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. 2025 Apr 30;5(4):e0004127. doi: 10.1371/journal.pgph.0004127

Association between national action and trends in antibiotic resistance: an analysis of 73 countries from 2000 to 2023

Peter Søgaard Jørgensen 1,2,3,*, Luong Nguyen Thanh 1,3, Ege Pehlivanoğlu 1, Franziska Klein 1,¤a, Didier Wernli 4, Dusan Jasovsky 5,¤b, Athena Aktipis 6, Robert R Dunn 7, Yrjö Gröhn 8, Guillaume Lhermie 8,¤c, H Morgan Scott 9, Eili Y Klein 10,11
Editor: Ashish KC12
PMCID: PMC12043137  PMID: 40305457

Abstract

The world’s governments have agreed on actions to address the challenge of antibiotic resistance. This raises the question of what level of national action is associated with improved outcomes, including both slower growth and lower levels of antibiotic resistance. Answering this question is challenged by variation in data availability and quality as well as disruptive events such as the COVID-19 pandemic. We investigate the association between level of national action and temporal trends in multiple indicators related to health system capacity, antibiotic use (ABU), absolute rates of resistance (ABR) and a Drug Resistance Index (DRI). Using the Global Database for Tracking Antimicrobial Resistance (TrACSS) to construct an index of national action, we apply cross-sectional regression across 73 countries to estimate the association between the level of action in 2016 and trends in national indicators (2000–2016). We find that national action is consistently associated with improved linear or categorical trends in all groups of indicators. Reductions are associated with a relatively high action index (range 0–4) for ABU (median 2.8, 25–75% quartile 2.6-3.3), ABR (3.0, 2.4-3.4), and DRI (3.5, 3.1-3.6). These associations are robust to the inclusion of other contextual factors related to socio-economic conditions, human population density, animal production and climate. Since 2016, a majority of both Low- and Middle-Income Countries (LMICs) and High-Income Countries (HICs) report increased action on repeated questions, while one third of countries report reduced action. The main limitations in interpretation are heterogeneity in data availability and in when actions have been implemented. Our findings highlight the importance of national action to address the domestic situation related to antibiotic resistance and indicate the value of both incremental changes in reducing adversity of outcomes and the need for high levels of action in delivering reduced levels of resistance.

Introduction

Antibiotic resistance (ABR) is a global public health challenge that in 2019 was estimated to contribute to 1.27 million deaths per year and was associated with a total of 4.95 million deaths [1]. In 2015, countries agreed a Global Action Plan to address the growing challenge of ABR, which was followed up in 2016 and 2024 with UN high-level meetings, where commitments were made to develop and implement national action plans (NAPs). The high burden of ABR and the increasing focus on national action highlights the importance of assessing the level of action that can be expected to lead to improvements in national conditions. However, such assessment is challenged by multiple factors, including the time it takes from policy adoption to effect of a policy, variation in data availability across countries, and the recent disruption to monitoring of the COVID-19 pandemic [2].

In 2016–17, the Global Database for Tracking Antimicrobial Resistance (TrACSS) completed its first survey of the presence and ambition of antibiotic resistance policies in more than 150 countries. Based on self-reporting, this database gives the first snapshot of the level of action taken to tackle antibiotic resistance around the world. Key indicators to consider the effects of policies on span from the upstream drivers that lead to increases in antibiotic use (ABU), ABU itself, levels of ABR and the exposure to and impact of resistant infections [3]. Among drivers, lack of health system capacity is a major contributor to inappropriate use [4,5]. For ABU, the total consumption of antibiotics adds selection pressures for resistance and the use of broad spectrum and last resort antibiotics are of particular concern [6]. For ABR, it is relevant to monitor effects of both common infections as well as resistance to last resort antibiotics. For exposure and impact, gaps in monitoring mean that good indicators are scarcely available [7].

In this paper we investigate the association of action reported in the TrACSS database with temporal trends in national indicators relating to antibiotic resistance from 73 countries (Fig 1). We apply a multi-indicator approach, covering indicators related to the health system, ABU, ABR and exposure to antibiotic resistant infections in humans (Drug Resistance Index, DRI).

Fig 1. Study design. (A) DPSE indicators (tier 1) and their tier 2 components (boxes with dashed-lines). “n” refers to number of countries, for detailed information on indicators see S1 Table, S2 Table, S3 Table. (B) Temporal overview of analysis showing the two periods across which the trend in DPSE indicators is calculated and the timing of the first (2016-17) and seventh (2023) TrACSS survey. (C) Governance syndrome. Categorical trends in DPSE indicators and the action index combine to form four types of governance syndrome.

Fig 1

Methods

Study design

We investigate national trends in indicators related to ABR by using a multi-indicator assessment approach according to a modified version of the Drivers-Pressure-State-Exposure-Effect-Action (DPSEEA) family of frameworks [8] (Fig 1, S1 Table, S2 Table, S3 Table). Such frameworks aim to assess how policies affects changes at multiple points in a system [3]. Similar frameworks, have been used to evaluate national progress on health and biodiversity issues [9], but also to understand the co-evolutionary dynamics of pesticide resistance [10].

Our main purpose is to understand to what degree self-reported policy action can help explain temporal trends in national indicators of drivers, pressures, state and exposure to antibiotic resistance, henceforth DPSE indicators (Fig 1A, see Variables and Indicators for details). Specifically, we construct an action index based on the first TrACSS survey in 2016–17. As 2016–17 was the first survey since the agreement of the Global Action Plan, the actions reported are assumed to mainly reflect measures implemented during the first decade and a half of the 21st century and to be relevant for temporal trends in indicators during this period. This is because countries will have had little time to take new large-scale action since 2015 and since any new action that has been taken since 2015, will have had little time to have a measurable effect. We therefore relate the action index to trends in DPSE indicators in the preceding 16 years (Fig 1B), specifically the change in indicators between the first and second half of the period 2000–2016. We also investigate the relative importance of action compared to covariates related to health systems, economy, human population, livestock production and climate (S4 Table). We apply cross-sectional regression and model selection to assess the strength of association with linear as well as categorical trends.

