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Determinants of patient satisfaction in ambulatory oncology: A cross sectional study based on the OUT-PATSAT35 questionnaire

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The aim of this study was to identify factors associated with satisfaction with care in cancer patients undergoing ambulatory treatment. We investigated associations between patients' baseline clinical and socio-demographic characteristics, as well as self-reported quality of life, and satisfaction with care. Patients undergoing ambulatory chemotherapy or radiotherapy in 2 centres in France were invited, at the beginning of their treatment, to complete the OUT-PATSAT35, a 35 item and 13 scale questionnaire evaluating perception of doctors, nurses and aspects of care organisation. Additionally, for each patient, socio-demographic variables, clinical characteristics and self-reported quality of life using the EORTC QLQ-C30 questionnaire were recorded. Among 692 patients included between January 2005 and December 2006, only 6 were non-responders. By multivariate analysis, poor perceived global health strongly predicted dissatisfaction with care (p < 0.0001). Patients treated by radiotherapy (vs patients treated by chemotherapy) reported lower levels of satisfaction with doctors' technical and interpersonal skills, information provided by caregivers, and waiting times. Patients with primary head and neck cancer (vs other localisations), and those living alone were less satisfied with information provided by doctors, and younger patients (< 55 years) were less satisfied with doctors' availability. A number of clinical of socio-demographic factors were significantly associated with different scales of the satisfaction questionnaire. However, the main determinant was the patient's global health status, underlining the importance of measuring and adjusting for self-perceived health status when evaluating satisfaction. Further analyses are currently ongoing to determine the responsiveness of the OUT-PATSAT35 questionnaire to changes over time.
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RESEARCH ARTICLE Open Access
Determinants of patient satisfaction in
ambulatory oncology: a cross sectional study
based on the OUT-PATSAT35 questionnaire
Thanh Vân France Nguyen
1,3*
, Jean-François Bosset
1,3
, Alain Monnier
2
, Jacqueline Fournier
1
, Valérie Perrin
2
,
Cédric Baumann
4
, Anne Brédart
5
and Mariette Mercier
3,6
Abstract
Background: The aim of this study was to identify factors associated with satisfaction with care in cancer patients
undergoing ambulatory treatment. We investigated associations between patients baseline clinical and socio-
demographic characteristics, as well as self-reported quality of life, and satisfaction with care.
Methods: Patients undergoing ambulatory chemotherapy or radiotherapy in 2 centres in France were invited, at
the beginning of their treatment, to complete the OUT-PATSAT35, a 35 item and 13 scale questionnaire evaluating
perception of doctors, nurses and aspects of care organisation. Additionally, for each patient, socio-demographic
variables, clinical characteristics and self-reported quality of life using the EORTC QLQ-C30 questionnaire were
recorded.
Results: Among 692 patients included between January 2005 and December 2006, only 6 were non-responders.
By multivariate analysis, poor perceived global health strongly predicted dissatisfaction with care (p < 0.0001).
Patients treated by radiotherapy (vs patients treated by chemotherapy) reported lower levels of satisfaction with
doctors technical and interpersonal skills, information provided by caregivers, and waiting times. Patients with
primary head and neck cancer (vs other localisations), and those living alone were less satisfied with information
provided by doctors, and younger patients (< 55 years) were less satisfied with doctors availabi lity.
Conclusions: A number of clinical of socio-demographic factors were significantly associated with different scales
of the satisfaction questionnaire. H owever, the main determinant was the patients global health status, underlining
the importance of measuring and adjusting for self-perceived health status when evaluating satisfaction. Further
analyses are currently ongoing to determine the responsivene ss of the OUT-PATSAT35 questionnaire to changes
over time.
Keywords: Patient satisfaction, Ambulatory oncology, Quality of life
Background
Patient satisfaction is recognised as a key performance
indicator in assessing quality of care, increasi ngly
required by accreditation agencies in the monitoring of
quality of hospital care in order to identify c are areas i n
need of improvement. Furthermore, satisfaction with
care may influence a patient s adherence to medical
treatment and consequently, impact on outcome.
Cancer treatments are often long, are associated with
frequent interactions and increased dependenc y on mul-
tidisciplinary healthcare services. In this context, patient
satisfaction with th eir experience of continuity of care, as
well as their relationships and communication with care-
givers, nee d to be evaluate d with a view to dete rmining
whether the patients expectations are being fulfilled.
Deter mining predictors of patient satisfaction has sev-
era l objectives. Firstly, identifying patient characteristics
(socio-demographic or clinical factors, baseline quality
of life (QOL)), should aid in interpreting questionnaire
results, by adjusting for these factors, particularly for
* Correspondence: nguyen_france@yahoo.fr
1
Oncology-Radiotherapy Department, Besançon University Hospital, 3
boulevard Fleming, 25030 Besançon, Cedex, France
Full list of author information is availabl e at the end of the article
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© 2011 Nguyen et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons
Attribution Licens e (http://creativecommons.org/license s/by/2.0), which pe rmits unrestricted use, distribution, an d reproduction in
any medium, provide d the original work is properl y cited.
benchmarking when comparing health care services
[1-3]. Furtherm ore, patient satisfaction surveys can help
to identify patient groups who need additional attention
or even targeted interventions, and bring to light areas
of the care process (e.g. organisation, providers commu-
nication skills) where there is room for improv ement
[4,5]. Socio-demographic charac teristics and health sta-
tus are the most w idely studied predictors of satisfac-
tion, with older age, low education and a good state of
health commonly reported to be associated with greater
satisfaction [ 6-11]. However, conflicting results have
been observed in this regard and especi ally the relation-
ship between these two conce pts, self-perceived qua lity
of life and satisfaction with care, remains debated.
In the setting of oncology, there has been an increase in
the use of ambulatory treatments, which represent a
completely differ ent cont ext to hospitalization. While
interpersonal (i.e. communication) o r technical (i.e. drug
administration) aspects of care, and multidisciplinary
teamwork are components common to patient satisfac-
tion in both in- and o ut-patients, other factors, such a s
hospital accessibility a nd t reatment en vironment (i.e.
location, appointment waiting lists, waiting times, park-
ing facilities) are concerns that are more specific to the
ambulatory setting [12]. A number of studies evaluating
patientsatisfactionquestionnaireresponsesinanambu-
latory oncology setting have been published [12-21]
focusing mainly on organisational aspects of care and the
quality of patient-caregiver relationships. However, none
of these studies attempted to ide ntify patient groups who
may be more at risk of dissatisfaction with care.
Theaimofthepresentstudywas,ontheonehand,to
identify patients clinic al and socio-demographic charac-
teristics as potential determinants of satisfaction with care
in cancer patients undergoing ambulatory chemo- or
radiotherapy. On the other hand, we investigated the influ-
ence of self-reported quality of life on satisfaction with
care, as measured by multi-dimensional questionnaires.
Methods
We conducted a multicenter, prospective cohort s tudy
of cancer outpatients from the beginning to 3 months
after the end of their treatment. The present analyses
were performed only on data collected at the beginning
of the treatment
The protocol was approved by the ethics committee of
the University Hospital of Besançon (Doubs, France),
the National French Data Protec tion Agency, and sup-
ported by a regional grant (Programme Hospitalier de
Recherche Clinique).
Patients
Patients were enrolled in two centres (one university
teaching hospital and one local (non-academic) hospital)
in eastern France between January 2005 and December
2006. Inclusion criteria were: patients aged over 18
years, able to understand written and spoken French,
able to provide written consent, able to com plete the
questionnaires, with a confirmed histological diagnosis
of cancer, and due to undergo ambulato ry treatment by
chemo- or radiotherapy,
The subsequent cancers were included in 9 treatment
groups: 2 prostate cancer groups (radiotherapy only or
surgery followed by radiotherapy), 3 breast cancer groups
(surgery plus radiotherapy, or surgery plus chemo and
radiotherapy, or chemotherapy alone), 2 head and neck
cancer groups (surgery plus radiotherapy or radiotherapy
with or without concurrent chemotherapy), 1 rectum
cancer group (radiochemotherapy plus surgery) a nd 1
lung cancer group (chemo and radiotherapy).
Study procedures and measures
Patients were invited to participate in the study at the
end of the first week of radiotherapy or at the second
cycle of chemotherapy . However, it was n ot technical ly
possible to meet all patients on a systematic basis.. Once
the patient agreed to participate and provided informed
consent, the socio-demographic questionnaire was com-
pleted with the research technician. The EORTC QLQ-
C30 and OUT- PATSAT35 questionnaires were given to
the patient to complete at home and mail back using a
pre-addressed, stamped envelope. Patients were
reminded to return the questionnaires on their next
visit, if they came back for radiotherapy treatment, or by
phone after 2 weeks, where necessary.
The EORTC IN-PATSAT32 questionnaire was devel-
oped by the EORTC QOL group in order t o assess
patient satisfaction with careinoncologyhospitals
[Additional file 1: Appendix A]. The OUT-PATSAT35
questionnai re was adapted from IN-PATSAT32, for use
among outpatients treated b y ambulatory chemotherapy
or radiotherapy [Additional file 2: Appendix B]. Ade-
quate psychometric properties have been reported in
French and Spanish language versions [22,23].
OUT-PATSAT35 contains 35 items covering 12
multi-item scales organized into three sections of fo ur
scales each: 2 sections evaluating doctors and nurses
(for chemotherapy) or radiation therapists (for radio-
therapy), as regards their technical skills (knowledge,
experience, assessment o f physical symptoms), i nterper-
sonal skills (int erest, wil ling ness to listen), provision of
information (about the disease, medical tests and treat-
ment), and a vailability (time devoted to patients); and a
third section evaluating the organization of the depart-
ment, the exchange of information between caregivers
(coherence, identification of the reference doctor), the
interpersonal skills and qua lity of infor mation pr ovided
by other hospital staff, waiting times (for consultation,
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medical tests, or treatment), the physical environment
(access, comfort, orientation), and lastly, a single-item,
overall satisfaction scale.
