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Abstract

Background: Current daily general practice has become increasingly technical and somatically oriented (where attention to patients' feelings is decreased) due to an increase in protocol-based guidelines. Priorities in GP-patient communication have shifted from a focus on listening and empathy to task-oriented communication. Aim: To explore what barriers GPs experience when applying empathy in daily practice, and how these barriers are managed. Design and setting: Thirty Dutch GPs with sufficient heterogeneity in sex, age, type of practice, and rural or urban setting were interviewed. Method: The consolidated criteria for reporting qualitative research (COREQ) were applied. The verbatim transcripts were then analysed. Results: According to participating GPs, the current emphasis on protocol-driven care can be a significant barrier to genuineness in communication. Other potential barriers mentioned were time pressures and constraints, and dealing with patients displaying 'unruly behaviour' or those with personality disorders. GPs indicated that it can be difficult to balance emotional involvement and professional distance. Longer consulting times, smaller practice populations, and efficient practice organisation were described as practical solutions. In order to focus on a patient-as-person approach, GPs strongly suggested that deviating from guidelines should be possible when necessary as an element of good-quality care. Joining intercollegiate counselling groups was also discussed. Conclusion: In addition to practical solutions for barriers to behaving empathically, GPs indicated that they needed more freedom to balance working with protocols and guidelines, as well as a patient-as-person and patient-as-partner approach. This balance is necessary to remain connected with patients and to deliver care that is truly personal.
INTRODUCTION
Caring for the ‘whole person’ in a holistic
manner is at the foundation of primary
care and is regarded as a basic expertise
for GPs.1 ‘Whole-person care’ means
‘…
integrating a biomedical, psychological,
social, cultural and holistic knowledge of
the patient and community and applying this
understanding to practical care planning
through person-centred approaches …’
.2
However, this person-centred approach
is under pressure nowadays. Over the
past decades, priorities in doctor–patient
communication in everyday practice have
shifted, from focusing on listening and
empathy to task-oriented communication.3
As a result of protocol-based guidelines,
daily practice has become increasingly
technical and somatically oriented.4 A
biomedical mainstream of care may be
life-saving and health-promoting but it
risks neglecting the patient’s experiences
of illness; understanding this is essential
to ensure shared decision making based
on the individual patient’s perspective,
preferences, and needs,5–9 and contributes
to effective health care.10
The emphasis in general practice on
evidence-based and protocol-driven care,
and the observed reduction in viewing the
patient as an individual, has caused an
ideological debate.6,11,12 To achieve insight
into different factors playing a role in GP–
patient communication, models of the
medical consultation were constructed.9,13
In these models, empathy was regarded
as an important tool to establish a person-
centred approach. By empathy the authors
mean that a physician:14,15
understands the patient’s situation,
perspective, and feelings;
communicates that understanding and
checks its accuracy; and
acts on that understanding in a helpful,
therapeutic way.
Empathy implies a morally valuable
aspect, namely the recognition of the other
as the centre of their own experience.16
The effectiveness of empathy on specific
clinical outcomes for patients has been
widely proven17 and GPs view empathy as an
important element during consultations.18
However, so far there have been no thorough
studies into what barriers GPs experience in
applying empathy in daily practice and how
they manage these barriers, especially in
the light of the aforementioned changes in
communication in the medical consultation.
Therefore, this study aims to examine
barriers to GPs expressing empathy and
how they manage these barriers.
METHOD
Study design
This study was carried out in the
Netherlands where primary care is
Research
FAWM Derksen, GP, Department of Primary and
Community Care, Gender and Women’s Health;
TC olde Hartman, MD, GP, Department of Primary
and Community Care; ALM Lagro-Janssen, MD,
PhD, GP, Department of Primary and Community
Care, Gender and Women’s Health, Radboudumc,
Nijmegen, the Netherlands. JM Bensing, PhD,
professor, Department of Psychology, Faculty
of Social and Behavioural Sciences, Utrecht
University, NIVEL, Netherlands Institute for Health
Services Research, the Netherlands.
Address for correspondence
Frans Derksen, Department of Primary and
Community Care, Gender and Women’s Health,
Radboudumc, PO Box 9101, 6500 HB Nijmegen,
the Netherlands.
E-mail: Frans.Derksen@radboudumc.nl
Submitted: 3 April 2016; Editor’s response:
20 June 2016; final acceptance: 8 July 2016.
©British Journal of General Practice
This is the full-length article (published online
11 Oct 2016) of an abridged version published in
print. Cite this version as: Br J Gen Pract 2016;
DOI: 10.3399/bjgp16X687565
Frans AWM Derksen, Tim C olde Hartman, Jozien M Bensing and Antoine LM Lagro-Janssen
Managing barriers to empathy in the
clinical encounter:
a qualitative interview study with GPs
Abstract
Background
Current daily general practice has become
increasingly technical and somatically oriented
(where attention to patients’ feelings is decreased)
due to an increase in protocol-based guidelines.
Priorities in GP–patient communication have
shifted from a focus on listening and empathy to
task-oriented communication.
Aim
To explore what barriers GPs experience when
applying empathy in daily practice, and how
these barriers are managed.
Design and setting
Thirty Dutch GPs with sufficient heterogeneity
in sex, age, type of practice, and rural or urban
setting were interviewed.
Method
The consolidated criteria for reporting
qualitative research (COREQ) were applied. The
verbatim transcripts were then analysed.
Results
According to participating GPs, the current
emphasis on protocol-driven care can
be a significant barrier to genuineness in
communication. Other potential barriers
mentioned were time pressures and
constraints, and dealing with patients
displaying ‘unruly behaviour’ or those with
personality disorders. GPs indicated that it can
be difficult to balance emotional involvement
and professional distance. Longer consulting
times, smaller practice populations, and
efficient practice organisation were described
as practical solutions. In order to focus on
a patient-as-person approach, GPs strongly
suggested that deviating from guidelines should
be possible when necessary as an element
of good-quality care. Joining intercollegiate
counselling groups was also discussed.
Conclusion
In addition to practical solutions for barriers to
behaving empathically, GPs indicated that they
needed more freedom to balance working with
protocols and guidelines, as well as a patient-
as-person and patient-as-partner approach.
This balance is necessary to remain connected
with patients and to deliver care that is truly
personal.
Keywords
empathic behaviour; empathy; patient-centred
care; primary health care; protocol-driven care;
shared responsibility.
1 British Journal of General Practice, Online First 2016
delivered by a GP and where patients are
registered on their practice list. Most GPs
cooperate in first-line health centres where
they often help out with other GPs and
health professionals such as specialised
practice nurses, with practice assistants.
After medical school and internships, GP
residents follow 3 years of postgraduate
vocational training. Since 1989 the Dutch
College of GPs has published more than
100 standardised protocols on different
diseases prevalent in primary care.19
For this study GPs were interviewed
between June 2012 and January 2013.
In-depth interviews were performed because
they enable experiences in daily practice
and the meanings interviewees attribute
to them to be explored. Furthermore, they
clarify participants’ opinions about their
own priorities.20,21 The consolidated criteria
for reporting qualitative research (COREQ)
were applied.22
Preparation and participants
Thirty-one interviews were conducted.
