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Longitudinal evaluation of a countywide alternative to the Quality and Outcomes Framework in UK General Practice aimed at improving Person Centred Coordinated Care

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Objectives To evaluate a county-wide deincentivisation of the Quality and Outcomes Framework (QOF) payment scheme for UK General Practice (GP). Setting In 2014, National Health Service England signalled a move towards devolution of QOF to Clinical Commissioning Groups. Fifty-five GPs in Somerset established the Somerset Practice Quality Scheme (SPQS)—a deincentivisation of QOF—with the goal of redirecting resources towards Person Centred Coordinated Care (P3C), especially for those with long-term conditions (LTCs). We evaluated the impact on processes and outcomes of care from April 2016 to March 2017. Participants and design The evaluation used data from 55 SPQS practices and 17 regional control practices for three survey instruments. We collected patient experiences (‘P3C-EQ’; 2363 returns from patients with 1+LTC; 36% response rate), staff experiences (‘P3C-practitioner’; 127 professionals) and organisational data (‘P3C-OCT’; 36 of 55 practices at two time points, 65% response rate; 17 control practices). Hospital Episode Statistics emergency admission data were analysed for 2014–2017 for ambulatory-sensitive conditions across Somerset using interrupted time series. Results Patient and practitioner experiences were similar in SPQS versus control practices. However, discretion from QOF incentives resulted in time savings in the majority of practices, and SPQS practice data showed a significant increase in P3C oriented organisational processes, with a moderate effect size (Wilcoxon signed rank test; p=0.01; r=0.42). Analysis of transformation plans and organisational data suggested stronger federation-level agreements and informal networks, increased multidisciplinary working, reallocation of resources for other healthcare professionals and changes to the structure and timings of GP appointments. No disbenefits were detected in admission data. Conclusion The SPQS scheme leveraged time savings and reduced administrative burden via discretionary removal of QOF incentives, enabling practices to engage actively in a number of schemes aimed at improving care for people with LTCs. We found no differences in the experiences of patients or healthcare professionals between SPQS and control practices.
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CloseJ, etal. BMJ Open 2019;9:e029721. doi:10.1136/bmjopen-2019-029721
Open access
Longitudinal evaluation of a
countywide alternative to the Quality
and Outcomes Framework in UK
General Practice aimed at improving
Person Centred Coordinated Care
James Close, 1 Ben Fosh,1 Hannah Wheat,2 Jane Horrell,1 William Lee,1
Richard Byng,3 Michael Bainbridge,4 Richard Blackwell,5 Louise Witts,5
Louise Hall,5 Helen Lloyd6
To cite: CloseJ, FoshB,
WheatH, etal. Longitudinal
evaluation of a countywide
alternative to the Quality and
Outcomes Framework in UK
General Practice aimed at
improving Person Centred
Coordinated Care. BMJ Open
2019;9:e029721. doi:10.1136/
bmjopen-2019-029721
Prepublication history and
additional material for this
paper are available online. To
view these les, please visit
the journal online (http:// dx. doi.
org/ 10. 1136/ bmjopen- 2019-
029721).
Received 7 February 2019
Revised 23 May 2019
Accepted 30 May 2019
For numbered afliations see
end of article.
Correspondence to
DrJames Close;
james. close@ plymouth. ac. uk
Research
© Author(s) (or their
employer(s)) 2019. Re-use
permitted under CC BY-NC. No
commercial re-use. See rights
and permissions. Published by
BMJ.
ABSTRACT
Objectives To evaluate a county-wide deincentivisation
of the Quality and Outcomes Framework (QOF) payment
scheme for UK General Practice (GP).
Setting In 2014, National Health Service England
signalled a move towards devolution of QOF to Clinical
Commissioning Groups. Fifty-ve GPs in Somerset
established the Somerset Practice Quality Scheme
(SPQS)—a deincentivisation of QOF—with the goal of
redirecting resources towards Person Centred Coordinated
Care (P3C), especially for those with long-term conditions
(LTCs). We evaluated the impact on processes and
outcomes of care from April 2016 to March 2017.
Participants and design The evaluation used data from
55 SPQS practices and 17 regional control practices for
three survey instruments. We collected patient experiences
(‘P3C-EQ’; 2363 returns from patients with 1+LTC; 36%
response rate), staff experiences (‘P3C-practitioner’; 127
professionals) and organisational data (‘P3C-OCT’; 36 of
55 practices at two time points, 65% response rate; 17
control practices). Hospital Episode Statistics emergency
admission data were analysed for 2014–2017 for
ambulatory-sensitive conditions across Somerset using
interrupted time series.
Results Patient and practitioner experiences were similar
in SPQS versus control practices. However, discretion from
QOF incentives resulted in time savings in the majority of
practices, and SPQS practice data showed a signicant
increase in P3C oriented organisational processes,
with a moderate effect size (Wilcoxon signed rank test;
p=0.01; r=0.42). Analysis of transformation plans and
organisational data suggested stronger federation-
level agreements and informal networks, increased
multidisciplinary working, reallocation of resources
for other healthcare professionals and changes to the
structure and timings of GP appointments. No disbenets
were detected in admission data.
Conclusion The SPQS scheme leveraged time savings
and reduced administrative burden via discretionary
removal of QOF incentives, enabling practices to engage
actively in a number of schemes aimed at improving
care for people with LTCs. We found no differences in
the experiences of patients or healthcare professionals
between SPQS and control practices.
BACKGROUND
The Quality and Outcomes Framework
(QOF) for UK General Practice (GP) is one
of the largest health-related pay-for-perfor-
mance (P4P) schemes in the world.1 Following
implementation in 2004, the scheme initially
had a positive impact on quality of care,
primarily achieved via establishment of
consistent procedural baselines in the clin-
ical management of incentivised (mostly
chronic) diseases.1–5 It reduced between-prac-
tice inequalities in care delivery,1–3 while
Strengths and limitations of this study
This study evaluated changes to service delivery,
conducted using two survey tools—offering a per-
spective on the experiences of both patients and
healthcare professionals.
These were supplemented with a longitudinal analy-
sis of organisational change (to measure alterations
to service deliver) and a timeseries of emergency
admissions for ambulatory-sensitive conditions (to
detect disbenets arising from the scheme).
Due to time and resource pressures on general
practice in the UK, we struggled to recruit controls
from within the same county (Somerset) or matched
controls from the region. As an alternative, we ob-
tained non-matched controls from the region.
No detectable improvements were established in
experiences of healthcare professionals or pa-
tients—this could be because the intervention had
no effect on these outcomes, the instruments were
not sensitive enough or changes to patient/practi-
tioner experiences were somewhat distal to the
intervention.
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Open access
also leading to improved disease registers, widespread
recording of clinical activities and adoption of electronic
medical record systems,1 leading to growth in GP data
and related research.6 7
Since the introduction of QOF, demographic shifts of
an aging population have continued to drive a shifting
clinical landscape,8 with the number of people with
three or more long-term conditions (mLTCs) thought
to have risen by one million over the last decade.9 The
subsequent rising demand for the management of long-
term conditions (LTCs) and mLTCs—requiring tailored
and coordinated support10 11—has led to QOF (with its
emphasis on processes for single disease guidelines)
being viewed as increasingly anachronistic.6 12–16 After
introduction of QOF, there was a significant reduction
in the continuity of care2 17 and the person-centeredness
of GP consultations,13 14 18 19 with a subsequent decline in
patients’ satisfaction.20 It has been argued that QOF does
not incentivise appropriate clinical care for people with
multimorbidity,6 12–16 who require individualised support,
greater continuity of care and a holistic, biopsychosocial
approach that is responsive and empowering.10 11 An
oft-quoted criticism is that QOF reduces consultations to
a ‘box-ticking’ exercise.21
In response to such criticisms, both the National
Health Service (NHS) Chief Executive and the General
Practitioners Committee Chairman previously backed
the removal of QOF.21 In 2014, NHS England signalled
a move towards devolution of QOF to Clinical Commis-
sioning Groups (CCGs), allowing organisations the
freedom to develop alternatives. Potential advantages
included the targeting of local health needs and greater
clinical engagement for quality improvement.22 In
response, the Somerset Practice Quality Scheme (SPQS)
was established as a deincentivisation of QOF. It arose
because GPs, the CCG and the Local Medical Committee
felt that QOF was not incentivising the highest value
clinical behaviour. The goal was to allow clinicians
the freedom to innovate, enable consultations to be
more person-centred and increase involvement with a
number of concurrent schemes aimed at improving
Person Centred Coordinated Care (P3C).23 The details
of the scheme were included in the SPQS contract24 and
local Sustainability and Transformation Plan (STP—
plans for reforming healthcare mandated by the Five-Year
Forward View25) of the GPs26 (see online supplementary
file 1 for a summary of Somerset STPs; box 1 for brief
details of the various schemes and references for details).
The contract removed incentives from QOF, although
Calculating Quality Reporting System (CQRS) remained
active in order to collect prevalence data for payment
calculations. The SPQS contract stated that the reduced
QOF overhead would be exploited to better meet the
needs of patients with LTCs by developing new models of
care. Implementation was specified in the locality STPs,
which included a patchwork of initiatives, most notably
the ‘Test and Learn pilots’, which encompassed three
distinct schemes (box 1), all of which had a shared vision
of targeting complex patients with care plans, multi-
disciplinary team input and single point of contact.27 28
Other schemes included a Village Agents service29 and
Health Connections Mendip (HCM)30—see box 1. Fifty-
five Somerset practices opted for SPQS, with 18 Somerset
practices (initially 20) retaining the existing QOF contract
(the SPQS practices increased to 57 in 2015/16; but two
mergers reduced it back to 55).
