The Effect of Health Education by Pharmacists on 10-Year Atherosclerotic Cardiovascular Disease Risk: A Cluster-Randomized Control Study in a Low Socioeconomic Status Javanese Population

Abstract

Background: Evidence from previous studies demonstrates that lifestyle modification reduces the incidence and complications of atherosclerotic cardiovascular disease. The study aimed to investigate the effect of a lifestyle intervention provided by pharmacists on the 10-year atherosclerotic cardiovascular disease (ASCVD) risk and quality of life (QoL) in a low socioeconomic status Javanese population. Methods: This research was a cluster-randomized controlled study of 1-year duration, conducted in a lower social economic community in the Sleman District of Yogyakarta, Indonesia. The eligible subjects were dichotomized into 2 groups: 40 to 55 years (n = 61 vs 65) and 56 to 70 years (n = 21 vs 43) for intervention and control subjects, respectively. The ASCVD score and risk factors within the age-based groups were analyzed using T test/Mann-Whitney test for continuous data or chi-square test for categorical data. Results: The intervention and control subjects had similar baseline characteristics (P > .05), including the ASCVD risk with the low- and high-risk classification for younger and elder subjects, respectively. At final follow-up, the younger intervention subjects had lower 10-year ASCVD risk (P = .001), higher high-density lipoprotein cholesterol (P = .02), smoking status (P = .001), persistence rate (P = .03), and QoL value for the physical and social function domains (P < .05) than the control subjects, whereas the elder intervention subjects only had better ASCVD risk score than controls (P = .03). Smoking interacting with intervention was the most influential variable on ASCVD risk in logistic regression analysis. Conclusion: The study demonstrates that the health education by the pharmacists produce significant outcomes of the ASCVD risk, smoking status, and QoL of physical and social function particularly in the younger group.

Keywords

pharmacist community pharmacist ASCVD risk low socioeconomic status health education

Introduction

Atherosclerotic cardiovascular diseases (ASCVDs), formerly known as cardiovascular diseases (CVDs),¹ showed a substantial decline worldwide due to the use of evidence-based therapy in heart disease.^2,3 Nevertheless, the highest mortality causes in Indonesia are related to the ASCVDs, including stroke, ischemic heart disease, and diabetes mellitus (DM), which are responsible for 21.2%, 8.9%, and 6.5%, respectively, of all death in Indonesia. High prevalence of hypertension, poor diet, and smoking status contribute to the development of the ASCVDs.⁴

Hypertension, DM, and hyperlipidemia are the most dominant ASCVD risk factors.⁵ The 10-year ASCVD risk can be predicted using pooled cohort equations.⁶ The risk prediction is effective to screen patient’s disease and to initiate therapy.⁷ The effect of therapy varies among different populations.² Pharmacists can participate in the ASCVD reduction with the lifestyle education, health promotion, and disease prevention.^8-12

A review study found no particular intervention method emerged with better impact.¹³ A community-based lifestyle intervention with a cultural approach showed greater reduction of the body mass index (BMI) and A1c than the education with printed materials among the lower health coverage subjects in the United States.¹⁴ To the contrary, an intensive lifestyle modification for weight loss failed to minimize the cardiovascular events among obese type 2 DM subjects.¹⁵ Regardless of the contradictive results, more evidence recently indicated that the ASCVDs were preventable with lifestyle modification.¹⁶

Sleman District, with 574 km² width and 1.1 million inhabitants, is the most populated district in the Yogyakarta Province, Indonesia. In a former research, Sleman population had high prevalence of hypertension, low disease awareness, and low blood pressure (BP) control rate despite the ownership of the universal health coverage.¹⁷ The patient and health care provider factors affect more on the health outcomes than the financing system.¹⁸ Based on the above description, we aimed to investigate the effect of a lifestyle modification with health education by pharmacists on the 10-year ASCVD risk and the quality of life (QoL) score. The health education was expected to be beneficial for the health knowledge enhancement and the ASCVD prevention in a low socioeconomic status population.

Methods

Design of Study and Intervention

This research was a cluster-randomized control study done of 1-year duration conducted in a lower socioeconomic community of the Sleman District of Yogyakarta. The study protocol was approved by the Ethics Committee of Universitas Gadjah Mada with Ref No. KE/FK/043/EC/2016. The open-labeled intervention involved with 2 main topics: (a) increase of cardiovascular risk awareness and (b) CVD prevention with healthy lifestyle and monitoring of BP, fasting blood glucose (FBG), high-density lipoprotein cholesterol (HDL-C), and total cholesterol (total-C).

The researchers, 3 pharmacists with 10 pharmacy students, conducted the intervention with 4 sessions of 90-minute long oral presentation and discussion, which were done consecutively every 1 to 2 months. Presentation covered the topics of hypertension, hyperlipidemia, and diabetes. Each of the subjects in the intervention group received 4 booklets covering the presentation topics and an activity manual, along with 3 posters about smoking cessation, exercise, and healthy food. The aforementioned printed materials were prepared to help the intervention subjects to better understand and maintain the knowledge. The intervention subjects were encouraged to participate in weekly exercise. We also recruited 5 active subjects in the intervention group as a local research team. The local team was trained for the measuring BP, peripheral FBG, and cholesterol technique by small group discussion with the aim to prepare them to continue the ASCVD prevention beyond the research period. The control subjects did not receive any health education, but obtained the monitoring report of HDL-C, total-C, and FBG.

