A Cross-Sectional Study of Antibiotic Self-Medication

authors:

avatar Fatemeh Mousavi ORCID 1 , avatar Parisa Shojaei ORCID 1 , * , avatar Azadeh Nazemi 2 , avatar Atefe Dadashi 3

Department of Community and Preventive Medicine, Faculty of Medicine, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran
Department of Computer Science and Engineering and IT, Shiraz University, Shiraz, Iran
Science and Research, Azad University, Tehran, Iran

how to cite: Mousavi F, Shojaei P, Nazemi A, Dadashi A. A Cross-Sectional Study of Antibiotic Self-Medication. Thrita. 2020;9(1):e105794. https://doi.org/10.5812/thrita.105794.

Abstract

Objectives:

This research has been conducted to study antibiotic self-medication, prevalence, and reasons.

Methods:

A questionnaire containing 30 comprehensive questions in terms of the experience of antibiotic self-medication was prepared. In this cross-sectional study, data were analyzed using analytical statistics bases on chi-square and logistic regression.

Results:

The results showed that 61.3% of the participants were self-antibiotic users. There was a significant difference only between gender and self-medication such that self-medication in males was more than females (P value = 0.027).

Conclusions:

Self-medication of antibiotics is almost high and requires more information about the side effects of these drugs in order to promote rational and physically prescribed use.

1. Background

Globally, antibiotics are one of the most commonly used medicines, specifically in developing countries where infectious diseases are still the most common cause of death (1). Self-medication refers to any attempt for self-treatment after self-diagnosis of the health issue or medical problem by taking medicines without any professional advice or authorized prescriptions (2). This type of medical solution is pervasive in most parts of the world, and 50% of all used antibiotics are purchased without any prescription (3). Antibiotic self-medication may lead to health hazards in developing countries that face poverty, inaccessibility, lack of medical professionals, poor quality of health equipment, irregular distribution of medicines, and decreasing patients’ trust in physicians (4). Considering the rapid growth of microbial resistance to antibiotics (5-7), the World Health Organization (WHO) has begun implementing a global program entitled Microbial Resistance to Microorganisms in 2001 (8). Despite these WHO activities, the use of antibiotics without prescriptions is increasing in developing countries (9).

Taking an inappropriate antibiotic and improper antibiotic usage may cause (1) microbial resistance, (2) spreading of some diseases such as pseudo-membranous colitis, (3) economically negative impact (8). Researchers previously found that self-treatment with antibiotics had a significant relationship with age, income, education, and patient satisfaction of former effective usage (10, 11). It can be the result of patients’ experience of the effectiveness of previous treatment (10). Increasing public knowledge of antibiotic treatment plays an important role in decreasing antibiotic resistance (12, 13). General awareness of antibiotic resistance in countries with high antibiotic resistance is not reasonable.

2. Objectives

considering the current situation of antibiotic resistance and demographic characteristics of visitors of a medical center located in the Northwest of Tehran, this research was conducted to investigate antibiotic self-treatment in the community.

3. Methods

This study was conducted to investigate antibiotic self-treatment in the community, initially considering the current situation of antibiotic resistance and the patients’ demographic characteristics of a medical center in the Northwest of Tehran. Three questionnaires were designed based on demographic characteristics of gender, occupation, education, marital status and health insurance (five questions), general knowledge about antibiotics (five questions), and the experience of antibiotics self-medication (24 questions). Between questionnaires 2 and 3, there is a filtering question of whether or not the participant has the experience of antibiotic self-medication. Based on the response to this question, the participants were categorized into two groups. If the answer was negative, so there was no need to answer the rest of the questions around the antibiotics self-medication in questionnaire 3. Otherwise, they have been asked to complete the questionnaire 3 that included 24 multiple-choice questions. To respond to some questions, the participants have the option to select more than one choice, such as experienced side effects or the type of used antibiotics. In this study, the participants who had experiences of antibiotic self-medication were called group two. All participants were informed of the method, background, target, implementation, information confidentiality, and releasing results conditions and completed written informed consent form before the study.