The initial phase of the scheme was previously evalu-
ated with a retrospective approach.31 This revealed early
stages of organisational change, including stronger feder-
ation-level agreements and informal networks, increased
multidisciplinary team working, reallocation of resources
towards healthcare assistants, nurses and others, and
changes to structure and timings of appointments with
GPs. From April 2016 to March 2017, we conducted
a longitudinal evaluation of the second full year of the
SPQS programme (see online supplementary file 2 for a
timeline of the SPQS scheme and associated evaluations).
This was commissioned with the aims of establishing the
nature and extent of P3C that has been implemented
Box 1 Initiative for implementation of SPQS.
Test and Learn:Comprises three similar initiatives (South Somerset
Symphony Vanguard, Taunton and Mendip—see below), which share
a common goal of targeting complex, multimorbid patients with a suite
of approaches including single personalised care plans, multidisci-
plinary team input and single point of access to provide PersonCentred
Coordinated Care.
Test and Learn—South Somerset Symphony Vanguard:A sym-
phony ‘hub’ system located at Yeovil District Hospital, where com-
plex patients receive extra support from health coaches(HCs)/Key
Workers at the Symphony hub service, although they remain under
management of general practice (GP).27 28
Test and Learn—Taunton: Operates under a ‘virtual hub’ model,
with complex/frail patients managed by a multidisciplinary team
moving between practices, with shared care plans and Well-being
Advisors.
Test and Learn—Frome Mendip, including ‘Health Connections
Mendip’: With loose eligibility criteria and a number of referral
routes, Community Practice Nurse and Health Connectors (based
at Frome) liaise regularly in multidisciplinary team input meetings.
There is a hub telephone line for single point of access. The mod-
el advocates using existing assets in the community. The Health
Connections team lead social prescribing work with a service direc-
tory to signpost patients to appropriate resources.30
Enhanced Primary Care (EPC): EPC is a subcomponent of the
Symphony Vanguard scheme that incorporates HCs into primary care,
focusing on less complex patients, allowing GPs to focus primarily on
medical problems.
Village Agents Service: Supports isolated, excluded and vulnerable
(including elderly and multimorbid) people by offering a signposting and
referral service. The service links with GPs.29
Living Better:A working partnership between the GP, AGE UK Somerset,
Social Care, Somerset Partnership, West Somerset District Council and
Somerset Clinical Commissioning Group. The project supports people
with one or more long-term conditions to better self-manage, helping
them build connections to the community and reducing dependency on
health and social care.
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since discretion from QOF, explore staff and patient
experiences of care delivery and examine non-elective
hospital admissions before and after inception of the
scheme.
METHODS
We conducted a mixed-methods evaluation of SPQS
which included a suite of quantitative and qualitative
tools. Analysis of quantitative data is described in this
paper. In-depth qualitative findings will be published in
a subsequent paper (including semistructured interviews
with practitioners, observations of consultations and facil-
itation workshops with practices). A schematic overview
of the full SPQS evaluation framework is provided in
figure 1. The quantitative evaluation included completion
of survey tools targeting patient experiences (P3C-EQ),
staff experiences (P3C-practitioner) and organisational
perspectives (P3C-OCT tool), alongside time series of
Hospital Episode Statistics (HES) for ambulatory-sensitive
conditions across Somerset. We chose not to use national
measures of GP (ie, GP Patient Survey and Friends and
Family Test): they have a broad sample and do not target
the patient group (ie, patients with LTCs) that are the
focus of SPQS. Furthermore, they do not target the
construct of interest (ie, P3C).
Samples
The 55 participating Somerset practices (mean list
size=7695; median=6515.5; smallest=1834; largest=29 078)
completed our evaluation tools (see below). While these
55 practices were incentivised to take part in our evalua-
tion (ie, by being part of SPQS), the non-SPQS Somerset
practices had no incentive to act as controls and did not
participate in this study. Therefore, for control practices,
we initially identified a cohort of non-Somerset control
practices matched for staffing data, list size, population
density, indices of multiple deprivation, QOF scores and
disease prevalence. However, the incentives available for
this evaluation (£200 per practice) were only sufficient to
recruit six practices by this method. We therefore supple-
mented this group with 11 unmatched practices from
across the Southwest, making a total of 17 control prac-
tices (mean list size=6714; median=4878; smallest=2678;
largest=4878). The control group therefore represents a
self-selected sample of practices that are likely to repre-
sent engaged, active practices (ie, with the resources to
engage with research). In contrast, completion of our
evaluation was mandatory for all SPQS practices.
Patient and public involvement
Patients were involved via the peninsula CLAHRC
patient involvement group (PenPig), who set priorities
for research objectives. Patients, public and healthcare
professionals were also involved in codesign workshops
to develop the measurement framework and individual
questionnaires (see papers for details23 32–37). Patients
also reviewed drafts of ethics approval applications
and all patient-facing communication. The work was
copresented with patients at the South West Society for
Academic Primary Care Regional Meeting 2018.
Figure 1 Our P3C mixed methods evaluation framework for SPQS2.LTC, long-term condition; P3C, Person Centred
Coordinated Care; QOF,Quality and Outcomes Framework; SPQS,Somerset Practice Quality Scheme.
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Survey tools
The P3C-Patient Experience Questionnaire (P3C-EQ) is a brief,
11-item patient-completed measure of patient experi-
ences of P3C delivery, which we have previously vali-
dated.32 38 39 The tool can be used to generate an aggregate
score of patient experience,32 with a range of score from
0 to 30, where a higher score indicates better experiences
of care.39 It can also be subscored to previously described
subdomains of P3C.23 32 34–37
The P3C-Practitioner Experience Survey is a 29-item instru-
ment that measures individual and managerial experience
of delivering P3C. Via a workshop with healthcare profes-
sionals, we selected the previously validated P3C-Practi-
tioner questionnaire (also known as the Person-Centred
Healthcare for Older Adults Survey40) as the most suit-
able instrument to examine practitioners’ perspectives
of P3C (see online supplementary file 3). A minimum of
two practitioners from each practice were requested to
respond. The instrument generates an aggregate score
with a range of 29–145, where a higher score indicates
better experiences of care.
The P3C-Organisational Change Tool (P3C-OCT) is an
evidenced-based measure of progress towards delivering
P3C from an organisational perspective.33 It was devel-
oped to support and measure P3C in line with Year of
Care34 and RCGP Principles of Collaborative Care and
Support Planning,41 thus providing a way to monitor
changes in line with policy directives which improve P3C.
The tool was designed to measure all core P3C routines,
which have been identified through research,42 43 patients’
accounts, policy documents34 and our own work.23 33 The
design of the P3C-OCT is based on a shared consensus of
the components of P3C (eg,35 36 44), which broadly corre-
spond to six domains: Information and Communication,
Care Planning, Goals and Outcomes, Transitions, Organ-
isational Process Activities and Decision Making. These
domains have been mapped to real-world actions that
support the delivery of P3C (eg, multidisciplinary team
meetings, care planning, provisions for information).
This allows the tool to translate concepts that are often
abstract and may be drawn from academic literature and
policy documents, into actionable, tangible processes
which a practice can implement. The result is a unique
29-question instrument with over 500 different possible
responses, which provides a detailed and practical inter-
rogation of P3C delivery. An equally weighted scoring
system allows results of the P3C-OCT to be aggregated
into a single composite score, or alternatively by subdo-
mains of P3C—generating a score of 0–20, with higher
scores indicating more P3C-related activity.
The P3C-OCT provides a detailed profile of care
delivery and organisation through 29 core questions.
All questions ask about objective activities (eg, processes
in place to deliver P3C) and subjective responses (eg,
how well these are working). Scores are given out of a
theoretical maximum of 20 points. The P3C-OCT was
also prepended by a series of SPQS-related questions
about administrative and consultation time savings from
discretion from QOF. Each SPQS practice was requested
to complete the P3C-OCT at two time points (from
February to August 2016 and December 2016 to March
2017). In contrast, control practices only completed the
P3C-OCT once (at time 2).
Data collection
All participating practices supported data collection
of the three survey tools. With the P3C-EQ, from each
practice, 100 patients with one or more LTCs, randomly
sampled from the practice list (using a customised EMIS
script), were invited to complete a postal questionnaire
at a single time point. Patients received an information
pack, consent sheet, demographic questionnaire and
P3C-EQ. All returned questionnaires were entered into a
Microsoft Access database prior to statistical analyses. For
the P3C-Practitioner, we obtained an opportunity sample
via both written and email communication with all partic-
ipating practices. For the P3C-OCT, all participating prac-
tices were offered an electronic or paper version, and we
requested that the tool was completed by a combination
of General Practitioner and Practice Manager (PM), thus
ensuring representation of front-facing and backend
operations of GP surgeries. Completion of the tool was
mandatory as part of the SPQS evaluation.
Analysis
SPQS and control practices were compared on the
P3C-Patient Experience Survey and the P3C-Practioner
Experience Survey (at time 2; 6–12 months after initiation
of second year/phase 2 of SPQS), with significance tested
using the non-parametric unmatched Mann–Whitney–
Wilcoxon (MWW) test taking into account within-practice
clustering by calculating Somers’ D statistic (non-para-
metric tests were used, as the scoring is a summation of
Likert responses, ie, data were ordinal). For the P3C-Or-
ganisational Change Tool, we compared time 1 (imme-
diately after implementation of second year/phase 2 of
SPQS) and time 2 (6–12 months later), with significance
evaluated by Wilcoxon signed-rank test.