Study Sites and Subject Selection

The study sites of 4 villages were selected with multistage randomization within 17 subdistricts and were grouped into west and east clusters before the submission of the protocol to the ethics committee. We interviewed some respondents to know their responses and appointed the more cooperative cluster from the west side as the intervention group.

At baseline, we invited all adults regardless of the characteristics to each study site within a week prior to the study and with the instruction of 8- to 10-hour fasting. The 10-year ASCVD risk calculator has the criteria of 90 to 200 mm Hg for systolic blood pressure (SBP), 130 to 320 mg/dL for total-C, and 20 to 100 mg/dL for HDL-C.¹⁹ All subjects who met the ASCVD calculator criteria and signed the informed consent were included, whereas pregnancy, CVDs (poststroke, myocardial infarction, and coronary stent), and nonfasting subjects were excluded.

At baseline, of the 201 eligible subjects, we matched the groups and dropped 11 younger candidates from the control group due to hyperthyroidism (n = 1), outliers of ASCVD score (>10%), and DM plus high cholesterol/BMI (n = 10). Diabetes has been associated with low life satisfaction.²⁰ The final number of subjects (n = 190) consisted of the intervention (n=82) and control (n = 108) groups. Furthermore, the subjects in each group were divided based on the ages of 40 to 55 and 56 to 70 years (Figure 1).

Figure 1.

Flow diagram of the sampling process and subject criteria.

Data Collection

Data collection was done at the study sites. Blood pressure (BP) was measured using digital sphygmomanometer Omron HEM-7120®. The second reading with <10 mm Hg difference from the first one was considered as BP, otherwise a third measurement was needed to determine mean BP from the 2 closest readings. High BP had the cut-point at ≥140/90 mm Hg and/or receiving hypertension medication. After collection of venous blood samples for FBG and cholesterol level, the samples were transported and analyzed in PL, an accredited clinical laboratory in Yogyakarta city. The FBG and cholesterol were determined with serum hexokinase and CHOD-PAP methods, respectively using the instrument of COBAS 311®. Diabetes was defined as blood glucose >125 mg/dL and/or receiving DM medication.

Variables

Variables of this study consisted of continuous data and categorical profiles. The continuous data were comprised the ASCVD risk score,¹⁹ age, BP, pulse, BMI, FBG, total-C, and HDL-C, and QoL using the SF-36 (Short Form–36 health questionnaire) instrument translated into Indonesian language; whereas the categorical profiles were comprised of gender, education background, hypertension medication, diabetes status, ASCVD classification, and control of BP, BMI, FBG, and cholesterol.

The QoL was assessed with the SF-36 instrument.^21,22 The instrument consists of 36 questionnaires divided into 8 domains, namely physical functions, physical role, pain free, general health, social health, vitality, mental health, and emotional role. The QoL evaluation is preferably done on each domain of the QoL instead of the total score of SF-36.^23-25

The BP target was standardized at <140/90 mm Hg and <150/90 mm Hg for <60 and ≥60 years subjects, respectively. The ASCVD risks were obtained from the ACC/AHA risk calculator¹⁹ and were classified into <5% (low risk) and ≥5% (moderate to high risk). There is no exact BMI cut-point for Asian population,²⁶ and BMI at ≥23.0 kg/m² is defined as overweight. Smoking status covered the active, including ever smoking in a previous year and/or passive smoking at work or at home.

Race was not analyzed because the all subjects were from Javanese ethnicity. The meal and salt intake were not evaluated because the subjects had consumed similar proportions and style of diet with the preference of sweet flavored meals. The Indonesian population has a higher cholesterol consumption in their diet than other Asian countries.⁴

Statistical Analysis

The data were analyzed by the Clinical Epidemiology & Biostatistics Unit, Faculty of Medicine, Universitas Gadjah Mada using the IBM program SPSS Statistics 22. The categorical data between groups were compared based on the odds ratio (OR) analyzed with either Pearson’s chi-square or Fisher’s exact test. Meanwhile, the continuous data were analyzed for the data normality with normal Q-Q plot description test and followed by either T test or Mann-Whitney test depending on the data normality. Finally, the logistic regression was performed to evaluate β coefficient (95% confident interval), P value, and coefficient determination of the variables in each age-based group. Prior to the regression analysis, bivariate analysis was done for the variables of age, SBP, Total-C, HDL-C, and FBG, BMI, education, gender, therapy of hypertension, and DM status and the variables in equations with P < .25 were continued for the regression analysis.

Results

Baseline Profiles

The characteristics of the overall and age-based subjects are presented in the categorical profiles (Table 1) and in the continuous data (Table 2). The analyses were done in the age-based group because the younger and older subjects had ASCVD score at <5% (low risk) and >7.5% (high risk), respectively. Moreover, age is a natural risk factor of ASCVD. The profiles of the intervention and control subjects within age-based groups were similar at baseline (P > .05) with 2 variables exceeded the normal range, namely mean SBP ≥140 mm Hg in younger subjects and BMI >23 kg/m².

Table 1.

