Abstract
Background
The overuse of antibiotics in primary healthcare settings (PHSs) has caused a serious public health problem in China. The outbreak of the Coronavirus Disease-19 (COVID-19) pandemic brought about dramatic changes in the supply of and demand for medical services in PHSs, possibly resulting in unprecedented changes in antibiotic use.
Objective
This study aims to assess the immediate and long-term impacts of the COVID-19 pandemic on the changes in antibiotic consumption in PHSs.
Method
The data on antibiotic consumption were collected from selected township hospitals in Shandong, China from January 2019 to December 2021. Antibiotic consumption was quantified by using the defined daily doses (DDDs) and the WHO Access, Watch, Reserve category. A segmented regression model was established to analyze the immediate and long-term impacts of the COVID-19 pandemic on antibiotic use by using the interrupted time series analysis.
Results
The overall antibiotic consumption in all PHSs decreased by 32.04% and 16.69% in 2020 and 2021 respectively compared to the corresponding period in 2019. Over the entire study period, the use of penicillins (J01C) and cephalosporins (J01D) accounted for more than 50% of the total antibiotic consumption. The average annual consumption of Watch category antibiotics decreased by 42.02% and 33.47% in 2020 and 2021 respectively compared to that in 2019. According to the interrupted time series analysis, the total antibiotic consumption decreased significantly immediately after the COVID-19 pandemic outbreak (coef. = − 2.712, p = 0.045), but it then increased significantly over a long-term (coef. = 0.205, p = 0.005). Additionally, the consumption of Access category antibiotics increased significantly in PHSs in the long-term (coef. = 0.136, p = 0.018). However, the consumption of Watch category antibiotics declined sharply immediately after the pandemic (coef. = − 1.222, p < 0.001), but then it increased slightly over a long-term (coef. = 0.073, p < 0.001).
Conclusion
The extensive use of penicillin and cephalosporins should be of great concern. After the outbreak of COVID-19 pandemic, the total antibiotic consumption decreased generally and the use pattern was improved to some extent in the PHSs in Shandong, China. This provides an opportunity for improving the misuse of antibiotics in PHSs in China.
Supplementary Information
The online version contains supplementary material available at 10.1186/s13756-022-01206-8.
Keywords: Antibiotic consumption, COVID-19, Primary healthcare settings, China
Introduction
Antimicrobial resistance (AMR) is a major urgent threat to global public health, and it has imposed a huge medical and economic burden on the whole society [1–3]. According to the report of the World Health Organization (WHO), antibiotic resistance has given rise to a global public health crisis, considering the fact that the public health is threatened, the use of antibiotics has to be optimized [4].
As one of the largest consumers of antibiotics, China plays an important role in containing and mitigating AMR [5]. Antibiotics are the most commonly prescribed drugs in PHSs [6, 7]. In China, more than 50% of outpatients have been prescribed antibiotics over the past decade [8], far above the level recommended by WHO (less than 30%) [9]. Therefore, it is necessary to optimize antibiotic use in PHSs for containing bacterial resistance [4, 6, 10].
The Coronavirus Disease-19 (COVID-19) pandemic swept across the world quickly and placed a heavy burden on the health systems globally. The impacts of the COVID-19 pandemic on antibiotic consumption and the risk of AMR have become a concern of many researchers of antibiotic resistance [11–19]. According to a report, after the outbreak of the COVID-19 pandemic in most European countries, the total consumption of antibiotics declined by more than 15%, which was mainly observed in PHSs [13]. Several national studies conducted in the USA, Portugal, Canada, and the UK also showed that the overall antibiotic consumption by outpatients or broad-spectrum antibiotic prescriptions decreased significantly during the COVID-19 pandemic. Especially, the number of prescriptions of certain categories of antibacterials (e.g., third-generation cephalosporins, fluoroquinolones) decreased significantly [11, 12, 14–16]. Similarly, several studies in China also found that there was a decline antibiotic consumption during the COVID-19 pandemic [17–19]. For example, a study from Yinchuan of China showed that the decrease in inappropriate antibiotic prescriptions in primary care settings may be associated with the COVID-19 pandemic [19]. Therefore, the antibiotic use pattern may have changed greatly during the COVID-19 pandemic. However, no adequate evidence has been found for the changes in antibiotic consumption in PHSs in China.
This study aimed to assess the immediate and long-term impacts of the COVID-19 pandemic on the changes in antibiotic consumption in PHSs in Shandong, China. The findings of this study may be conducive to developing and implementing intervention and management policies for antibiotic consumption in PHSs to further improve the misuse of antibiotics.