Items a re rated on a 5-level Likert scale as follows:
poor, fair, good, very good, excellent. All scores
are linearly transformed to a 0 -100 scale, with a higher
score reflecting a higher level of satisfaction.
The EORTC QLQ-C30 (versio n 3.0) is a 30-item self-
assessment of 15 scales of quality of life: 5 functional scales
(physical, ro le, emotional, cognitive, social) , 9 sympt om
scales (fatigue, nausea or vomiting, pain, dyspnoea, insom-
nia, constipation, diarrhoea, financial difficulties) and
finally, a global health scale. All measures range from 0 to
100. High scores on the functional scales represent a heal-
thier level of functioning, whereas high scores on the
symptom scales represent a higher level of symptoms.
The following variables were collected by self-adminis-
tered questionnaire and f rom medical records: gender,
age (in years), marital status, level of education (primary,
secondary, high school diploma or highe r), number of
children, occupation (employed versus unemployed/
retired), monthly income (i n Euro), distan ce from home
to hospital (in kilometres (km)), means of transport
(personal car versus other), leisure activities (yes/no),
number of co morbidities (renal, cardiac, respiratory,
hepatic, diabetes), primary cancer site (prostate, head
and neck, breast, rectum, lung), treatment mo dality
(chemotherapy and/or radiotherapy).
Statistical methods
Thesamplesizeof520patients was calculated acc ord-
ing to Cohens procedure based on multiple regression
with a b risk of 20%, an a risk of 1%, a participation
rate of 90% and a ΔR
2
of 0.05 [24].
Patient characteristics were compared using Fisher s
exact test, or Chi square for categorical data, and the
Student t test for continuous data. Continuous data
were subsequently coded into 2 or more classes catego-
rical variables for the further analyses.
Bivariate analysis
The associations between EORTC QLQ-C30 and OUT-
PATSAT35 scores were analysed by Pearson correlation
and general linear regression. Then, we assessed the
relationship bet ween eac h categoric al vari able (cl inical
and socio-demographic data) and all OUT-PATSAT35
scores (considered as dependent variables) using analysis
of variance (MANOVA model). We investigated colli-
near r elationships between sex, chemo- or radiotherapy,
and primary cancer localization.
Multivariate analysis
Significant categorical and cont inuous variables (QLQ-
C30 scores) by bivariate analysis, were introduced into
the multivariate models using analysis of variance
(ANOVA) for each scale score of the OUT-PATSAT35
questionnaire.
The significance level for bivariate analysis was set at
a = 0.05 and for multivariate analysis at a =0.01(to
correct for multiple testing). All tests were two-sided.
For the in terpretation of the scores, we considered the
minimal difference defined as clinically meaningful by
Osoba et al as a mean change of at least 5 points [25].
Statistical analysis was performe d using Sta tistical
Analysis Software (version 9.1, SAS Institute, Cary, NC).
Results
Patient characteristics
733 patients met the eligibility criteria and were invited
to participate in the study: 41 patients (5.6%) declined.
Thus, 692 patients were included. of whom 2 patients
failed to answer both questionnaires OUT-PATSAT35
and QLQ-C30 and 4 patients for the OUT-PATSAT35
(0.9% of non respondents). The characteristics of the
study population are shown in Tabl e 1. Median age var-
ied from 63 to 66 years (range 29-88), with a balanced
proportion of ma les and females. The percentage of sin-
gle patients was 18% and 21% in the local and university
teaching hospitals respectively, while monthly income
waslessthan1500Eurofor42%and41%ofpatients,
respectively. Most significant differences between the
two centres were observed for the distribution of the
primary cancer site, the number of patients treated by
radiotherapy and the distance fr om home to hospital (p
< 0.0001). All patients were treated in a curative intent
except for 5 patients who had metastases.
EORTC QLQ-C30 and OUT-PATSAT35 scores
Mean scores for the OUT-PATSAT35 sc ales ranged
from 61.7 to 71.3 for the evaluation of doctors, from
58.5 to 72.5 for nurses or radiation therapists, from 59.8
to 64.6 for the organization or physical environment,
while the mean overall satisfaction score was 72.5. Mean
scores for the EORTC QLQC30 functio nal scales ranged
from 63.6 (global health) to 82.7 (cognitive functioning)
and for symptom scales from 8.7 ( financial difficulties)
to 33.5 (fatigue) (Table 2).
Bivariate analysis
Correlation coefficients were significant between almost
all OUT-PATSAT35 scales and the QLQ-C30 functional
scales, fatigue, pain and sleep. The highest correlation
coefficients (0.20 < r < 0.30, p < 0.000 1) were observed
between global health and almost all OUT-PATSAT35
scales (the maximal correlation was between gl obal
health and the doctors technical skills), between emo-
tional functioning and nurse or radiation therapist avail-
ability, and doctors provision of information scales.
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Table 1 Socio-demographic and clinical characteristics of the study population
Characteristics Local hospital Teaching hospital p
309 383
Sex male/female 157 (51) 198 (51.7) 0.88
Age Median [min;max] 66 [29;88] 63 [31;84] 0.06
30-55 65 (21) 87 (22.7)
56-65 72 (23.3) 114 (29.8)
66-75 118 (38.2) 138 (36)
76-88 54 (17.5) 44 (11.5)
Marital status Single or separated 55 (18.2) 81 (21.2) 0.34
Living with partner, or family 248 (81.8) 301 (78.8)
Education level primary 149 (50.5) 169 (44.6) 0.01
secondary 80 (27.1) 87 (23)
high school diploma or higher 66 (22.4) 123 (32.4)
Employment status Employed 64 (21.1) 111 (29.1) 0.02
Retired or unemployed 239 (78.9) 270 (70.9)
Children No 28 (10.3) 47 (12.5) 0.52
Yes (not dependent) 193 (70.7) 268 (71.1)
Yes (still dependent) 52 (19) 62 (16.4)
Distance home-hospital Number of km: Median [min;max] 15 [1;160] 35 [1;145] < 0.0001
20 203 (65.7) 146(38.1) < 0.0001
> 20 106 (34.3) 237(61.9)
Means of tranport Personal car 135 (48.8) 120(31.3) 0.0007
Other (taxi, ambulance, bus) 173 (56.2) 263(68.7)
Monthly income In Euro 0.03
MW or less 34 (13) 36 (9.8)
MW-1499 103 (39.3) 115(31.4)
1500-2999 96 (36.6) 152(41.5)
3000 29 (11.1) 63 (17.2)
Leisure activities Yes/no 178 (59.3) 242 (64.2) 0.20
Localization treated Prostate 76 (24.6) 52 (13.6) < 0.0001*
RT
Surgery+RT 32 (10.4) 50 (13)
Head and neck 6 (1.9) 16 (4.2)
Surgery+RT
RT+/-CT 26 (8.4) 45 (11.8)
Breast 72 (23.3) 133 (34.8)
Surgery+RT
Surgery+CT+RT 66 (21.4) 35 (9.1)
CT 5 (1.6) 0
Rectum 5 (1.6) 18 (4.7)
RT+CT+surgery
Lung 21 (6.8) 34 (8.9)
CT+RT
Chemotherapy Yes 111 (36) 111 (29) 0.048
Radiotherapy Yes 236 (77.1) 347 (90.6) < 0.0001
Number of comorbidities 0 94 (30.4) 107 (27.9) 0.24
1 132 (42.7) 142 (37.1)
2 63 (20.4) 97 (25.3)
3 20 (6.5) 37 (9.7)
RT = radiotherapy; CT = chemotherapy; MW = minimum wage.
*p for heterogeneity between primary localizations
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We identified primary localization, type of treatment,
age, sex, marita l status, leisure activities, home-hospital
distance and monthly income as variables significantly
associated with at least one OUT-PATSAT35 scale (p <
0.05, Tabl e 3) . Considering the min imal clinicall y mean-
ingful differenc e score, patients treated for head and
neck cancer appeared to be less satisfied with the tech-
nical skills, information and a vailabilit y of doctors, pro-
vision of info rmation by nurses or r adiati on therap ists,
exchange of information between caregivers, physical
environment and overall satisfaction than those treated
for prostate cancer. Patients receiving radiotherapy
reported less satisfaction with doctors technical s kills,
interpersonal skills, provis ion of information, nurses or
radiation therapists interpersonal skills, provision of
information, availability, and waiting times than those
treated by chemotherapy. Patients who had leisure activ-
ities reported more satisfacti on on doctors evaluation
scales and exchange of information between caregivers.
Patients < 55 years old were less satisfied with doctors
availability. Patients living alone were less sati sfied with
doctors information than those living with family.
Multivariate analysis
The linear regression between the QLQC30 and the
OUT-PATSAT35 scales selected the following signifi-
cant scales for subsequent analyses: global health status,
emotional and social functional scales, and sleep, pain
and fatigue for symptom scales.
In mult ivariate mo dels, lo calization of the primary
cancer (breast, prostate, head and neck, rectum, or lung)
and type of treatment received (radiotherapy and/or
chemothera py) were included in two separ ate models
because a collinear relationship was observed between
these two variables. In the first model (Table 4), head
and neck cancer, compared to prostate cancer, ap peared
to be the primary localization where patients were sig-
nificantly less satisfied with doctors provision of infor-
mation and the physical environment (mean score
differences were 10 and 9 respectively).