Age-Based and Overall Subjects’ Characteristics at Baseline and Final Follow-up.^a

Characteristics	Overall Subjects			40- to 55-Year-Old Subjects			56- to 70-Year-Old Subjects
Characteristics	n (%)	n (%)	P; OR (95% CI)	n (%)	n (%)	P; OR (95% CI)	n (%)	n (%)	P; OR (95% CI)
Profiles at baseline
Gender	Male	Female	.01; 0.35 (0.17-0.75)	Male	Female	.13; 0.47 (0.18-1.26)	Male	Female	.05; 0.30 (0.09-1.03)
Interventions	11 (13.4)	71 (86.6)		7 (11.5)	54 (88.5)		4 (19.0)	17 (81.0)
Controls	33 (30.6)	75 (69.4)		14 (21.5)	51 (78.5)		19 (44.2)	24 (55.8)
Diabetes	DM	No	.35; 0.56 (0.17-1.90)	DM	No	.12^b; 0.16 (0.02-1.40)	DM	No	.39^b; 2.22 (0.41-12.1)
Interventions	4 (4.9)	78 (95.1)		1 (1.6)	60 (98.4)		3 (14.3)	18 (85.7)
Controls	9 (8.3)	99 (91.7)		6 (9.2)	59 (90.8)		3 (7.0)	40 (93.0)
Education	≤Junior high	>Junior high	.36; 0.76 (0.41-1.38)	≤Junior high	>Junior high	.89; 0.95 (0.47-1.93)	≤Junior high	>Junior high	.43^b; 0.69 (0.17-2.77)
Interventions	51(62.2)	31(37.8)		34 (55.7)	27(44.3)		17(81.0)	4(19.0)
Controls	74(68.5)	34(31.5)		37(56.9)	28(43.1)		37(86.0)	6(14.0)
Hypertension therapy	Therapy	No	.98; 0.99 (0.40-2.47)	Therapy	No	.40; 0.58 (0.16-2.10)	Therapy	No	.28^b; 2.38 (0.60-9.35)
Interventions	9 (11.0)	73 (89.0)		4 (6.6)	57 (93.4)		5 (23.8)	16 (76.2)
Controls	12 (11.1)	96 (88.9)		7 (10.8)	58 (89.2)		5 (11.6)	38 (88.4)
Smoking	Smoking	No	.59; 0.85 (0.48-1.52)	Smoking	No	.83; 0.93 (0.46-1.87)	Smoking	No	.66; 0.79 (0.28-2.25)
Interventions	37 (45.1)	45 (54.9)		27 (44.3)	34 (55.7)		10 (47.6)	11 (52.4)
Controls	53 (49.1)	55 (50.9)		30(46.2)	35 (53.8)		23 (53.5)	20 (46.5)
ASCVD Risk <5%	Risk <5%	No	.01; 2.35 (1.27-4.36)	Risk <5%	No	.07; 2.52 (0.90-7.05)	Risk <5%	No	.47^b; 1.61 (0.44-5.84)
Interventions	60 (73.2)	22 (26.8)		55 (90.2)	6 (9.8)		5 (23.8)	16 (76.2)
Controls	58 (53.7)	50 (46.3)		51 (78.5)	14 (21.5)		7 (18.8)	36 (83.7)
Outcomes at final follow-up
Hypertension therapy	Therapy	No	.93 1.04 (0.44-2.46)	Therapy	No	.37; 1.78 (0.49-6.44)	Therapy	No	.79^b; 0.84 (0.22-3.12)
Interventions	11 (13.4)	71 (86.6)		7 (11.5)	54 (88.5)		4 (19.0)	17 (81.0)
Controls	13 (13.0)	87 (87.0)		4 (6.8)	55 (93.2)		9 (22.0)	32 (78.0)
Blood pressure	Good control	No	.03; 1.98 (1.07-3.67)	Good control	No	.10; 2.26 (1.04-4.91)	Good control	No	.13; 2.38 (0.77-7.35)
Interventions	58 (70.7)	24 (29.3)		44 (72.1)	34 (57.6)		15 (71.4)	6 (28.6)
Controls	55 (55.0)	45 (45.0)		17 (27.9)	25 (42.4)		21 (51.2)	20 (48.8)
Blood glucose	<126 mg/dL	≥126 mg/dL	.28; 1.93 (0.57-6.51)	<126 mg/dL	≥126 mg/dL	.38^b; 2.15 (0.38-12.18)	<126 mg/dL	≥126 mg/dL	.75^b; 1.32 (0.23-7.45)
Interventions	78 (95.1)	4 (4.9)		59 (96.7)	2 (3.3)		19 (90.5)	2 (9.5)
Controls	91 (91.0)	9 (9.0)		55 (93.2)	4 (6.8)		36 (87.8)	5 (12.2)
Total cholesterol	<200 mg/dL	≥200 mg/dL	.69; 0.89 (0.49-1.59)	<200 mg/dL	≥200 mg/dL	.45; 0.76 (0.37-1.56)	<200 mg/dL	≥200 mg/dL	.94; 0.96 (0.33-2.77)
Interventions	41 (50.0)	41 (50.0)		32 (52.5)	29 (47.5)		9 (42.9)	12 (57.1)
Controls	53 (53.0)	47 (47.0)		35 (59.3)	24 (40.7)		18 (43.9)	23 (56.1)
HDL cholesterol	≥40 mg/dL	<40 mg/dL	.34; 1.71 (0.56-5.22)	≥40 mg/dL	<40 mg/dL	.17^b; 2.6 (0.64-10.59)	≥40 mg/dL	<40 mg/dL	.76^b; 0.75 (0.12-4.88)
Interventions	77 (93.9)	5 (6.1)		58 (95.1)	3 (4.9)		19 (90.5)	2 (9.5)
Controls	90 (90.0)	10 (10.0)		52 (88.1)	7 (11.9)		38 (92.7)	3 (7.3)
Smoking status	Nonsmoking	Smoking	.07; 1.71 (0.95-3.08)	Nonsmoking	Smoking	.001; 3.76 (1.76-8.03)	Nonsmoking	Smoking	.12; 2.31 (0.79-6.76)
Interventions	47(57.3)	35 (42.7)		38 (62.3)	23 (37.7)		12 (57.1)	9 (42.9)
Controls	44 (44.0)	56 (56.0)		18 (30.5)	41 (69.5)		15 (36.6)	26 (63.4)
ASCVD score	Low risk	Medium-high risk	<.001; 4.01 (2.14-7.51)	Low risk	Medium-high risk	.001; 4.23 (1.71-10.51)	Low risk	Medium-high risk	.03 ^b ; 5.07 (1.12-22.92)
Interventions	59 (72.0)	23 (28.0)		53 (86.9)	8 (13.1)		6 (28.6)	15 (71.4)
Controls	39(39.0)	61 (61.0)		36 (61.0)	23 (39.0)		3 (7.3)	38 (92.7)
Persistence^c	Persistence	No	.01; 1.08 (1.02-1.14)	Persistence	No	.03 ^b ; 1.10 (1.02-1.19)	Persistence	No	.32; 1.05 (0.98-1.20)
Interventions	82 (100.0)	0 (0.0)		61 (100.0)	0 (0.0)		21(100.0)	0 (0.0)
Controls	100 (92.6)	8 (7.4)		59 (90.8)	6 (9.2)		41 (95.3)	2 (4.7)