Methods
Study setting and design
This study was conducted in Shandong province in eastern China, which had a total population of 101, 699, 900 at the end of 2021 [20]. The method of purpose sampling was used in the study. Two counties S and Y in City L located in the western area of Shandong Province were selected as the target locations. The two counties have similar mid-level development indexes in terms of Gross Domestic Product (GDP), number of permanent residents, number of health technicians, and number of township hospitals. In addition, the pandemic prevention and control policies were highly synchronized during the COVID-19 pandemic in PHSs in Shandong, China. Therefore, the sample township hospitals are representative of the majority of township hospitals in rural Shandong. They can representatively display the changes of antibiotic consumption trend and the use pattern before and after the outbreak of the COVID-19 pandemic.
Township hospitals are primary healthcare centers in rural China. Their primary missions are to provide rural population with extensive primary outpatient services (i.e., establishment resident health records, common diseases treatment, non-communicable diseases control, vaccination and health education) and limited inpatient service (i.e., basic clinical examination, surgical treatment for a few diseases). Antibiotics are used by inpatients and outpatients, but most of them are consumed by outpatients of the township hospitals in Shandong, China. During the early period of the COVID-19 pandemic, the township hospitals changed their daily work and business hours. For example, they greatly shortened their opening hours, and most of the medical staff were deployed to assist in tracking down infected individuals and conduct epidemiological investigation. At the same time, the number of patients in township hospitals decreased sharply, for those, patients with fever were transferred to COVID-19 pandemic specific clinics. In addition, antibiotics in pharmacies were not available for patients without physicians’ prescription. Instead, antibiotics were mostly prescribed in PHSs in rural China.
Data were collected from all township hospitals (38 in total) in counties S and Y in City L in Shandong Province. In Shandong Province, PHSs are only allowed to purchase, store and distribute drugs listed in the Regulations on Drug Administration based on the zero price difference policy. At the same time, doctors in PHSs are only permitted to prescribe antibiotics listed in the List of Essential Drugs [21].
We conducted a 3-year natural, before and after, quasi-experimental study in the real world. A controlled interruption time series design was used to collect data at several time points before and after the COVID-19 pandemic outbreak, aiming to investigate the immediate and long-term impacts of the pandemic on antibiotic consumption. In this study, the effectiveness of data was estimated by controlling the baseline level and the trend [22], the longitudinal characteristics of the data ensured the robustness of results [23].
Data collection and management
We retrospectively collected aggregated monthly antibiotic consumption data from 38 township hospitals in counties S and Y of City L in Shandong, China, from January 2019 to December 2021. The data were collected with the following method. Two researchers were responsible for preparing Excel forms with headers. These persons emailed feedback to the researchers. At the end of December 2019, and then it spread to Shandong Province due to population migration during Chinese New Year holidays [24]. Therefore, the antibiotic consumption data over 12 months before and 24 months after the outbreak of the COVID-19 pandemic was included. The antibiotic consumption data mainly included the following variables: names of township hospitals, manufacturer of antibiotics, unique chemical substance name, generic name, dosage form, unit strength, specification, unit (by box, bottle, or ampoule), price per unit, inventory at the beginning of the month, monthly purchase quantity, monthly ex-warehouse quantity, monthly inventory at the end of the month, etc.
The original data were managed in Microsoft Excel (version 2019). We strictly controlled the quality of the data, carefully sorted and summarized them after receiving the emails from the persons in charge of the township hospitals. The validity of the data was assessed by two researchers engaged in antibiotic resistance research. They mainly made logic proofreading and supplemented outliers or missing values. During the process of cleaning data, the data with problems were separately listed and sent back to the corresponding persons in charge via emails for supplementing or correction. For example, they should supplement monthly usage, specifications, and dosage forms of drug, and check whether the end-of-month inventory of the drugs as consistent with the beginning-of-month inventory of the next month.
We assessed antibiotic consumption data according to Anatomical Therapeutic Chemical (ATC) classification J01 (i.e., antibacterial for systemic use) [25]. Additional file 1: Table S1 provides a full list of antibiotics analyzed in this study. A total of 55 unique chemical substance names (55 ATC-5 codes) were identified for single or combined antibiotics; they were first classified into 19 ATC-4 classes and secondly into 6 ATC-3 groups. At the same time, antibiotics were classified according to the WHO AWaRe categories (version 2021), aiming to analyze the use patterns of antibiotics [26]. Only one type of antibiotic, Fosfomycin, was classified as Reserve. Therefore, the antibiotics of the Reserve category were not included in the analysis. Instead, only Access and Watch category antibiotics were included. The Access category antibiotics are recommended by the WHO as the first or second choice for empirical treatment, whereas the increased consumption of Watch category antibiotics will aggravate antibiotic resistance.
Outcome measures
The study assessed the immediate and long-term impacts of the COVID-19 pandemic on the changes in antibiotic use. The primary outcome indicator of interest was the monthly antibiotic consumption. Antibiotic consumption was measures using Defined Daily Dose (DDD), an assumed average maintenance dose developed by WHO to compare drug consumptions [25]. In this study, the DDD value of each drug was determined according to the Guidelines for ATC classification and DDD assignment 2021 [26]. The DDD equivalence per package [DPP = (unit strength * package size/DDD)] of drugs was calculated according to ATC templates. The total consumption of each group of procured drugs (DDDs) was estimated as the summed DPPs of all-inclusive products [27].
where Ni represents the number of packages of a certain antibiotic product(i) used in the township hospitals.