To establish the appropriateness of the
questions, four test interviews were
performed by three authors before the
interviews; these were audiotaped and
discussed by the first author within the
research group.
Participants were recruited using a step-
by-step procedure. To avoid the possibility of
interviews taking place between people who
knew each other, a statistical employee
performed a systematic random sampling
from the NIVEL (Netherlands Institute for
Health Services Research) GP register
(which includes all practising Dutch GPs).
To produce a maximum variation sample,
characteristics such as age (<45, 45–55,
>55 years), sex, practice type (solo, being
one GP in a practice and duo being two, or
a group practice), and grade of urbanisation
were taken into account. A total number of
147 GPs were selected and approached by
letter, explaining the subject of the study and
the duration of the interview. Some weeks
after this letter was sent, the GPs were
contacted by telephone. After 100 telephone
calls, 31 GPs with sufficient variety in
the aforementioned characteristics had
consented to take part and signed an
informed consent form. The 47 GPs who
were not telephoned were placed on a
reserve list (Figure 1). Appointments were
made with the 31 GPs; anonymity and
confidentiality were guaranteed.
Data collection
The interviews were held face to face at
the GPs’ own practices and lasted between
45 and 70 minutes. All fieldwork was
conducted by one author with a background
in general practice who was an experienced
interviewer.
The interviews were based on an interview
guide formulated by the lead author and
based on literature and expert opinions
(Appendix 1). No repeat interviews were
carried out. At the end of each interview
the interviewee was given a short summary
and was asked if they agreed with it. All
interviews were recorded on audiotape
and transcribed verbatim (in Dutch). After
the first eight interviews, the interviewing
style was analysed. After this, more open-
ended questions were introduced to achieve
more probing interviews and more room for
reflection.
After 20 interviews it became clear that no
new issues were arising. Although the first
20 interviews approached various aspects
of empathy, the issue of barriers to empathy
and how to manage these turned out to be
the topic that came up the most. Therefore,
the final 10 interviews were used to focus
even more on the barriers GPs experienced
in applying empathy during consultations
and the way they managed these barriers.
Data analysis
To analyse the data, iterative content
analysis was employed.23 The systematic
examination of transcripts was undertaken
by the interviewer and two doctoral medical
students trained in qualitative analysis. This
team of researchers was formed to minimise
the influence of personal characteristics on
How this fits in
Priorities in GP–patient communication
have shifted from focusing on listening and
empathy to task-oriented communication
and protocol-driven care. The effectiveness
of empathy on specific clinical outcomes
for patients has been widely proven and
GPs appreciate empathy as an important
element during consultations. There are
limited data concerning what barriers
GPs experience in applying empathy in
daily practice and how they manage these
barriers. This study indicates that GPs use
different ways to manage barriers in order
to preserve the role of empathy in GP–
patient communication. For example, GPs
may deviate from the recommendations
described in the guidelines, to deliver high-
quality person-centred care and to show
genuine interest in their patients. More
work is needed to resolve the barriers
experienced by GPs.
British Journal of General Practice, Online First 2016 2
the analysis and thus the possibility of
bias. Atlas.ti (version 7) was used to assist
with registering, searching, and coding the
data. The researchers, independently of one
another, read and re-read the transcripts,
and met regularly to discuss the subjects
and interpretations. In addition, after the
third, twelfth, and thirtieth interview, the
coding process was discussed with one
author acting as supervisor. By using axial
and selective coding, codes and super
codes were attributed to text segments.
Codes referring to the same phenomenon
were grouped in categories and significant
themes were made explicit. These themes
formed the structure of the final result;
quotations were used to explicate the
themes. The original quotations were in
Dutch and were translated into English with
the help of a native speaker.
RESULTS
Overview of the results
Thirty-one GPs participated but, because
one recording failed, the study was based
on 30 interviews. The demographics of the
participants show variability concerning sex,
age, degree of urbanisation, and practice
type (Table 1). An algorithm showing the
procedure by which participants were
recruited and information about those GPs
not willing to participate is presented in
Figure 1.
GPs indicated that they encounter barriers
when they apply empathic behaviour in daily
practice. However, because they consider
empathy in the clinical encounter to be
very important, they emphasised ways to
manage these barriers. Four main barriers
were distinguished:
a conflict between protocol-driven care
and showing genuine interest;
a tension between professional distance
and emotional involvement;
patients behaviour threatening
connectedness within the GP–patient
communication; and
a conflict between time pressures
and constraints and the GPs’ need for
personal space, peace, and need to
regroup after each encounter.
These barriers and the ways that GPs
manage them so that they can continue to
show empathy are described below.
Protocol-driven care versus showing
genuine interest
GPs considered empathy to be an important
prerequisite for humane care. However,
they found that guideline-driven care results
in a disease-centred emphasis rather
than a person-centred way of thinking
and working. The increased number of
guidelines and bureaucratic requirements
were seen as significant barriers to behaving
empathically during the consultation.
Six GPs also mentioned that therapeutic
regimens and ‘programmed asking’ (a
list of standard questions) from evidence-
based guidelines and protocols hamper
Data
147 GPs selected and sent a letter
100 GPs were telephoned
47 GPs put on reserve list
31 GPs consented to participate
and 30 interviews
were recorded
Drop out
13 GPs did not call back
19 GPs had no time for participation
2 GPs no affinity for the subject
2 GPs bad health
33 GPs wrong address or
telephone number
Figure 1. Participants flowchart.
Table 1. Characteristics of the
participating GPs
Characteristics of the 31a
participating GPs
N
(%)
Sex
Male 14 (45)
Female 17 (55)
Age, years
<45 13 (42)
45–55 10 (32)
>55 8 (26)
Practice type
Sole 8 (26)
Two partners (duo) 14 (45)
Group 9 (29)
Urbanisation
Rural area 12 (39)
Urban area 19 (61)
Mean experience as GP, 16 (2–33)
years (range)
a
Thirty-one GPs participated but, because one
recording failed, the study was based on 30
interviews.
3 British Journal of General Practice, Online First 2016
genuine reactions, interest, and creativity,
thereby reducing the effectiveness of their
empathic behaviour. This programmed way
of working in the current medical system
was identified as an external barrier to
providing empathic care:
‘… that we’re working in an extremely
protocolised way, in fact being the doormat
of the health insurance companies,
that when I witness a resident doing a
cardiovascular risk protocol, reading out
30 questions to the patient and looking at
the computer screen all the time, and I tell
them they were doing that, they will hate it
as much as I do, but that is the danger of
working with protocols … and it causes you
to completely miss out on contact with the
patient, and empathy suffers enormously, I
think.’
(GP 12, male, age 40 years)
‘In my experience, the more you’re doing
your own thing, like I want this and I need
that, the more you’re doing that, the less
you really listen. That way you run the risk
of missing things in a patient and later you
think, if I had just kept quiet for a moment
and listened, if I had just taken a little bit
more time, I would have picked up on things
that would have changed the situation and
the patient would have been more satisfied.’
