ArticlePDF AvailableLiterature Review

Patient expectations of treatment for back pain: a systematic review of qualitative and quantitative studies

Authors:

Abstract

A systematic review of qualitative and quantitative studies. To summarize evidence from studies among patients with low back pain on their expectations and satisfaction with treatment as part of practice guideline development. Patients are often dissatisfied with treatment for acute or chronic back pain. We searched the literature for studies on patient expectations and satisfaction with treatment for low back pain. Treatment aspects related to expectations or satisfaction were identified in qualitative studies. Percentages of dissatisfied patients were calculated from quantitative studies. Twelve qualitative and eight quantitative studies were found. Qualitative studies revealed the following aspects that patient expectation from treatment for back pain or with which they are dissatisfied. Patients want a clear diagnosis of the cause of their pain, information and instructions, pain relief, and a physical examination. Next, expectations are that there are more diagnostic tests, other therapy or referrals to specialists, and sickness certification. They expect confirmation from the healthcare provider that their pain is real. Like other patients, they want a confidence-based association that includes understanding, listening, respect, and being included in decision-making. The results from qualitative studies are confirmed by quantitative studies. Patients have explicit expectations on diagnosis, instructions, and interpersonal management. New strategies need to be developed in order to meet patients' expectations better. Practice guidelines should pay more attention to the best way of discussing the causes and diagnosis with the patient and should involve them in the decision-making process.
SPINE Volume 29, Number 20, pp 2309–2318
©2004, Lippincott Williams & Wilkins, Inc.
Patient Expectations of Treatment for Back Pain
A Systematic Review of Qualitative and Quantitative Studies
Jos Verbeek MD, PhD,* Marie-Jose´ Sengers, MSc,* Linda Riemens,† and
Joke Haafkens, PhD*
Study Design. A systematic review of qualitative and
quantitative studies.
Objectives. To summarize evidence from studies
among patients with low back pain on their expectations
and satisfaction with treatment as part of practice guide-
line development.
Summary of Background Data. Patients are often dis-
satisfied with treatment for acute or chronic back pain.
Methods. We searched the literature for studies on
patient expectations and satisfaction with treatment for
low back pain. Treatment aspects related to expectations
or satisfaction were identified in qualitative studies. Per-
centages of dissatisfied patients were calculated from
quantitative studies.
Results. Twelve qualitative and eight quantitative
studies were found. Qualitative studies revealed the fol-
lowing aspects that patient expectation from treatment
for back pain or with which they are dissatisfied. Patients
want a clear diagnosis of the cause of their pain, informa-
tion and instructions, pain relief, and a physical examina-
tion. Next, expectations are that there are more diagnos-
tic tests, other therapy or referrals to specialists, and
sickness certification. They expect confirmation from the
healthcare provider that their pain is real. Like other pa-
tients, they want a confidence-based association that in-
cludes understanding, listening, respect, and being in-
cluded in decision-making. The results from qualitative
studies are confirmed by quantitative studies.
Conclusions. Patients have explicit expectations on di-
agnosis, instructions, and interpersonal management.
New strategies need to be developed in order to meet
patients’ expectations better. Practice guidelines should
pay more attention to the best way of discussing the
causes and diagnosis with the patient and should involve
them in the decision-making process.
Key words: back pain treatment, patient satisfaction,
patient expectations, quality of health care, systematic
review, qualitative research, practice guidelines. Spine
2004;29:2309 –2318
Low back pain is one of the most common health prob-
lems for which people consult their physician.
1
It is not
surprising that many practice guidelines have been pub-
lished in recent years to support physicians in their man-
agement of back pain.
2,3
Two of the authors (J.V. and
L.R.) were also involved in the development of such a
guideline. This was a multidisciplinary clinical practice
guideline for back pain that was intended to be comple-
mentary to existing guidelines for specific disciplines
such as general practitioners and occupational physi-
cians.
4
The focus was to be on the patients’ views. The
clinical parts of the guideline are typically based on sys-
tematic reviews of the literature. In line with this ap-
proach, we decided to apply the same method to find out
about patients’ perceptions.
For a practice guideline, patient satisfaction with
treatment is a relevant outcome measure. It is known
that when patients are satisfied with the encounter with
the physician they are more likely to comply and coop-
erate with treatment, thus promoting treatment effec-
tiveness.
5
There are many studies from other fields of
medicine that support this relation between patient-
with-provider-satisfaction and compliance-with-drug-
treatment.
6–9
The same has not been shown for back
pain, although more positive patient expectations were
related to a better outcome in back pain treatment in one
study.
10
The study also showed that being optimistic
regarding a specific treatment was not the same as being
optimistic in general. However, in back pain treatment,
it is not too difficult to imagine that a patient who is
dissatisfied about the encounter with the physician,
would not be willing to comply with the advice “to stay
active” as it is generally recommended in practice guide-
lines.
The theoretical framework on which patient satisfac-
tion and patient expectations are based is not very well
elaborated yet. Intuitively, we all have ideas about causes
and meanings of satisfaction of patients with contacts
with healthcare providers. Satisfaction with health care
can best be defined as a positive feeling of the patient
toward an aspect of the process or outcome of health
care.
11
Some researchers have named those factors in
health care that are related to satisfaction “dimensions”
of satisfaction.
12
The strongest dimension of satisfaction
is usually to be treated with respect or in a humane way
by the provider of care. The outcome can be less impor-
tant. Apparently, this positive feeling of satisfaction is
due to expectations that we have about the care to be
provided. There is a close link between these expecta-
tions and the dimensions of satisfaction. Usually, pa-
tients are dissatisfied because the treatment did not meet
their expectations.
13,14
Therefore, aspects of care about
From the *Coronel Institute for Work, Environment and Health, Am-
sterdam, The Netherlands; and †Stichting Patie¨ntenbelangen Orthope-
die, Westervoort, The Netherlands. Drs. Verbeek and Sengers contrib-
uted equally in the development of the manuscript.
Acknowledgment date: January 15, 2003. First revision date: Septem-
ber 18, 2003. Second revision date: November 3, 2003. Acceptance
date: November 17, 2003.
The manuscript submitted does not contain information about medical
device(s)/drug(s).
Institutional funds were received in support of this work. No benefits in
any form have been or will be received from a commercial party related
directly or indirectly to the subject of this manuscript.
Address correspondence and reprint requests to Jos H.A.M. Verbeek,
MD, PhD, Coronel Institute for Work, Environment and Health,
Meibergdreef 15, 1105 AZ Amsterdam, The Netherlands; E-mail:
j.h.verbeek@amc.uva.nl
2309
which patients have specific expectations or with which
they express satisfaction or dissatisfaction are of impor-
tance to providers of care who wish to improve patient
satisfaction. To find out about these aspects, both qual-
itative and quantitative studies that report on patient
satisfaction or on expectations of treatment can be
used.
15,16
A synthesis of these studies could indicate a
more complete picture of what patients expect from their
healthcare providers, than that acquired through single
studies. The results of this synthesis could lead to specific
recommendations as part of practice guidelines in addi-
tion to evidence about the effectiveness of interventions.
We wish to report here the results of our study on what
patients with nonspecific low back pain expect from
treatment for back pain, and with which aspects of their
treatment they are dissatisfied.
Materials and Methods
Search Strategy and Study Selection. MEDLINE, Psy-
cINFO, Embase dating from years 1966 to 2001 were searched
electronically using the keywords (MeSH terms) “backache” or
“back pain” combined with the terms “patient satisfaction,”
“physician-patient relationship,” “doctor-patient relation-
ship,” “patient expectation,” or “patient preferences.” In ad-
dition, the reference lists of retrieved reviews and articles were
screened for relevant titles. To find out if we had missed arti-
cles, we searched the Spine journal separately. These searches
yielded 330 articles. The titles and abstracts of the articles were
screened to determine their relevancy. The articles were subse-
quently read to determine whether they met the following in-
clusion criteria: the publication had to be a report of an empir-
ical study; studies had to concern patients older than 18 with
acute or chronic nonspecific low back pain; studies had to re-
port on aspects of the treatment with which dissatisfaction was
expressed or that were part of the expectation of the patients.
Nonspecific back pain was defined as pain in the back with or
without radiation and without specific systemic disease as the
underlying cause of the symptoms.
17
Back pain lasting longer
than 3 months was defined as chronic.
18
Study Categories. We classified studies into qualitative and
quantitative studies following the authors description. If it was
not clear from that description, we categorized a study by
means of the sort of questions that were asked. If the research-
ers asked the same closed questions among all the patients and
included figures indicating the percentage of patients that were
dissatisfied or that had specific expectations, a study was clas-
sified as quantitative, regardless of the means of gathering the
data. We categorized a study as qualitative if satisfaction or
expectations were ascertained by means of interviews or open-
ended questions. In addition, studies were categorized into
those about acute patients, chronic patients, or a mixture of
these. The studies were also grouped according to the provider
of the treatment.
Treatment Aspects. To collect data about expectations or
dissatisfaction, we used a list with all possible aspects of treat-
ment or themes that were reported to be related to patients’
expectations and satisfaction in general (Table 1).
12,13,19
The
observation list was the same for both quantitative and quali-
tative studies. If a study contained new aspects of treatment
they were subsequently added to the list in line with the ap-
proach of grounded theory.
