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, Antihistamines in the pediatric population: Achieving optimal outcomes Schad & Skoner
, Pediatric allergic rhinitis: Current and future state of the art Carr
REVIEW
" Elucidating the mechanism underlying the ocular symptoms of allergic rhinitis Naclerio et al.
ORIGINAL ARTICLES
" Prevalence of allergic sensitization to indoor fungi in West Virginia Beezhold et al.
l Late phase allergic reaction in nasal provocation with fungal allergens Niedoszytko et al.
l Dust mite avoidance measures in patients on immunotherapy White et al.
, Mattress risk factors for sudden infant death syndrome Jenkins
" Exhaled breath condensate pH in the evaluation of asthma Coop et al.
a Pharmaceutical care for asthma patients: A community pharmacy based project Petkova
, Emergency dept utilization by patients not meeting HED1Scriteria for persistent asthma Hsu et al.
a Mycobacterium vaccae ameliorates airway histo1?athology in asthma Yazi et al.
l Serum 19Elevels in pregnant women and their infants De Amici et al.
l Antigenic extracts from pollen & seeds of mustard (brassica) Shahi et al.
l Causes of moderate to severe angioedema Banerji et al.
l POPs Case: A is-year old girl with recurrent pneumonia DiDario et al.
armaceutical care for asthma patients: A community
harmacy-based pilot proj ect
alentina B. Petkova, Ph.D.
. Asthma is a clinical problem with social, psychological, and economic burdens. To improve patient disease management and
quality of life (QOL), different education programs have been developed. The purpose of this study is to adapt and implement
. (? community-based educational program for patients with asthma. A prospective, randomized, controlled trial was performed.
Fifty individuals with mild asthma (aged 18-40 years) that have been attending pharmacies were included in the sample. The
duration of the disease was 9 :!:: 4.21 years. A 4-month study was conducted on essence of asthma and factors that can intensify
;1; nourishing facts, allergens, and physical activities; self-management and use of tobacco;and pharmacotherapy, inhalation
technique, and possible adverse drug reactions. Patient's health-related QOL was assessed in the beginning and at the end of
the survey. Parameters assessed during the four stages of the program were patients' peak expiratory flow (PEF); inhaler
technique; severe asthma symptoms, including breathlessness, hospitalization rates,frequency of urgent medical aid calls, and
frequency of general practitioner visits; compliance with therapy; and satisfaction with pharmacy services. Health-related QOL
of the intervention patients was improved at 4 months and there was improvement in the PEF rate, decrease in patients'
breathlessnessand wheezing rate, decreasein the reported hospitalizations rate becauseof the disease, decreasein the physician's
visits, and increase in satisfaction with pharmacist-provided information. The positive results from the educational approach
show a potential to decreaseasthma disease complications and show a positive impact on patients' inhaler technique, patients'
opinions about the pharmacy services, and information obtained.
(Allergy Asthma Proc 29:55-61,2008;doi: 10.2500/aap2008.29.3083)
Key words: Asthmatic quality of life, bronchial asthma, Bulgaria, educational program for asthma patients, patient
knowledge, pharmaceutical care, pharmaceutical education '
here has been a significant increase in the prev- viders.8-10 But community pharmacists are consid-
T alence of allergy and especially of bronchial
asthma in the past 20 years. Asthma seems to be
ered to be in a unique position to support asthma
patients with the management of their chronic illness
associated with an enormous social, psychological, because of their permanent contact with the patients
and economic burden as it is responsible for many and their drug knowledge, authority, and easy ac-
deaths and expenditure of health care expenses. 1,2 cessibility. The pharmacists are well educated and
Despite the innovations in the availability and effi- can be trained easily, especially in asthma, to be able
cacy of asthma drug treatment, the quality of health to provide specialized care to asthmatic patients.
care provided to this group of chronic patients seem Training provided to pharmacists has a long-term
to be suboptimal, and asthma mortality and morbid- effect on their knowledge and proficiency and can
ity rates remain unacceptably high.3-5 There are improve patient drug knowledge, inhaler technique,
many reports of noncompliance to asthma treatment, and level of compliance. In the United States, phar-
which leads to poor quality of asthma care and in- macists' instructions in metered-dose inhalers im-
creases in asthma exacerbations that lead to hospi- proved patient skills.ll,12Pharmacists play an impor-
talizations, GP visits, extra use of drugs, and increase tant role in asthmatic patients' treatment, focused on
in asthma treatment cost.6,7
the safe and effective use of drugs.13 According to
There are many educational programs for patients
the European Therapeutic Outcome Monitoring
with asthma, provided by different health care pro-
studies, pharmacists not only improved patients'
drug knowledge, inhalator skills, and patients' com-
pliance with the prescribed therapy, but they also
From the Faculty of Pharmacu, Department of Social Pharmacy, Medical University- work and improve the drug therapy together with
Sofia, Sofia, Bulgaria the general practitioner (GP)Y-16 The pharmacist's
Address correspondenceand reprint requests to Valentina Petkoua, Ph.D., Faculty of
Pharmacy, Department of Social Pharmacy, Medical Uniocreitv-Sofia, 2-Dunav sir., contribution to patient care through education and
Sofia-lOOO,Bulgaria monitoring and through assessing and optimizing
E-mail address:petkovav1972@yahoo.com the drug therapy leads, in general, to improvement
Copyright © 2008, OceanSide Publications, Inc., U.S.A.
