Skip to main content
Tanaffos logoLink to Tanaffos
. 2024 Apr;23(4):376–391.

Predictors of Quality of Life in Patients with Asthma in Ahvaz, Iran

Ahmad Tahmasebi Ghorrabi 1,2, Hanieh Raji 3, Amin Torabipour 4,5,✉, Seydeh Maryam Mousavi 2, Zahara Oraman 2, Parisa Badiei Nasab 2, Mohammad Hosein Haghighizadeh 6
PMCID: PMC12464841  PMID: 41018940

Abstract

Background:

Asthma impacts the quality of life (QOL) of patients and their families. The magnitude of this morbidity is influenced by several factors, including age, disease duration, and others. This study was conducted to determine the predictors of quality of life in patients with asthma in Ahvaz, Iran.

Materials and Methods:

This cross-sectional study was conducted among patients referred to the pulmonary clinics of Imam Khomeini and Golestan hospitals in Ahvaz in 2022. The quality of life was assessed using the SF-36v2 questionnaire. The effect of socio-demographic characteristics on quality-of-life scores was examined by t-test, one-way variance (ANOVA), Pearson’s correlation coefficient, and regression models.

Results:

From a total of 204 studied asthmatic patients, the average age of patients was 43.22±15.17 years. The average QOL in patients was 57.69±22.97. Physical role and social functioning had the lowest and highest mean scores among SF-36 dimensions, respectively. A significant difference was observed between the average QOL score and the variables of age, gender, education level, employment status, illness costs, illness severity, daily exercise, and number of visits (P<0.05). Most clinical, socio-demographic, and economic variables were predictors of SF-36, PCS, MCS, and QOL dimensions (P<0.05).

Conclusion:

This study showed that the quality of life in asthmatic patients is affected by the severity of the disease, number of visits, age, sex, and education. By performing appropriate interventions on social and economic factors, the quality of life of asthmatic patients can be improved.

Keywords: Risk factors, Quality of life, Asthma

INTRODUCTION

Chronic respiratory diseases affect more than one billion people worldwide, including three hundred million people with asthma (1). Asthma is one of the most common chronic diseases in Iran and the world, the most important reason for referring to the emergency department, and the cause of significant disability, complications, and scattered deaths at all ages (2, 3). Global Burden of Disease studies have estimated that approximately 339 million people worldwide have asthma, and this number is expected to reach 400 million by 2025. Also, this disease causes the death of more than 1000 people per day (4, 5). The prevalence of asthma in women, men, and in general around the world is 10.28%, 9.32%, and 9.79%, respectively. Also, the prevalence of asthma in Iran is between 7.7 and 9.3%, and in the Eastern Mediterranean region, between 5 and 10% (6, 7). The prevalence of asthma in the west of Iran, which includes Khuzestan, is also 4% (7). Also, the prevalence of asthma in Ahvaz city was between 10 and 12.5% (8).

The goal of health care for patients with chronic diseases is not only to reduce mortality but also to improve the quality of life (5). Asthma is a disease that can lead to different degrees of limitations in the physical, emotional, and social areas of the patient’s life (2). This disease has an increasing burden in terms of complications, health care costs, and health-related quality of life (9), which harms the quality of life (10, 11). Quality of life is defined as a person’s perspective of their position within the culture and value system in which they live, as well as their goals, expectations, standards, and concerns. For a complete picture of the patient’s health status, conventional clinical indicators and health-related quality of life (HRQoL) should be evaluated (12). Health-related quality of life is defined as the functional effect of a disease and subsequent treatment as perceived by the patient. Health-related quality of life is considered a key indicator in guiding health policies (13). Also, measuring the quality of life is used for clinical decision-making and evaluating the effects of chronic diseases and various treatments (13, 14).

Asthma is affected by several factors that can aggravate or improve the condition and thus improve the patient’s quality of life (5). Identifying predictive factors related to the quality of life of patients with asthma is essential for understanding the disease and its treatment it should provide meaningful information about the impact of the disease and its treatment on the perceived health of patients (9). Factors such as gender, age, body mass index (BMI), education level, place of residence, and socio-demographic parameters are related to the quality of life in patients with asthma (3, 9). Also, demographic characteristics (older age, female gender, low education level, and unemployment), clinical conditions (severity, hospitalization, and high safety level indicators), poor control and management, and co-morbidities are factors related to low quality of life in patients with asthma. (15–17). Lázár et al.’s study showed that gender, comorbidities, disease symptoms, and smoking are relevant factors affecting the quality of life (18). Also, Shi et al.’s study showed that gender and income are related factors and predictors of quality of life in patients with asthma (19).

Measuring and identifying factors related to and predicting health-related quality of life is based on the recognition that health care should not only focus on patient survival but should also focus on quality of life. Also, this information can help guide clinical management, develop clinical guidelines, and allocate resources fairly (20).

Khuzestan province has been exposed to various pollutants for many years, the most important sources of which are fine, industrial, and non-industrial pollutants. The pollution level in Ahvaz (the capital of Khuzestan province) is getting more and more severe every day (8). According to a report by the World Health Organization in 2013, Ahvaz City was the most polluted city in the world in terms of the annual average of suspended particles less than 10 micrometers (372 micrograms per cubic meter) (21). Therefore, conducting a detailed study on the quality of life of asthma patients in Ahvaz seemed necessary. Therefore, this study was conducted to determine the related and predictive factors of health-related quality of life in asthma patients in Ahvaz City.

MATERIALS AND METHODS

Study setting and samples

This cross-sectional study was conducted over six months, from May 2022 to November 2022. The time of conducting the study was the conditions of the COVID-19 pandemic in the world. This study was conducted in the clinics of Imam Khomeini and Golestan general and teaching hospitals (a referral medical center for respiratory patients) in Ahvaz. Ahvaz, the capital of Khuzestan province, with an area of 185 square kilometers, is located at the geographical coordinates of 31.20 degrees north and 48.40 degrees east. With a population of over 1,300,000 people, Ahvaz is the seventh most populated city in Iran (22, 23).

At first, according to the size of the research population, the sample size was calculated as 195 people using Cochran’s formula. Three hundred fifty people were asked to enter the study. Then, eligible patients who met the inclusion criteria were identified and included in the study with the diagnosis of the study team doctor. The criteria for entering the study were having asthma for at least one year, being under active follow-up, and willingness to participate in the study. Also, the exclusion criteria of pregnant women (due to different effects of pregnancy on asthma), suffering from other respiratory diseases (pneumonia, COPD) and unstable heart failure (due to co-founding effects), missing or incomplete data, the existence of psychiatric problems or cognitive disorder, those who were unable to understand or complete the questionnaire and unwillingness to participate in the study. Finally, 204 patients were included in the study based on the inclusion and exclusion criteria.

Procedure

The data were collected by trained interviewers who visited the clinics of the specified hospitals daily, utilizing the available sampling methods. After receiving the necessary permits and going to the predetermined sampling centers, the patients who met the inclusion criteria were selected. Then, the interviewers collected data by introducing themselves and stating the study’s objectives. Patients who did not read and write were informed with the help of the patient’s companion or their parents. The data was collected during the COVID-19 pandemic. Due to the limitations of the COVID-19 pandemic and the special conditions of the population under study, compliance with prevention protocols was put on the agenda. A two-part questionnaire including demographic characteristics and SF-36 v2 was used to collect data. The demographic characteristics section of the questionnaire includes questions about social and economic characteristics [age, sex, education level, residential status, size of household, type of insurance, employment status, personal income (Riyals), and cost of illness (Riyals)], and clinical characteristics. The severity of the disease, the number of times the drug was taken (per day), smoking, family history, the number of visits (per month), underlying disease, the duration of daily exercise (in minutes), and the duration of the disease (in years) of the patients were evaluated. SF-36 v2 questionnaire was also used for patients’ quality of life. SF-36 v2 questionnaire was used in various studies aimed at evaluating the quality of life of asthma patients (1, 3, 24).