20
The main aspects were divided
into subcategories if necessary. Aspects of treatment that re-
lated to dissatisfaction and those that related to expectations
were both processed in the same way as aspects that determined
patient satisfaction. All articles were read and data extracted by
two reviewers independently. If there was initial disagreement,
the results were discussed until consensus was reached.
Expectations and Satisfaction. In qualitative studies, as-
pects of expectations or dissatisfaction that were mentioned by
patients and considered important by the authors, were in-
cluded in the results of this review. For example, if a study
reported that patients wanted to know the cause of the pain,
the main item “clinical management” and the subitem “diag-
nosis/finding cause of pain” were scored as an expectation. For
qualitative studies, satisfaction was defined as a patient’s eval-
uation of aspects of treatment by means of a positive feeling or
attitude toward these aspects of treatment.
11
A study could only contribute once to an item. The number of
studies in which a treatment aspect was mentioned was used to
synthesize study results and is therefore an indicator of the
importance patients ascribe to a certain aspect of treatment. To
illustrate these numbers, the actual words used by patients are
quoted from the qualitative articles that scored on the corre-
sponding treatment aspect (Table 1).
In quantitative studies, the frequency of answers to ques-
tions about dissatisfaction or expectations was used to discover
relevant treatment aspects. For questions about satisfaction,
percentages were recalculated into percentages of dissatisfac-
tion or negative answers. Next, 95% confidence intervals were
calculated to account for differences in population size that
would lead to a low power of the study. If more than a statis-
tically significant 10% of the patients were dissatisfied with an
aspect of care, it was scored as an aspect of care that patients
were dissatisfied with. We chose to search for aspects of treat-
ment with which patients were dissatisfied because it is known
that patients are inclined to give an ingratiating response about
questions related to treatment, which leads to less informative
high levels of satisfaction. We further inferred that aspects that
patients would be willing to report on as dissatisfying would be
the most important. For the same reasons, we selected the low
criterion of 10%.
13
If more than one question in a study fitted
into the same item of care, the average of the percentages for
those questions was used.
We wanted to take the methodologic quality of the individ-
ual studies into account in the synthesis since low quality stud-
ies will provide less evidence than high quality studies. There-
fore, two reviewers assessed independently the quality of the
qualitative and quantitative studies. If there was initial dis-
agreement, the item was discussed until consensus was reached.
For qualitative articles, a scoring list of seven items from vari-
ous authors was adapted.
21–24
For quantitative studies, the
scoring list consisted of six items.
17,25
If a study scored more
than four points, it was considered to be of high quality (Ap-
pendix A).
Results
Twelve qualitative and eight quantitative articles, origi-
nating from several countries, met the inclusion criteria
(Table 2). Authors reported on the same population in
two articles on two different occasions. In one case, an
2310 Spine
Volume 29
Number 20
2004
Table 1. Aspects of Treatment for Back Pain About Which Patients Have Expectations or Express Satisfaction in
Qualitative Studies (N 12) and Quantitative Studies (N 8) According to Type of Back Pain*
Treatment Aspect
Qualitative Studies: Expectations or Satisfaction Quantitative Studies: Dissatisfaction
Quotations
Acute
(N 1)
Mixed Acute
and Chronic
(N 5)
Chronic
(N 6)
Acute
(N 1)
Mixed Acute
and Chronic
(N 6)
Chronic
(N 1)
Clinical management
Diagnoses/finding cause of
pain
(30) (31) (34) (28) (29) (39) (33) (32) (43) (45) “The initial diagnosis was just-well you
know, there really wasn’t one. I had
some x-rays and they said they
weren’t really certain what was
going on.” (29)
Technical competence (34) (28) (29) (42) (26) (43) “My back was hurting. I tell the
doctor what’s up. And he still
won’t examine me to see if I’m
telling the truth or notѧyou can’t
fix a car just by looking at it.” (28)
Information/instructions (36) (31) (34) (35) (37) (29) (33) (32) (42) (26) (27) (41) (43) “I need more knowledge or directions
from somebody. I need to know
what to do.” (29)
Convenience of treatment (29) About TENS:“I use it when pain is
severe, but batteries only last for 1
day and that gets expensive.(29)
Pain relief (36) (30) (28) (29) (39) (33) (42) (26) (44) (43) “I am not getting anywhere. I’ve had
all these different things, the TENS
machine and the physio and I’m
still back at square one.” (39)
Facilities
Diagnostic test (31) (28) (29) “With an x-ray you know more, you
know your body better.” (31)
Other therapy (31) (34) (29) (32) “I came to be referred (to
physiotherapist). . . it is already 7
years ago.” (31)
Specialty consultations (29) “..it just hurt too much. So I started my
little quest of trying to find another
doctor to help me.”(29)
Sickness certification/job (34) (35) (37) (38) (43) My GP told me: When I have back
pain myself, I have to keep
working (37)
Interpersonal management
Communication (30) (34) (39) (32) “They treat you as if you don’t
understand what they’re talking
about. I’d like to be spoken to on
my own level.” (39)
Congruency/confirmation (33) (26) (41) Congruent patients had expectations
centered on pain that could be
fulfilled by the therapist. (33)
Being included in decision
making
(36) (35) “I need to makeѧinformed choices
about what I am going to doѧit is
up to me to make those kinds of
decisions.”(35)
Listening (34) (28) (32) “..people have a problem talking to
their doctorsѧThey don’t listen to
what you say.” (28)
Respect (39) “It is as if he (physician) is saying to
me: Well I’ve been to college and
university and you are just a lowly
person.” (39)
Confidence based
relationship
(36) (37) (28) (39) (32) (26) (27) (41) “I don’t have any faith really, what I
want to find out is what is causing
the pain all through my body and I
seem to meet a blank wall.” (39)
Time/effort (34) (28) (32) (27) (41) She might be a good doctor, but I
don’t think she’s got time for
patients. (34)
Understanding (39) (32) (26) (27) (41) (45) Being believed is the most
important. (32)
Continuity of care
Waiting time (39) She was kept waiting for an hour and
a half andѧwithout apology. (39)
Finances
*References are in parentheses.
2311Patient Expectations
Verbeek et al
article described satisfaction levels at the beginning of
treatment,
26
and a second article reported on satisfaction
after a 1-year follow-up of participants in the same
study.
27
In the other case, two articles described studies
using the same population but reported on different as-
pects of low back pain and its care.
28,29
These articles
were analyzed separately. Ten of the qualitative studies
were of high quality, with two studies scoring the maxi-
mum 7 points (Appendix A). In only four studies, the
data were analyzed by two researchers; and in six stud-
ies, someone else than the healthcare providers recruited
participants.
Only one of the eight quantitative studies scored low
on quality assessment, with four studies achieving the
maximum score. One qualitative and one quantitative
study were restricted to acute patients. Nine studies in-
cluded care by chiropractors or compared care between
different providers.
Qualitative Studies
Within the area of clinical management, two treatment
aspects occurred most frequently: patients want to know
the cause of their pain and patients want information or
instruction (Table 1). They expect an accurate diagno-
sis,
30–32
so that they can prove to others that their pain is
real. Therefore, patients are often dissatisfied either
about not receiving a diagnosis, inadequate diagnoses, or
different diagnoses over time.
29,33
Patients blame their
healthcare provider for the care provider’s inability to
explain the cause of pain and feel that their pain is not
legitimate. The process of delegitimization is described as
an experience of a series of negative consequences, from
not being seen to not being heard, to a sense of deficiency
and shame.
28
Even when an explanation was given, some
patients doubted its validity because it conflicted with
their own prior understanding or because they believed it
was based on inadequate investigation.
28
Two studies
also reported dissatisfaction with superficiality of exam-
inations.
29,34
From eight studies, it can be concluded that patients
also expect instructions or advice regarding their back
pain management. Advice seemed to be especially impor-
tant for patients for whom management of pain was a
Table 2. Qualitative (n 12) and Quantitative (n 8) Studies on Satisfaction With and Expectations of Treatment of
Patients With Back Pain, Included in the Review
Author and Year (reference) Population (N) Country
Study Design and
Measurement Treatment/Intervention Quality
Qualitative studies
Cedraschi 1996 (33) Chronic (71) Switzerland Semi-structured
interview
General care by chiropractor/
rheumatologist
High
Skelton 1996 (34) Acute and chronic (52) UK In-depth interview GP care High
Chew 1997 (38) Chronic (20) UK Semi-structured
interview
GP care High
McPhillips-Tangum 1998 (29) Chronic (54) USA In-depth interview General primary care from
medical doctors
High
Åbyholm 1999 (32) Chronic (22) Norway In-depth interview Physicians High
Walker 1999 (39) Chronic (20) UK Interpretation of
narrative accounts
Pain clinic High
Grimmer 1999 (36) Acute (45) Australia In-depth interview, focus
groups, questionnaires
Physiotherapeutic care High
Rogers 1999 (35) No information (17) Australia Semi-structured
interview
GP care Low
Rhodes 1999 (28) Chronic (54) USA In-depth, semi-structured
interviews
Diagnostic tests High
Sigrell 2001 (30) Acute and chronic (93) Sweden Questionnaires Chiropractic care Low
Ostlund al 2001 (37) Acute and chronic (20) Sweden In-depth interviews Rehabilitation High
Schers 2001 (31) Acute and chronic (20) The Netherlands In-depth interviews GP care High
Quantitative studies
Deyo 1986 (45) Acute and chronic (140) USA Observational,
questionnaire
House staff physicians Low
Cherkin 1989 (41) Acute and chronic (457) USA Observational,
questionnaire
Chiropractic/GP care High
Carey 1995 (42) Acute (1,633) USA Observational,
questionnaire
Primary care practitioners/
orthopaedic
care/chiropractor
High
Carey 1996 (44) Acute and chronic (180) USA Observational, telephone
interviews
Chiropractor/physicians High
Curtis 2000 (43) Acute and chronic (311) USA Observational and RCT,
questionnaire
GP/chiropractic physicians/
orthopaedic surgeons
High
Nyiendo 2000 (26) Acute and chronic (139) USA Observational,
questionnaire
Chiropractic/GP care High
Pincus 2000 (40) Chronic (60) UK Observational,
questionnaire
GP/osteopaths High
Nyiendo 2001 (27) Acute and chronic (835) USA Observational,
questionnaire
Chiropractic/GP care High
RCT randomized controlled trial; GP general practitioner.
