Abstract
Objectives
To quantify the association between income and antibiotic misuse including unprescribed use, storage of antibiotics and non-adherence.
Methods
We identified pertinent studies through database search, and manual examination of reference lists of selected articles and review reports. We performed a dose–response meta-analysis of income, both continuous and categorical, in relation to antibiotic misuse. Summary odds ratios (ORs) and their 95% confidence intervals (CIs) were estimated under a random-effects random effects model.
Results
Fifty-seven studies from 22 countries of different economic class were included. Overall, the data are in agreement with a flat linear association between income standardized to socio-economic indicators and antibiotic misuse (OR per 1 unit increment = 1.00, p-value = 0.954, p-value non-linearity = 0.429). Data were compatible with no association between medium and high income with general antibiotic misuse (OR 1.04; 95% CI 0.89, 1.20 and OR 1.03; 95% CI 0.82, 1.29). Medium income was associated with 19% higher odds of antibiotic storage (OR 1.19; 95% CI 1.07, 1.32) and 18% higher odds of any aspect of antibiotic misuse in African studies (OR 1.18; 95% CI 1.00, 1.39). High income was associated with 51% lower odds of non-adherence to antibiotic treatment (OR 0.49; 95% CI 0.34, 0.60). High income was also associated with 11% higher odds of any antibiotic misuse in upper-middle wealth countries (OR 1.11; 95% CI 1.00, 1.22).
Conclusions
The association between income and antibiotic misuse varies by type of misuse and country wellness. Understanding the socioeconomic properties of antibiotic misuse should prove useful in developing related intervention programs and health policies.
Keywords: Income, Antibiotics, Misuse, Meta-analysis, Dose–response
Introduction
The misuse of antibiotics is defined as the intake of these drugs without medical advice (self-prescription) or their use when prescribed by the physician but without compliance with the physician’s instructions for treatment regimen in terms of timing, dosage and duration [1, 2]. It is a salient problem worldwide, irrespective of the country economy and wealth. Antibiotic misuse has led to antibiotic resistance, a universal public health problem with high socioeconomic and clinical burdens. Different systematic reviews and meta-analyses reported the high prevalence of antibiotic misuse. In their study, Morgan et al. reviewed publications from five continents and concluded that the use of antibiotics without prescription is wide-reaching and accounts for 19 to 100% of antibiotic use outside Northern Europe and North America [3]. Gualano et al. also reported that almost half of the individuals stop taking antibiotics upon improvement [4]. Another review estimated that the mean use of leftover antibiotics worldwide is 29%, and that of compliance with antibiotic therapy is only 62% [5]. A recent meta-analysis of studies from low- and middle- income countries found that the pooled prevalence of non-prescribed use of antibiotics is considerably high (78%) in these countries [6]. Antibiotic misuse is also frequent in high- income countries, including the United States where the prevalence of antibiotic use without prescription is as high as 66% in some instances, and that of storage of antibiotics for future use ranges between 14 and 48% [7].
Antibiotic resistance causes at least 700,000 annual deaths worldwide [8], more than 35,000 in the United States alone [9]. A similar record is registered in Europe [10]. The impact of antibiotics resistance on the economy is also expanding with disturbing figures [11]. By 2050, the annual mortality rate from antibiotic resistance is projected to exceed that of major causes of death like cancer and diabetes [8], and the provoked economic shortfalls will be as large as that of the 2008–2009 global financial crisis [12].
Several determinants of antibiotic misuse have been identified. These are mainly sociodemographic, including female gender, young adults and elderly, low educational level, difficult access to the healthcare system, unaffordability of the cost of physicians visit and accessibility to antibiotics [7, 13, 14].
In 2012, a narrative review report about self-medication with antibiotics in developing countries analysed data of five studies and concluded that middle income is associated with antibiotic misuse [15]. Studies that evaluated the association of income with antibiotic misuse showed divergent results. Some studies reported up to six-fold increased odds of misuse in high- income individuals [16, 17], while other studies did not find any association [18–20], or detected lower odds of misuse [21, 22]. It is also unclear whether the association between income and antibiotic misuse holds at different social classes and in regions with different levels of access to healthcare and in which regulations about antibiotic dispensing might vary. To the best of our knowledge, there is no meta-analysis that evaluates the association of income with antibiotic misuse worldwide.
To address this gap, we aimed in this study to carry out a meta-analysis of the association of income with antibiotic misuse. We present analyses standardized for socio-economic indicators.
Materials and methods
PRISMA guidelines were followed for the conduct and reporting of this meta-analysis, and the study protocol was registered in the PROSPERO database (ID: number deleted for blinding purposes). The outcome, antibiotic misuse, was defined as the use or purchase of non-prescribed antibiotics to treat oneself or another person, storage of leftover antibiotics, or nonadherence to the physicians’ instructions regarding the dosage, timing and treatment duration. Storage of antibiotics facilitates access to them and therefore is the first step towards their use without prescription [23].
Literature search and study selection
Medline, EMBASE, Conference Proceedings Citation Index-Science, the Open Access Theses and Dissertations, and the five regional bibliographic databases of the World Health Organization (WHO) were searched since their inception until January 2021. The following search syntax was applied in Medline: (Socioeconomic Factors OR income) AND (antibiotic*) AND ((drug storage [MeSH]) OR (compliance) OR (adherence) OR (Nonprescription Drugs/administration & dosage* [MeSH]) OR (misuse) OR (irrational use) OR (left-over)) and adapted for the other databases. We complemented our search by using free text words as follows: antibiotics AND (misuse OR "unprescribed use" OR leftover OR "adherence to treatment") AND (income OR "socioeconomic status" OR "socioeconomic level"). The reference lists of related reviews [3–7, 13–15, 24, 25] and those of included studies were manually checked to supplement database searches. The search was carried out without any language or date restrictions.
Studies that met the following criteria were included: (1) reporting at least two levels of income with defined boundaries as an exposure, and (2) providing Odds Ratio (OR) or Risk Ratio (RR) and their 95% Confidence Interval (CI) as a measurement of the association of income and misuse of antibiotics by the general population, or sufficient data for their calculation.
Data extraction and synthesis
From each included study, we extracted: (1) general study characteristics: author’s last name and year of publication, study period, participants characteristics (age and gender), and country where the study took place, (2) exposure: levels of monthly income, (3) measures of association: for each income level: number of subjects who practiced antibiotic misuse, total sample size, adjusted ORs and 95%CIs, and restriction, adjustment, or matching variables. When adjusted ORs were not provided, the crude estimates were registered, and (4) Type of antibiotic misuse: use without prescription, non-adherence, and storage of antibiotic leftover. When data was were provided for more than one type of antibiotic misuse, we extracted the data of all types of misuse. When the number of events of antibiotic misuse per income level was not available, we contacted the authors to request this information, but no reply was received [26–28]. We then deemed the number of events missing for those studies. We also inquired about the reference group used in a sub-analysis of one study [29], but due to lack of answer, we did not consider that subgroup.
We standardized the income to country-specific socio-economic indicators using two approaches. In the first approach, income was standardized to gross domestic product (GDP) per capita based on purchasing power parity (PPP) [30]. PPP is a currency conversion rate that is used to equalise the purchasing power of different monetary units. It allows to compare standards of living and economic productivity between countries [31]. In the second approach, the income level was standardized to the adjusted net national income per capita, expressed in US dollars [30]. The historical country-specific values of PPP, GDP per capita based on PPP, and adjusted net national income per capita were extracted from their specific portals in the World Bank [31–33].
Besides data reported in the studies, the classification of countries by economy [34], geographic distribution [35], and literacy rate [36] was obtained.
Statistical analysis
Studies included in this meta-analysis presented income categorized into 2 to 6 levels, with an average of 3 levels. As an estimate of the dose, we used the midpoint assigned to an estimated contrast given the upper and lower boundaries of the income.
We carried out dose–response meta-analysis of income standardized to: (1) gross domestic product (GDP) per capita based on (PPP) and (2) adjusted net national income per capita.
The dose–response meta-analysis was performed using a one-stage mixed-effects model taking into account heterogeneity across studies [37, 38].
We first used a linear function to estimate a summary OR of antibiotic misuse associated with an increase of 1 unit in income. We next flexibly modelled income using restricted cubic splines with 3 knots fixed at 10th, 50th and 90th percentiles of its distribution. Tests of hypothesis about the regression coefficients of the dose–response model were conducted using a large sample Wald-type test. To facilitate tabular presentation of the summary odds ratios, we further categorized income into tertiles using the lowest as referent.
We stratified the dose–response analysis by type of antibiotic misuse (unprescribed use, storage of leftover, non-adherence); WHO geographic classification, country economy (low wealth, lower–middle wealth, upper–middle wealth and high-wealth); literacy rate (≥ 90%, < 90%); exposure ascertainment (use of pretested or validated questionnaire; untested questionnaire or not reported); comparability (control for age, sex, educational level and household size; incomplete control); and publication year (≤ 2015, > 2015). In 2015, WHO published the global action plan to combat the problem of antibiotic resistance [39].