3.1. Statistical Analysis

Categorical variables were expressed as frequencies, whereas numerical variables (age) were presented as means and standard deviation (SD) as data were normally distributed. We used the chi-square test (Fisher’s exact) for comparing the study variables such as gender, education level, marital status, insurance status, and occupation. Based on collected data, at least 1,024 records were required to make a predictable model, and 434 records were not sufficient for this purpose. All statistical analyses were performed using STATA software (version 22), and only p-values less than 0.05 were considered significant.

4. Results

The average age of participants was between 23 and 49, and most of them were married and high-educated. The participants were asked what the main side effect or adverse reaction of antibiotics was. The first group without antibiotic self-medication experience declared vaginal thrush and antibiotic resistance as antibiotic side effects. The second group who experienced antibiotic self-medication pointed to nausea and vomiting as antibiotics side effects.

As the first row of Figure 1 illustrates, 61.3% of the participants had the experience of antibiotics self-medication (group 2). Moreover, 0.85% of the group 2 kept some medicines at home (second row), and 54.9 % of them recommend the used antibiotic to others (third row). The reason for antibiotic self-medication for 66.2%of them was convenience, for 23.3% of them were cost-saving, and for 11.4% was the lack of trust in physicians (last row). As Figure 2 illustrates, 46.6% sometimes switched antibiotics, and their reason was lack of efficiency. 45.9% never switched antibiotics (left) 60.2% had the experience of taking the same medicines with different names at the same time (right). When the participants were asked about the efficiency of antibiotic self-medication, 48.1% believed that it was inefficient, 16.5% were not sure, while 35.3% found it efficient (Figure 3). Figure 4 on the left side shows that 65% know about side effects, whereas the right side indicates that 75% believe antibiotics affect bacterial infections. Figure 5 illustrates 144 out of 266 participants of the group two switched to other antibiotics, it also shows their reasons. Figure 6 illustrates 128 out of 266 participants of the group two changed the dosage of antibiotics, it also shows their reasons. Correspondingly, 56.6% never changed the dosage of antibiotics deliberately, while 36.9% occasionally changed the dosage. Condition improvement was their reason for changing the dosage. Figure 7 illustrates the antibiotic providers for 266 participants of the group two. Accordingly, 83.5% usually provided antibiotics from community pharmacies, while 23.8% used leftover medicine.

Self-medication population, keeping medicine at home, medication. Recommendation to others, antibiotics self-medication reason.
Self-medication population, keeping medicine at home, medication. Recommendation to others, antibiotics self-medication reason.
Left-switch antibiotics, same antibiotics type different names-right.
Left-switch antibiotics, same antibiotics type different names-right.
Evaluation-top-the efficiency of antibiotic self-medication, bottom-fighting against infections.
Evaluation-top-the efficiency of antibiotic self-medication, bottom-fighting against infections.
Knowledge-side effects-left-effects with antibiotics-right.
Knowledge-side effects-left-effects with antibiotics-right.
Here, 144 participants switched to another antibiotic.
Here, 144 participants switched to another antibiotic.
Here, 128 participants changed the dosage of antibiotics.
Here, 128 participants changed the dosage of antibiotics.
Shows antibiotic provider for self-medication.
Shows antibiotic provider for self-medication.

Figure 8 illustrates 144 out of 266 participants of the group two had adverse reaction experiences and what they did after these experiences. Most participants stopped taking medicines after an adverse reaction. In this study, 71.4% of self-medicated participants (group 2) used antibiotics to treat sore throat, 51.2% of them in the self-medication group chose the medicines for treatment based on the last prescribed medicine, and 45.6% relied on their own former experience. In selecting antibiotics, 53.4% considered the type of medicines, 56.6 % occasionally checked the instructions on the medicine package, 30.3% always checked this instruction, 53% of the group two participants fully understood the instructions, 35.9% partially understood, and 11.1% did not understand at all. Also, 46.6% stopped taking antibiotics when their illness symptoms disappeared (19.5%). Amoxicillin, Co-amoxiclav, and Cefixime were the most common antibiotics used, respectively. Table 1 summarizes the comparison of different five factors, including gender, occupation, education, marital status, and health insurance cover in the self-medication and non-self-medication groups. These results were not significant at P < 0.05.

