Abstract
Despite several initiatives to benchmark national action in responding to antimicrobial resistance (AMR), no comprehensive inventory exists of indicators used across these efforts. We present a scoping review that maps and synthesises existing indicators used to assess national performance in addressing AMR. We conducted a review of academic and grey literature to identify quantitative and qualitative indicators used to assess national AMR performance across animal, environmental, and human health sectors. The academic search was conducted across MEDLINE, EMBASE, and Global Health. The grey literature search was conducted across multilateral organisations (e.g., WHO, FAO, WOAH, UNEP, OECD) and think-tanks. We categorised indicators into a thematic framework spanning 19 subdomains within three overarching domains: Governance & Leadership, Action Areas, and Monitoring & Evaluation. From 184 academic studies, we identified 2311 indicators, and 1406 from 48 grey literature sources. In total, 2101 were in human health, 675 in animal health, 232 in environmental health, and 709 were multisectoral. Within the three overarching domains, 281 were Governance & Leadership, 1907 were Action Areas, and 1671 were Monitoring & Evaluation indicators. When grouping indicators by subdomain, Surveillance & Laboratory (1427), Stewardship (765), and Prevention & Control (365) accounted for the largest volumes, followed by Social Determinants (232), Reporting (141), and Workforce (140), in contrast to Accountability (22), Transparency (22), and Equity (29). This comprehensive scoping review provides a One Health inventory of 3717 indicators used to assess national performance in responding to AMR. While revealing robust Surveillance & Laboratory, Prevention & Control, and Stewardship metrics, we identify critical gaps in Accountability, Transparency, and Equity. These measures comprise the Governance & Leadership domain, which is essential for policy implementation.
Subject terms: Health care, Medical research
Introduction
Antimicrobial resistance (AMR), leading to an estimated 1.14 million deaths worldwide in 2021 alone1, is a critical, complex public health issue. By 2035, the global economy is projected to incur additional healthcare costs of $412 billion, and losses of $443 billion from reduced workforce productivity2.
International efforts to combat AMR have intensified since 2011, when the WHO Regional Office for Europe (WHO Europe) and the European Commission adopted regional action plans for AMR3,4. This was followed by the WHO 2015 Global Action Plan (GAP) and the 2016 and 2024 United Nations (UN) political declaration on AMR5. In 2023, the WHO Europe member states endorsed an AMR roadmap to identify, prioritise, implement, and monitor high-impact interventions to tackle AMR6. Despite these initiatives, countries are inconsistent when translating global and regional commitments into practice due to differing political priorities, economic constraints, and healthcare infrastructure capacities7.
In response, stakeholders have advocated for target-based approaches, such as the global 10–20–30 targets for 2030, the targets within the 2024 UN political declaration on AMR (UNGA), and the EU’s One Health Action Plan goals5,8,9. Targets provide specific, measurable objectives that can unify and accelerate country-level efforts, but reliance on targets alone risks oversimplifying the multifactorial drivers of and policy responses to AMR10. Several initiatives exist that monitor different aspects of AMR national policy, such as the Global Database for Tracking AMR Country Self-Assessment Survey (TrACSS)11, IHR States Parties Self-Assessment Annual Report (SPAR)12, WHO Infection Prevention and Control Assessment Tool 2 (IPCAT2)13 the Joint External Evaluation (JEE)14, the Global Coalition on Aging and Infectious Disease Society of America AMR Preparedness Index15, the AMR Governance Framework16, FAO’s Assessment Tool for Laboratories and AMR Surveillance Systems (ATLASS)17, and the WOAH Observatory Monitoring Reports18. However, these initiatives are sometimes conducted and interpreted in isolation, resulting in a fragmented evidence base that limits the ability of policymakers to form a comprehensive, cross-sectoral view of national AMR policy responses.
We conducted a literature review to identify and consolidate existing quantitative and qualitative indicators currently used, or proposed, to compare national performance in addressing AMR. We aimed to highlight best practices, uncover gaps in indicator coverage, and identify candidates for inclusion within a novel proposed One-Health AMR Accountability Index19. While previous reviews examine selected aspects of AMR policy implementation, this study encompasses academic and grey literature to map indicators across the full One Health spectrum and, to our knowledge, constitutes the most comprehensive resource to date that identifies gaps, reduces duplication, and helps develop balanced, multisectoral indicators to measure national performance in addressing AMR.
Results
Scoping review
Our academic search identified 9361 results (Fig. 1). Following title and abstract screening, 1087 results remained. We further excluded 468 (wrong outcomes), 126 (wrong comparator), and 309 (wrong study design). This resulted in 184 academic studies and 48 grey literature sources. Levels of interrater-reliability observed were substantial, for abstract and title screening (0.78), and fair, for full text screening (0.30). The lower agreement at the full-text stage is consistent with the greater complexity of eligibility decisions required at this level, where a more nuanced judgement was required regarding the inclusion and exclusion criteria. All disagreements were resolved through adjudication by a third independent reviewer (MA).
Fig. 1. PRISMA flow diagram of studies included in scoping review.
Authors’ creation.
Supplementary Table 1 lists grey literature and source links, while Supplementary Tables 2 and 3 summarise the literature included. From these sources, 6645 indicators were initially extracted (Fig. 2). During screening, 2928 indicators were excluded: 1011 (not considered cross-national measures of performance in addressing AMR); 1547 (duplicates); 370 (not specific to AMR). This resulted in 3717 indicators eligible for inclusion.