Quality appraisal
As all studies retrieved were eventually of cross-sectional nature, we appraised the quality of the studies using the Newcastle–Ottawa Scale for cross-sectional studies [40]. One point was given for the fulfilment of each of the following criteria: (1) well- defined target population; (2) reported response rate; (3) well described and appropriate statistical analysis; (4) justified sample size; (5) studies adjusted, matched or restricted for age, sex, educational level and household size; (6) use of previously tested or validated questionnaire; and (7) outcome ascertainment carried out using external assessment in addition to self-reporting. When information on a specific criterion was not given, it was graded with 0 point. The grades across items were then summed to obtain a quality score of a maximum of seven points. Two epidemiologists (NM and AF) carried out the quality assessment, and disagreements were resolved by referring to a third epidemiologist (BT).
Publication bias
Publication bias was checked visually using funnel plot and formally through Egger’s test [41], and the trim-and-filltrim and fill method [42].
Results
Literature search and study
Figure 1 represents the flow diagram of the selection of studies about income level and misuse of antibiotics. One thousand four hundred fifty-three publications were identified from the literature search, out of which 314 were selected for full- text review (Fig. 1). Fifty-one studies published between 2001 and 2021 met our inclusion criteria (Table 1). Five studies provided data for several types of misuse [20, 27, 28, 43, 44]. We treated each type of misuse as a separate study, making a total of 57 studies introduced in the dose–response analysis. All studies were of cross-sectional design. They involved a total population of 51,008 individuals from 22 countries and 18,094 events of antibiotic misuse. Forty-nine studies were published in English, one in Spanish [45] and one in Croatian [46].
Fig. 1.
Flow diagram of the selection of studies about income level and misuse of antibiotics
Table 1.
General characteristics of studies included the dose-–response meta-analysis of income level and antibiotic misuse
Author, Year | Country | Setting | Age (Years) |
Sex | Outcome | Mean Income (USD) |
Total N/level | Outcome/level | OR point estimate | Adjustment, restriction or matching variables |
---|---|---|---|---|---|---|---|---|---|---|
Moktan 2021[63] | India | Attendants of public hospital | 18–90 |
M: 309 F: 195 |
Use without prescription | 37.50 | 137 | 41 | Reference category | Age, gender, educational level, marital status, public and private clinics, frequency of doctors’ consultation, family/friend influence (other family members self-medicating with antibiotics), symptoms (minor illness) |
112.51 | 185 | 59 | 1.10 (0.68–1.77) | |||||||
225.01 | 129 | 52 | 1.58 (0.95–2.63) | |||||||
375.01 | 53 | 19 | 1.31 (0.67–2.56) | |||||||
Bulabula 2020 [26] | South Africa | Pregnant women attending public hospital |
Mean (SD): 29 (6.1) |
F: 301 | Use without prescription | 49.50 | – | – | Reference category | Age, gender, educational level, residential location, knowledge about antibiotics, attitudes towards antibiotics |
174.50 | – | – | 5.40 (0.90–29.90) | |||||||
375.00 | – | – | 4.10 (0.80–19.40) | |||||||
625.00 | – | – | 6.40 (1.20–35.20) | |||||||
Chen 2020 [43] | Mali | Medical university students |
Mean (SD) 21.3 (2.4) |
M:310 F:136 |
Storage of antibiotics | 82.95 | 290 | 168 | Reference category | Age |
506.50 | 114 | 77 | 1.51 (0.96–2.38) | |||||||
1181.60 | 42 | 27 | 1.31 (0.67–2.56) | |||||||
Use without prescription | 82.95 | 290 | 73 | Reference category | ||||||
506.50 | 114 | 29 | 1.01 (0.62–1.67) | |||||||
1181.60 | 42 | 19 | 2.46 (1.27–4.77) | |||||||
Elmahi 2020 [64] | Sudan | General population | ≥ 18 |
M: 130 F: 116 |
Use without prescription | 49.50 | 182 | 110 | 1.05 (0.59–1.87) | Age, pregnancy, current antibiotic use |
149.50 | 64 | 38 | Reference category | |||||||
Mallah 2020 [59] | Lebanon | Children´s caregivers | ≥ 18 |
M:276 F:1092 |
Any misuse practice | 249.50 | 21 | 2 | Reference category | Age, sex, educational level, area of residence, alcohol consumption, access to medical care facilities, and frequency of telephone medical consultation |
999.50 | 260 | 34 | 1.43 (0.32–6.41) | |||||||
2000.00 | 223 | 17 | 0.78 (0.17–3.65) | |||||||
3000.50 | 808 | 36 | 0.44 (0.10–1.98) | |||||||
Nusair 2020 [65] | Jordan | General population | 0 to > 65 |
M: 674 F: 1169 |
Use without prescription | 88.75 | 175 | 61 | Reference category | Past month antibiotic use |
266.61 | 659 | 253 | 1.16 (0.82–1.65) | |||||||
444.11 | 1042 | 458 | 1.47 (1.05–2.05) | |||||||
Rathish 2020 [18] | Sri Lanka | General population |
Mean (SD): 36 (21) |
M: 181 F: 203 |
Use without prescription | 150.00 | 267 | 263 | Reference category | NA |
450.00 | 117 | 111 | 2.15 (0.37–12.54) | |||||||
Xu 2020 [28] | China | Children´s caregivers | Parents with children < 13 years old |
M: 1344 F: 4935 |
Use without prescription | 377.50 | – | – | Reference category | Age, gender, educational level, medical background, residential location |
1132.58 | – | – | 0.76 (0.57–1.03) | |||||||
1887.58 | – | – | 0.81 (0.54–1.21) | |||||||
Storage of antibiotics | 377.50 | – | – | Reference category | ||||||
1132.58 | – | – | 1.03 (0.91–1.17) | |||||||
1887.58 | – | – | 1.16 (0.99–1.36) | |||||||
Ateshim 2019 [66] | Eritrea | General population |
Median (IQR): 37 (24) |
M: 238 F: 339 |
Use without prescription | 0.00 | 291 | – | Reference category | Age, gender, educational level, marital status, occupational status, knowledge about antibiotics, attitudes towards antibiotics |
32.53 | 92 | – | 0.92 (0.54–1.56) | |||||||
113.78 | 136 | – | 1.22 (0.78–1.19) | |||||||
211.28 | 58 | – | 1.43 (0.75–2.73) | |||||||
Benameur 2019 [67] | Saudi Arabia | University students |
Mean (SD): 20.96 (0.148) |
M:166 F:69 |
Use without prescription | 133.37 | 164 | 95 | Reference category | Age, gender, educational level, marital status, speciality (medical vs non-medical), residential location, health insurance |
667.50 | 50 | 26 | 0.79 (0.42–1.49) | |||||||
1468.63 | 18 | 14 | 2.54 (0.80–8.06) | |||||||
Bogale 2019 [19] | Ethiopia | General population | 18 to > 60 |
M: 246 F: 349 |
Use without prescription | 10.75 | – | 46 | Reference category | Age, gender, educational level, marital status, residential location, occupational status, healthcare profession |
32.27 | – | 74 | 2.55 (1.18–5.50) | |||||||
64.52 | – | 42 | 1.08 (0.47–2.46) | |||||||
107.52 | – | 92 | 1.42 (0.62–3.25) | |||||||
Mate 2019 [44] | Mozambique | General population |
Median (IQR): 33 (IQR: 25–47) |
M:294 F:797 |
Use without prescription | 21.24 | 528 | 108 | Reference category | Age |
63.75 | 224 | 45 | 0.98 (0.66–1.44) | |||||||
127.51 | 183 | 40 | 1.09 (0.72–1.64) | |||||||
212.51 | 117 | 26 | 1.11 (0.68–1.80) | |||||||
Incomplete course of treatment | 21.24 | 506 | 150 | Reference category | ||||||
63.75 | 215 | 68 | 1.10 (0.78–1.55) | |||||||
127.51 | 175 | 60 | 1.24 (0.86–1.79) | |||||||
212.51 | 114 | 21 | 0.54 (0.32–0.89) | |||||||
Mukattash 2019 [68] | Jordan | Children´s caregivers | 20 to ≥ 50 |
M: 134 F: 712 |
Use without prescription | 352.50 | 94 | 41 | Reference category | Age |
1058.21 | 325 | 141 | 0.99 (0.62–1.57) | |||||||
1763.21 | 427 | 150 | 0.70 (0.44–1.10) | |||||||
Sun 2019 [69] | China | Children´s caregivers | Parents with children < 13 years old |
M: 2243 F: 7283 |
Storage of antibiotics | 230.50 | 2102 | 874 | Reference category | Age, gender of the parents, gender of the child, educational level, socioeconomic characteristics (residential location and GDP per capita), health insurance, specialty (medical vs non-medical) |
