Abstract
The general population has been excessively using antibiotics during the COVID-19 pandemic. Therefore, the use of antibiotics for any reported illnesses in the preceding four weeks and knowledge of antibiotics among the general population in the community were assessed for possible interventions. A mobile phone survey among a general population across eight administrative divisions of Bangladesh was conducted during January–March 2021. Reported illness episodes irrespective of COVID-19 in the preceding four weeks of the interview, use of antibiotics for the illnesses, and knowledge on antibiotics among the general population were recorded. Descriptive analyses were performed. We randomly interviewed 1854 participants, with a mean age of 28.5 years (range: 18–75 years); 60.6% were male. Among all participants, 86.3% (95% CI: 84.7–87.8) heard names of antibiotics, but only 12.1% reported unspecified harmful effects, and 3.5% reported antimicrobial resistance when antibiotics were taken without a physician’s prescription. Among 257 (13.9%) participants, who consumed medicines for their recent illness episode, 32.7% (95% CI: 27.2–38.6) reported using antibiotics. Of those who could recall the names of antibiotics prescribed (n = 36), the most frequently used was azithromycin (22.2%) followed by cefixime (11.1%) and ciprofloxacin (5.6%). Our findings show an increased antibiotic use for illnesses reported in the preceding four weeks and an elevated knowledge at the community level during the COVID-19 pandemic compared with the pre-pandemic period.
Keywords: antibiotic resistance, COVID-19, pandemic, antibiotic awareness, antibiotic use
1. Introduction
Modern healthcare is predominantly reliant on antibiotic treatment [1], but there has been a phenomenal and imprudent use of antibiotics leading to the advent of resistant strains of bacteria [2,3]. To address the antimicrobial resistance (AMR) as a whole, with more emphasis on antibiotic resistance, the World Health Organization (WHO) initiated a range of AMR-related activities, including the development of the Global Action Plan on Antimicrobial Resistance (GAP-AMR) by the 68th World Health Assembly in May 2015 [4]. Published literatures exhibit a high proportion of inappropriate use of antimicrobials, and, as a result, optimizing the use of antimicrobial agents is one of the five key strategic objectives outlined in the GAP-AMR [4].
In late 2019, a novel coronavirus (SARS-CoV-2) was identified as the cause of an outbreak of disease named COVID-19 (coronavirus disease 2019), causing pneumonia in severe cases [5] further complicating as an acute respiratory distress syndrome (ARDS), a hyperinflammatory state and ultimately a multiorgan dysfunction with fatal consequences [6,7]. It was subsequently characterized as a pandemic on 11 March 2020 by the WHO [8]. Despite being a viral disease, it mimicked clinical symptoms of bacterial pneumonia; hence, different antimicrobials, especially antibiotics, were used as empirical therapy [9,10,11,12,13]. Furthermore, during the initial stages of the pandemic, there was a lack of proper antivirals with proven efficacy, and this, compounded by the anxiety and uncertainty of available treatment, led to the empirical but rather widespread and excessive use of antibiotics [13]. A study in Italy showed that, during lockdown for COVID-19, there was a relevant reduction in antibiotic consumption among children, due to closed daycare centers and schools, except for a relative increase in azithromycin use in adults [14]. However, there was no strong justification for routine use of azithromycin for reducing time to recovery or risk of hospitalization from the suspected COVID-19 in the community [15].
During the COVID-19 pandemic, the general population has likely been sensitized about using antibiotics for treating COVID-19. According to web-based surveillance on the COVID-19 pandemic and antibiotics used in Malaysia, 37% of the participants were aware that using antibiotics could not speed up recovery from all infections [16]. Still, 49% of the respondents reported that antibiotics were effective against bacterial infection only [16]. Dispensing of antibiotics was increased profoundly in Egypt during the early period of the COVID-19 pandemic without proper clinical evaluation, and azithromycin, ceftriaxone, and linezolid were the major antibiotics used [17]. Approximately, 93% of the presumptive COVID-19 patients received antibiotics with official prescriptions and without prescriptions, of which 18% comprised of pharmacist and patient’s recommendations [17]. Before the COVID-19 pandemic, studies in Bangladesh reported that 48% of adult respondents heard about antibiotics, 70% of children of those parents who were aware of antibiotics had received it previously, and 28% of study participants took antibiotics before presenting at the hospital for acute febrile illness [18,19]. During the first wave of the COVID-19 pandemic in Bangladesh, a study among suspected COVID-19 patients found that the use of antibiotics was 92% during their overall suspected phase. Among them, 89% were prescribed antibiotics on hospital admission, while 47% of COVID-19 suspected patients received antibiotics 24 h before hospital admission [20]. A prime contributor to antibiotics overuse in Bangladesh is perhaps the availability of over-the-counter dispensed antibiotics through unregulated drug stores (pharmacies) [19,21]. Therefore, assessing the use of antibiotics and the relevant knowledge on antibiotics among the general population irrespective of hospitalization, especially during the COVID-19 pandemic, is imperative in order to formulate policy interventions regarding the rational use of antibiotics.