(GP 3, male, age 58 years)
‘People with diabetes, for instance, they
have to record about 73 items in a list
and I thoroughly dislike that, because you’re
spending most of your time looking at the
computer screen instead of at the patient,
so, yes, the increase in administrative tasks
does influence my communication …’
(GP 2,
male, age 40 years)
To maintain their humane, empathic
behaviour, GPs suggested that it is more
effective and natural to combine the
recommendations in the guidelines with
questions about the patient’s personal
situation. GPs indicated that they considered
patients as equal human beings, and that
they wanted to treat them with respect
and to show genuine interest, for example,
by telephoning patients proactively in case
of hospital admissions or life events, or
by reflecting on previous situations.
Furthermore, according to GPs, it helps
to mutually value each other’s expertise:
the GP with regard to medical knowledge
and the patient with regard to their specific
situation and illness experiences. This
patient-as-person approach contributed, in
their view, to an innately humane form of
contact, enhancing mutual understanding,
shared responsibility, and commitment, and
it helped to develop a trusting relationship:
‘Empathy also means asking further
questions: how are the kids, or if you know
the husband is recovering from an illness,
how is your husband doing? When the
woman is visiting you to have her blood
pressure checked, it is interesting to let go
of protocol for a minute and ask after her
husband, thereby showing interest in her
context and broadening the picture; I can
see that it’s greatly appreciated, and it also
gives me a lot of information about how
she’s doing.’
(GP 13, male, age 37 years)
‘Empathy also involves a certain disposition,
an outlook on how you want to deal with
a person … I believe that patients can put
forward their own expertise, to which I add
mine, and together we can then explore
the problem and get to work … it’s like
building a foundation for cooperation with
the patient.’
(GP 23, female, age 55 years)
Professional distance versus emotional
involvement
The risks of getting too close to and
emotionally involved with patients emerged
during the interviews, with GPs concluding
that such relationships may interfere with
their objective judgement with regard to
diagnosis and treatment. At the same
time, GPs stated that they needed a certain
level of involvement in order to behave
empathically. Furthermore, according
to GPs, when involvement becomes too
intense, they risk developing burnout:
‘That sometimes you start to cry when
something is really tough, that has
happened to me a few times. It makes me
think less clearly and that is not good, so
for me that’s a boundary I don’t want to
cross. I think it’s fine to be sympathetic with
someone, but I shouldn’t start blubbering
along, that’s not what I’m there for and I
don’t want to go there, and I think I can be
more empathetic when I’m not eaten up by
it.’
(GP 9, female, age 55 years)
GPs mentioned ways to protect their
professionalism, for example, by setting
clear boundaries and creating distance in
their doctor–patient contact by behaving in
a business-like way.
Furthermore, they were convinced that
intercollegiate counselling groups offer an
excellent opportunity to discuss this issue
in depth:
‘Of course, there are moments when
British Journal of General Practice, Online First 2016 4
there is a lot of pressure, for example
during palliative care … when a different
connection with someone develops, you
must try to remain professional, which is
quite difficult and I try not to show that to
my patient. When necessary I can show
my emotions to my partner at home or
during counselling with colleagues.’
(GP 17,
female, age 36 years)
‘There is a boundary and I can work with
that. I think it’s OK to have emotions, as
a GP it’s OK to show you have feelings
and you’re not a business-like person, you
can express your feelings, but there is a
boundary and that is your professionalism.’
(GP 18, female, age 34 years)
Patients’ behaviour threatening
connectedness within GP–patient
communication
GPs indicated that certain patients
characteristics can hamper GP–patient
contact and complicate spontaneous and
honest empathic communication. GPs
specifically mentioned problems with the
‘unruly behaviour’ of some patients, such
as those who argue aggressively with
the reception staff, patients who keep an
emotional distance, those with personality
disorders, or patients who cross moral
boundaries such as actively engaging in
sexual abuse or drug dealing:
‘They sometimes fend it off, they build up
a wall, like “What is it, what do they want.”
That occurs pretty regularly here, with older
men of the rough-diamond type, they don’t
say much but do come, and I think that can
be tough, but if you approach them more
quietly, you do sometimes get through to
them, but I do find it tough sometimes.’
(GP
17, female, age 36 years)
‘When I get the feeling … it does happen
that you have to deal with someone and you
just don’t click. “You can’t please them all.”
So there are people you just don’t get along
with, but that usually filters itself out, people
switch to another GP and so they should.’
(GP 5, male, age 65 years)
As a prerequisite for empathic behaviour
in these situations, GPs emphasised that
they need to be able to communicate in
a free and honest way. They stated that
their residency training in communication
styles and intervision courses (Balint
groups or coaching groups) help them to
stay on speaking terms with these patients,
preserving a trusting doctor–patient
relationship:
‘Really wishing the other person to have
a good consultation, even if they enter all
grumpy. It can be pretty tough in a situation
like that to find out what is bothering them.’
(GP 23, female, age 55 years)
‘What I want to say is that it doesn’t simply
happen by “switching on”, so yes, I’m all for
supervision and intervision for GPs. In my
opinion it is very important to experience
personal growth, you could say that
“growing and pruning” is my motto.’
(GP 8,
female, age 37 years)
Everyday time pressures and constraints
versus GPs’ personal space and peace
GPs indicated that it is more difficult to
pay empathic attention to the patient when
the consultation schedule is overloaded.
Overcrowded waiting rooms and large
numbers of patients get in the way of empathy.
Disturbance to the consultation itself, for
example, because of incoming telephone
calls, has a negative influence on GPs’
attention and communication. Furthermore,
GPs indicated that personal factors also play
an important role in hindering empathic
attention. For example, reduced physical
fitness, personal difficulties, or a recent night
shift can result in a decrease in a GP’s ability
to show empathy:
‘Well, it is affected by how you feel, how
well you’ve slept … you do have an off-day
sometimes, and if you’re doing consultations
with a splitting headache, you know, it can
be difficult to be really empathic; so yes, it
does have to do with the condition you’re in
yourself.’
(GP 29, female, age 64 years)
‘Being distracted, someone entering
when you’re distracted it’s hard to focus on
a conversation, whether it be from being
tired, or busy, or having all sorts of thoughts
running through your head, there are phone
calls and messages all the time. I think all
those things can interfere.’
(GP 9, female,
age 45 years)
To manage these barriers, GPs stated that
they try to plan longer consultation times for
specific patients. In addition, they indicated
that having a thoughtful and committed
practice assistant who predicts patients’
required consultation times helps them
apply empathy. Furthermore, optimising
the organisation of the consultation hours
by structured deliberations between GPs
and practice assistants was regarded by
some as useful. Others saw a reduction
in the number of registered patients as an
opportunity to create extra time:
5 British Journal of General Practice, Online First 2016
‘Wouldn’t it be an idea to switch to smaller
practices and to spend 15 minutes on each
patient, while keeping your income that
way you’d actually facilitate empathy by
keeping incomes at the same level … I
think there’s certainly a case for setting
a 15-minute consultation time for many
complaints.’