The above analysis is limited to the human health sector as monitoring in the animal sector is currently too sparse. To complement this analysis, we assess the degree to which production of animal protein is correlated with level of policy action. We correlate the volume of production with level of action taken in the human and animal sector. Finally, we assess the extent to which changes in DPSE indicators are associated with subsequent changes in level of action from 2016 up until 2023 (Fig 1B). Here, a positive cycle is defined as a country experiencing decreases in DPSE indicators during the 2000–2016 period and subsequent increased action during the period 2016–2022 and a negative cycle if the DPSE indicator increased and action decreased. Increases in DPSE indicators and increased action were categorized as “Meeting the challenge” and decreases in DPSE indicators and decreased action were categorized as “Relaxed responses” (Fig 1B).

Setting

A total of 73 countries were included in the analyses (S5 Table). The countries represent all inhabited continents, in order of sample size: Europe (n = 35), Asia (n = 20), South America (n = 7), Africa (n = 5), North America (n = 4), Oceania (n = 2). These were divided between 37 High-Income Countries (HICs) and 36 Low- and Middle-Income Countries (LMICs).

Variables and indicators

DPSE categories capture indicators of health system development (Drivers), ABU (Pressures), ABR (State), and antibiotic resistance relative to use of an antibiotic as measured by the DRI (Exposure). Composite DPSE indicators vary in the number of levels (tiers) at which they can be disaggregated, from one (Exposure), over two (Pressure and State), to three (Drivers), for additional details see S1 Text.

Drivers – health system.

We included fifteen variables relating to the general state of the human health system across four tier 2 indicator groups: infection prevalence (Infection), sanitation standards (Sanitation), vaccination coverage (Vaccination), and health care workforce (Workforce). Each consists of two to four tier-3 indicators (S1 Table).

Pressure – antibiotic use (ABU).

We include antibiotic consumption data for humans for the years 2000–2015. Data are obtained for three tier-2 indicators: use of six broad-spectrum antibiotics [11], measured as percent of total use; use of 25 newly available antibiotics [12]; and total per capita use (total), measured as the Daily Defined Dose (DDD) per 1000 inhabitants per day (S2 Table).

State – absolute rates of resistance (ABR).

We include three groups of tier-2 indicators for antibiotic resistance: Methicillin-resistant Staphylococcus aureus, Carbapenem resistance in Enterobacteriaceae (CRE) and in other bacteria (CRO), and Streptococcal resistance to macrolides and penicillin (S2 Table).

Exposure – relative rates of resistance (DRI).

We use the DRI as an indicator of exposure as it takes into account resistance relative to the use of antibiotics in a country, both of which are important factors in determining likely exposures to resistant infections [13]. For this index we include 16 drug and bacterial combinations including the bacteria: Enterococcus faecalis/faecium, Escherichia coli, Klebsiella pneumonia, Pseudomonas aeruginosa and Staphylococcus aureus (S3 Table). Although the DRI index has been critiqued previously as a standalone indicator [14], we here use it as a part of a multi-indicator analysis to complement patterns in absolute rates of use and resistance.

Action – self-assessment survey.

Selected questions from the AMR TrACSS dataset (S6 Table) were divided into five thematic categories: Awareness & Education, Monitoring & Surveillance, Prevention, Regulation, and General questions(S7 Table). For each country, action scores within categories were calculated by a simple average with individual responses ranging from 0 to 4, in order of increasing ambition. The action index was calculated as the average of all five categories equally weighted. The action index used for the governance syndrome analysis include questions that were asked repeatedly over the years 2016–17 to 2022–23 (S6 Table). Here we calculated the difference between the last year of response (2022–23 for all except 2021–22 for Romania) and the first year of response (2016–17).

Data sources

A variety of data sources was used for measuring the DPSE indicators (S1 Table, S2 Table, S3 Table), explanatory covariates (S4 Table), and the action index (S6 Table). Data for health system drivers came from the United Nations, the World Bank, and the World Health Organization. Data for ABU were obtained the IQVIA database [15] for the years 2000–2015. Data for ABR came from ResistanceMap [16]. Data sources for the DRI were identical to those for ABU (IQVIA [15]) and ABR (ResistanceMap [16]). Data for the action index came from the Global Database for TrACSS survey in 2016–17 and 2022–23. Data for covariates came from The Eora Global Supply Chain Database (GDP), World Income Inequality Database – WIID (Gini index), NASA Center for Climate Simulation – BioClim (mean temperature), Gridded Livestock of the World – GLW (animal production), and NASA’s Socioeconomic Data and Applications Center – SEDAC (human population density).

Bias

Countries are only included if they have sufficient data for the Drivers indicator group and at least one of the other DPSE indicators (ABU, ABR or DRI). This reduces the number of LMICs that can be investigated and biases the sample towards well monitored, often HICs.

Study size

Countries included in the analyses were filtered based on two criteria. First, answering the TrACSS survey in 2016–17 (S6 Table). Second, reporting at minimum three years in the period 2000–2008 as well as in 2008–2016 for ABU or ABR indicators. Applying these criteria, we are able to analyse 73 countries in total (drivers n = 73, ABU n = 65, ABR n = 35, DRI n = 25, Fig 1A).

Quantitative variables

Linear and categorical trends.

We calculated the average for each DPSE indicator at tier 1–3 (S1 Table, S2 Table, S3 Table) across the years 2000–2008 (henceforth baseline) and 2008–2016. First, raw data were standardized by their standard deviation (s.d.= 1), which allow for comparing indicators that use different units of measurement. Then the national changes in means between two periods was calculated as:

  • (1) Linear trend=X20082016X20002008

Henceforth referred to as the linear trend (abbreviated l.t.). We also analyzed countries based on the sign of change of the linear trend (increasing vs. decreasing), henceforth referred to as the categorical trend (abbreviated c.t.).