Higher-income countries have used telephone surveys to collect real-time data on population-level estimates of health and demographics [22,23,24]. Bangladesh had a mobile phone teledensity of 103% in 2021 [25], with over 175 million subscribers registered in May 2021 [26]. We utilized this opportunity and conducted a mobile-phone-based survey to obtain real-time data during the COVID-19 pandemic. In this study, we aimed to assess antibiotic use for any reported illnesses in the preceding four weeks and knowledge regarding antibiotics among the general population in Bangladesh.
2. Methods
2.1. Study Design and Study Population
We conducted a cross-sectional mobile-phone-based survey during the COVID-19 pandemic for eight weeks between mid-January 2021 and mid-March 2021 to assess antibiotic use and relevant knowledge on antibiotic use in Bangladesh utilizing the Computer-Assisted Telephone Interviewing (CATI) system [27,28]. The target population was adult individuals (aged 18 years and above) with a mobile phone subscription across all eight administrative divisions in Bangladesh to ensure a national geographical representation.
2.2. Data Collection
A mobile phone database (containing only numbers and locations from where the subscription was registered) of a mobile-phone survey platform of the Programme for Emerging Infections at International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b) was used as the sample population. The CATI software randomly picked up mobile phone numbers from that database for the interviews. Two interviewers made phone calls to random numbers from 9.00 AM to 5.00 PM throughout the weekdays (Sunday to Thursday). If any respondent could not speak during the call time but agreed to take part at a later convenient date and time, the interviewer fixed an appointment for the interview, especially on weekends. On weekends (Friday and Saturday), phone calls were made from 10:00 AM to 12:00 PM for those working adults who had earlier scheduled the interviews. Data through mobile phone calls were collected using a tablet device and entered in real-time into the icddr,b server. Each phone call started with greetings stating the objective of the call and informing that the names of the interviewee would not be asked, data would be confidential, and an age screening question would be asked followed by a verbal consent to start the interview. Interviews only progressed if the respondent agreed to participate and was 18 years of age or older. For social acceptance during the interview, we used the common term “corona” instead of “COVID-19”.
2.3. Data Collection Tool
We used a structured questionnaire to register socio-demographic variables followed by the experience of general illnesses, including any COVID-19 disease in the preceding four weeks and the healthcare-seeking pattern during the pandemic period. Subsequently, the frequency of healthcare-seeking for the illness was documented, including the frequency of antibiotic use. Information on knowledge on antibiotics such as any antibiotic name recalled spontaneously, the name with the duration of antibiotic, if used, and any adverse effects known if taken without a doctor’s prescription were also collected. In total, 60 pilot interviews were conducted in two rounds (30 in each round) before initiating the study to validate the tool used, and study variables were restructured based on feedback from the pilot interviews. A response rate and a cooperation rate (defined later) of the survey conducted were determined.
2.4. Computer-Assisted Telephone Interviewing (CATI) System
The CATI system integrated the data collection tool with the mobile phone database over the internet. It also provided an interface on a handheld tablet device for making calls, scheduling repeat calls, selecting mobile interviewee numbers randomly, and logging the interviewers’ activities [29]. In addition, the system had inbuilt algorithms to perform automated variables’ check and facilitated direct data entry. On a typical workday, the interviewer logged into the system with a unique ID and password on a tablet device into the web interface of the CATI system, and it randomly selected the phone numbers to be dialed. Once the call was connected, the interview progressed with the interviewer registering entries concurrently in the data server where all the responses were stored. Subsequently, more interviews were conducted in the same manner.