SF-36 questionnaire v2

SF-36 v2 questionnaire includes 36 items and eight dimensions of physical performance (10 items) (PF), physical role (4 items) (RP), body pain (2 items) (BP), general health (5 items) (GH) vitality (4 items) (VT), social functioning (2 items) (SF), emotional role (3 items) (RE) and mental health (5 items) (MH) evaluate health-related quality of life. In addition, the SF-36 includes a question about the change in general health status compared to the previous year. Each concept can be scored from 0 to 100, where a higher score subjectively indicates a better quality of life. The questions of this questionnaire are on a Likert scale, where the number of answer options varies from two to six points depending on the item. For example, items 3 and 6 measuring physical functioning ranged from 1 (Yes, I am constrained) to 3 (Not limited at all). Items measuring physical role, such as 13 and 14, show dichotomous responses (1 yes and 2 no). Items measuring physical pain, such as the 22, show scores ranging from 1 (none) to 5 (extreme). Finally, items like 28 and 29, which measure mental health and quality of life, are scored from 1 (always) to 6 (never), respectively. Items are reverse-coded to have the same meaning. This questionnaire provides a complete assessment of overall quality of life (OQOL), physical component summary (PCS), and mental component summary (MCS). PF, RP, BP, and GH subscales form the physical component summary (PCS), and VT, SF, RE, and MH subscales form the mental component summary (MCS). Also, the sum of the physical component summary (PCS) and mental component summary (MCS) constitute the overall quality of life (OQOL) (1, 3, 24–28). The validity and reliability of the questionnaire were confirmed previously (27, 29). Cronbach’s alpha for the eight subscales of this questionnaire in An et al.’s study was between 0.73 and 0.90 (27). Oliveira et al.’s study also calculated Cronbach’s alpha for the eight subscales of this questionnaire between 0.7 and 0.9 (1). Also, in Chow et al.’s study, the Cronbach’s alpha of this questionnaire was 0.88 (29). In Iran, the use and scientific validity of this questionnaire have been tested in several studies, and its reliability has been reported as 0.82 according to Cronbach’s alpha (30).

Statistical analysis

In this study, statistical analysis was done using SPSS Ver 22 software. Mean and standard deviation were used for descriptive data. Also, t-test, one-way variance (ANOVA), and Pearson’s correlation coefficient were used to compare SF-36 scores with each other and their dimensions with socio-demographic, economic, and clinical variables. To identify variables predicting the quality of life of the studied patients, linear multivariate regression analysis was used in a step-by-step method. Regression coefficients were determined using the least squares method. Separate models were examined for SF-36, PCS, MCS, and OQOL dimensions.

Ethics approval

This study was approved by the Medical Ethics Committee of Ahvaz Jundishapur University of Medical Sciences with code IR.AJUMS.REC.1397.034. The confidentiality of patients’ information, obtaining patients’ consent, and receiving written consent from patients were observed. Patients consented to the clinical data and health outcomes they reported being used for research purposes.

RESULTS

The average age of patients was 43.22±15.17 years. The age of the patients was at least five, and at most 79 years. The highest treatment costs for patients had a median of 137.14 dollars, with 39.2% falling between 100 and 199 dollars. The highest individual income among patients was $400 or more, with a median of $342.86 and an interquartile range of 0, which represents 81.4% of the participants. The average number of family members of the patients was 5.01 people. Female patients (55.4%), diploma (36.8%), living in the city (83.3%), having social security insurance (59.8%), not having supplementary insurance (53.3%), and working (50.5%) were the most frequent patients (Table 1). Most patients had moderate disease severity (36.8%). However, patients with high disease severity (33.3%) also had a significant percentage, and the distribution of patients according to disease severity was close to each other. The findings in the clinical characteristics section showed that there was no family history (55.4%), no smoking (84.8%), and the presence of underlying disease (69.1%) in the majority of patients. The average number of drug intakes per day, the number of visits per month (Min=1, Max=10), the duration of exercise in minutes (Min=0, Max=120), and the duration of illness in years (Min=1, Max=60) were 1.76±2.37, 1.15±1.54, 24.86±12.95 and 7.83±7.20, respectively. 40.7% of patients took medicine twice a day, and 70.1% were visited by a doctor once a month. The findings showed that 64.7% of patients did not exercise at all. Also, the disease duration was 72.1% of patients under ten years (Table 2).

Table 1.

Socio-demographic and economic characteristics of patients with asthma in Ahvaz, Iran (N=204)

Variables Frequency Percentage
Age (year) <18 11 5.4
18–39 72 35.3
40–59 91 44.6
≥60 30 14.7
Gender Female 113 55.4
Male 91 44.6
Level of Education Illiterate 34 16.7
Elementary 38 18.6
Diploma 75 36.8
University degree 57 27.9
Residence Rural 34 16.7
Urban 170 83.3
Family size <3 37 18.1
3–5 103 50.5
>5 64 31.4
Type of Insurance Social Security 122 59.8
Healthcare Service 22 10.8
Armed Forces 10 4.9
Health of Iranians 26 12.7
Other 24 11.8
Employment Status Unemployed 101 49.5
Employed 103 50.5
Personal income (dollars) <400 166 81.4
≥400 38 18.6
<100 70 34.3
Cost of illness (dollars) 100–199 80 39.2
≥200 54 26.5

Table 2.

Clinical characteristics of asthma patients in Ahvaz, Iran (N=204)

Variables Frequency Percentage
Illness Severity Mild 61 29.9
Medium 75 36.8
Severe 68 33.3
No. of Times to Take Medicine (per day) 1 59 28.9
2 83 40.7
3≥ 62 30.4
Smoking No 173 84.8
I quit 17 8.3
Yes 14 6.9
Family History Yes 91 44.6
No 113 55.4
Number of Visits (per month) 1 143 70.1
2 37 18.1
3≥ 24 11.8
Underlying Disease Yes 141 69.1
No 63 30.9
Nothing 132 64.7
Daily Exercise Duration (in minutes) <20 34 16.7
20–60 31 15.2
60≥ 7 3.4
Duration of Illness (in years) <10 147 72.1
≥10 57 27.9

The findings showed that the average OQOL of the study participants was 22.97 ± 57.69. Also, the mean of PCS and MCS were 25.27±54.43 and 24.53±60.95, respectively. Among the dimensions of quality of life, they had the lowest and highest mean (44.18±45.10) RP and (31.01±70.23) SF, respectively. All dimensions of quality of life had a significant relationship and direct correlation with total quality of life (Table 3).

Table 3.

Quality of life questionnaire dimensions score (SF-36) and its relationship with total quality of life (OQOL) in patients with asthma in Ahvaz, Iran (N=204).

Dimensions of Quality of Life Mean (SD) Min Max P value Pearson correlation coefficient
Physical Functioning PF 61.60(28.50) 0 100 0.001 0.74**
Role Physical RP 45.10(44.18) 0 100 0.001 0.76**
Bodily Pain BP 63.73(31.63) 0 100 0.001 0.74**
General Health GH 47.30(22.00) 0 100 0.001 0.68**
Role Emotional RE 57.68(46.21) 0 100 0.001 0.76**
Vitality VT 56.13(23.62) 0 100 0.001 0.76**
Mental Health MH 59.77(22.88) 0 100 0.001 0.67**
Social Functioning SF 70.23(31.01) 0 100 0.001 0.70**
Physical Component Summary PCS 54.43(25.27) 3.75 100 0.001 0.92**
Mental Component Summary MCS 60.95(24.53) 0 99 0.001 0.92**
Overall Quality of Life OQOL 57.69(22.97) 2.5 98.89 - -