Time series of emergency admissions to hospital
A multigroup interrupted time-series analysis (ITS)
was conducted to identify whether deincentivisation
of QOF and the introduction of SPQS were associated
with changes in emergency admissions to acute hospitals
with a primary diagnoses for four long-term, ambulatory
care sensitive conditions (ACSCs). HES were obtained
for patients from all 55 GP practices enrolled in the
SPQS scheme (actually 56 practices in 2015/15) and
18 Somerset QOF practices (ie, Somerset practices not
enrolled in SPQS; initially 20). Data were obtained for a
70-month period from April 2011 to May 2018. This time
period is divided into 38 months preintervention (April
2011 to May 2014) and 48 months postintervention (June
2014 to May 2018; SPQS contract went live in June 2014,
month 39). Data include monthly admission counts for
four ACSCs: Acute Myocardial Infarction (AMI), Chronic
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Obstructive Pulmonary Disease (COPD), Diabetes and
Stroke. We selected these ACSCs as a proxy for prevent-
able admissions and an indicator of any deteriorating
quality of care associated with SPQS. Due to the differ-
ence in number of practices between SPQS and QOF
practices, admissions were divided by the number of prac-
tices, thus providing an average of emergency admissions
(expressed as admissions per month per practice). Anal-
ysis was performed using the itsa command45 on STATA
(StataCorp Ltd). This uses regression-based model with
Newey-West standard errors. Preintervention and postin-
tervention slopes/intercepts of the sample (SPQS prac-
tices) were compared with controls (QOF practices). Lag
period was set to 1 month.
RESULTS
Person Centred Coordinated Care-Patient Experience
Questionnaire
There were 1752 responses received from 49 (89%) of
the 55 practices enrolled in SPQS and 611 responses
from patients enrolled in the 17 control (QOF) practices
(36% response rate and similar to other studies46). The
responses of the two groups were compared in table 1.
The mean global aggregated scores for the P3C-EQ for
SPQS (23.39, n 1752) and QOF controls (23.68, n 611)
were not significantly different (MWW U test; p=0.346)
and indicate generally positive experiences of care across
both samples.
P3C-Practitioner results
Full results of the P3C-Practioner are provided in online
supplementary file 3. We received 98 responses from 55
SPQS practices and 29 responses from 18 control prac-
tices from a mix of healthcare professionals—62 GPs
(49%); 35 nurses (27%); 12 well-being advisors; 7 LTC
nurse; 11 others. The mean global aggregated scores for
the P3C-EQ for SPQS (23.39, n 1752) and QOF controls
(23.68, n 611) were not significantly different (MWW test;
p=0.405). Return rates are not applicable, as this was a
convenience sample where we requested response from
at least two different professionals at each practice.
P3C-OCT results
To evaluate changes to P3C during the SPQS scheme, we
undertook an analysis of the organisation and delivery
of care using the P3C-OCT. Of 55 practices enrolled in
the scheme, 36 practices provided admissible data (ie,
complete and timely) at the two evaluation time-points
(time 1: 2/2016–8/2016 and time 2 was 12/2016-5/2017;
65% response rate). This revealed an increase (0.9;
p=0.034) in aggregate scores on the P3C-OCT between
T1 (5.8) to T2 (6.7). This therefore represents a measur-
able increase in activity towards P3C delivery and organi-
sation (see table 2), with a moderate effect size (r=0.42).
To determine the specific areas of P3C that improved
during the evaluation, this was examined by domains
of P3C.34–36 When broken into subdomains of P3C,
Table 1 Demographic prole of responses to P3C-EQ as percentages
Participant demographics as a percentage
Age(years) Education Gender Multimorbidity
QOF SPQS QOF SPQS QOF SPQS No. LTCs QOF SPQS
<=24 0.3 0.4 None 1.0 1.3 Male 44.0 43.4 1 19.6 20.1
25–34 2.5 1.3 Primary 3.1 2.1 Female 53.8 53.9 2 19.6 23.8
35–44 2.5 2.6 Secondary 33.7 34.6 Non-response 2.2 2.7 3 20.6 17.8
45–54 8.8 5.3 College/vocational 26.4 28.1 4 11.3 13.7
55–64 18.3 13.3 Undergraduate 11.5 10.8 5 9.3 7.5
65–74 25.7 29.2 Postgraduate 8.2 7.8 6 4.7 5.1
75–84 29.3 32.7 Non-response 16.2 15.3 7 2.8 2.8
>=85 12.1 14.1 >=8 4.2 2.8
Non-response 0.5 1.0 Non-response 7.9 6.4
LTC, long-term conditions; P3C-EQ, PersonCentred Coordinated Care-Patient Experience Questionnaire; QOF, Quality and Outcomes Framework; SPQS, Somerset Practice Quality Scheme.
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significant improvements were delivered in areas related
to ‘Goals and Outcomes’ (eg, goal setting with patients;
1.7 increase, p=0.00; large effect size r=0.61).
Further to the longitudinal analysis, SPQS practices
were also compared with a cohort of 17 non-SPQS prac-
tices from the South West (all control practices returned
data at time 2). Aggregate results for the P3C-OCT
revealed that control practices had an aggregate score
of 6.2 on the P3C-OCT, with no significant difference
between SPQS and control practices either before (a
score of 5.8 vs 6.2; p=0.64) or after (6.7 vs 6.2; p=0.41) the
intervention.
Discretion from QOF and time savings
When asking SPQS practices to complete the P3C-OCT,
we also included a number of additional questions
related to the SPQS scheme. We asked SPQS practices a
subjective appraisal of time savings (both in GP consulta-
tions and administration) from enrolment in the scheme.
These are shown in figure 2. More than half (55%) of
the practices (28 of 51 practices that completed these
questions) agreed that time had been freed up within the
10 min standard consultation time.
With regard to administrative time savings, more than
three quarters of SPQS practices (40/51; 78%) reported
administrative (non-consultation time for practitioners)
time savings since initiation of the scheme, with just over
one third of these practices (14/51; 27%) reporting gains
of more than 2 hours per week. For administrators and
non-clinical staff, SPQS was reported to free up time
for more than 86% (44/51) of practices with only 13%
(7/51) reporting a negligible effect. Free text response
boxes confirmed the plans of the STPs (see introduc-
tion and online supplementary file 1), stating that effi-
ciency had been leveraged for increased collaborative
and federation-level working, including engagement with
a number of schemes in Somerset designed to improve
P3C, for example, ‘Better use of Symphony’, ‘Engage-
ment with EPC’, ‘Rural Practice Network’, ‘Health
coaches’, ‘Huddles’, ‘P3C relevant training’, ‘Replaced
by other work such as Symphony/health coaching’. ‘This
hasn't shown a reduction in workload but rather a change
in workload.’ In this manner, the time savings leveraged
from QOF were not hypothesised to lead to an improve-
ment of experiences for practitioners, but instead a shift
in workload.
Retention of QOF elements
When asking SPQS practices to complete the P3C-OCT,
we also included a number questions specific to the
implementation of SPQS. When asked ‘Are you still
using components of the QOF?’, nearly all practices
enrolled in SPQS continued to use at least some aspects
of QOF (only 1 out of 51 respondents to this question
stated ‘none’; 86% of practices used ‘Some’, ‘Most’ or
‘All’). We further investigated the continued utilisation
of QOF via a free-text response in the P3C-OCT ques-
tionnaire. This revealed that QOF was still (according to
one practice) used by ‘applying individually’, not 'point
scoring’. A common aspect that was dropped was excep-
tion reporting, with time also being saved by avoiding
‘target chasing’. Elements of QOF were also contractually
retained such as the CQRS. This remained active under
the SPQS contract to allow data on prevalence and key
indicators to be collected from practices via GP Extraction
System (GPES), where prevalence figures are used in the
SPQS payments calculation.
QOF also continued to be used for the monitoring
of LTCs and recall of patients with LTCs for routine
check-ups. Around a half of SPQS practices (n=25) still
use QOF for recall of at least some (or all) conditions (eg,
checking for recall requirements for patients with LTCs
and the management of specific chronic diseases). Free
text responses suggested that while recall was an essen-
tial function, the implementation under QOF was overly
burdensome and not tailored for multiple morbidities.
Some practices countered this by running in-house devel-
oped searches with a priority to ‘concentrate on an inte-
grated LTC system’. This suggests that there is scope for
collaboration to design an overhauled, integrated recall
system that is specifically designed for efficient manage-
ment of multiple LTCs (as previously proposed47 48).
Time series of hospital episode statistics
Results of the ITS are shown in figure 3. No significant
increases were detected in the slope postintervention (ie,
after the initiation of the SPQS contract in June 2014) in
emergency admissions for patients with a primary diag-
nosis of four ACSCs in SPQS practices. Full results of
Table 2 Mean changes in P3C-OCT scores between time 1
and time 2 for 36 paired practices
Time 1 Time 2
Change T1 T2
(pvalue; effect size)
Total OCT Score 5.8 6.7 0.9 (p=0.01; r=0.42)*
Information and
Communication
7.4 8.1 0.7 (p=0.25; r=0.19)
Care Planning 6.6 7.2 0.6 (p=0.14; r=0.25)
Goals and
Outcomes
6.1 7.8 1.7 (p<0.001; r=0.61)*
Transitions 4.9 5.2 0.3 (p=0.43;r=013)
Organisational
Process Activities
4.3 5.2 0.9 (p=0.03;r=0.36)
Decision Making 3.8 4.4 0.6 (p=0.07;r=0.3)
The top row provides the total OCT score (out of a maximum of
20), followed by domains of P3C. The OCT score for each domain
is given for time 1, time 2 and the difference between time 1 and
2. The statistical signicance of these differences is indicated by
p value from Wilcoxon signed-rank test. Statistically signicant
results (at the level p<0.008; corresponding to a Bonferroni
adjustment for six tests at the p<0.05 signicance level) are
indicated in bold font and with * next to the p value. Effect sizes
were calculated as test statistic z by the square root of the number
of pairs.