Data analysis
This study used the descriptive statistical method to quantify the patterns and trends of antibiotic consumption. First, the relative changes in the overall antibiotic consumption among all PHSs in 2020 and 2021 compared to the corresponding periods in 2019 were described. Second, a monthly antibiotic consumption trend chart based on ATC classification and WHO AWaRe category was prepared to observe and describe changes in antibiotic consumption from January 2019 to December 2021, respectively.
By using interrupted time series analysis, the immediate and long-term impacts of the COVID-19 pandemic on the trends of antibiotic consumption in PHSs were assessed [23, 28]. The time unit in this study was month, for all the data were collected monthly at even intervals. With December 2019 taken as the intervention time point, the data over 12 months before the intervention and 24 months after the intervention was finally included in the study. A segmented regression model was established as follows:
where is the independent outcome variable of month t (antibiotic consumption DDDs); where is a continuous time series variable (1,2,3… 36); Covid-19t represents the intervention time indicator before and after the outbreak of the COVID-19 pandemic. The intervention time nodes lie in the 12th month before the outbreak of COVID-19 pandemic (t = 0) and the 24th after the outbreak of COVID-19 pandemic (t = 1); where Long-termt represents the time since the outbreak of the COVID-19 pandemic; its value before the outbreak of COVID-19 pandemic is 0, while its value after the outbreak of COVID-19 pandemic is 1, 2, 3, …24, corresponding to January 2020 to December 2021 (long-term effect). In addition, a dummy variable Cold was set to control the extreme value of antibiotic consumption during the coldest period of Chinese Spring Festival, which was the wild data point of this study [28–31]. By referring to previous studies, we assigned 1 to the variable Cold in December and January of each year, and 0 for the rest of months of these the year [32].
In this model, β0 is used to estimate the level of antibiotic consumption at the beginning of the time series. β1 is used to estimate the change trends of antibiotic consumption prior to the outbreak of the COVID-19 pandemic. β2 is used to assess the changes immediately after the outbreak of the COVID-19 pandemic. β3 reflects the monthly changes in antibiotic consumption after the outbreak of the COVID-19 pandemic. If it is different from the trend before the outbreak of the COVID-19 pandemic, it suggests that the outbreak of the COVID-19 pandemic has a long-lasting impact on the antibiotic consumption. β4 is used to estimate the weather effect of the coldest period. is an estimate of the random error at time t. In addition, Durbin–Watson test was performed to verify the existence of the first-order autocorrelation (if the value is about 2, it indicates that there is no autocorrelation) [33]. In case of an autocorrelation, the regression will be estimated using the Prais-Winsten method [32].
All statistical analyses were performed in STATA version 15.0 (STATA Crop LP, College Station, TX, USA), and P < 0.05 was considered statistically significant.
Results
Overall antibiotic consumption
Generally, the antibiotic consumption decreased by 32.04% and 16.69% from January to December in 2020 and 2021 compared to the corresponding periods in 2019, respectively (Table 1).
Table 1.
Monthly comparative analysis of overall antibiotic consumption in PHSs
| Before | During the COVID-19 pandemic | % Relative change (2020 vs 2019) | %Relative change (2021 vs 2019) | ||
|---|---|---|---|---|---|
| 2019 | 2020 | 2021 | |||
| Antibiotic consumption (ten thousand DDDs) | |||||
| Total | 170.36 | 115.78 | 141.93 | − 32.04 | − 16.69 |
| January | 19.14 | 12.47 | 12.95 | − 34.85 | − 32.34 |
| February | 16.71 | 9.69 | 10.56 | − 42.01 | − 36.80 |
| March | 14.81 | 9.69 | 11.48 | − 34.57 | − 22.48 |
| April | 13.64 | 8.43 | 10.17 | − 38.20 | − 25.44 |
| May | 13.91 | 8.43 | 10.17 | − 39.40 | − 26.89 |
| June | 12.15 | 8.12 | 10.59 | − 33.17 | − 12.84 |
| July | 12.37 | 8.58 | 11.31 | − 30.64 | − 8.57 |
| August | 13.07 | 8.92 | 12.99 | − 31.75 | − 0.61 |
| September | 12.29 | 9.86 | 8.81 | − 19.77 | − 28.32 |
| October | 13.04 | 9.86 | 13.07 | − 24.39 | 0.23 |
| November | 13.35 | 9.59 | 14.49 | − 28.16 | 8.54 |
| December | 15.88 | 12.14 | 15.34 | − 23.55 | − 3.40 |
DDDs defined daily doses
Antibiotic consumption by ATC classification
In this study, the categories of the most frequently used antibiotics were J01C (beta-lactam antibacterials, penicillins), followed by J01D (cephalosporins, other beta-lactam antibacterials), J01F (macrolides, lincosamides and streptogramins) and J01M (quinolone antibacterials).