(GP 12, male, age 40 years)
‘So that is an important prerequisite, you
know, having peace of mind, things running
smoothly in the practice. Your staff need to
understand when they can interrupt you and
when they cannot, and that some questions
are worth an interruption and others are
not; that’s a matter of fine-tuning things.’
(GP 16, male, age 45 years)
DISCUSSION
Summary
This study describes the barriers GPs
encounter when applying empathy in
daily practice and how they manage these
barriers. GPs perceive the current emphasis
on protocol-driven care with guidelines,
bureaucratic requirements, pay-for-
performance, and quality-of-care indicators
to be an important barrier to remaining
genuinely patient-oriented during the
consultation. Although the government is
not driving these changes, health insurance
organisations use, for example, blood levels
(an HbA1c value from the diabetes protocol)
as quality-of-care indicators.
To manage these barriers GPs try to
combine a patient-as-person approach with
the recommendations given in the guidelines.
GPs mentioned overcrowded office hours
and disturbances in consultations as
factors hampering empathic behaviour.
Longer consulting times, smaller practice
populations, and efficient practice
organisation were described as practical
solutions. Furthermore, GPs argued that
approaching patients as partners with
mutual expertise can result in shared
responsibility. Conversely, they described
how having to deal with transgressive
behaviour in patients, those exhibiting
unruly behaviour, those with personality
disorders, and those keeping an emotional
distance presented a barrier to displaying
empathy in a spontaneous way. GPs also
discussed their own internal difficulties
in balancing emotional involvement and
professional distance.
Strengths and limitations
GPs’ experiences with barriers to
empathetic behaviour and the ways they
manage these barriers during consultations
are, to the best of the authors’ knowledge,
hitherto under-researched aspects of GPs’
everyday practice. Previous studies have
explored the views of GP trainees, medical
educators, and hospital specialists, or have
approached the subject theoretically.9,24
Being interviewed by a colleague has
possibly affected the data collection.25
Negatively, it could result in a lack of
objectivity and possible bias, and, with
respect to the participants, the possibility
of them providing ‘desirable’ answers.
Positively, being interviewed by a trustworthy
colleague may have led GPs to give more
personally detailed information.
Empathy can be considered a ‘container’
concept. Some interviewees merged it
with aspects of general communication or
patient-centredness. Qualitative studies are
limited in their generalisability. However,
compared with quantitative studies, they can
provide richer insights. By using a cyclical
and iterative way of collecting and analysing
data, ‘progressive focusing’ on the barriers
that GPs encounter and on the way these
barriers are managed was realised. The
GPs who participated did so as volunteers.
Accepting a time-consuming interview may
imply that GPs had some sympathy with
the subject and may have under-exposed
negative thoughts. Therefore, caution
should be taken in generalising conclusions
beyond this study.
Although the qualitative method is
appropriate to explore and clarify GPs’
opinions, it does not provide insight into
the GPs’ actual behaviour. However, tape-
recording the interviews, multiple coding
during analysis, and member checks added
to the rigour of the study.
Comparison with existing literature
Previous research has pointed out that
communication styles of GPs have changed
from focusing on listening and empathy
towards task-oriented communication.26 It
can be assumed that this task-oriented
communication originates from the ever-
expanding numbers of standardised
protocols and guidelines. Recently, health
insurance companies have focused on the
GP guidelines which were not intended
to be used in this way27 — in order to define
quality-of-care indicators for primary care.
These indicators are mostly somatically
oriented. Van Os and colleagues pointed
out that merely following guidelines is not
enough to deliver good-quality care.28 The
best outcome will be gained when doctors
follow the professional guidelines and are
able to build a trustful and personal doctor–
patient relationship with their patients as
well. Therefore, evaluating the quality of
British Journal of General Practice, Online First 2016 6
health care simply by measuring adherence
to the guidelines is not appropriate at all.10,29
This explains the tension GPs face when
they try to deliver good-quality health care.
It is also in line with what patients expect:
they count on a humane and personal
approach from their GP, who shows an
affective attitude and who is aware of the
latest evidence available, and who takes the
needs and consequences of their illness
into account.10,30,31 In this regard patients
have previously identified certain types
of non-verbal behaviour of GPs, such as
being occupied by the computer screen, as
negative.31
Furthermore, this study highlights that
empathy helps GPs to consider patients as
so-called cooperating experts, an approach
with shared responsibility and expertise,
enabling tailor-made solutions. Previous
research has defined the mutual-expert
approach as partnership-building, a working
alliance, or as achieving collaboration.9,32,33
To choose the best course of action for
the individual patient, Greenhalgh and
colleagues argue that evidence-based
medicine should reintroduce its founding
principles, that is, a strong interpersonal,
humanistic, and professional relationship,
empathetic listening, and a collaboration
between an expert physician and an expert
patient.34 GPs expressed exactly the same
opinion in this study.
Preserving a more emotionally
involved GP–patient relationship does
have consequences. GPs in this study
experienced tension between behaving
empathically and remaining professional.
They described how engaging empathy
brings with it a need to create a balance
between involvement and preserving some
distance. The authors are not aware of
recent general-practice-oriented studies
analysing GPs’ experiences regarding these
aspects. Ethicists such as Gelhaus point
to the depth of emotional participation
of GPs in enabling adequate empathic
understanding.35 Previous theoretically
oriented studies describe similar ideas
about working on the boundary of self–
other awareness. It is stated that mental
flexibility, self-critical analysis, and self-
knowledge help in maintaining a clear self–
other separation. Self-knowledge allows
one to have a controlled, balanced, and
efficient regulatory process of empathy-
related responding.35–37
Implications for research and practice
Given the results of this study, there is a
need to get quantitative insight into the
prevalence and relevance of barriers to
empathic behaviour in daily practice. The
consequences of overly biomedical protocol-
driven care especially should be studied in
depth, as well as the influence of the role
of health insurance companies on patient-
centred care.38 The urgency of resolving the
barriers experienced by GPs should also be
determined. Further research in this area
may be helpful to convince policymakers
and health insurance companies to take
action and to stimulate positive conditions
for empathic behaviour in GPs. Because
patients are considered important judges
on healthcare issues,39,40 and research into
patient outcomes has been performed,41
the authors advocate more detailed
research into patients’ experiences and
opinions with regard to GPs’ empathetic
behaviour. Insight into patients’ points of
view gives physicians the opportunity to act
on them.42
According to GPs, empathy is a requisite
for high-quality person-centred care, GP
education should then focus on this to
show students and residents the added
value of empathetic behaviour. Teaching
and practising this behaviour should be
embedded explicitly in the current teaching
models on GP–patient communication.
A focus on personal development and
the introduction of humanities within GP
education and residency may preserve
and strengthen empathy as a humanising
communication skill in general practice.43
Furthermore, continuous medical education
and organising intercollegiate counselling
groups may help GPs in preserving an
effective GP–patient relationship and in
managing involvement with patients, while
at the same time maintaining professional
objectivity.
