ARTICLE
Increasing
attention to health care quality has led to a renewed interest in patients'
satisfaction, regarded as one of the principal elements for obtaining patients'
evaluation of the services they received [1-3].
Several authors underscored the importance of evaluating in different
settings (e.g. primary care, inpatient and outpatient hospital care) the
patient's opinion about the care received. Many physicians are reluctant
to accept data generated from patients' satisfaction surveys or to have
their patients participating in such surveys, discounting the importance
of the patient perspective [4]. On the other hand, the results of satisfaction
surveys clearly showed how this kind of research improves the physician
patient interaction and the outcome of patients, especially those affected
by chronic diseases [5] requiring long term treatment and regular follow-up.
The patient perceived quality of care or patient satisfaction is considered
a legitimate measure of health care quality and should be included together
with other measures in quality improvement programs [6, 7].
In order to improve perceived quality of health care, it is important
to understand which are the main factors influencing patient satisfaction.
These can include factors related to the health care provider such as
infrastructures and access to care, interpersonal skills of personnel,
and patient related factors such as socio-demographic characteristics
of patients, disease severity and health related quality of life.
A recent study evaluating this topic in a dermatological setting among
outpatients concluded that improving physician's interpersonal skills
could increase patient satisfaction which was observed to have a positive
effect on treatment adherence and health outcomes [8].
To the best of our knowledge, there are no published studies examining
factors related to the satisfaction of dermatological inpatients. Even
if improved outpatient care represents the core of dermatological treatment,
inpatient care remains essential especially for those who have extensive
skin disease, are physically frail, or have disabilities and lack of social
support [9]. The elderly, in particular, may require inpatient care to
ensure adequate treatment of their skin disorders.
Even more than in other specialties, dermatological inpatients need emotional
support because the disfigurement caused by their diseases may often result
in an attribution of negative or denigrating qualities by society and
by the patient himself [10] and is also associated with increased psychiatric
morbidity [11].
The specific aim of the present study was to evaluate the independent
effect on patient satisfaction of patient characteristics and of specific
aspects of health care (competence and efficiency of caregivers; information
about the clinical status, progress and prognosis; physical comfort with
pain management; emotional support, hospital success in involving patient's
family and friends; information about treatment and follow-up), with the
practical purpose to help the Hospital Management to intervene in the
identified critical areas of care.
Materials and methods
We studied a sample of consecutive dermatological inpatients, recruited
from October 1st to November 30th 2001, at the Istituto
Dermopatico dell'Immacolata (IDI IRCCS) (Rome, Italy). IDI IRCCS is a
large research hospital and a referral point for dermatological patients
from Central and Southern Italy. In 2001, there were 170,000 outpatients,
while there were 17,000 inpatients.
The patients' eligibility criteria for this study were: a) age ³ 18 years
b) ability to read Italian c) no major cognitive deficits precluding questionnaire
completion. The study protocol was approved by the Institutional Ethical
Committee. A nurse invited participants to complete a self-administered
questionnaire originally elaborated by Picker Institute and validated
in the U.S.A. in multiple settings [12, 13]. Our version, already used
on vascular patients [14], included 23 neutrally worded questions:
14 to be answered on a five point scale ranging from totally positive
to totally negative opinions, 7 on a yes/no response, and 2 questions
about patient "overall satisfaction" of care and "access"
on a 0/10 points scale. It was possible to mark the response "not
applicable" for each of the questions. All of the questions were
part of 7 different dimensions of care: respect for patient preference,
co-ordination of care; information and education, physical comfort and
pain relief, emotional support, involvement of family and friends, continuity
and transition out of the hospital (the questionnaire is available upon
request). The non-anonymous questionnaire was completed by the patient
on the last day of hospital stay, just before discharge.
Patients were categorized as satisfied or not
satisfied with regards to each single dimension, considering as satisfied
those who rated at the maximum level at least 75 % of the questions
included in each dimension.
In order to identify the dimension most related to overall satisfaction
and to assess if it was influenced by potential confounding factors, patients'
demographic characteristics (age, sex, educational level, region of residence)
and specific aspects of care known to be associated with satisfaction
(length of stay, severity of disease, multiple hospital admissions) were
analyzed and a regression analysis was performed.
Disease severity was defined by means of All Patient Refined Diagnosis-Related
Group (APR DRG) [15-17] because by adding subgroups to the basic DRG it
allows us to address differences in patients' severity of illness and
risk of mortality. The APR DRG classifies the disease in four subgroups
or classes: minor, moderate, major and extreme according to the
extent of organ-system loss of function or physiologic decompensation.