According to Fig. 1, the consumption of J01C antibiotics (beta-lactam antibacterial, penicillins) fluctuated throughout the study period. It declined sharply in December 2019. Then, it fluctuated steadily on a relatively low level. However, it increased significantly in September 2021. This trend mainly affected the change of the total consumption of J01 antibiotics during this period.
Fig. 1.
Monthly changes in antibiotic consumption by ATC classification
Antibiotic consumption by the WHO AWaRe category
According to Table 2, the average annual consumption of Watch category antibiotics decreased by 42.02% and 33.47% in 2020 and 2021 compared to the same periods in 2019, respectively. Figure 2 illustrates that before the outbreak of COVID-19, Watch category antibiotics were consumed much more than Access category antibiotics. However, in December 2019 (after the outbreak of COVID-19), the trend of antibiotic consumption was reversed. It suggests that the outbreak of the COVID-19 pandemic may have improves the improper antibiotic consumption patterns in PHSs.
Table 2.
Annually comparative analysis of antibiotic consumption by WHO AWaRe category in PHSs
| AWaRe category | Before | During the COVID-19 pandemic | % Relative change (2020 vs 2019) | %Relative change (2021 vs 2019) | |
|---|---|---|---|---|---|
| 2019 | 2020 | 2021 | |||
| Access antibiotics (ten thousand DDDs) | 74.91 | 60.27 | 78.62 | − 19.54 | 4.95 |
| Watch antibiotics (ten thousand DDDs) | 95.44 | 55.34 | 63.50 | − 42.02 | − 33.47 |
DDDs defined daily doses
Fig. 2.
Monthly changes in antibiotic consumption by WHO AWaRe category
Impacts of the COVID-19 pandemic on antibiotic consumption
As shown in Table 2, after the outbreak of the COVID-19 pandemic, the consumption of J01 antibiotics (antibacterials for systemic use) in PHSs showed a significant immediate decline immediately (coef. = − 2.712, p = 0.045), followed by a low-level increase with significance in the long-term (coef. = 0.205, p = 0.005). At the same time, the immediate impact of the outbreak of the COVID-19 pandemic on the consumption of J01C antibiotics (beta-lactam antibacterials, penicillins) had no statistical significance in the short term However, its consumption had a low-level increase in the long-term (coef. = − 0.117, p = 0.031). Similarly, the consumption of J01D antibiotics (cephalosporins, other beta-lactam antibacterial), J01M antibiotics (quinolone antibacterial) and J01F antibiotics (macrolides, lincosamides and streptogramins) all showed significant immediate declines in the short term after the COVID-19 pandemic outbreak (coef. = − 0.405, p = 0.020; coef. = − 0.083, p = 0.026; coef. = − 0.740, p < 0.001). It is particularly worth noting that there was no statistical significance in the immediate impact of COVID-19 on Access category antibiotic consumption, but a significant and rapid increase was observed in the long-term (coef. = 0.136, p = 0.018).On the contrary, the pandemic caused a significant immediate decrease of the consumption of Watch category antibiotics in the immediate (coef. = − 1.222, p < 0.001) and a slight increase in the long-term (coef. = 0.073, p < 0.001), with significant statistical differences (Figs. 3, 4, and Table 3).
Fig. 3.
Monthly consumption trend of antibiotics from the Access category in PHSs
Fig. 4.
Monthly consumption trend of antibiotics from the Watch category prescribed in PHSs
Table 3.
The segmented regression time series analysis of the antibiotic consumption in PHSs
| Outcome indicators | Immediate effect | Long-term effect | ||||||
|---|---|---|---|---|---|---|---|---|
| Coef. | 95% CI | P | Coef. | 95% CI | P | |||
| J01 Antibacterials for systemic use (ten thousand DDDs) | − 2.712 | − 46.327 | 50.671 | 0.045* | 0.205 | − 3.150 | 2.740 | 0.005** |
| J01C Beta-lactam antibacterials, Penicillins (ten thousand DDDs) | − 0.850 | − 31.172 | 32.872 | 0.918 | 0.117 | − 1.724 | 1.489 | 0.031* |
| J01D Cephalosporins, Other Beta-lactam antibacterials (ten thousand DDDs) | − 0.405 | − 12.792 | 13.601 | 0.020* | 0.025 | − 0.912 | 0.863 | 0.133 |
| J01F Macrolides, lincosamides and streptogramins (ten thousand DDDs) | − 0.740 | − 1.416 | 2.897 | < 0.001** | 0.012 | − 0.516 | 0.491 | < 0.001** |
| J01G Aminoglycoside antibacterials (ten thousand DDDs) | − 0.114 | − 0.705 | 0.932 | 0.005** | − 0.002 | − 0.104 | 0.109 | 0.000** |
| J01M Quinolone antibacterials (ten thousand DDDs) | − 0.083 | − 8.613 | 8.778 | 0.026* | 0.033 | − 0.719 | 0.653 | 0.844 |
| J01X Other antibiotics in J01 (ten thousand DDDs) | − 0.001 | − 3.550 | 3.552 | 0.632 | 0.023 | − 0.965 | 0.918 | 0.927 |
| Access category antibiotics (ten thousand DDDs) | − 0.970 | − 29.687 | 31.627 | 0.931 | 0.136 | − 1.976 | 1.704 | 0.018* |
| Watch category antibiotics (ten thousand DDDs) | − 1.222 | − 18.900 | 21.345 | < 0.001** | 0.073 | − 1.317 | 1.171 | < 0.001** |
DDDs defined daily doses, Coef. non-standardized coefficient, CI confidence interval
*p < 0.05; **p < 0.01
Discussion
Our study assessed changes in antibiotic use during the COVID-19 pandemic. The segmented regression model revealed that antibiotic consumption declined significantly and the use pattern has changed before and after the COVID-19 pandemic outbreak.
