Introduction to panel where Standards Developing Organization and National Competence Centers discuss the scope of the European SDO platform reflecting on earlier presentations.
3. Moderator
• Michiel Sprenger
• Strategy adviser @Nictiz, the National
Competence Center of the Netherlands (NCC-
NL)
• Teacher in Clinical Informatics at Eindhoven
Technical University
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4. Remember the stakeholders
• Citizens (sometimes patients)
• Health professionals
• Health system
• Market
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5. Remember the layered model for interoperability
ReEIF
Policy
IT Infrastructure
Care Process Health professionals
Board members, C-level mgmt
Applications Procurers, software suppliers
ICT development and management
Legal and regulatory Regulatory bodies
Information Health professionals, Informaticians
Actors
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6. Scene of collaboration
• Three geographic layers
– Global
– Europe (main focus of today)
– National
• Partners (for this discussion)
– SDOs and Profiling Organisations:
• Develop base standards on international scale
• Assist localisation on national level
– National Competence Centres (NCCs)
• Localise standards
• Combine standards to new national specifications and/or
standards
– Policy:
• Member states (MoH)
• eHealth Network (eHN, JAseHN)
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7. Panellists
• Christof Gessner, NCC-DE, HL7-DE and
European HL7-SAB
• Pim Volkert, NCC-NL, SNOMED-NL
• Manne Andersson, NCC-SE and JAseHN
• Karima Bourquard, IHE-EU
• Catherine Chronaki, HL7-EU
• Robert Stegwee, CEN-TC251 EU
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8. Panel discussion
• Panellists: introduce yourself
• Answer the following questions:
• What is, or are, your main collaboration issues
• How should we pick them up
• What should be the result
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9. Related questions:
• Do we really need European standards?
• How to liaise with industry ?
• How to liaise with stakeholders like citizens
and professionals
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10. Eleven Draft Recommendations (Part 1: on Standards)
1. Make it easier to refer to specific standards and
specifications in eHealth (public) procurement –
establish a standards sets repository
2. Develop free and open tools-based access to
standards for implementation and deployment
3. Increase the visibility of clinical best practices in
terms of professional guidelines linked to generic
workflows and information sets
4. Detail a clear governance and maintenance process
for each set of standards related to an identified
combination of use cases
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11. Eleven Draft Recommendations (Part 2: on Data)
5. Support the flow of health data between record
systems and (mobile) devices (break down the silos)
6. Make it safe and easy to migrate to the cloud for
health and healthcare data to become interoperable
7. Provide guidance on the interpretation of the medical
device directive in case of personal use of eHealth
and mHealth services (Active Assisted Living)
8. Consider broadening the scope of the European
Health Terminology Services (being developed under
CEF) to include the full range of health data, including
patient generated, sensor and medical device data
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12. Eleven Draft Recommendations (Part 3: on Usage)
9. Clinical model content should be shared
internationally, irrespective of the particular paradigm
used in its creation, and the incorporation of such
content in clinical applications should be encouraged
10. Localisation of standards sets should be supported
and guided to prevent local adaptation of the
underlying standards that “break” cross-border or
cross-realm interoperability
11. Establish an eHealth Standards Observatory, for the
purpose of monitoring
– the use of standards sets related to use cases
– the use of terminologies in data capture and data exchange
– the adoption of cross-border guidelines
(including patient summary)
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