The relationship between SF-36 scores and socio-demographic and economic characteristics in Table 4 showed that with increasing age, the score of PF, GH, MH, PCS, and MCS decreased (p=0.001). The difference in scores of PF, RP, BP, VT, MH, SF (p=0.05), PCS, and MCS was greater in men than in women (p=0.001). Increasing the level of education in patients had a positive effect on PF, VT, MH, and MCS scores (p=0.001). VT score (p=0.02) was higher in people living in the city than in rural people. No significant difference was found between the dimensions of the household and the type of insurance with the scores of the SF-36 dimensions (P>0.05). Employed people had significantly better scores in BP (p=0.02), VT (p=0.04), MH (p=0.001, and MCS (p=0.02) than unemployed people. Scores of high-income patients compared to low-income patients in BP (p=0.02) and MH (p=0.001) had a significant difference. With increasing patient treatment costs, the scores of PF (p=0.00), RP (p=0.01), BP (p=0.001), GH (p=0.01), PCS (p=0.001), and MCS (p=0.001) decreased significantly (Table 4). Also, the relationship between SF-36 scores and clinical characteristics of patients in Table 5 showed that there was a significant difference between the scores of all eight dimensions of quality of life, PCS, and MCS with the severity of the disease (p=0.001). So, the scores decreased with the increase in the severity of the disease. With the increase in the number of drug doses, scores of PF (p=0.02), BP (p=0.02), GH (p=0.001), SF (p=0.05), and PCS (p=0.001) decreased significantly. No significant difference was found between smoking in patients with SF-36 dimension scores (p>0.05). BP score (p=0.02) was significantly higher in people without a family history (Table 5). With the increase in the number of patient visits per month, the scores of PF (p=0.001), BP (p=0.04), VT (p=0.001), SF (p=0.01), PCS (p =0.02), and MCS (p=0.001) decrease significantly. With increasing the duration of daily exercise of the patients, the scores of PF (p=0.001), GH (p=0.01), VT (p=0.04), and PCS (p=0.001) increase significantly. There was a significant difference between the duration of the patient’s illness and the scores of GH (p=0.01) and PCS (p=0.001) (Table 5).

Table 4.

Quality of life dimension score (SF-36) based on socio-demographic and economic characteristics in patients with asthma (N=204)

Variables PF RP BP GH PCS

Mean (SD) P Mean (SD) P Mean (SD) P Mean (SD) P Mean (SD) P
Age <18 89.09(20.71) 0.001 77.27(36.15) 0.08 77.95(28.06) 0.32 64.54(24.23) 0.01 77.22(24.90) 0.001
18–39 66.53(22.99) 43.40(44.80) 64.48(33.03) 47.36(21.80) 55.44(24.43)
40–59 61.48(28.13) 44.78(44.02) 63.52(30.92) 47.75(20.71) 54.38(24.16)
≥60 40.00(30.96) 38.33(42.92) 57.33(31.17) 39.50(22.68) 43.79(25.80)
Gender Female 54.74( 30.04) 0.001 38.05(42.92) 0.01 55.44(31.37) 0.001 44.82(22.51) 0.07 48.26(25.70) 0.001
Man 70.11( 24.02) 53.85(44.40) 74.01(28.95) 50.38(21.06) 62.09(22.61)
Level of Education Illiterate 42.79(31.31) 0.001 41.91(42.95) 0.3 57.50(33.13) 0.12 44.26(22.73) 0.43 46.62(26.89) 0.06
Elementary 66.97(25.18) 46.05(48.11) 65.53(35.51) 43.95(22.84) 55.62(28.49)
Diploma 62.00(27.75) 39.33(42.74) 60.60(30.15) 47.93(22.21) 52.47(23.23)
University degree 68.69(25.38) 53.95(43.76) 70.35(29.34) 50.53(20.71) 60.88(23.51)
Residence Rural 56.18(32.38) 0.23 42.65(43.31) 0.72 64.34(35.73) 0.90 44.85(22.44) 0.48 52.00(28.12) 0.54
Urban 62.68(27.64) 45.59(44.46) 63.60(30.85) 47.79(21.94) 54.92(24.72)
Family size <3 53.51(28.98) 0.13 38.51(44.3) 0.50 55.54(33.39) 0.07 40.00(21.85) 0.08 46.90(25.43) 0.08
3–5 62.28(28.07) 44.90(43.77) 62.72(32.40) 48.59(23.34) 54.62(25.76)
>5 65.16(28.45) 49.22(44.97) 70.08(28.36) 49.45(19.13) 58.48(23.72)
Type of Insurance Social Security 63.00(28.06) 0.91 46.93(43.66) 0.5 66.19(31.76) 0.34 47.70(21.96) 0.5 55.95(25.25) 0.51
Healthcare Service 61.60(27.22) 47.73(42.89) 62.04(26.59) 50.23(21.35) 55.40(18.35)
Armed Forces 56.00(31.78) 30.00(43.77) 44.75(32.07) 36.50(22.97) 41.81(27.45)
Health of Iranians 59.42(27.83) 34.62(45.32) 63.17(34.51) 49.42(19.45) 51.66(25.37)
Other 59.17(32.82) 51.04(47.47) 61.25(31.32) 44.79(25.08) 54.06(29.77)
Employment Status Unemployed 58.12(30.73) 0.08 42.57(44.93) 0.42 58.74(32.80) 0.02 45.74(23.17) 0.32 51.29(27.20) 0.08
Employed 65.00(25.83) 47.57(43.51) 68.62(29.78) 48.83(20.78) 57.50(22.93)
Personal Income <400 60.28(29.17) 0.18 42.53(43.44) 0.09 61.00(32.23) 0.01 47.65(22.17) 0.65 52.87(25.72) 0.07
≥400 67.00(25.16) 55.63(46.16) 74.94(26.51) 45.87(21.50) 60.86(22.47)
Cost of Illness <100 71.57(24.69) 0.001 55.22(44.06) 0.04 75.70(26.37) 0.001 55.52(19.63) 0.001 64.50(23.27) 0.001
100–199 58.82(27.34) 43.44(43.34) 58.34(30.96) 44.81(19.60) 51.35(22.49)
≥200 53.77(31.28) 35.53(43.80) 57.19(34.60) 41.14(25.08) 46.91(27.74)
Variables RE VT MH SF MCS
Mean (SD) P Mean (SD) P Mean (SD) P Mean (SD) P Mean (SD) P
Age <18 90.91(30.15) 0.45 85.00(17.03) 0.16 84.36(11.38) 0.001 79.77(29.48) 0.30 85.01(15.07) 0.001
18–39 61.11(44.76) 57.08(21.26) 58.44(23.29) 70.83(31.82) 61.87(24.04)
40–59 53.48(47.11) 54.72(23.37) 58.90(21.67) 71.57(30.17) 59.67(23.86)
≥60 50.00(47.75) 47.50(24.56) 56.57(24.27) 61.25(31.72) 53.83(25.94)
Gender Female 52.51(46.89) 0.07 49.91(24.07) 0.001 55.80(23.16) 0.001 66.48(32.18) 0.05 56.17(24.82) 0.001
Man 64.10(44.79) 63.84(20.71) 64.70(21.66) 74.89(28.99) 66.89(22.94)
Level of Education Illiterate 44.12(46.94) 0.13 46.18 (24.00) 0.04 52.24(20.79) 0.04 64.71(29.75) 0.37 51.81(22.01) 0.03
Elementary 54.39(49.27) 55.00 (25.97) 56.11(25.67) 67.17(36.66) 58.17(27.82)
Diploma 58.22(46.20) 58.87 (22.88) 60.71(24.45) 70.17(32.28) 62.00(25.46)
University degree 67.25(42.48) 59.21 (21.58) 65.47(18.43) 75.66(25.37) 66.90(20.83)
Residence Rural 50.98(48.01) 0.36 47.79(25.64) 0.02 54.47(24.71) 0.14 65.44(33.85) 0.32 54.67(27.90) 0.10
Urban 59.02(45.87) 57.79(22.91) 60.83(22.42) 71.19(30.42) 62.21(23.69)
Family size <3 53.15(47.44) 0.34 53.24(23.63) 0.71 57.30(25.29) 0.77 69.59(31.53) 0.63 58.32(25.61) 0.54
3–5 55.01(45.90) 56.94(24.51) 60.50(23.97) 68.59(32.63) 60.26(25.49)
>5 64.58(45.95) 56.48(22.35) 60.01(19.67) 73.24(28.16) 63.58(22.36)
Type of Insurance Social Security 54.92(47.12) 0.4 57.25(23.75) 0.25 60.95(22.42) 0.08 71.52(31.21) 0.84 61.16(24.88) 0.3
Healthcare Service 75.76(37.34) 60.68(21.39) 68.00(21.05) 73.30(29.45) 69.43(22.80)
Armed Forces 56.67(49.81) 49.00(27.76) 53.60(28.97) 66.25(29.49) 56.38(24.71)
Health of Iranians 53.85(45.29) 47.88(20.84) 50.46(20.95) 64.90(30.82) 54.27(22.98)
Other 59.72(48.13) 58.12(25.22) 58.87(24.03) 68.33(33.72) 61.26(25.24)
Employment Status Unemployed 51.82(48.64) 0.07 52.77(25.68) 0.04 54.98(24.13) 0.001 67.97(31.87) 0.3 56.88(25.63) 0.02
Employed 63.43(43.16) 59.42(21.01) 64.46(20.64) 72.45(30.13) 64.94(22.82)
Personal income <400 57.11(46.37) 0.72 55.27(24.15) 0.3 58.20(23.20) 0.04 68.61(31.82) 0.13 59.80(24.97) 0.17
≥400 60.00(46.03) 59.63(21.22) 66.20(20.55) 76.87(26.78) 65.67(22.28)
Cost of illness <100 66.17(43.22) 0.15 61.27(22.16) 0.08 63.52(19.02) 0.14 75.60(25.38) 0.17 66.64(20.85) 0.04
100–199 55.83(46.77) 54.62(23.02) 59.71(22.21) 69.22(31.19) 59.85(23.58)
≥200 50.29(48.02) 52.19(25.40) 55.44(27.21) 65.35(35.98) 55.82(28.57)

Table 5.