In this study, a significant decline was observed in the overall antibiotic consumption in PHSs in 2020 and 2021 compared to the corresponding period in 2019, respectively. Interestingly, the interrupted time series analysis showed a significant immediate decline in overall antibiotic consumption, but a slow increase in the long-term. It is worth noting that antibiotics were partially unavailable in PHSs in China early in the pandemic. Physicians prescribed these drugs carefully, fearing delays in identifying potential COVID-19 patients due to insufficient diagnostic capabilities. The increasing antibiotic consumption after the effective control of the COVID-19 pandemic was potentially associated with the gradual restoration of medical order. According to previous studies in the UK [34] and Portugal [16], the number of antibiotic prescriptions and antibiotic consumption decreased in PHSs after the outbreak of the COVID-19 pandemic. However, the research report in Portugal [16] showed that the slight upward trend of the overall antibiotic consumption in the long-term was not statistically significant, which differs from the results of our study. We found that the overall antibiotic consumption had a statistically significant upward trend over the long-term. This result may be caused by the prevention and control policies on the COVID-19 pandemic in China. In the early stage of the COVID-19 pandemic, China issued many strict isolation and protection measures, such as requiring “Isolation at home,” and promoting “Do not go to hospitals unless indeed necessary” [17]. These measures reduced the number of outpatient visits and the incidence of influenza to some extent, causing antibiotics consumed in PHSs to drop sharply [17, 18]. However, after China successfully contained the COVID-19 pandemic rapidly and began to adopt normalized pandemic prevention and measures, antibiotic consumption began to rise again. This was possibly due to the gradual removal of a series of pandemic containing measures.
Moreover, after the COVID-19 pandemic outbreak, the consumption of Access category antibiotics in PHSs increased significantly in the long-term. However, the consumption of Watch category antibiotics decreased immediately but increased slightly in the long-term. Similarly, a previous study also demonstrated that the consumption of Watch category antibiotics declined after the COVID-19 pandemic outbreak [16]; and another study suggested that the proportion of the consumption of Access category antibiotics used in PHSs rise significantly during the COVID-19 pandemic [17]. This may be related to the strict restrictions and increased hygiene measures adopted during the COVID-19 pandemic, as well as the reduction of medical service contact and irrational prescriptions of antibiotics. Therefore, the COVID-19 pandemic may have optimized the use pattern of antibiotics and sent a positive signal for the management of antibiotic resistance in China [17, 32]. By assessing the changes in the consumption of three classes of antibiotics, i.e., J01D antibiotics (cephalosporins, other beta-lactam antibacterials), J01F antibiotics (macrolides, lincosamides and streptogramins) and J01M antibiotics (quinolone antibacterials), we found a significant immediate decrease of the consumption of all antibiotic classes in the short-term, which contributed to reducing antibiotic resistance [35, 36]. According to a study conducted in South Korea [37], the consumption of penicillin, cephalosporins and fluoroquinolones decreased during the COVID-19 pandemic, decreased by 54%, 32%, and 15%, respectively, compared to those in the previous year. This may be mainly attributed to the declined infectious diseases incidence caused by non-pharmaceutical interventions (i.e., hand-washing, face masks, physical distancing and travel restrictions), as well as the decline in medical services of PHSs due to the COVID-19 pandemic. However, it is worth noting that antibiotic use rebounded from the low level and increased slightly in the long term, indicating that the decline of antibiotic use during the pandemic may not last for a long time. The COVID-19 pandemic may have some positive impact on improving antibiotic misuse in PHSs [38]. At the same time, considering the fact that the majority of antibiotics are prescribed in PHSs in China [6–8], the declined antibiotic consumption and improved use patterns due to the COVID-19 pandemic bring a new opportunity for future policymakers to improve their antibiotic stewardship.