Statistical method

Model formulation.

We fitted gaussian mixed effect regressions models with the linear trend (equation 2) and the action index as response variable (equation 3), the latter to assess the ability of the categorical trend to explain variation in action (S8 Table). We also fitted binomial mixed effect models with the proportion of declining tier 2 indicators as the response variable, weighted by the availability of indicators (equation 4, S9 Table). All models included baselines (Baseline) as covariates and equation 2 and 3 a random grouping variable (Income) indicating income level (HIC vs LMIC).

  • (2) Linear trend ~ Action + Baseline + (1|Income)

  • (3) Action ~ Categorical trend + Baseline + (1|Income)

  • (4) Proportion in decline ~ Action + Baseline

To explore how action various with size of animal production we also fit a model with action as response variable and action in the human and animal health sector as explanatory variables. For this analysis, we used questions that were asked in parallel for the two sectors (S6 Table).

Sensitivity analysis.

We applied model selection to assess the relative importance of action variables compared to other covariates (S10 Table). Here we fitted gaussian models to the linear trend and binomial models to the categorical trend and we included countries as random effects, the type of DPSE indicator and country income level as factorial variables and covariates relating to the health system, economic condition, human population, animal production mass, and annual mean temperature (S11 Table). We also allow for pairwise interactions between factorial variables and covariates. All global model formulas are detailed in S11 Table. We tested the sensitivity to various combinations of country and indicator subsets, resulting in a total of 17 model selection procedures for the linear trend and 16 for the categorial trend where we did not fit models to the Exposure data as there was too little variation in the response variable outcome. We used the R package “MuMIn” [17] and applied the Akaike’s information criterion corrected for small sample sizes (AICc). We report averaged effects for the 95% Akaike weighted subset as well as coefficients from the models with lowest AICc. All statistical analyses were carried out in R 4.3.1 [18].

Results

Trends in DPSE indicators

The four tier-1 DPSE indicators exhibit mixed 16-year trends with health system drivers improving (linear trend = -0.126 ± 0.017 s.d., p < 0.001, categorical trend = 6/73 countries increasing, p < 0.001), ABU and DRI increasing (ABU: l.t. = 0.289 ± 0.048, p < 0.001, c.t. = 55/65, p < 0.001; DRI: l.t. = 0.184 ± 0.065, p = 0.01, c.t. = 21/25, p = 0.002), and non-significant trends in ABR (l.t. = 0.019 ± 0.069, p = 0.8, c.t. = 16/32, p = 1). The increase in ABU is also seen for three of the four tier 2 indicators (total per capita use: l.t. = 0.329 ± 0.065 p < 0.001, c.t. = 50/65, p < 0.001; broad-spectrum antibiotics: l.t. = 0.278 ± 0.069, p < 0.001, 47/65, p = 0.001; newly available antibiotics: l.t. 0.232 ± 0.061, p < 0.001, c.t. = 55/63, p < 0.001). The only tier-2 ABR indicator that showed a consistent increase over time across countries was resistance to last resort carbapenems (c.t. = 20/28, p = 0.028).

Association between DPSE trends and action

At the tier-1 level, action is negatively correlated with three of four DPSE indicators for both linear and categorical trend (Fig 2, S12 Table, S13 Table). For the linear trend, action is negatively associated with health system drivers, ABU and DRI (Fig 2A, Fig 2B, Fig 2D, p < 0.05). For the categorical trend, action is negatively associated with ABU, ABR and DRI (Fig 2F, Fig 2G, Fig 2H, p < 0.05).

Fig 2. Association between action index and linear trend (A, B, C, D), and categorical trend (E, F, G, H).

Fig 2

Indicator p-values are from linear mixed models with country income group as random effect. For detailed formulas, see S8 Table. Blue represents drivers of antibiotics resistance, purple represents antibiotics use, orange represents resistance, and red represents DRI.

Complementary analyses indicate that the overall explanatory ability of the action index is (a) not due to a correlation with the baseline state of the indicators (S14 Table), is (b) highest at the level of tier 1 (S12 Table, S13 Table), and (c) outperforms individual components of the action index (S15 Table, S16 Table, S17 Table, S18 Table, S19 Table, S20 Table, S21 Table, S22 Table, S23 Table, S24 Table). Thus, individual action components are on average associated with 1 (linear trend) and 1.4 (categorical trend) DPSE indicators, respectively. Of these, the Monitoring and Surveillance component is most commonly associated with DPSE indicators (two of four indicators in both types of models) while Prevention is not associated with any indicators.

The level of action required for consistent negative categorical trend varies widely between DPSE categories (Fig 3, S25 Table, S26 Table). Here, DRI and ABU exhibits the largest needs for action, converging around an action index of 3.5-3.6 out of 4 for 50% probability (Fig 3). DRI showed signs of a threshold behaviour, with very low probabilities of improvement with action below 2 and 50% chance of improvement with an action index above 3.5. For ABU, reduction in 25% of variables was achieved at an action score of 2.5 and 50% at 3.5. We found a 30% chance for reduction in ABR at 1.5 and 50% chance at 2.5. Drivers show overall high probabilities of improvement irrespective of action, but with a slight negative trend as action increases.

Fig 3. Proportion of declining indicators as a function of the action index.

Fig 3

Shown is the proportion of lower-level indicators within a category that have witnessed a reduction from 2000 to 2016. Weight refers to the proportion of variables avaiable for a given country. Uncertainty bands indicate standard errors.