615.50 | 2889 | 1434 | 1.22 (1.08–1.38) | |||||||
1154.00 | 2749 | 1355 | 1.17 (1.02–1.33) | |||||||
1923.00 | 1786 | 917 | 1.36 (1.16–1.60) | |||||||
Hu 2018 [70] | China | Medical university students |
Mean (SD): 22 (1.5) |
M: 661 F: 1158 |
Use without prescription | 768.50 | 1565 | 59 | Reference category | Age, gender, educational level, parents’ educational level, parents medical background, residential location, knowledge–attitudes–and practice score, center of recruitment |
2306.50 | 254 | 18 | 1.95 (1.13–3.36) | |||||||
Tong 2018 [71] | China | Attendants of primary care clinics | < 45 to > 60 |
M:340 F:374 |
Noncompliance | 153.20 | 162 | 150 | Reference category | Age, gender, educational level, residential location, occupation, employment status, knowledge about antibiotics |
344.78 | 180 | 163 | 0.72 (0.33–1.57) | |||||||
651.18 | 187 | 158 | 0.40 (0.20–0.82) | |||||||
880.98 | 185 | 150 | 0.33 (0.16–0.66) | |||||||
Peng 2018 [20] | China | University students |
Guizhou Mean (SD): 21.3 (2.1) Zhejiang Mean (SD): 19.7 (2.6) |
M: 2035 F: 1960 |
Use without prescription | 230.92 | – | – | Reference category | Age, socioeconomic characteristics (GDP per capita and residential location) |
1001.00 | – | – | 0.65 (0.39–1.09) | |||||||
2079.08 | – | – | 0.66 (0.33–1.31) | |||||||
Storage of antibiotics | 230.92 | – | – | Reference category | ||||||
1001.00 | – | – | 1.30 (1.10–1.53) | |||||||
2079.08 | – | – | 1.14 (0.90–1.43) | |||||||
Buying without prescription | 230.92 | – | – | Reference category | ||||||
1001.00 | – | – | 1.14 (0.90–1.44) | |||||||
2079.08 | – | – | 1.05 (0.76–1.46) | |||||||
Redzick 2018 [46] | Croatia | Attendants of primary care clinics | – |
M: 142 F: 402 |
Use without prescription | 84.62 | 88 | 5 | Reference category | Age |
226.12 | 55 | 13 | 5.14 (1.72–15.38) | |||||||
339.32 | 97 | 4 | 0.71 (0.19–2.75) | |||||||
452.52 | 100 | 15 | 2.93 (1.02–8.42) | |||||||
594.02 | 199 | 25 | 2.39 (0.88–6.45) | |||||||
Wang 2018 [27] | China | University students |
Mean (SD): 20.7 (2.7) |
M: 5515 F: 5677 |
Storage of antibiotics | 230.92 | 3417 | – | Reference category | Age, gender, educational level, parents’ educational level, parents medical background, residential location, speciality (medical vs non-medical) |
1001.00 | 5823 | – | 1.15 (1.04–1.27) | |||||||
2310.08 | 1435 | – | 1.02 (0.88–1.19) | |||||||
3850.08 | 517 | – | 1.00 (0.81–1.23) | |||||||
Use without prescription | 230.92 | 3417 | – | Reference category | ||||||
1001.00 | 5823 | – | 0.89 (0.67–1.19) | |||||||
2310.08 | 1435 | – | 1.13 (0.75–1.71) | |||||||
3850.08 | 517 | – | 0.93 (0.53–1.63) | |||||||
Abdelrahman 2017 [60] | Saudi Arabia | General population | < 18 to > 65 |
M: 735 F: 293 |
Use without prescription | 200.12 | 368 | 112 | Reference category | Age |
867.62 | 146 | 60 | 1.59 (1.07–2.37) | |||||||
2002.50 | 198 | 72 | 1.31 (0.91–1.88) | |||||||
3337.63 | 316 | 146 | 1.96 (1.43–2.69) | |||||||
Albawani 2017 [72] | Yemen | Attendants of pharmacies |
Mean (SD): 28.6 (7.7) |
M: 204 F: 159 |
Use without prescription | 116.80 | 268 | 229 | Reference category | Age |
352.80 | 51 | 46 | 1.57 (0.59–4.19) | |||||||
581.90 | 44 | 41 | 2.33 (0.69–7.89) | |||||||
Erku 2017 [73] | Ethiopia | General population |
Mean (SD): 33.19 (10.82) |
M: 163 F: 487 |
Any misuse practice | 50.00 | 331 | 282 | Reference category | Age, gender, educational level, marital status, employment status, household size, frequency of visiting health care institutions, satisfaction about healthcare service |
125.50 | 201 | 170 | 0.95 (0.58–1.55) | |||||||
175.50 | 118 | 83 | 0.41 (0.25–0.68) | |||||||
Gebrekirstos 2017 [74] | Ethiopia | Attendants of pharmacies |
Median (IQR): 30 (16) |
M: 473 F: 307 |
Use without prescription | 3.26 | 130 | 76 | 1.67 (1.13–2.48) | Age, gender, educational status, marital status, employment status, household size, residential location, type of illness, healthcare insurance, previous experience with antibiotics, access to healthcare |
13.00 | 92 | 41 | 0.96 (0.61–1.50) | |||||||
26.00 | 81 | 32 | 0.78 (0.48–1.26) | |||||||
39.02 | 477 | 218 | Reference category | |||||||
Gillani 2017 [75] | Pakistan | Non-medical university students |
Mean (SD): 23.0 (3.4) |
M:352 F:375 |
Use without prescription | 75.00 | 245 | 110 | Reference category | Age, specialty (non-medical) |
225.00 | 180 | 80 | 0.98 (0.67–1.45) | |||||||
400.00 | 136 | 54 | 0.81 (0.53–1.24) | |||||||
600.01 | 166 | 82 | 1.20 (0.81–1.78) | |||||||
Hassali 2017 [76] | Malaysia | General population |
Mean (SD): 28.7 (7.4) |
M: 171 F: 229 |
Any misuse practice | 124.88 | 231 | 82 | Reference category | Age, gender, educational level, marital status, race, healthcare related occupation, employment status, health insurance |
499.88 | 94 | 29 | 0.51 (0.27–0.98) | |||||||
1000.00 | 47 | 13 | 0.40 (0.16–0.78) | |||||||
1500.13 | 28 | 7 | 0.42 (0.13–1.34) | |||||||
Jamhour 2017 [29] | Lebanon | General population | > 18 |
M: 182 F: 218 |
Use without prescription | 499.50 | 88 | 36 | Reference category | Age, gender, educational level, specialty (unrelated to health care) |
1500.00 | 97 | 54 | 1.81 (1.01–3.25) | |||||||
Kajeguka 2017 [77] | Tanzania | General population |
Mean (SD): 35.4 (13.4) |
M:144 F:156 |
Use without prescription | 49.50 | 162 | 70 | 2.82 (0.47–16.68) | Age, gender, educational level, marital status, employment status, self-treated condition |
300.50 | 102 | 74 | 1.02 (0.22–4.76) | |||||||
700.50 | 36 | 23 | Reference category | |||||||
Kurniawan 2017 [78] | Indonesia | Attendants of primary care clinics |
Median (IQR): 45 (18–49) |
M: 137 F: 263 |
Use without prescription | 87.50 | 186 | 146 | Reference category | Age, gender, educational level, marital status, employment status, health insurance |
262.50 | 54 | 34 | 0.52 (0.24, 1.12) | |||||||
Nuñez 2017 [79] | Perú | University students | Mean: 19.82 |
M: 492 F: 508 |
Use without prescription | 462.00 | 321 | 204 | Reference category | Age |
1386.62 | 322 | 211 | 1.09 (0.79–1.51) | |||||||
2772.62 | 178 | 119 | 1.16 (0.79–1.70) | |||||||
4620.62 | 179 | 120 | 1.17 (0.79–1.72) | |||||||
Senadheera 2017 [80] | Sri Lanka | General population | ≥ 18 |
M: 190 F: 174 |
Use without prescription | 87.50 | 292 | 15 | Reference category | Age, gender, educational level, employment status, health insurance, household size, receiving medical treatment in the last three months, knowledge of antibiotic name |
262.51 | 288 | 26 | 1.83 (0.95–3.54) | |||||||
Torres 2017 [45] | Ecuador | General population | 18–64 |
M:97 F:110 |
Use without prescription | 349.50 | 200 | 98 | Reference category | Age |
1100.00 | 132 | 68 | 1.11 (0.71–1.72) | |||||||
1775.00 | 36 | 14 | 0.66 (0.32–1.37) | |||||||
2250.50 | 8 | 2 | 0.35 (0.07–1.76) | |||||||
Aleem 2016 [21] | Saudi Arabia | Children´s caregivers | < 25 to ≥ 55 |
M: 249 F: 382 |
Use without prescription | 667.50 | 91 | 17 | Reference category | Age, gender, educational level, household size |
2002.63 | 519 | 54 | 0.50 (0.26, 0.95) | |||||||
Bilal 2016 [81] | Pakistan | Attendants of public hospital |
Mean (SD): 48.6 (4.4) |
M: 263 F: 137 |
Use without prescription | 35.00 | 180 | 172 | Reference category | Age, residential location, specialty (non-medical related participants) |
105.00 | 73 | 62 | 0.26 (0.10–0.68) | |||||||
210.00 | 49 | 36 | 0.13 (0.05–0.33) | |||||||
415.00 | 36 | 29 | 0.19 (0.06–0.57) | |||||||
685.01 | 62 | 26 | 0.03 (0.01–0.08) | |||||||
Zhu 2016 [82] | China | University students |
18–45 (IQR: 21–22) |
M: 369 F: 291 |