2.5. Sample Size Calculation
According to recent studies, 48% of the respondents were found to hear about antibiotics in 2018, and 40% of the respondents used antibiotics for respiratory illness during 2012–2013 [18,30]. Based on the statistics above, we conservatively expected that antibiotics might be known and consumed by 20% general population consisting of those with illnesses, fear of having illnesses, and/or presumed illnesses in Bangladesh. Therefore, assuming a 95% confidence level with 5% absolute precision and 20% expected to be aware and used antibiotics, we required a minimum sample size of 246 individuals. This sample size would be sufficient to detect any prevalence of antibiotic awareness and use of 20% to 80% with the 95% confidence level [31]. Since we wanted to have a national representative sample, we opted to cover each of the eight administrative divisions of Bangladesh. Therefore, we targeted a minimum sample size of (246 × 8 = 1968) respondents across Bangladesh.
2.6. Data Analysis
From the CATI software system, we calculated the response rate and cooperation rates as following:
Interview data were stored in icddr,b local server. Stata v.13 (StataCorp LP, College Station, TX, USA) was used to perform descriptive analysis to summarize the categorical variable based on frequency distribution with percentage and 95% confidence interval. For continuous variables, we used descriptive statistics (mean, standard deviation (SD), and range) for symmetric distribution and median and interquartile range (IQR) for asymmetric distribution. We also used Python 3.6 to create maps illustrating study findings.
3. Results
A total of 2183 respondents were reached in our study. On average, there were 280 calls made per week and 1854 complete interviews conducted from 62 districts of Bangladesh. Therefore, the cooperation rate was 85% for this study (Figure 1). The average duration of calls was 8 (range: 3–16) min.
Among the 1854 complete interviews conducted, 60.6% were male, and the mean age was 28.5 years ranging from 18 to 75 years. The majority (45.4%) of them were students, followed by homemakers (23.3%) and service holders (16.7%). The median household size was 5 members, and 50.7% were living in urban areas. The division-wise response proportions are listed in Table 1.
Table 1.
Demographic Characteristics (N = 1854) | N | % (95% CI) |
---|---|---|
Age (Years) | ||
18–30 | 1239 | 66.8 (64.7, 68.9) |
31–40 | 347 | 18.7 (17, 20.6) |
41–50 | 191 | 10.3 (9, 11.8) |
50+ | 77 | 4.2 (3.3, 5.2) |
Mean age in years (Range) | 28.5 (18–75) | |
Gender | ||
Male | 1124 | 60.6 (58.4, 62.8) |
Female | 649 | 35.0 (32.9, 37.2) |
Not willing to disclose | 81 | 4.4 (3.5, 5.4) |
Occupation | ||
Student | 842 | 45.4 (43.2, 47.7) |
Homemaker | 432 | 23.3 (21.4, 25.3) |
Service holder | 309 | 16.7 (15, 18.4) |
Businessman | 104 | 5.6 (4.7, 6.8) |
Skilled worker | 50 | 2.7 (2.1, 3.5) |
Farmer | 43 | 2.3 (1.7, 3.1) |
Unemployed | 34 | 1.8 (1.3, 2.6) |
Retired | 14 | 0.8 (0.5, 1.3) |
Doctor | 7 | 0.4 (0.2, 0.8) |
Others | 12 | 0.6 (0.4, 1.1) |
No Response | 7 | 0.4 (0.2, 0.8) |
Median household size, members (IQR) | 5 (4–6) | |
Place of residence | ||
Urban | 939 | 50.6 (48.4, 52.9) |
Rural | 876 | 47.2 (45, 49.5) |
Not willing to disclose | 39 | 2.1 (1.5, 2.9) |
Division name of the residence | ||
Dhaka | 535 | 28.9 (26.8, 31) |
Chattogram | 403 | 21.7 (19.9, 23.7) |
Khulna | 353 | 19.0 (17.3, 20.9) |
Rangpur | 202 | 10.9 (9.6, 12.4) |
Barishal | 199 | 10.7 (9.4, 12.2) |
Sylhet | 84 | 4.5 (3.7, 5.6) |
Rajshahi | 17 | 0.9 (0.6, 1.5) |
Mymensingh | 15 | 0.8 (0.5, 1.3) |
Missing/No response | 46 | 2.5 (1.9, 3.3) |
Among those consuming medicines (n = 257, 13.9%) for their general illness reported in the preceding four weeks, 4.7% did not know whether they were taking antibiotics together, with another 4.7% missing/no responses. The proportion of respondents using antibiotics was 32.7% (95% CI: 27.2–38.6, n = 84) for general illnesses in the preceding four weeks. Among the COVID-19 patients (n = 16), this proportion of use of antibiotics was only 12.5% (n = 2). Purchase of antibiotics (n = 84) was advised by the seller at pharmacies (33.3%) as over-the-counter sales, on the prescription of formal private clinics (21.4%), on the prescription of formal (MBBS/MD) doctors (15.5%), and those from public healthcare facilities (14.3%). Thirteen percent of the respondents also reported purchasing antibiotics advised by village doctors (quacks). Among respondents purchasing antibiotics, 17.9% reported purchasing a partial number of antibiotics of the prescribed antibiotics. Of those who could recall the names of antibiotics (n = 36), the most frequently consumed was azithromycin (22.2%) followed by cefixime (11.1%) and ciprofloxacin (5.6%) (Table 2).