Model selection

Action variables had relatively high levels of importance in model selection usually ranking in top 3 (Fig 4, S1 Fig, S27 Table), and with consistent negative associations with worsened outcomes (S2 Fig, S3 Fig). For linear trends, the general action variable often had a higher importance score than the action index. Here, health system indicators such as workforce were also important and associated with increasing trends for ABU, ABR and DRI. For categorical trends, the action index repeatedly featured in the best selected models (negative coefficients) along with animal production (positive coefficients) and mean temperature (interaction with DPSE) (S3 Fig). Similar effects were also visible when limiting the analysis to HICs, but almost absent within LMICs, potentially due to their larger heterogeneity and data scarcity (S4 Fig, S5 Fig, S6 Fig).

Fig 4. Most important variables in model selection.

Fig 4

The rank of the five most important variables (rows) is shown using color coding. Each column represents a unique model selection procedure on the linear trend (17 procedures) or the categorical trend (16 procedures). Model names refers to the subset of DPSE indicators included D (Driver), P (Pressure), S (State), E (Exposure). In model names, "noDr" indicates exclusion of health system variables as explanatory variables and "aX" refers to analysis of DPSE for country subsets with X variable available. See S10 Table, S11 Table for details on each model selection procedure.

Action in the animal vs human health sector

Countries with larger animal production generally take more ambitious action on animal as well as human health specific issues (slope = 0.60, s.e. = 0.1, t = 6.1, p < 0.001, Fig 5). This is true especially in HICs, where animal health specific action was more sensitive to tonnage of animal protein produced than in LMICs (slope difference = -0.61, F = 12.6, df = 129, p < 0.001, Fig 5). Thus, in HICs, large producers of animal protein had a higher action index on specific animal health questions than they had for human health questions, whereas small producers had a higher action index for the human health questions (slope difference = -0.52, p = 0.01, df = 80, F = 6.2, Fig 5A). In LMICs on the other hand, the human action index was generally higher than the animal action index (mean difference = 0.25, p = 0.02, df = 179, F = 5.8, Fig 5B) with both increasing for bigger producers (slope = 0.29, p < 0.001, df = 179, t = 5, Fig 5B). The level of action in the largest LMIC producers is significantly lower than in the largest HIC producers pointing to a need for further strengthening action in several of the world’s largest producing countries (Fig 5).

Fig 5. Animal production and the action index.

Fig 5

Action level of countries on human (red) and animal (blue) specific issues in relation to total production of vertebrate biomass (mammals, birds and fish) for high-income (HIC) and low- and middle-income countries (LMIC).

Changes in action over time

Three quarters (76%) of countries analysed for association with DPSE indicators in 2016–17 report increased action between 2016–17 and 2023. This is the case in both HICs (70%) as well as in LMICs (83%). However, almost 25% of countries lowered their ambition including almost 30% of HICs (all = 23%, HIC = 30%, LMIC = 17%, Fig 6). For drivers, we see that more than half of HICs and LMICs are in a positive cycle with improved conditions and subsequent increased policy ambition. However, this proportion drops markedly for ABU, ABR, and DRI. For ABU in LMICs, 3 out of 31 countries (10%) are in a positive cycle and 6 in a negative cycle, but 70% are meeting the challenge of increasing ABU with increased policy responses. For HICs, negative cycles are fairly frequent for ABU (24%, n = 34) and DRI (32%, n = 22) and positive cycles very rare for DRI (5%, n = 22).

Fig 6. Governance syndrome.

Fig 6

(A) Trend in DPSE indicators as a function of change in action index. Countries in negative cycle are named with ISO3 codes (see S5 Table). (B) Distribution of governance syndrome by DPSE indicator and country income level.

Discussion

Our results show associations between self-reported action on antibiotic resistance in 2016–17 and trends in the preceding 16 years in health system drivers, ABU, ABR and DRI. These results are robust to inclusion of other contextual variables in multivariate models, strongest at the aggregate scale of both DPSE and action indicators, and not due to a correlation with the baseline state of indicators. The results indicate that every step of improved action is important to reduce the magnitude of increases in ABU and DRI (Fig 2B, Fig 2D), and that high levels of action can help achieve reductions in ABU, ABR and DRI (Fig 2F, Fig 2G, Fig 2H). Here we discuss the interpretation of the results, some potential limitations as well as consequences for policy.

National action and DPSE indicators

National action on antibiotic resistance has been critiqued for not being well enough funded and national action plans (NAPs) for not being fully developed and operationalized, with some indications of adoption of standard templates [1922]. These concerns about the state of national action increase the uncertainty and potential discrepancy between data reported and action taken on the ground. We would expect, such default, template responses to make it harder to detect an association between reported actions and DPSE indicator trends. That is because, such responses make it harder to distinguish between countries with well-implemented and poorly-implemented policies. As we compare trends in DPSE indicators leading up to the 2016–17 survey, some recently taken action will likely not have had an effect on the trends. On the other hand, some policies will have been implemented for several years prior. That we detect these associations even with the above-mentioned uncertainties indicates that well implemented action probably has fairly large and measurable effects with the time needed for achieving the intended effect being the major unknown. It also implies that the estimated levels of action needed to reduce ABU, ABR, and DRI, given sufficient time, are likely safe levels and that reductions might be achievable at lower levels.

We find that the action index more consistently explains univariate changes in the four composite DPSE indicators than any of the individual components of the index and that the explanatory ability of the action index is most consistent at the highest level of aggregation of the DPSE indicators. These results indicate the importance of assessing aggregate policy responses and evaluating their potential impacts on combined indices of multiple indicators. This approach helps account for cross-country variation in social, economic and environmental context and related variation in needs for action. Monitoring and surveillance and general action (such as early progress on NAP development) also explain variation in trends in several multivariate models. Here, general action likely indicates the importance of responding systemically through coordinated responses across sectors e.g., through NAPs [21,23]. The monitoring and surveillance variable performs well in model selection for several models limited to ABU and ABR well as models limited to HICs. The importance of this variable could indicate its importance in enabling informed decision making as well as the adaptive management of both the use of antibiotics and containment of resistant variants [24].