Use without prescription | 40.00 | 45 | 28 | Reference category | Age, gender, educational level, major, healthcare insurance, residential location |
120.08 | 423 | 192 | 0.50 (0.27–0.95) | |||||||
240.08 | 173 | 83 | 0.56 (0.29–1.10) | |||||||
400.08 | 19 | 13 | 1.32 (0.42–4.11) | |||||||
Ding 2015 [83] | China | Children´s caregivers | ≤ 29 to ≥ 50 |
M: 70 F: 652 |
Noncompliance | 67.08 | 78 | 15 | Reference category | Age, access to healthcare (number of clinics) |
268.33 | 384 | 111 | 1.71 (0.93–3.13) | |||||||
536.66 | 260 | 76 | 1.73 (0.93–3.24) | |||||||
Gebeyehu 2015 [84] | Ethiopia | General population |
Mean (SD): Urban 34.1 (12.9) Rural 34.5 (11.5) |
M:263 F:819 |
Any misuse practice | 25.47 | 108 | 30 | Reference category |
Age, gender, educational level, marital status, employment status, residential location, household size Level of healthcare service satisfaction, knowledge on antibiotics use |
76.50 | 177 | 59 | 1.30 (0.77–2.20) | |||||||
127.53 | 77 | 26 | 1.33 (0.70–2.50) | |||||||
178.53 | 19 | 3 | 0.49 (0.13–1.79) | |||||||
229.53 | 7 | 2 | 1.04 (0.19–5.65) | |||||||
Yousif 2015 [85] | Saudi Arabia | General population | ≥ 18 |
M: 228 F: 172 |
Use without prescription | 1335.00 | 219 | 173 | Reference category | Age, gender, educational level, marital status, employment status, residential location |
4005.13 | 172 | 142 | 0.80 (0.50–1.30) | |||||||
Cheaito 2014 [86] | Lebanon | Attendants of pharmacies |
Mean (SD): 38.24 (13.7) |
M: 143 F: 176 |
Use without prescription | 1000.00 | 278 | 117 | Reference category | Age, gender, educational level, marital status, employment status, health insurance, having a reference doctor and frequency of consultation |
3000.00 | 40 | 17 | 1.02 (0.52–1.99) | |||||||
Eticha 2014 [87] | Ethiopia | University students |
Mean (SD): 21 (2.06) |
M: 267 F: 140 |
Use without prescription | 6.28 | 159 | 42 | Reference category | Age, gender, university year, religion, residential location |
18.92 | 160 | 38 | 0.87 (0.52–1.44) | |||||||
31.56 | 88 | 32 | 1.59 (0.91–2.79) | |||||||
Hu 2014 [22] | Australia | General population |
Mean (SD): 33 (8.2) Range: 14–63 |
M: 170 F: 258 |
Storage of antibiotics | 1904.13 | 150 | 85 | Reference category | Age, gender, educational level, residential location, employment status, marital status, parental status, language proficiency, main language spoken at home, health insurance |
5712.46 | 278 | 118 | 0.56 (0.38–0.84) | |||||||
Lv 2014 [88] | China | University students | NA |
M:341 F:390 |
Any misuse practice | 41.00 | 139 | 58 | Reference category | Gender, university year, residential location, major (medical vs non-medical), health insurance |
123.08 | 447 | 175 | 1.14 (0.76–1.71) | |||||||
246.08 | 131 | 56 | 1.00 (0.59–1.67) | |||||||
410.08 | 14 | 5 | 1.26 (0.39–4.13) | |||||||
Mihretie 2014 [89] | Ethiopia | General population |
Mean (SD): 37.8 (12.2) |
M: 34 F: 17 |
Use without prescription | 13.75 | 14 | 9 | Reference category | Age |
38.78 | 10 | 8 | 2.22 (0.33–14.80) | |||||||
67.53 | 10 | 8 | 2.22 (0.33–14.80) | |||||||
102.53 | 14 | 6 | 0.42 (0.09–1.91) | |||||||
Shah 2014 [90] | Pakistan | University students |
Mean (SD): 20.04 (1.74) |
M: 253 F: 178 |
Use without prescription | 250.00 | 115 | 51 | Reference category | Age, specialty (non-medical) |
750.00 | 139 | 73 | 1.39 (0.85–2.28) | |||||||
1250.00 | 70 | 38 | 1.49 (0.82–2.71) | |||||||
1750.01 | 73 | 28 | 0.78 (0.43–1.42) | |||||||
Abobotain 2013 [61] | Saudi Arabia | Children´s caregivers | < 25 to ≥ 55 |
M:241 F:369 |
Use without prescription | 667.37 | 91 | 17 | Reference category | Age, educational level, marital status, household size, number of children < 12 years old, healthcare related profession |
2002.50 | 519 | 54 | 0.50 (0.26, 0.95) | |||||||
Pan 2012 [17] | China | University students |
Mean (SD): 22.3 (2.6) |
M:745 F:555 |
Use without prescription | 38.75 | 548 | 215 | Reference category | Age, gender, major, residential location, healthcare insurance |
116.33 | 668 | 352 | 1.73 (1.37–2.17) | |||||||
232.58 | 74 | 46 | 2.54 (1.54–4.20) | |||||||
387.58 | 10 | 8 | 6.20 (1.30–29.45) | |||||||
Widayati 2011 [91] | Indonesia | General population |
Median (Range) Prescribed 40.5 (18–69) Self-medicated 43 (18–66) |
M: 309 F: 250 |
Use without prescription | 74.50 | 41 | 19 | Reference category | Age, gender, educational level, marital status, household size, employment status, healthcare insurance |
224.50 | 24 | 15 | 1.93 (0.69–5.40) | |||||||
550.00 | 5 | 1 | 0.29 (0.03–2.82) | |||||||
1050.50 | 4 | 2 | 1.16 (0.15–9.03) | |||||||
Ilhan 2009 [16] | Turkey | Attendants of primary care clinics |
Mean (SD) 39.5 (15.2) |
M:1652 F:1044 |
Use without prescription | 157.43 | 272 | 46 | Reference category | Age, gender, educational level, marital status, employment status, household size, healthcare insurance (social security), perceived health status, presence of chronic diseases |
472.93 | 1148 | 188 | 0.96 (0.67–1.39) | |||||||
788.43 | 505 | 107 | 1.32 (0.89–1.97) | |||||||
1103.93 | 265 | 61 | 1.73 (1.11–2.70) | |||||||
1419.43 | 350 | 84 | 1.55 (1.02–2.36) | |||||||
Hadi 2008 [92] | Indonesia | Attendants of primary care clinics |
Median (range) 31 (0–87) |
M: 1147 F: 1849 |
Use without prescription | 13.50 | 192 | 30 | Reference category | Age, gender, educational level, residential location, ethnicity, household size, healthcare insurance |
40.50 | 274 | 42 | 0.98 (0.59, 1.63) | |||||||
Al-Azzam 2007 [93] | Jordan | General population | ≥ 17 to > 60 |
M:1040 F:1093 |
Use without prescription | 88.75 | 606 | 204 | Reference category | NA |
266.61 | 721 | 309 | 1.48 (1.18–1.85) | |||||||
444.11 | 806 | 329 | 1.36 (1.09–1.69) | |||||||
Sawair 2007 [94] | Jordan | Attendants of primary care clinics | ≤ 16 to > 65 |
M: 220 F: 257 |
Use without prescription | 139.30 | 140 | 46 | Reference category | Age, gender, educational level, marital status, employment status, healthcare insurance, smoking habits, self-reported health status, chronic comorbidities |
420.00 | 133 | 63 | 1.94 (1.18–3.21) | |||||||
700.70 | 204 | 85 | 1.35 (0.85–2.14) | |||||||
Awad 2005 [95] | Sudan | General population | ≤ 20 to > 60 |
M: 790 F: 960 |
Use without prescription | 19.25 | – | – | Reference category | Age, gender, educational level |
67.40 | – | – | 0.78 (0.59–1.00) | |||||||
125.15 | – | – | 0.61 (0.42–0.87) |
Income level and antibiotic misuse: continuous analysis
Overall, the data from these 57 studies were compatible with a flat linear association between income standardized to GDP per capita based on PPP and antibiotic misuse (OR 1.00; p-value = 0.954, p-value non-linearity = 0.452). Similar results were obtained for the association of income standardized to adjusted net national income per capita and antibiotic misuse (OR 1.00; p-value = 0.940).
As a graphical presentation of the trend, Fig. 2 shows the estimated summary odds ratio of antibiotic misuse conferred by income standardized to GDP per capita based on PPP.
Fig. 2.
Trend of the association of income level standardized to GDP per capita based on PPP and antibiotic misuse. Solid line represents the linear trend. Long-dashed line represents the non-linear restricted cubic spline approach. Short-dashed lines represents 95% CI
Income level and antibiotic misuse: categorical and stratified analysis
In the categorical approach of income standardized to GDP per capita based on PPP, overall, as compared to low (1st tertile), no association between income and general antibiotic misuse was observed: medium income (2nd tertile): OR 1.04; 95% CI 0.89, 1.20, and high income (3rd tertile): OR 1.03; 95% CI 0.82, 1.29 (Table 2).
Table 2.