2312 Spine
Volume 29
Number 20
2004
priority
35
and for patients with a longer experience in the
healthcare system.
36
Moreover, patients wanted a com
-
prehensive approach to management.
34
That might be
the reason why patients often had the feeling that many
questions remained unanswered
29
and that information
and recommendations were not given to them.
31–33,37
This was especially the case with patients whose opin-
ions differed from that of the physicians, the so-called
noncongruent patients.
Pain relief is a treatment aspect that comes up in many
interviews. It can be regarded as the driving force for
seeking treatment or for returning for subsequent treat-
ment.
36
Patients want an effective treatment,
30
designed
to decrease difficulties with normal activities.
28
Chronic
patients who had gone through many experiences with
the healthcare system did not expect anymore that med-
ical interventions would alleviate their symptoms
38
as
opposed to patients who were more inexperienced with
the healthcare system and still expected pain relief.
36
However, in one study, chronic patients wanted to im-
prove their health and still hoped that the physician
would discover the right remedy,
39
which was often not
the case. As a result, dissatisfaction with pain relief is
often mentioned. Patients assessed treatments as ineffec-
tive because these did not alleviate their symp-
toms.
28,29,39
Patients have the feeling that their condition
deteriorates as a result of continued treatment.
39
Con
-
gruency between patient and healthcare provider is prob-
ably related to the effectiveness of the treatment. Con-
gruent patients experienced more pain relief than
noncongruent patients.
33
Apart from the outcome of treatment, one study
showed that patients were also dissatisfied with the pro-
cess because the treatment was too inconvenient.
29
Sickness certification was mentioned as an important
aspect of treatment in four of the 12 qualitative studies.
Some patients seemed even to be primarily concerned
with sickness certification,
34
which was described as so
-
cial recognition and a legitimization of social and eco-
nomic inactivity.
37,38
Even when patients were confident
of their own body, a formal validation was often de-
sired.
35
Two studies reported that to get a diagnosis or sick-
ness certification patients wanted diagnostic tests.
28,29
Therefore, some patients made efforts to convince their
healthcare provider that tests were needed.
31
Dissatisfac
-
tion with diagnostic tests is a major theme in one study
because such tests did not turn out to provide the solu-
tion or diagnoses that patients desired.
28
In addition to sickness certification, patients consider
a consultation as an opportunity to explore possibilities
of alternative management
29,31,32,34
or referral to medi
-
cal or surgical specialist treatment.
29
In none of the studies did the patients mention expec-
tations about or dissatisfaction with medication.
With respect to interactions with healthcare provid-
ers, the dominant expectation of patients, especially ex-
perienced patients, was a confidence-based associa-
tion.
28,32,36,37,39
Reasons why a confidence-based
relationship could not be established were healthcare
providers failed to diagnose and treat the pain
39
or pa
-
tients felt that the healthcare provider did not believe
they were in pain.
28,32
In addition to confidence, patients also expect a
healthcare provider to communicate well.
30
Therefore,
patients were dissatisfied about poor communication
skills
34
and understanding.
32,39
Patients expected to be
treated with respect
39
and wanted to be listened to rather
than be given a nonexistent “magical cure.”
34
Patients
did not feel that the treatment came up to their expecta-
tions because healthcare providers did not listen and did
not spend enough time with them.
28,32,34
Finally, it is
reported that especially experienced patients wish to be
involved in the decision-making process. When this does
not happen they become frustrated. These patients state
that they are the best judges of what is good for them.
When patients are included in the decision-making pro-
cess, there is a greater chance of congruency between
patient and healthcare provider.
35,36
One study reported that patients were dissatisfied
with the continuity of care, which means that patients
were often kept waiting for referrals, investigations or
the results thereof, appointments, surgery, further opin-
ions, or a pain clinic.
39
No study mentioned expectations about or dissatis-
faction with the “location of the treatment,” “access to
care,” or the “costs” involved.
Quantitative Studies
Percentages of dissatisfied patients varied to a large ex-
tent. In one study on chronic patients, there was no dis-
satisfaction beyond our 10% criterion.
40
Variation
seemed to be related to type and formulation of questions.
Large differences in dissatisfaction occurred between differ-
ent types of healthcare providers (Appendix B).
In most studies, patients were dissatisfied with the
amount of information they received from their health-
care provider.
26,27,41–43
Next in rank was lack of pain
relief as the most dissatisfying aspect of the treat-
ment.
26,42–44
Patients of general practitioners wanted in
-
formation about diagnostics and specialist consulta-
tions, whereas chiropractors’ patients wanted more
diverse information.
41
Moreover, high proportions of
patients reported receiving a lack of instruction about
how to take care of their back, such as back exercises,
postures, and lifting.
27,41,43
Especially acute patients had little trust in the provid-
ers’ technical competence. They noticed the absence of a
detailed back history and physical examination.
26,42
According to the patients, physical ability did not im-
prove after treatment, and there was a lack of help with
their job situation.
43
In none of the quantitative studies were questions
asked about facilities such as diagnostic tests, referrals,
or sickness certification.
2313Patient Expectations
Verbeek et al
In some studies, up to 80% of the patients complained
about not being understood by their provider
26,41,45
and
stated a lack of confidence in provider or treat-
ment.
26,27,41
Comparisons on this subject between gen
-
eral practitioners and chiropractors were all in favor of
the chiropractors. High proportions of patients had little
confidence in the treatment only a year after starting
treatment
26,27,41
or felt that the provider was not confi
-
dent of the diagnosis or treatment.
27
Communication, listening, and respect were not mea-
sured or mentioned in the quantitative studies as aspects
of dissatisfaction.
In none of the studies was continuity of care or costs
mentioned as causes of dissatisfaction.
Discussion
This review reveals that there is a gap between what is
offered by healthcare providers and what is expected by
patients. It shows that patients with back pain expect an
explanation for their pain (diagnosis), instructions and
advice on back pain management, pain relief, and sick-
ness certification. Like patients with other disorders, they
appreciate a confidence-based relationship with a pro-
vider who communicates well and listens to them. Pa-
tients are dissatisfied with treatment for the same rea-
sons. Therefore, they feel delegitimized and lose their
confidence in the healthcare provider. Results of qualita-
tive studies are confirmed by quantitative studies. Vari-
ations in satisfaction with treatment between different
care providers are explained by the same items.
No established methods for reviews of qualitative re-
search exist as yet.
16
Some advocate the use of ethno
-
graphic methods to synthesize qualitative studies
46
and
others use the term metasynthesis to this end.
47
We used
a combination of techniques in which findings from
qualitative studies were supported by the results from
quantitative research. Because we used a list based on an
extensive review of patient satisfaction and expectations,
we were comprehensive in listing aspects of patient sat-
isfaction. In 10 of the 12 qualitative studies, participant
selection had been described and patients represented a
wide range of patients with low back pain. This guaran-
tees that a wide range of ideas about satisfaction with or
expectations about back pain treatment was included in
our review.
48
In addition, the methodologic quality of
most studies was high, which supports our conclusions.
A weak point in most qualitative studies was that care
providers recruited their own patients, which could re-
sult in selection bias. However, we found no indication
that patients who were recruited by their own care pro-
vider showed higher satisfaction levels. The studies orig-
inated from several countries, which could have resulted
in culturally determined reasons for satisfaction. How-
ever, all studies were from developed Western countries,
and we did not find aspects of satisfaction that were
pertinent to a specific culture. We found few studies that
consisted only of patients with either acute or chronic
back pain. From these studies, we could not conclude
that there were different expectations among acute or
chronic patients. There was a gradual difference between
more and less experienced patients. More experienced
patients expected more information and made higher de-
mands on the interpersonal association with their health-
care provider than new patients. Analysis of the results
according to the methodologic quality of the studies did
not change the results since almost all studies were of
high quality.
Other studies that used different methods to relate
patient satisfaction to aspects of care support the find-
ings from this review that patients are more satisfied with
technically competent physicians and extensive diagnos-
tics such as radiographs.
49,50
Another study showed that
concordance, defined as concordance between physi-
cians’ recommendations and patients’ adherence to
them, was as low as one third of all cases with back
pain.