OCT,Organisational Change Tool; P3C, Person Centred
Coordinated Care.
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Open access
significance tests are provided in online supplementary
file 4. The removal of QOF has had no significant effect
on emergency admissions for these four ACSCs at the
time of intervention or in the 2 years following. However,
for the non-SPQS Somerset practices, a significant slope
change (increase) in admissions for AMI and diabetes
was observed, and a significant slope change (decrease)
for admissions for stroke was observed. These changes in
admissions are therefore unrelated to the SPQS contract
(see discussion below).
DISCUSSION
We observed a variety of responses to deincentivisation
of QOF in Somerset. Some QOF-related components
remained mandatory (prevalence reporting). Some
‘desirable’ features of the QOF system were still used
(eg, prompts during consultation), others were adapted
(eg, patient recall) and some burdensome components
dropped altogether (eg, exception reporting).
Practices reported that these alterations had led to
time and resource savings in both GP consultations
and administration. These time savings were used to
increase involvement in implementation projects such
as Symphony Test and Learn, Village Agents, Health
Connections and the South Somerset Vanguard. These
were planned as part of the SPQS contract and associ-
ated ongoing healthcare reforms. These local imple-
mentation projects are actively targeting service redesign
for complex patient needs, using P3C across practice
contexts. These projects have involved stronger federa-
tion-level agreements and informal networks, increased
multidisciplinary team working, reallocation of resources
for healthcare assistants (including Health and Well-being
Advisors and Health Coaches), nurses and others, single
points of access for the patient, shared electronic record
systems, increased use of care planning and changes to
structure and timings of GP appointments. The results
of our longitudinal P3C-OCT survey confirm significant
improvements in P3C, suggesting that SPQS has been
successful in its stated aims as a system lever for service
redesign aimed at the delivery of greater person-centred
and coordinated primary care.
While there is emerging evidence that P3C approaches
can improve outcomes (particularly for complexity/
Figure 2 Consultation time savings (top left), administrative GP time savings (top right) and non-GP administrative time
savings (bottom left). Percent responses for 51 practices enrolled in Somerset Practice Quality Scheme.GP,General Practice;
QOF,Quality and Outcomes Framework.
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8CloseJ, etal. BMJ Open 2019;9:e029721. doi:10.1136/bmjopen-2019-029721
Open access
multimorbidity),36 49 we could not establish that the
changes introduced via SPQS are leading to better
outcomes for patients. Patient experience is downstream
of the organisational changes occurring in Somerset, and
any detectable improvement in patient outcomes may
be delayed. The results of the patient P3C-EQ experi-
ence established a similar experience of care in Somerset
compared with the control QOF practices (who repre-
sent active, research engaged organisations, whereas
completion of the survey was mandatory for SPQS prac-
tices; see Methods). Similarly, comparison of practitioner
perspective of P3C to the control group revealed similar
experiences in SPQS versus the control practices. These
findings are broadly reflective of results from other initia-
tives, where—for example—patient-centred care for
multimorbid patients recently revealed mixed effects on
processes of care, but was not associated with measur-
able improvements in quality of life or other secondary
outcomes, with the authors concluding that the initia-
tive ‘supported changes in organisation more than it
supported changing the clinicians' attitudes on which
patient-centredness depends.’50
In reference to disbenefits, we could find no evidence of
increased admissions associated with SPQS. However, ITS
did establish trend changes in admissions in non-SPQS
Somerset practices (eg, those practices that retained the
QOF contract). A significant increase was observed in
admissions with a primary diagnosis of AMI and Diabetes,
and a significant decrease observed for those with a
primary diagnosis of Stroke. It is, however, unlikely that
relatively minor changes to QOF in the years 2014/15 and
2015/1651 52 have led to these observed trend changes in
emergency admission.
While the time series did not establish any disbenefits in
SPQS practices, earlier evaluation of SPQS established that
deincentivisation of QOF leads to inconsistent recording
of QOF data. Subsequently, analysis of QOF scores have
little utility in assessing the quality of care in Somerset.31
This paucity of data represents a major disbenefit of QOF
deincentivisation: one of the primary benefits of QOF has
been the widespread recording of clinical activities1 and
availability of GP data and research.6 7 It is not currently
clear how ‘quality’ could be assessed in the post-QOF
landscape—a question that has major implications for
research, evaluation, healthcare management.
Limitation of the study
The ability to draw firm conclusions from this study was
limited by several factors. Due to time and resource pres-
sures on GP in the UK, we struggled to recruit controls
from within the same county (Somerset) or matched
controls from the region. As an alternative, we obtained
Figure 3 Results of interrupted time-series analysis. The four graphs show the ITS for the four ACSCs (from left to right,
top to bottom, the graphs are: Acute Myocardial Infarction (AMI), Chronic Obstructive Pulmonary Disease (COPD), Diabetes
and Stroke). Data starts at April 2011 and ends at January 2017. The SPQS contract was live from June 2014 (ie, intervention
start time, indicated by vertical dashed line). Y-axis gives the number of admissions, normalised as admissions per month per
practice. Black circles indicate the average number of emergency admissions in each month for SPQS practices; white circles
are average admissions for QOF Somerset practices. The regression lines preintervention and postintervention are shown
unbroken (for SPQS) and dashed (for QOF Somerset practices). All changes between preintervention and postintervention
between SPQS and QOF practices are non-signicant (see online supplementary le 4).ACSCs,ambulatory care sensitive
conditions; ITS,interrupted time-series analysis; QOF,Quality and Outcomes Framework; SPQS,Somerset Practice Quality
Scheme.
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Open access
non-matched controls from the region. These repre-
sented a biased cohort of research-engaged practices. We
could not detect improvements in experiences of health-
care professionals or patients—this could be because
the intervention had no effect on these outcomes, the
instruments were not sensitive enough, the controls were
unsuitable or changes to patient/practitioner experi-
ences were somewhat distal to the intervention. A further
limitation of the study methods was that P3C-OCT was
only administered to control practices at the second time-
point, meaning that we cannot determine if significant
improvements of P3C-OCT score in SPQS practices might
also have been present in controls.
Implications for the future
While previous calls for the removal of QOF in England53
have not been reiterated, recent policy has moved towards
a reformed, streamlined version of QOF.54 55 With QOF
continuing to evolve, lessons from SPQS have implica-
tions for UK policy. We have previously made a number
of suggestions for the future landscape of QOF.47 48 These
include retaining limited components of QOF (eg, those
elements that are desirable by GPs; ‘QOF-Lite’), the
development of novel systematic data capture (including
GP contact data) or collaboration on an overhauled, inte-
grated recall system that is specifically designed for effi-
cient management of multiple LTCs.47 48 GP, however, is
under huge time and resource pressures.56 Any proposed
alternatives will have to fulfil the primary requirements of
being a streamlined process for supporting coordination
of care, especially for those with complex health needs.
The recent national review of QOF concluded that QOF
should be reformed to become more person-centred,
create space for professionalism and optimally impact
wider population health and system resource utilisation.57
Author afliations
1Community and Primary Care Research Group, University of Plymouth, Plymouth,
UK
2Sociology, Philosophy and Anthropology Department, University of Exeter, Exeter,
UK
3Peninsula Schools of Medicine and Dentistry, University of Plymouth, Plymouth, UK
4NHS Somerset Clinical Commissioning Group, Yeovil, UK
5South West Academic Health Science Network, Exeter, UK
6Psychology, University of Plymouth, Plymouth, UK
Acknowledgements This research was supported by the National Institute for
Health Research (NIHR) Collaboration for Leadership in Applied Health Research
and Care South West Peninsula. The views expressed are those of the author(s) and
not necessarily those of the NHS, the NIHR or the Department of Health and Social
Care. Funding for this evaluation was also provided South West Academic Health
Sciences Network (SWAHSN). We would also like to extend a very grateful thanks
to all the healthcare professionals and patients who gave their precious time to
support this evaluation.
Contributors JC corresponded with partaking practices, collected data, analysed
data and compiled manuscript. BF input, validated and analysed data. HW
corresponded with partaking practices and collected data. JH corresponded with
partaking practices and collected data. WL supported the Interrupted Time Series
analysis. RBy aided study design and conception. MB corresponded with partaking
practices and data collection. LW helped with study design, data collection and
corresponded with partaking practices. RBl collected and analysed data for Hospital
Episode Statistics. LH corresponded with partaking practices and collected data.
HL designed and oversaw the study from inception to completion. All authors read,
contributed to and approved the manuscript.
Funding This research was supported by the National Institute for Health Research
(NIHR) Collaboration for Leadership in Applied Health Research and Care South
West Peninsula. Funding for this evaluation was provided by South West Academic
Health Sciences Network (SWAHSN). BF was supported by additional funding from
the University of Gothenburg Centre for Person-centred Care (GPCC)
Competing interests None declared.