Meta-analysis of the association of income level represented as units of GDP per capita based on PPP with antibiotic misuse
Number of studies | Medium income OR (95%CI) | High income OR (95% CI) | |
---|---|---|---|
All studies | 57 | 1.04 (0.89, 1.20) | 1.03 (0.82, 1.29) |
Type of misuse | |||
Use without prescription | 43 | 1.06 (0.87, 1.28) | 1.07 (0.84, 1.37) |
Storage of antibiotics | 6 | 1.19 (1.07, 1.32) | 1.04 (0.92, 1.17) |
Non-adherence | 3 | 1.10 (0.89, 1.35) | 0.49 (0.34, 0.70) |
Country economy | |||
Low | 16 | 1.02 (0.83, 1.24) | 0.90 (0.59, 1.37) |
Lower-middle | 11 | 1.14 (0.73, 1.80) | 0.92 (0.46, 1.84) |
Upper-middle | 25 | 1.17 (0.91, 1.49) | 1.11 (1.00, 1.22) |
High | 5 | 0.90 (0.44, 1.85) | 1.04 (0.33, 3.28) |
WHO Region | |||
African | 14 | 1.18 (1.00, 1.39) | 0.96 (0.67, 1.38) |
Eastern Mediterranean | 17 | 0.92 (0.65, 1.32) | 0.95 (0.58, 1.57) |
South-East Asian | 6 | 1.11 (0.62, 2.00) | 1.53 (0.81, 2.92) |
Western Pacific | 16 | 0.99 (0.82, 1.20) | 1.05 (0.92, 1.19) |
Survey year | |||
Until 2015 | 29 | 0.95 (0.75, 1.20) | 0.91 (0.62, 1.35) |
After 2015 | 28 | 1.12 (0.99, 1.26) | 1.15 (0.93, 1.41) |
Literacy rate | |||
< 90% | 20 | 1.03 (0.82, 1.29) | 1.02 (0.68, 1.54) |
≥ 90% | 37 | 1.09 (0.93, 1.28) | 1.02 (0.84, 1.23) |
Pre-tested or validated questionnaire | |||
No | 10 | 1.02 (0.51, 2.06) | 0.90 (0.34, 2.36) |
Yes | 47 | 1.06 (0.91, 1.24) | 1.04 (0.85, 1.27) |
Adjustment | |||
Incomplete | 47 | 1.09 (0.95, 1.24) | 1.05 (0.84, 1.31) |
Complete | 10 | 0.90 (0.71, 1.15) | 0.60 (0.30, 1.23) |
Quality Score | |||
Lower quality (≤ 3 points) | 24 | 0.99 (0.75, 1.31) | 1.09 (0.72, 1.66) |
Higher quality (> 3 points) | 33 | 1.04 (0.86, 1.25) | 1.03 (0.81, 1.31) |
Stratified analysis revealed that medium income was associated with 19% higher odds of storage of antibiotics (OR 1.19; 95% CI 1.07, 1.32),); nonetheless, we did not observe any significant association between high income and this type of misuse (OR 1.04; 95% CI 0.92, 1.17). It is noteworthy to mention that storage of antibiotics was evaluated in five studies carried out in China [20, 27, 28, 43, 44] and in a sixth study that was undertaken in Australia but involved Chinese immigrants [22]. High income was associated with 51% lower odds of non-adherence to antibiotics treatment (OR 0.49, 95% CI 0.34, 0.70) (Table 2). When restricting the analysis to low-wealth countries, high- income individuals were at 11% higher odds of antibiotic misuse than those with low income in upper–middle wealth countries (OR 1.11; 95% CI 1.00, 1.22) (Table 2). Our findings also suggested an association between medium-income medium income level and antibiotic misuse in African countries (OR 1.18; 95% CI 1.00, 1.39) (Table 2). After 2015, the odds of misuse of antibiotics in medium- income individuals increased when compared with studies undertaken until 2015 (ORuntil 2015 0.95; 95% CI 0.75, 1.20 and ORafter 2015 1.12; 95% CI 0.99, 1.26). Similar findings were obtained for high- income individuals (ORuntil 2015 0.91; 95% CI 0.62, 1.35 and ORafter 2015 1.15; 95% CI 0.93, 1.41) (Table 2). No meaningful difference in the odds of antibiotic misuse by medium- and high- income individuals was observed when countries were grouped according to literacy rate (Table 2).
The categorical approach of income standardized to net national income per capita showed similar results to that of income standardized to GDP per capita based on PPP (data not shown).
Methodological characteristics of the studies
Restricting the analysis to those studies that used pretested or validated questionnaires did not yield any substantial modification in the pooled OR estimates (ORmedium 1.06; 95% CI 0.91, 1.24 and ORhigh 1.04; 95% CI 0.85, 1.27) (Table 2).
Studies that incompletely controlled for sex, age, educational level and household size showed higher pooled estimates than those with complete control of those variables in medium income (ORincomplete 1.09; 95% CI 0.95, 1.24 and ORcomplete 0.90; 95% CI 0.71, 1.15) and in high income (ORincompletz 1.05; 95% CI 0.84, 1.31 and ORcomplete 0.60; 95% CI 0.30, 1.23) (Table 2).
No notable difference was observed between pooled estimates from studies with lower-quality (≤ 3 points) and those from studies with higher-quality score (> 3 points) (Table 2).
Publication bias
The funnel plot (Fig. 3) and Egger’s test of the null hypothesis (p-value = 0.39) did not suggest evidence of publication bias. These findings were further confirmed by the Trim-and-Fill analysis that did not yield to the addition of any study.
Fig. 3.
Funnel plot of studies about income and antibiotic misuse
Discussion
Antibiotic resistance is an internationally growing multifaceted emergency that has been exacerbated by antibiotic misuse and has left devastating impact at the clinical, health and socio-economic levels. If not controlled, antibiotic resistance will convert into the major cause of death in 2050 [8].
To the best of our knowledge, this is the first meta-analysis that assesses the dose–response association between income level and misuse of antibiotics. Our results agree well with the hypothesis of no association between income level and misuse of antibiotics. Subgroup analyses reveal a dose–response association of medium- and high- income levels with specific types of antibiotic misuse, i.e., storage of drug leftover and non-adherence, country wealth, geographic region and study period.
Our primary findings suggest that the odds of misuse of antibiotics do not differ between poor and wealthy people. This is in line with the fact that both low- and high- income individuals tend to self-medicate. On the one hand, under constrained financial resources, especially in less developed economies where access to health facilities is limited, self-medication is the only available option of healthcare [47]. By self-medicating, individuals with low income avoid expenses of medical consultation and subsequent lab tests. Low- income households report forgone care more often than those with high- income level [48]. They often cut -back basic needs and take less medication than prescribed, due to cost [49, 50], explaining therefore the observed higher likelihood of adherence to treatment by high- income than by low- income individuals. On the other hand, people with high- income level tend to medicate themselves as they have easier access to sources of information including internet to seek health information [51], can afford purchasing non-reimbursed medicines, and have more social support that increases their access to unprescribed medicines including through sharing with families and friends [52].
Our dose–response meta-analysis also showed that medium- income individuals have higher odds of storing antibiotic leftover than those with low income. This could be related to higher financial affordability by medium-income medium income individuals to purchase and store antibiotics. Our results also show a higher likelihood of misuse by high-income individuals in upper–middle wealth countries. Consistent with our findings, an earlier report about the economy of self-medication in general, indicated that the demand for self-medication declines with rising the income level of high- income individuals, but increases with increasing the income of low-income individuals, resulting in a null pooled effect between income and self-medication [47].
We also reported that medium- income individuals in Africa have higher chances of antibiotic misuse, probably due to the poor enforcement of antibiotic dispensing regulations in those regions.
We observed a marginal increase in the odds of misuse of antibiotics by medium- income and high- income individuals after 2015 than before this period. This could be related to two main motives;: first, as concluded by WHO in its report Global Spending on Health, the expenditure on health is growing faster than economies, leading to a doubling of the out-of-pocket spending and very large differences between high- and low-wealth countries concerning health expenditure [53], second, not all countries have developed and implemented sufficient measures to control the dispensing of antibiotics, and thus people with greater financial resources continued using antibiotics without prescription. A recent review report indicated that more than half of the antibiotics worldwide are dispensed without prescription [54]. Consequently, the WHO placed a new urgent call to control antibiotics resistance crisis on 2019 [55].
The findings of this meta-analysis are unlikely to be affected by publication bias as revealed by the negative result of Egger’s test and the trim-and-fill analysis that did not suggest imputation of any additional study.
This meta-analysis suffers from several limitations. All eligible studies were of cross-sectional design, which, theoretically, limited any causal inference. However, income is a relatively stable variable through time and, which mitigates this limitation. Furthermore, only one-fifth of included studies performed a complete control for socio-demographic variables, and higher OR estimates were obtained from studies with incomplete adjustment than in studies with complete adjustment. This reveals that our findings could be overestimated due to incomplete adjustment. Additional studies that control adequately for all potentially related socio-demographic variables are needed to confirm our results. Also, one-sixth of studies did not employ a pretested or validated questionnaire to ascertain the exposure and the outcome. However, this was unlikely to affect our results as constraining the analysis to the remaining studies did not introduce any change in the overall effect.
Our analysis was based on random-effect models to account for heterogeneity between studies [56–58]. Heterogeneity was expected in our study due to difference in the defined levels of income, period of antibiotic use (for example, use in the past month [59], past 3 months [60] and past year [61]), and settings. Experts in meta-analysis emphasize that heterogeneity is the expectation in any meta-analysis rather than the exception [62] and that no amount of heterogeneity is considered unacceptable as long as the inclusion criteria are clearly defined and the data are correctly analysed [56].
Understanding the socioeconomic properties of antibiotic misuse is crucial to develop related intervention programs and health policies, yet addition of high-quality studies that control for socio-demographic and socio-economic indicators are needed to confirm our findings.
Acknowledgements
Mrs Narmeen Mallah received a Grant for her internship at Karolinska Institutet from Erasmus+ KA103 Erasmus European Mobility Program. The authors would like to thank to Mr. Luís Cea and Dr. Sami Ashour for their help with economic concepts.