Quality of life dimension score (SF-36) based on clinical characteristics in patients with asthma (N=204)

Variables PF RP BP GH PCS

Mean (SD) P Mean (SD) P Mean (SD) P Mean (SD) P Mean (SD) P
Illness Severity Mild 77.95(25.40) 0.001 68.03(41.36) 0.001 75.45(25.43) 0.001 60.49(18.34) 0.001 70.48(21.54) 0.001
Medium 65.34(23.73) 50.00(41.71) 72.50(29.27) 49.80(18.62) 59.41(21.29)
Severe 42.79(25.36) 19.12(35.64) 43.53(29.67) 32.72(20.02) 34.54(18.81)
Number of Times to Take Medicine (per day) 1 65.68(26.33) 0.02 52.54(46.35) 0.06 70.12(31.22) 0.02 52.88(20.55) 0.001 60.31(24.13) 0.001
2 65.06(28.18) 47.89(44.03) 66.02(31.48) 48.67(22.53) 56.91(25.33)
3≤ 53.06(29.49) 34.27(40.79) 54.55(30.62) 40.16(21.01) 45.51(24.21)
Smoking No 62.81(28.52) 0.35 47.54(44.43) 0.15 63.66(30.35) 0.09 47.54(21.97) 0.66 55.39(25.10) 0.44
I quit 55.88(30.06) 35.29(44.24) 61.91(39.37) 42.94(27.38) 49.00(28.65)
Yes 53.57(25.97) 26.79(37.29) 66.79(38.85) 49.64(14.73) 49.20(23.35)
Family History Yes 59.51(29.87) 0.35 48.08(44.91) 0.39 58.82(33.29) 0.04 47.53(23.73) 0.89 53.48(26.88) 0.63
No 63.28(27.37) 42.70(43.64) 67.68(29.79) 47.12(20.60) 55.19(23.99)
Number of Visits (per month) 1 64.89(26.49) 0.001 48.43(44.32) 0.07 67.15(30.95) 0.04 48.08(21.08) 0.72 57.14(24.79) 0.02
2 59.18(32.47) 44.59(45.69) 58.31(31.70) 44.86(23.81) 51.74(27.70)
3≤ 45.62(29.01) 26.04(37.21) 51.67(32.71) 46.46(24.99) 42.45(20.75)
Underlying Disease Yes 64.08(27.21) 0.06 46.28(44.41) 0.57 64.80(30.67) 0.47 49.11(22.49) 0.08 56.07(25.20) 0.17
No 56.03(30.69) 42.46(43.91) 61.31(33.81) 43.25(20.46) 50.76(25.23)
Daily Exercise Duration (in minutes) Nothing 57.53(28.72) 0.001 42.61(44.52) 0.22 61.65(30.95) 0.07 45.16(22.20) 0.03 51.74(24.72) 0.01
<20 64.27(27.47) 40.44(43.08) 60.15(36.13) 47.35(23.03) 53.05(26.58)
20–60 69.03(25.27) 55.64(43.16) 70.88(29.393) 51.61(16.40) 61.79(23.38)
60≤ 92.14(18.67) 67.86(42.60) 88.58(16.57) 68.57(24.95) 79.28(21.58)
Duration of Illness (in years) <10 63.64(26.68) 0.1 46.94(43.88) 0.34 66.02(32.14) 0.09 50.24(21.17) 0.001 56.71(24.33) 0.04
≥10 56.32(32.39) 40.35(45.00) 57.80(29.72) 39.74(22.48) 48.55(26.87)
Variables RE VT MH SF MCS
Mean (SD) P Mean (SD) P Mean (SD) P Mean (SD) P Mean (SD) P
Illness Severity Mild 74.32(40.54) 0.001 68.20(22.45) 0.001 69.90(19.05) 0.001 81.80(22.37) 0.001 73.55(20.55) 0.001
Medium 64.44(43.61) 56.53(20.26) 60.05(22.23) 72.00(30.05) 63.26(22.23)
Severe 35.29(45.66) 44.85(22.88) 50.37(23.07) 57.90(34.48) 47.10(23.52)
Number of Times to Take Medicine (per day) 1 59.88(45.81) 0.88 55.76(24.27) 0.59 59.45(22.38) 0.61 72.25(30.00) 0.05 61.84(24.41) 0.78
2 55.82(46.00) 58.01(22.85) 58.27(23.95) 74.73(29.77) 61.71(24.01)
3≤ 58.06(47.50) 53.95(24.17) 62.06(22.04) 62.30(32.52) 59.09(25.60)
Smoking No 58.38(46.19) 0.45 57.43(23.61) 0.16 61.25(22.04) 0.09 70.90(30.70) 0.24 61.99(23.98) 0.26
I quit 45.09(48.50) 50.88(23.66) 52.47(28.10) 58.82(34.73) 51.82(31.23)
Yes 64.29(44.26) 46.43(22.13) 50.29(24.03) 75.89(29.19) 59.22(21.42)
Family History Yes 60.81(45.43) 0.39 56.04(25.45) 0.96 60.71(24.42) 0.59 66.20(33.25) 0.09 60.94(27.04) 0.99
No 55.16(46.88) 56.19(22.15) 59.00(21.65) 73.47(28.82) 60.96(22.43)
Number of Visits (per month) 1 62.00(45.20) 0.07 59.37(20.59) 0.001 62.16(21.41) 0.07 73.27(29.07) 0.01 64.20(22.33) 0.001
2 52.25(48.77) 51.62(28.31) 55.13(24.35) 69.93(32.73) 57.23(27.53)
3≤ 40.28(45.02) 43.75(28.17) 52.67(27.19) 52.60(34.77) 47.32(27.61)
Underlying Disease Yes 60.28(46.10) 0.23 58.09(23.69) 0.08 61.30(23.30) 0.18 73.78(29.80) 0.01 63.34(24.45) 0.04
No 51.85(46.28) 51.74(23.05) 56.52(21.73) 62.30(32.41) 55.60(24.04)
Daily Exercise Duration (in minutes) Nothing 57.07(46.51) 0.44 53.37(23.90) 0.001 57.77(23.29) 0.06 69.60(31.16) 0.63 59.45(24.63) 0.09
<20 54.90(46.33) 54.71(22.72) 59.76(25.04) 66.54(33.67) 58.98(26.06)
20–60 56.99(46.50) 63.23(19.68) 63.74(16.49) 75.40(27.85) 64.84(20.61)
60≤ 85.71(37.80) 83.57(17.49) 80.00(20.26) 77.14(30.63) 81.61(24.62)
Duration of Illness (in years) <10 59.64(45.53) 0.33 57.52(22.38) 0.18 60.24(22.85) 0.63 71.79(30.71) 0.25 62.30(24.07) 0.21
≥10 52.63(47.95) 52.54(26.42) 58.54(23.13) 66.23(31.69) 57.49(25.55)

The relationship between OQOL and socio-demographic and economic variables showed that as the age of patients increases, OQOL decreases significantly (p=0.001). So, patients under 18 years old and over 60 years old had the highest and lowest quality of life, respectively. There was a significant difference between the gender (p=0.001) and the employment status (p=0.03) of the patients with the OQOL score. So, OQOL is more prevalent in male and working patients. As the level of education in patients increases, OQOL increases significantly (p=0.03). The treatment costs of patients harmed OQOL (p=0.001), and with the increase in treatment costs, OQOL decreased significantly. No significant difference was found between the variables of residence status, size of household, type of insurance, and individual income of patients with OQOL (P>0.05) (Table 6).