DRI is the hardest of the indicators to achieve reductions in, followed by ABU and ABR. Taken together, we interpret these patterns as indications that absolute rates of resistance can more easily be mitigated by e.g., cycling antibiotics, while reducing use requires a wider infection prevention and control strategy. Reducing relative rates of resistance may also require improving use of antibiotics across the board to mitigate selection pressures on resistance e.g., when a new antibiotic is adopted. The linear trend in ABR shows fairly weak correlation with action, whereas the categorical trend is consistently correlated. The former pattern could be an indication of (1) a non-linear association between action and ABR; (2) that bacteria targeted for management vary by country and potentially go beyond the three indicators available for this analysis, or; (3) that absolute rates of resistance can be circumvented through various aforementioned strategies. The latter pattern could indicate a threshold of action above which such reductions are more likely to be achieved. Overall, national action has a fairly small effect size on the linear trend in health system drivers at ca. 0.25 s.d. across the range of the action index compared to 0.5 s.d. for ABU and DRI. This could be because health system improvements are driven by other policy instruments rather than AMR specific policy. The weakly negative association between action and proportion of improving drivers might be due to such improvements being much harder to achieve for countries with more developed health systems, i.e., countries where almost the entirely population has access to sanitation and vaccines, infection rates are low and where health care workforces are already high.

Health systems, climate and animal production

Model selection reveals that multiple contextual factors help explain additional variation in DPSE indicator trends. These include variables related to health system development, climate and animal production. The relationship between health systems and antibiotic resistance is multifaceted. While the highest burden of antibiotic resistance is often due to lack of access to healthcare and antibiotics, health systems are also associated with higher levels of regulated use [2527]. These consequences for equitable access might be driving the positive association between health workforce and the linear trend in ABU, ABR and DRI in multivariate models.

A positive association between warmer mean temperatures and the categorical trend of DPSE indicators is likely not due to collinearity with GDP per capita, inequality, or country income level as these are all considered as covariates (Fig 4). Possible explanations include a potential non-linear effect of climate on biological factors such as bacterial growth rates [28] or horizontal gene transfer [29]. Alternatively, one or more social, economic or environmental factors that we were not able to include in this analysis could be correlated with our climate indicator.

Animal production is positively associated with the categorical trend of DPSE indicators in four models that do not include health system indicators as explanatory variables (Fig 4). While the importance of animal production is lower when health system variables are included, the pattern is still worth examining given the potential concern about any spillover effect from the animal sector to the human health sector. Multiple explanations can be hypothesized for such patterns, including spillover of residues, resistance genes, or cultural factors relating to antibiotic use, to name a few [30]. Whatever any potential causal explanations might be, these patterns indicate that additional action in both the animal and human sectors may be needed to achieve indicator reductions in large animal producing countries. This challenge should not be underestimated as countries with large animal production are already reporting higher levels of actions in both the human and animal health sector (Fig 5). Reducing the variation in action across countries by elevating the lower level of action of large producers could help address any spillover effects.

Changes in action

While most countries increase their level of action in 2023 compared with 2016–17, around a quarter reduce their levels of action. Reductions in the action index might reflect reduced prioritisation of the policies in the ABR area e.g., during and after the pandemic [2], but might also be due to enhanced accuracy of the data reported in the TrACSS survey compared to the first years. Improved accuracy in reporting would influence findings regarding governance syndromes by inflating the number of countries in the ‘relaxed response’ or ‘negative cycle’ categories. Given the high levels of action associated with reductions of ABU and DRI, it is expected that positive cycles are the least common in these two categories. That is in part due to countries with high levels of action that reduced ABU and DRI having less options to improve their score in 2023. Going forward it will be important to find governance mechanisms, that enable countries to progress in taking new action while focusing on implementing and securing sustainable funding for currently planned actions.

Limitations

Our study has several limitations that should be taken into account when interpreting the results. First, our study is limited by the data availability in countries, which vary by indicator group and is generally biased towards HICs. Care should be taken when interpreting the results to not transfer them outside of their context. For application to specific income-settings, results relating to the specific HIC model and LMIC model should be used. The level of action is self-reported by countries and does not necessarily reflect the actual level of policies implemented in the country. Further, we cannot account for how long policies have been implemented. For example, it is reasonable to assume that countries with higher policy ambition levels have been frontrunners in the field for some time, policies therefore have been in place longer, and potentially showing a larger effect compared to countries who have recently implemented such policies. Our data is limited to antibiotic indicators in the human sector and does not necessarily say anything about the level of action needed for reducing adversity or improving trends in crop or animal health systems.

Conclusions

In conclusion, our analysis indicates the importance of governments taking ambitious and comprehensive action on antibiotic resistance across sectors to improve the national situation. At the same time, in cases where reductions cannot yet be achieved, each additionally implemented action is likely to help reduce the severity of trends in antibiotic use and relative rates of resistance, stressing the need for continuously increased action. Future studies should assess the association between national action and trends in the DPSE indicators during the time period following the agreement of the Global Action Plan.

Supporting information

S1 Text. Supplementary Methods.

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pgph.0004127.s001.pdf (142.2KB, pdf)
S1 Fig. Importance Scores of Variables in Model Selection from Averaged Models.

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pgph.0004127.s002.pdf (386.9KB, pdf)
S2 Fig. Coefficient Estimates of Averaged Models for All Countries in Linear Trend and Categorical Trend Models.

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pgph.0004127.s003.pdf (420.2KB, pdf)
S3 Fig. Coefficient Estimates of Variables from Best Selected Models from Model Selection.

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pgph.0004127.s004.pdf (366KB, pdf)
S4 Fig. Rank of Variables in Averaged Models for Different Income.

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pgph.0004127.s005.pdf (283.8KB, pdf)
S5 Fig. Importance Scores of Variables in Model Selection from Averaged Models for Different income Groups.

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S6 Fig. Coefficient Estimates of Averaged Models for Countries with Different Income Groups.

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pgph.0004127.s007.pdf (238.7KB, pdf)
S1 Table. Indicator selection for Driver categories.