The dimensions with the strongest association to the outcome of interest
were in turn considered as dependent variables, and the distribution of
satisfied patients for each of them studied in respect to the principal
diagnosis of hospital admission (according to the ICD9 CM classification
system). For this purpose, the sample recruited for the study was divided
in three main categories: patients with acute skin diseases, patients
with chronic skin diseases, and patients with tumors. A fourth category
was added and defined as "others" (i.e., when the dermatological
diagnosis was the second or the third diagnosis in the hospital discharge
reports).
The statistical analysis was performed using the STATA 7 statistical
package (College Stata,TX, USA: Stata Corporation 1999).
Results
Six hundred and seventy two consecutive inpatients were recruited and
completed the questionnaire. Of these, 16 were excluded because younger
than 18 years. Eight were excluded because they completed less than
70 % of the items. The mean age of the 648 eligible patients
was 49.9 years (sd ± 17.6); 266 (41.1 %) were males
and 382 (58.9 %) females. In order to verify whether our sample was
comparable with the total population of IDI patients, we used the hospital
administrative data to assess the sex and age distribution of all patients
who attended the dermatological units the year 2001 and matched our
inclusion criteria. The mean age of all dermatological patients was 50.7 year
(sd ± 16.3); 42.9 % were males and 57.1 % were females.
Twenty-two percent of the patients were affected by a tumor, 17.9 %
by an acute dermatological disease, 47.9 % by a chronic skin condition,
the remaining 11.7 % had a non-dermatological principal diagnosis.
According to the ICD9-CM international classification system of diseases
the most frequent acute disease was dermatitis (61 cases), the most
common chronic skin disease was urticaria (78 cases), while 57 patients
were admitted with a diagnosis of tumor.
The APR-DRG classification attributed 482 patients to class I - minor
- (74.4 %), 158 (24.4 %) to class II - moderate -
and 8 (1.2 %) to class III - major -. Class II and III here
were grouped and classified as "moderate" (25.6 %).
Figure 1 shows the "overall
satisfaction" data. A total of 60.2 % of patients rated the
care received as excellent.
This group was considered for the further analysis as "satisfied"
whith the others as "not satisfied". We decided to be conservative,
because the non-anonymous nature of the questionnaire could have induced
patients to attribute particularly high scores.
Table I shows the prevalence
of "overall satisfaction" according to patients characteristics
(age, sex, educational level, region of residence), specific aspects of
care (length of stay, multiple access, disease severity) and type of disease.
The oldest and less educated patients as well as those with an intermediate
duration of hospital stay are more frequently "overall satisfied".
As for the class of disease, patients with a tumor were more satisfied,
whereas those with an acute disease were less satisfied.
Figure 2 shows the proportion
of satisfied patients with regards to each dimension studied, except overall
satisfaction. The dimension with the highest prevalence of satisfaction
refers to "physical comfort" (89.6 %) while the lowest
prevalence of satisfaction refers to "emotional support" (47.8 %)
and "family involvement" (54.6 %).
To ascertain the dimension most closely related to the "overall satisfaction"
a strategy suggested by Gunby et al. was performed [18]. It consists
of repeated multiple logistic regression models where the single dimension
is in turn removed if it reaches the higher X value. In our study "information
and education" and "co-ordination of care" were the dimensions
most closely related to overall satisfaction (data not shown). In order
to see if these dimensions were affected by potential confounding factors,
patients' demographic and clinical characteristics were added in the analysis
individually and in combination. There was no evidence to suggest that
the final choice of criteria was confounded. The selected dimensions were
then further explored: Table
II shows that patients with an intermediate length of stay (LOS) are
the least satisfied regarding both dimensions while individuals aged ³
65 years are more satisfied compared to younger regarding the "coordination
of care". Residents in the same region as IDI and at their first
admission are instead more satisfied with the information received during
their stay. Patients with tumors compared to those affected by other diseases
seem to be more satisfied for the two dimensions under study. Patients
with chronic diseases show the lowest prevalence of satisfaction with
coordination of care.
Furthermore, logistic regression analyses were performed with information
and subsequently coordination of care as outcomes. The disease was included
as independent variable and the results adjusted for the patient's characteris
tics. The results represented as O.R. and 95 % CI are displayed in
Figure 3. Patients with
tumors are more likely to be satisfied with the information received than
those with acute diseases.