In the second model (Table 5), patients treated by
radiotherapy were signif icantly less satisfied with doc-
tors technical skills, interpersonal skills, provision of
information by doctors, nurses or radi ation therapists
(mean score difference > 10 for information provision),
Table 2 Number of patients, mean score and standard deviation for each scale of the OUT-PATSAT35 and QLQC30
questionnaires
OUT-PATSAT35 QLQC30
Scale Number of patients Mean score (SD) Scale Number of patients Mean score (SD)
Overall satisfaction Functional scales
SATGEN 669 72.5 (19.7) Global health 679 63.6(19.8)
Evaluation of Doctors Physical 685 82.6 (18.6)
SATDTS 661 71.3 (20.3) Role 682 78.7 (27.6)
SATDIS 659 67 (24.1) Emotional 684 75 (23.1)
SATDIP 668 65.1 (25) Cognitive 684 82.7 (20.9)
SATDAV 671 61.7 (23.6) Social 681 80.4 (25)
Evaluation of Nurses or radiation therapists Symptom scales
SATNTS 679 72.5 (21.1) Fatigue 680 33.5 (25.6)
SATNIS 676 71.6 (20.5) Nausea 684 10 (20.7)
SATNIP 640 58.5 (26.4) Pain 685 19.4 (24.7)
SATNAV 653 66.1 (23) Dyspnoea 674 18.4 (27.9)
Organization, physical environment Sleep 679 30 (31.7)
SATEXE 609 64.6 (23.1) Appetite 671 16.5 (28)
SATOTH 634 63.7(21.9) Constipation 678 17.6 (28.8)
SATWAI 625 60.6 (20.6) Diarrhoea 670 9.50 (20.4)
SATPE 674 59.8 (20.1) Financial difficulties 675 8.74 (20.9)
SATGEN = overall satisfaction; SATDTS doc tors technical skills; SATDIS = doctors interpersonal skills; SATDIP = do ctors provision of information; SATDAV doctors
availability; SATNTS = nurses or radiation therapists technical skills; SATNIS = nurses or radiation therapists interpersonal skills; SATNIP = nurses or radiation
therapists provision of information; SATNAV = nurses or radiation therapists availability; SATEXE = exchange of information between caregivers; SATOTH = other
personnels interpersonal skills and provision of information; SATWAI = waiting time; SATPE = physical environment. OUT-PATSAT35 scales: SATGEN = overall
satisfaction, SATDTS doctorstechnical skills, SATDIS = doctors interpersonal skills, SATDIP = doctors information provision, SATDAV doctorsavailability, SATNTS =
nurses or technologists technical skills, SATNIS = nurses or technologists interpersonal skills SATNIP = nurses or technologists information provision, SATNAV =
nurses or technologists availability, SATEXE = exchange of information between caregivers, SATOTH = other personal interpersonal skills and information
provision, SATWAI = waiting-time, SATPE = physical environment
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Table 3 Univariate analysis (Manova model) between each clinical and sociodemographic variable and all OUT-PATSAT35 scales
SATGEN SATDTS SATDIS SATDIP SATDAV SATNTS SATNIS SATNIP SATNAV SATEX SATOTH SATWAI SATPE
Center 0.93 0.46 0.98 0.85 0.78 0.80 0.35 0.33 0.30 0.41 0.43 0.93 0.40
Teaching hospital 72.5 (19.8) 71.6 (20.7) 68.3 (23.9) 66.0 (24.4) 61.8 (23.9) 73.1 (20.9) 72.0 (19.9) 60.2 (25.0) 66.6 (22.1) 64.2 (22.5) 63.9 (21.4) 60.4 (20.7) 59.3 (21.1)
Local hospital 74.7 (19.7) 73.4 (19.7) 67.9 (24.0) 67.7 (24.7) 63.4 (24.3) 73.3 (21.2) 72.8 (21.1) 61.0 (26.6) 66.5 (23.6) 65.7 (23.6) 65.7 (22.5) 63.2 (20.8) 61.9 (20)
Localization 0.01 0.005 0.09 < 0.0001 0.002 0.14 0.12 0.004 0.09 0.03 0.40 0.61 < 0.0001
prostate 77.6 (18.6) 74.6 (19.6) 70.3 (23.9) 69.4 (24.6) 68.0 (22.9) 76.0 (19.9) 75.7 (20.0) 61.1 (26.3) 68.6 (22.6) 68.4 (23.7) 67.4 (22.6) 63.4 (20.8) 66.3 (20.0)
head neck 69.1 (21.6) 64.8 (22.1) 61.2 (26.3) 54.1 (29.4) 55.0 (25.4) 69.3 (22.2) 69.8 (20.7) 53.7 (27.6) 60.4 (22.9) 58.8 (23.1) 62.6 (22.1) 59.2 (21.6) 52.4 (18.9)
breast 72.1 (18.2) 73.9 (19.3) 68.9 (22.1) 70.4 (20.8) 61.6 (23.1) 73.0 (20.5) 71.4 (19.9) 64.1 (23.7) 67.8 (22.3) 65.1 (21.9) 63.5 (21.3) 60.8 (20.3) 58.9 (20)
rectum 75.0 (21.1) 72.2 (24.3) 71.1 (26.3) 61.7 (25.9) 60.0 (25.5) 75.0 (21.7) 68.9 (23.6) 51.1 (30.7) 62.5 (25.4) 65.8 (20.3) 62.2 (25.2) 62.8 (19.9) 57.8 (24.3)
lung 71.7 (25.3) 68.6 (20.4) 66.1 (27.4) 59.7 (26.5) 59.4 (26.5) 69.4 (24.5) 69.9 (21.7) 53.7 (25.3) 64.4 (23.8) 60.1 (24.6) 65.1 (20.6) 63.0 (22.9) 60.6 (22.2)
Radiotherapy 0.64 0.0004 0.009 < 0.0001 0.17 0.05 0.04 0.0002 0.02 0.03 0.23 0.003 0.63
No 74.4 (16.8) 79.4 (16.9) 74.2 (18.1) 76.6 (17.6) 65.7 (20.3) 77.1 (19.3) 76.5 (18.4) 69.8 (20.7) 71.6 (20.5) 69.6 (20.5) 67.3 (17.8) 67.6 (19.7) 59.6 (19.9)
yes 73.4 (20.3) 71.1 (20.6) 67 (24.8) 64.7 (25.4) 61.8 (24.7) 72.4 (21.3) 71.6 (20.6) 58.8 (26.2) 65.7 (23.1) 63.9 (23.4) 64.2 (22.6) 60.5 (20.9) 60.7 (20.8)
Sex 0.07 0.56 0.99 0.05 0.17 0.33 0.10 0.02 0.72 0.56 0.27 0.45 0.19
female 71.8 (19.1) 72.9 (20.1) 68.1 (23.2) 68.9 (22.5) 61.0 (23.2) 72.2 (21.2) 70.8 (20.4) 63.2 (24.8) 67.0 (23.1) 64.2 (22.7) 63.6 (21.4) 60.9 (20.3) 59.2 (20)
male 74.9 (20.2) 71.9 (20.5) 68.1 (24.6) 64.8 (26.2) 63.8 (24.7) 74.0 (20.9) 73.7 (20.3) 58.1 (26.3) 66.3 (22.6) 65.4 (23.3) 65.7 (22.3) 62.3 (21.2) 61.5 (21.1)
Age 0.09 0.06 0.06 0.06 0.0002 0.04 0.03 0.07 0.01 0.20 0.07 0.21 0.001
[30;55] 70.4 (19.7) 72.0 (21.3) 64.7 (25.5) 64.4 (25.3) 54.0 (23.4) 74.3 (21.5) 71.9 (20.4) 60.9 (25.0) 65.5 (21.9) 63 (22.8) 61 (22.3) 59.1 (22) 55.7 (21.3)
[55;65] 75.7 (19.3) 75.5 (20.3) 71.5 (23.1) 71.3 (24.1) 64.9 (24.2) 75.7 (19.3) 75.0 (19.2) 64.4 (24.5) 70.0 (21.9) 68 (23.5) 67.5 (20.3) 63.5 (20.2) 59.5 (19.6)
[65;75] 72.8 (20.1) 69.6 (20.0) 66.7 (23.9) 64.9 (23.7) 65.0 (23.1) 69.7 (22.0) 69.3 (21.4) 56.9 (26.5) 63.0 (23.6) 63.2 (23) 63.9 (22.6) 60.8 (20.6) 61.6 (20.3)
[75;88] 76.1 (19.1) 74.1 (18.3) 70.9 (22.0) 66.1 (25.6) 65.1 (24.4) 75.2 (20.2) 75.5 (19.0) 61.5 (26.5) 70.8 (22.6) 65.9 (21.8) 67.3 (21.6) 64.3 (20) 67.5 (20.5)