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pgph.0004127.s008.pdf (109.7KB, pdf)
S2 Table. Indicator selection for Use and Resistance categories.

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pgph.0004127.s009.pdf (101.3KB, pdf)
S3 Table. Indicator selection for DRI (exposure) category.

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pgph.0004127.s010.pdf (102.2KB, pdf)
S4 Table. Ecological variables used as covariates.

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pgph.0004127.s011.pdf (99.9KB, pdf)
S5 Table. List of countries included in the study.

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pgph.0004127.s012.pdf (101.6KB, pdf)
S6 Table. Governance Syndrome questions.

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pgph.0004127.s013.pdf (122.2KB, pdf)
S7 Table. Questions used for calculating the action index.

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pgph.0004127.s014.pdf (122.3KB, pdf)
S8 Table. Model Formulas for Association between Action and Indicator Linear Trend and Categorical Trend.

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pgph.0004127.s015.pdf (81.3KB, pdf)
S9 Table. De-escalation plot formulas for univariate models.

(PDF)

pgph.0004127.s016.pdf (81KB, pdf)
S10 Table. Global Models Data Subset Formulas for The Model Selection.

(PDF)

pgph.0004127.s017.pdf (82.8KB, pdf)
S11 Table. Model selection global model formulas.

(PDF)

pgph.0004127.s018.pdf (115.7KB, pdf)
S12 Table. Association Between Linear Trend and Action.

(PDF)

pgph.0004127.s019.pdf (104.8KB, pdf)
S13 Table. Association Between Categorical Trend and Action.

(PDF)

pgph.0004127.s020.pdf (93.4KB, pdf)
S14 Table. Association Between Baseline and Action.

(PDF)

pgph.0004127.s021.pdf (106.2KB, pdf)
S15 Table. Linear Trend and Awareness and Education.

(PDF)

pgph.0004127.s022.pdf (92.1KB, pdf)
S16 Table. Categorical Trend and Awareness and Education.

(PDF)

pgph.0004127.s023.pdf (93.3KB, pdf)
S17 Table. Linear Trend and General.

(PDF)

pgph.0004127.s024.pdf (90KB, pdf)
S18 Table. Categorical Trend and General.

(PDF)

pgph.0004127.s025.pdf (92.5KB, pdf)
S19 Table. Linear Trend and Monitoring and Surveillance.

(PDF)

pgph.0004127.s026.pdf (91.7KB, pdf)
S20 Table. Categorical Trend and Monitoring and Surveillance.

(PDF)

pgph.0004127.s027.pdf (92.8KB, pdf)
S21 Table. Linear Trend and Prevention.

(PDF)

pgph.0004127.s028.pdf (90KB, pdf)
S22 Table. Categorical Trend and Prevention.

(PDF)

pgph.0004127.s029.pdf (90.2KB, pdf)
S23 Table. Linear Trend and Regulation.

(PDF)

pgph.0004127.s030.pdf (91.9KB, pdf)
S24 Table. Categorical Trend and Regulation.

(PDF)

pgph.0004127.s031.pdf (91KB, pdf)
S25 Table. De-escalation Merged Model Comparison Results.

(PDF)

pgph.0004127.s032.pdf (94.5KB, pdf)
S26 Table. De-escalation Merged Model Results.

(PDF)

pgph.0004127.s033.pdf (77.8KB, pdf)
S27 Table. Model selection table including variables for best selected models and null models.

(PDF)

pgph.0004127.s034.pdf (324.6KB, pdf)

Acknowledgments

The manuscript is a product of the SESYNC Pursuit, Living with Resistance, we thank all participants for their contributions to discussions during the meetings.

Data Availability

All code and data necessary to carry out the analyses are publicly available at https://github.com/PSJorgensen/national-actions-and-trends-in-antibiotic-resistance. Results can be viewed interactively at https://gedb.shinyapps.io/amr_trend.

Funding Statement

We acknowledge funding from the Erling-Persson Family Foundation (P.S.J., L.N.T., E.P., F.K.), the European Union (ERC, INFLUX, 101039376, P.S.J.), the IKEA Foundation (P.S.J.), the Marianne and Marcus Wallenberg Foundation (P.S.J) and the Uppsala Antibiotic Centre (UAC, L.N.T.). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Views and opinions expressed are, however, those of the author(s) only and do not necessarily reflect those of the European Union or the European Research Council. Neither the European Union nor the granting authorities can be held responsible for them. We thank SESYNC for support for the Living with Resistance pursuit, which this paper is a product of.

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PLOS Glob Public Health. 2025 Apr 30;5(4):e0004127. doi: 10.1371/journal.pgph.0004127.r001

Author response to Decision Letter 0


Transfer Alert

This paper was transferred from another journal. As a result, its full editorial history (including decision letters, peer reviews and author responses) may not be present.

26 Jul 2024

PLOS Glob Public Health. doi: 10.1371/journal.pgph.0004127.r002

Decision Letter 0

Ashish KC

3 Sep 2024

PGPH-D-24-01686

Association between national policy and trends in antibiotic resistance: an analysis of 73 countries from 2000 to 2023

PLOS Global Public Health

Dear Dr. Søgaard Jørgensen,

Thank you for submitting your manuscript to PLOS Global Public Health. After careful consideration, we feel that it has merit but does not fully meet PLOS Global Public Health’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

Please submit your revised manuscript by Oct 18 2024 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at globalpubhealth@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pgph/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

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Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

We look forward to receiving your revised manuscript.

Kind regards,

Ashish KC

Academic Editor

PLOS Global Public Health

Journal Requirements:

1. We ask that a manuscript source file is provided at Revision. Please upload your manuscript file as a .doc, .docx, .rtf or .tex.