Abbreviations: OR, odds ratio; CI, confidence interval; DM, diabetes mellitus; HDL, high-density lipoprotein; ASCVD, atherosclerotic cardiovascular disease.

P values calculated using chi-square. Values in boldface indicate statistical significance. OR > 1: interventions with higher proportion than controls. Hypertension therapy: good control of blood pressure <140/90 mm Hg except for ≥60-year-old subjects <150/90 mm Hg.

P values calculated using Fisher’s exact test.

RR relative risk; persistence rate: comparison between final follow-up and baseline.

Table 2.

Subjects’ Characteristics of the Overall and Age-Based Group Subjects at Baseline and Final Follow-up.^a

Characteristics	Baseline (Mean ± SD)			Final Follow-up (Mean ± SD)
Characteristics	Overall Subjects	40- to 55-Year-Old Subjects	56- to 70-Year-Old Subjects	Overall Subjects	40- to 55-Year-Old Subjects	56- to 70-Year-Old Subjects
Age (years)
Interventions	50.4 ± 7.6	46.8 ± 5.0	60.7 ± 3.5	50.4 ± 7.6	46.8 ± 5.0	60.7 ± 3.5
Controls	52.3 ± 8.6	46.3 ± 4.7	61.4 ± 3.4	52.6 ± 8.5	46.5 ± 4.8	61.3 ± 3.4
Systolic BP (mm Hg)
Interventions	138.0 ± 20.5	134.0 ± 18.0	149.4 ± 23.2	132.8 ± 19.2	128.8 ± 16.4	144.5 ± 22.2
Controls	142.4 ± 22.6	137.8 ± 22.4	150.4 ± 21.1	136.6 ± 20.4	131.8 ± 19.3	143.4 ± 20.2
Diastolic BP (mm Hg)
Interventions	80.4 ± 10.4^b	80.3 ± 10.1	80.7 ± 11.6	83.5 ± 10.3	83.6 ± 10.4	83.2 ± 10.2
Controls	83.8 ± 12.2	82.7 ± 12.8	85.7 ± 10.9	85.7 ± 11.5	85.8 ± 12.8	85.7 ± 9.5
Pulse (/min)
Interventions	83.4 ± 11.2	83.4 ± 11.6	83.2 ± 10.3	80.6 ± 13.2	80.6 ± 13.4	80.7 ± 12.9
Controls	82.2 ± 13.7	83.2 ± 15.0	80.7 ± 11.3	79.3 ± 14.0	79.7 ± 16.2	79.2 ± 10.3
BMI (kg/m²)
Interventions	23.6 ± 4.7	23.0 ± 4.5	22.1 ± 4.8	24.1 ± 4.5	24.7 ± 4.4	22.4 ± 4.4
Controls	23.8 ± 4.7	24.4 ± 4.7	22.8 ± 4.7	24.0 ± 4.4	24.8 ± 4.3	22.8 ± 4.4
FBG (mg/dL)
Interventions	92.9 ± 23.6	91.8 ± 24.9	96.1 ± 19.1	92.5 ± 19.9	90.7 ± 19.0	97.6 ± 22.1
Controls	99.9 ± 44.5	101.4 ± 53.0	97.0 ± 26.5	94.7 ± 40.6	92.9 ± 42.1	97.4 ± 38.7
Total-C (mg/dL)
Interventions	193.1 ± 34.0^c	192.3 ± 33.4	195.2 ± 36.3	200.1 ± 32.8	196.4 ± 30.1	210.9 ± 38.2
Controls	204.9 ± 36.4	199.8 ± 33.1	213.2 ± 39.7	200.5 ± 32.9	199.5 ± 34.0	201.9 ± 31.8
HDL-C (mg/dL)
Interventions	55.7 ± 13.1	56.1 ± 12.7	54.5 ± 14.4	57.7 ± 12.9^d	57.5 ± 12.8^f	58.2 ± 13.5
Controls	56.4 ± 12.3	55.0 ± 11.7	58.2 ± 13.0	52.3 ± 11.9	52.0 ± 11.9	52.8 ± 11.9
ASCVD risk (%)
Interventions	5.0 ± 7.9	2.5 ± 1.9	12.4 ± 12.7	4.2 ± 4.8^e	2.4 ± 1.9^g	9.3 ± 6.8^h
Controls	7.2 ± 7.6	3.3 ± 2.5	13.2 ± 8.8	8.1 ± 7.3	4.1 ± 2.9	13.8 ± 7.9