Table 2.
Antibiotic Use | N | % (95% CI) |
---|---|---|
Antibiotics used for reported illness (n = 257) | ||
Yes | 84 | 32.7 (27.2, 38.6) |
No | 149 | 58.0 (51.9, 63.9) |
Don’t know | 12 | 4.7 (2.7, 8) |
Missing/no response | 12 | 4.7 (2.7, 8) |
Source of antibiotic prescription (n = 84) | ||
Pharmacy | 28 | 33.3 (24.2, 43.9) |
Formal private clinic | 18 | 21.4 (14, 31.3) |
Formal (MBBS/MD) doctor | 13 | 15.5 (9.3, 24.7) |
Public healthcare facility | 12 | 14.3 (8.4, 23.3) |
Quack, village doctor | 11 | 13.1 (7.5, 21.9) |
Self-medication | 2 | 2.4 (0.7, 8.3) |
Recalled names of antibiotics prescribed (n = 84) | ||
Yes | 36 | 42.9 (32.8, 53.5) |
No | 15 | 17.9 (11.1, 27.4) |
No response/don’t know | 33 | 39.3 (29.5, 50) |
Names of the prescribed antibiotics recalled (n = 36) | ||
Azithromycin | 8 | 22.2 (11.7, 38.1) |
Cefixime | 4 | 11.1 (4.4, 25.3) |
Ciprofloxacin | 2 | 5.6 (1.5, 18.1) |
Co-trimoxazole | 1 | 2.8 (0.1, 14.2) |
Flucloxacillin | 1 | 2.8 (0.1, 14.2) |
Metronidazole | 1 | 2.8 (0.1, 14.2) |
Tetracycline | 1 | 2.8 (0.1, 14.2) |
Purchase of prescribed antibiotics (n = 84) | ||
Full course purchased | 69 | 82.1 (72.6, 88.9) |
Partial purchase | 15 | 17.9 (11.1, 27.4) |
Duration of antibiotics taken (n = 84) | ||
3–5 | 37 | 44.0 (33.9, 54.7) |
6–7 | 27 | 32.1 (23.1, 42.7) |
8–14 | 6 | 7.1 (3.3, 14.7) |
14+ | 6 | 7.1 (3.3, 14.7) |
<3 | 5 | 6.0 (2.6, 13.2) |
Missing/No response | 3 | 3.6 (1.2, 10) |
Median duration of antibiotics taken (IQR) | 5 (3–7) | |
Antibiotics used for COVID-19 positive (n = 16) | ||
Yes | 2 | 12.5 (3.5, 36) |
No | 1 | 6.3 (0.3, 28.3) |
Missing/No response | 13 | 81.3 (57, 93.4) |
About one-fifth (18.5%, n = 343) of all the respondents reported symptoms of general illness in the past four weeks of the interview. Among those who reported illness, runny nose (9.3%) was mainly reported, followed by fever (2.3%), cough (1.6%), and diarrhea (1.2%). The COVID-19 specific symptom of anosmia/ageusia, sore throat, and headache were reported by 0.7%, 0.6%, and 0.6% of the respondents, respectively. Only 13.9% (n = 257) of all study participants sought healthcare for their illness. Among them, 46.7% went to medicine shops (pharmacies) for treatment. The healthcare-seeking respondents also sought healthcare from private clinics (16.0%), formal (MBBS/MD) doctors (12.1%), took self-medication (8.6%), went to village doctors (7.8%), followed by resorting to public healthcare facilities (7.0%) for their illnesses. The majority reported consuming one−three medicines (77.8%), four−five medicines (12.1%), and six medicines or more (2.3%) for their recent episode of illness in the last four weeks. Two percent of respondents reported hospitalizations due to any disease among those who sought healthcare (Table 3).
Table 3.