Marital status 0.03 0.79 0.54 < 0.05 0.76 0.11 0.18 0.07 0.16 0.27 0.37 0.89 0.93
Living with partner/family 74.4 (19.4) 72.6 (20.2) 68.6 (24) 67.8 (24.0) 62.7 (24.4) 73.9 (20.4) 72.9 (20.0) 61.5 (24.9) 67.2 (22.2) 65.4 (22.6) 65.1 (21.5) 61.8 (20.5) 60.4 (20.4)
Single/separated 69.7 (20.9) 72.0 (20.4) 66.9 (23.5) 62.3 (28.5) 61.9 (22.2) 70.1 (23.6) 69.8 (22.2) 56.3 (28.8) 63.6 (25.0) 62.6 (24.5) 62.9 (23.4) 61.5 (22.1) 60.6 (21.9)
Distance 0.73 0.03 0.19 0.09 0.16 0.52 0.37 0.07 0.23 0.14 0.58 0.05 0.04
[1; 20] 73.7 (20.7) 74.2 (20.6) 69.4 (25.1) 68.5 (25.6) 63.9 (24.6) 73.7 (23.0) 73.1 (21.7) 62.4 (26.3) 67.7 (24.0) 66.3 (24.1) 65.2 (22.5) 63.3 (21) 58.7 (21.2)
[20; 145] 73.1 (18.7) 70.4 (19.7) 66.7 (22.5) 64.9 (23.3) 60.9 (23.3) 72.5 (18.7) 71.5 (18.8) 58.5 (25.0) 65.3 (21.4) 63.3 (21.6) 64.1 (21.2) 59.8 (20.5) 62.3 (19.8)
Leisure activities 0.20 0.007 0.004 0.0001 0.006 0.01 0.09 0.14 0.04 0.009 0.22 0.82 0.25
no 71.9 (20.8) 69.3 (21) 64.2 |(24.9) 61.4 (26.3) 58.7 (24.8) 69.9 (22.0) 70.3 (20.8) 58.2 (26.1) 63.7 (22.7) 61.4 (24.3) 63.1 (22.6) 61.4 (21.7) 59.1 (21.4)
yes 74.2 (19.2) 74.3 (19.5) 70.4 (22.7) 69.8 (22.8) 64.7 (23.1) 74.8 (20.3) 73.4 (20.0) 61.7 (25.4) 68.1 (22.8) 66.8 (22) 65.5 (21.3) 61.8 (20.4) 61.3 (20.2)
Monthly income 0.32 0.06 0.60 0.10 0.64 0.05 0.37 0.15 0.33 0.16 0.65 0.94 0.37
MW or less 75.0 (21.8) 67.5 (23.2) 64.5 (28.2) 62.4 (29.3) 60.5 (24.9) 74.8 (20.6) 73.2 (21.4) 62.1 (25.0) 64.7 (24.6) 61.9 (26.8) 64.1 (26.6) 60.1 (24) 63.4 (21.6)
MW-1499 71.8 (19.3) 70.9 (19.6) 67.7 (21.7) 64.9 (23.8) 61.1 (24.8) 69.8 (21.4) 70.9 (19.8) 58.3 (26.0) 64.5 (21.9) 62.7 (21.3) 63.9 (21.1) 61.6 (21.9) 58.5 (21.2)
1500-2999 75.1 (19.0) 73.6 (20.5) 68.5 (23.9) 68.5 (23) 63.4 (23.0) 75.6 (20.8) 74.4 (20.5) 63.7 (26.0) 68.5 (22.7) 66 (22.7) 66.4 (21.5) 61.8 (19.2) 61.5 (18.7)
?3000 71.9 (18.6) 76.1 (18.6) 70.1 (25.2) 71.5 (25.8) 64.4 (24.1) 75.0 (20.3) 71.2 (20.9) 57.5 (25.7) 68.2 (22.9) 69 (23.6) 63.3 (21) 60.7 (20.1) 60.5 (22.9)
SATGEN = overall satisfaction; SATDTS doctors technical skills; SATDIS = doctors interpersonal skills; SATDIP = doctors provision of information; SATDAV doctors availability; SATNTS = nurses or radiation therapists
technical skills; SATNIS = nurses or radiation therapists interpersonal skills; SATNIP = nurses or radiation therapists provision of information; SATNAV = nurses or radiation therapists availability; SATEXE = exchange
of information between caregivers; SATOTH = other personnels interpersonal skills and provision of information; SATWAI = waiting time; SATPE = physical environment. MW = minimum wage.
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Table 4 OUT-PATSAT35 scales mean score, mean difference and p values for clinical, socio-demographic factors and QLQC30 scales by multivariate analysis:
model with primary localization *
$
SATGEN SATDTS SATDIS SATDIP SATDAV SATNTS SATNIS SATNIP SATNAV SATEX SATOTH SATWAI SATPE
Monthly income (euros) 0.17 0.43 0.59 0.44 0.17 0.02 0.1 0.008 0.45 0.56 0.28 0.92 0.07
MW or less
a
73.3 68.6 67.9 62.8 60.8 76.1 72.9 57.7 64.9 62.5 65.5 60.2 64.7
MW-1499 -4.8 0.1 -4.5 -5.3 -5.3 -8.1 -4.7 -6.9 -3.4 -0.9 -3.5 -0.2 -7.6
1500-2999 -2.2 2.4 -3.4 -3.3 -1.1 -3.3 -1.2 -2.7 0 2 -1.4 1 -5.4
? 3000 -5.4 3.9 -2.3 -3.6 -1.3 -5 -5.6 -12.5 -1.3 2.8 -6 1.5 -4.5
Age 0.33 0.19 0.05 0.02 0.001 0.11 0.14 0.02 0.11 0.42 0.14 0.44 0.03
30-55
a
67.9 69.4 61.4 58.5 51.9 73.6 70.6 53 63.1 62.5 59.7 58.7 56
56-65 4.1 3.3 7.5 6.5 9.2 0.4 2.1 3.95 3.3 3 5.7 4 3.7
66-75 2.9 -1 4.3 0 10 -4.6 -2.7 -4.6 -2.4 -0.9 2.5 1.8 4.6
76-88 2.3 0.9 3.8 -1.5 8.8 -2.3 -1.7 -2.8 1.6 1.8 4.1 2.5 8.9
Marital status 0.04 0.96 0.28 0.003 0.36 0.20 0.37 0.01 0.11 0.29 0.23 0.94 0.89
Living with partner or family
a
72.3 70.3 66.7 63.4 60 73.4 71 55.6 65.6 64.8 64.2 60.7 60.5
Single or separated -4.2 -0.2 -2.7 -7.3 -2.2 -2.8 -1.9 -6.9 -3.8 -2.6 -2.8 0.2 -0.3
Localization
Prostate
a
74.2 73.5 66.7 64.2 64.5 75.8 74.5 57.5 66.9 66.1 64 62 65.5
Head and neck 0.03 0.03 0.13 0.002 0.02 0.04 0.11 0.02 0.09 0.04 0.47 0.46 0.002
-6 -6.3 -5.1 -10.4 -7.9 -6 -4.5 -9.1 -5.6 -6.9 -2.3 -2.3 -9.2
Breast 0.06 0.54 0.82 0.37 0.1 0.02 0.02 0.53 0.67 0.43 0.61 0.51 0.01
-3.7 -1.2 0.6 2.2 -4 -4.9 -4.8 1.8 -1.1 -1.9 -1.2 -1.5 -5.1
Rectum 0.23 0.19 0.67 0.11 0.04 0.43 0.03 0.04 0.23 0.69 0.34 0.67 0.22
-5.7 -6.3 -2.4 -9.1 -11.1 -4 -10.7 -13.8 -6.9 -2.2 -5.1 -2.3 -5.9
Lung 0.20 0.44 0.98 0.24 0.23 0.26 0.52 0.26 0.59 0.61 0.50 0.998 0.11
-4.5 -2.7 0.1 -4.9 -5 -4.2 -2.3 -5.55 -2.2 -2.1 2.7 0 -5.7
QLQC30 scales
Global health status < 0.0001 < 0.0001 < 0.0001 < 0.0001 0.004 0.0004 < 0.0001 < 0.0001 < 0.0001 < 0.0001 0.0001 0.001 0.003
*adjusted for center, leisure activities, distance from home to hospital and QLQC30 scales (emotional, social, sleep, pain, fatigue). $numbers in bold correspond to p values, numbers in italic correspond to mean
scores, otherwise numbers correspond to mean difference compared to the reference class. a: reference class. SATGEN = overall satisfaction; SATDTS doctors technical skills; SATDIS = doctors interpersonal skills;
SATDIP = doctors provision of information; SATDAV doctors availability; SATNTS = nurses or radiation therapists technical skills; SATNIS = nurses or radiation therapists interpersonal skills; SATNIP = nurses or
radiation therapists provision of information; SATNAV = nurses or radiation therapists availability; SATEXE = exchange of information between caregivers; SATOTH = other personnel s interpersonal skills and
provision of information; SATWAI = waiting time; SATPE = physical environment. MW = minimum wage.