in patient quality of life (QOL).12,17,18
tions, and urgent medical aid (UMA) calls in the past ance coverage and were educated-the secondary and
4 weeks. That information was obtained in the be- higher education predominates in both groups. Five
ginning and at the end of the study. patients from group 1 and six patients from group 2
Patient satisfaction with the services provided by phar- were current cigarette smokers. The duration of the
macists was assessed by a directed interview. It was asthma since diagnosis is comparatively equal in both
provided in the beginning of the project and after the groups. The severity of patients' asthma is shown in
education process. the Table 1.
PEF rate measurements, inhaler technique assess- Table 2 represents the influence of the education on
ments, and data obtained from QOL instruments were the studied parameters: PEF rate, inhaler technique,
analyzed using repeated-measures analysis of variance asthma self-monitoring, quality of services provided,
(ANOVA). In addition, changes between baseline and and patients' QOL. It is clear that there are some dif-
4 months for the various measures were compared ferences between the two groups at baseline: the hos-
within and between the two groups of patients using pitalization rate and the frequency of UMA calls are
t-tests and the Mann-Whitney U-test (between-group lower in the intervention group than in the control
analysis), as appropriate. A value of p < 0.05 was group. Although the results for asthma self-monitor-
considered statistically significant. Statistics were per- ing, shortness of breath, and availability of cough are
formed by using SPSS/version 12.0 (SPSS Inc., Chi- nearly equal in the two groups. The purpose of the
cago,IL). study was to assess if there was any alteration in the
results between the two groups because of the educa-
RESULTS tion program.
Fifty patients were eligible to participate in the The results of the PEF rate from the patient's diaries
study, 22 in the intervention group (group 1) and 28 in show that at baseline, the mean PEF of the patients in
the control group (group 2). The separation is based on both groups were comparatively equal (335.45 ± 15.73
patient willingness to take part in the education pro- L/minute for group 1 versus 332.14 ± 14.49L/minute
gram. Table 1 gives demographic information about for group 2). After ANOVA analysis with gender and
the two groups. age as covariates (predictors), it was proven that PEF
The number of women is equal in the two groups was not significantly different in the two groups (p >
and statistically there is no significant difference be- 0.05). These PEF values are the mean for both groups
tween the number of men in the intervention and without taking in mind the influence of patients' age
control groups (p > 0.05). The intervention group also and height.
had a significantly younger mean age compared with During the education process fluctuation still is ob-
the control group. All of the patients had health insur- served in the control group PEF values whereas after
PEF rate (L/min) 335.45 ± 15.73 332.14 ± 14.49 338.64 ± 12.55 333.57 ± 14.00
Inhaler technique 0.41 ± 0.5 0.46 ± 0.5 0.55 ± 0.51 0.46 ± 0.51
Asthma self-monitoring
Availability of cough, shortness of 90.9% 96.4% 68.2% 96.4%
breath
Hospitalization rate 36.4% 85.7% 13.6% 78.6%
Frequency of UMA calls 54.5% 89.3% 18.2% 78.6%
Visit to GP
<2-3 times 63.7% 17.9% 86.4% 21.4%
>6 times 9.1% 3.6% 4.5% 3.6%
QOL 3.55 ± 1.335 3.39 ± 0.685 3.77 ± 1.020 3.00 ± 0.903
Quality of health services provided
Information provided from the 1.45 ± 0.510 1.71 ± 0.460 1.23 ± 0.429 1.57 ± 0.504
pharmacist
Satisfaction from the services provided 1.55 ± 0.510 1.71 ± 0.460 1.27 ± 0.456 1.75 ± 0.441
Necessity of additional information 1.18 ± 0.395 1.36 ± 0.488 1.45 ± 0.510 1.29 ± 0.460
Table 3 PEF rate alterations (L/min) At baseline, both groups had similar inhaler scores,
and a relatively low percentage of patients was as~
Group 1 Group 2 sessed with "correct" for their inhaler techniques (9
Baseline 335.45 ± 15.73 332.14 ± 14.49 [40.9%] for group 1 and 13 [46.4%] for group 2). After
After 1 mon 336.59 ± 14.09 326.07 ± 12.86 the education session the patients in group 1 showed a
After 2 mon, 338.86 ± 12.53 331.61 ± 13.95 trend to improve their techniques (12 [54.5%]).There is
After 3 mon 338.41 ± 12.19 322.32 ± 12.36 no improvement observed in the control group. The
After 4 mon 338.64 ± 12.55 333.57 ± 14.00 difference between the 4-month score and the baseline
score was significantly higher in the intervention
group than in the control group (,1-test).