Symptoms Reported for the Current Episode of Illness (N = 1854) | N | % (95% CI) |
---|---|---|
Runny nose | 173 | 9.3 (8.1, 10.7) |
Fever | 42 | 2.3 (1.7, 3) |
Cough | 29 | 1.6 (1.1, 2.2) |
Loose motion/dysentery | 23 | 1.2 (0.8, 1.9) |
Loss of smell/taste | 13 | 0.7 (0.4, 1.2) |
Sore throat | 11 | 0.6 (0.3, 1.1) |
Headache | 11 | 0.6 (0.3, 1.1) |
Injury/accident | 8 | 0.4 (0.2, 0.8) |
Urinary tract infection | 7 | 0.4 (0.2, 0.8) |
Allergy | 5 | 0.3 (0.1, 0.6) |
Difficulty breathing | 4 | 0.2 (0.1, 0.6) |
Any others | 17 | 0.9 (0.6, 1.5) |
No symptoms | 1454 | 78.4 (76.5, 80.2) |
Missing/no response | 57 | 3.1 (2.4, 4) |
Healthcare seeking behavior for the current episode of illness (n = 1854) | ||
Healthcare sought | ||
Yes | 242 | 13.1 (11.6, 14.7) |
Self-medication | 15 | 0.8 (0.5, 1.3) |
No | 1546 | 83.4 (81.6, 85) |
Missing/no response | 51 | 2.8 (2.1, 3.6) |
Healthcare seeking point (n = 257) * | ||
Pharmacy | 120 | 46.7 (40.7, 52.8) |
Formal private clinic | 41 | 16.0 (12, 20.9) |
Formal (MBBS/MD) doctor | 31 | 12.1 (8.6, 16.6) |
Self | 22 | 8.6 (5.7, 12.6) |
Quack, village doctor | 20 | 7.8 (5.1, 11.7) |
Public healthcare facility | 18 | 7.0 (4.5, 10.8) |
Followed the previous prescription | 0 | - |
Others (NGO and Homeopathy) | 5 | 1.9 (0.8, 4.5) |
Hospitalization required (n = 257) | ||
Yes | 5 | 1.9 (0.8, 4.5) |
No | 252 | 98.1 (95.5, 99.2) |
Medicine taken (n = 257) | ||
Yes | 246 | 95.7 (92.5, 97.6) |
No | 11 | 4.3 (2.4, 7.5) |
Number of medicines taken (including Antibiotic) (n = 257) | ||
1–3 | 200 | 77.8 (72.4, 82.5) |
4–5 | 31 | 12.1 (8.6, 16.6) |
>6 | 6 | 2.3 (1.1, 5) |
Missing/no response | 20 | 7.8 (5.1, 11.7) |
* inclusive of those (n = 257) who sought health care (n = 242) and self-medicated (n = 15).
Most (86.3%, 95% CI: 84.7–87.8, n = 1600) of the respondents heard names of antibiotics in their lifetime, and the division-wise proportionate responses are illustrated in Figure 2. They could state names of azithromycin (12.0%), ciprofloxacin (6.6%), cefixime (4.8%), and amoxycillin (2.8%), spontaneously. When interviewed for dosage of antibiotics, 48.3% (n = 772) reported that they knew the dosage and reported antibiotic use duration as one week (68.9%), three to five days (17.2%), two weeks (9.1%), more than two weeks (3.4%), and less than three days (1.4%). Unspecified harmful effects were stated by 12.1% of the respondents, kidney problems by 5.5% of the respondents, and 3.5% of the respondents reported antibiotic resistance as the effect of taking antibiotics without consulting a physician (Table 4).
Table 4.