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Table 5 OUT-PATSAT35 scales mean score. mean difference and p values for clinical. socio-demographic factors and QLQC30 scales by multivariate analysis:
model with treatment*$
SATGEN SATDTS SATDIS SATDIP SATDAV SATNTS SATNIS SATNIP SATNAV SATEX SATOTH SATWAI SATPE
Monthly income 0.22 0.28 0.49 0.28 0.13 0.02 0.16 0.01 0.40 0.40 0.30 0.89 0.08
MW or less
a
74.9 72.3 71.5 69.9 64.6 77.5 75.7 66 68.7 64.7 67.2 62.5 65.8
MW-1499 -4.6 0.2 -4.6 -5.9 -5.4 -7.7 -4.5 -7 -3.4 -0.7 -3.8 -0.1 -7.3
1500-2999 -1.9 2.7 -3.1 -2.9 -0.9 -2.9 -1.5 -2.5 0.1 2.5 -1.9 1 -4.8
? 3000 -4.8 4.7 -1.5 -2.5 -0.6 -4.2 -5.2 -11.4 -0.8 3.8 -6 2 -3.5
Age 0.11 0.23 0.02 0.08 < 0.0001 0.41 0.31 0.1 0.15 0.43 0.07 0.22 0.001
30-55
a
68.5 72.1 64 64.9 54.2 73.6 71.6 60.5 65.8 63.8 60.2 59.9 56.1
56-65 4.9 4.1 8.3 6.3 10.2 1.7 3.5 4 4 3.7 6.5 4.9 4.8
66-75 4.9 1 6.2 1.7 12.8 -1.8 0.1 -2.8 -0.5 1.2 4 3.7 7.1
76-88 4.4 3.3 6.1 0.7 11.8 0.9 1.6 -0.1 4 4.3 5.8 4.8 11.3
Marital status 0.03 0.84 0.22 0.004 0.26 0.12 0.21 0.01 0.07 0.24 0.16 0.89 0.74
Living with partner or family
a
74.3 74.4 70.7 70.7 64.2 75.5 74.2 64.2 69.8 67.6 65.9 63.4 62.3
Single or separated -4.5 -0.4 -3 -7.2 -2.7 -3.4 -2.6 -6.9 -4.2 -3 -3.2 -0.3 -0.8
Radio-therapy 0.25 0.003 0.003 0.0001 0.03 0.06 0.03 < 0.0001 0.01 0.03 0.20 0.007 0.44
no
a
73.4 77.8 73.4 72.6 65.9 76.1 75.5 67 71.2 69.1 66 66.7 62.8
yes -2.7 -7.1 -8.4 -11 -6 -4.6 -5.2 -12.4 -7 -6 -3.4 -6.9 -1.8
QLQC30 scales
Global health status < 0.0001 < 0.0001 < 0.0001 < 0.0001 0.002 0.0002 < 0.0001 < 0.0001 < 0.0001 < 0.0001 0.0002 0.001 0.0009
*adjusted for center. leisure activities. distance from home to hospital. and QLQC30 scales (emotional. social. sleep. fatigue. pain) $numbers in bold correspond to p values, numbers in italic correspond to mean
scores, otherwise numbers correspond to mean difference compared to the reference class. a: reference class SATGEN = overall satisfaction; SATDTS doctors technical skills; SATDIS = doctors interpersonal skills;
SATDIP = doctors provision of information; SATDAV doctors availability; SATNTS = nurses or radiation therapists technical skills; SATNIS = nurses or radiation therapists interpersonal skills; SATNIP = nurses or
radiation therapists provision of information; SATNAV = nurses or radiation therapists availability; SATEXE = exchange of information between caregivers; SATOTH = other personnels interpersonal skills and
provision of information; SATWAI = waiting time; SATPE = physical environment. MW = minimum wage.
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and waiting times (the first questionnaire was often
delivered during the first week of treatment).
Socio-demographic determinants significantly linked to
dissatisfaction with care, in both models, were marital
status (living alone) associated with doctors information
provision, and young age (< 55 years) with doctors avail-
ability. A monthly income > 3000 Euro was associated
with less satisfaction with nurses or radiation therapists
information provision, but this was only significant in the
model with primary cancer (Tables 4 and 5).
The centre was not found to be a significant determi-
nant of patient satisfaction.
Poorer perceived global health status, in both models,
was significantly associated with lower levels on OUT-
PATSAT35 scales: regression coefficient ranged from
0.17 to 0.34 (p < 0.0001, Tables 4 and 5).
Discussion
Using the OUT-PATSAT35 questionnaire, we identified
clinical (global health sta tus, primary cancer, tre atment
modalities) and socio-demographic factors (marital sta-
tus, age) significantly associated with different domains
of satisfaction with care among cancer outpatients at
the beginning of their ambulatory treatment.
None of the OUT-PATSAT35 scales correlated highly
with the EORTC QLQ-C30 (all r < 0.30; p < 0.0001).
The same findings were observed in t he French and
Spanish [22,23] validation studies of the OUT-PAT-
SAT35 questionnaire, underlining the fact that these
two questionnaires probably assess complementary
concepts.
Using the EORTC IN- PATSAT32 and QLQ-C30
questionnaires, Avery et al investigated associations
between patient satisfa ction with care and surgical mor-
bidity among inpatients undergoing surgery for oesopha-
geal or gastric cancer [ 26]. Among the 181 patients
included, r esults showed that patient satisfaction scores
remained high and were not associated with the pre-
sence of major postoperative complications. These latter
were, however, related to worse quality of life. Unfortu-
nately, the authors did not directly assess relationships
between QOL and satisfaction scores.
Indeed, the relationship between QOL and satisfaction
with care remains unclear [10,27]. Previous studies have
reported contradictory results, depending on whether
functional or symptom scales were considered (global
health, physical functioning or pain), underlining the
complexity of patient satisfaction interpretation. Despite
the multidimensional co ncept of QOL, in our study,
poor global health status was the main determinant of
low levels of satisfaction with care. Similar findings were
observed by Bredart et al among cancer inpatients
[6,28]. Our methodology su ggests that health status may
influence patient satisfaction, and not the other way
around. Different explanations have been proposed for
this relationship; for example, poorer health may nega-
tively influence ones attitude towards medical care, or
caregivers may respond less positively to patients with
poor health, thus resulting in lower satisfaction levels
[18]. In any case, this effect has not been confirmed in
longitudinal studies with repeated measures of global
health, in order to assess whether higher levels of satis-
faction can result from interventions aimed at improving
quality of life.
Patients treated for a head and neck cancer reported
less satisfaction with the level of information provided
by doctors. Patients who start radiotherapy for head and
neck cancer are those who e xperience the most symp-
toms associated with their illness (such as pain, dyspha-
gia, dysphonia), or may have complications linked to
previous treatment (such as mutilating surgery). This
can lead to aesthetic or functional problems and co nse-
quently, difficulties in patient-doctor communication.
Moreover, because this type of cancer is usually related
to an addiction to tobacco and alcohol, it may be
hypothesised that this negatively influences care provi-
ders att itude toward thes e patie nts com pared t o those
treated for other cancer sites.
Radiotherapy, as compared to chemotherapy, was sig-
nificantly linked to lower satisfaction scores in most
scales. These results should be interpreted with caution
because the few patients receiving chemotherapy were
those treated for breast cancer and these two variables
(namely treatment modality and cancer localization),
were not entered into the same model. The first ques-
tionnaire was co mpleted during the first week of radio-
therapy treatme nt, when mo st patients had experie nced
very few side effects, and thus, treatment related toxicity
cannot be the reason behind their dissatisfaction. Radia-
tion therapists, as opposed to nurses in ambulatory che-
motherapy, spend less time with patients during each
radiation session, and the care pathway in a radiother-
apy department is co mplex, requiring sever al appoint-
ments for preparation, and the time to the definitive
start of treatment may be long. Moreover, radiation
treatment is stressful in itself: patients have reported
fears about the size and possible fall of the machine, the
delivery of co rrect radiation doses, their ability to stay
unmoved in uncomfortable positions and being shut up
alone during the radiation session. Thus, the dissatisfac-
tion with care observed among radiotherapy patients
could be explained by a discrepancy between care
expectations and the perception of care received, high-
lighting the importance of delivering adequate informa-
tion [29].
Patients living alone seem to be less satisfied with doc-
tors information provision. Cancer patients understand-
ing is often affected by anxiety or denial then the
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Page 9 of 11
presence of relatives, ab le to repeat and to discuss the
information given during the consultation, should facili-
tate the doctor-patient communication.
Age was a minor determinant of satisfaction, with
patients < 55 years old less satisfied with doctors avail-
ability. Other studies using similar questionnaires did
not find any relationship between age and satisfaction
scores [6,23,26]. Poinsot et al suggest a cultural evolu-
tion in French cancer patients to wards increased knowl-
edge of the medical aspects of their disease, and thus, a
greater homogeneity in their care expectation [23].
Level of education was not associated with satisfaction
scores, in our s tudy. Poinsot et al observ ed similar find-
ings to ours [23], although other reports have shown
that a higher level of education was associated with
higher expectations as regards quality of care [6,14].
It is like ly that our study is not representative of all
patients seen in oncology practice, since we did not
include some common primary localizations such as
uterine or upper gastrointestinal tract cancer, and meta-
static patients.
Nevertheless, our results confirm the acceptability of
the OUT-PATSAT35 questionnaire in a large outpatient
sample. A number of clinical (primary site, radiotherapy)
and socio-demographic factors (marital status, age) were
significantly associated with different scales of the satis-
faction questionnaire. However, t he major determinant
of satisfaction was patients global health status, suggest-
ing that self-reported quality of life is a key element in
understanding cancer patient satisfaction.
Conclusions
Our findings brought to light a number of patient charac-
teristics that are associated with dissatisfaction with care,
as well as concerns about specific aspects of care. Health-
care providers should use such results to target these
patient groups, who ar e at risk of experiencing less satis-
faction with their pathway of care (in particular, head and
neck cancer patients, patients treated by radiotherapy).
Our o bservations also highlight some aspects of health
professionals behaviour that may leave room for improve-
ment (e.g. providing adequate information to patients).
Lastly, our results underscore the importance of mea-
suring and adjusting for self-perceived health status
when comparing patient satisfaction with care between
hospitals or assessing variations in patient satisfaction
over time.
Further analyses are currently ongoing to determine
the responsiveness of this questionnaire to changes over
time, and to evaluate whether improvements in patients
quality of life c ould lead to impro ved satisfaction with
car e. Indeed, if this relationship is confirmed, initiatives
targeting patients with poorer health status should gen-
erate greater returns in patient satisfaction.
Additional material
Additional file 1: Appendix A. EORTC IN-PATSAT32.
Additional file 2: Appendix B. OUT-PATSAT35.