During the study, patient self-monitoring was pre-
the second month and especially after the third month sented, which included patient's report about the exis-
there are stable values of the PEF rate in group 1. After tence, duration, and severity of asthma crisis; hospital-
the education process, stable values of the PEF rate are ization and duration of hospitalization if needed; and
observed for group 1 (338.64 ± 12.55)and there are still compliance with the drug treatment. Patients reported
fluctuations in the PEF rate of the patients in group 2 frequency of cough, chest tightness, and shortness of
(333.57 ± 14.00; Table 3) breath. Over 90% of patients inboth the control and the
For the patients in the control group the mean PEF at intervention groups reported that they have experi-
baseline (332.14. ± 14.49 L/minute) was almost equal enced these symptoms most of the time. Up to 50%
to the mean PEF after 4 months (333.57 ± 14.00 reported feeling these symptoms three to six times a
L/minute). The corresponding comparison for the in- week or more frequently. After the education session
tervention group shows improvement in the PEF rate significantly more patients in the intervention group
after the program (335.45 ± 15.73 in the beginning and than in the control group (32% versus 4%) reported no
338.64 ± 12.55 at the end of the project). The difference availability of these symptoms at all (p = 0.013;,1-test).
between the 4-month PEF and the baseline PEF was A significant part of the control group (85.7%) in
significantly higher in the intervention group than in comparison with the intervention group (36.4%) was
the control group (ANOVA with gender and age as hospitalized because of asthma crisis and the length of
covariates). hospital stay was from 2-5 days. They reported that
The inhaler technique scores were calculated based they were hospitalized once (57.1% versus 18.2%) or
on observation of patients' skills. Their inhaler tech- more then once (28.6%versus 18.2%). After the educa-
niques were ranked with "1" for correct and "0" for tion process there was a decrease in the hospitalization
incorrect. rate in the intervention group. The patients reported
that during the observed period they were hospitalized Analysis of the Asthma Assessment form showed no
only once (13.6%). The rest of the patients from this significant differences in the patients' QOL over the
group were not hospitalized. Although the results in 4-month period. Approximately 27.2% of the interven-
the control group show a decrease in the rate of the tion group and only 7.1% of the control group said that
polyhospitalizations from 28.6 to 21.4%, there is con- they had fully experienced day most of the time and
stant rate of 57.1% in the single hospitalizations. There their disease did not interfere in their daily routine.
is an increase in the number of patients from this group After the program, there is no significant change ob-
that were not hospitalized (from 14.3 to 21.4%). The served in the answers of the patients: ~25.0% of the
self-reported hospitalization rates were significantly intervention group and 3.6% of the control group an-
different between the two groups (p = 0.001; paired swered that they have had fully experienced days most
t-test). All of the patients claimed that they were com- of the time for the last 4 weeks (Tables 2 and 4).
pliant with the prescribed therapy and all of the pa- From the analysis of the data of each group over
tients said that they strictly followed the physicians' time, it is evident that for the 22 patients in the inter-
instructions. vention group who completed the study, the mean
A significant decrease in the frequency of UMA calls score at the end of the program (3.77 ± 1.020) was
was observed. Inthe beginning of the study ~45.5% of significantly higher than at baseline (3.55 ± 1.355;P <
patients from the intervention group were not calling 0.0001;paired t-test), indicating that there is improve-
for UMA, and the remaining patients needed UMA ment in the QOL over the duration of the study (the
once (27.3%)or more then once (27.2%);only 10.7% of scoring was from I, "interference all of the time," to 5,
the patients from the control group did not need UMA. "interference none of the time"). The corresponding
The rest called UMA only once (71.4%)or more times comparison for the control group showed that there
(17.9%). After the education process there was a de- was worsening in the patients' QOL: from 3.39 ± 0.685,
crease in the UMA calling rate in the intervention the results decreased to 3.00 ± 0.903 (p = 0.039;paired
group. The patients reported that during the observed t-test).
period they needed their services only once (18.2%). Data regarding patient satisfaction with the services
The rest of the patients from this group did not have provided by pharmacists were collected by interview.
any disease complications that called for UMA inter- It was provided in the beginning of the project and
vention. The results in the control group showed a after the education process. The patients' responses
decrease in the rate of the calls from 89.3 to 78.6%.The were based on the services provided by the private
difference between the 4-month results and the base- community pharmacists included in the project phar-
line was not significant in the two groups (p > 0.05; macies.
Mann-Whitney U-test). The intervention group was more satisfied with the
After the education process there was no significant information that was provided by their pharmacists in
difference in the results of the control group regarding the beginning of the program, whereas the patients
the frequency of GP visits-3.6% declared that they from the control group were not so satisfied (54.5%
have visited their physician more then six times and from the intervention group were positive vs. 28.6%for
21.4% visited their physician less then two to three the control group). After the education process both
times. Although there are significant differences in the groups showed increase in their satisfaction (77.3%for
intervention group, 86.4% have visited their physician the intervention group vs. 42.9%for the control group).
less then two to three times and only 4.5% visited their After the analysis of the data for each group, over
physician more then six times for the last 4 weeks (p = time, it is evident that for the intervention group, the
0.018; _i-testt mean score at 4 months (1.23 ± 0.429)was significantly