Author contributions
NM and BT conceived the research idea, carried out the literature review and extracted the data. AF participated in quality assessment of retrieved studies. NM carried out data analysis and interpretation and designed and wrote the manuscript. BT and NO supervised data analyses. All authors reviewed and revised the manuscript and approved it for publication.
Funding
Open Access funding provided thanks to the CRUE-CSIC agreement with Springer Nature.
Data availability
The data generated and analyzed in the meta-analysis are included in the article. The data are available by accessing the cited references.
Declarations
Conflict of interest
The authors declare no conflict of interest.
Footnotes
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.Centers for Disease Control and Prevention: Antibiotic use questions and answers. https://www.cdc.gov/antibiotic-use/community/about/should-know.html#anchor_1572453021219 (2019). Accessed 21 Apr 2021
- 2.United Nations Office on Drugs and Crime: The non-medical use of prescription drugs: Poliy direction issues. https://www.unodc.org/documents/drug-prevention-and-treatment/nonmedical-use-prescription-drugs.pdf (2011). Accessed 20 Aug 2021
- 3.Morgan DJ, Okeke IN, Laxminarayan R, Perencevich EN, Weisenberg S. Non-prescription antimicrobial use worldwide: a systematic review. Lancet Infect. Dis. 2011;11(9):692–701. doi: 10.1016/S1473-3099(11)70054-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Gualano MR, Gili R, Scaioli G, Bert F, Siliquini R. General population's knowledge and attitudes about antibiotics: a systematic review and meta-analysis. Pharmacoepidemiol. Drug Saf. 2015;24(1):2–10. doi: 10.1002/pds.3716. [DOI] [PubMed] [Google Scholar]
- 5.Kardas P, Devine S, Golembesky A, Roberts C. A systematic review and meta-analysis of misuse of antibiotic therapies in the community. Int. J. Antimicrob. Agents. 2005;26(2):106–113. doi: 10.1016/j.ijantimicag.2005.04.017. [DOI] [PubMed] [Google Scholar]
- 6.Torres NF, Chibi B, Kuupiel D, Solomon VP, Mashamba-Thompson TP, Middleton LE. The use of non-prescribed antibiotics; prevalence estimates in low-and-middle-income countries. A systematic review and meta-analysis. Arch. Public Health. 2021;79(1):2. doi: 10.1186/s13690-020-00517-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Grigoryan L, Germanos G, Zoorob R, Juneja S, Raphael JL, Paasche-Orlow MK, et al. Use of antibiotics without a prescription in the U.S. population: a scoping review. Ann. Intern. Med. 2019;171(4):257–263. doi: 10.7326/M19-0505. [DOI] [PubMed] [Google Scholar]
- 8.Wellcome Trust: Review on antimicrobial resistance. Tackling drug-resistant infections globally: Final report and recommendations. https://amr-review.org/sites/default/files/160525_Final%20paper_with%20cover.pdf (2016). Accessed 21 Apr 2021
- 9.Centers for Disease Control and Prevention: Antibiotic resistance threats in the United States. www.cdc.gov/DrugResistance/Biggest-Threats.html (2019). Accessed 21 Apr 2021
- 10.European Center for Disease Prevention and Control & Organization for Economic Co-operation and Development: Antimicrobial resistance tackling the burden in the European Union. A Briefing note for EU/EEA countries. https://www.ecdc.europa.eu/en/antimicrobial-resistance (2019). Accessed 21 Apr 2021
- 11.Spellberg B, Blaser M, Guidos RJ, Boucher HW, Bradley JS, Eisenstein BI, et al. Combating antimicrobial resistance: policy recommendations to save lives. Clin. Infect. Dis. 2011;52(Suppl 5):S397–428. doi: 10.1093/cid/cir153. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.World Bank: Drug-resistant infections: A threat to our economic future. Washington, DC. https://documents.worldbank.org/en/publication/documents-reports/documentdetail/323311493396993758/final-report (2017). Accessed 21 Apr 2021
- 13.Alhomoud F, Aljamea Z, Almahasnah R, Alkhalifah K, Basalelah L, Alhomoud FK. Self-medication and self-prescription with antibiotics in the Middle East-do they really happen? A systematic review of the prevalence, possible reasons, and outcomes. Int J Infect Dis. 2017;57:3–12. doi: 10.1016/j.ijid.2017.01.014. [DOI] [PubMed] [Google Scholar]
- 14.Torres NF, Chibi B, Middleton LE, Solomon VP, Mashamba-Thompson TP. Evidence of factors influencing self-medication with antibiotics in low and middle-income countries: a systematic scoping review. Public Health. 2019;168:92–101. doi: 10.1016/j.puhe.2018.11.018. [DOI] [PubMed] [Google Scholar]
- 15.Ocan M, Obuku EA, Bwanga F, Akena D, Richard S, Ogwal-Okeng J, et al. Household antimicrobial self-medication: a systematic review and meta-analysis of the burden, risk factors and outcomes in developing countries. BMC Public Health. 2015;15:742. doi: 10.1186/s12889-015-2109-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Ilhan MN, Durukan E, Ilhan SO, Aksakal FN, Ozkan S, Bumin MA. Self-medication with antibiotics: questionnaire survey among primary care center attendants. Pharmacoepidemiol. Drug Saf. 2009;18(12):1150–1157. doi: 10.1002/pds.1829. [DOI] [PubMed] [Google Scholar]
- 17.Pan H, Cui B, Zhang D, Farrar J, Law F, Ba-Thein W. Prior knowledge, older age, and higher allowance are risk factors for self-medication with antibiotics among university students in southern China. PLoS ONE. 2012;7(7):e41314. doi: 10.1371/journal.pone.0041314. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Rathish D, Wickramasinghe ND. Prevalence, associated factors and reasons for antibiotic self-medication among dwellers in Anuradhapura: a community-based study. Int. J. Clin. Pharm. 2020;42(4):1139–1144. doi: 10.1007/s11096-020-01065-6. [DOI] [PubMed] [Google Scholar]
- 19.Bogale AA, Amhare AF, Chang J, Bogale HA, Betaw ST, Gebrehiwot NT, et al. Knowledge, attitude, and practice of self-medication with antibiotics among community residents in Addis Ababa, Ethiopia. Expert Rev. Anti Infect Ther. 2019;17(6):459–466. doi: 10.1080/14787210.2019.1620105. [DOI] [PubMed] [Google Scholar]
- 20.Peng D, Wang X, Xu Y, Sun C, Zhou X. Antibiotic misuse among university students in developed and less developed regions of China: a cross-sectional survey. Glob. Health Action. 2018;11(1):1496973. doi: 10.1080/16549716.2018.1496973. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Aleem MA, Rahman M, Ishfaq M, Mehmood K, Ahmed SS. Determinants of antibiotics misuse by the parents in children: a survey from Northern Region of Saudi Arabia. Bangladesh J. Child Health. 2016;40(2):64–71. doi: 10.3329/bjch.v40i2.31560. [DOI] [Google Scholar]
- 22.Hu J, Wang Z. In-home antibiotic storage among Australian Chinese migrants. Int. J. Infect. Dis. 2014;26:103–106. doi: 10.1016/j.ijid.2014.04.017. [DOI] [PubMed] [Google Scholar]
- 23.Grigoryan L, Monnet DL, Haaijer-Ruskamp FM, Bonten MJ, Lundborg S, Verheij TJ. Self-medication with antibiotics in Europe: a case for action. Curr. Drug Saf. 2010;5(4):329–332. doi: 10.2174/157488610792246046. [DOI] [PubMed] [Google Scholar]
- 24.De Sanctis V, Soliman AT, Daar S, Di Maio S, Elalaily R, Fiscina B, et al. Prevalence, attitude and practice of self-medication among adolescents and the paradigm of dysmenorrhea self-care management in different countries. Acta Biomed. 2020;91(1):182–192. doi: 10.23750/abm.v91i1.9242. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Xu R, Mu T, Wang G, Shi J, Wang X, Ni X. Self-medication with antibiotics among university students in LMIC: a systematic review and meta-analysis. J. Infect. Dev. Countries. 2019;13(8):678–689. doi: 10.3855/jidc.11359. [DOI] [PubMed] [Google Scholar]
- 26.Bulabula ANH, Dramowski A, Mehtar S. Antibiotic use in pregnancy: knowledge, attitudes and practices among pregnant women in Cape Town South Africa. J. Antimicrob. Chemother. 2020;75(2):473–481. doi: 10.1093/jac/dkz427. [DOI] [PubMed] [Google Scholar]
- 27.Wang X, Lin L, Xuan Z, Li L, Zhou X. Keeping antibiotics at home promotes self-medication with antibiotics among Chinese university students. Int. J. Environ. Res. Public Health. 2018;15(4):687. doi: 10.3390/ijerph15040687. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Xu Y, Lu J, Sun C, Wang X, Hu YJ, Zhou X. A cross-sectional study of antibiotic misuse among Chinese children in developed and less developed provinces. J. Infect. Dev. Countries. 2020;14(2):129–137. doi: 10.3855/jidc.11938. [DOI] [PubMed] [Google Scholar]
