Area in the Finnish strategy document | Relation to scope in the Nordic e-health policies |
Digital health and social services centre and customer and service counselling | Relates to Shifting towards prevention and digital first |
From digitalisation of information to digital operating models | Relates to Supporting health operations |
Giving customers access to their own data | Relates to Empowering and activating citizens |
Customer participation in services | Relates to Empowering and activating citizens |
Digital wellbeing operating models and service task | Relates to Empowering and activating citizens |
Ensuring data quality | Relates to Supporting health operations and Making health data more available in research and innovation workflows |
Interoperability policies and selection of data models | Relates to Doing the groundwork |
Evaluating and updating the Kanta information system services | Relates to Supporting health operations |
Strengthening the benefits of Kanta data | Relates to Supporting health operations |
National and regional steering and management of the service system by developing secondary use of health and social services data | Relates to Supporting health operations and Making health data more available in research and innovation workflows |
Use of information in research, development and innovation activities | Relates to Making health data more available in research and innovation workflows |
Developing a management and steering model for digitalisation and information management | Not relevant outside Finland |
Digital security | Relates to Doing the groundwork |
Area for indicator development | Value chain | ||
Health- care | Education and training | Research and innovation | |
Scope: Empowering an activating citizens | |||
Patients scheduling and rescheduling of appointments for consultations | x | ||
Patients bringing self-measurements to the consultation | x | ||
Patients’ collection and use of digital health data | x | x | |
Patients’ belief in own ability to access, understand and make use of digital health data | x | ||
Patients bringing knowledge and reasoning services to the consultation room | x | ||
Patients access to decision support tools including tools for shared decision making | x | ||
Patients’ interaction with digital care pathways in which they are enrolled and are to benefit from | x | ||
Patients’ discovery, inquiry and engagement in clinical trials | x | x | |
Patients’ attitudes towards the digital healthcare system | |||
Scope: A shift towards prevention and digital first | |||
Citizens and patients use of knowledge sources that are curated and published by health authorities and made available in patient portals | x | ||
Synchronous and asynchronous digital consultations | x | (x) | |
Next generation digital consultation tools | x | x | |
Building down the barriers between health information silos that are constrained by geography or by healthcare subsector (for primary use) | |||
Provision of relevant knowledge at Point of care. Knowledge-support Clinical decision support | x | x | |
Helping health professionals gain an overview of the situation of the patient | x | x | |
Availability and use of order sets | x | ||
Repertoire of digital care pathways that are available to clinicians and their value as tools to improve quality, completeness and continuity of care | x | ||
Documentation support | x | x | |
Outcome assessment | x | x | x |
Supporting for interprofessional collaboration | x | x | |
Support for quality and safety monitoring of healthcare performance (including cohort-specific aggregation of healthcare data on national, Nordic and European levels). | x | x | |
Unresolved health problem to research workflows (e.g. discovery, inclusion into and conductance of clinical trials in oncology) | X | x | |
Scope: Doing the groundwork | |||
Development, maintenance and expansion of IT-infrastructure and information infrastructure that is specific to the health domain. | x | x | x |
Development and implementation of service models that reimburse digitized care | x | ||
Standardisation work | x | x | |
Work on legislation (e.g. to allow for secondary use of health data) | x | x | |
Improving procurement practices | x | ||
Information security, cybersecurity. | x | x | x |
Scope: Making health data more available in research and innovation workflows | |||
Increasing availability and quality of data (e.g. structured documentation, use of terminology systems) | x | x | x |
Data to knowledge workflows, e.g. Number of ethically approved biomedical research projects that utilize data that originates from healthcare or self-care. | x | x | |
Knowledge to innovation workflows (e.g. multicenter international clinical trials of medicinal products or medical devices). | x | x | |
Siloed health data to aggregated health data workflows (nationally and internationally) e.g. Nordic or European research registries dedicated to a particular patient cohort such as long Covid, patients with rare diseases. | x | x | |
Scope: Supporting health personnel | |||
Implementing Healthcare information systems that are easy to learn, easy to memorize and that does not require the development of workarounds | x | x | |
The governing of knowledge content in Clinical decision-support systems to optimize the relevance of CDS and minimize alert fatigue | x | x | |
IT support for representing the state of the patient and the care that was provided to ease the documentation burden for health personnel. | x | x | |
Sufficient and competent IT-support for healthcare personnel | x | x | |