Indicates 144 participants’ actions after an adverse reaction.
Indicates 144 participants’ actions after an adverse reaction.
Table 1.

The Comparison of Different Variables in the Two Groups of Antibiotic Self-Medication and Non-Self-Medication

Variable Non Self-Medication, No. (%)Self-Medication, No. (%)TotalChi-SquareP Value
Gender1.210.027
Male122 (116.45) [0.26]68 (73.55) [.42]190
Female144 (149.55) [0.21]100 (94.45) [0.33]244
Occupation0.120.72
Medical100 (101.74) [0.03]66 (64.26) [0.05]166
Non-medical166 (164.26) [0.02]102 (103.74) [0.03]268
Health insurance0.1070.74
Yes234 (232.9) [0.01]146 (147.1) [0.01]380
No32 (33.1) [0.04]22 (20.9) [0.06]54
Marital status3.310.19
Married148 (142.85) [0.19]84 (89.15) [0.30]232
Widow14 (18.47) [1.08]16 (11.53) [1.74]30
Single104 (104.68) [0.00]66 (65.32) [0.01]170
Education5.640.059
Undergrad10 (9.81) [0.00]6 (6.19) [0.01]16
Graduated50 (60.06) [1.69]48 (37.94) [2.67]98
Post-grad206 (196.13) [0.50]114 (123.87) [0.79]320

5. Discussion

Most researchers focused on patients’ views and their opinions regarding antibiotic self-medication (14-17). Healthcare professionals and medical advisers, particularly pharmacists, play a significant role in modifying these beliefs and habits (18). The frequency of self-medication in this survey (61.3%) was more than the mean estimation of antimicrobial self-medication in the countries with low and middle-range income (38.8%) (15).

5.1. Prevalence Variation

The results of recent research indicate that the prevalence of self-medication varies between 7.3% to 85.59%, with an overall prevalence of 42.64% (19).

5.2. Reasons for Prevalence Variation

The reasons for this prevalence variation are differences in social determinants of health, tradition, culture, economic, developmental status, socioeconomic culture, personal traits, and the healthcare system (20, 21). On the other hand, methodology, study prevalence variation, sample population, and recall time may cause this variation. The other series of parameters for the prevalence of self-medication include the short distance between pharmacies and residential area or long distance to the healthcare facility, negligence, minor illness, inappropriate attitude of health workers (impolite, corrupt, unclean), re-treatment of similar disease, and lack of health personnel (19).

5.3. Variation

Research results of Aziz et al. (2018) confirmed the researches findings in developing countries (18). Based on these researches, the prevalence of antibiotic self-medication is 17% in Pavyde et al. (15), 52% in Kandelaki et al. (19), 4.4% in Widayati et al. (20), and 3.4% in Gilani et al. studies (21).

5.4. Age

In our study, antibiotic self-medication had no significant relationship with age. In the study of Al-Azzam et al. in Jordan, the highest frequency of antibiotic self-medication was at 18 to 39 years. Study results of Bulario et al. (2018) indicated that age was the only factor significantly associated with antibiotic self-medication (22, 23).

5.5. Children

Based on studies of Togoobaatar et al. and Alele, treating a child with a non-prescribed antibiotic is increased with the child’s age (24, 25). The reason underlying this increase is mothers’ cautiousness and fears to take medicines for infants or early-stage children. Alele (25) described since mothers are cautious, or have various fears to take medicines for infants or early-stage children, so antibiotic self-medication increases with the child’s age.

5.6. Knowledge

According to reports of studies, mothers without jobs and mothers with higher education without any health insurance cover more than mothers who employed attempt to treat their children by antibiotic self-medication. Based on Lithuania’s research, there is no relation between knowledge about antibiotics and self-medication (16). On the other hand, free study results in the USA indicate that the lack of sufficient knowledge is one of the reasons behind antibiotics self-medication (26).