- 29.Jamhour A, El-Kheir A, Salameh P, Hanna PA, Mansour H. Antibiotic knowledge and self-medication practices in a developing country: a cross-sectional study. Am. J. Infect. Control. 2017;45(4):384–388. doi: 10.1016/j.ajic.2016.11.026. [DOI] [PubMed] [Google Scholar]
- 30.The World Bank: Metadata glossary. https://databank.worldbank.org/metadataglossary/world-development-indicators/series/NY.ADJ.NNTY.CD. Accessed 1 Mar 2021
- 31.The World Bank: Price level ratio of PPP conversion factor (GDP) to market exchange rate. https://data.worldbank.org/indicator/PA.NUS.PPPC.RF?view=chart. Accessed 8 Feb 2021
- 32.The World Bank: GDP per capita, PPP (current international $). https://data.worldbank.org/indicator/NY.GDP.PCAP.PP.CD. Accessed 8 Feb 2021
- 33.The World Bank: Adjusted net national income per capita (current US$). https://data.worldbank.org/indicator/NY.ADJ.NNTY.PC.CD. Accessed 8 Feb 2021
- 34.The World Bank: World Bank country and lending groups, country classification. https://datahelpdesk.worldbank.org/knowledgebase/articles/906519-world-bank-country-and-lending-groups. Accessed 24 Feb 2021
- 35.World Health Organization: Countries. https://www.who.int/countries/. Accessed 18 Feb 2021
- 36.United Nations Educational Scientific and Cultural Organization: Education and literacy. http://uis.unesco.org/en/country/lb (2018). Accessed 21 Apr 2021
- 37.Orsini N. Weighted mixed-effects dose-response models for tables of correlated contrasts. Stata J. 2021;21:320. doi: 10.1177/1536867X211025798. [DOI] [Google Scholar]
- 38.Crippa A, Discacciati A, Bottai M, Spiegelman D, Orsini N. One-stage dose-response meta-analysis for aggregated data. Stat. Methods Med. Res. 2019;28(5):1579–1596. doi: 10.1177/0962280218773122. [DOI] [PubMed] [Google Scholar]
- 39.World Health Organization: Global action plan on antimicrobial resistance. https://www.who.int/antimicrobial-resistance/publications/global-action-plan/en/. (2015). Accessed 21 Apr 2021 [DOI] [PubMed]
- 40.Modesti PA, Reboldi G, Cappuccio FP, Agyemang C, Remuzzi G, Rapi S, et al. Panethnic differences in blood pressure in Europe: a systematic review and meta-analysis. PLoS ONE. 2016;11(1):e0147601. doi: 10.1371/journal.pone.0147601. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Egger M, Davey Smith G, Schneider M, Minder C. Bias in meta-analysis detected by a simple, graphical test. BMJ. 1997;315(7109):629–634. doi: 10.1136/bmj.315.7109.629. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Duval S, Tweedie R. Trim and fill: a simple funnel-plot-based method of testing and adjusting for publication bias in meta-analysis. Biometrics. 2000;56(2):455–463. doi: 10.1111/j.0006-341x.2000.00455.x. [DOI] [PubMed] [Google Scholar]
- 43.Chen J, Sidibi AM, Shen X, Dao K, Maiga A, Xie Y, et al. Lack of antibiotic knowledge and misuse of antibiotics by medical students in Mali: a cross-sectional study. Expert Rev. Anti Infect. Ther. 2020;19:1–8. doi: 10.1080/14787210.2021.1857731. [DOI] [PubMed] [Google Scholar]
- 44.Mate I, Come CE, Goncalves MP, Cliff J, Gudo ES. Knowledge, attitudes and practices regarding antibiotic use in Maputo City, Mozambique. PLoS ONE. 2019;14(8):e0221452. doi: 10.1371/journal.pone.0221452. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Torres KS, Ochoa A, Encalada D, Quizhpe A. Prevalence of self-medication with antibiotics in the urban parishes of the city of Cuenca, 2016–2017 [Prevalencia de la automedicacion con antibioticos en las parroquias urbanas de la ciudad de Cuenca, 2016–2017] Archivos Venezolanos de Farmacología y Terapéutica. 2017;36(4):130–136. [Google Scholar]
- 46.Redzic L, Zalihic A. Self-medication with antibiotics in family practice in patients and parents [Samomedikacija antibioticima među pacijentima] Croat. J. Infect. [Infektološki glasnik] 2018;38(3):69–73. [Google Scholar]
- 47.Chang FR, Trivedi PK. Economics of self-medication: theory and evidence. Health Econ. 2003;12(9):721–739. doi: 10.1002/hec.841. [DOI] [PubMed] [Google Scholar]
- 48.Mielck A, Kiess R, von dem Knesebeck O, Stirbu I, Kunst AE. Association between forgone care and household income among the elderly in five Western European countries–analyses based on survey data from the SHARE-study. BMC Health Serv. Res. 2009;9:52. doi: 10.1186/1472-6963-9-52. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Mojtabai R, Olfson M. Medication costs, adherence, and health outcomes among Medicare beneficiaries. Health Aff. (Millwood) 2003;22(4):220–229. doi: 10.1377/hlthaff.22.4.220. [DOI] [PubMed] [Google Scholar]
- 50.Piette JD, Heisler M, Wagner TH. Cost-related medication underuse among chronically ill adults: the treatments people forgo, how often, and who is at risk. Am. J. Public Health. 2004;94(10):1782–1787. doi: 10.2105/ajph.94.10.1782. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 51.Renahy E, Parizot I, Chauvin P. Health information seeking on the Internet: a double divide? Results from a representative survey in the Paris metropolitan area, France, 2005–2006. BMC Public Health. 2008;8:69. doi: 10.1186/1471-2458-8-69. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Vanhaesebrouck A, Vuillermoz C, Robert S, Parizot I, Chauvin P. Who self-medicates? Results from structural equation modeling in the Greater Paris area, France. PLoS ONE. 2018;13(12):e0208632. doi: 10.1371/journal.pone.0208632. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 53.World Health Organization: Global spending on health: a world in transition. https://www.who.int/health_financing/documents/health-expenditure-report-2019/en/. (2019). Accessed 21 April 2021
- 54.Batista AD, Rodrigues DA, Figueiras A, Zapata-Cachafeiro M, Roque F, Herdeiro MT. Antibiotic dispensation without a prescription worldwide: a systematic review. Antibiotics (Basel) 2020;9(11):786. doi: 10.3390/antibiotics9110786. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55.Interagency Coordination Group on Antimicrobial Resistance: No time to wait: Securing the future from drug-resistant infections. Report to the secretary-general of the United Nations.: World Health Organization. https://www.who.int/antimicrobial-resistance/interagency-coordination-group/final-report/en/. (2019). Accessed 21 Apr 2021
- 56.Higgins JP. Commentary: heterogeneity in meta-analysis should be expected and appropriately quantified. Int. J. Epidemiol. 2008;37(5):1158–1160. doi: 10.1093/ije/dyn204. [DOI] [PubMed] [Google Scholar]
- 57.National Research Council . Combining Information: Statistical Issues and Opportunities for Research. Washington, DC: The National Academies Press; 1992. [Google Scholar]
- 58.Murad MH, Montori VM, Ioannidis JPA, et al. Fixed-effects and random-effects models. In: Guyatt G, Rennie D, Meade MO, et al., editors. Users’ Guide to the Medical Literature A Manual for Evidence-Based Clinical Practice. 3. New York: McGraw-Hill; 2015. p. 885. [Google Scholar]
- 59.Mallah N, Badro DA, Figueiras A, Takkouche B. Association of knowledge and beliefs with the misuse of antibiotics in parents: a study in Beirut (Lebanon) PLoS ONE. 2020;15(7):e0232464. doi: 10.1371/journal.pone.0232464. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 60.Abdelrahman TM, Al Saeed MS, Karam RA, Alkhthami AM, Alswat OB, Alzahrani AA, et al. Misuse of antibiotics and antibiotic resistance: a public population-based health survey in al Taif- Saudi Arabia. WJPMR. 2017;3(2):54–62. [Google Scholar]
- 61.Abobotain AH, Sheerah HA, Alotaibi FN, Joury AU, Mishiddi RM, Siddiqui AR, et al. Socio-demographic determinants of antibiotic misuse in children. A survey from the central region of Saudi Arabia. Saudi Med. J. 2013;34(8):832–840. [PubMed] [Google Scholar]
- 62.Berlin JA. Invited commentary: benefits of heterogeneity in meta-analysis of data from epidemiologic studies. Am. J. Epidemiol. 1995;142(4):383–387. doi: 10.1093/oxfordjournals.aje.a117645. [DOI] [PubMed] [Google Scholar]
- 63.Moktan D, Shehnaz SI. Factors driving self-medication with antimicrobials in Karaikal, Puducherry India. J. Pharmacol. Pharmacother. 2021;11:64–71. doi: 10.4103/jpp.JPP_21_20. [DOI] [Google Scholar]
- 64.Elmahi OKO, Balla SA, Khalil HA. Self-medication with antibiotics and its predictors among the population in Khartoum Locality, Khartoum State, Sudan in 2018. Int. J. Trop. Dis. Health. 2020;41(4):17–25. doi: 10.9734/IJTDH/2020/v41i430267. [DOI] [Google Scholar]