Antibiotic Knowledge | N | % (95% CI) |
---|---|---|
Ever heard any name of antibiotics (N = 1854) | ||
Yes | 1600 | 86.3 (84.7, 87.8) |
No | 254 | 13.7 (12.2, 15.3) |
Name of antibiotics recalled spontaneously (n = 1600) | ||
Azithromycin | 192 | 12.0 (10.5, 13.7) |
Ciprofloxacin | 106 | 6.6 (5.5, 8) |
Cefixime | 76 | 4.8 (3.8, 5.9) |
Amoxicillin | 45 | 2.8 (2.1, 3.7) |
Flucloxacillin | 20 | 1.3 (0.8, 1.9) |
Cefradine | 9 | 0.6 (0.3, 1.1) |
Metronidazole | 4 | 0.3 (0.1, 0.6) |
Ceftriaxone | 3 | 0.2 (0.1, 0.5) |
Tetracycline | 2 | 0.1 (0, 0.5) |
None | 1143 | 71.4 (69.2, 73.6) |
Knowledge of antibiotics use duration (n = 1600) | ||
Yes | 772 | 48.3 (45.8, 50.7) |
No | 821 | 51.3 (48.9, 53.8) |
Missing/no response | 7 | 0.4 (0.2, 0.9) |
Knowledge of duration (days) of antibiotics use (n = 772) | ||
1–7 | 532 | 68.9 (65.6, 72.1) |
3–5 | 133 | 17.2 (14.7, 20.1) |
8–14 | 70 | 9.1 (7.2, 11.3) |
14+ | 26 | 3.4 (2.3, 4.9) |
<3 | 11 | 1.4 (0.8, 2.5) |
Median (IQR) | 7 (3–7) | |
Knowledge of side effects of taking antibiotics without consulting a doctor (n = 1600) | ||
Harmful effects (unspecified) | 194 | 12.1 (10.6, 13.8) |
Kidney problem | 88 | 5.5 (4.5, 6.7) |
Antibiotic resistance | 56 | 3.5 (2.7, 4.5) |
Liver problem | 29 | 1.8 (1.3, 2.6) |
Heart problem | 21 | 1.3 (0.9, 2) |
Headache | 21 | 1.3 (0.9, 2) |
Fatigue | 19 | 1.2 (0.8, 1.8) |
Neurological problem | 15 | 0.9 (0.6, 1.5) |
Nausea, vomiting | 10 | 0.6 (0.3, 1.1) |
Loose motion/abdominal discomfort | 15 | 0.9 (0.6, 1.5) |
Infection | 8 | 0.5 (0.3, 1) |
Cancer, stroke liver & kidney problem | 8 | 0.5 (0.3, 1) |
Lung problem | 7 | 0.4 (0.2, 0.9) |
Death | 7 | 0.4 (0.2, 0.9) |
Fever | 5 | 0.3 (0.1, 0.7) |
Stroke | 2 | 0.1 (0, 0.5) |
Allergy/rash | 2 | 0.1 (0, 0.5) |
Gynecological problem | 2 | 0.1 (0, 0.5) |
Mineral deficiency | 1 | 0.1 (0, 0.4) |
No response | 1090 | 68.1 (65.8, 70.4) |
Among all the respondents, 6% (n = 111) reported that they underwent COVID-19 testing, and most (81.1%, 95% CI: 72.8–87.3) availed public facilities for it. Among those who tested for COVID-19 (n = 111), 14% (n = 16) were tested positive, and 4% (n = 4) were hospitalized. A small proportion (8%, n = 141) of all respondents stated that their family members underwent COVID-19 testing; 13% tested positive, while 9% did not respond to this question, and 5% of COVID-19 affected family members were admitted to the hospital. Five deaths (4%) among family members with COVID-19 disease were also reported (Table 5).
Table 5.
COVID-19 Illness | n | % (95% CI) |
---|---|---|
Tested for COVID-19 since the start of COVID-19 pandemic (Self) | ||
Yes | 111 | 6.0 (5.0, 7.2) |
No | 1665 | 89.8 (88.3, 91.1) |
Missing/no response | 78 | 4.2 (3.4, 5.2) |
COVID-19 test result (n = 111) (self) | ||
Positive | 16 | 14.4 (9.1, 22.1) |
Unknown | 2 | 1.8 (0.5, 6.3) |
COVID-19 testing facility type (n = 111) (self) | ||
Public | 90 | 81.1 (72.8, 87.3) |
Private | 18 | 16.2 (10.5, 24.2) |
Both | 3 | 2.7 (0.9, 7.6) |
Hospitalization required for COVID-19 (n = 111) (self) | ||
Yes | 4 | 3.6 (1.4, 8.9) |
No | 107 | 96.4 (91.1, 98.6) |
COVID-19 information of other family members | ||
Number of family members tested for COVID-19 since the start of the COVID-19 pandemic | ||
1 | 68 | 3.7 (2.9, 4.6) |
2 | 25 | 1.3 (0.9, 2) |
3 | 20 | 1.1 (0.7, 1.7) |
4 | 11 | 0.6 (0.3, 1.1) |
>5 | 16 | 0.9 (0.5, 1.4) |
No | 1633 | 88.1 (86.5, 89.5) |
Missing/no response | 81 | 4.4 (3.5, 5.4) |
Mean Number of family members tested for COVID-19 (Range) | 2.3 (1–15) | |
The COVID-19 test result of family members (n = 141) | ||
Negative | 111 | 78.7 (71.3, 84.7) |
One to three members positive | 18 | 12.8 (8.2, 19.3) |
Missing/no response | 12 | 8.5 (4.9, 14.3) |
Hospitalization of family members due to Corona (n = 141) | ||
Yes | 7 | 5.0 (2.4, 9.9) |