GPs described different kinds of barriers
to their empathetic behaviour. They pointed
out different ways to manage these barriers
to preserve the role of empathy in GP–
patient communication. In a healthcare
system in which protocol-driven care and
quality indicators have become increasingly
important, GPs consider empathy as a
fundamental tool in their patient-as-
person and patient-as-partner approach.
GPs in this study also stated that it is
sometimes necessary to deviate from the
recommendations described in the
guidelines, in order to deliver high-quality
person-centred care and to show a genuine
interest in their patients.
Funding
This research received no specific grant
from any funding agency in public,
commercial, or not-for-profit sectors.
Ethical approval
Interviewing healthcare professionals with
respect to professional beliefs does not
require approval of an ethics committee
according to Dutch legislation.
Provenance
Freely submitted; externally peer reviewed.
Competing interests
The authors have declared no competing
interests.
Acknowledgements
The authors thank the participants who were
interviewed and the two medical students,
Sascha Kuiper and Milou Van Meerendonk.
The authors also thank Judith Tijman,
translator, and Rosamund Havardre, native
English speaker.
Discuss this article
Contribute and read comments about this
article: bjgp.org/letters
7 British Journal of General Practice, Online First 2016
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British Journal of General Practice, Online First 2016 8
Appendix 1. Interview guidelines
Introduction
My name is Frans Derksen and I am a retired GP. I conduct scientific research on empathy in GP–patient communication. As I mentioned in my letter of introduction,
I am interested in the personal opinions, experiences, and perceptions of both GPs and patients on the role of empathy during consultations. This part of my research
focuses on GPs; in a later phase the opinions of patients will be investigated. I have chosen face-to-face interviews as the method to collect the data for this research.
Names and addresses of GPs to approach were obtained through taking a sample from the NIVEL GP file. You were in that sample and you have shown yourself
willing to get involved with this research. Thank you for that. In the interview I would like to talk to you about the following topics: background information about your
practice, your views on general practice, your views on empathy in communication with the patient, and, finally, the conditions you believe play a role when working with
empathy. I would like to stress that in this interview there will be plenty of space for your thoughts. My aim is to let the interview take up to about 1 hour (15 minutes per
topic). As we have agreed, I will audiotape the entire interview and I will make some notes and check my list of questions. Everything you say is strictly confidential; the
research findings will be anonymised.
Do you have any questions at this point?
Some questions to gain background information on your practice: Do you work in an urban or a rural area? When did you start working as a GP? Do you train GP
students? Could you tell me something about your practice organisation (sole, two partners, group) and about your patient population?
A. First your own general views on general practice:
1. At some point in your life you chose to become a GP. How did you come to that choice?
2. What aspects would you describe as the core of your job?
3. What important developments have you noticed during the time you have been a GP?
4. What do you think of these developments?
5. How do you feel now about your choice to become a GP, taking into account the developments that you just outlined?
B. Now I would like to talk to you about empathy:
1. What does the concept of empathy mean to you as a GP?
2. Can you specify the way you use it? How do you use it? What do you find difficult or easy? Do you feel capable of providing it and are you skilled at it? Can you give me
any examples? How do you experience empathy yourself?
3. Does the special feature of the GP with its longstanding contact with the patient play a role in the implementation of empathy?
4. There is a lot of talk about sex differences in the use of empathy. Do you have any opinion on that?
5. How much importance do you attach to the use of empathy in your relationship with your patients? Can you indicate this on a scale of 1 to 10? What if you relate it
specifically to evidence-based medicine and/or protocol-based medicine?
6. Can you give any examples of your personal experiences with empathy during the consultation? Were they positive or negative?
7. In general, GPs are highly esteemed by their patients; if they complain about anything it is a lack of communication skills and empathy in their GP. Do you recognise
this? Can you tell me anything about that?
8. How do you think patients experience empathy?
C. Preconditions and barriers to empathy:
1. Do you think there are preconditions and barriers to being empathic? If so, what are they?
2. Is it possible to facilitate its use? How? Can GP training play a role in this? What was it like during your own training?
3. Do health insurance companies and the government show enough interest in the role of empathy in your opinion?
4. Is there enough, or too much, attention being paid to empathy in medical literature, during refresher courses, and by professional associations? If so, how could this be
improved?
D Final question:
1. We have talked at length about your views on general practice and empathy. Would you like to add anything, anything that we have not covered, but that in your view is
important in this context?
These were the questions I wanted to put to you. Thank you very much for replying and for your cooperation.
9 British Journal of General Practice, Online First 2016
... A recent systematic review identifying the predictors of physician compassion and related constructs (Pavlova et al., 2021) found that compassion was lower for less educated patients (Batley et al., 2016;Bertakis & Azari, 2011) and minoritized racial and ethnic groups (Foo et al., 2017;Park et al., 2018;Porthe et al., 2018), but more likely for patients reporting higher socio-economic status (Batley et al., 2016;Bertakis & Azari, 2011) as well as the elderly and children (Bayne et al., 2013;Zandbelt et al., 2007). Unsurprisingly, crosssectional evidence also suggests that compassion is greater for patients who are cooperative or thankful (Picard et al., 2016;Porthe et al., 2018;Street Jr et al., 2007) but is challenged by patients seen as 'difficult'-aggressive or angry, demanding or having crossed some moral boundary (e.g., drunk drivers, drug dealers or perpetrators of family violence; Derksen et al., 2016Derksen et al., , 2018Sandikci et al., 2017). In some views, 'patients who are rude, demanding or difficult suck the oxygen from compassion' (Fernando et al., 2016). ...
... However, while the two vignette scenarios were designed to depict comparably difficult patients, our findings suggest that more urgent patient presentations were also perceived as less difficult. Exploratory analyses showed that greater patient difficulty was associated with lower compassion, particularly for the less urgent patient, in line with prior studies (Derksen et al., 2016(Derksen et al., , 2018Fernando et al., 2016;Sandikci et al., 2017;Wang et al., 2022). ...
... Studies show that health care professionals often experience anxiety when managing complex and possibly ineffective treatments, or having a risk of misdiagnosing someone or appearing incompetent in front of colleagues (Sutherland & Cooper, 1992;Tallentire et al., 2017). Consequently, this might trigger 'fight or flight' response (Gilbert, 2020) and maladaptive coping (i.e., avoidance, detachment and other blaming; Davidsen & Fosgerau, 2014;Peng et al., 2018), explaining why both patients who are perceived as non-urgent (Batley et al., 2016;Bayne et al., 2013;Bishop et al., 2014;Zandbelt et al., 2007) and those perceived as more 'difficult' often elicit lower compassion response (Derksen et al., 2016(Derksen et al., , 2018Fernando et al., 2016;Sandikci et al., 2017), and why non-urgent patients are often pejoratively labelled (e.g., 'attention-seekers' and 'time-wasters'; Batley et al., 2016;Bayne et al., 2013;Sandikci et al., 2017;Stein, 1986). Depending on a particular context, such a dynamic may then be suggestive of compassion operating via different behavioural mechanisms, a possibility we give greater attention to below. ...