- 65.Nusair MB, Al-Azzam S, Alhamad H, Momani MY. The prevalence and patterns of self-medication with antibiotics in Jordan: a community-based study. Int. J. Clin. Pract. 2021;75:e13665. doi: 10.1111/ijcp.13665. [DOI] [PubMed] [Google Scholar]
- 66.Ateshim Y, Bereket B, Major F, Emun Y, Woldai B, Pasha I, et al. Prevalence of self-medication with antibiotics and associated factors in the community of Asmara, Eritrea: a descriptive cross sectional survey. BMC Public Health. 2019;19(1):726. doi: 10.1186/s12889-019-7020-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 67.Benameur T, Al-Bohassan H, Al-Aithan A, Al-Beladi A, Al-Ali H, Al-Omran H, et al. Knowledge, attitude, behaviour of the future healthcare professionals towards the self-medication practice with antibiotics. J. Infect. Dev. Countries. 2019;13(1):56–66. doi: 10.3855/jidc.10574. [DOI] [PubMed] [Google Scholar]
- 68.Mukattasha TL, Alkhatatbeha MJ, Andrawosa S, Jaraba AS, AbuFarhab RK, Nusair MB. Parental self-medication of antibiotics for children in Jordan. JPHSR. 2019 doi: 10.1111/jphs.12331. [DOI] [Google Scholar]
- 69.Sun C, Hu YJ, Wang X, Lu J, Lin L, Zhou X. Influence of leftover antibiotics on self-medication with antibiotics for children: a cross-sectional study from three Chinese provinces. BMJ Open. 2019;9(12):e033679. doi: 10.1136/bmjopen-2019-033679. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 70.Hu Y, Wang X, Tucker JD, Little P, Moore M, Fukuda K, et al. Knowledge, attitude, and practice with respect to antibiotic use among Chinese medical students: a multicentre cross-sectional study. Int. J. Environ. Res. Public Health. 2018;15(6):1165. doi: 10.3390/ijerph15061165. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 71.Tong S, Pan J, Lu S, Tang J. Patient compliance with antimicrobial drugs: a Chinese survey. Am. J. Infect. Control. 2018;46(4):e25–e29. doi: 10.1016/j.ajic.2018.01.008. [DOI] [PubMed] [Google Scholar]
- 72.Albawani SM, Hassan YB, Abd-Aziz N, Gnanasan S. Self-medication with antibiotics in Sana’a City, Yemen. Trop. J. Pharm. Res. 2017;16(5):1195. doi: 10.4314/tjpr.v16i5.30. [DOI] [Google Scholar]
- 73.Erku DA, Mekuria AB, Belachew SA. Inappropriate use of antibiotics among communities of Gondar town, Ethiopia: a threat to the development of antimicrobial resistance. Antimicrob. Resist. Infect. Control. 2017;6:112. doi: 10.1186/s13756-017-0272-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 74.Gebrekirstos NH, Workneh BD, Gebregiorgis YS, Misgina KH, Weldehaweria NB, Weldu MG, et al. Non-prescribed antimicrobial use and associated factors among customers in drug retail outlet in Central Zone of Tigray, Northern Ethiopia: a cross-sectional study. Antimicrob. Resist. Infect. Control. 2017;6:70. doi: 10.1186/s13756-017-0227-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 75.Gillani AH, Ji W, Hussain W, Imran A, Chang J, Yang C, et al. Antibiotic self-medication among non-medical university students in Punjab, Pakistan: a cross-sectional survey. Int. J. Environ. Res. Public Health. 2017;14(10):1152. doi: 10.3390/ijerph14101152. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 76.Hassali MA, Arief M, Saleem F, Khan MU, Ahmad A, Mariam W, et al. Assessment of attitudes and practices of young Malaysian adults about antibiotics use: a cross-sectional study. Pharm. Pract. (Granada) 2017;15(2):929. doi: 10.18549/PharmPract.2017.02.929. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 77.Kajeguka DC, Moses EA. Self-medication practices and predictors for self-medication with antibiotics and antimalarials among community in Mbeya City, Tanzania. Tanzan. J. Health Res. 2017 doi: 10.4314/thrb.v19i4.6. [DOI] [Google Scholar]
- 78.Kurniawan K, Posangi J, Rampengan N. Association between public knowledge regarding antibiotics and self-medication with antibiotics in Teling Atas Community Health Center East Indonesia. Med. J. Indones. 2017;25:62–69. doi: 10.13181/mji.v26i1.1589. [DOI] [Google Scholar]
- 79.Nuñez M, Tresierra-Ayalab M, Gil-Olivares F. Antibiotic self-medication in university students from Trujillo, Peru. Medicina Universitaria. 2017;18(73):205–209. doi: 10.1016/j.rmu.2016.10.003. [DOI] [Google Scholar]
- 80.Senadheera GP, Sri Ranganathan S, Gunawardane NS, Fernando GH, Fernandopulle BM. Practice of self-medication with antibiotics in the Colombo district, Sri Lanka. Ceylon Med. J. 2017;62(1):70–72. doi: 10.4038/cmj.v62i1.8439. [DOI] [PubMed] [Google Scholar]
- 81.Bilal M, Haseeb A, Khan MH, Arshad MH, Ladak AA, Niazi SK, et al. Self-medication with antibiotics among people dwelling in rural areas of Sindh. J. Clin. Diagn. Res. 2016;10(5):08–13. doi: 10.7860/JCDR/2016/18294.7730. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 82.Zhu X, Pan H, Yang Z, Cui B, Zhang D, Ba-Thein W. Self-medication practices with antibiotics among Chinese university students. Public Health. 2016;130:78–83. doi: 10.1016/j.puhe.2015.04.005. [DOI] [PubMed] [Google Scholar]
- 83.Ding L, Sun Q, Sun W, Du Y, Li Y, Bian X, et al. Antibiotic use in rural China: a cross-sectional survey of knowledge, attitudes and self-reported practices among caregivers in Shandong province. BMC Infect Dis. 2015;15:576. doi: 10.1186/s12879-015-1323-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 84.Gebeyehu E, Bantie L, Azage M. Inappropriate use of antibiotics and its associated factors among urban and rural communities of Bahir Dar City administration, Northwest Ethiopia. PLoS ONE. 2015;10(9):e0138179. doi: 10.1371/journal.pone.0138179. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 85.Yousif MA, Abubaker IE. Prevalence, determinants and practices of self-medication with antibiotics: a population based survey in Taif, Kingdom of Saudi Aarabiaksa. Int. J. Res. Pharm. Sci. 2015;5(2):51–56. [Google Scholar]
- 86.Cheaito L, Azizi S, Saleh N, Salameh P. Assessment of self-medication in population buying antibiotics in pharmacies: a pilot study from Beirut and its suburbs. Int. J. Public Health. 2014;59(2):319–327. doi: 10.1007/s00038-013-0493-y. [DOI] [PubMed] [Google Scholar]
- 87.Eticha T, Araya H, Alemayehu A, Solomon G, Ali D. Prevalence and predictors of selfmedication with antibiotics among Adi-haqi Campus students of Mekelle University, Ethiopia. IJPSR. 2014;5(10):678. [Google Scholar]
- 88.Lv B, Zhou Z, Xu G, Yang D, Wu L, Shen Q, et al. Knowledge, attitudes and practices concerning self-medication with antibiotics among university students in western China. Trop. Med. Int. Health. 2014;19(7):769–779. doi: 10.1111/tmi.12322. [DOI] [PubMed] [Google Scholar]
- 89.Mihretie TM. Self-Medication Practices with Antibiotics Among Urban Dwellers of Bahir Dar Town, North West Ethiopia. Addis Ababa: Addis Ababa University; 2014. [Google Scholar]
- 90.Shah SJ, Ahmad H, Rehan RB, Najeeb S, Mumtaz M, Jilani MH, et al. Self-medication with antibiotics among non-medical university students of Karachi: a cross-sectional study. BMC Pharmacol. Toxicol. 2014;15:74. doi: 10.1186/2050-6511-15-74. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 91.Widayati A, Suryawati S, de Crespigny C, Hiller JE. Self medication with antibiotics in Yogyakarta City Indonesia: a cross sectional population-based survey. BMC Res. Notes. 2011;4:491. doi: 10.1186/1756-0500-4-491. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 92.Hadi U, Duerink DO, Lestari ES, Nagelkerke NJ, Werter S, Keuter M, et al. Survey of antibiotic use of individuals visiting public healthcare facilities in Indonesia. Int. J. Infect. Dis. 2008;12(6):622–629. doi: 10.1016/j.ijid.2008.01.002. [DOI] [PubMed] [Google Scholar]
- 93.Al-Azzam SI, Al-Husein BA, Alzoubi F, Masadeh MM, Al-Horani MA. Self-medication with antibiotics in Jordanian population. Int. J. Occup. Med. Environ. Health. 2007;20(4):373–380. doi: 10.2478/v10001-007-0038-9. [DOI] [PubMed] [Google Scholar]
- 94.Sawair FA, Baqain ZH, Abu Karaky A, Abu ER. Assessment of self-medication of antibiotics in a Jordanian population. Med. Princ. Pract. 2009;18(1):21–25. doi: 10.1159/000163041. [DOI] [PubMed] [Google Scholar]
- 95.Awad A, Eltayeb I, Matowe L, Thalib L. Self-medication with antibiotics and antimalarials in the community of Khartoum State, Sudan. J. Pharm Pharm Sci. 2005;8(2):326–331. [PubMed] [Google Scholar]
Associated Data
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Data Availability Statement
The data generated and analyzed in the meta-analysis are included in the article. The data are available by accessing the cited references.