Abbreviations: BP, blood pressure; BMI, body mass index; FBG, fasting blood glucose; Total-C, total cholesterol; HDL-C, high-density lipoprotein cholesterol; ASCVD, atherosclerotic cardiovascular disease.

P values calculated using T test

P = .04.

P = .02.

P = .004.

P < .001.

P = .02.

P < .001.

P = .03.

Outcomes at Final Follow-up

All intervention subjects completed the study. Whereas, the control group was less persistent with a drop-out rate of 6 (9.2%) from the younger (P = .03) and 2 (4.7%) from the older including 1 deceased subject (P = .32) (Table 1). At final follow-up, the younger intervention subjects had better outcomes for the mean 10-year ASCVD score (P < .001) and mean HDL-C (P = .02) (Table 2) and proportion of ASCVD score <5% (P = .001), and smoking status (P = .001) (Table 1); whereas the older intervention subjects had only better outcome for the ASCVD risk score (P = .03) (Table 1).

We performed the logistic regression to evaluate the most influential variables on ASCVD. In the younger subjects, the variables of intervention, age, smoking status, SBP, total-C, HDL-C, gender, FBG, and therapy for hypertension had significant correlation with ASCVD risk in bivariate analysis (P < .25) and the variables were input for regression analysis. Pharmacist intervention in bivariate analysis has significant effect on ASCVD (P = .002 and R² = 12.6%), when the intervention was adjusted with other variables, it became insignificant for ASCVD (P = .71). Finally, the intervention was found interacting significantly with age, SBP, HDL-C, and smoking status, and these variables together with total-C and gender produced significant outcome on ASCVD risk (P = .01 and R² = .859). In this study, the variables of the intervention interacting with smoking contributed the greatest effect on ASCVD according to the β coefficient in the logistic regression. In the older subjects, the variables intervention, age, smoking status, SBP, BMI, categorical total-C, and HDL-C had significant effect on ASCVD in bivariate analysis, but all variables were insignificant in logistic regression analysis (Supplementary File: Table of Logistic Regression Summary).

Quality of Life

The QoL values were similar between groups at baseline except for a higher score of vitality among older intervention subjects (P < .02). At final follow-up, the QoL increased for the physical (P = .005) and social function domains (P = .008) among the younger intervention subjects; whereas the QoL were similar among the older subjects (P > .05) (Table 3).

Table 3.

The Age-Based and Overall Subjects’ Quality of Life at Baseline and Final Follow-up.^a

Quality of Life Domain	Baseline			Final Follow-up
Quality of Life Domain	Overall Subjects	40- to 55-Year-Old Subjects	56- to 70-Year-Old Subjects	Overall Subjects	40- to 55-Year-Old Subjects	56- to 70-Year-Old Subjects
Physical function
Interventions	95 (10-100)	95 (10-100)	80 (10-100)	100 (50-100)^b	100 (60-100)^c	100 (50-100)
Controls	95 (0-100)	95 (40-100)	90 (0-100)	100 (0-100)	100 (0-100)	95 (0-100)
Physical role
Interventions	100 (0-100)	100 (0-100)	100 (0-100)	100 (0-100)	100 (0-100)	100 (0-100)
Controls	100 (0-100)	100 (0-100)	100 (0-100)	100 (0-100)	100 (0-100)	100 (0-100)
Pain free
Interventions	67.5 (10-100)	100 (0-100)	67.5 (10-100)	80 (32.5-100)	80 (32.5-100)	80 (42.5-100)
Controls	67.5 (0-100)	100 (0-100)	67.5 (10-100)	70 (0-100)	77.5 (20-100)	67.5 (0-100)
General health
Interventions	62.5 (25-90)	60 (25-90)	65 (25-80)	70 (25-95)	70 (25-95)	70 (30-90)
Controls	60 (25-90)	65 (25-90)	60 (30-90)	65 (15-100)	65 (25-100)	65 (15-95)
Social health
Interventions	100 (25-100)	100 (25-100)	100 (37.5-100)	100 (50-100)^d	100 (50-100)^e	100 (50-100)
Controls	67.5 (25-100)	87.5 (37.5-100)	87.5 (25-100)	100 (0-100)	87.5 (0-100)	100 (12.5-100)
Vitality
Interventions	75(30-100)	75 (30-100)	85 (45-100)^f	80 (40-100)	80 (40-100)	85 (50-100)
Controls	70 (30-100)	70 (30-100)	75 (30-100)	75 (20-100)	75 (20-100)	75 (30-100)
Mental health
Interventions	84 (32-100)	80 (32-100)	92 (56-100)	88 (36-100)	88 (36-100)	100 (40-100)
Controls	80 (28-100)	76 (28-100)	84 (35-100)	86 (40-100)	84 (48-100)	88 (40-100)
Emotional role
Interventions	100 (0-100)	100 (0-100)	100 (0-100)	100 (0-100)	100 (0-100)	100 (0-100)
Controls	100 (0-100)	100 (0-100)	100 (0-100)	100 (0-100)	100 (0-100)	100 (0-100)

P values calculated using Mann-Whitney test.

