draft policy framework being developed for discussion with Ministerial Group
Current LTSF focus cont’d
Service planning
defining district, regional and national level responsibilities
developing planning methodologies, tools and capabilities
strong fit with networks and decision making
supporting emerging DHB regional service planning, and existing national tertiary planning
Decision making
what key decisions will need to be made in the system over the next 5-10 years?
equity of access, affordability, vulnerability, quality & safety, new technologies and services, workforce, ICT
accountability and decision structures currently decentralised to individual DHBs
most of the key future decisions will need to be made across DHB boundaries
likely rebalancing of decisions towards regions, and to the centre
important role for clinical leadership at regional and national levels
linkage with shared services for backroom functions, and aggregation of P & F
options being explored with the Ministerial Group
Current focus cont’d
Engaging the community and health professionals
communications strategy to build awareness of challenges and trends
provide context for specific change proposals
provide opportunity to shape the future system
being scoped in discussion with National Health Committee
Longer term work programme
Seven response areas identified for co-ordinated response through the LTSF :
long term service planning
quality, safety and innovation
new models of care
performance
leadership and decision making
workforce
information systems
Key elements of the LTSF work programme from 09/10 will be defined through Ministry SOI process and with DHB CEOs
New models of care
Review of trends in models of care and service configuration:
Acute secondary and tertiary inpatient services will consolidate into a smaller number of centres
Smaller district hospitals will use clustering, regional services and networks to expand their critical mass
Services will shift between professional groups
Services will shift between settings: from tertiary to secondary, from there to primary and community, and into the home
Primary care will have greater role in prevention, delivery of traditionally secondary services, and improved access to specialist diagnostic testing
Increase in integration and self management will be enabled by information technology
What will the cost impacts be?
How will change be managed?
What does this mean for ICT development?
Direction from the new Government
“ It will be critical to re-orient the health service in a way that fosters quality, is patient-centred and provider-friendly.”
Hon Tony Ryall
Minister of Health
February 2009
Goal of a nationwide Health ICT effort
Develop a sustainable and effective information management and technology environment…
that stimulates, enables and supports…
re-orienting the health system in a way that
fosters quality
is person-centred
is provider-friendly
increases productivity of the system as a whole
Person-centred
Services organised around the needs of each person and family/whānau
Information systems and processes centred on the person
The right care can be provided by the right professional/provider at the right place and the right time
Person/citizen is a participant (‘co-producer’) in the health care process
Provider friendly
Simple, automated processes, where ‘compliance costs’ for providers are minimised
Providers only required to collect and report information that really matters
Clinical delivery tasks are made easier and safer through the use of supportive technologies (such as clinical decision support systems)
Clinical networking is made easy
Information Management Principles (NIHI, 2008)
Health information should be recorded in a form that allows all relevant actors to be able to trust that information where appropriate
Health information must always identify source and method of derivation
Health information should be encoded to international standards wherever practical
Primacy of patient safety
All individual health information will be made available to all clinicians engaged in care of a patient (subject to audit trails)
Information Management Principles cont’d
Health information of all individuals will be shared in privacy-protected form to support healthcare quality improvement
Statutory adherence
People can access their own health information
People can contribute to their own health record
People can define additional access rights on their health information for other people (e.g. family members)
People can review who has accessed their health information and have a clear and effective means of directing queries concerning such access
Current state evidence (NZ)
‘ Connected Health’ quantitative survey (2008, to be published) found:
79% of surveyed clinicians agreed that better access to electronic healthcare information held by other organisations could improve the way they provide health services
48% of surveyed clinicians were unable to find the electronic information they needed from other organisations at least once a day
Among DHB employed clinicians, this number rises to 75%
nearly 15% report they are unable to find this information more than 10 times every day
Current state evidence (NZ) cont’d
‘ Connected Health’ quantitative survey also found:
Surveyed clinicians wanted electronic access to:
Patient medication information 68%
Diagnostic test results 66%
Discharge summaries 61%
Clinical guidelines 57%
Wanted day-to-day tasks handled electronically:
Diagnostic test results 47%
Discharge summaries 44%
Patient medication information 42%
Patient referrals 34%
85% of clinicians strongly agreed that having improved e-access to health information would
Improve coordination of care between practitioners
Help achieve better outcomes for health organisations
Emerging evidence in favour of EHR outcomes
Amarasigham, R. et al. (2009). Clinical information technologies and inpatient outcomes. Archives of Internal Medicine, 169, 2:
In hospitals where more doctors used computerised data, there were 16% fewer medical complications than in hospitals where less computerised data was used
More computerised hospitals also tended to have lower costs because medical complications can add dramatically to the cost of hospitalisation
The Commonwealth Fund (In-the–Literature, January 2009):
31% of primary care physicians with high IT capability and 28% of those with medium IT capacity reported their ability to provide quality medical care had improved over the past five years
By contrast, just 22% of those with low IT capability reported similar views
Ministry of Health priority areas
Provide better information for the public
Provide on-line directories of providers and guidance on service options
Improve the use of national data collections
Foster development of personal health ‘portals’
Ensure smarter investment in information technology
Provide a national ‘blueprint’ for health information systems
Develop a common decision-making process
Accelerate progress through collaboration and sharing
Strengthen the national health information infrastructure
Strengthen identity management (NHI, HPI)
Provide a ‘core clinical record’ capability for safety and continuity of care
Provide facilities for finding and sharing information nationally
Simplify agreement, payment and reporting systems
Rationalise service agreements
Automate administrative and payment processes
Make performance monitoring and reporting meaningful
Accelerating progress - critical enablers
National health information architecture
National health information infrastructure
Shared services
Spreading innovations
Community dialogue on safe sharing of health information
Common decision making framework
National health information architecture
An overarching architecture for the New Zealand health system – developed jointly with DHBs, PHOs, NGOs, private providers
Describes how business processes, systems, information components and technical standards will combine and work together
Provides a context for the development of enterprise architectures at organisational levels
Ensures alignment and re-usability of artefacts
Enables smarter IT investment decisions
It is supported by:
A set of collaborative tools
A common repository
A joint governance mechanism
Health System Architecture
National health information infrastructure
Provide a nationwide coverage
Provide a platform for regional and local developments
Provide better information to the public
Support collaboration and clinical networking
Examples:
National directories (NHI, HPI)
‘ Core clinical record’ (replacing the Medical Warning System) clinicians to define ‘core clinical data set’ first
Data warehousing, analysis and reporting (focus on quality improvement)
- includes public reporting of provider performance
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