51
Hazard et al did not find a relation between out
-
come and satisfaction, which was explained by a differ-
ence in treatment goals of practitioners and patients.
52
It is unclear if, or to what extent, expectations of and
dissatisfaction with the interpersonal relationship with
the care provider are specific for back pain patients. Pa-
tients with other diseases have similar expectations such
as an effective treatment or help with their job situa-
tion.
53,54
Even if this is a factor specific to back pain
treatment, it is of importance to take into account be-
cause there is evidence that better interpersonal manage-
ment leads to better outcomes.
55
It is interesting to note that patients were more satis-
fied with chiropractic care. There is evidence that this is
not related to the provider himself or the content of care
but to the better management of expectations of diagno-
sis, information, clinical skills, and the patient-provider
relationship.
41,56
If the treatment of healthcare providers does not meet
the expectations of back pain patients, practice guide-
lines could be a means to help professionals in improving
the quality of care. It has been suggested that patient
preferences should be taken into account when develop-
ing guidelines.
57
However, most guidelines only provide
recommendations on technical skills for physicians such
as diagnostic criteria and effective interventions.
2
This
places the practitioner in a highly unenviable position.
On the one hand, the practice guideline recommends re-
fraining from diagnostic tests in patients with nonspecific
back pain and stresses that there is no underlying patho-
logic cause known. On the other hand, patients are more
satisfied with extensive diagnostics and wish to know the
cause of their back pain. There is an urgent need to fill
this gap, either through the development and training of
communication skills for physicians or through public
information campaigns.
31
Results of research in both ar
-
eas are promising.
58–60
Moreover, practice guidelines
should pay more attention to the best way of discussing
2314 Spine
Volume 29
Number 20
2004
the causes and diagnosis with the patient and should
involve them in the decision-making process.
Key Points
There is an extensive literature of qualitative
studies on patients’ expectations of treatment for
back pain of generally good methodologic quality.
The treatment aspects that emerge from the qual-
itative studies are better diagnosis, need for instruc-
tions and pain relief, and confirmation that pain is
real and legitimate.
Better strategies are needed to meet patients’
expectations.
Acknowledgments
The authors thank Marjolein Godfroij and Nico Sten-
vers for their help in the collecting the data, and Lilian
Åmre, Daphne Lees, and Kumar Jamdagni for help in
translation and editing.
References
1. Carey TS, Evans A, Kalsbeek W, et al. Care-seeking among individuals with
low back pain. Spine 1995;20:312–7.
2. Koes BW, van Tulder MW, Ostelo R, et al. Clinical guidelines for the man-
agement of low back pain in primary care: an international comparison.
Spine 2001;26:2504–13.
3. Tuut MK, van Tulder MW, van Everdingen JJE, et al. Aspecifieke lage-
rugklachten. Bestaande Nederlandse en buitenlandse richtlijnen vergeleken.
[Non-specific low-back pain: a comparison of Dutch and foreign guidelines].
Medisch Contact 2002;26:1016–9.
4. Dutch Institute for Healthcare Improvement CBO. Richtlijn aspecifieke rug-
klachten. [Clinical practice guideline non-specific low-back pain]. Utrecht,
The Netherlands: CBO, 2002.
5. Hall JA, Roter DL, Milburg MA, et al. Why are sicker patients less satisfied
with their medical care? Tests of two explanatory models. Health Psychol
1998;17:70–5.
6. Murphy DA, Roberts KJ, Martin DJ, et al. Barriers to antiretroviral adher-
ence among HIV-infected adults. AIDS Patient Care STDS 2000;14:47–58.
7. O’Malley AS, Forrest CB, Mandelblatt J. Adherence of low-income women
to cancer screening recommendations. J Gen Intern Med 2002;17:144–54.
8. Arnsten JH, Gelfand JM, Singer DE. Determinants of compliance with anti-
coagulation: a case-control study. Am J Med 1997;103:11–7.
9. Williams B, Coyle J, Healy D. The meaning of patient satisfaction: an expla-
nation of high reported levels. Soc Sci Med 1998;47:1351–9.
10. Kalauokalani D, Cherkin DC, Sherman KJ, et al. Lessons from a trial of
acupuncture and massage for low back pain: patient expectations and treat-
ment effects. Spine 2001;26:1418–24.
11. Goldstein MS, Elliot SD, Guccione AA. The development of an instrument to
measure satisfaction with physical therapy. Phys Ther 2000;80:853–62.
12. Hall JA, Dornan MC. What patients like about their medical care and how
often they are asked: a meta-analysis of the satisfaction literature. Soc Sci
Med 1988;27:935–9.
13. Verbeek J, van Dijk F, Ra¨sa¨nen K, et al. Consumer satisfaction with occu-
pational health services: should it be measured? Occup Environ Med 2001;
58:06.
14. Thompson AGH, Sunol R. Expectation as determinants of patients satisfac-
tion: concepts, theory and evidence. Int J Qual Health Care 1995;7:127– 41.
15. NHS Centre for Reviews and Dissemination. Undertaking Systematic Re-
views of Research on Effectiveness: CRD’s Guidance for Those Carrying out
or Commissioning Reviews, 4th ed, 2nd report. NHS Centre for reviews and
dissemination, University of York, York, UK, 2001.
16. Dixon-Woods M, Fitzpatrick R, Roberts K. Including qualitative research in
systematic reviews: opportunities and problems. J Eval Clin Pract 2001;7:
125–33.
17. Borghouts JAJ, Koes BW, Bouter LM. The clinical course and prognostic
factors of non-specific neck pain: a systematic review. Pain 1998;77:1–13.
18. Verbeek JH. Vocational rehabilitation of workers with back pain. Scand J
Work Environ Health 2001;27:346–52.
19. Grol R, Wensing M, Mainz J, et al. Patients’ priorities with respect to general
practice care: an international comparison. Fam Pract 1999;16:4–11.
20. Barbour RS, Barbour M. Evaluating and synthesizing qualitative research:
the need to develop a distinctive approach. J Eval Clin Pract 2003;9:17986.
21. Popay J, Rogers A, Williams G. Rationale and standards of the systematic
review of qualitative literature in health services research. Qual Health Res
1998;8:341–51.
22. Mays N, Pope C. Qualitative Research in Health Care. London: BMJ, 1996.
23. BSA Medical Sociology Group. Criteria for the evaluation of qualitative
research papers. Med Sociol News 1996;22:68–71.
24. Giacomini MK, Cook DJ. Users’ guides to the medical literature: XXIII.
Qualitative research in health care. A. Are the results of the study valid?
Evidence-Based Medicine Working Group. JAMA 2000;284:357–62.
25. van Tulder MW, Assendelft WJJ, Koes BW, et al. Method guidelines for
systematic reviews in the Cochrane Collaboration back review group for
spinal disorders. Spine 1997;22:2323–34.
26. Nyiendo J, Haas M, Goodwin P. Patient characteristics, practice activities,
and one-month outcomes for chronic, recurrent low-back pain treated by
chiropractors and family medicine physicians: a practice-based feasibility
study. J Manipulative Physiol Ther 2000;23:23945.
27. Nyiendo J, Haas M, Goldberg B, et al. Pain, disability, and satisfaction
outcomes and predictors of outcomes: a practice-based study of chronic low
back pain patients attending primary care and chiropractic physicians. J
Manipulative Physiol Ther 2001;24:433–9.
28. Rhodes LA, McPhillips-Tangum CA, Markham C, et al. The power of the
visible: the meaning of diagnostic tests in chronic back pain. Soc Sci Med
1999;48:1189–203.
29. McPhillips-Tangum CA, Cherkin DC, Rhodes LA, et al. Reasons for re-
peated medical visits among patients with chronic back pain. J Gen Intern
Med 1998;13:289–95.
30. Sigrell H. Expectations of chiropractic patients: the construction of a ques-
tionnaire. J Manipulative Physiol Ther 2001;24:4404.
31. Schers H, Wensing M, Huijsmans Z, et al. Implementation barriers for gen-
eral practice guidelines on low back pain a qualitative study. Spine 2001;26:
E348–53.
32. Abyholm AS, Hjortdahl P. Being believed is what counts: a qualitative study
of experiences with the health service among patients with chronic back
pain. Tidsskr Nor Laegeforen 1999;119:1630–2.
33. Cedraschi C, Robert J, Perrin E, et al. The role of congruence between patient
and therapist in chronic low back pain patients. J Manipulative Physiol Ther
1996;19:244–9.
34. Skelton AM, Murphy EA, Murphy RJ, et al. Patients’ views of low back pain
and its management in general practice. Br J Gen Pract 1996;46:153–6.
35. Rogers WA. Beneficence in general practice: an empirical investigation.
J Med Ethics 1999;25:388–93.
36. Grimmer K, Sheppard L, Pitt M, et al. Differences in stakeholder expecta-
tions in the outcome of physiotherapy management of acute low back pain.
Int J Qual Health Care 1999;11:155–62.
37. O
¨
stlund G, Cedersund E, Alexanderson K, et al. “It was really nice to have
someone”; lay people with musculoskeletal disorders request supportive re-
lationships in rehabilitation. Scand J Public Health 2001;29:285–91.
38. Chew CA, May CR. The benefits of back pain. Fam Pract 1997;14:461–5.
39. Walker J, Holloway I, Sofaer B. In the system: the lived experience of chronic
back pain from the perspectives of those seeking help from pain clinics. Pain
1999;80:621–8.