Acknowledgements
The authors are grateful to Fiona ECARNOT and Marc PUYRAVEAU.
This publication was supported by Programme Hospitalier de Recherche
Clinique (PHRC 2004 - France).
Part of this work was presented in poster presentation of ESMO in Berlin,
september 2009: Nguyen TV, Bosset JF, Monnier A, Perrin V, Fournier J.
Determinants of patient satisfaction in ambulatory oncology: a prospective
study based on the EORTC OUT-PATSAT 35 questionnaire. Eur J Cancer
Suppl 2009;7:241; in oral presentation of 10
th
Biennal ESTRO in Maastricht,
September 2009: Nguyen TV, Bosset JF, Monnier A, Mercier M. Determinants
of satisfaction with care in cancer outpatients: a prospective study based on
the EORTC OUT-PATSAT35 questionnaire. Radiother Oncol 2009;92:S106; In
oral presentation of 16
th
ISOQOL in New Orleans, October 2009: Nguyen TV,
Bosset JF, Monnier A, Mercier M: Determinants of patient satisfaction in
ambulatory oncology: a prospective study based on the EORTC OUT-
PATSAT35 questionnaire. In ISOQOL conference Abstracts Issue. Qual Life Res
2009;A-38
Author details
1
Oncology-Radiotherapy Department, Besançon University Hospital, 3
boulevard Fleming, 25030 Besançon, Cedex, France.
2
Radiotherapy
Department, Montbéliard Hospital, 25200 Montbéliard, France.
3
Clinical
Research Department, EA 3181, Université de Franche Comté, 25030
Besançon, France.
4
Nancy University, Paul Verlaine Metz University, Paris
Descartes University, EA 4360 Apemac, Nancy, France - INSERM, CIC-EC CIE6,
Nancy, France.
5
Psycho-Oncolog Unit, Institut Curie, 75 231 Paris cedex,
France.
6
Health-Related Quality of Life in Oncology Platform, Nancy
University, Cancéropole Grand Est, France.
Authors contributions
TVFN participated to the coordination of the study, performed the statistical
analysis, the interpretation of data and drafted the manuscript. JFB and AM
participated in the conception and design of the study. JF and VP
contributed to the acquisition of data. CB and AB revised the manuscript
critically for important intellectual content. MM participated in the
conception and coordination of the study, and helped to the statistical
analysis and the interpretation of data. All authors read and approved the
final manuscript.
Competing interests
The authors declare that they have no competing interests.
Received: 7 June 2011 Accepted: 28 December 2011
Published: 28 December 2011
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Nguyen et al. BMC Cancer 2011, 11:526
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... Recent data on patient satisfaction with care revealed positive experiences of many cancer patients in Europe [33][34][35] but also demonstrated persisting unmet needs concerning communication and coordinated supportive psychosocial care [34][35][36]. Despite the shift towards patient-centred care and numerous changes within the oncology care system, studies suggest that the quality of cancer care in some European countries is still determined by patient characteristics such as age, educational background and time to treatment [34,[37][38][39]. For Germany, current data assessing patient satisfaction and determinants of quality cancer care is limited. ...
... Better choice of comprehensive therapy 125 "Rehabilitation for follow-up treatment". Improved patient-oriented physician-patient communication 39 "Patient-oriented communication; the conversations were often demoralising". Greater social support 33 "Support by social services (did not take place! ...
... The findings propose that contrary to previous data [34,[37][38][39], the quality of physician-patient interaction is not so much determined by the social characteristics of the patients. This is indicated by the non-significant results for the variables age and education alongside insurance type. ...
Article
Full-text available
Background Patient-centredness has become a central quality indicator for oncology care. Elements include shared decision-making, patient navigation and integration of psychosocial care, which impact patient-reported and clinical outcomes. Despite efforts to promote patient-centred care in Germany in recent decades, implementation remains fragmented. Further, research on patient experiences with cancer care and its determinants is limited. Therefore, this study examines which patient- and facility-specific factors are associated with patient-centred quality care delivery. Methods A cross-sectional study was conducted among 1,121 cancer patients in acute treatment, rehabilitation, and aftercare for different cancer entities across Germany. A participatory developed questionnaire was used. Outcome measures were the quality of physician-patient interaction and provision of psychosocial care during acute care. Predictors comprised patient-specific characteristics and treatment facility-specific factors. Multiple linear regression and multivariate binary logistic regression analyses were performed. In addition, a content analysis of open-ended comments on the patients’ overall cancer care needs was applied. Results Multiple linear regression analysis showed recent diagnosis (β=−0.12, p = < 0.001), being male (β=−0.11, p = 0.003), and having a preference for passive decision-making (β=−0.10, p = 0.001) to be significantly associated with higher interaction quality, but not age, education and health insurance type. An overall low impact of patient characteristics on interaction quality was revealed (adj. R² = 0.03). Binary logistic regression analysis demonstrated the availability of central contact persons (OR = 3.10, p < 0.001) followed by recent diagnosis (p < 0.001), having breast cancer (p < 0.001) and being female (OR = 1.68, p < 0.05) to significantly predict offering psycho-oncological counselling to patients in acute care facilities. The availability of peer support visiting services (OR = 7.17, p < 0.001) and central contact persons (OR = 1.87, p < 0.001) in the care facility, breast cancer diagnosis (p < 0.001) and a higher level of education (p < 0.05) significantly increased the odds of patients receiving information about peer support in the treatment facility. Despite relatively satisfactory quality of physician-patient interactions in cancer care (M = 3.5 (± 1.1)), many patients expressed that better patient-centred communication and coordinated, comprehensive cancer care are needed. Conclusion The findings reflect effective developments and improvements in cancer care and suggest that patients’ social characteristics are less decisive for delivering patient-centred quality care than systemic factors surrounding the care facilities. They can serve to inform oncology care in Germany.
... The primary outcome of this study is the experience lived by the patient during their chemotherapy treatment. To quantify this experience, the use of the OUT-PATSAT-35 questionnaire has been established, an adapted version of the European Organisation for Research and Treatment of Cancer OUT-PATSAT-35 questionnaire focused on evaluating the satisfaction of cancer patients regarding their healthcare [37,38]. This questionnaire contains 35 items referring to 12 multi-item scales divided into 3 sections [38]. ...
... To quantify this experience, the use of the OUT-PATSAT-35 questionnaire has been established, an adapted version of the European Organisation for Research and Treatment of Cancer OUT-PATSAT-35 questionnaire focused on evaluating the satisfaction of cancer patients regarding their healthcare [37,38]. This questionnaire contains 35 items referring to 12 multi-item scales divided into 3 sections [38]. The first two sections evaluate the medical and nursing staff in the chemotherapy-oriented version regarding their technical expertise, interpersonal skills, information delivery, and availability. ...
... Based on estimators from the literature [38,39], it was calculated that 80 participants (40 per group) will be required for this study. This estimation considers a between-group difference in the OUT-PATSAT-35 score of 10 points with symmetric standard deviations of 15 points between groups, a target statistical power of 80%, and standard significance levels (5% two-tailed alpha). ...
Article
Full-text available
Chemotherapy requires careful monitoring, but traditional follow-up approaches face significant challenges that were highlighted by the COVID-19 pandemic. Hence, exploration into telemonitoring as an alternative emerged. The objective is to assess the impact of a telemonitoring platform that provides clinical data to physicians overseeing solid tumor patients, aiming to enhance the care experience. The methodology outlines a parallel-group randomized clinical trial involving recently diagnosed patients with solid carcinomas preparing for curative intent chemotherapy. Eligible adult patients diagnosed with specific carcinoma types and proficient in Spanish, possessing smartphones, will be invited to participate. They will be randomized using concealed allocation sequences into two groups: one utilizing a specialized smartphone application called Contigo for monitoring chemotherapy toxicity symptoms and accessing educational content, while the other receives standard care. Primary outcome assessment involves patient experience during chemotherapy using a standardized questionnaire. Secondary outcomes include evaluating severe chemotherapy-associated toxicity, assessing quality of life, and determining user satisfaction with the application. The research will adhere to intention-to-treat principles. This study has been registered at ClinicalTrials.gov (NCT06077123).
... Other frequent socio-demographic determinants of patient experiences reported in the literature were area of residence [5,13,16], education level [5,6,10], and level of social support [6,11]. Regarding health characteristics, poorer health status or quality of life was one of the most important determinants of reporting lower ratings and poorer experiences [5,6,9,10,12,15,[17][18][19]. Finally, studies looking at clinical characteristics of cancer have found that experiences varied by type of cancer and prognosis [4,6,9,13,16], treatments [8,9] and time since diagnosis [12]. ...
... The most important determinant was self-reported health status, where individuals with poor health status were systematically more likely to report a low rating of overall cancer care and problematic experiences of care. Arditi This finding concurs with those from previous studies [5,6,9,10,12,15,[17][18][19]. Although our cross-sectional design does not allow to infer the direction of the relationship, other authors have suggested that health status may influence rating of care [17,18]. ...
... Arditi This finding concurs with those from previous studies [5,6,9,10,12,15,[17][18][19]. Although our cross-sectional design does not allow to infer the direction of the relationship, other authors have suggested that health status may influence rating of care [17,18]. One of their explanation is that individuals in poorer health may rate their care more poorly as care is not helping them to improve their health, leading them to have a more negative attitude towards medical care. ...