Additional Editor Comments (if provided):

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Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. Does this manuscript meet PLOS Global Public Health’s publication criteria ? Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe methodologically and ethically rigorous research with conclusions that are appropriately drawn based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

**********

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: Yes

**********

3. Have the authors made all data underlying the findings in their manuscript fully available (please refer to the Data Availability Statement at the start of the manuscript PDF file)?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception. The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: No

**********

4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS Global Public Health does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: No

Reviewer #2: Yes

**********

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: Thank you very much for inviting me to review this interesting work on assessing the national government reporting on AMR action and the change in terms of prevention, mitigation, restoration and adaptation. I must applaud the self-explanatory figures used to explain the process and analysis. However, I have major concern on the clarity of paper been written, presented and the conclusion made.

Abstract

I could not understand what DPSEEA framework is as it was provided for the first time. The study design is not avialable as well as the number of countries included in the analysis. How were the countries selected, I guess it was based on the TrACCS. What is the source of government reported policy action and the source of different indicators.

I could not understand the research question until I saw figure 1. Can authors keep it simple

Association of government reported AMR action on the prevention, mitigation, restoration and adaptation. OR Association of government reported AMR action on the health system strengthening, anti-microbial use, anti-biotic resistance and drug resistance.

In the abstract, the second and third sentence is confusing and does not provide good information of the work you are doing, can you please remove it.

Main text

Introduction- The first paragraph is well written and explains the context. I got lost while reading the second paragraph. In the second para you mention drivers and indicator. Can you please provide the name of indicator. I think there should be a good amount of explanation of four indicators.

The third paragraph is more of method, it should be in method section. Also, please provide the full form such as DPSEEA, as the acronym is used for the first time.

Please provide your research objective clearly, the research objective as in abstract is not well stated.

Method

Can you please use a STROBE checklist to ensure that you do not miss the manuscript reporting. For example, the design is missing. Study setting- The different countries included are missing

Selection criteria

Framework- Figure 1 can be one.

Data analysis

I am confused why you did an association of action done in 2016 as exposure while the health system strengthen, ABU, AMR as outcome. The reason I can asking this, the Global action plan was endorsed in 2015 and reporting of action was done a year after. How can a any action taken in a year, change the vaccination coverage, sanitation coverage, ABU as these are systematic level changes that requires an optimal years duration. Can you do the validation/reliability assessment instead to see, whether the action reported is true in terms of actions in place. If you keep action as exposure and try to see the temporal trend, it does not fit the standard epidemiological definition.

I really like the indicators selection, can you please make a table and show within each drivers what were the indicators (denominator, numerator) and source of data.

Result- The result are well presented especially with the graphs.

Discussion

Can you please method a section on methodological consideration, which is missing.

Reviewer #2: I must commend the ingenuity in applying regression statistical analysis to the DPSEEA framework to assess the association between national policies and trends in antibiotic resistance for 23 years across 73 countries. This approach not only adds a novel dimension to antibiotic resistance research but also provides valuable insights that could guide future interventions.

While your manuscript provides a comprehensive overview of the indicators and data sources, I noticed that specific datasets or versions are not always mentioned (e.g., Lines 125 and 160). Perhaps, you could state, 'The data used for antibiotic consumption trends were sourced from the QuintilesIMS MIDAS database, version X.Y (DOI: xxxx).'

Explicitly providing DOIs, URLs, and any conditions for data access would greatly enhance the transparency and reproducibility of your study, in line with PLOS’s data policy. Including these details will not only strengthen your manuscript but also make it easier for other researchers to build on your work.

Moreover, I recommend explicitly referencing the datasets where not already done (line 125 and 160) or including all of them in supplementary materials. This additional detail will further solidify your manuscript’s contribution to the field and ensure that it is a model of transparency in antibiotic resistance research.

**********

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Reviewer #1: No

Reviewer #2: Yes:  Emmanuel Ifechukwude Benyeogor

**********

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PLOS Glob Public Health. doi: 10.1371/journal.pgph.0004127.r004

Decision Letter 1

Ashish KC

19 Mar 2025

Association between national action and trends in antibiotic resistance: an analysis of 73 countries from 2000 to 2023

PGPH-D-24-01686R1

Dear Dr. Søgaard Jørgensen,

We are pleased to inform you that your manuscript 'Association between national action and trends in antibiotic resistance: an analysis of 73 countries from 2000 to 2023' has been provisionally accepted for publication in PLOS Global Public Health.

Before your manuscript can be formally accepted you will need to complete some formatting changes, which you will receive in a follow up email. A member of our team will be in touch with a set of requests.

Please note that your manuscript will not be scheduled for publication until you have made the required changes, so a swift response is appreciated.

IMPORTANT: The editorial review process is now complete. PLOS will only permit corrections to spelling, formatting or significant scientific errors from this point onwards. Requests for major changes, or any which affect the scientific understanding of your work, will cause delays to the publication date of your manuscript.

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Thank you again for supporting Open Access publishing; we are looking forward to publishing your work in PLOS Global Public Health.

Best regards,

Ashish KC, PhD

Academic Editor

PLOS Global Public Health

***********************************************************

Reviewer Comments (if any, and for reference):

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #1: All comments have been addressed

Reviewer #2: All comments have been addressed

**********

2. Does this manuscript meet PLOS Global Public Health’s publication criteria ? Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe methodologically and ethically rigorous research with conclusions that are appropriately drawn based on the data presented.

Reviewer #1: Yes

Reviewer #2: (No Response)

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: Yes

**********

4. Have the authors made all data underlying the findings in their manuscript fully available (please refer to the Data Availability Statement at the start of the manuscript PDF file)?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception. The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS Global Public Health does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: The title and the abstract reads very well.

The introduction section in the main text reads very well.

The method section now provides research design, the settings, the data collection and extraction process.

The results have now been provided succinctly and intelligently.

The methodological consideration is now added and provides the limitation

Reviewer #2: Thank you for addressing my comments and your efforts in enhancing the transparency and clarity of the manuscript. The inclusion of explicit dataset references, citations, reordering of supplementary tables and improved descriptions further improve the manuscript's organization. These revisions will undoubtedly enhance the study’s impact and usability for future research in antibiotic resistance.