Advantages and limitations
As for the strengths of this study, first we adopted a strong quasi experimental design, based on interrupted time series analysis, to assess the immediate and long-term impacts of the COVID-19 pandemic on antibiotic use by ATC classification and AWaRe category. When making antibiotic data analysis, we considered the seasonal factors and made corresponding adjustment. In addition, we completed an autocorrelation test to ensure the robustness of the results. This study provided the latest evidence for the changes in antibiotic use patterns in PHSs in Shandong Province of China.
However, there are several limitations in this study. First, due to the limited time and funds, we only obtained a small sample size for this study, and only collected the monthly antibiotic consumption data of 38 township hospitals. Second, as the data on patients and prescriptions were not available, we did not analyze the specific influencing factors causing the changes in antibiotic use patterns. Third, as the COVID-19 pandemic had a complex impact on the antibiotic consumption in each specific region or setting, the findings may not be extrapolated to other settings or regions. Therefore, it is necessary to carry out more researches in different settings.
Conclusion
To sum up, our study suggests that the COVID-19 pandemic has an in-depth impact on antibiotic consumption in PHSs in Shandong, China. After the outbreak of COVID-19 pandemic, the overall antibiotic consumption declined significantly in the short-term. However, it showed a increase over the long-term. Consistent priority use of penicillin and cephalosporin should be of great concern in the PHSs in Shandong, China. In addition, the COVID-19 pandemic caused a rapid increase in the consumption of Access category antibiotics in the long-term but an immediate significant decrease in the consumption of Watch category antibiotics. This may have improved the antibiotic use patterns in PHSs to some extent. Therefore, the COVID-19 pandemic may bring an opportunity for better management of antibiotics use in China. In future studies, it is necessary to monitor antibiotic consumption and collect data on patients using antibiotics and related prescriptions s to better explore the impact of the COVID-19 pandemic on antibiotic use. In this way, we may find the direct factors causing the aforementioned changes. Policy-makers should seize the opportunity to overcome the challenges faced by antibiotic use under the COVID-19 pandemic in PHSs in China to improve their management to a higher level.
Supplementary Information
Additional file 1. Table S1. List of the antibiotics analyzed in this study.
Acknowledgements
We thank all the participants for their contribution and the Center for Health Management and Policy Research, School of Public Health, Cheeloo College of Medicine, Shandong University, (NHC Key Laboratory of Health Economics and Policy Research, Shandong University).
Abbreviations
- PHSs
Primary healthcare settings
- COVID-19
Coronavirus Disease-19
- DDDs
Defined daily doses
- AWaRe
Access, Watch, Reserve
- AMR
Antimicrobial resistance
- WHO
World Health Organization
- ATC
Anatomical Therapeutic and Chemical
- GDP
Gross Domestic Product
- DDD
Defined daily dose
- DPP
DDD equivalence per package
- J01
Antibacterials for systemic use
- J01C
Beta-lactam antibacterials, penicillins
- J01D
Cephalosporins, other beta-lactam antibacterials
- J01F
Macrolides, lincosamides and streptogramins
- J01G
Aminoglycoside antibacterials
- J01M
Quinolone antibacterials
- J01X
Other antibiotics in J01
- Coef.
Non-standardized coefficient
- CI
Confidence interval
Author contributions
TW and LS contributed equally to this work and share first authorship. TW and LS contributed to the study design, data analysis, and drafting of the manuscript. QS and JY made substantial contributions to the conception, design, and revision of the manuscript. LZ participated in the extraction and the revision of the manuscript. All authors have seen and approved the final manuscript.
Funding
This research was supported by the National Natural Science Foundation of the Republic of China (Grant number 71774103). The funding body played no role in study design, data collection and analysis, manuscript preparation, or decision to publish the results.
Availability of data and materials
The datasets used and analyzed during the current study are available from the corresponding author upon reasonable request.
Declarations
Ethics approval and consent to participate
Not applicable.
Consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
Footnotes
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Ting Wang and Liyan Shen have contributed equally to this work
References
- 1.Laxminarayan R, Duse A, Wattal C, Zaidi AKM, Wertheim HFL, Sumpradit N, et al. Antibiotic resistance—the need for global solutions. Lancet Infect Dis. 2013 doi: 10.1016/S1473-3099(13)70318-9. [DOI] [PubMed] [Google Scholar]
- 2.Meeker D, Linder JA, Fox CR, Friedberg MW, Persell SD, Goldstein NJ, et al. Effect of behavioral interventions on inappropriate antibiotic prescribing among primary care practices: a randomized clinical trial. JAMA. 2016 doi: 10.1001/jama.2016.0275. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Zhao H, Wei L, Li H, Zhang M, Cao B, Bian J, et al. Appropriateness of antibiotic prescriptions in ambulatory care in China: a nationwide descriptive database study. Lancet Infect Dis. 2021 doi: 10.1016/S1473-3099(20)30596-X. [DOI] [PubMed] [Google Scholar]
- 4.World Health Organization. Global action plan on antimicrobial resistance. Geneva: World Health Organization. 2015. https://www.who.int/publications/i/item/9789241509763. Accessed 20 May 2022.