Patient consent for publication Not required.
Ethics approval Ethical clearance was obtained from the Plymouth University
Ethics Committees (FREC). All participants were given an information pack about
the study and gave informed consent.
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement All data relevant to the study are included in the article or
uploaded as supplementary information.
Open access This is an open access article distributed in accordance with the
Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which
permits others to distribute, remix, adapt, build upon this work non-commercially,
and license their derivative works on different terms, provided the original work is
properly cited, appropriate credit is given, any changes made indicated, and the use
is non-commercial. See: http:// creativecommons. org/ licenses/ by- nc/ 4. 0/.
REFERENCES
1. Langdown C, Peckham S. The use of nancial incentives to help
improve health outcomes: is the quality and outcomes framework t
for purpose? A systematic review. J Public Health 2014;36:251–8.
2. Campbell SM, Reeves D, Kontopantelis E, et al. Effects of pay for
performance on the quality of primary care in England. N Engl J Med
2009;361:368–78.
3. Doran T, Kontopantelis E, Valderas JM, et al. Effect of nancial
incentives on incentivised and non-incentivised clinical activities:
longitudinal analysis of data from the UK Quality and Outcomes
Framework. BMJ 2011;342:d3590.
4. Fleetcroft R, Cookson R. Do the incentive payments in the new NHS
contract for primary care reect likely population health gains? J
Health Serv Res Policy 2006;11:27–31.
5. Kontopantelis E, Reeves D, Valderas JM, et al. Recorded quality
of primary care for patients with diabetes in England before and
after the introduction of a nancial incentive scheme: a longitudinal
observational study. BMJ Qual Saf 2013;22:53–64.
6. McShane M, Mitchell E. Person centred coordinated care: where
does the QOF point us? BMJ 2015;350:h2540.
7. Staa TP, Goldacre B, Gulliford M, et al. Pragmatic randomised trials
using routine electronic health records: putting them to the test. BMJ
2012;344:e55.
8. A Century of Change. 1999 researchbriengs. les. parliament. uk/
documents/ RP99- 111/ RP99- 111. pdf.
9. Department of Health. Long Term Conditions Compendium of
Information. 3rd edn, 2012 https:// assets. publishing. service. gov. uk/
government/ uploads/ system/ uploads/ attachment_ data/ le/ 216528/
dh_ 134486. pdf.
10. Coulter A, Entwistle VA, Eccles A, et al. Cochrane Consumers
and Communication Group. Personalised care planning for adults
with chronic or long-term health conditions. In: The Cochrane
Collaboration. 85. Chichester, UK: John Wiley & Sons, Ltd, 2015.
11. Peckham S, Wallace A. Pay for performance schemes in primary
care: what have we learnt? Qual Prim Care 2010;18:111–6.
12. Kontopantelis E, Springate DA, Ashworth M, et al. Investigating the
relationship between quality of primary care and premature mortality
in England: a spatial whole-population study. BMJ 2015;350:h904.
13. Siriwardena AN. The ethics of pay-for-performance. Qual Prim Care
2014;22:53–5.
14. Checkland K, Harrison S, McDonald R, et al. Biomedicine, holism
and general medical practice: responses to the 2004 General
Practitioner contract. Sociol Health Illn 2008;30:788–803.
15. Petersen LA, Woodard LD, Urech T, et al. Does pay-for-performance
improve the quality of health care? Ann Intern Med 2006;145:265–72.
16. Christianson J. Financial incentives, healthcare providers and quality
improvements. 2007.
17. Campbell SM, Kontopantelis E, Reeves D, et al. Changes in patient
experiences of primary care during health service reforms in England
between 2003 and 2007. Ann Fam Med 2010;8:499–506.
on 23 July 2019 by guest. Protected by copyright.http://bmjopen.bmj.com/BMJ Open: first published as 10.1136/bmjopen-2019-029721 on 23 July 2019. Downloaded from
10 CloseJ, etal. BMJ Open 2019;9:e029721. doi:10.1136/bmjopen-2019-029721
Open access
18. Maisey S, Steel N, Marsh R, et al. Effects of payment for
performance in primary care: qualitative interview study. J Health
Serv Res Policy 2008;13:133–9.
19. Saultz JW, Albedaiwi W. Interpersonal continuity of care and patient
satisfaction: a critical review. Ann Fam Med 2004;2:445–51.
20. Gillam SJ, Siriwardena AN, Steel N. Pay-for-performance in the
United Kingdom: impact of the quality and outcomes framework: a
systematic review. Ann Fam Med 2012;10:461–8.
21. Blackburn P. QOF to end in ‘bold, overdue step’ welcomed by GPs.
Br Med Assoc 2016 https://www. bma. org. uk/ news/ 2016/ october/
qof- to- end- in- bold- overdue- step- welcomed- by- gps.
22. Millett C, Majeed A, Huckvale C, et al. Going local: devolving national
pay for performance programmes. BMJ 2011;342:c7085.
23. Lloyd HM, Pearson M, Sheaff R, et al. Collaborative action for
person-centred coordinated care (P3C): an approach to support
the development of a comprehensive system-wide solution to
fragmented care. Health Res Policy Syst 2017;15:98.
24. Somerset LMC. Somerset Practice Quality Scheme. https://www.
somersetlmc. co. uk/ some rset prac tice qual itys cheme.
25. Five Year Foward View. 2014.
26. Close J, Witts L, Horrell JL, et al. Evaluation of the Somerset Practice
Quality Scheme (SPQS): PHASE 2. http:// p3c. org. uk/ SPQS_ Phase2_
ExecSummary. pdf.
27. South Somerset Symphony Programme. https://www. england. nhs.
uk/ ourwork/ new- care- models/ vanguards/ care- models/ primary-
acute- sites/ south- somerset/.
28. Symphony Integrated Healtchare. http://www. symp hony inte grat edhe
althcare. com/.
29. Somerset Village Agents Service. http:// somersetrcc. org. uk/ our_
work/ supporting- individuals/ somerset- village- agents- project/.
30. Health Connections Mendip. https:// heal thco nnec tion smendip.
org/.
31. Lloyd H. Evaluation of the Somerset Practice Quality Scheme
(SPQS). 2015 http://www. swahsn. com/ wp- content/ uploads/ 2016/ 06/
Evaluation- of- the- Somerset- Practice- Quality- Scheme- July- 2015. pdf
http:// www. webcitation. org/ 6s3E0utpO.
32. Sugavanam T, Fosh B, Close J, et al. Codesigning a Measure of
Person-Centred Coordinated Care to Capture the Experience
of the Patient: The Development of the P3CEQ. J Patient Exp
2018;5:201–11.
33. Horrell J, Lloyd H, Sugavanam T, et al. Creating and facilitating
change for Person-Centred Coordinated Care (P3C): The
development of the Organisational Change Tool (P3C-OCT). Health
Expect 2018;21.
34. House of Care model – background. 2016 https://www. england. nhs.
uk/ resources/ resources- for- ccgs/ out- frwrk/ dom- 2/ house- of- care/
house- care- mod/.
35. A narrative for Person-Centred Coordinated Care. 2013 http://
www. nationalvoices. org. uk/ sites/ www. nationalvoices. org. uk/ les/
what_ patients_ want_ from_ integration_ national_ voices_ paper. pdf
(Accessed 31 Jan 2016).
36. Harding E, Wait S, Scrutton J. The State of Play in Person Centred
Care. 2015 http://www. heal thpo licy part nership. com/ wp- content/
uploads/ State- of- play- in- person- centred- care- full- report- Dec- 11-
2015. pdf.
37. Lloyd H, Wheat H, Horrell J, et al. Patient-Reported Measures for
Person-Centered Coordinated Care: a comparative domain map and
web-based compendium for Supporting Policy Development and
Implementation. J Med Internet Res 2018;20:e54.
38. Sugavanam T, Lloyd H, Horrell JL, et al. The Development of the
P3CEQ: a Generic Measure to Probe Person Centred Coordinated
Care. Health Qual Life Outcomes Rev 2016.
39. Lloyd H, Fosh B, Whalley B, et al. Validation of the person-centred
coordinated care experience questionnaire (P3CEQ). Int J Qual
Health Care 2018 (Published Dec 2018).
40. Dow B, Fearn M, Haralambous B, et al. Development and initial
testing of the Person-Centred Health Care for Older Adults Survey.
Int Psychogeriatr 2013;25:1065–76.
41. Royal College of General Practitioners. Collaborative Care and
Support Planning Guidance. http://www. rcgp. org. uk/ clinical-
and- research/ resources/ toolkits/ collaborative- care- and- support-
planning- toolkit. aspx.
42. Olsson LE, Jakobsson Ung E, Swedberg K, et al. Efcacy of person-
centred care as an intervention in controlled trials - a systematic
review. J Clin Nurs 2013;22:456–65.
43. Fors A, Ekman I, Taft C, et al. Person-centred care after acute
coronary syndrome, from hospital to primary care - A randomised
controlled trial. Int J Cardiol 2015;187:693–9.
44. Horrell JL, Sugavanam T, Close J, et al. Creating and Facilitating
Change for Person Centred Coordinated Care (P3C): The
Development of the Organisational Change Tool (P3C-OCT).
Implement Sci Rev 2016.
45. Linden A. Conducting interrupted time-series analysis for single- and
multiple-group comparisons. Stata J 2015;15:480–500.
