3. NHS 1997-2010
NSH Plan
National Service Frameworks
National Institute of Clinical Excellence
Healthcare Commission
National Patient Surveys
National Staff Surveys
Foundation Trusts
QIPP / QSIP / CQUIN
4. NHS 1997-2010 – what changed?
Waiting times
Deaths from cancer & CV disease
Health care associated infections
National standards of care for major diseases
Information on performance
Smoking rates
5. Mental Health Services 1997-2010
Suicide Prevention Toolkit
Assertive Community Treatment
Crisis Resolution & Home Treatment
Early Intervention in Psychosis
Payment by Results
HoNOS PbR / Care Packages Programme /
MH Clustering
6. A high performing NHS
Access
Safety
Clinical effectiveness
Patient experience
Equity
Efficiency
Accountability
Health promotion
Management of long-term conditions
8. Liberating the NHS and an Information Revolution
The White Paper ‘Liberating the NHS’, published on the 12th July,
outlined government plans for a new direction for the NHS, including
an ‘information revolution’ and greater patient choice and control.
Vision for an information revolution
People have access to their health records and the information they
need to make informed choices about their health and care.
“No decision about me, without me”
Liberating NHS information will help drive better care, improving
outcomes , innovation and the better use of resources.
9. What does this mean for clinicians
• Patient access to the whole of their records electronically
• Initially in primary care but later all records
• More patient and public facing information about health and care
options
• Information derived from care records to be harnessed
• To assess care quality – and to help improve it
• To find and disseminate best practice
• To highlight areas of poor performance or waste
10. Care records
your records
form the
primary
source of data
Creating
intelligence
as data is
analysed
and
interpreted
The
Information
revolution
The
Information
Revolution
11. Creating
intelligence
as data is
analysed
and
interpreted
Care records
your records
form the
primary
source of data
The
Information
revolution
1.4
Leading to
patient-centred
care
Improving
service quality
and outcomes
for you
Giving you greater
ownership & control
over your care
Encouraging
clinicians and care
professionals
to respond to your
needs and capture
data at the point
of care
Enabling you
to make properly
informed
choices
Leading to
easily understandable
Information
published by a range
of organisations to
meet your needs
Improving
data quality
as data is exposed
to professional scrutiny
and the quality of
data improves
Leading to
greater
transparency
through routine
publication of
core data
The main source for
aggregate data
for secondary uses
such as research
Enabling
more direct
communication
between you &
your professional
Allowing you to
share information
from your record
with others
Promoting
benchmarking of
outcomes
by clinicians
Promoting
benchmarking of
outcomes
by clinicians
12. Creating
intelligence
as data is
analysed
and
interpreted
Care records
your records
form the
primary
source of data
The
Information
revolution
1.5
Leading to
patient-centred
care
Giving you greater
ownership & control
over your care
Encouraging
clinicians and care
professionals
to respond to your
needs and capture
data at the point
of care
Enabling you
to make properly
informed
choices
Leading to
easily understandable
Information
published by a range
of organisations to
meet your needs
Improving
data quality
as data is exposed
to professional scrutiny
and the quality of
data improves
Leading to
greater
transparency
through routine
publication of
core data
The main source for
aggregate data
for secondary uses
such as research
Enabling
more direct
communication
between you &
your professional
Allowing you to
share information
from your record
with others
Promoting
benchmarking of
outcomes
by clinicians
Improving
service quality
and outcomes
for you
Improving
service quality
and outcomes
for you
13. Creating
intelligence
as data is
analysed
and
interpreted
Care records
your records
form the
primary
source of data
The
Information
revolution
2.4
Giving you greater
ownership & control
over your care
Encouraging
clinicians and care
professionals
to respond to your
needs and capture
data at the point
of care
Enabling you
to make properly
informed
choices
Enabling
more direct
communication
between you &
your professional
Allowing you to
share information
from your record
with others
Promoting
benchmarking of
outcomes
by clinicians
Improving
service quality
and outcomes
for you
Leading to
patient-centred
care
The main source for
aggregate data
for secondary uses
such as research
Leading to
greater
transparency
through routine
publication of
core data
Improving
data quality
as data is exposed
to professional scrutiny
and the quality of
data improves
Leading to
easily understandable
Information
published by a range
of organisations to
meet your needs
Leading to
easily understandable
Information
published by a range