Table 6.

Total quality of life score (OQOL) based on socio-demographic and economic variables in patients with asthma in Ahvaz, Iran (N=204)

Variables Classification Mean SD Confidence interval (95 percent) T or F P value

High Low
Age <18 81.11 19.31 94.09 68.13 5.75 0.001
18–39 58.66 21.39 63.68 53.62
40–59 57.03 22.18 61.64 52.40
≥60 48.81 25.00 58.14 39.47
Gender Female 52.22 23.39 −6.10 −18.43 −3.92 0.001
Man 64.49 20.62
Level of Education Illiterate 49.21 22.80 57.17 41.25 3.04 0.03
Elementary 56.90 26.74 65.68 48.10
Diploma 57.23 21.78 62.24 52.21
University degree 63.89 20.58 69.34 58.42
Residence Rural 53.33 26.33 3.27 −13.72 −1.21 0.23
Urban 58.56 22.22
Family Size <3 52.60 23.42 60.41 44.79 1.60 0.21
3–5 57.44 23.90 62.11 52.77
>5 61.03 20.86 66.24 55.81
Type of Insurance Social Security 58.55 23.02 62.68 54.42 0.90 0.47
Healthcare Service 62.41 18.54 70.63 54.19
Armed Forces 49.09 24.52 66.63 31.55
Health of Iranians 52.96 22.05 61.87 44.05
Other 57.66 26.62 68.90 46.42
Employment Status Unemployed 54.09 24.65 −.85 −13.41 −2.24 0.03
Employed 61.22 20.71
Personal Income <400 56.33 23.34 1.01 −14.88 −1.72 0.09
≥400 63.26 20.73
Cost of Illness <100 65.57 20.29 70.52 60.62 6.81 0.001
100–199 55.60 20.98 60.27 50.92
≥200 51.36 26.17 58.30 44.41

The relationship between OQOL and clinical variables showed that the severity of the disease (p=0.001) and the number of visits per month (p=0.001) have a negative effect on the patients’ OQOL. So, with the increase in the severity of the disease and the number of visits, the OQOL of the patients decreases significantly. The findings showed that the OQOL (p=0.02) in the patients increases significantly with the increase in the duration of the patients’ exercise per day. No significant difference was found between the variables of number of times of drug use (per day), smoking, family history, underlying disease, and duration of disease with OQOL (P>0.05) (Table 7).

Table 7.

Total quality of life score (OQOL) based on clinical variables in patients with asthma in Ahvaz, Iran (N=204)

Variables Classification Mean SD Confidence interval (95 percent) T or F P value

High Low
Illness Severity Mild 72.01 19.27 76.95 67.08 44.46 0.001
Medium 61.33 19.95 65.92 56.74
Severe 40.82 18.34 45.26 36.38
Number of Times to Take Medicine (per day) 1 61.07 22.92 67.04 55.09 2.60 0.08
2 59.31 23.03 64.34 54.28
3≤ 52.30 22.34 57.97 46.63
Smoking No 58.69 22.49 62.06 55.31 1.18 0.31
I quit 50.41 29.22 65.44 35.38
Yes 54.20 20.08 65.81 42.61
Family History Yes 57.21 24.72 5.53 −7.26 −0.27 0.80
No 58.07 21.56
Number of Visits (per month) 1 60.67 21.29 64.19 57.15 5.52 0.001
2 54.49 26.54 63.33 45.64
3≤ 44.88 22.69 54.47 35.30
Underlying Disease Yes 59.70 22.71 13.34 −0.30 1.89 0.06
No 53.18 23.08
Daily Exercise Duration (in minutes) Nothing 55.59 22.41 59.45 51.73 3.46 0.02
<20 56.02 24.64 64.61 47.41
20–60 63.32 21.02 71.03 55.60
60≤ 80.45 21.49 100.00 60.56
Duration of Illness (in years) <10 59.50 22.02 13.51 −0.54 1.82 0.07
≥10 53.02 24.87

Finally, to identify each independently related variable and predict the quality of life of the participants, linear multivariate regression analysis was used in a step-by-step method. Table 8 shows the coefficients of the multivariate linear regression models that evaluate the association and prediction of the study variables for each dimension of SF-36, PCS, MCS, and OQOL. The results showed that the clinical variables of disease severity, number of visits per month, smoking, family history, duration of disease, number of drug intakes per day, and background patient and socio-demographic and economic variables of gender, age, cost of disease, education level and employment status are predictors of SF-36, PCS, MCS and OQOL dimensions (Table 8).

Table 8.

Predictors of health-related quality of life in patients with asthma (N=204)

Dependent variable predictor variables B Beta P Confidence interval (95 percent) R2

Low High
PF Constant 109.84 0.001 92.47 127.20 0.40
Illness severity −15.69 −0.43 0.001 −19.62 −11.75
Age −9.78 −0.27 0.001 −13.75 −5.80
gender 12.36 0.21 0.001 6.11 18.60
Number of visits per month −5.60 −0.13 0.02 −10.08 −1.09
RP Constant 80.47 0.001 58.03 102.91 0.24
Illness severity −23.20 −0.42 0.001 −29.98 −16.42
gender 18.86 0.21 0.001 7.49 30.22
Smoking −12.65 −0.16 0.01 −22.86 −2.44
BP Constant 57.63 0.001 38.80 76.46 0.26
Illness severity −16.02 −0.40 0.001 −20.78 −11.26
gender 17.11 0.27 0.001 9.50 24.73
family history 8.97 0.14 0.02 1.35 16.58
GH Constant 92.18 0.001 82.28 102.08 0.33
Illness severity −12.29 −0.44 0.001 −15.57 −9.00
duration of illness −6.95 −0.23 0.001 −10.30 −3.60
cost of illness −3.74 −0.13 0.03 −7.07 −0.40
RE Constant 78.44 0.001 55.32 101.55 0.14
Illness severity −19.42 −0.34 0.001 −26.92 −11.93
Level of Education 6.79 0.15 0.02 1.05 12.54
VT Constant 83.39 0.001 68.03 98.76 0.32
Illness severity −9.60 −0.32 0.001 −13.09 −6.11
gender 15.09 0.32 0.001 9.22 20.96
Smoking −7.84 −0.18 0.001 −13.13 −2.54
Number of visits per month −5.96 −0.17 0.001 −9.93 −1.99
Age −4.29 −0.14 0.02 −7.87 −0.72
MH Constant 81.21 0.001 69.06 93.36 0.23
Illness severity −10.02 −0.35 0.001 −13.67 −6.38
Employment status 12.40 0.27 0.001 6.65 18.16
Smoking −7.05 −0.17 0.001 −12.25 −1.85
Number of visits per month −4.89 −0.15 0.02 −9.04 −0.75
Number of times to take the medicine per day 4.09 0.14 0.03 0.32 7.86
SF Constant 92.50 0.001 74.85 110.15 0.16
Illness severity −10.79 −0.28 0.001 −15.81 −5.76
Number of visits per month −1.28 −0.17 0.02 −2.24 −0.32
gender −6.73 −0.15 0.03 −12.50 −0.96
PCS Constant 88.32 0.001 73.15 103.48 0.42
Illness severity −16.93 −0.53 0.001 −20.37 −13.50
gender 11.85 0.23 0.001 6.40 17.31
Age −4.08 −0.12 0.02 −7.55 −0.61
Number of visits per month −3.95 −0.10 0.04 −7.88 −0.03
MCS Constant 81.20 0.001 68.23 94.16 0.28
Illness severity −12.20 −0.39 0.001 −15.89 −8.50
gender 10.66 0.22 0.001 4.76 16.56
Number of visits per month −5.92 −0.16 0.001 −10.15 −1.67
The underlying patient −0.09 −0.15 0.01 −1.59 −0.18
OQOL Constant 90.00 0.001 76.00 104.00 0.40
Illness severity −14.45 −0.50 0.001 −17.62 −11.28
gender 10.41 0.22 0.001 5.38 15.45
Number of visits per month −4.94 −0.15 0.001 −8.56 −1.32
Age −4.08 −0.14 0.01 −7.29 −0.88