46. Peters M, Crocker H, Jenkinson C, et al. The routine collection
of patient-reported outcome measures (PROMs) for long-
term conditions in primary care: a cohort survey. BMJ Open
2014;4:e003968.
47. Close J, Byng R, Valderas JM, et al. Quality after the QOF? Br J Gen
Pract.
48. Close J, Valderas JM, Byng R, et al. Adapting QOF to focus on
wellbeing and health. BMJ 2017;359:j5541.
49. Richards T, Coulter A, Wicks P. Time to deliver patient centred care.
BMJ 2015;350:h530.
50. Salisbury C, Man MS, Bower P, et al. Management of multimorbidity
using a patient-centred care model: a pragmatic cluster-randomised
trial of the 3D approach. Lancet 2018;392:41–50.
51. Changes to QOF 2014/15. http://www. nhsemployers. org/-/ media/
Employers/ Documents/ Primary- care- contracts/ QOF/ 2014- 15/
Summary- of- changes- to- QOF- 14- 15- England- only. pdf? la= en& hash=
3F34 6851 ACED EF66 54FA FC33 57B4 7314 19B462ED.
52. Changes to QOF 2015/16. http://www. nhsemployers. org/-/ media/
Employers/ Documents/ Primary- care- contracts/ QOF/ 2014- 15/
Summary- of- changes- to- QOF- 1516. pdf? la= en& hash= 9125 2299
83CF 5DE4 4134 D5EF DA70 A58B E7E76658.
53. Bostock N. GPC backs ‘bold step’ as Simon Stevens says QOF has
reached end of the road. GP Online 2016.
54. Mahase E. QOF will be reformed to remove ‘unnecessary indicators’.
Pulse 2019.
55. Wickware C. Quarter of QOF indicators to be scrapped under new
proposals. Pulse 2018.
56. Baird B, Charles A, Honeyman M, et al. Understanding pressures in
general practice:King’S Fund. 2016 https:// pdfs. semanticscholar.
org/ b187/ cb50 f66c 1357 95c9 3864 5c8a a1e2 c428719a. pdf (Accessed
23 Mar 2017).
57. NHS. Report of the Review of the Quality and Outcomes Framework
in England. https://www. england. nhs. uk/ publication/ report- of- the-
review- of- the- quality- and- outcomes- framework- in- england/.
on 23 July 2019 by guest. Protected by copyright.http://bmjopen.bmj.com/BMJ Open: first published as 10.1136/bmjopen-2019-029721 on 23 July 2019. Downloaded from
... Directing resources towards coordinated care was the aim of the Somerset Practice Quality Scheme reported by Close et al., in 2019(Close et al., 2019. Ultimately, time savings and MDT improvements were recorded, and decreased administrative work was appreciated by disincentivising quality and outcome framework targets (QOFs) and redirecting resources to target complex patients with multi-morbidities. ...
... Directing resources towards coordinated care was the aim of the Somerset Practice Quality Scheme reported by Close et al., in 2019(Close et al., 2019. Ultimately, time savings and MDT improvements were recorded, and decreased administrative work was appreciated by disincentivising quality and outcome framework targets (QOFs) and redirecting resources to target complex patients with multi-morbidities. ...
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Objective The potential for data collected in general practice to be linked and used to address health system challenges of maintaining quality care, accessibility and safety, including pandemic support, has led to an increased interest in public acceptability of data sharing, however practitioners have rarely been asked to share their opinions on the topic. This paper attempts to gain an understanding of general practitioner’s perceptions on sharing routinely collected data for the purposes of healthcare planning and research. It also compares findings with data sharing perceptions in an international context. Materials and methods A mixed methods approach combining an initial online survey followed by face-to-face interviews (before and during COVID-19), designed to identify the barriers and facilitators to sharing data, were conducted on a cross sectional convenience sample of general practitioners across Western Australia (WA). Results Eighty online surveys and ten face-to-face interviews with general practitioners were conducted from November 2020 – May 2021. Although respondents overwhelmingly identified the importance of population health research, their willingness to participate in data sharing programs was determined by a perception of trust associated with the organisation collecting and analysing shared data; a clearly defined purpose and process of collected data; including a governance structure providing confidence in the data sharing initiative simultaneously enabling a process of data sovereignty and autonomy. Discussion Results indicate strong agreement around the importance of sharing patient’s medical data for population and health research and planning. Concerns pertaining to lack of trust, governance and secondary use of data continue to be a setback to data sharing with implications for primary care business models being raised. Conclusion To further increase general practitioner’s confidence in sharing their clinical data, efforts should be directed towards implementing a robust data governance structure with an emphasis on transparency and representative stakeholder inclusion as well as identifying the role of government and government funded organisations, as well as building trust with the entities collecting and analysing the data.
... The reports provided by the PHN allow general practices to review and improve their data quality, with some practitioners hesitantly anticipating these payments to ultimately be associated to outcomes as was implemented in the UK with the Quality Outcomes Framework (QOF). Although the bene ts of the QOF are yet to be determined (32,33), the adoption of a pay for performance program was unpopular with many practitioners at the time, which could be a contributing factor to the low uptake of voluntary secondary use data programs. A similar observation was shared amongst several Australian practitioners that participated in a national study related to the PIP QI implementation (34) generating division and confusion across general practice in participation of the program. ...
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Objective The potential for data collected in general practice to be linked and used to address health system challenges of maintaining quality care, accessibility and safety, including pandemic support, has led to an increased interest in public acceptability of data sharing, however practitioners have rarely been asked to share their opinions on the topic. This paper attempts to gain an understanding of general practitioners’ perceptions on routinely sharing practice data for both population health planning and healthcare research both from an Australian and international perspective. Materials and Methods A mixed methods approach combining an initial online survey followed by face-to-face interviews (before and during COVID-19), designed to identify the barriers and facilitators to sharing data, were conducted on a representative sample of general practitioners across Western Australia (WA). Results Eighty online surveys and ten face-to-face interviews with general practitioners were conducted from Nov 2020 – May 2021. Although respondents overwhelmingly identified the importance of population health research, their willingness to participate in data sharing programs was determined by a perception of trust associated with the organisation collecting and analysing shared data; a clearly defined purpose and process of collected data; including a governance structure providing confidence in the data sharing initiative simultaneously enabling a process of data sovereignty and autonomy. Discussion Results indicate strong agreement around the importance of sharing patient’s medical data for population and health research and planning. Concerns pertaining to lack of trust, governance and secondary use of data continue to be a setback to data sharing with implications for primary care business models being raised. Conclusion To further increase general practitioner’s confidence in sharing their clinical data, efforts should be directed towards implementing a robust data governance structure with an emphasis on transparency and representative stakeholder inclusion as well as identifying the role of government and government funded organisations, as well as building trust with the entities collecting and analysing the data.
... Previously reported examples of communication initiatives that may enhance integration include improved eRefferal (Bouamrane and Mair, 2014) and electronic discharge (Murphy et al., 2017) systems. Likewise, Close et al. (2019) demonstrated improved care coordination with their 'Somerset Practice Quality Scheme', and the country of New Zealand showed considerable gains with regards to responsibility and accountability among care providers as a result of alliances between District Health Boards and Primary Health Organisations (Gauld, 2014). The implementation and evaluation of similar initiatives globally may yield benefits. ...
Article
Purpose “Integrated care” (IC) is an approach to health and social care delivery that aims to prevent problems arising from fragmented care systems. The collective content of the IC literature, whilst valuable, has become extensive and wide-ranging to such a degree that knowing what is most important in IC is a challenge. This study aims to address this issue. Design/methodology/approach A scoping review was conducted using Arksey and O'Malley's framework to determine IC priority areas. Findings Twenty-one papers relevant to the research question were identified. These included studies from many geographical regions, encompassing several study designs and a range of populations and sample sizes. The findings identified four priority areas that should be considered when designing and implementing IC models: (1) communication, (2) coordination, collaboration and cooperation (CCC), (3) responsibility and accountability and (4) a population approach. Multiple elements were identified within these priorities, all of which are important to ensuring successful and sustained integration of care. These included education, efficiency, patient centredness, safety, trust and time. Originality/value The study's findings bring clarity and definition to what has become an increasingly extensive and wide-ranging body of work on the topic of IC. Future research should evaluate the implementation of these priorities in care settings.
... The averaging step was performed in 47 (78%) of the studies. One example of this is illustrated by Close et al. 18 (Table 3). However, descriptions about how they tested and handled autocorrelation were sporadic. ...
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Objective Missing data can produce biased estimates in interrupted time series (ITS) analyses. We reviewed recent ITS investigations on health topics for determining 1) the data management strategies and statistical analysis performed, 2) how often missing data were considered and, if so, how they were evaluated, reported and handled. Study Design and Setting This was a scoping review following standard recommendations from the PRISMA Extension for Scoping Reviews. We included a random sample of all ITS studies that assessed any intervention relevant to health care (eg, policies or programmes) with individual-level data, published in 2019, with abstracts indexed on MEDLINE. Results From 732 studies identified, we finally reviewed 60. Reporting of missing data was rare. Data aggregation, statistical tools for modelling population-level data and complete case analyses were preferred, but these can lead to bias when data are missing at random. Seasonality and other time-dependent confounders were rarely accounted for and, when they were, missing data implications were typically ignored. Very few studies reflected on the consequences of missing data. Conclusion Handling and reporting of missing data in recent ITS studies performed for health research have many shortcomings compared with best practice.