Patients classified as "others" were significantly more likely
to be satisfied than those with chronic dermatological diseases where
no significant difference was found between different diseases.
Discussion
The objective of the study was to examine the perceived quality of health
care among dermatological inpatients to identify bottle necks in the quality
perceived areas and to suggest positive solutions to the Hospital Management.
Increasing interest in patient perceived quality of care or patient satisfaction
can be accounted for by numerous developments, including concerns over
health care costs, informed consumerism and heightened awareness of the
influence of psychosocial factors in the process and outcome of medical
care [19]. A growing body of research has also shown that patient dissatisfaction
with health care is related to patient non compliance with medical treatment,
discontinuation of care and frequent changing of health care providers
[20-23].
The majority of studies have focused exclusively on the role of health
status and demographic variables when identifying predictors of patient
satisfaction with health care. Others reported inconsistent findings regarding
the influence of demographic variables such age, income, education, race
and sex on patient satisfaction [21, 24].
Among the socio-demographic variables examined in this study, educational
level was associated with overall patient satisfaction, confirming what
was reported in a non dermatological meta analysis [24]. In particular,
patients with less education were more satisfied with the general aspect
of medical care. A possible explanation for the relationship between education
and satisfaction with care is that less educated patients are not as knowledgeable
about various aspects of medical care and thus apply less stringent criteria
when judging health care compared with more educated patients.
Also the length of stay was related to overall satisfaction particularly
for patients who have a short or a long stay. Out-patient care is considered
the best approach for treating dermatological diseases but in settings
where this is not possible a reduction of hospital stay is appreciated
by the patients. Almost 40 % of IDI patients are from regions other
than Lazio, with evident logistic problems. Patients with longer hospital
stay were the most satisfied, and this perhaps reflected the peculiarity
of some dermatological diseases. Serious diseases or disorders involving
the entire body can be perceived as a stigma and the patient might prefer
to be cured in a hospital environment [9].
Reports have demonstrated that there is a highly significant association
between patient satisfaction and the amount of information given. In a
previous study [25] on dermatological patients, those with chronic diseases
asked for more information from care givers than those with tumors (63 %
versus 37 %). Younger patients requested more information than older
ones. In our study patients with tumors were more satisfied than those
affected by acute or chronic diseases or by non-dermatological diseases.
The likelihood of overall satisfaction increased with increased disease
severity also in outpatients [8]. Patients with tumors usually receive
special attention in order to facilitate their access and treatment and
are better followed in time (scheduled visits for therapy or surgery,
follow-up etc.). On the other hand, patients with chronic dermatological
diseases often know almost everything about their disease and particularly
with recurrent access to the hospital they have very low expectations
and show a low overall satisfaction.
Among the seven dimensions of satisfaction, emotional support has the
lowest percentage of maximum satisfaction (less than 50 %). The Hospital
Management has recognized this as a critical area and promoted training
in improving communication skills [26-28].
Actions are expected with staff dedicating greater attention to patients'
fears and anxiety associated to the skin diseases, such as patients' worries
about the impact of the illness on their ability to care for themselves
or about the effects on interpersonal relationships. Patient satisfaction
will be monitored over time and the impact of the interventions will be
evaluated.
The performed analyses preserve details and reduce the amount of data
presented offering composite scores. Each score represents a critical
component of quality of care as defined by the patients. The Picker Institute
developed this paradigm for synthesizing the information provided by patients
in order to categorize the aspect of care they found especially critic.
This allows each patient to suggest how the hospital might address his
needs and preferences.
This level of detail contrasts sharply with other patient survey reports,
which rely principally on global satisfaction.
In our Institute "coordination of care", "information and
education" appeared to be strongly associated with overall satisfaction.
In order to achieve satisfaction with the coordination of care, patients
would expect to be able to identify a specific doctor in charge of their
care, to receive from doctors and nurses consistent information, to perceive
the admission process as good. In order to be satisfied with the education
and information, patients expect doctors and nurses to answer their questions
about the disease, the treatments, the diagnostic exams.
A modified "patient chart", new information sheets for the admission
and round table discussions between health personnel are among the initiatives
implemented by the Health Management following this survey.
Article accepted on 18/12/2002
CONCLUSION
The study was partially supported by Italian Ministry of Health. We thank
L. Sobrino (HIS) for providing administrative data, Head Nurses of Clinical
Units for assisting in data collection and S. Bolli, V. Salvatori, N. Salcedo
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