Article
Full-text available
Background Understanding how patient-reported experiences of care and overall rating of care vary among patients with different characteristics is useful to help interpret results from patient experience surveys and design targeted improvement interventions. The primary objective of this paper was to identify the socio-demographic and health-related characteristics independently associated with overall rating of cancer care. The secondary objective was to explore if and how these characteristics were associated with specific experiences of cancer care. Methods This cross-sectional multicenter study analyzed self-reported data collected from 2696 patients diagnosed with breast, prostate, lung, colorectal, skin, or hematological cancer from four large hospitals in French-speaking Switzerland. Multivariate logistic regressions with purposeful stepwise selection of independent variables were used to identify the socio-demographic and health-related characteristics independently associated with overall rating of cancer care in the primary analyses. In the secondary analyses, we ran the multivariate model from the primary analyses with specific experiences of care as outcomes to estimate the adjusted odds ratios (OR) and 95% confidence intervals (CI) of the selected characteristics. Results Respondents’ mean rating of overall cancer care was 8.5 on a scale from 0 to 10, with 17% categorized as reporting a low rating (0–7 rating). Being a woman (OR 1.43, 95% CI 1.12–1.83), not being Swiss (OR 1.47, 95% CI 1.12–1.94), reporting lower health literacy (OR 1.95, 95% CI 1.54–2.47), preferring making medical decisions alone (OR 1.92, 95% CI 1.38–2.67), having forgone care due to cost (OR 1.72, 95% CI 1.29–2.29), having used complementary medicine (OR 1.55, 95% CI 1.22–1.97), and reporting poorer health (OR 3.12, 95% CI 2.17–4.50) were all independently associated with a low rating of overall cancer care. Poorer health, lower health literacy, and having forgone care were the three characteristics most often associated with problematic experiences of care. Conclusions Our results identified several patient characteristics consistently associated with lower overall rating of care and specific experiences of cancer care. Among these determinants, health literacy and financial hardship emerged as key recurring factors shaping poor patient experiences that should be prioritized for attention by cancer care services.
... A patient's self-reported physical health status was found to be related with patient satisfaction (Hekkert et al., 2009;Larsson & Wilde-Larsson, 2010;Nguyen et al., 2011) as was a patient's selfreported mental health status (Chen et al., 2018;Larsson & Wilde-Larsson, 2010;Westaway et al., 2003). Westaway et al. (2003) and Chen et al. (2018), on the other hand, found no relationship with self-reported physical health status, and Larrabee et al. (2004) found no relationship with self-reported mental health status but did find a relationship with self-reported quality of life. ...
... In France, patients receiving radiotherapy treatments for cancer and patients with head and neck cancers had lower patient satisfaction scores (Nguyen et al., 2011). Patients who viewed doctors more favourably or were extraverted and emotionally stable had higher patient satisfaction (Larsson & Wilde-Larsson, 2010). ...
... Chen et al., 2018;Findik et al., 2010;Hekkert et al., 2009;Larrabee et al., 2004;Larsson & Wilde-Larsson, 2010;Nguyen et al., 2011;Westaway et al., 2003;Yen & Lo, 2004), whileOzturk et al. (2020) found an inverse relationship between age and patient satisfaction, andTang et al. (2013) found no relationship.SexA number of articles found sex to be an element of patient satisfaction. Women had higher reported satisfaction than men in articles byChen et al. (2018) andHekkert et al. (2009), while men had higher reported satisfaction than women in an article byFindik et al. (2010). ...
Article
Full-text available
Aim: To summarize the scientific literature on the elements essential to understanding a nursing definition of patient satisfaction. Design: Whittemore and Knafl's methodology was used for this integrative review. Methods: Articles were included if the studies they explored patient satisfaction in patient populations and measured patient satisfaction using standardized, validated instruments. Elements in this review were defined as the essential components that create the complex concept of patient satisfaction. Results: Thirty articles were found and analysed in full. Five definitions of patient satisfaction were used, all of which were at least 20 years old. Twenty-two different measures of patient satisfaction were used, six of which were nursing-specific. Sixty-eight elements of patient satisfaction were studied in the included articles. Forty-three elements were reported as having a significant relationship with patient satisfaction, 25 were reported as having no significant relationship. Eight elements had both significant and non-significant relationships.
... While there is some literature exploring the experiences of older patients and their families in acute care [13], there is little research that focuses specifically on older patients with cancer, and this research has been limited to the contexts of ambulatory [15] and palliative care [16]. Providing quality care is a challenge, and it is important to understand the perceptions that older patients with cancer and their families have of both the quality of care and their satisfaction with it [5,17]. ...
Article
Full-text available
Background The unique life situations of older patients with cancer and their family members requires that health care professionals take a holistic approach to achieve quality care. The aim of this study was to assess the perceptions of older patients with cancer and family members about the quality of care received and evaluate differences between their perceptions. A further aim was to examine which factors explain patients’ and family members’ levels of satisfaction with the care received. Methods The study was descriptive and cross-sectional in design. Data were collected from patients (n = 81) and their family members (n = 65) on four wards in a cancer hospital, using the Revised Humane Caring Scale (RHCS). Data were analysed using descriptive statistics, crosstabulation, Wilcoxon signed rank test, and multivariable Analysis of Covariance (ANCOVA). Results Family members had more negative perceptions of the quality of care than patients did. Dissatisfaction was related to professional practice (p < 0.001), interaction between patient and health care professionals (p < 0.001), cognition of physical needs (p = 0.024), and human resources (p < 0.001). Satisfaction with overall care was significantly lower among those patients and family members who perceived that they had not been involved in setting clear goals for the patient's care with staff (p = 0.002). Conclusions It is important that older patients with cancer and family members receive friendly, respectful, individual care based on their needs and hopes, and that they can rely on professionals. Health care professionals need more resources and education about caring for older cancer patients to provide quality care.
... This is consistent with the previous observations that individuals living alone were more dissatisfied with doctors' information than those living with family. 24 This finding appears to be in line with the previous reports that showed that social support is positively related with health outcomes and quality of life of chronic disease patients, 25,26 which in turn could add on the satisfaction profile with regard to patient care. Finally, this study indicated that having access to a nearby diagnostic laboratory and pharmacy contributed to increased satisfaction levels among caregivers. ...
Article
Full-text available
Background: The COVID-19 pandemic led to a paradigm shift in routine care delivery with the widespread transition to virtual care without demanding preconditions. Caregivers' satisfaction is a critical parameter to ensuring the quality of clinical service in the pediatric population. Despite this fact, such patient-related factors are under-investigated and poorly documented in developing countries such as Ethiopia. The study was aimed to assess caregivers' satisfaction regarding teleconsultations and associated factors during COVID-19 pandemic at Tikur Anbessa Specialized Hospital, Addis Ababa, Ethiopia. Methods: Health institution-based cross-sectional survey was conducted in randomly selected caregivers who were served with phone-based medical consultations during the pandemic. Data were collected by means of a pretested, structured interviewer-administered questionnaire. Data were entered into Excel 2016 and analyzed using SPSS version 26. Logistic regression models were used to predict the association of study variables and adjusted for possible confounders. Results: Overall, 177 (61.5%) of participants reported satisfaction with the teleconsultation. Female caregivers (AOR=1.78; 95% CI 1.05, 3.01), having family support (AOR=2.6; 95% CI 1.45, 4.65), access to a nearby laboratory (AOR=2.18; 95% CI 1.24, 3.83), having access to nearby pharmacy (AOR=2.82; 95% CI 1.63, 4.86) were found to be predictors of caregivers' satisfaction with teleconsultation in the study area. Conclusion: A considerable number of caregivers were satisfied with the teleconsultation service during the COVID-19 pandemic. It is important for healthcare providers and policy makers to strengthen the provision of teleconsultation service options for caregivers including women and those with better access to diagnostic centers and pharmacies. They should try to make teleconsultation caregiver-friendly.
... [13]. Several patient satisfaction surveys [14] have been developed for use with patients diagnosed with cancer; [15] similar instruments have been developed for use in the area of nursing. When patients are satisfied with their treatment results and their interactions with their therapists, they are more likely to return for continued therapy and to follow their therapist's recommendations [16]. ...
... [13]. Several patient satisfaction surveys [14] have been developed for use with patients diagnosed with cancer; [15] similar instruments have been developed for use in the area of nursing. When patients are satisfied with their treatment results and their interactions with their therapists, they are more likely to return for continued therapy and to follow their therapist's recommendations [16]. ...
Article
Key Words: Validity, Reliability, Arabic version of MedRisk questionnaire, Patient satisfaction, Physical therapy services, Low back pain. Background: One measure of care quality is a patient's level of satisfaction with their treatment. Maintaining a focus on patient satisfaction as a way to evaluate the effectiveness of physiotherapy is important. Providers of healthcare and researchers in the field of health services continue to place an emphasis on learning more about how to improve the quality of care they offer for their patients. Patients' expectations of receiving good value for their time, money, and effort while receiving medical care are equally essential. Aim: The purpose of this study is to evaluate the Arabic translation of the MedRisk questionnaire with regard to its face & content validity, factor analysis, feasibility, internal consistency reproducibility, as well as test-retest reliability. Subjects: 300 individuals, from both genders, aged from 18 to 60, all having LBP (mechanical or discogenic) were enrolled. Methods: In a cross-sectional study, investigators used an Arabic translation of the MedRisk Questionnaire to evaluate patient satisfaction. Results: The first expert panel found a value of 74.17% for face validity, whereas the second found a value of 97.50%. Experts agreed that the content validity was very high (97.5%). It was determined that 61.1% of the total variance in the questionnaire can be accounted for by a single factorial structure. Cronbach's was used to evaluate the internal consistency. Since then, the Cronbach has reduced from 0.939 to 0.937. The Arabic translation of the MedRisk questionnaire took an average of 5.33 minutes (SD 1.04) to complete and has excellent test-retest reliability. There were no substantial changes in either the floor or the ceiling. Conclusion: The Arabic translation of the MRPS is simplified, easy to apply, fast, as well as comprehensive scale. Consequently, it might be an appropriate scale for clinical evaluation of Arabic-speaking patients suffering from low back pain.