The determination coefficients (R2) in multiple regression models of SF-36 dimensions showed that PF (R2=0.40) and RE (R2=0.14) had the highest and lowest determination coefficients (R2), respectively. The determination coefficients for PCS, MCS, and OQOL were 0.42, 0.28, and 0.40, respectively. This means that 42% of PCS changes, 28% of MCS changes, and 40% of OQOL changes are explained by variables in specific models (Table 8). Disease severity is present as a predictor variable in all multiple regression models. So, the severity of the disease from B=−9.60 to B=−23.20 causes a decrease in SF-36, PCS, MCS, and OQOL dimensions. After the severity of the disease, gender, number of visits per month, age, and smoking are the most essential variables in predicting OQOL, SF-36 dimensions, PCS, and MCS, respectively. The variables of disease severity, sex, age, and number of visits per month together predict 42% of PCS changes, and the variables of disease severity, sex, number of visits per month, and having an underlying disease together predict 28% of MCS. According to the value of B per unit of increase in disease severity, age and number of visits per month decrease OQOL by −4.08, −14.45, and −4.94, respectively. The variables of disease severity, sex, age, and number of visits per month together predict 40% of the changes in OQOL (Table 8).

DISCUSSION

Asthma is a chronic and non-communicable disease with a high global burden, which leads to a high rate of absenteeism from work and school, as well as an increase in emergency room visits and hospitalizations (12). Quality of life (QoL) is a term that has been widely studied in asthma because it allows the impact of the disease on the patient’s life to be evaluated through the patient’s perception (31). In the last two decades, HRQoL assessment has gained a prominent role in the management (treatment and control) of asthma. Adherence to drug treatment and symptom control, as well as self-perceived physical, emotional, and social well-being, play an essential role in effective disease management (12). The purpose of this study was to determine the related and predictive factors of health-related quality of life in asthma patients in Ahvaz.

Based on the results of this study, the quality of life score of the studied participants was 57.69. Also, the scores of PCS and MCS were 54.43 ± 25.27 and 60.95 ± 24.53, respectively. Many studies have been conducted on the quality of life of patients. The study of Rabitabar et al. (32) and Abbasi et al. (33) showed different results in this regard, 56.32 ± 11.69 and 70.47 ± 9.30, respectively. Also, in the study of Kalmarzi et al. (34), the quality of life score of patients in a pilot study in the experimental and control groups was reported to be 51.50 ±19.78 and 46.25 ± 18.26, respectively. Also, different results were reported in the studies regarding the score of different aspects of the patient’s quality of life according to the factors affecting them. PCS and MCS scores in the study of Rask-Andersen et al. (35), Song et al. (36), and Patil et al. (37) were (49.1±10.7, 59±5.15), (43.2±0.3, 48.4±0.2) and (47.43 ± 15.56, 66.71±13.59), respectively. In a study in Iran, the PCS and MCS scores were reported to be 58.8±18.3 and 57.3±17, respectively. It was consistent with the results of the present study.

The results of this study showed that RP (45.10± 44.18) and SF (70.23 ± 31.01) had the lowest and highest scores among the dimensions of quality of life. In the study by Malek et al. (3), BP (73.8±22) and RE (46±31) they have had the highest and lowest scores, respectively. Also, Adams et al. (39) showed that BP (67±30.8) and PF (24 ± 25.1) had the highest and lowest scores among other aspects of patients’ quality of life. However, another study (37) showed that GH (39.11±12.79) and RE (80.86±28.17) had the lowest and highest scores, respectively. The difference in the results of studies evaluating the quality of life of patients is caused by the influence of different variables. The severity of disease, delivery of medical services, and sociocultural conditions are the key factors that affect the quality of life score. In this study and other similar studies, the minimum and maximum scores belonged to the physical and mental dimensions, respectively. Physical dimensions have a more significant impact on the quality of life due to the effects of the disease on the body and physical limitations. Therefore, by improving physical performance and taking measures to reduce the effects of disease on the body, the quality of life can be increased. Also, physical dimensions have a significant impact on psychological dimensions.

The findings showed that there was a significant difference among all the variables (except for the household size, type of insurance, and smoking), at least with the score of one of the dimensions, components, and overall quality of life. No significant difference was observed between the score of variables of the household dimension, type of insurance, and smoking with any of the dimensions and components and the total score. A study showed that there was a significant difference between PCS and MCS scores and age, and no significant difference was found with smoking, which is consistent with the results of the present study (35). Another study showed that no significant difference was found between the PCS and MCS scores with the residence status and education level, while there was a significant difference with age, which is consistent with the results of the present study (3). Contrary to the result of the present study, in one study, no significant difference was found between PCS and MCS scores with gender (3). A study showed that there was a significant difference between the average scores of the quality of life in all dimensions, PCS and MCS, with the severity of asthma, so that the quality of life decreased with the severity of the disease (1), which was consistent with the results of the present study. Another study showed the same as the present study, the duration of the illness, and unlike our study, marital status, education level, employment status, residence status, and income were related to the PCS score (38). Also, in the present study, gender, education level, unlike previous studies, and employment status, as in previous studies, were related to the MCS score (38). A study showed that no significant difference was found between the average OQOL and the variables of age, sex, and residence status. At the same time, there was a significant difference between the variables of income, marital status, and daily exercise (40). Another study showed that no significant difference was found between the average OQOL and the variables of age, gender, and marital status. At the same time, there was a significant difference in the variables of education level, type of insurance, income, smoking, and daily exercise (24). In a study, it was observed that there was no significant difference between the average OQOL and the variables of gender, age, income, education level, marital status, employment status, smoking, and sports activities, while there was a significant difference with underlying diseases (13). The study of Santos et al. (42), unlike the present study, showed that smoking has a significant relationship with the OQOL of the patients and causes a decrease in their OQOL. Although in this study, the quality of life in non-smoking patients is higher than in smoking patients, no statistically significant relationship was found. Contrary to this study, another study (43) showed that there is no significant relationship between the variables of age, sex, marital status, education level, and employment status with patients’ OQOL. The review of various studies showed that the quality of life in patients with asthma, like this study, had a significant relationship with age, gender, marital status, education level, employment status, and disease severity (20, 45, 46, 47). Also, the results of other studies, contrary to the results of this study, showed that age, sex, income, and smoking were not related to the quality of life in patients (9, 20, 47). In general, poor economic and social status and low educational level are the factors influencing the low quality of life of asthma patients, which is consistent with the results of the present study (41).

The comparison of the results of this study with other studies shows that social, economic, and clinical variables are related to PCS, MCS, and OQOL scores and affect the quality of life. The reason for the similarities and differences in the results of the studies can be due to the difference in the population under study, the severity and stage of the disease in the patients, the living environment, and individual conditions. Also, the level of expectations, the level of general well-being, and the physical and mental resilience of people can be adequate in relating these variables to the quality of life, and one of the reasons for the similarities and differences between the results of this study and other studies. Therefore, to improve and increase the quality of life of patients, interventions and programs should be done according to the role and influence of these factors.

The present study showed that disease severity, gender, number of visits per month, and age are predictors of OQOL and PCS. Also, variables of disease severity, sex, underlying disease, and number of visits per month are predictors of MCS. In the present study, predictive variables were identified for all SF-36 dimensions. Adams et al.’s study (39) showed that the age variable was predictive of patients’ quality of life in all dimensions of SF-36, and the gender variable was predictive of quality of life in PF and MH dimensions. In the present study, age was only a predictor of the dimensions of PF and VT, and the gender variable in this study was the predictor of PF, as in the mentioned study (39). Song et al.’s study (36) showed that the variables of age, gender, and severity of the disease were predictors of PCS as in the present study. Also, unlike the present study, residence status, education level, income, insurance (general type), and smoking were among the predictors of PCS. This study (36) showed that the variables of age, gender, as in the present study, and the level of income and smoking were predictors of MCS, unlike the present study. In various studies, the variables of age, sex, education level, income, and severity of asthma are predictive factors of the quality of life in patients with asthma, as in the present study (11, 19, 45, 48). Unlike the present study, other studies showed that the variables of age, gender, economic status, smoking, disease duration, and disease severity are not predictors of quality of life in asthmatic patients (11, 48). The comparison of the results of this study and other studies shows that socio-demographic, economic, and clinical factors predict the quality of life in asthma patients. Therefore, the quality of life of these patients can be increased with appropriate changes and interventions on the variables.