- 5.Zhang QQ, Ying GG, Pan CG, Liu YS, Zhao JL. Comprehensive evaluation of antibiotics emission and fate in the river basins of china: source analysis, multimedia modeling, and linkage to bacterial resistance. Environ Sci Technol. 2015 doi: 10.1021/acs.est.5b00729. [DOI] [PubMed] [Google Scholar]
- 6.Dyar OJ, Beović B, Vlahović-Palčevski V, Verheij T, Pulcini C. How can we improve antibiotic prescribing in primary care? Expert Rev Anti Infect Ther. 2016 doi: 10.1586/14787210.2016.1151353. [DOI] [PubMed] [Google Scholar]
- 7.Peñalva G, Fernández-Urrusuno R, Turmo JM, Hernández-Soto R, Pajares I, Carrión L, et al. Long-term impact of an educational antimicrobial stewardship programme in primary care on infections caused by extended-spectrum β-lactamase-producing Escherichia coli in the community: an interrupted time-series analysis. Lancet Infect Dis. 2020 doi: 10.1016/S1473-3099(19)30573-0. [DOI] [PubMed] [Google Scholar]
- 8.Sulis GAP, Nafade V, Gore G, Daniels B, Daftary A, et al. Antibiotic prescription practices in primary care in low- and middle-income countries: a systematic review and meta-analysis. PLoS Med. 2020 doi: 10.1371/journal.pmed.1003139. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.World Health Organization. Using indicators to measure country pharmaceutical situations: fact book on who level I and level II monitoring indicators. Geneva: World Health Organization. 2006. https://apps.who.int/iris/handle/10665/354554. Accessed 20 May 2022.
- 10.Wang X, Tang Y, Liu C, Liu J, Cui Y, Zhang X. Effects of restrictive-prescribing stewardship on antibiotic consumption in primary care in China: an interrupted time series analysis, 2012–2017. Antimicrob Resist Infect Control. 2020 doi: 10.1186/s13756-020-00821-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Borek AJ, Maitland K, McLeod M, Campbell A, Hayhoe B, Butler CC, et al. Impact of the COVID-19 pandemic on community antibiotic prescribing and stewardship: a qualitative interview study with general practitioners in England. Antibiotics (Basel). 2021;10:1531. doi: 10.3390/antibiotics10121531. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Buehrle DJ, Wagener MM, Nguyen MH, Clancy CJ. Trends in outpatient antibiotic prescriptions in the United States during the COVID-19 pandemic in 2020. JAMA Netw Open. 2021 doi: 10.1001/jamanetworkopen.2021.26114. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Högberg LD, Vlahović-Palčevski V, Pereira C, Weist K, Monnet DL, ESAC-Net Study Group Decrease in community antibiotic consumption during the COVID-19 pandemic, EU/EEA, 2020. Euro Surveill. 2021 doi: 10.2807/1560-7917.ES.2021.26.46.2101020. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.King LM, Lovegrove MC, Shehab N, Tsay S, Budnitz DS, Geller AI, et al. Trends in US outpatient antibiotic prescriptions during the coronavirus disease 2019 pandemic. Clin Infect Dis. 2020 doi: 10.1093/cid/ciaa1896. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Kitano T, Brown KA, Daneman N, MacFadden DR, Langford BJ, Leung V, et al. The impact of COVID-19 on outpatient antibiotic prescriptions in Ontario, Canada; an interrupted time series analysis. Open Forum Infect Dis. 2021 doi: 10.1093/ofid/ofab533. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Silva TM, Estrela M, Gomes ER, Piñeiro-Lamas M, Figueiras A, Roque F, et al. The impact of the COVID-19 pandemic on antibiotic prescribing trends in outpatient care: a nationwide, quasi-experimental approach. Antibiotics (Basel) 2021 doi: 10.3390/antibiotics10091040. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Yang Y, Geng X, Liu X, Wen X, Wu R, Cui D, et al. Antibiotic use in China’s public healthcare institutions during the COVID-19 pandemic: an analysis of nationwide procurement data, 2018–2020. Front Pharmacol. 2022 doi: 10.3389/fphar.2022.813213. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Zhang T, Shen X, Liu R, Zhao L, Wang D, Lambert H, et al. The impact of COVID-19 on primary health care and antibiotic prescribing in rural China: qualitative study. BMC Health Serv Res. 2021 doi: 10.1186/s12913-021-07082-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Zhao H, Wang S, Meng R, Liu G, Hu J, Zhang H, et al. Appropriateness of antibiotic prescriptions in Chinese primary health care and the impact of the COVID-19 pandemic: a typically descriptive and longitudinal database study in Yinchuan city. Front Pharmacol. 2022 doi: 10.3389/fphar.2022.861782. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.National Bureau of Statistics of China . China statistical yearbook 2021. Beijing: China Statistics Press; 2021. [Google Scholar]
- 21.Ministry of Health of the People’s Republic of China. Administrative measures for the clinical use of antibacterial drugs. In: Ministry of Health of the People’s Republic of China, editor. 2012.
