • Interoperability • Integration

  15. Are we nearly there yet???? • Standards …. Good progress • Interoperability …… in some contexts • Integration ……. Limited • We are missing too many opportunities to engage and empower the patient!

  16. Personal Digital Health Robert A. Stegwee, PhD, FHL7

  17. Personal Health Records and the capabilities they provide to citizens • A personal health record is more than a viewer and organizer of personal health information • It provides treatment support, including self management options • It facilitates the exchange of health information with health care providers • It supports healthy lifestyle options and the tracking of personal fitness

  18. Adoption of Personal Health Records is very limited • Survey among invited experts in 25 countries across 6 continents • No individual PHR systems are reported that currently reach a million users or more • Many PHR systems are still in a pilot phase with user numbers in the 100s or 1000s

  19. Different strategies are being implemented, with no clear differentiation in success • Having a strategy leads to more scale and more exchange of health information between citizen and other stakeholders in the health system • Government led initiatives have the best track record in realizing exchange, often realized within a government led health system • Apparently the consumer market lifestyle focus of tech companies is not perceived as a contribution to the PHR initiatives in different countries

  20. Leadership and commitment of providers are key to success of Personal Health Records • Top three barriers to success of Personal Health Records adoption mentioned: Legislation and Citizen interest are not identified as key barriers

  21. A vision on the role of personal health information for future delivery of health care • Personal experience is key in understanding • The perceived impact on a person’s life • The progression of a disease for an individual patient • The outcome of different treatment options • In relation to individual lifestyle choices • Tools for capturing, analysing, and relating all this data are becoming available – with the person at the centre! Experience experts are those people who are suffering from cognitive impairments and who are willing to share with us the effects of the disease on their lives. They are the ones who can tell us the real story behind the effects of this disease and its diagnosis, from their own perspective. www.cottonwoolinmyhead.org

  22. Catherine Chronaki, MS, will speak on initiatives for patient engagement, where myHealthData,quantified self measures and Participatory Medicine, are included to deliver tailored, adaptive and actionable health experience for individuals, families and communities. PLEASE ADD approx 8 slides

  23. Digital health literacy Power of knowledge to use my data Engage in health – data care between care Co-producers

  24. Prof. Ed Hammond, MD, PhD, FACMI, FHIMSS, will speak on new initiatives in standards, seeking to liberate data for population health and precision medicine in the learning health system. He will be using HL7 FHIR (Fast Healthcare Interoperability Resources and standards) as an example of recent development. PLEASE ADD approx 8 slides

  25. FHIR is FREE!!! F – Fast (to design & to implement) H – Healthcare I – Interoperable R – Resources (Building blocks)

  26. What is FHIR? • Based on a set of modular components called “Resources” • Resources refer to each other using URLs • Small discrete units of exchange with defined behaviour and meaning • Have known identity and behaviour • Extensions permit adding data not part of core • Resources are combined into “Profiles” to solve clinical and administrative problems in a practical way. • Parties exchanging data define the specific way they want to use resources and their relations using Profiles. • Profiles are the framework for defining services. • Exchange resources between systems • Using a RESTful API (e.g. web approach) • As a Bundle of resources (messages, documents) • Positives • Service driven • Modify components with changing need • Portability of components by moving program code with the data

  27. Prof. Christian Lovis, MD, MPH, will address means for the industry to engage with health professionals and policy makers to contribute to research strategies that alleviate disparities with digital health literacy. PLEASE ADD approx 8 slides

  28. Extra

  29. Holistic approach • Citizens • Community • Health policy • Research • Industry • Peer learning • Co-design • Personal circumstances • Health events

  30. Digital Health Literacy Expert Empower Engage Equity Enable Educate Evolve Evaluate Standards

  31. My Data – My Decision Our ePower Enable Educate Evaluate Evolve Engage Expert Empower Equity

  32. Expert Empower Engage Health & Digital Health Literacy Digital literacy, eSkills Equity Enable Personal characteristics health & wellness Health Experience Educate Evolve Evaluate

  33. OLD Expert Empower Engage Health & Digital Health Literacy Digital literacy, eSkills Equity Enable Personal characteristics health & wellness Health Experience Equip/Educate Evolve Evaluate

  34. Expert Empower Engage Health & Digital Health Literacy Digital literacy, eSkills Digital Health Compass Enable Equity Personal characteristics health & wellness Health Experience Educate Evolve Evaluate

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