of organisations to
meet your needs
14. Moving away from targets to outcomes
• New frameworks for measuring NHS, social care and public health
outcomes create new opportunities for improvement and
accountability*
• We will consider how outcomes information may be mandated in
Quality Accounts
• We are undertaking a fundamental review of data collections in health
and social care. There will be a public consultation on this in 2011
• This will introduce a new focus on patient and service-user generated
information such as patient reported outcomes measures (PROMS),
patient and service user experience, ratings and real-time feedback
• Information must support GPs to take commissioning decisions and
local authorities to integrate health and social care
*Transparency in Outcomes – a framework for the NHS’ consultation launched 19 July
20. Information for autonomy, accountability and
democratic legitimacy
• A ‘presumption of openness’ when publishing data is crucial for
accountability
• Wider availability of data will allow ‘information intermediaries’ to
cater for people with a range of needs (including people who do
not themselves presently use computers)
• We are identifying national data sets for early release
• We attach great importance to ensuring trust in published data
21. Jul 2010 Oct 2011 Jan Apr Jul Oct 2012 Jan Apr
Provisional overall timeline: July 2010 - June 2012Keymilestones
Overall
White Paper
Published
Health Bill
Public
health White
Paper
NHS Board
begins. in
shadow form
NHS Board and
economic
regulator take up
full powers
New public
health service
operational
2012/132011/12
Report on
funding of long-
term care and
support
White Paper on
social care
reform (during
2011)
Shadow health
and wellbeing
partnerships
begin
Publications on social care,
choice, information,
education and data returns
Spending
Review
released
New
Spending
Review
period
begins
2011/12
allocations
11/12
QIPP/
operational
planning
complete
2012/13
allocations
12/13
QIPP/
operational
planning
complete
First GP
Consortia start
work in shadow
form (from
2011/12)
Finance and efficiency Autonomy and accountabilityPolicy and legislation
Additional
White Paper
Consultations
Local health and
wellbeing boards
and HealthWatch
established
Choice extended
to long-term
conditions and
diagnostics (from
2011)
Choice of
consultant-led
team; expansion
of PROMs
Free choice of
GP practiceExtension of
choice in mental
health (ongoing)
A patient-led NHS
Outcomes
Framework fully
implemented
Outcomes
Framework
comes into use
Further
publication on
Outcomes
Framework
Initial
consultation
on Outcomes
Framework
Improving healthcare
outcomes
22. Jul 2010 Aug Sep Oct Nov Dec Jan Feb Mar
Early engagement and action timeline: July 2010 – Mar 2011
Planning, performance and QIPP
First submission QIPP and
Reform plan and QIPP tertial
review at SHA level
QIPP and Reform
plan and QIPP
tertial review at
SHA level
White Paper consultation processes
NHS Chief Executive
visits every region
National stakeholder engagement
Regional and local stakeholder engagement
Development of QIPP
plans to include reform
New commissioner / provider leads and bridging
functions in place at DH and in SHAs
DH planning with Monitor and CCP for creation of Economic Regulator
Identification of likely first GP
commissioning consortia
Development process for first GP
commissioning consortia
Capability development for GP commissioning consortia
(ongoing)
Engagement and consultation
Policy design and implementation
Work to drive and accelerate the Foundation Trust pipeline
23. Fact and Facade
Information Revolution another NPfIT?!
Liberating – from jobs?!
Demand to reduce £20 billion AND
coalition promise: “no clinical services will be
cut” …
“may be cut” …
“will have to be cut” …
“these are the cuts!”
25. Monitoring
Where you are?
What are you doing?
How are you doing it?
How much of it are you doing?
Big Brother is watching you!
26. Unique Selling Product
What is your NHS Trust selling?
Your Expertise
Your Credentials
Your Experience
Do you know that they know?
27. The new drivers
Current changes:
What ideology?
What place for ideology?
What attachment NHS staff can have / afford?
Stock market – the new god that failed
Time for psychiatrists to
reconsider their options
28. Local options
PBC
Specialist commissioning
Local types of specialist commissioning
What out of county expenditure on each?
What are your local PBC priorities?
29. Enter the saviour!
Meet the commissioner(s)
Identify needs of specialist commissioning in
your area
30. Think outside the box!
Create a consortium
Create a social enterprise
Employee-Employer partnership
Develop new businesses
None of these options possible
without YOUR clinical leadership
31. Think of business within …
… and business without NHS
32. Your unique value
Practice based experience
Experience based evidence
Basis for a new model of delivery
How will you market the new model?
33. Marketing the new model
Your organisation
Others
Yourself, your ideas
Coherently expressed in business jargon
