Digital health involves using technology to improve health and wellbeing at individual and population levels.
Increasing costs/expenditure
Population Health & Societal Changes
Population growth - ageing populations
Increasing chronic and comorbid conditions
Increasing demand for healthcare
Increasing demand from ‘expert patients’
Lifestyle risk factors
'Digital' life – inactive lifestyles
Unequally distributed in the population
Health and social care crisis
Waiting lists
Staff shortages
Improve access to healthcare
Development of new treatments and interventions
Personalised and precision medicine
Share and coordinate patient information
Support and improve collaboration
Improve care coordination
Improve the quality and efficiency of care
Improve assessment, decision-making, treatment and monitoring
Improve quality and safety
Evidence-based medicine (EBM)
Reduce inefficiencies and costs in the healthcare system
Support achievement of policy aims
Framework for digital equity (Richardson et al. 2022)
A person’s capability to understand, read, use and obtain health care information.
Communication, collaboration and participation
Teaching, learning and self-development
Information, data and content literacies
Creation, innovation and research
Digital identity, wellbeing, safety and security
Technical proficiency
Ability to access, manage, evaluate, and create information safely and effectively using digital technologies.
Ensures effective use of digital tools while maintaining privacy, security, and ethical standards.
Confidence in using digital technologies, willingness to embrace change, digital resilience.
Understanding the adverse side of digital literacies such as cyber threats and misinformation.
Knowing when not to use digital sources.
Those capabilities that fit someone for living, learning, working, participating and thriving in a digital society (Health Education England, 2018)
Consideration of confounding factors (e.g., education, digital divide, health conditions) when analyzing correlation between age and digital skills.
Privacy, security, information governance.
UK GDPR and DPA 2018.
Right to be let alone, free from interference or intrusion.
Rights of an individual or an organisation - Access and control.
How (and what) information is collected, stored, processed, used and shared.
Situated – depends on context.
Bodily, spatial, communicational, informational, intellectual, decisional, associational, behavioral.
Standards and technologies protecting data from destruction, modification, or disclosure.
Confidentiality (C): prevention of unauthorized disclosure.
Integrity (I): guarantee that information isn't modified in transit.
Availability (A): information is available when needed.
Resilience: systems continue operating under adverse conditions.
External: Malware, hacking, phishing.
Internal: Insider threats, loss of devices.
Unsecured networks.
Encryption, access control, data backups, data masking, data erasure, network protections (VPN, firewalls).
Framework: legal, ethical, and quality standards supporting high-quality care.
Physical harm, privacy breach, data loss, identity theft, emotional distress, fines, reputational damage.
Justify the purpose
Do not use PII unless it is absolutely necessary
Minimise PII
Restrict access
Everyone should be aware of their responsibilities
Understand and comply with the law
Principle 7: The duty to share information can be as important as the duty to protect patient confidentiality
Principle 8: Inform patients and service users about how their confidential information is used
Patients have the right to opt out of their confidential information being used beyond their own care
Sets out principles, rights, and obligations for processing personal data.
Process of protecting data, relationship between data collection, privacy expectations, and relevant laws.
Information that directly or indirectly identifies an individual.
Special categories (e.g., race, health data) require higher protection.
Right to be informed
Right of access
Right to rectification
Right to erasure
Right to restrict processing
Right to data portability
Right to object
Rights related to automated decision making including profiling
Consent
Contract
Legal Obligation
Vital interests
Public task
Legitimate interests
Freely given, specific, informed, and unambiguous agreement to the processing of personal data.
Patient autonomy, confidentiality, risk of harm, equity, data exploitation, bias.