40. Pincus T, Vogel S, Savage R, et al. Patients’ satisfaction with osteopathic and
GP management of low back pain in the same surgery. Complement Ther
Med 2000;8:1806.
41. Cherkin DC, MacCornack FA. Patient evaluations of low back pain care
from family physicians and chiropractors. West J Med 1989;150:351–5.
42. Carey TS, Garrett J, Jackman A, et al. The outcomes and costs of care for
acute low back pain among patients seen by primary care practitioners,
chiropractors, and orthopedic surgeons: the North Carolina Back Pain
Project. N Engl J Med 1995;333:913–7.
43. Curtis P, Carey TS, Evans P, et al. Training in back care to improve outcome
and patient satisfaction: teaching old docs new tricks. J Fam Pract 2000;49:
786–92.
44. Carey TS, Evans AT, Hadler NM, et al. Acute severe low back pain: a
population-based study of prevalence and care-seeking. Spine 1996;21:
33944.
45. Deyo RA, Diehl AK. Patient satisfaction with medical care for low-back
pain. Spine 1986;11:28–30.
46. Paterson BL, Thorne S, Dewis M. Adapting to and managing diabetes. Image
J Nurs Sch 1998;30:57–62.
2315Patient Expectations
Verbeek et al
47. Sandelowski M, Docherty S, Emden C. Focus on qualitative methods:
qualitative metasynthesis: issues and techniques. Res Nurs Health 1997;
20:365–71.
48. Greenhalgh T, Taylor R. Papers that go beyond numbers (qualitative re-
search). Br Med J 1997;315:740–3.
49. van der Weide WE, Verbeek JH, van Dijk FJ. Relation between indicators for
quality of occupational rehabilitation of employees with low back pain.
Occup Environ Med 1999;56:488–93.
50. Kendrick D, Fielding K, Bentley E, et al. Radiography of the lumbar spine in
primary care patients with low back pain: randomised controlled trial. Br
Med J 2001;322:400–5.
51. Hermoni D, Borkan JM, Pasternak S, et al. Doctor-patient concordance and
patient initiative during episodes of low back pain. Br J Gen Pract 2000;50:
809–10.
52. Hazard RG, Haugh LD, Green PA, et al. Chronic low back pain: the rela-
tionship between patient satisfaction and pain, impairment, and disability
outcomes. Spine 1994;19:881–7.
53. Bredart A. Assessment of Satisfaction With Cancer Care: Development,
Cross-cultural Psychometric Analysis and Application of a Comprehensive
Instrument. Amsterdam: University of Amsterdam, 2001.
54. Maunsell E, Brisson C, Dubois L, et al. Work problems after breast cancer:
an exploratory qualitative study. Psychooncology 1999;8:467–73.
55. Di Blasi Z, Harkness E, Ernst E, et al. Influence of context effects on health
outcomes: a systematic review. Lancet 2001;357:757–62.
56. Cherkin DC, Deyo RA, Battie M, et al. A comparison of physical therapy,
chiropractic manipulation, and provision of an educational booklet for the
treatment of patients with low back pain. N Engl J Med 1998;339:1021–9.
57. Owens DK. Spine update: patient preferences and the development of prac-
tice guidelines. Spine 1998;23:1073–9.
58. Klein BJ, Radecki RT, Foris MP, et al. Bridging the gap between science and
practice in managing low back pain: a comprehensive spine care system in a
health maintenance organization setting. Spine 2000;25:73840.
59. Phelan EA, Deyo RA, Cherkin DC, et al. Helping patients decide about back
surgery: a randomized trial of an interactive video program. Spine 2001;26:
206–11.
60. Buchbinder R, Jolley D, Wyatt M. 2001 Volvo Award Winner in Clinical
Studies: effects of a media campaign on back pain beliefs and its potential
influence on management of low back pain in general practice. Spine 2001;
26:2535–42.
12
2316 Spine
Volume 29
Number 20
2004
Appendix A. Quality Assessment
Qualitative Studies
(39) (30) (34) (33) (36) (35) (38) (28) (29) (32) (37) (31)
Subjects
1. Description of inclusion, exclusion
criteria and selection of study
population is described.
101110111111
2. Description of the subjects in
detail (age, gender, social
position, acute or chronic back
pain).
101110011111
3. Someone other than their care
provider recruited the patients.
100000111110
Data collection/procedure
4. Method of data collection is
described in detail (recruitment,
condition in which data were
collected and listed).
111111111111
5. The treatment is described and
when more than one treatment is
studied, these are analyzed in
separate categories.
111011111101
Theoretical framework
6. There is a clear connection to a
wider theoretical
framework/existing body of
knowledge.
111111111011
Analysis & conclusions
7. Two researchers have
independently analysed the data.
100000001011
Total score () 735453467566
Conclusion quality H L H H H L HHHHHH
High quality: number of 4
Low quality: number of 3
Quantitative Studies
(45) (42) (26) (27) (41) (43) (40) (44)
Subjects
1. Description of inclusion, exclusion
criteria and selection of study
population is described.
01111111
2. Description of the subjects in
detail (age, gender, social
position, acute or chronic back
pain).
01111111
3. Someone other than their care
provider recruited the patients.
00011101
Data collection/procedure
4. Method of data collection is
described in detail (recruitment,
condition in which data were
collected and listed).
11111111
5. The treatment is described and
when more than one treatment is
studied, these are analyzed in
separate categories.
00111111
Analysis & conclusions
6. Procedure of statistical analysis is
described detailed (reproducible
process).
11011101
Total score () 24466646
Conclusion quality L HHHHHHH
High quality: number of 4
Low quality: number of 3
2317Patient Expectations
Verbeek et al
Appendix B. Questions About Treatment That Provoked Dissatisfied or Negative Answers Among Significantly More
Than 10% of Patients Treated for Back Pain in Quantitative Studies of Satisfaction With Back Pain Treatment (N 8)
Aspects of treatment/Questions % Reference Provider
1. Clinical management
Diagnosis/cause of pain
Did not explain cause of back pain 19 (43) Phys man
Did not explain cause of back pain 20 (43) Phys
Cause of problem not clearly explained 25 (43) Phys var
Did not give an adequate explanation of my problem 25 (45) Phys hosp
Technical competence
No careful examination of the back performed 20 (42)
Overall treatment result not excellent 25 (43) Phys man
No detailed history of back pain taken 32 (42) Phys var
Overall not excellent treatment 34 (43) Phys train
Not satisfied with treatment condition/overall 41 (26) GP
Overall not excellent treatment 45 (43) Phys
Not satisfied with treatment of back problem 68 (42)
Information/education
No advice on pain/prevention 20 (43) Phys
Not sufficient information about cause of back pain 21 (26) Chir
Patient not given sufficient information 27 (27) Chir
Not sufficient information about cause of back pain 34 (26) Chir
Not satisfied with information and idea about recovery time 52 (41) Chir
Not satisfied with information given 53 (42) Chir
Patient not given sufficient information 60 (27) GP
Not satisfied with information given 70 (42) Phys var
Not satisfied with information and idea about recovery time 84 (41) GP
Instructions
Patient knew how to care for back 18 (27) Chir
No instructions on exercises, lifting, don’t know what to do 29 (41) Chir
Patient knew how to care for back 49 (27) GP
No advice on sitting/sleeping/back exercise 50 (43) Phys
No instructions on exercises, lifting, don’t know what to do 62 (41) GP
Pain relief
Treatment not helpful 20 (44) Phys
Result of pain relief not excellent/good 32 (43) Phys man
No improvement in low back pain after 1 month 44 (26) GP
Result of pain relief not excellent/good 45 (43) Phys train
Result of pain relief not excellent/good 56 (43) Phys
Not satisfied with overall results of treatment 58 (42) Chir
Not satisfied with overall results of treatment 73 (42) Phys var
No improvement in low back pain after 1 month 87 (26) GP
Improvement physical ability
Did not improve ability to perform social activities/walk/work 38 (43) Phys train
Did not improve ability to perform social activities/walk/work 45 (43) Phys man
Did not improve ability to perform social activities/walk/work 52 (43) Phys
2. Facilities for patients
Did not help with job situation 59 (43) Phys train
Did not help with job situation 59 (43) Phys man
Did not help with job situation 65 (43) Phys
3. Interpersonal management
Confirmation
Doctor did not agree that pain was real 22 (27) GP
Did not believe that my pain was real 29 (41) Chir
Did not believe that my pain was real 62 (41) GP
Confidence
Not confident that treatment was working 26 (27) Chir
Not confident that recommended treatment would work 47 (26) GP
Doctor not confident/comfortable about diagnosis/treatment 35 (27) GP
Provider did not seem confident 40 (41) Chir
Not confident that treatment was working 64 (27) GP
Provider did not seem confident 79 (41) GP
Time/effort
Time spent listening by doctor not adequate 36 (27) GP
Not very satisfied with amount of time spent 47 (41) Chir
Not very satisfied with amount of time spent 72 (41) GP
Understanding
Doctors did not understand what was bothering 19 (45) Phys hosp
Doctor did not understand concerns about pain 25 (26) GP
Doctors did not understand patients’ concerns 40 (27) GP
Did not understand my concerns 45 (41) Chir
Did not understand my concerns 75 (41) GP
Concern care provider
Not concerned about pain 42 (41) Chir
Not concerned about pain 80 (41) GP
Phys physicians; phys man physicians instructed in manual therapy; Phys var physicians from various specialties; Phys hosp physicians from a hospital
setting; GP general practitioner; Chir chiropractor.