5.7. Gender

In our study, the rate of antibiotic self-medication in the male population is 64.2%, and in the women population, is 59.1%. These results were confirmed by Grigoryan et al. (27) and Widayati et al. (28). They established that antibiotic self-medication in men population is higher than the women population.

5.8. Cause

The most common cause of self-medication in our study is the ease of access to these medicines. Whereas, Horumpende et al. confirmed that the lack of knowledge, the urgent need to treat illness, and the expense of access to health requirements lead to self-using of antibiotics (29). In the Ershadpour survey, most people believe that there is no risk for antibiotic self-medication (30). Some of the other reasons for antibiotic self-medication in Iran are patients’ lack of trust in the quality of medicine, preferring the imported brand and the availability of over the counterantibiotics (29). The result of our study showed that 46.6% of the participants stopped taking antibiotics when their symptoms had disappeared. Many researchers studied to find out why people stop taking medicines after their symptoms disappeared. Their results indicate that people have not sufficient knowledge about improper treatment taking antibiotics and adverse reactions caused by it (31).

5.9. Affect

In the current study, 73% of participants in the group two believe that antibiotics can affect bacterial infections. Ekambi et al. and Bulario et al. (2018) have reported that in the opinion of 74.7 % of their survey participants, antibiotics have affected bacterial infection (20, 23). Generally, most people do not have accurate and comprehensive information regarding antibiotics, their properties, side effect, and fighting against microbes and infections (20). A community-based study in developing countries has reported that most adult people believe that bacteria and viruses are the same, and antibiotics can kill both of them (32).

5.10. Type

The most commonly used antibiotic in our study was amoxicillin, which is consistent with the results of the Nepal (1), whereas, in the study of Ajibola et al., the most common antibiotic was ampicillin (33).

5.11. Health Issue

In our study, most people took antibiotics to treat sore throat, and the most common side effect was nausea. According to the study by Bulario et al., most participants took antibiotics for fever, cough, and cold (23). According to Horumpende et al. research, in Barangay Tandang Sora, Quezon City cough, throat irritation, fever, and gastrointestinal tract diseases such as diarrhea and vomiting mostly make people take antibiotics without physician advice (29). Based on Gebeyehu study, health issues, which lead people to take antibiotics without prescription are tract symptoms (74.6%), diarrhea (74.4%), and physical injury/wound (64.3%), respectively (31).

In fact, self-medication has some advantages for healthcare systems in some cases. It may reduce pressure on medical services, leading to optimal utilization of facilities and clinical skills. These clinical skills are associated with general practitioners and specialist pharmacists, paramedics, and those who prescribe medicines. Antibiotic resistance is a modern medical challenge (15, 17, 34); thus, the prevalence of antibiotics self-medication needs to be controlled. Nowadays, due to the access to all available information on the internet, some patients tend to use self-medications. The lack of knowledge of some patients about some medicines, the treatment period, and its side effects may increase the risk of self-medication. Totally, 61.3% of the participants of the present study had the experience of self-medication with antibiotics. It means almost a large number of people prescribe and consume antibiotics for themselves without authorized prescriptions and they do not need it. Although most of them evaluate that the final treatment result was not successful, the lack of knowledge of some patients about some medicines, the treatment period, and its side effects may increase the risk of self-medication (20, 35).

5.12. Conclusion

Antibiotic self-medication can cause some severe adverse reactions. Obtained results from participants’ responses highlighted the role of local community pharmacy as an available and reliable health advisor and medicine supplier. In conclusion, pharmacies can support community health by providing medicine leaflets. These leaflets include information about the proper dosage of medicine, instruction, the treatment period, side effects, and adverse reactions.

Acknowledgements

References

  • 1.

    Nepal G, Bhatta S. Self-medication with antibiotics in WHO Southeast Asian Region: a systematic review. Cureus. 2018;10(4).

  • 2.

    Hart CA, Kariuki S. Antimicrobial resistance in developing countries. Bmj. 1998;317(7159):647-50.

  • 3.