... Primary data were collected between 2014 and 2018 during mixed methods formative evaluations of five primary care interventions, which aimed to promote PCC for individuals with multi-morbidity living in the community. The evaluations assessed patient outcomes in health and well-being, implementation barriers and facilitators and addressed the research question of whether the interventions were aligned with the GPCC routines (Close et al., 2019;Lloyd et al., 2015;Sugavanam et al., 2018). Approval was obtained from the Health Research Authority to integrate and publish work from the five evaluations as part of our programme of work (Ref: 18/NE/0143, Tyne and Wear). ...
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Evidence is emerging of the potential of person-centred approaches to create partnerships between professionals and patients while also containing healthcare costs. This is important for enhancing outcomes in individuals with complex needs, who consistently report poor experiences with care. The shift towards person-centred care (PCC) is, however, a radical departure from the norm, with increased expectations of both professional and patient. Although there have been studies on the ways in which health care professionals can modify practice to enhance PCC, not all patients welcome changes to their care delivery or understand the aim of the new approach. Without engagement and understanding from the patient, a PCC approach will fail to initiate. Few studies explore how, why and in what circumstances patients become more involved in their care and what professionals can do to enhance participation. We conducted a secondary analysis of qualitative data to examine this issue. Data were collected between 2014 and 2018 from primary care-based PCC projects across the southwest of England. Supported by people with experience (practitioners and those receiving treatment), theory building workshops developed an explanatory framework that identified contextual factors and mechanisms likely to contribute to effective engagement. Our results show that engagement in a care partnership is achieved through trust and a patient's sense of candidacy. Shared understanding of purpose, clarity of expectations and power sharing were found to facilitate trusted relationships between professional and patient and encourage candidacy. Only then is it possible to develop goals that are meaningful to the patient. Our theory of engagement applies to professionals and patients alike but places the initial burden of responsibility on those who hold the most power: the professional and the system. This theory has the potential to explain patient engagement in PCC and a range of other service interventions, treatments and intervention research.
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Background Countries are adapting their health and social care systems to better meet the needs of growing populations with (multiple) chronic conditions. To guide this process, assessment of the ‘patient experience’ is becoming increasingly important. For this purpose, the Person‐Centred Coordinated Care Experience Questionnaire (P3CEQ) was developed in the United Kingdom, and translated into several languages. Aim This study aimed to assess the internal and construct validity of the Dutch P3CEQ to capture the experience of person‐centred coordinated care of people with chronic conditions in the Netherlands. Participants and Methods Adults with chronic conditions (N = 1098) completed the Dutch P3CEQ, measures of health literacy and patient activation, and reported the use and perceived quality of care services. Data analysis included Principal Component and reliability analysis (internal validity), analysis of variance and Student's T‐tests (construct validity). Results The two‐component structure found was pretty much the same as in the UK validation study. Sociodemographic correlates also resembled those found in the United Kingdom. Women, persons who were less educated, less health‐literate or less activated experienced less person‐centred coordinated care. P3CEQ scores correlated positively with general practitioner performance scores and quality ratings of the total care received. Conclusion The Dutch P3CEQ is a valid instrument to assess the experience of person‐centred coordinated care among people with chronic conditions in the Netherlands. Awareness of inequity and more attention to communication skills in professional training are needed to ensure that care professionals better recognize the needs of women, lower educated or less health‐literate persons, and improve their experiences of care. Patient Contribution The P3CEQ has been developed in collaboration with a range of stakeholders. Eighteen persons with (multiple) chronic conditions participated as patient representatives and codesign experts in (four) codesign workshops. Other patient representatives participated in cognitive testing of the English‐language instrument. The usability of the P3CEQ to capture the experience of person‐centred coordinated care of older persons has been examined by interviewing 228 older European service users, including 13 living in the Netherlands, as part of the SUSTAIN project. More than a thousand persons with chronic conditions participated in the validation study of the Dutch P3CEQ.
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Background Using computer software in general practice to predict patient risk of emergency hospital admission has been widely advocated, despite limited evidence about effects. In a trial evaluating the introduction of a Predictive Risk Stratification Model (PRISM), statistically significant increases in emergency hospital admissions and use of other NHS services were reported without evidence of benefits to patients or the NHS. Aim To explore GPs’ and practice managers’ experiences of incorporating PRISM into routine practice. Design and setting Semi-structured interviews were carried out with GPs and practice managers in 18 practices in rural, urban, and suburban areas of south Wales. Method Interviews (30–90 min) were conducted at 3–6 months after gaining PRISM access, and ∼18 months later. Data were analysed thematically using Normalisation Process Theory. Results Responders ( n = 22) reported that the decision to use PRISM was based mainly on fulfilling Quality and Outcomes Framework incentives. Most applied it to <0.5% practice patients over a few weeks. Using PRISM entailed undertaking technical tasks, sharing information in practice meetings, and making small-scale changes to patient care. Use was inhibited by the model not being integrated with practice systems. Most participants doubted any large-scale impact, but did cite examples of the impact on individual patient care and reported increased awareness of patients at high risk of emergency admission to hospital. Conclusion Qualitative results suggest mixed views of predictive risk stratification in general practice and raised awareness of highest-risk patients potentially affecting rates of unplanned hospital attendance and admissions. To inform future policy, decision makers need more information about implementation and effects of emergency admission risk stratification tools in primary and community settings.
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Higher incidences of fractures are seen in people with type 1 diabetes (T1D), but knowledge on different fracture sites is sparse. We found a higher incidence mainly for distal fracture sites in people with T1D compared to controls. It must be further studied which fractures attributed to the higher incidence rates (IRs) at specific sites.IntroductionPeople with T1D have a higher incidence of fractures compared to the general population. However, sparse knowledge exists on the incidence rates of individual fracture sites. Therefore, we examined the incidence of various fracture sites in people with newly treated T1D compared to matched controls.Methods All people from the UK Clinical Practice Research Datalink GOLD (1987–2017), of all ages with a T1D diagnosis code (n = 6381), were included. People with T1D were matched by year of birth, sex, and practice to controls (n = 6381). Fracture IRs and incidence rate ratios (IRRs) were calculated. Analyses were stratified by fracture site and sex.ResultsThe IR of all fractures was significantly higher in people with T1D compared to controls (IRR: 1.39 (CI95%: 1.24–1.55)). Compared to controls, the IRR for people with T1D was higher for several fracture sites including carpal (IRR: 1.41 (CI95%: 1.14–1.75)), clavicle (IRR: 2.10 (CI95%: 1.18–3.74)), foot (IRR: 1.70 (CI95%: 1.23–2.36)), humerus (IRR: 1.46 (CI95%: 1.04–2.05)), and tibia/fibula (IRR: 1.67 CI95%: 1.08–2.59)). In women with T1D, higher IRs were seen at the ankle (IRR: 2.25 (CI95%: 1.10–4.56)) and foot (IRR: 2.11 (CI95%: 1.27–3.50)), whereas in men with T1D, higher IRs were seen for carpal (IRR: 1.45 (CI95%: 1.14–1.86)), clavicle (IRR: 2.13 (CI95%: 1.13–4.02)), and humerus (IRR: 1.77 (CI95%: 1.10–2.83)) fractures.Conclusion The incidence of carpal, clavicle, foot, humerus, and tibia/fibula fractures was higher in newly treated T1D, but there was no difference at other fracture sites compared to controls. Therefore, the higher incidence of fractures in newly treated people with T1D has been found mainly for distal fracture sites.
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Background: Measuring patient experiences of healthcare is increasingly emphasized as a mechanism to measure, benchmark and drive quality improvement, clinical effectiveness and patient safety at both national and local NHS level. Person-centred coordinated care (P3C) is the conjunction of two constructs; person-centred care and care coordination. It is a complex intervention requiring support for changes to organizational structure and the behaviour of professionals and patients. P3C can be defined as: 'care and support that is guided by and organized effectively around the needs and preferences of individuals'. Despite the vast array of PRMS available, remarkably few tools have been designed that efficiently probe the core domains of P3C. This paper presents the psychometric properties of a newly developed PREM to evaluate P3C from a patient perspective. Methods: A customized EMIS search was conducted at 72 GP practices across the South West (Somerset, Devon and Cornwall) to identify 100 patients with 1 or more LTCs, and are frequent users of primary healthcare services. Partial Credit Rasch Modelling was conducted to identify dimensionality and internal consistency. Ecological validity and sensitivity to change were assessed as part of intervention designed to improve P3C in adults with multiple long-term conditions; comparisons were drawn between the P3CEQ and qualitative data. Results: Response rate for the P3CEQ was 32.82%. A two-factor model was identified. Rasch analysis confirmed unidimensionality of each factor (using infit MSQ values between 0.5 and 1.5). High internal consistency was established for both factors; For the Person-centred scale Cronbach's Alpha = 0.829, Person separation = 0.756 and for the coordination scale Cronbach's alpha = 0.783, person separation = 0.672. Conclusions: The P3CEQ is a valid and reliable measure of P3C. The P3C is considered to have strong face, construct and ecological validity, with demonstrable sensitivity to change in a primary healthcare intervention.