No | 133 | 94.3 (89.2, 97.1) |
Missing/no response | 1 | 0.7 (0, 3.9) |
Death of family members due to COVID-19 (n = 141) | ||
Yes | 5 | 3.5 (1.5, 8) |
No | 133 | 94.3 (89.2, 97.1) |
Missing/no response | 3 | 2.1 (0.7, 6.1) |
4. Discussion
Our study found 32.7% (95% CI: 27.2–38.6) of the general population who reported illness in the preceding four weeks of the interview using antibiotics in the community. This proportion of antibiotic use for illnesses was higher than a pre-pandemic study in a community setting in Bangladesh during 2018, reporting (21%) antibiotics use within the last month [18]. The COVID-19 pandemic may have influenced this rise in the proportion of antibiotic use in Bangladesh. However, the proportion of antibiotics used among COVID-19 patients was much low (12.5%) in our findings. However, determining the proportion of antibiotic use among COVID-19 cases was not the study’s objective. Yet, this study finding is much lower than 47% among the suspected COVID-19 cases reported in a previous hospital-based study from Bangladesh [20]. The proportion of antibiotics used for COVID-19 respondents in our study is also much lower than the study conducted in Egypt during the COVID-19 pandemic [17]. This may be likely to the fact that a very low number of COVID-19 cases were detected through this survey.
This study also measured the relevant knowledge regarding antibiotics irrespective of any respondents suffering from COVID-19 illness. The basic knowledge regarding antibiotics was very high among our survey respondents. Our study found a very high proportion (86.3%, 95% CI: 84.7–87.8) of respondents reported to know names of antibiotics compared with the previously reported proportion of 48% in Bangladesh before the COVID-19 pandemic [18]. Furthermore, azithromycin, a macrolide antibiotic, was found as the most frequently (12%) recalled/reported antibiotic. This is perhaps because azithromycin was the most commonly prescribed antibiotics by physician’s advice and self-medication during the COVID-19 pandemic situation in Bangladesh [32] and other countries in Europe and Asia [33]. An online survey conducted at the end of March 2020 on 6227 physicians in 30 countries revealed that, after some common analgesics, azithromycin was the second-highest prescribed drug for COVID-19 [34]. Earlier reports on antibiotics awareness in Bangladesh stated the most frequent (11%) antibiotic reported to be a fluoroquinolone named ciprofloxacin [35]. Although our study participants mentioned several unspecified harmful effects of antibiotics if taken without a physician’s prescription, very few (4%) could expressly state about antibiotic resistance. This rate is much lower than previous reports from Bangladesh, where 60% of the respondents stated antibiotic resistance [35]. Overall, our findings illustrate that the general population was more knowledgeable about antibiotics during the COVID-19 pandemic compared with the pre-pandemic period.
Drug shops (pharmacies) contributed to the lion’s share (33.3%) of antibiotic dispensing without a prescription, and village doctors also contributed a handsome proportion (13.1%) in prescribing antibiotics in our study. Recent past studies in Bangladesh reported proportions as high as 43% [36] and 16% from drug shops (pharmacies), and 18% from village doctors [35]. Bangladesh’s common practice is to fetch over-the-counter medicines and even antibiotics regardless of consulting any qualified healthcare providers and the socio-economic status and education of the buyer [37,38]. Our findings and this intrinsic nature of the population regarding procuring antibiotics raise a flag to immediately adopt and strengthen “prescription-only from formal providers” for antibiotic purchase [20].