P = .003.

P = .01.

P = .005.

P = .008.

P = .02.

Discussion

The study was held in a low socioeconomic status setting. More than 50% of the younger subjects and >80% of the elder subjects had the formal education of junior high school or lower similar in intervention and control groups (Table 1). Mostly, the male subjects had the profession as farmers or construction workers. Meanwhile, the female subjects were housewives with sedentary lifestyle and only small proportion worked as part-time farmers. Some negative lifestyles included smoking in public areas or in the house and no routine exercise. Activities in daily work were considered to be a form of exercise for most subjects.

The intervention produced more intense outcomes among the younger than older subjects in both intervention and control groups due to poorer education background in the elder subjects. Moreover, the younger subjects were likely have better capacity to absorb the information and the physiological factors.

Prevalence of hypertension and diabetes in Yogyakarta Province in 2013 based on the National Basic Health Research (Riskesdas 2013) were 25.7% and 2.6%, respectively.²⁷ At the final follow-up, the proportion of subjects with uncontrolled BP and FBG were higher than the provincial morbidity rate for both intervention and control groups. The low socioeconomic status including education background became an obstacle in the absorption of information provided for the intervention subjects.

Positive Outcome of Intervention

At final follow-up, the intervention subjects had fewer smokers and the subjects persistently participated in the weekly exercise established during the baseline period. The intervention subjects also had significantly higher mean HDL-C, though the HDL-C increase was not as good as the finding from a CVD prevention research which showed the biggest contribution of exercise on HDL-C with up to 53% elevation.¹¹

Better mean ASCVD risk scores among the intervention subjects were attributed to the improvement of the healthy lifestyle and some ASCVD variables. Although the mean ASCVD risk score was significantly lower in the intervention than the control subjects in each age-based groups, the ASCVD risk classification within each age-based group was not different between groups, being low risk for the younger subjects (ASCVD <5%) and high to extremely high risk for the older subjects (ASCVD score at >7.5%).

Exercise was significantly correlated to higher life satisfaction.²⁰ In this study, the exercise activity among the intervention subjects were likely related to the higher QoL particularly among the younger group. The finding was even superior to a previous study that demonstrated that the exercise improved only the physical function.²⁸ The result was also similar to another study that showed that a supervised exercise improved the subject’s functional capacity.²⁹ Interestingly, the weekly exercise among the intervention subjects still continues at the time of this article’s submission. The higher persistent rate at final follow-up in the intervention subjects was supported by the active subjects.

Less Successful Outcome of Intervention

The proportion of subjects who received routine therapy for hypertension remained the same at final follow-up. The subjects who were not in routine therapy, they only took the antihypertensive medicine for the symptoms of headaches and neck stiffness. One former study in the district showed that the universal health coverage increased the proportion of hypertension therapy.¹⁷ The ownership of health financial support was similar between groups, but there were fewer healthcare facilities near the intervention than the control group. The control subjects had 2 hospitals with 30 beds, whereas the intervention subjects had only the primary care center as their nearest health care facility.

Previous references have demonstrated that physical activities improve the ASCVD outcomes,^16,30 as well as produce greater reductions in all ASCVD risk except for LDL-C levels and the primary ASCVD outcome.¹⁵ The intervention in this study covered the education about fat and calorie restriction and physical exercise, but it did not reduce the BMI and total-C. The subjects were aware of being overweight but were not successful in the BMI and total-C control.

The intervention and control groups were not statistically different in mean BP at final follow-up. These results were similar to a previous study done in the Sleman District that revealed the BP control deficiency among the subjects.¹⁷ The result was inferior to another study done among DM with hypertension patients which had demonstrated significant BP improvement after a pharmacist intervention.³¹

We hope that the improvement of the ASCVD risk will lead to the decline of ASCVD morbidity and mortality rate. Further study is needed to observe the long-term impact of the pharmacist intervention on the ASCVD outcomes in the Sleman District of Yogyakarta.

Limitation of the Study

The simple randomization method could not be applied in this study because the ASCVD risk profiles were not available in the population. Determination of the intervention group was done with nonproprietary method. At baseline, the overall subjects in the intervention group had lower DBP, total-C, and lower score of ASCVD risk than the control group, though the variables were not statistically different within the age-based groups. The analysis was performed within the age-based group in this study.

Conclusion

The younger intervention subjects had better 10-year ASCVD risk, smoking status, HDL-cholesterol, and quality of life for the physical and social function domains than the controls, whereas the elder intervention subjects had lower 10-year ASCVD risk than the controls. Although the health promotion and education provided by the pharmacists in this study produced a positive outcome on the ASCVD risk, the results of this study cannot be generalized to other population or different setting.