Article
Full-text available
Objectives: To experimentally investigate whether more urgent patient presentations elicit greater compassion from health care professionals than less urgent, facilitating future research and thinking to address systemic barriers to compassion in health care. Design: This is a pre-registered online study with an experimental, within-subjects repeated-measure study design. Two clinical vignettes that systematically varied the urgency of patient presentation were utilized. Both vignettes depicted a patient with difficult behaviours typically associated with lower compassion. Methods: Health care professionals (doctors, nurses and allied health practitioners) recruited from all 20 District Health Boards across Aotearoa/New Zealand completed two vignettes in a counterbalanced order. Paired-sample t-tests were used to test the effect of the presentation urgency on indices of compassion. Results: A total of 939 participants completed the vignettes (20% doctors, 47%, nurses and 33% allied health professionals). As expected, participants reported greater care and motivation to help the more urgent patient. However, the more urgent patient was also perceived as less difficult, and exploratory analyses showed that perceived patient difficulty was associated with lower caring and motivation to help, particularly in the less urgent patient. Conclusions: This is the first work to experimentally test the relationship between the urgency of patient presentation and compassion in health care. Although the association between urgency and difficulty is complex, our findings are consonant with evolutionary views in which urgent distress elicits greater compassion. A system-wide orientation towards efficiency and urgency may exacerbate this 'bias' which must be addressed to ensure more equitable compassion in health care.
... Systematic reviews (Pavlova et al. 2021;Wang et al. 2022) outline a growing body of qualitative evidence showing that healthcare-specific beliefs about compassion may impact the expression of it. For example, believing that compassion can help achieve better treatment outcomes and make one's work more enjoyable predicts reports of greater compassion (Derksen et al. 2016;Swendiman et al. 2019;Uygur, Brown, and Herbert 2019). Conversely, believing that compassion negatively affects objectivity and professionalism, career progression or mental health predicts reports of lower compassion (Carmel and Glick 1996;Lyness 1993;Stratta, Riding, and Baker 2016). ...
... Finally, and potentially related to the previous comment, there was a lack of an association between the belief that compassion is harmful and ratings of compassion. In other words, healthcare professionals might "feel the fear and do it anyway," as it seems likely that a belief in compassion's importance may outweigh the healthcare push for objectivity or professionalism (Derksen et al. 2016). In other words, healthcare professionals are likely able to compromise some professional and personal outcomes in order to avoid distress from the inability to express compassion (Sinclair et al. 2017). ...
Article
Full-text available
Aims To develop and preliminarily validate a measure of beliefs about compassion in health care and assess whether and which beliefs may predict compassion. Design Pre‐registered cross‐sectional online survey study with a repeated‐measures vignette component. Method Exploratory and Confirmatory Factor analyses were performed on a split sample of 890 healthcare professionals in Aotearoa New Zealand (NZ). Links with fears of compassion for others, burnout, trait compassion, compassion competency and ability and self‐efficacy were used to assess convergent and divergent validity. Linear mixed model regression analyses were used to assess relationships between beliefs and compassion. In writing this report, we adhered to the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) guidelines. Results Four‐factor structure featuring three negative (compassion as harmful, not useful, draining) and one positive (compassion is important) type of beliefs was established. Confirmatory factor analysis indicated a good fit and subscales indicated good measures of validity. Internal consistency was achieved for the subset of beliefs (harmful, not useful). Regression analyses indicated negative effects of the belief that compassion is draining on caring, motivation to help and compassion overall; negative effects of the belief that compassion is not useful on the motivation to help and a positive effect of the belief that compassion is important on caring and compassion overall. There was no effect of beliefs that compassion is harmful on compassion measures. Conclusion This report extends prior qualitative studies of beliefs about compassion in a large healthcare sample, offering a way to measure these potentially malleable factors that might be targeted in education, interventions and future research. Patient or Public Contribution The study was designed in consultation with healthcare and compassion research professionals, including substantial input from Indigenous Māori healthcare professionals.
... Indeed, PWUD are first of all people with multiple vulnerabilities who need a human and person-centered approach. The participants expressed needs that correspond to the definition of empathy used by Derksen et al. [33]: "empathy as the competence of a physician to understand the patient's situation, perspective, and feelings; to communicate that understanding and check its accuracy; and to act on that understanding in a helpful therapeutic way". Indeed, it can increase patient satisfaction, reduce stress and anxiety, and lead to better clinical outcomes [33]. ...
... The participants expressed needs that correspond to the definition of empathy used by Derksen et al. [33]: "empathy as the competence of a physician to understand the patient's situation, perspective, and feelings; to communicate that understanding and check its accuracy; and to act on that understanding in a helpful therapeutic way". Indeed, it can increase patient satisfaction, reduce stress and anxiety, and lead to better clinical outcomes [33]. Furthermore, the participants emphasized the importance of not being stigmatized or categorized by doctors. ...
Article
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Background People who use illicit drugs cumulate medical and psychosocial vulnerabilities, justifying a rounded health approach. Both caregivers and patients can form barriers to accessing care, leading to inadequate care. This study aimed to identify the needs and expectations of such patients in general practice. Methods Qualitative research was conducted using semi-structured interviews with 23 people with illicit substance use disorder in Brussels in 2020. Multicentric recruitment was conducted to obtain a heterogeneous mix of sociodemographic profiles and care trajectories. Thematic analysis was performed using RQDA package software. Results Participants highlighted several vulnerabilities. These include the presence of significant self-stigmatization and guilt, sometimes to the extent of self-dehumanization, even after years of care, and overdoses masking suicide attempts and early memory disorders. Multiple substance use, smoking in almost all participants, and misuse of benzodiazepines were also noted. The majority of participants expressed the need for an open-minded, non-stigmatizing and empathic GP with a holistic approach that could guide them throughout their life course. The competencies of the GPs in the field of addiction seemed secondary to the participants. Knowledge and good collaboration with the mental health network were assets. Conclusion Participants expressed the need for GPs with good interpersonal skills, including a non-stigmatizing attitude. The care coordinator role of the GP was highlighted as a key element, as it was a holistic approach focusing on global health (including the social determinants of health) and not only on substance use disorders.
... Indeed, PWUD are rst of all people with multiple vulnerabilities who need a human and person-centered-approach. The participants expressed needs that correspond to the de nition of empathy used by Derksen et al. (33) : "empathy as the competence of a physician to understand the patient's situation, perspective, and feelings; to communicate that understanding and check its accuracy; and to act on that understanding in a helpful therapeutic way". Indeed it cans bring greater patient satisfaction, reduces stress and anxiety, and leads to better clinical outcomes (33). ...
... The participants expressed needs that correspond to the de nition of empathy used by Derksen et al. (33) : "empathy as the competence of a physician to understand the patient's situation, perspective, and feelings; to communicate that understanding and check its accuracy; and to act on that understanding in a helpful therapeutic way". Indeed it cans bring greater patient satisfaction, reduces stress and anxiety, and leads to better clinical outcomes (33). Furthermore, participants emphasized the importance of not being stigmatized or categorized by doctors. ...