2318 Spine
Volume 29
Number 20
2004
... It has been acknowledged by both researchers and clinicians that health services for tinnitus requires significant improvement Langguth et al., 2011;Martinez et al., 2015;Searchfield, 2011). Tinnitus is like other 'invisible' chronic health issues such as back pain, insomnia and migraine (Benca, 2005;Bigal et al., 2008;Verbeek et al., 2004) in that they are self-reported. Dissatisfaction with the perceived lack of information has been consistently reported by those who experience these types of chronic conditions (Benca, 2005;Bigal et al., 2008;Verbeek et al., 2004). ...
... Tinnitus is like other 'invisible' chronic health issues such as back pain, insomnia and migraine (Benca, 2005;Bigal et al., 2008;Verbeek et al., 2004) in that they are self-reported. Dissatisfaction with the perceived lack of information has been consistently reported by those who experience these types of chronic conditions (Benca, 2005;Bigal et al., 2008;Verbeek et al., 2004). Tinnitus, in common with these other chronic health issues, is often associated with co-occurring health conditions and psychological symptoms, some of which compound the tinnitus or complicate treatment . ...
... Studies on help-seeking for chronic conditions such as back pain, insomnia and migraine have reported similar barriers upon seeking help and reasons for patient (dis)satisfaction to those found in this review. Help seekers for these other conditions reported no physical examination, greater satisfaction from allied health professionals rather than GPs, (Butler & Johnson, 2008;Verbeek et al., 2004) lack of knowledge of effective treatments, (Benca, 2005;Bigal et al., 2008) uninformed in regards to referrals, (Cheung et al., 2014) reluctance to provide recommended care or treatment (Bigal et al., 2008;Dodick et al., 2016) and incorrect diagnosis (Dodick et al., 2016). These studies all highlight the difficult process faced by people with chronic conditions to obtain a diagnosis and an informed approach to management of the condition. ...
Article
The objective of this scoping review was to describe the extent and type of evidence related to seeking help for tinnitus and satisfaction with healthcare providers including diagnosis, services and treatments along the clinical pathway. The selection criteria were adults aged 18 and over with tinnitus who sought help and where patient satisfaction with healthcare providers was reported. Online databases MEDLINE (OvidSP), Embase (OvidSP), PsycINFO (OvidSP) and CINAHL plus (EBSCO) were searched for original studies in English. The search had no date limit. Twenty-one records were eligible for data extraction. Studies reported that the most common healthcare providers seen were general practitioners, ear, nose and throat specialists and audiologists. Depression and tinnitus severity were related to an increase in the number of times help was sought and the type of healthcare provider seen may also impact patient satisfaction. The majority of participants were unlikely to receive a referral to a specialist at the initial GP consultation. Although there is limited research in this area, help-seekers for tinnitus were generally dissatisfied and reported negative interactions with healthcare providers. However, once in a specialised tinnitus clinical setting, studies reported that most help-seekers were satisfied and had positive interactions with healthcare providers.
... Bei bis zu 80 % der Betroffenen [5] lassen sich keine eindeutigen morphologischen Ursachen für den Rückenschmerz finden. Auch Personen, die unter unspezifischen Rückenschmerzen leiden, wünschen sich eine morphologische Erklärung und Diagnose ihrer Beschwerden [26]. ...
... An Patientenerwartungen, gewonnen aus qualitativen und quantitativen Untersuchungen, wurden beschrieben: klare Ursachendiagnose der Schmerzen, schmerzbezogene Informationen und Anweisungen, Schmerzlinderung, körperliche Übungen, differenzierte und weiterführende Diagnostik, Zuweisung zu anderen Therapieformen und Spezialisten sowie Krankschreibungen. Zwischenmenschlich besteht die Erwartung nach einer vertrauensvollen Verbindung mit Verstehen, Zuhören, Respekt und Beteiligung an Entscheidungsprozessen [26]. Rückenschmerzbetroffene in Rehabilitationseinrichtungen zeigen hohe Behandlungserwartungen in den Bereichen Erholung, Gesundheit und Krankheitsbewältigung [6,7]. ...
... myofasziale Befunde oder Gelenkfunktionsstörungen wurden offenbar nicht als Schmerzursache und mitgeteilte Diagnose wahrgenommen. In einem Review qualitativer und quantitativer Studien wurde dies ebenfalls beschrieben [26]: Die Patienten erwarten eine genaue Diagnose und den Nachweis, unter realen Schmerzen zu leiden. Auch Schmerzpatienten einer spezialisierten Schmerzklinik hofften, dass die morphologische Ursache ihrer Beschwerden gefunden wird und ihnen in der Bildgebung demonstriert werden kann. ...
Article
Background Apart from rehabilitation research, there have been no studies regarding the expectations of patients with chronic back pain in terms of inpatient multimodal pain therapy. The aim of this naturalistic longitudinal study is to explore treatment expectations, their fulfilment, and influence on the treatment success of inpatient multimodal pain therapy.Methods This study included 118 patients with chronic back pain who were physically examined and assessed for their psychological comorbidity. They were interviewed pre and post pain therapy. Treatment expectations were recorded via the questionnaire for assessing rehabilitational expectations and motivations (FREM-17), and further variables via the Pain Disability Index (PDI, german version) and the german Hospital Anxiety and Depression Scale (HADS-D).ResultsThe results show that treatment expectations have an impact on therapy success or failure. In particular, patients’ expectations of coping with illness and recovery could be met by inpatient multimodal pain therapy, whereas health and pension-related expectations remained unfulfilled. In addition to the treatment expectations, the therapy result was primarily determined by the patient’s ability to perform before the therapy.Conclusions From the clinical side, treatment expectations should be explored and checked for feasibility to avoid patient disappointment.
... As patients with chronic pain often tend to approach their pain from a biomedical perspective and dismiss the role of social and psychological factors in their pain complaints (De Oliveira et al., 2020;Kenny, 2004), this discussion is regarded as an important step in preparing them for treatment taking a biopsychosocial approach. In addition, it is considered important that patients and their practitioners develop a shared understanding of the causal and maintaining factors that have contributed, and still contribute, to their pain and pain-related disability (Frantsve & Kerns, 2007;Oosterhof et al., 2014;Verbeek et al., 2004). After all, if patients and practitioners reach a shared understanding about the nature of the pain problem, they are more likely to reach agreement on the treatment goals and the most appropriate treatment plan (see also McCabe, 2021). ...
... Thus, this study adds to this body of research and shows that the way in which patients and practitioners orient to the problem analysis may depend on the specific medical context. From a clinical perspective, it is considered highly important that patients and practitioners agree that the pain problem should be approached from a biopsychosocial perspective (Frantsve & Kerns, 2007;Oosterhof et al., 2014;Verbeek et al., 2004). Moreover, it is considered important that they reach a sufficiently shared understanding of the causal and maintaining factors involved in the pain and pain-related disability before they move on to treatment (Verbunt et al., 2019). ...
Article
Full-text available
Before patients with chronic pain enter an interdisciplinary chronic pain rehabilitation programme, a team of various healthcare professionals performs a biopsychosocial analysis of their pain problem. To enhance patients’ engagement, the problem analysis is thoroughly discussed with them in order to gain a shared understanding of the nature of their pain problem. This study explores how patients and practitioners talk through their rehabilitation team’s hypotheses regarding the psychosocial factors involved in these patients’ health situation. Nine consultations were recorded at various Dutch interdisciplinary chronic pain rehabilitation units. The recordings were transcribed and analysed, combining an applied conversation analytic research approach with discursive psychology. Patients and practitioners are found to orient to ensuring consensus on the problem analysis as a relevant activity and tend to avoid or minimize the articulation of differences in perspectives. This study also shows that this orientation to consensus involves a delicate management of issues of accountability and blame. Findings can be used by practitioners to consider communication practices that are more likely to encourage patients to voice potential concerns regarding their rehabilitation team’s findings.
... Expectations of the visit were met to a greater extent in the standard care group. When consulting a caregiver (PT or physician), it has previously been reported that the most important expectation is not to recover but to have their disorder confirmed [28][29][30]. In the present study, all the patients had knowledge of their diagnosis prior to being referred for an orthopedic assessment. ...