**********

7. PLOS authors have the option to publish the peer review history of their article (what does this mean? ). If published, this will include your full peer review and any attached files.

Do you want your identity to be public for this peer review? If you choose “no”, your identity will remain anonymous but your review may still be made public.

For information about this choice, including consent withdrawal, please see our Privacy Policy .

Reviewer #1: No

Reviewer #2: No

**********

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    S1 Text. Supplementary Methods.

    (PDF)

    pgph.0004127.s001.pdf (142.2KB, pdf)
    S1 Fig. Importance Scores of Variables in Model Selection from Averaged Models.

    (PDF)

    pgph.0004127.s002.pdf (386.9KB, pdf)
    S2 Fig. Coefficient Estimates of Averaged Models for All Countries in Linear Trend and Categorical Trend Models.

    (PDF)

    pgph.0004127.s003.pdf (420.2KB, pdf)
    S3 Fig. Coefficient Estimates of Variables from Best Selected Models from Model Selection.

    (PDF)

    pgph.0004127.s004.pdf (366KB, pdf)
    S4 Fig. Rank of Variables in Averaged Models for Different Income.

    (PDF)

    pgph.0004127.s005.pdf (283.8KB, pdf)
    S5 Fig. Importance Scores of Variables in Model Selection from Averaged Models for Different income Groups.

    (PDF)

    pgph.0004127.s006.pdf (299.8KB, pdf)
    S6 Fig. Coefficient Estimates of Averaged Models for Countries with Different Income Groups.

    (PDF)

    pgph.0004127.s007.pdf (238.7KB, pdf)
    S1 Table. Indicator selection for Driver categories.

    (PDF)

    pgph.0004127.s008.pdf (109.7KB, pdf)
    S2 Table. Indicator selection for Use and Resistance categories.

    (PDF)

    pgph.0004127.s009.pdf (101.3KB, pdf)
    S3 Table. Indicator selection for DRI (exposure) category.

    (PDF)

    pgph.0004127.s010.pdf (102.2KB, pdf)
    S4 Table. Ecological variables used as covariates.

    (PDF)

    pgph.0004127.s011.pdf (99.9KB, pdf)
    S5 Table. List of countries included in the study.

    (PDF)

    pgph.0004127.s012.pdf (101.6KB, pdf)
    S6 Table. Governance Syndrome questions.

    (PDF)

    pgph.0004127.s013.pdf (122.2KB, pdf)
    S7 Table. Questions used for calculating the action index.

    (PDF)

    pgph.0004127.s014.pdf (122.3KB, pdf)
    S8 Table. Model Formulas for Association between Action and Indicator Linear Trend and Categorical Trend.

    (PDF)

    pgph.0004127.s015.pdf (81.3KB, pdf)
    S9 Table. De-escalation plot formulas for univariate models.

    (PDF)

    pgph.0004127.s016.pdf (81KB, pdf)
    S10 Table. Global Models Data Subset Formulas for The Model Selection.

    (PDF)

    pgph.0004127.s017.pdf (82.8KB, pdf)
    S11 Table. Model selection global model formulas.

    (PDF)

    pgph.0004127.s018.pdf (115.7KB, pdf)
    S12 Table. Association Between Linear Trend and Action.

    (PDF)

    pgph.0004127.s019.pdf (104.8KB, pdf)
    S13 Table. Association Between Categorical Trend and Action.

    (PDF)

    pgph.0004127.s020.pdf (93.4KB, pdf)
    S14 Table. Association Between Baseline and Action.

    (PDF)

    pgph.0004127.s021.pdf (106.2KB, pdf)
    S15 Table. Linear Trend and Awareness and Education.

    (PDF)

    pgph.0004127.s022.pdf (92.1KB, pdf)
    S16 Table. Categorical Trend and Awareness and Education.

    (PDF)

    pgph.0004127.s023.pdf (93.3KB, pdf)
    S17 Table. Linear Trend and General.

    (PDF)

    pgph.0004127.s024.pdf (90KB, pdf)
    S18 Table. Categorical Trend and General.

    (PDF)

    pgph.0004127.s025.pdf (92.5KB, pdf)
    S19 Table. Linear Trend and Monitoring and Surveillance.

    (PDF)

    pgph.0004127.s026.pdf (91.7KB, pdf)
    S20 Table. Categorical Trend and Monitoring and Surveillance.

    (PDF)

    pgph.0004127.s027.pdf (92.8KB, pdf)
    S21 Table. Linear Trend and Prevention.

    (PDF)

    pgph.0004127.s028.pdf (90KB, pdf)
    S22 Table. Categorical Trend and Prevention.

    (PDF)

    pgph.0004127.s029.pdf (90.2KB, pdf)
    S23 Table. Linear Trend and Regulation.

    (PDF)

    pgph.0004127.s030.pdf (91.9KB, pdf)
    S24 Table. Categorical Trend and Regulation.

    (PDF)

    pgph.0004127.s031.pdf (91KB, pdf)
    S25 Table. De-escalation Merged Model Comparison Results.

    (PDF)

    pgph.0004127.s032.pdf (94.5KB, pdf)
    S26 Table. De-escalation Merged Model Results.

    (PDF)

    pgph.0004127.s033.pdf (77.8KB, pdf)
    S27 Table. Model selection table including variables for best selected models and null models.

    (PDF)

    pgph.0004127.s034.pdf (324.6KB, pdf)
    Attachment

    Submitted filename: Response to Reviewers after Ege 241127 - Peter submit 241213.pdf

    pgph.0004127.s036.pdf (128.2KB, pdf)

    Data Availability Statement

    All code and data necessary to carry out the analyses are publicly available at https://github.com/PSJorgensen/national-actions-and-trends-in-antibiotic-resistance. Results can be viewed interactively at https://gedb.shinyapps.io/amr_trend.


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