The antibiotic azithromycin was the most frequently prescribed/used, followed by cefixime—a third-generation cephalosporin. For treating suspected or confirmed mild-to-moderate COVID-19 cases without clinical suspicion of bacterial infections, antibiotics were discouraged from using for empirical treatment by WHO [39]. However, due to overburdened laboratories for testing microbiological samples and lack of recommended antiviral therapy for COVID-19 infection, there was an increased empirical use of antimicrobials, including broad-spectrum antibiotics, by the clinicians [13,40]. In Spain, a biphasic use of antibiotics was observed during the COVID-19 pandemic during 2020, along with amoxicillin/clavulanic acid and broad-spectrum antibiotics in public referral hospitals [40]. Physicians reported the widespread use of broad-spectrum antibiotics in 23 countries [9]. Moreover, the most common antibiotic classes prescribed were macrolides, fluoroquinolones, β-lactam/β-lactamase inhibitors, and cephalosporins in North America, Europe, China, and Asia [33]. The use of macrolide and cephalosporins were similar to the results from a recent study conducted across Bangladesh during the first wave of the COVID-19 pandemic, where macrolide was the most frequently (27%) used antibiotic followed by cephalosporin (16%) among suspected COVID-19 patients before hospital admission [20]. However, both azithromycin and cefixime belong to the Watch group antibiotic, which is not recommended according to the WHO AWaRe classification/tool [41]. This non-compliance in antibiotic use also flags a concern for antimicrobial resistance.
Although we were able to cover respondents from across eight administrative divisions of Bangladesh, while interpreting our study findings, several limitations must be kept in consideration. The majority of our study respondents were males aged 18–40 years; therefore, our sampled respondents may not represent Bangladesh’s demographic profile. Furthermore, antibiotics were more likely to be used in extremes of age while we had no respondents <5 years, and only 4.2% were above 50 years. It was a survey based on mobile phone, and hence there may be recall bias in the responses leading to data loss and distortion. Furthermore, knowledge questions on antibiotics were limited to basic ones such as names, dosage, and harmful effects. Lastly, there were minimal opportunities to cross-validate responses, and only 5% of the complete interviews were randomly cross checked by repeat interviews. Overall, our results may be an underestimate of our actual prevalence of antibiotic use and knowledge.
In conclusion, our study findings underscored the increased proportion of antibiotic use for recent illnesses and raised knowledge about antibiotics at the community level during the COVID-19 pandemic in Bangladesh. Overuse of antibiotics, widespread availability, and generalized access to all types of antibiotics as over-the-counter drugs in the community surface raise concerns for antibiotic resistance in the near future. A robust monitoring system supported by policy and law is highly recommended to delimit over-the-counter antibiotic sales. Together with building community awareness on AMR, precisely due to the irrational use of antibiotics, it is imperative to promote, standardize, and strengthen antimicrobial stewardship within the health system of Bangladesh.
Acknowledgments
We are grateful to our survey participants for providing their valuable time and information. We also thank Hafizur Rahman, Anik Palit, Probir Kumar Ghosh, and Faiza Tasfia for their contribution to this project.
Author Contributions
Conceptualization, M.R., F.C. and Z.A.; methodology, M.R. and Z.A.; software, Z.A. and S.M.-E.-M.; validation, Z.A., M.M.R. and M.S.A.; formal analysis, M.S.A. and Z.A.; data curation, Z.A., M.M.R. and M.S.A.; writing—original draft preparation, Z.A., M.M.R. and S.M.-E.-M.; writing—review and editing, Z.A., F.C., M.R., M.Z.H., S.C., S.P., M.A.I., N.D., K.I. and Z.K.; visualization, M.S.A. and Z.A.; supervision, F.C.; project administration, Z.A., M.M.R. and S.M.-E.-M.; funding acquisition, F.C. All authors have read and agreed to the published version of the manuscript.
Funding
This study was funded by the Fleming Fund Country Grant to Bangladesh Bangladesh (FF48-416 FFCGB 1). icddr,b is grateful to the governments of Bangladesh, Canada, Sweden, and the UK for providing core/unrestricted support.
Institutional Review Board Statement
The survey was conducted according to the guidelines of the Declaration of Helsinki and approved by the Institutional Review Board consisting of the Research Review Committee and Ethical Review Committee of icddr,b (protocol code PR-20116).
Informed Consent Statement
All study participants have provided informed consent for participating in the mobile phone survey.
Data Availability Statement
The data presented in this survey are available on reasonable request from icddr,b’s research administration through the corresponding author. The data are not publicly available due to privacy restrictions and icddr,b policy.
Conflicts of Interest
The authors declare no conflict of interest. The funders had no conflict of interest with the study and contents of the manuscript.
Footnotes
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The data presented in this survey are available on reasonable request from icddr,b’s research administration through the corresponding author. The data are not publicly available due to privacy restrictions and icddr,b policy.