    Högberg LD, Muller A, Zorzet A, Monnet DL, Cars O. Antibiotic use worldwide. The Lancet Infectious Diseases. 2014;14(12):1179-80.

  • 4.

    Loyola Filho AID, Lima-Costa MF, Uchôa E. Bambuí Project: a qualitative approach to self-medication. Cadernos de saude publica. 2004;20(6):1661-9.

  • 5.

    Eticha T, Mesfin K. Self-medication practices in Mekelle, Ethiopia. PLoS One. 2014;9(5). e97464.

  • 6.

    Arshad MS, Ijaz MFRM, Hussain A. Evaluation of antibiotic use behavior in cold and flu amongst the students of Bahauddin Zakariya University Multan Pakistan. Pak. J. Pharm. 2007;2010(20-23):15-22.

  • 7.

    Aqeel T, Shabbir A, Basharat H, Bukhari M, Mobin S, Shahid H, et al. Prevalence of self-medication among urban and rural population of Islamabad, Pakistan. Tropical Journal of Pharmaceutical Research. 2014;13(4):627-33.

  • 8.

    Alghadeer S, Aljuaydi K, Babelghaith S, Alhammad A, Alarifi MN. Self-medication with antibiotics in Saudi Arabia. Saudi Pharmaceutical Journal. 2018.

  • 9.

    Moise K, Bernard JJ, Henrys JH. Evaluation of antibiotic self-medication among outpatients of the state university hospital of Port-Au-Prince, Haiti: a cross-sectional study. Pan African Medical Journal. 2017;28(1).

  • 10.

    Al-Azzam S, Al-Husein B, Alzoubi F, Masadeh M, Ali M. Self-medication with antibiotics in Jordanian population. International journal of occupational medicine and environmental health. 2007;20(4):373-80.

  • 11.

    Fadare JO, Tamuno I. Antibiotic self-medication among university medical undergraduates in Northern Nigeria. Journal of public health and Epidemiology. 2011;3(5):217-20.

  • 12.

    Almohammed RA, Bird EL. Public knowledge and behaviours relating to antibiotic use in Gulf Cooperation Council countries: A systematic review. J Infect Public Health. 2018. [PubMed ID: 30245158]. https://doi.org/10.1016/j.jiph.2018.09.002.

  • 13.

    Varadarajan V, Paul CMP, Swapna S, Preethi S, Kumar K, PU DD. A cross sectional study on the prevalence of self-medication in a Chennai based population, Tamil Nadu, India. International Journal of Community Medicine and Public Health. 2017;4(2):418-23.

  • 14.

    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 C hina. Tropical Medicine & International Health. 2014;19(7):769-79.

  • 15.

    Salm F, Ernsting C, Kuhlmey A, Kanzler M, Gastmeier P, Gellert P. Antibiotic use, knowledge and health literacy among the general population in Berlin, Germany and its surrounding rural areas. PLoS One. 2018;13(2). e0193336. [PubMed ID: 29474470]. [PubMed Central ID: PMC5825110]. https://doi.org/10.1371/journal.pone.0193336.

  • 16.

    Pavydė E, Veikutis V, Mačiulienė A, Mačiulis V, Petrikonis K, Stankevičius E. Public knowledge, beliefs and behavior on antibiotic use and self-medication in Lithuania. International journal of environmental research and public health. 2015;12(6):7002-16.

  • 17.

    Torres NF, Chibi B, Middleton LE, Solomon VP, Mashamba-Thompson T. Evidence of factors influencing self-medication with antibiotics in LMICs: a systematic scoping review protocol. Systematic reviews. 2018;7(1):102.

  • 18.

    Lescure D, Paget J, Schellevis F, Van Dijk L. Determinants of Self-medication with Antibiotics in European and Anglo-Saxon countries: a Systematic Review of the Literature. Frontiers in public health. 2018;6:370.

  • 19.

    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. International Journal of Infectious Diseases. 2017;57:3-12.

  • 20.