Life with asthma has many aspects and different variables affect the person in this regard. Psychological factors, physical health factors, and multifactorial aspects are among the factors that affect asthma patients and their quality of life, and it was found that these factors directly and indirectly affect self-management. Also, the level of activity and other outcomes have a significant impact on the quality of life of patients with asthma (49). The findings indicate the complex and negative effects of health and psychological factors on the quality of life in asthma. Also, self-management with regular support reduces the use of healthcare resources and improves the quality of life at all levels of asthma severity (50). Therefore, investing in self-management and self-care skills training can be one of the most essential measures to improve the quality of life of asthma patients.

This study had some limitations and strengths. This study was conducted cross-sectionally, and it was impossible to measure changes in the quality of life during different stages of the disease. Also, due to difficult access, the physical and mental conditions of the patients were not assessed in a large volume. Another limitation of this study was the cultural and ethnic differences of the participants. One of the strengths of this study was the use of the SF-36 questionnaire as a valid tool to assess the quality of life, its implementation in the only treatment centers for respiratory patients in Ahvaz, and the examination of numerous demographic, social, and clinical variables in the patients.

CONCLUSION

Despite effective treatments for asthma patients, the results of the present study showed that the HRQOL of patients is poor. The low quality of life in patients with severe asthma, with a high number of visits, the elderly, women, people with low education, and high treatment costs is significant. PCS quality of life score in patients was lower than MCS, which shows that physical dimensions have a more significant impact on low quality of life in patients than mental dimensions. This result shows that it is necessary to focus on the physical health of patients to improve HRQOL. Clinical variables (severity of the disease, number of visits per month, smoking, family history, duration of the disease, number of drug intakes per day, and background patient) and socio-demographic and economic variables (gender, age, cost of the disease, education level and employment status) were among the predictors of SF-36, PCS, MCS and OQOL dimensions. Suitable interventions can significantly improve patient outcomes. These can include training on how to manage the disease, reducing physical symptoms, preventing disease progression, and enhancing living conditions. Additionally, providing financial aid through pharmaceutical, therapeutic, and nutritional packages can help increase resilience. Overall, these methods can lead to improvements in patients’ health-related quality of life HRQOL.

Acknowledgments

This article is based on the research project approved under the number NCRCCD-9701, with the ethics code IR.AJUMS.REC.1397.034, at the Research Center for Nursing Care in Chronic Diseases (NCRCCD) of Jundishapur University of Medical Sciences in Ahvaz. The authors would like to express their gratitude to everyone who participated in this project, especially the patients.

Footnotes

Conflict of interest

The authors of this article have no conflict of interest.