Preprint
Full-text available
Background: People who use illicit drugs cumulate medical and psychosocial vulnerabilities which justify a rounded health approach. Both caregivers and patients can form barriers to accessing care which can lead to inadequate care. We tried with this study to identify the needs and expectations of these patients in general practice. Methods: Qualitative research using semi-structured interviews was conducted on 23 people with illicit substance use disorder in Brussels in 2020. A multicentric recruitment was performed to obtain a heterogeneous mix of socio-demographic profiles and care trajectories. A thematic analysis was performed using RQDA package software. Results: Several vulnerabilities were highlighted by the participants. These include the presence of significant self-stigmatization and guilt, sometimes to the extent of self-dehumanization even after years of care; overdoses masking suicide attempts and early memory disorders. Multiple substance use, smoking in almost all participants and significant misuse of benzodiazepines were also noted. The majority of participants expressed the need for an open-minded, non-stigmatizing and empathic GP with a holistic approach who could guide them throughout their life course. The competences of GPs in the field of addiction seemed secondary for the participants. Knowledge and good collaboration with the mental health network was an asset. Conclusion: The participants expressed the need for GPs with good interpersonal skills including a non-stigmatizing attitude. The care coordinator role of the GP was highlighted as a key element, as was a holistic approach focusing on global health (including the social determinants of health) and not only on the substance use disorder.
... Keine Angst vor Emotionen im Sprechzimmer! ▶ Tab. 2 WWSZ-Gesprächstechnik in der patientenzentrierten Kommunikation mit Beispielen [7, 14, 15].Merke Die PZK eignet sich vor allem für den Beziehungsaufbau, für eine ganzheitliche Exploration zur Hypothesenbildung und für stützende Gespräche.Wir gehen insbesondere bei der PZK als Behandelnde engere Beziehungen zu unseren Patientinnen/Patienten ein und investieren Zeit und Mühe[18]. Auch erleben wir zwischendurch Frustrationen, wenn unsere Beziehungsangebote nicht angenommen werden oder wir uns nicht genug abgrenzen können. Neben dem Erlernen spezifischer Techniken ist es wichtig, einen professionellen Umgang mit und eine Haltung zu dem Erleben der uns aufsuchenden Menschen zu finden. ...
... The extra time in a naturopathic consultation is used to take a full case history, explore the complex multifactorial needs of patients and provide an individualised approach to treatment [21]. Longer consultations have the potential to strengthen the patient-provider relationship by allowing a safe space for patients to speak freely, sharing of knowledge and involving patients' preferences in decision making [22,23]. ...
... Empathy in GP-patient interactions is a cornerstone of effective, high quality care, 38 though a number of barriers are known to prevent empathic communication in practice. 39 Few studies have explored strategies to preserve or increase empathy in practicing GPs, despite a wealth of research reporting these for medical students. Findings from this study may go some way to understanding the trajectory of empathy in GPs, as well as ways to enhance or maintain it over time. ...
Article
Phenomenon: There is a paucity of research reporting the experiences of general practitioner clinical educators. Providing education for students could lead to better clinical skills and greater job satisfaction for the educator. However, it could also result in increased stress and mental fatigue, adding to what is an already pressured situation in the current primary care climate. Clinical Debrief is a model of case-based learning with integrated supervision developed to prepare medical students for clinical practice. This study aimed to explore the experiences of general practitioners who facilitate Clinical Debrief. Approach: Eight general practitioner educators with experience of facilitating Clinical Debrief participated in semi-structured qualitative interviews. Results were analyzed using Reflexive Thematic Analysis, and four main themes were developed. Findings: Themes included: Personal enrichment: psychological "respite" and wellbeing; Professional enrichment: Clinical Debrief as a "two-way" door; Becoming a facilitator: a journey; and, Relationships in teaching: blurred boundaries and multiple roles. Insights: Being a Clinical Debrief facilitator had a transformative impact on the personal and professional lives of the GPs who participated in this study. The implications of these findings for individual GPs, their patients, and the wider healthcare system, are discussed.
... This result is contrary to study of persons with burnout who felt mistrust, misunderstood and rejected in health care encounters, by Engebretsen and Bjorbaekmo (2019). The differences with these results may result from person-centred care being overshadowed by overly result-oriented, time-limited and depersonalized care, as indicated in a study with general practitioners (Derksen et al., 2016). Furthermore, previous research based on the person's own perspectives highlights the importance of humanistic needs where the persons whole lifeworld is considered (Alsén et al., 2020(Alsén et al., , 2022Arman et al., 2011;Engebretsen & Bjorbaekmo, 2019;Jingrot & Rosberg, 2008). ...
Article
Full-text available
Purpose The study aimed to describe primary health care professionals lived experiences of supporting recovery in persons with stress-related disorders. Methods This study was based on a phenomenological approach known as reflective lifeworld research (RLR). Seventeen health care professionals working in primary health care were included in the study. Lifeworld interviews were conducted to collect data. The data were analysed in accordance with the phenomenological RLR principles of openness, flexibility and bridling. Results Health care professionals experienced supporting recovery as a complex process with a need for a tailored approach, regardless of profession. In an alliance, the health care professionals encounter the persons where they are based on their own narratives about their life situation. In an interpersonal platform, the health care professionals use a lingering and flexible approach. Support is provided by encouraging existential reflection and learning as well as guiding the person to consider their own needs. This supports the person’s quest for a sustainable recovery process in his/her life situation. Conclusions We conclude that supporting recovery requires a genuinely person-centred care in which elements of existential care are crucial. Primary health care for persons with stress-related disorders could benefit from the development of additional research and models for such an approach.