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Background: The management of people with multiple chronic conditions challenges health-care systems designed around single conditions. There is international consensus that care for multimorbidity should be patient-centred, focus on quality of life, and promote self-management towards agreed goals. However, there is little evidence about the effectiveness of this approach. Our hypothesis was that the patient-centred, so-called 3D approach (based on dimensions of health, depression, and drugs) for patients with multimorbidity would improve their health-related quality of life, which is the ultimate aim of the 3D intervention. Methods: We did this pragmatic cluster-randomised trial in general practices in England and Scotland. Practices were randomly allocated to continue usual care (17 practices) or to provide 6-monthly comprehensive 3D reviews, incorporating patient-centred strategies that reflected international consensus on best care (16 practices). Randomisation was computer-generated, stratified by area, and minimised by practice deprivation and list size. Adults with three or more chronic conditions were recruited. The primary outcome was quality of life (assessed with EQ-5D-5L) after 15 months' follow-up. Participants were not masked to group assignment, but analysis of outcomes was blinded. We analysed the primary outcome in the intention-to-treat population, with missing data being multiply imputed. This trial is registered as an International Standard Randomised Controlled Trial, number ISRCTN06180958. Findings: Between May 20, 2015, and Dec 31, 2015, we recruited 1546 patients from 33 practices and randomly assigned them to receive the intervention (n=797) or usual care (n=749). In our intention-to-treat analysis, there was no difference between trial groups in the primary outcome of quality of life (adjusted difference in mean EQ-5D-5L 0·00, 95% CI -0·02 to 0·02; p=0·93). 78 patients died, and the deaths were not considered as related to the intervention. Interpretation: To our knowledge, this trial is the largest investigation of the international consensus about optimal management of multimorbidity. The 3D intervention did not improve patients' quality of life. Funding: National Institute for Health Research.
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Background Person-centred coordinated care (P3C) is a priority for stakeholders (ie, patients, carers, professionals, policy makers). As a part of the development of an evaluation framework for P3C, we set out to identify patient-reported experience measures (PREMs) suitable for routine measurement and feedback during the development of services. Methods A rapid review of the literature was undertaken to identity existing PREMs suitable for the probing person-centred and/or coordinated care. Of 74 measures identified, 7 met our inclusion criteria. We critically examined these against core domains and subdomains of P3C. Measures were then presented to stakeholders in codesign workshops to explore acceptability, utility, and their strengths/weaknesses. Results The Long-Term Condition 6 questionnaire was preferred for its short length, utility, and tone. However, it lacked key questions in each core domain, and in response to requests from our codesign group, new questions were added to cover consideration as a whole person, coordination, care plans, carer involvement, and a single coordinator. Cognitive interviews, on-going codesign, and mapping to core P3C domains resulted in the refinement of the questionnaire to 11 items with 1 trigger question. The 11-item modified version was renamed the P3C Experiences Questionnaire. Conclusions Due to a dearth of brief measures available to capture people’s experience of P3C for routine practice, an existing measure was modified using an iterative process of adaption and validation through codesign workshops. Next steps include psychometric validation and modification for people with dementia and learning difficulties.
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Background Fragmented care results in poor outcomes for individuals with complexity of need. Person-centred coordinated care (P3C) is perceived to be a potential solution, but an absence of accessible evidence and the lack of a scalable ‘blue print’ mean that services are ‘experimenting’ with new models of care with little guidance and support. This paper presents an approach to the implementation of P3C using collaborative action, providing examples of early developments across this programme of work, the core aim of which is to accelerate the spread and adoption of P3C in United Kingdom primary care settings. Methods Two centrally funded United Kingdom organisations (South West Collaboration for Leadership in Applied Health Research and Care and South West Academic Health Science Network) are leading this initiative to narrow the gap between research and practice in this urgent area of improvement through a programme of service change, evaluation and research. Multi-stakeholder engagement and co-design are core to the approach. A whole system measurement framework combines outcomes of importance to patients, practitioners and health organisations. Iterative and multi-level feedback helps to shape service change while collecting practice-based data to generate implementation knowledge for the delivery of P3C. The role of the research team is proving vital to support informed change and challenge organisational practice. The bidirectional flow of knowledge and evidence relies on the transitional positioning of researchers and research organisations. Results Extensive engagement and embedded researchers have led to strong collaborations across the region. Practice is beginning to show signs of change and data flow and exchange is taking place. However, working in this way is not without its challenges; progress has been slow in the development of a linked data set to allow us to assess impact innovations from a cost perspective. Trust is vital, takes time to establish and is dependent on the exchange of services and interactions. If collaborative action can foster P3C it will require sustained commitment from both research and practice. This approach is a radical departure from how policy, research and practice traditionally work, but one that we argue is now necessary to deal with the most complex health and social problems.
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Background: Patient-reported measure (PRM) questionnaires were originally used in research to measure outcomes of intervention studies. They have now evolved into a diverse family of tools measuring a range of constructs including quality of life and experiences of care. Current health and social care policy increasingly advocates their use for embedding the patient voice into service redesign through new models of care such as person-centered coordinated care (P3C). If chosen carefully and used efficiently, these tools can help improve care delivery through a variety of novel ways, including system-level feedback for health care management and commissioning. Support and guidance on how to use these tools would be critical to achieve these goals. Objective: The objective of this study was to develop evidence-based guidance and support for the use of P3C-PRMs in health and social care policy through identification of PRMs that can be used to enhance the development of P3C, mapping P3C-PRMs against an existing model of domains of P3C, and integration and organization of the information in a user-friendly Web-based database. Methods: A pragmatic approach was used for the systematic identification of candidate P3C-PRMs, which aimed at balancing comprehensiveness and feasibility. This utilized a number of resources, including existing compendiums, peer-reviewed and gray literature (using a flexible search strategy), and stakeholder engagement (which included guidance for relevant clinical areas). A subset of those candidate measures (meeting prespecified eligibility criteria) was then mapped against a theoretical model of P3C, facilitating classification of the construct being measured and the subsequent generation of shortlists for generic P3C measures, specific aspects of P3C (eg, communication or decision making), and condition-specific measures (eg, diabetes, cancer) in priority areas, as highlighted by stakeholders. Results: In total, 328 P3C-PRMs were identified, which were used to populate a freely available Web-based database. Of these, 63 P3C-PRMs met the eligibility criteria for shortlisting and were classified according to their measurement constructs and mapped against the theoretical P3C model. We identified tools with the best coverage of P3C, thereby providing evidence of their content validity as outcome measures for new models of care. Transitions and medications were 2 areas currently poorly covered by existing measures. All the information is currently available at a user-friendly web-based portal (p3c.org.uk), which includes all relevant information on each measure, such as the constructs targeted and links to relevant literature, in addition to shortlists according to relevant constructs. Conclusions: A detailed compendium of P3C-PRMs has been developed using a pragmatic systematic approach supported by stakeholder engagement. Our user-friendly suite of tools is designed to act as a portal to the world of PRMs for P3C, and have utility for a broad audience, including (but not limited to) health care commissioners, managers, and researchers.
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Background: Person Centred Coordinated Care (P3C) is a UK priority for patients, carers, professionals, commissioners and policy makers. Services are developing a range of approaches to deliver this care with a lack of tools to guide implementation. Methodology: A scoping review and critical examination of current policy, key literature and NHS guidelines, together with stakeholder involvement led to the identification of domains, subdomains and component activities (processes and behaviours) required to deliver P3C. These were validated through codesign with stakeholders via a series of workshops and cognitive interviews. Results: Six core domains of P3C were identified as follows: (i) my goals, (ii) care planning, (iii) transitions, (iv) decision making (v), information and communication and (vi) organizational support activities. These were populated by 29 core subdomains (question items). A number of response codes (components) to each question provide examples of the processes and activities that can be actioned to achieve each core subdomain of P3C. Conclusion: The P3C-OCT provides a coherent approach to monitoring progress and supporting practice development towards P3C. It can be used to generate a shared understanding of the core domains of P3C at a service delivery level, and support reorganization of care for those with complex needs. The tool can reliably detect change over time, as demonstrated in a sample of 40 UK general practices. It is currently being used in four UK evaluations of new models of care and being further developed as a training tool for the delivery of P3C.
Technical Report
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An evaluation of the SPQS pilot was conducted by the SW Academic Health Science Network (AHSN) and the SW Peninsula CLAHRC (Collaboration for Leadership in Applied Health Research and Care) on behalf of NHS England. SPQS arose out of concern felt by some general practices in Somerset that person centred and coordinated care for people with complex conditions is hampered by current GP contracting conditions. Fifty-five out of 75 general practice providers in Somerset joined the SPQS which allowed them to test an alternative to the Quality & Outcomes Framework (QOF) element of the General Medical Services contract. The SWAHSN and CLAHRC collaborative led by Dr Helen Lloyd and Louise Witts conducted primary and secondary research between November 2014 and July 2015 to explore the implementation of SPQS and any resultant changes in clinical and organizational behaviour following inception of the scheme. This report details our findings and suggests recommendations for the longitudinal evaluation of the SPQS and QOF.
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This is the protocol for a review and there is no abstract. The objectives are as follows: To assess the effects of personalised care planning for patients with long-term health conditions, as compared to forms of care in which active involvement of patients in treatment and management decisions (at least in goal setting and action planning) is not explicitly attempted or achieved. We will address the following primary research questions: Is personalised care planning effective for improving physical health (e.g. lipid measurements)? Is personalised care planning effective for improving psychological health (e.g. anxiety and depression)? Is personalised care planning effective for improving psychosocial health (e.g. quality of life)? Is personalised care planning effective for improving patients' capabilities for self-managing their condition? We will also look for evidence to address the following secondary research questions: Is personalised care planning effective for improving patients' health-related behaviours? How does personalised care planning impact on rates of use and costs of formal health services? What is the relative effectiveness of different types of intervention used to promote personalised care planning?