REFERENCES

  • 1.Brasil-Oliveira R, Cruz ÁA, Souza-Machado A, Pinheiro GP, Inácio DDS, Sarmento VA, et al. Oral health-related quality of life in individuals with severe asthma. J Bras Pneumol 2020;47(1):e20200117. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Battula M, Arunashekar P, Nagarajan VP. A Prospective Study to Assess the Quality of Life in Children with Newly Diagnosed Asthma and Their Caregivers using the Pediatric Asthma Quality of Life Questionnaire. J Prim Care Community Health 2020;11:2150132720961272. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Malek F, Khalil Sayah S, Kia NS, Ghods E. The Relationship Between Sleep Quality and Quality of Life Among Patients With Asthma. Cureus 2022;14(3):e23402. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Behniafard N, Nafei Z, Mirzaei M, Karimi M, Vakili M. Prevalence and Severity of Adolescent Asthma in Yazd, Iran: Based on the 2020 Global Asthma Network (GAN) Survey. Iran J Allergy Asthma Immunol 2021;20(1):24–32. [DOI] [PubMed] [Google Scholar]
  • 5.Fazel N, Kundi M, Jensen-Jarolim E, Pali-Schöll IM, Kazemzadeh A, Esmaily H, et al. Quality of life and asthma control in pregnant women with asthma. BMC Pulm Med 2021;21(1):415. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Song P, Adeloye D, Salim H, Dos Santos JP, Campbell H, Sheikh A, et al. Global, regional, and national prevalence of asthma in 2019: a systematic analysis and modelling study. J Glob Health 2022;12:04052. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Rahimian N, Aghajanpour M, Jouybari L, Ataee P, Fathollahpour A, Lamuch-Deli N, et al. The Prevalence of Asthma among Iranian Children and Adolescent: A Systematic Review and Meta-Analysis. Oxid Med Cell Longev 2021;2021:6671870. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Idani E, Raji H, Madadizadeh F, Cheraghian B, Haddadzadeh Shoshtari M, Dastoorpoor M. Prevalence of asthma and other allergic conditions in adults in Khuzestan, southwest Iran, 2018. BMC Public Health 2019;19(1):303. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Louis G, Pétré B, Schleich F, Zahraei HN, Donneau AF, Silvestre A, et al. Predictors of asthma-related quality of life in a large cohort of asthmatics: A cross-sectional study in a secondary care center. Clin Transl Allergy 2021;11(7):e12054. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Chiner E, Hernández C, Blanco-Aparicio M, Funenga-Fitas E, Jiménez-Ruiz C. Patient perspectives of the influence of severe and non-severe asthma on their quality of life: A national survey of asthma patients in Spain. Clin Respir J 2022;16(2):130–41. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Ali R, Ahmed N, Salman M, Daudpota S, Masroor M, Nasir M. Assessment of Quality of Life in Bronchial Asthma Patients. Cureus 2020;12(10):e10845. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Roncada C, Medeiros TM, Strassburger MJ, Strassburger SZ, Pitrez PM. Comparison between the health-related quality of life of children/adolescents with asthma and that of their caregivers: a systematic review and meta-analysis. J Bras Pneumol 2020;46(3):e20190095. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Lee GN, Koo HYR, Han K, Lee YB. Analysis of Quality of Life and Mental Health in Patients With Atopic Dermatitis, Asthma and Allergic Rhinitis Using a Nation-wide Database, KNHANES VII. Allergy Asthma Immunol Res 2022;14(2):273–83. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Abedi Yekta AH, Poursaeid Esfahani M, Salehi S, Hassabi M, Khosravi S, Kharabian S, et al. Assessment of the Effects of Inspiratory Muscle Training (IMT) and Aerobic Training on the Quality of Life of Patients with Chronic Obstructive Pulmonary Disease. Tanaffos 2019;18(3):223–9. [PMC free article] [PubMed] [Google Scholar]
  • 15.Stern J, Pier J, Litonjua AA. Asthma epidemiology and risk factors. Semin Immunopathol 2020;42(1):5–15. [DOI] [PubMed] [Google Scholar]
  • 16.Phan HT, Vu GV, Vu GT, Ha GH, Pham HQ, Latkin CA, et al. Global Mapping of Research Trends on Interventions to Improve Health-Related Quality of Life in Asthma Patients. Int J Environ Res Public Health 2020;17(10):3540. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Mansouri M, Sharifi F, Tabatabaee SS, Heidari E, Yaghubi H, Keshtkar A, et al. Prevalence of Ever Self-Reported Asthma and Associated Factors among University Students in Iran: A Population-Based Study. Int J Prev Med 2020;11:54. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Lázár Z, Horváth A, Tomisa G, Tamási L, Müller V. Impact of Clinical Factors on Generic and Disease-Specific Quality of Life in COPD and Asthma-COPD Overlap with Exacerbations. Pulm Med 2020;2020:6164343. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Shi M, Liang L, Wang Y, Yu Y. Risk factors associated with health-related quality of life in pediatric asthma. Sci Prog 2021;104(2):368504211013657. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Akhiwu HO, Dami N, Oguche S. Assessment of the health related quality of life in children with asthma in a tertiary hospital in North Central, Nigeria. Pan Afr Med J 2022;41:58. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Dastoorpoor M, Idani E, Goudarzi G, Khanjani N. Acute effects of air pollution on spontaneous abortion, premature delivery, and stillbirth in Ahvaz, Iran: a time-series study. Environ Sci Pollut Res Int 2018;25(6):5447–58. [DOI] [PubMed] [Google Scholar]
  • 22.Borsi SH, Khanjani N, Nejad HY, Riahi A, Sekhavatpour Z, Raji H, et al. Air pollution and hospital admissions due to deep vein thrombosis (DVT) in Ahvaz, Iran. Heliyon 2020;6(8):e04814. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Dastoorpoor M, Khanjani N, Khodadadi N. Association between Physiological Equivalent Temperature (PET) with adverse pregnancy outcomes in Ahvaz, southwest of Iran. BMC Pregnancy Childbirth 2021;21(1):415. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Lee LK, Ramakrishnan K, Safioti G, Ariely R, Schatz M. Asthma control is associated with economic outcomes, work productivity and health-related quality of life in patients with asthma. BMJ Open Respir Res 2020;7(1):e000534. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Lins-Kusterer L, Valdelamar J, Aguiar CVN, Menezes MS, Netto EM, Brites C. Validity and reliability of the 36-Item Short Form Health Survey questionnaire version 2 among people living with HIV in Brazil. Braz J Infect Dis 2019;23(5):313–21. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Socha M, Sobiech KA. Socio-Demographic and General Health Factors Associated with Quality of Life in Long-Term Breast Cancer Survivors from Southwestern Poland. Int J Environ Res Public Health 2021;18(17):9321. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.An J, Zhou K, Li M, Li X. Assessing the relationship between body image and quality of life among rural and urban breast cancer survivors in China. BMC Womens Health 2022;22(1):61. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Aguirre SI, Ornelas M, Blanco H, Jurado-García PJ, Benavides EV, Rodríguez-Villalobos JM, et al. Quality of Life in Mexican Older Adults: Factor Structure of the SF-36 Questionnaire. Healthcare (Basel) 2022;10(2):200. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Chow WL, Tan SM, Aung KCY, Chua SYN, Sim HC. Factors influencing quality of life of Asian breast cancer patients and their caregivers at diagnosis: perceived medical and psychosocial needs. Singapore Med J 2020;61(10):532–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Montazeri A, Goshtasebi A, Vahdaninia M, Gandek B. The Short Form Health Survey (SF-36): translation and validation study of the Iranian version. Qual Life Res 2005;14(3):875–82. [DOI] [PubMed] [Google Scholar]
  • 31.Valero-Moreno S, Montoya-Castilla I, Pérez-Marín M. Quality of life in patients with asthma: Medical indicators and psychological variables. J Pediatr Nurs 2023;69:e136–e144. [DOI] [PubMed] [Google Scholar]
  • 32.Rabitabar A, Bigdeli S, Souraki AD, Borimnejad L. Parents’ medication beliefs, quality of life and adherence to medication in children referring to asthma and allergy centers located in the Mazandaran province, Iran. Journal of Pediatric Nursing 2021;8(1):86–94. [Google Scholar]
  • 33.Abbasi F, Moradi Manesh F, Naderi F, Bakhtiyarpour S. The effectiveness of schema therapy on cognitive emotion regulation and quality of life in asthmatic individuals. Medical Journal of Mashhad University of Medical Sciences 2020;63(2):2446–54. [Google Scholar]
  • 34.Kalmarzi RN, Moradi G, Majd SA, Khanpuor F. The effect of mindfulness-based cognitive therapy on mindfulness and quality of life for patients with asthma. Shenakht J Psychol Psychiatry 2018;5(5):1–4. [Google Scholar]
  • 35.Rask-Andersen A, Leander M, Sundbom F, Lampa E, Oudin A, Leynaert B, et al. Health-related quality of life as associated with asthma control, psychological status and insomnia. Ups J Med Sci 2022;127. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Song HJ, Blake KV, Wilson DL, Winterstein AG, Park H. Health-Related Quality of Life and Health Utilities of Mild, Moderate, and Severe Asthma: Evidence from the Medical Expenditure Panel Survey. J Asthma Allergy 2021;14929–41 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Patil SS, Oggu A, Jayachandran S, Patil N, Doddayya H. Assessment of health related quality of life of asthma patients in a tertiary care teaching hospital. International Journal of Community Medicine and Public Health 2019;6(2):654. [Google Scholar]
  • 38.Kia NS, Malek F, Ghods E, Fathi M. Health-related quality of life of patients with asthma: a cross-sectional study in Semnan, Islamic Republic of Iran. East Mediterr Health J 2017;23(7):500–6. [DOI] [PubMed] [Google Scholar]
  • 39.Adams S, Rajani M, Baatjies R, Omar F, Jeebhay MF. Health-Related Quality of Life (HRQoL) of Residents with Persistent Lower Respiratory Symptoms or Asthma Following a Sulphur Stockpile Fire Incident. Int J Environ Res Public Health 2022;19(5):2915. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Rajabi S, Kamali M, Mousavi SK. Relationship between Lifestyle and Quality of Life in Patients with Asthma Referred to Medical Centers in Zanjan Province. Journal of Health and Care 2021;23(2):110–20. [Google Scholar]
  • 41.Plaza-González S, Zabala-Baños MDC, Astasio-Picado Á, Jurado-Palomo J. Psychological and Sociocultural Determinants in Childhood Asthma Disease: Impact on Quality of Life. Int J Environ Res Public Health 2022;19(5):2652. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Santos VCHD, Moreira MAF, Rosa AVD, Sobragi SM, Silva CAJD, Dalcin PTR. Association of quality of life and disease control with cigarette smoking in patients with severe asthma. Braz J Med Biol Res 2022;55:e11149. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Kazemi M, Barkhordari-Sharifabad M, Nasiriani KH, Fallahzadeh H. The Correlation of Health Literacy with Quality of Life in Asthmatic Patients. Iran Journal of Nursing 2019;32(121):54–67. [Google Scholar]
  • 44.Tavakol M, Sharafian S, Shaker Y, Alizadeh M, Keikavoosi-Arani L, Ghorbani M, et al. Quality of Life in 8–12-year-old Children with Asthma in Karaj. Medical Journal of Mashhad university of Medical Sciences 2022;65(1):247–56. [Google Scholar]
  • 45.Kharaba Z, Feghali E, El Husseini F, Sacre H, Abou Selwan C, Saadeh S, et al. An Assessment of Quality of Life in Patients With Asthma Through Physical, Emotional, Social, and Occupational Aspects. A Cross-Sectional Study. Front Public Health 2022;10:883784. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Ozoh OB, Aderibigbe SA, Ayuk AC, Dede SK, Egbagbe E, Babashani M. Health-related quality of life in asthma measured by the World Health Organization brief questionnaire (WHO-BREF) and the effect of concomitant allergic rhinitis-A population-based study. Clin Respir J 2023; 1–10. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Malik M, Khan A, Hussain A, Hashmi A. Assessment of Health-related Quality of Life Among Asthmatic Patients: The Need for Structured Pharmaceutical Care Delivery System in Pakistan. J Pharm Bioallied Sci 2017;9(4):272–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 48.Zeru TG, Engidawork E, Berha AB. Assessment of Asthma Control and Quality of Life among Asthmatic Patients Attending Armed Forces Referral and Teaching Hospital, Addis Ababa, Ethiopia. Pulm Med 2020;2020:5389780. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Stanescu S, Kirby SE, Thomas M, Yardley L, Ainsworth B. A systematic review of psychological, physical health factors, and quality of life in adult asthma. NPJ Prim Care Respir Med 2019;29(1):37. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Hodkinson A, Bower P, Grigoroglou C, Zghebi SS, Pinnock H, Kontopantelis E, et al. Self-management interventions to reduce healthcare use and improve quality of life among patients with asthma: systematic review and network meta-analysis. BMJ 2020;370:m2521. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Tanaffos are provided here courtesy of National Research Institute of Tuberculosis and Lung Disease

RESOURCES