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Author Information 1 University of Oxford, Health Services Research Unit, Nuffield Department of Population Health, Oxford, UK 2 University of Aberdeen, Health Services Research Unit, Aberdeen, UK 3 University of Oxford, Department of Primary Care Health Sciences, Oxford, Oxfordshire, UK 4 University of Oxford, Quality and Outcomes Research Unit and Health Experiences Research Group, Oxford, Oxfordshire, UK 5 University of Oxford, Nuffield Department of Population Health, Oxford, Oxfordshire, UK 6 University of Oxford, Nuffield Department of Primary Care Health Sciences, Oxford, UK *Angela Coulter, Health Services Research Unit, Nuffield Department of Population Health, University of Oxford, Old Road Campus, Headington, Oxford, OX3 7LF, UK. angela.coulter@dph.ox.ac.uk. Abstract Background Personalised care planning is a collaborative process used in chronic condition management in which patients and clinicians identify and discuss problems caused by or related to the patient's condition, and develop a plan for tackling these. In essence it is a conversation, or series of conversations, in which they jointly agree goals and actions for managing the patient's condition. Objectives To assess the effects of personalised care planning for adults with long-term health conditions compared to usual care (i.e. forms of care in which active involvement of patients in treatment and management decisions is not explicitly attempted or achieved). Search methods We searched the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, EMBASE, PsycINFO, ProQuest, clinicaltrials.gov and WHO International Clinical Trials Registry Platform to July 2013. Selection criteria We included randomised controlled trials and cluster-randomised trials involving adults with long-term conditions where the intervention included collaborative (between individual patients and clinicians) goal setting and action planning. We excluded studies where there was little or no opportunity for the patient to have meaningful influence on goal selection, choice of treatment or support package, or both. Data collection and analysis Two of three review authors independently screened citations for inclusion, extracted data, and assessed risk of bias. The primary outcomes were effects on physical health, psychological health, subjective health status, and capabilities for self management. Secondary outcomes included effects on health-related behaviours, resource use and costs, and type of intervention. A patient advisory group of people with experience of living with long-term conditions advised on various aspects of the review, including the protocol, selection of outcome measures and emerging findings. Main results We included 19 studies involving a total of 10,856 participants. Twelve of these studies focused on diabetes, three on mental health, one on heart failure, one on end-stage renal disease, one on asthma, and one on various chronic conditions. All 19 studies included components that were intended to support behaviour change among patients, involving either face-to-face or telephone support. All but three of the personalised care planning interventions took place in primary care or community settings; the remaining three were located in hospital clinics. There was some concern about risk of bias for each of the included studies in respect of one or more criteria, usually due to inadequate or unclear descriptions of research methods. Physical health Nine studies measured glycated haemoglobin (HbA1c), giving a combined mean difference (MD) between intervention and control of -0.24% (95% confidence interval (CI) -0.35 to -0.14), a small positive effect in favour of personalised care planning compared to usual care (moderate quality evidence). Six studies measured systolic blood pressure, a combined mean difference of -2.64 mm/Hg (95% CI -4.47 to -0.82) favouring personalised care (moderate quality evidence). The pooled results from four studies showed no significant effect on diastolic blood pressure, MD -0.71 mm/Hg (95% CI -2.26 to 0.84). We found no evidence of an effect on cholesterol (LDL-C), standardised mean difference (SMD) 0.01 (95% CI -0.09 to 0.11) (five studies) or body mass index, MD -0.11 (95% CI -0.35 to 0.13) (four studies). A single study of people with asthma reported that personalised care planning led to improvements in lung function and asthma control. Psychological health Six studies measured depression. We were able to pool results from five of these, giving an SMD of -0.36 (95% CI -0.52 to -0.20), a small effect in favour of personalised care (moderate quality evidence). The remaining study found greater improvement in the control group than the intervention group. Four other studies used a variety of psychological measures that were conceptually different so could not be pooled. Of these, three found greater improvement for the personalised care group than the usual care group and one was too small to detect differences in outcomes. Subjective health status Ten studies used various patient-reported measures of health status (or health-related quality of life), including both generic health status measures and condition-specific ones. We were able to pool data from three studies that used the SF-36 or SF-12, but found no effect on the physical component summary score SMD 0.16 (95% CI -0.05 to 0.38) or the mental component summary score SMD 0.07 (95% CI -0.15 to 0.28) (moderate quality evidence). Of the three other studies that measured generic health status, two found improvements related to personalised care and one did not. Four studies measured condition-specific health status. The combined results showed no difference between the intervention and control groups, SMD -0.01 (95% CI -0.11 to 0.10) (moderate quality evidence). Self-management capabilities Nine studies looked at the effect of personalised care on self-management capabilities using a variety of outcome measures, but they focused primarily on self efficacy. We were able to pool results from five studies that measured self efficacy, giving a small positive result in favour of personalised care planning: SMD 0.25 (95% CI 0.07 to 0.43) (moderate quality evidence). A further five studies measured other attributes that contribute to self-management capabilities. The results from these were mixed: two studies found evidence of an effect on patient activation, one found an effect on empowerment, and one found improvements in perceived interpersonal support. Other outcomes Pooled data from five studies on exercise levels showed no effect due to personalised care planning, but there was a positive effect on people's self-reported ability to carry out self-care activities: SMD 0.35 (95% CI 0.17 to 0.52). We found no evidence of adverse effects due to personalised care planning. The effects of personalised care planning were greater when more stages of the care planning cycle were completed, when contacts between patients and health professionals were more frequent, and when the patient's usual clinician was involved in the process. Authors' conclusions Personalised care planning leads to improvements in certain indicators of physical and psychological health status, and people's capability to self-manage their condition when compared to usual care. The effects are not large, but they appear greater when the intervention is more comprehensive, more intensive, and better integrated into routine care. Plain language summary Effects of personalised care planning for people with long-term conditions Background People with long-term health conditions play an important part in managing their own health. But some of the tasks involved can be complicated, and require confidence and skill. Such tasks include taking medicines properly, monitoring symptoms, adopting or maintaining healthy lifestyles, managing their emotions, solving practical problems, knowing when and how to seek medical advice or community support, and coping with the impact of the condition(s) on their daily lives. Personalised care planning aims to provide support from health professionals that is tailored to the needs of individual patients. Such support recognises patients’ concerns, and helps them become more able to manage their own health. Personalised care planning is a conversation, or series of conversations, between a patient and a clinician when they jointly agree on goals and actions for managing the patient's health problems. Review question We carried out this systematic review to find out whether a personalised approach, in which patients are encouraged to participate in setting goals and action plans and determining their support needs, leads to better outcomes than when these decisions are taken by health professionals alone. Results We found 19 randomised trials published before July 2013 that addressed this issue, involving 10,856 participants with conditions such as diabetes, mental health problems, heart failure, kidney disease, and asthma. The studies looked at a range of different interventions designed to involve patients and support self management. We combined and summarised results from studies that measured similar outcomes and found that involvement in personalised care planning probably led to small improvements in some indicators of physical health (better blood glucose levels, lower blood pressure measurements among people with diabetes, and control of asthma). It also probably reduced symptoms of depression, and improved people's confidence and skills to manage their health. We observed no effect on cholesterol, body mass index or quality of life. We found no evidence of any harms arising from personalised care planning. We found that the process worked best when it included preparation, record-sharing, care co-ordination and review, involved more intensive support from health professionals, and was integrated into routine care. However, the quality of evidence was only moderate, meaning that further research might change these findings. Conclusion We concluded that personalised care planning is a promising approach that offers the potential to provide effective help to patients, leading to better health outcomes. More research is needed to work out which aspects are most effective for specific patient groups.
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To examine whether GPs' communication styles have changed since the introduction and implementation of clinical guidelines for psychosocial problems in Dutch general practice in the 1990s. From a database of 5184 consultations videotaped between 1977 and 2008, 512 consultations assessed by GPs as 'completely psychosocial' were coded with RIAS (Roter Interaction Analysis System). The 121 consultations prior to and 391 consultations after implementation of guidelines were analyzed whether communication styles have changed over time. We found that GPs were more likely to consider consultations to be mainly (17%) or completely (12%) psychosocial after the implementation of guidelines. They gave more biomedical and psychosocial information and advice in the second period compared to the first period. We also found that empathy decreased over time (frequency of empathic statements by GPs changed from 2.9-3.2 to 1.4-1.6 between periods). Communication in psychosocial consultations has changed; GPs have become more focused on task-oriented communication (asking questions, giving information and advice) and less on showing empathy. GPs face the challenge of integrating an evidence-based approach of applying guidelines that promote active symptom exploration with understanding patients' personal contexts and giving room to their emotions.