Supplemental Material

Supplementary_file_SAGE_EFFECT_OF_PHARMACIST_INTERVENTION – Supplemental material for The Effect of Health Education by Pharmacists on 10-Year Atherosclerotic Cardiovascular Disease Risk: A Cluster-Randomized Control Study in a Low Socioeconomic Status Javanese Population

Supplemental material, Supplementary_file_SAGE_EFFECT_OF_PHARMACIST_INTERVENTION for The Effect of Health Education by Pharmacists on 10-Year Atherosclerotic Cardiovascular Disease Risk: A Cluster-Randomized Control Study in a Low Socioeconomic Status Javanese Population by Rita Suhadi, Dita Maria Virginia and Christianus Heru Setiawan in Journal of Primary Care & Community Health

Footnotes

Acknowledgements

The authors would to like to express their gratitude to Mr Erik Hookom for his kind assistance in the manuscript English editing.

Declaration of Conflicting Interests

The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Funding

The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: The Director General of Higher Education, Indonesian Ministry of Research, Technology and Higher Education for the research grant of the Penelitian Terapan Unggulan Perguruan Tinggi (PTUPT) scheme in the year 2016-2017. No: 027 a /Penel.LPPM USD/IV 12016 and No: 075 /Penel.LPPM USD/IV/2017.

Supplemental Material

Supplementary material is available for this article online.

ORCID iD

Rita Suhadi

Author Biographies

Rita Suhadi is a senior lecturer in the Division of Pharmacology and Clinical Pharmacy at the Faculty of Pharmacy, Sanata Dharma University. Her research focuses on the outcome research in hypertension and cardiovascular disease, specifically in the area of disease awareness and therapy adherence.

Dita Maria Virginia is a junior lecturer in the Division of Pharmacology and Clinical Pharmacy at the Faculty of Pharmacy, Sanata Dharma University. Her main research interest is pharmacotherapy in female health, including issue of obesity and reproduction.

Christianus Heru Setiawan is a junior lecturer in the Division of Pharmacology and Clinical Pharmacy at the Faculty of Pharmacy, Sanata Dharma University. He has some researches in the stroke issue, on both the treatment and prevention. He is also active in the community service in the health care center that serve lower socioeconomic status patients.

References

Stone

Robinson

Lichtenstein

et al ; American College of Cardiology/American Heart Association Task Force on Practice Guidelines. 2013 ACC/AHA guideline on treatment of blood cholesterol to reduce atherosclerotic cardiovascular risk in adults: a report of the American College of Cardiology/American Heart Association Task Force on practice guidelines. Circulation. 2014;129(25 suppl 2):S1-S45. doi:10.1161/01.cir.0000437738.63853.7a.

Ford

Capewell

Proportion of the decline in cardiovascular mortality disease due to prevention versus treatment: public health versus clinical care. Annu Rev Public Health. 2011;32:5-22. doi:10.1146/annurev-publhealth-031210-101211.

Mensah

Wei

Sorlie

et al . Decline in cardiovascular mortality: possible causes and implications. Circ Res. 2017;120:366-380. doi:10.1161/CIRCRESAHA.116.309115.

World Atlas. Leading causes of death in Indonesia. https://www.worldatlas.com/articles/leading-causes-of-death-in-indonesia.html. 2017. Accessed March 13, 2018.

Quintana

Janszky

Gigante

et al . Diabetes, hypertension, overweight and hyperlipidemia and 7-day case-fatality in first myocardial infarction. IJC Metab Endocr. 2016:12;30-35. doi:10.1016/j.ijcme.2016.05.009.

Goff

Jr Llyod-Jones

Bennett

et al ; American College of Cardiology/American Heart Association Task Force on Practice Guidelines. 2013 ACC/AHA guideline on the assessment of cardiovascular risk: a report of the American College of Cardiology/American Heart Association Task Force on practice guidelines. Circulation. 2013;129(25 suppl 2):S49-S73. doi:10.1161/01.cir.0000437741.48606.98.

Gluckman

Kovacs

Stone

Damalas

Mullen

Oetgen

WJ.

The ASCVD risk estimator app: from concept to the current state. J Am Coll Cardiol. 2016;67:343-352. doi:10.1016/j.jacc.2015.10.068.

Lee

Choi

Wong

Chung

Cheng

FW.

Pharmacist intervention in the prevention of heart failure for high-risk elderly patients in the community. BMC Cardiovasc Disord. 2015;15:178. doi:10.1186/s12872-015-0173-3.

Omboni

Sala

The pharmacist and the management of arterial hypertension: the role of blood pressure monitoring and telemonitoring. Expert Rev Cardiovasc Ther. 2015;13:209-221. doi:10.1586/14779072.2015.1001368.

10.

Iso

Lifestyle and cardiovascular disease in Japan. J Atheroscler Thromb. 2011;18:83-88. doi:10.5551/jat.6866.

11.

Noé

Dósa

Ránky

Pavlik

Cardiovascular results of an individually controlled complex prevention. Acta Physiol Hung. 2014;101:1-12. doi:10.1556/APhysiol.101.2014.1.1

12.

Zullig

LL.

Melnyk

Stechuchak

et al . The Cardiovascular Intervention Improvement Telemedicine Study (CITIES): rationale for a tailored behavioral and educational pharmacist-administered intervention for achieving cardiovascular disease risk reduction. Telemed J E Health. 2014;20:135-143. doi:10.1089/tmj.2013.0145.

13.