Thesis
La satisfaction des patients est un des éléments d’évaluation de la qualité des soins. Elle est un concept subjectif qui témoigne de l’adéquation entre ce qu’un patient attend du système de soins et des professionnels de santé et sa perception de la qualité des soins reçus. Son évaluation repose sur l’utilisation d’outils tels que des auto-questionnaires. Son amélioration dépend de l’identification des attentes et des besoins de soins des patients. En cancérologie, et notamment en situation palliative, elle témoigne d’une prise en charge globale et personnalisée. L’objectif principal de cette thèse était de développer et de valider des outils en langue française d’évaluation de la satisfaction et d’identification des besoins de soins des patients atteints de cancer. Pour ce faire, une traduction et une adaptation transculturelle du questionnaire anglais de satis- faction FAMCARE-Patient ont été effectuées. La validité de contenu et la validité de face de l’outil obtenu (FFP-16) ont été vérifiées. Les analyses statistiques ont mis en évidence de bonnes propriétés psychométriques de l’outil. Nous avons également développé à partir de la littérature un outil d’identification des besoins de soins (ACCOmPAgNE) combinant quatre approches complémentaires : l’importance d’un domaine donné, l’intensité et la pénibilité d’une difficulté rencontrée et le besoin d’aide exprimé. La validité de contenu et la validité de face ont été vérifiées. En utilisant ces outils, il serait possible de faciliter la communication entre patients et professionnels de santé, favoriser des actions adaptées à la singularité d’un patient donné et améliorer la qualité des soins reçus et la satisfaction de celui-ci.
Thesis
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The predominant theme of this research is to examine, in addition to age, what other factors affect the quality of life for Canadians living with neurological conditions. In this research, we conduct a systematic review of the literature and examine population-based survey data, which is nationally representative, to identify risk factors, trends, health care and general life satisfaction for select neurological conditions found among Canadians. This thesis focuses on reducing the existing gaps in research on the experiences of Canadians living with select neurological conditions.
Article
Objectives. Based on Donabedian's structure, process, and outcome model, this study was conducted to identify the underlying dimensions of patient satisfaction for diabetic patients and determine the effects of demographic characteristics and health status on these dimensions. Design. A cross-sectional analytical research design was used with a questionnaire, comprising demographic characteristics, the general and mental health items from the SF-20, and a 25-item patient satisfaction scale. Setting and study participants. The questionnaire was administered to 263 South African black diabetic outpatients from the diabetic clinics at two hospitals. There were 174 females and 89 males, aged between 16 and 89 years (mean = 53.5, sd = 13.9). The average number of years of schooling was 6.3 (sd = 4.1). Main outcome measure. A reliable and valid patient satisfaction scale. Results. Factor analysis was conducted on the patient satisfaction scale and two factors, accounting for 71.6% of the variance, were extracted. The major items on Factor I were support, consideration, friendliness, and encouragement, labelled the interpersonal dimension. Factor II emphasized availability of a seat and toilet in the waiting area and cleanliness, labelled the organizational dimension. The two factors had very good reliability coefficients: 0.85 (organizational) and 0.98 (interpersonal). Multi-trait scaling showed that all items exceeded the item convergent (r>0.40) and discriminant (Z>1.96) validity criteria. Patients in poor general health were significantly less satisfied (P = 0.007) with the organizational quality of their care than patients in good health; patients in poor mental health were significantly less satisfied (P = 0.04) with the interpersonal quality of their care than patients in good mental health. Conclusions. The findings provided support for Donabedian's model. They demonstrated that attributes of providers and settings are major components of patient satisfaction, and showed that the scale is a reliable and valid measure of patient satisfaction for this South African population.
Article
The EORTC OUT-PATSAT35 RT questionnaire evaluates the satisfaction with care (SC) expressed by cancer outpatients treated with radiotherapy. In this study we assess the psychometric properties of the OUT-PATSAT35 RT when applied to a sample of Spanish patients. A total of 100 patients with different tumor sites completed the EORTC core questionnaire, QLQ-C30, the OUT-PATSAT35 RT, the Oberst patients' perception of care quality and satisfaction scale (OS) and the item on intention to recommend the hospital (IR). Psychometric evaluation of the structure, reliability and validity of the questionnaire was conducted. Multitrait-scaling analysis showed that 33 out of 34 item-scale correlation coefficients met the standards for convergent validity and that many of them met the standards for discriminant validity. Cronbach's coefficients were good (0.70-0.97) for all scales except environment. Correlations between the areas of the QLQ-C30 and OUT-PATSAT35 RT were generally low (<0.40). Correlations between the OS and the IR were moderate with the EORTC OUT-PATSAT35 RT. Areas whose contents were more related had higher correlation coefficients (>0.50), and vice versa (<0.20). Patients with higher scores on the OS and the IR, patients who had more visits to the doctor and patients who had a better performance status showed higher SC levels in 12, 8 and 1 OUT-PATSAT35 RT areas, respectively. The OUT-PATSAT35 RT appears to be a reliable and valid instrument when applied to a sample of Spanish cancer patients. These results are in line with those of the validation study conducted by the authors of the questionnaire.
Article
We evaluated the longitudinal course of the relationship between patient satisfaction and quality of life (QoL) in Chinese breast and nasopharyngeal cancer patients. A sample of Chinese breast (n = 250) and nasopharyngeal (n = 242) cancer patients were assessed during their first outpatient visit (baseline) and at 2 follow-up interviews (FU1 and FU2). The Chinese version of the Functional Assessment of Cancer Therapy-General Scale (FACT-G (Ch)) was adopted to assess QoL. Patient satisfaction was assessed by the 9-item Chinese Patient Satisfaction Questionnaire (ChPSQ-9) and the cognitive subscale of the Medical Interview Satisfaction Scale (MISS-Cog). Linear mixed effects models were fitted to identify predictors of patient satisfaction and QoL. Recurrence after baseline (std beta = 0.58; 95% CI: 0.17, 0.98; P < 0.05) was the only predictor of MISS-Cog, age (std beta = 0.01; 95% CI: 0.00, 0.02; P < 0.05) and depressed mood (std beta = 0.20; 95% CI: 0.10, 0.30; P < 0.001) of ChPSQ-9. After adjusting for sociodemographic and psychosocial variables, both ChPSQ-9 (std beta = 0.13; 95% CI: 0.07, 0.19; P < 0.001) and MISS-Cog (std beta = 0.07; 95% CI: 0.02, 0.12; P < 0.05) independently predicted FACT-G (Ch) scores. These findings suggest both general emotional support and informational support are important in predicting QoL among Chinese breast and nasopharyngeal cancer patients.
Article
Assessment of the quality of care and patients' satisfaction has become an increasingly needed area of research. The present study investigated various qualitative and quantitative aspects of provision of care and interaction between cancer outpatients and medical and nursing staff within a radiotherapy department in Pordenone, north-eastern italy. A total of 368 outpatients were contacted: 258 completed the questionnaire (response rate 70%). No difference emerged between respondents and non-respondents as concerning age, sex, marital status, clinical stage, cancer type and reason for referral. Significant differences were found for education and type of work, white collar and better educated patients being more frequent among respondents. Most of the patients reported good or very good levels of satisfaction with major aspects of care provision and relationship with medical and nursing staff. Length of time spent in various administrative procedures, cost of the therapy and change of attending physician in different examinations were the issues commented upon relatively less favourably. Reported waiting time for each medical examination exceeded 1 hour in approximately half of the patients. Improvement in hospital services constituted the priority, according to male patients. Public transportation concerned most women's and elderly patients' attention. Among elderly patients, the need for better provision of care at home was also deeply felt.
Article
A meta-analysis was performed to examine the relation of patients' sociodemographic characteristics to their satisfaction with medical care. The sociodemographic characteristics were age, ethnicity, sex, socioeconomic status (three indices), marital status, and family size. Greater satisfaction was significantly associated with greater age and less education, and marginally significantly associated with being married and having higher social status (scored as a composite variable emphasizing occupational status). The average magnitudes of relations were very small, with age being the strongest correlate of satisfaction (mean r = 0.13). No overall relationship was found for ethnicity, sex, income, or family size. For all sociodemographic variables, the distribution of correlations was significantly heterogeneous, and statistical contrasts revealed the operation of several moderating variables. The meaning of the overall results and their relation to earlier reviews is discussed.
Article
A diagnosis of cancer places considerable stress on patients and requires them to make major adjustments in many areas of their lives. As a consequence, considerable demands are placed on health care providers to satisfy the complex care needs of cancer patients. Currently, there is little available information to indicate the extent to which cancer patients are satisfied with the quality of care they receive. The present study assessed the perceptions of 232 ambulatory cancer patients about the importance of and satisfaction with the following aspects of care: doctors technical competence and interpersonal and communication skills, accessibility and continuity of care, hospital and clinic care, nonmedical care, family care, and finances. The results indicate that all 60 questionnaire items used were considered to reflect important aspects of care, but that greater importance was given to the technical quality of medical care, the interpersonal and communication skills of doctors, and the accessibility of care. Most patients were satisfied with the opportunities provided to discuss their needs with doctors, the interpersonal support of doctors, and the technical competence of doctors. However, few patients were satisfied with the provision of information concerning their disease, treatment, and symptom control and the provision of care in the home and to family and friends.