    Ekambi GE, Ebongue CO, Penda IC, Nga EN, Mpondo EM, Moukoko CEE. Knowledge, practices and attitudes on antibiotics use in Cameroon: Self-medication and prescription survey among children, adolescents and adults in private pharmacies. PloS one. 2019;14(2). e0212875.

  • 21.

    Garofalo L, Di Giuseppe G, Angelillo IF. Self-medication practices among parents in Italy. BioMed Research International. 2015;2015.

  • 22.

    Aziz MM, Masood I, Yousaf M, Saleem H, Ye D, Fang Y. Pattern of medication selling and self-medication practices: A study from Punjab, Pakistan. PloS one. 2018;13(3). e0194240.

  • 23.

    Bulario JS, Cruz ILP, Pilapil MC, Gutierrez MM. Factors Associated with Parental Self-medication of Antibiotics in Health Centers of Manila. KnE Social Sciences. 2018;3(6):891-910.

  • 24.

    Togoobaatar G, Ikeda N, Ali M, Sonomjamts M, Dashdemberel S, Mori R, et al. Survey of non-prescribed use of antibiotics for children in an urban community in Mongolia. Bulletin of the World Health Organization. 2010;88:930-6.

  • 25.

    Alele PM. Self-Medication Practices by Caretakers for Children. International Invention Journal of Medicine and Medical Sciences. 2015;2(11):165-71.

  • 26.

    Kariyawasam SH, Nanayakkara DN, Mohottiarachchi MACP, Nandasena YLS. A Descriptive Cross sectional Study on Mothers Self- Medicating Children. Sri Lanka Journal of Child Health. 2005:7-12.

  • 27.

    Grigoryan L, Burgerhof JG, Degener JE, Deschepper R, Lundborg CS, Monnet DL, et al. Attitudes, beliefs and knowledge concerning antibiotic use and self‐medication: a comparative European study. Pharmacoepidemiology and drug safety. 2007;16(11):1234-43.

  • 28.

    Widayati A, Suryawati S, de Crespigny C, Hiller JE. Self medication with antibiotics in Yogyakarta City Indonesia: a cross sectional population-based survey. BMC research notes. 2011;4(1):491.

  • 29.

    Horumpende PG, Said SH, Mazuguni FS, Antony ML, Kumburu HH, Sonda TB, et al. Prevalence, determinants and knowledge of antibacterial self-medication: A cross sectional study in North-eastern Tanzania. PloS one. 2018;13(10). e0206623.

  • 30.

    Ershadpour R, Zare H, Kalani N. systematic review of drug selfmedication prevalence in general population of Iran. research commitee journal of Mashhd University of Medical Sciences. 2014;18(60):16-23.

  • 31.

    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. Public Library of Science ONE. 2015. https://doi.org/10.1371/journal.pone.0138179.

  • 32.

    El Zowalaty ME, Belkina T, Bahashwan SA, El Zowalaty AE, Tebbens JD, Abdel-Salam HA, et al. Knowledge, awareness, and attitudes toward antibiotic use and antimicrobial resistance among Saudi population. Int J Clin Pharm. 2016;38(5):1261–1268. https://doi.org/10.1007/s11096-016-0362-x.

  • 33.

    Ajibola O, Omisakin O, Eze A, Omoleke S. Self-medication with antibiotics, attitude and knowledge of antibiotic resistance among community residents and undergraduate students in Northwest Nigeria. Diseases. 2018;6(2):32.

  • 34.

    El Zowalaty ME, Belkina T, Bahashwan SA, El Zowalaty AE, Tebbens JD, Abdel-Salam HA, et al. Knowledge, awareness, and attitudes toward antibiotic use and antimicrobial resistance among Saudi population. International journal of clinical pharmacy. 2016;38(5):1261-8.

  • 35.

    Riaz H, Finlayson AE, Bashir S, Hussain S, Mahmood S, Malik F, et al. Prevalence of Vitamin D deficiency in Pakistan and implications for the future. Expert Rev Clin Pharmacol. 2016;9(2):329-38. [PubMed ID: 26582317]. https://doi.org/10.1586/17512433.2016.1122519.