- 22.Sruamsiri R, Wagner AK, Ross-Degnan D, Lu CY, Dhippayom T, Ngorsuraches S, et al. Expanding access to high-cost medicines through the E2 access program in Thailand: effects on utilisation, health outcomes and cost using an interrupted time-series analysis. BMJ Open. 2016 doi: 10.1136/bmjopen-2015-008671. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Kontopantelis E, Doran T, Springate DA, Buchan I, Reeves D. Regression based quasi-experimental approach when randomisation is not an option: interrupted time series analysis. BMJ (Clinical Research Ed) 2015;350:h2750. doi: 10.1136/bmj.h2750. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Li Q, Guan X, Wu P, Wang X, Zhou L, Tong Y, et al. Early transmission dynamics in Wuhan, China, of novel coronavirus–infected pneumonia. N Engl J Med. 2020 doi: 10.1056/NEJMoa2001316. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.World Health Organization. The anatomical therapeutic chemical classification system with defined daily doses (ATC/DDD). https://www.who.int/standards/classifications/other-classifications/the-anatomical-therapeutic-chemical-classification-system-with-defined-daily-doses. Accessed 20 May 2022.
- 26.World Health Organization. WHO Access, watch, reserve (aware) classification of antibiotics for evaluation and monitoring of use. 2021. https://www.who.int/publications/i/item/2021-aware-classification. Accessed 20 May 2022.
- 27.Lin H, Dyar OJ, Rosales-Klintz S, Zhang J, Tomson G, Hao M, et al. Trends and patterns of antibiotic consumption in Shanghai Municipality, China: a 6 year surveillance with sales records, 2009–14. J Antimicrob Chemother. 2016 doi: 10.1093/jac/dkw013. [DOI] [PubMed] [Google Scholar]
- 28.Wagner AK, Soumerai SB, Zhang F, Ross-Degnan D. Segmented regression analysis of interrupted time series studies in medication use research. J Clin Pharm Ther. 2002 doi: 10.1046/j.1365-2710.2002.00430.x. [DOI] [PubMed] [Google Scholar]
- 29.Chen M, Wang Q, Shen H. Analysis on seasonal change rule of antibiotic use in our hospital. China Pharm. 2012;21:52–53. [Google Scholar]
- 30.Zhen L, Qu B, Hu M, Guo C, Chen L, Jin C. The impact of a peer review and feedback intervention on antibiotic prescribing: Interrupted time series analysis at village clinics in Qingdao, Shangdong Province. Chin J Health Policy. 2013;6:54–59. [Google Scholar]
- 31.Zhen L, Jin C, Xu HN. The impact of prescriptions audit and feedback for antibiotic use in rural clinics: interrupted time series with segmented regression analysis. BMC Health Serv Res. 2018 doi: 10.1186/s12913-018-3602-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Yang Y, Chen L, Ke X, Mao Z, Zheng B. The impacts of Chinese drug volume-based procurement policy on the use of policy-related antibiotic drugs in Shenzhen, 2018–2019: an interrupted time-series analysis. BMC Health Serv Res. 2021 doi: 10.1186/s12913-021-06698-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Draper N, Smith H. Applied regression analysis. Wiley series in probability and statistics. 3. New York: John Wiley & Sons; 1998. [Google Scholar]
- 34.Hussain AZ, Paudyal V, Hadi MA. Impact of the COVID-19 pandemic on the prescribing patterns of first-line antibiotics in English primary care: a longitudinal analysis of national prescribing dataset. Antibiotics (Basel) 2021 doi: 10.3390/antibiotics10050591. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Knight GM, Glover RE, McQuaid CF, Olaru ID, Gallandat K, Leclerc QJ, et al. Antimicrobial resistance and COVID-19: intersections and implications. Elife. 2021 doi: 10.7554/eLife.64139. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Monnet DL, Harbarth S. Will coronavirus disease (COVID-19) have an impact on antimicrobial resistance? Euro Surveill. 2020 doi: 10.2807/1560-7917.ES.2020.25.45.2001886. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Ryu S, Hwang Y, Ali ST, Kim D-S, Klein EY, Lau EHY, et al. Decreased use of broad-spectrum antibiotics during the coronavirus disease 2019 epidemic in South Korea. J Infect Dis. 2021 doi: 10.1093/infdis/jiab208. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Blix HS, Høye S. Use of antibiotics during the COVID-19 pandemic. Tidsskr Nor Laegeforen. 2021 doi: 10.4045/tidsskr.20.1003. [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Additional file 1. Table S1. List of the antibiotics analyzed in this study.
Data Availability Statement
The datasets used and analyzed during the current study are available from the corresponding author upon reasonable request.