Evans

Watson

Eurich

et al . Diabetes and cardiovascular disease interventions by community pharmacists: a systematic review. Ann Pharmacother. 2011;45;615-628. doi:10.1345/aph.1P615.

14.

Kandula

Dave

De Chavez

et al . Translating a heart disease lifestyle intervention into the community: the South Asian Heart Lifestyle Intervention (SAHELI) study; a randomized control trial. BMC Public Health. 2015;15:1064. doi:10.1186/s12889-015-2401-2.

15.

Look AHEAD Research Group; Wing

Bolin

et al . Cardiovascular effects of intensive lifestyle intervention in type 2 diabetes. N Engl J Med. 2013:11;369:145-154. doi:10.1056/NEJMoa1212914.

16.

Altowaijri

Phillips

Fitzsimmons

A systematic review of the clinical and economic effectiveness of clinical pharmacist intervention in secondary prevention of cardiovascular disease. J Manag Care Pharm. 2013;19:408-416. doi:10.18553/jmcp.2013.19.5.408.

17.

Suhadi

Linawati

Virginia

Setiawan

CH.

Early implementation of universal health coverage among the hypertension subjects in Sleman District of Yogyakarta. Acta Med Indones. 2015;47:311-319.

18.

Ogedegbe

Barriers to optimal hypertension control. J Clin Hypertens (Greenwich). 2008;10:644-646. doi:10.1111/j.1751-7176.2008.08329.x.

19.

American College of Cardiology. ASCVD Risk Estimator Plus: estimate risk. http://tools.acc.org/ASCVD-Risk-estimator/. Accessed March 10, 2017.

20.

Baumann

Tchicaya

Lorentz

Le Bihan

Life satisfaction and longitudinal changes in physical activity, diabetes and obesity among patients with cardiovascular diseases. BMC Public Health. 2017;17:925. doi:10.1186/s12889-017-4925-0.

21.

Carvalho

MAN

Silva

IBS

Ramos

SBP

Coelho

Gonçalves

Neto

FJA

. Quality of life of hypertensive patients and comparison of two instruments of HRQOL measure [in Portuguese]. Arq Bras Cardiol. 2012;98:442-451. doi:10.1590/S0066-782X2012005000032.

22.

Lins

Carvalho

FM.

SF-36 total score as a single measure of health-related quality of life: scoping review. SAGE Open Med. 2016;4:2050312116671725. doi:10.1177/2050312116671725.

23.

Boesten

JEJ

Kaper

Stoffers

HEJH

Kroon

van Schayck

. Rimonabant improves obesity but not the overall cardiovascular risk and quality of life; results from CARDIO-REDUSE (CArdiometabolic Risk reDuctIOn by Rimonabant: the Effectiveness in Daily practice and its USE). Fam Pract. 2012;29:521-527. doi:10.1093/fampra/cms013.

24.

Latas

Stojkovic

Ralic

Jovanović

Spirić

Milovanović

Medical students’ health related quality of life—a comparative study. Vojnosanit Pregl. 2014;71:751-756. doi:10.2298/VSP1408751L.

25.

RAND Corporation. 36-Item short form survey instrument (SF-36). https://www.rand.org/content/dam/rand/www/external/health/surveys_tools/mos/mos_core_36item_survey.pdf. Accessed July 14, 2017.

26.

WHO Expert Consultation. Appropriate body-mass index for Asian populations and its implications for policy and intervention strategies. Lancet. 2004;363:157-163.doi:10.1016/S0140-6736(03)15268-3.

27.

Badan Penelitian Dan Pengembangan Kesehatan, Kementerian Kesehatan RI. Riset kesehatan dasar Riskesdas 2013 (National Basic Health Research Report). http://www.depkes.go.id/resources/download/general/Hasil%20Riskesdas%202013.pdf. Published December 1, 2013. Accessed July 13, 2016.

28.

Benda

NMM

Seeger

JPH

Stevens

GGCF

et al . Effects of high-intensity interval training versus continuous training on physical fitness, cardiovascular function and quality of life in heart failure patients. PLoS One. 2015;10:e0141256. doi:10.1371/journal.pone.0141256.

29.

Guidon

McGee

One-year effect of a supervised exercise programme on functional capacity and quality of life in peripheral arterial disease. Disabil Rehabil. 2013;35:397-404. doi:10.3109/09638288.2012.694963.

30.

Osbak

Mourier

Henriksen

Kofoed

Jensen

GB.

Effect of physical exercise training on muscle strength and body composition, and their association with functional capacity and quality of life in patients with atrial fibrillation: a randomized controlled trial. J Rehabil Med. 2012;44:975-979. doi:10.2340/16501977-1039.

31.

Houle

SKD

Chuck

McAlister

Tsuyuki

. Effect of a pharmacist-managed hypertension program on health system costs: an evaluation of the Study of Cardiovascular Risk Intervention by Pharmacists-Hypertension (SCRIP-HTN). Pharmacotherapy. 2012;32:527-537. doi:10.1002/j.1875-9114.2012.01097.x.

Supplementary Material

Please find the following supplemental material available below.

For Open Access articles published under a Creative Commons License, all supplemental material carries the same license as the article it is associated with.

For non-Open Access articles published, all supplemental material carries a non-exclusive license, and permission requests for re-use of supplemental material or any part of supplemental material shall be sent directly to the copyright owner as specified in the copyright notice associated with the article.

0.00 MB

0.39 MB