Article
Full-text available
Background Physical therapy-led orthopedic triage is a care model used to optimize pathways for patients with hip or knee osteoarthritis. However, scientific evidence of the effectiveness of this model of care is still limited and only a few studies report patients’ perception of it. The aim of this study was to compare patients’ perceived quality of care after physical therapy-led triage with standard practice in a secondary care setting for patients with primary hip or knee osteoarthritis. Methods In this randomized study, patients with hip or knee osteoarthritis referred for an orthopedic consultation received either physical therapy-led triage (n = 344) or a standard care assessment by an orthopedic surgeon (n = 294). To evaluate the patients’ perceived quality of care, a short version of the Quality from the Patient’s Perspective (QPP) questionnaire was sent to the patients within a week after their assessment. The primary outcome was the statement “I received the best examination and treatment” on QPP. Results A total of 348 patients (70%, physical therapy-led triage: n = 249, standard care: n = 199) answered the questionnaire. No significant difference was found in the primary outcome between the groups (p = 0.6). Participants in the triage group perceived themselves to have received significantly better information about how to take care of their osteoarthritis (p = 0.017) compared with the standard care group. The standard care group reported that they participated in the decision-making process to a greater extent (p = 0.005), that their expectations were met to a greater degree (p = 0.013), and that their care depended more on their need for care rather than the caregivers’ routines (0.007). Conclusion Both groups report high perceived quality of care. Significant differences were found in four of 14 questions, one in favor of the physical therapist and three in favor of the standard care group. The findings of this study are in line with previous research and support the use of this care model for patients with hip or knee OA in secondary care. However, due to the dropout size, the results should be interpreted with caution. Trial registration Clinical Trials NCT04665908, registered 14/12/2020.
... 19 Expectations can be positively modulated using verbal suggestions with instructions about the benefits of an individual intervention. [20][21][22] Another mechanism underlying placebo effects involves classical conditioning. 16 For example, in the context of placebo hypoalgesia, classical conditioning is typically induced in the laboratory using a 'response conditioning' paradigm, where treatment cues (eg, cream or injection) are paired with surreptitious reductions in the intensity of painful stimuli. ...
Article
Full-text available
Introduction Placebo effects are responses capable of modulating pain and influencing treatment response. Two mechanisms are commonly related to placebo effects: expectations and conditioning. However, the research in this field is focused on laboratory studies with healthy participants. This study aims to identify whether a conditioning procedure with positive induced expectations about spinal manipulative therapy (SMT) will result in greater hypoalgesic effects in adults with chronic low back pain (CLBP) in a clinical trial design. Methods and analysis This trial will enrol 264 patients with non-specific CLBP, aged 18–60 years. Patients will undergo a calibration test to determine the thermal pain threshold for the hidden pain conditioning procedure. Afterward, they will be randomised to one of the three groups: hidden pain conditioning with positive induced expectations—group one (G1); positive expectations—group two (G2) and neutral expectations—group three (G3). Patients will receive instructions to manipulate the expectations. The pretreatment heat pain test will be performed before the SMT and after the intervention patients will undergo again the heat pain intensity test. However, only patients in G1 will receive hidden pain conditioning to reinforce the association between SMT and pain intensity reduction. All patients will undergo five sessions of SMT. The outcomes will be assessed immediately after the last session and at the 6 weeks and 3-month follow-ups. All statistical analyses will be conducted following intention-to-treat principles, and the treatment effects will be determined with linear mixed models. Ethics and dissemination The Federal University of São Carlos approved this research (Process n° 52359521.1.0000.5504). All participants will give written informed consent. Dissemination of the results will include publications in peer-reviewed journals and presentations at conferences. If positive expectations and classical conditioning improve outcomes, it may support the administration of such intervention. Trial registration number NCT05202704 .
... Expectations of the visit were met to a greater extent in the standard care group. When consulting a caregiver (PT or physician), it has previously been reported that the most important expectation is not to recover but to have their disorder con rmed [19][20][21]. In the present study, all the patients had knowledge of their diagnosis prior to being referred for an orthopedic assessment. ...
Preprint
Full-text available
Background: Physical therapy-led orthopedic triage is a care model used to optimize pathways for patients with hip or knee osteoarthritis. However, scientific evidence of the effectiveness of this model of care is still limited and only a few studies report patients’ perception of it. The aim of this study was to compare patients’ perceived quality of care after physical therapy-led triage with standard practice in a secondary care setting for patients with primary hip or knee osteoarthritis. Methods: In this randomized study, patients with hip or knee osteoarthritis referred for an orthopedic consultation received either physical therapy-led triage (n=344) or a standard care assessment by an orthopedic surgeon (n=294). To evaluate the patients’ perceived quality of care, a short version of the Quality from the Patient’s Perspective questionnaire was sent to the patients within a week after their assessment. The primary outcome was the statement “I received the best examination and treatment”. Results: A total of 348 patients (70%, Physical therapy-led triage: n=249, Standard care: n=199) answered the questionnaire. No significant difference was found in the primary outcome between the groups (p=0.6). Participants in the triage group perceived themselves to have received significantly better information about how to take care of their osteoarthritis (p=0.017) compared with the standard care group. The standard care group reported that they participated in the decision-making process (p=0.005) to a greater extent, that their expectations were met (p=0.013) to a greater degree and that their care depended more on their need for care rather than the caregivers’ routines. Conclusion: Both groups report high perceived quality of care. Significant differences were found in four of 14 questions, one in favor of the physical therapist and three in favor of the standard care group. The results in the present study suggest that physical therapy-led triage can be implemented for patients with hip or knee osteoarthritis at a secondary care unit. Trial registration: Clinical Trials NCT04665908, registered 14/12/2020
... Patient satisfaction can be interpreted as a level of patient satisfaction with the care provided. According to expectations theory, satisfaction is the correlation between what the patient wants and the extent to which his desire has been satisfied, but it is necessary to know the needs of patients (Verbeek et al., 2004). ...
Chapter
Full-text available
This study has been focused on examining examine the dynamics of liberalization, privatization, and globalization in relation to export performance for Ethiopian privatized manufacturing firms since 1991. To achieve these objectives, cross-sectional data was collected from 114 fully privatized manufacturing firms through key informant approaches and structural equation modelling (SEM) was used. This model identified liberalization, privatization, and globalization as independent variable under competitive priority mediating role for export performance. The model tells that all the predicting variables (LPG) in the hypothesized model were significant at P< 0.05 and this shows that economic liberalization, privatization, and economic globalization affect export performance under all competitive priority. The finding shows that LPG stimulates export performance under firm’s competitive priority an intervening role. The competitive priority of firms comprises cost, flexibility, and quality priority. Those measures confine arouses export performance in terms of both quantitative (market share, profit) and subjective measures (export satisfaction) indicators. The extent of law-and-order commitment towards financial and non-financial incentives) and the overall trade openness use as liberalization indicator.
... Patient satisfaction can be interpreted as a level of patient satisfaction with the care provided. According to expectations theory, satisfaction is the correlation between what the patient wants and the extent to which his desire has been satisfied, but it is necessary to know the needs of patients (Verbeek et al., 2004). ...
... However, already prior to the consultation, when both diagnosis and available treatment options are still unknown, patients may have developed a firm set of expectations for the treatment of their condition, as well as for the anticipated outcomes of this treatment [10,14,15]. Because of these expectations, patients can develop a preference for a specific treatment option. ...
Article
Full-text available
Objective Existing studies on shared decision-making (SDM) have hardly taken into consideration that patients could have independently developed expectations prior to their consultation with a healthcare provider, nor have studies explored how such expectations affect SDM. Therefore, we explore how pre-consultation expectations affect SDM in patients with low back pain. Methods We performed a qualitative study through telephone interviews with 10 patients and seven care professionals (physicians, nurse, physician assistants) and 63 in-person observations of patient-physician consultations in an outpatient clinic in the Netherlands. Transcripts were analyzed through an open coding process. Results A discrepancy existed between what patients expected and what care professionals could offer. Professionals perceived they had to undertake additional efforts to address patients' ‘unrealistic’ expectations while attempting SDM. Patients, in turn, were often dissatisfied with the outcomes of the SDM encounter, as they believed their own expectations were not reflected in the final decision. Conclusion Unaddressed pre-consultation expectations form a barrier to constructive SDM encounters. Practical implications Patients’ pre-consultation expectations need to be explored during the SDM encounter. To achieve decisions that are truly shared by care professionals and patients, patients’ pre-consultation expectations should be better incorporated into SDM models and education.
Article
Purpose A narrative review was conducted to identify, critically appraise, and synthesise primary research on the lived experiences of postmenopausal women with osteoporosis. Materials and methods A systematic search of qualitative studies published between January 1960 and August 2021 was conducted across seven databases. The selected qualitative studies reported the lived experiences of postmenopausal women with osteoporosis, both with and without a history of fragility fractures. Results A total of 17 publications (n = 334) were identified. These results suggest that osteoporosis and fragility fractures significantly affected postmenopausal women’s lives. They reported difficulties in carrying out daily activities due to pain and change in their routines to cope with health problems. Some women were satisfied with the information provided by healthcare professionals. Their medicine adherence was also determined by their belief in the importance of their scheduled treatment for osteoporosis. Conclusion Qualitative studies that explored the lived experiences of postmenopausal women with osteoporosis can provide important insights into the impact of the disease on women’s lives and potential pathways for improving care and management. • Implications for rehabilitation • Osteoporosis and fragility fractures affect the quality of life of postmenopausal women worldwide. • The provision of targeted and tailored health information for postmenopausal women with osteoporosis is paramount in improving their health literacy and aiding in the long-term management of their bone health. • What is already known • Osteoporosis and related fragility fractures are common, affecting more than 200 million people worldwide, including three million people in the UK. • Osteoporotic fractures have significant clinical and public health impacts. • What this study adds • Osteoporosis, particularly fragility fractures, has a significant impact on the lives of postmenopausal women, including pain and functional impairment. • Women’s belief in the importance of their scheduled treatment plays a significant role in their concordance with the prescribed medications for osteoporosis. • Provision of targeted health information for postmenopausal women with osteoporosis is key to their involvement in decision-making and disease management.
Article
Full-text available
To advance understanding of the lived experience of diabetes as described in published research and theses. Meta-analysis extends the analysis of individual research studies beyond individual experience to incorporate dominant system beliefs and health system ideologies. Curtin and Lubkin's (1990) conceptualization of the experience of chronic illness. Forty-three qualitative interpretive research reports in six computerized data bases 1980-1996 pertaining to the lived experience of diabetes and published in nursing, in the social sciences, and in allied health journals were used. Meta-ethnography in which trustworthiness was achieved by using multiple researchers, identifying negative or disconfirming cases, and testing rival hypotheses Balance is the determinant metaphor of the experience of diabetes. People learn to balance diabetes through their experience and experimentation with strategies for managing their illness. Learning to balance is a developmental process in which one learns to assume control of diabetes management. Support for such development requires that nurses know their clients as individuals and value the expertise they have gained in living with diabetes. Control of blood sugar levels within a prescribed range may be a goal established by professionals, but the goal of healthy balance determines a person's willingness to assume an active role in self-care.
Article
Full-text available
Background and objectives. Improving the sensitivity of general practice to Patients' needs demands a good understanding of Patients' expectations and priorities in care provision. Insight into differences in expectations of patients in different cultures and health care systems may support decision-making on desirable models for care provision in general practice. An international study was conducted to determine priorities of patients in general practice care: which views do patients in different countries have in common and which views differ? Methods. Written surveys in general practices in the UK, Norway, Sweden, Denmark, The Netherlands, Germany, Portugal and Israel were performed. Samples of patients from at least 12 practices per country, stratified according to area and type of practice, were included. Patients rated the importance of 38 different aspects of general practice care, selected on the basis of literature analysis, qualitative studies and consensus discussions. Rankings between countries were compared. Results. A total number of 3540 patients (response rate on average 55%) completed the questionnaire. Patients in different countries had many opinions in common. Aspects that got the highest ranking were: getting enough time during the consultation; quick services in case of emergencies; confidentiality of information on patients; telling patients all they want to know about their illness; making patients feel free to talk about their problems; GPs going to courses regularly; and offering preventive services. However, differences between opinions of patients in different countries were also found for some of the selected aspects. A confounding effect of Patients' characteristics may have played a role in these differences. Discussion. The study provides information on what patients expect of and value in general practice care. It shows that patients in different cultures and health care systems may have different views on some aspects of care, but most of all that they have many views in common, particularly as far as doctor–patient communication and accessibility of services are concerned.
Article
Full-text available
Objective: To test the hypothesis that radiography of the lumbar spine in patients with low back pain is not associated with improved clinical outcomes or satisfaction with care. Design: Randomised unblinded controlled trial. Setting: 73 general practices in Nottingham, north Nottinghamshire, southern Derbyshire, north Lincolnshire, and north Leicestershire. 52 practices recruited participants to the trial. Subjects: 421 patients with low back pain of a median duration of 10 weeks. Intervention: Radiography of the lumbar spine. Main outcome measures: Roland adaptation of the sickness impact profile, visual analogue scale for pain, health status, EuroQol, satisfaction with care, use of primary and secondary care services, and reporting of low back pain at three and nine months after randomisation. Results: The intervention group were more likely to report low back pain at three months (relative risk 1.26, 95% confidence interval 1.00 to 1.60) and had a lower overall health status score and borderline higher Roland and pain scores. A higher proportion of participants consulted their doctor in the three months after radiography (1.62, 1.33 to 1.97). Satisfaction with care was greater in the group receiving radiography at nine but not three months after randomisation. Overall, 80% of participants in both groups at three and nine months would have radiography if the choice was available. An abnormal finding on radiography made no difference to the outcome, as measured by the Roland score. Conclusions: Radiography of the lumbar spine in primary care patients with low back pain of at least six weeks' duration is not associated with improved patient functioning, severity of pain, or overall health status but is associated with an increase in doctor workload. Guidelines on the management of low back pain in primary care should be consistent about not recommending radiography of the lumbar spine in patients with low back pain in the absence of indicators for serious spinal disease, even if it has persisted for at least six weeks. Patients receiving radiography are more satisfied with the care they received. The challenge for primary care is to increase satisfaction without recourse to radiography.
Article
Background: Chronic lower back pain (CLBP), without definable cause, is a symptom commonly presented to GPs, accounting for a significant proportion of their workload; it is also a common reason for sickness absence, and thus of national economic importance. Objectives: This qualitative study aims to explore how sufferers of CLBP describe their pain and its impact on their lives, and how their problem is dealt with in the consultation with their family doctor. Method: Semi-structured interviews were carried out with a sample of attenders at a back pain clinic set up in general practice. Transcription and analysis was carried out using a grounded-theory approach. Results: Sufferers of CLBP describe withdrawal from normal social obligations, including work. They view their GP as being unable to help and, because of this, the doctor becomes a resource through which their social and economic inactivity can be legitimated. Conclusions: Presenting with CLBP permits the patient a good deal of power over the GP: it is difficult for the GP to challenge the patient's ideas without damaging the relationship. GPs are forced to collude with the patient's definition of ill-health, which may not be in the best interests of the patient or society.
Article
In this document, the framework for carrying out systematic reviews is described in three stages: planning, reviewing and disseminating. The need for a review should be established before commissioning or commencing review work. The methodology of the review should be documented and working arrangements should be put in place to ensure that the methods can be followed. Finally, there should be a strategy for putting together a report of the review and disseminating its findings to relevant audiences, and if possible, updating the review. The stages of a review and the phases within them are described consecutively. However, this chronology may vary during the review. It will not always be possible to complete one phase before another has to be started, and sometimes it will be more efficient to work on several phases simultaneously. It is essential that good communication is maintained between those commissioning or supervising the review and those carrying it out. To aid the process, this framework includes agendas for some joint meetings. These meetings help set a timetable and ensure that the review work receives the required direction and support. The number of meetings and their schedule may have to be tailored to suit the requirements of a given review. The content of this report draws on information from several sources. All the steps necessary to undertake a systematic review have been listed, but it is not possible to provide definitive advice on all of the methods. This is because the science of systematically reviewing the literature is relatively young, and many methodological issues are still being explored. Therefore this guidance is to assist those conducting reviews to reach a minimum standard based on the understanding of the subject at the time of writing. Reviewers wishing to obtain up-to-date information in this area should look at the Cochrane Methodology Database and systematic reviews of empirical methodological research in the Cochrane Library. New advice is incorporated in updates of the Cochrane Reviewers' Handbook (URL: http://www.updatesoftware. com/ccweb/cochrane/hbook.htm) and the ‘Resources available at the CRD’ web site (URL: http:// www.york.ac.uk/inst/crd/).
Article
This paper concerns the concepts and practices currently in use in occupational health for the rehabilitation of workers with back pain. No conclusive evidence exists for an etiologic model for nonspecific back pain. A difference between acute and chronic back pain is backed up by evidence from the literature. Apart from having the patient stay active and return to ordinary activities as early as possible, there are no significant forms of intervention for acute back pain that effectively decrease the time off work. For chronic back pain multidisciplinary treatment in an occupational setting is effective in enhancing return to work. Clinical practice guidelines consist of diagnostic triage, the assessment of "red flags" for medical emergencies, and guidance in the appropriate application of diagnostic facilities. Occupational health guidelines concentrate on gradual return to work, psychosocial issues, and multidisciplinary rehabilitation facilities.
Article
People treated for cancer have reported a variety of problems at work. However, there is little data on work experience after breast cancer, particularly for women treated in recent years. This exploratory qualitative study was conducted among 13 breast cancer survivors who had paid employment at diagnosis, returned to work afterwards, and mentioned work-related problems to a clinic nurse or physician. Unstructured, thematic interviews were undertaken. Qualitative thematic content analysis was conducted to identify and group themes which emerged from participants' discourse. Women in various types of jobs reported experiencing job loss, demotion, unwanted changes in tasks, problems with the employer and co-workers, personal changes in attitudes to work and diminished physical capacity. These work problems also preoccupied people treated for cancer more than two decades ago. New areas of concern also emerged: possible positive and negative effects of learning (implicitly or explicitly) about the diagnosis while at work and lack of discussion with health professionals about work and return-to-work issues, suggesting that health professionals' behaviour may influence women's work experience right from diagnosis. The identification of these new problems and confirmation of previously reported ones underlines the pertinence of determining how important and widespread these problems are in women now being treated for breast cancer.
Article
We compare health maintenance organization enrollees' evaluations of the care they received from family physicians and chiropractors for low back pain. Patients of chiropractors were three times as likely as patients of family physicians to report that they were very satisfied with the care they received for low back pain (66% versus 22%, respectively). Compared with patients of family physicians, patients of chiropractors were much more likely to have been satisfied with the amount of information they were given, to have perceived that their provider was concerned about them, and to have felt that their provider was comfortable and confident dealing with their problem. Although the more positive evaluations of chiropractors may be related to differences in the patient populations served by the two providers or to benefits of spinal manipulation, it is suggested that a potentially more potent force--the therapeutic effect of the patient and provider interaction itself--may explain the observed differences.