Fig. 2. PRISMA flow diagram of indicators included in scoping review.
Authors’ creation.
We identified 2311 unique indicators from academic studies and 1406 from grey literature sources (outlined in Supplementary Data 1 and 2). Table 1 provides the number of academic studies, grey literature sources, indicators identified, and example indicators within each AMR policy subdomain. A summary visualisation of indicator density across the 19 subdomains illustrates substantial concentration in Surveillance & Laboratory, Stewardship, Prevention & Control, and comparatively few indicators for Accountability, Transparency, and Equity subdomains (Fig. 3). Since indicators could be grouped under multiple subdomains, in some instances the totals exceed the number of unique indicators identified (n = 3717). Supplementary Figure 1 visualises indicator groupings by sector (animal, environmental, human health, multisectoral). We provide below an in-depth narrative synthesis of indicators grouped under their subdomains, with notable findings. Supplementary Figure 2 displays the distribution of academic studies by publication year; most appeared within the past five years.
Table 1.
Overview of subdomains showing the number of academic studies and grey literature sources reviewed
| Domain | Sub-domain | Definition | Academic indicators | Academic studies | Grey literature indicators | Grey literature studies | Example indicator |
|---|---|---|---|---|---|---|---|
| Monitoring & Evaluation | Surveillance & Laboratory | Indicators that assess the comprehensiveness of surveillance programmes and the capacity and quality of laboratory systems across all sectors. | 941 | 118 | 486 | 32 | What is the status of the national surveillance system for antimicrobial resistance in live aquatic animals?11 |
| Reporting | Mechanisms for communicating progress on the national AMR strategy to external stakeholders, including annual progress reports and formal submissions to international and regional surveillance initiatives (e.g., GLASS, ECDC, CAESER, EARS-Net) | 56 | 18 | 85 | 12 | Does the country report use of antibiotics (ATC classes J01, A07AA, P01AB) and do they report route of administration (oral, parenteral, inhalation, rectal)?63 | |
| Feedback Mechanisms | Indicators that capture the existence and quality of processes for relaying surveillance data and performance information back to regional, organizational, and individual stakeholders | 16 | 6 | 50 | 13 | Select all that apply: 1) Quality audits of long-term care facilities (LTCFs) include AMR. 2) There is monitoring and evaluation of AMR in LTCFs44. | |
| Effectiveness | Indicators examine whether structured mechanisms exist at the national level to evaluate if policies or interventions achieve their intended health and economic outcomes. | 19 | 9 | 17 | 8 | Estimation of the incidence of patients acquiring at least one hospital-acquired infection (HAI) in acute care hospitals per 1000 hospital admissions. Estimation of all types of HAIs per year in acute care hospitals per 1000 hospital admissions13. | |
| Governance & Leadership | Regulations & Legislation | Covers all forms of legislation, incentives, and penalties in place for the containment of AMR. | 74 | 13 | 54 | 14 | Does the country have legislation in place that limits or prohibits the over-the-counter sale of antibiotics without a prescription?49 |
| Strategic Vision | Indicators that measure the extent to which there exists a national long-term strategy that has been informed by a situational analysis, with specific, measurable, actionable, relevant and time-bound (SMART) aims for the containment of AMR. | 88 | 26 | 25 | 13 | Is there a national strategic plan for hospital-acquired infection surveillance (with a focus on priority infections based on the local context) developed by the multidisciplinary technical group?48 | |
| Participation | Indicators that evaluate the extent of inclusive involvement of all relevant stakeholders in development, implementation, monitoring and evaluation of national strategies to address AMR. | 47 | 19 | 11 | 7 | Who is involved & what is the role for priority setting regarding AMR action and standards?20 | |
| Coordination | Indicators that measure the comprehensiveness of mechanisms in place for coordination across One Health sectors. | 30 | 14 | 42 | 16 | What is the level of effective integration of laboratories in AMR surveillance in the animal health and food safety sectors?48 | |
| Accountability | Indicators that measure whether responsibility is allocated to deliver objectives and activities listed within the NAP, and whether agreements exist if actions are not undertaken or targets not met. | 15 | 9 | 7 | 6 | What is the number of focal persons in the network who are reference persons for AMR activities?23 | |
| Transparency | Indicators that measure the extent to which NAPs, progress reports, funding information and other data are publicly available and accessible. | 6 | 6 | 16 | 7 | Is the information on the national action plan, including progress reports, AMR surveillance data, funding allocation, responsible body, and responsible person/sector within the country, publicly available?75 | |
| Sustainability | Assesses the commitment of relevant stakeholders, the degree to which adequate budgets for present and future activities are allocated, and the consistency with which support is provided for AMR policy development, implementation and monitoring. | 18 | 9 | 28 | 14 | Is the country’s funding for One Health initiatives in government budget? If Yes, what is the amount of funding? Describe the extent of technical support provided to build capacities to address AMR through support for implementation of international standards and action plans, trainings, and R&D80. | |
| Equity | Indicators that measure the extent to which AMR policy facilitates equitable access to antimicrobials or mitigates the impact of AMR on disadvantaged and vulnerable populations. | 11 | 3 | 18 | 3 | Does the country promote equal participation of women, men and other vulnerable groups and/or groups facing discrimination in the multisectoral AMR coordination mechanism and technical working groups?85 | |
| Action Areas | Prevention & Control | Measures of the comprehensiveness of IPC programmes, biosecurity mechanisms, and access to clean water, sanitation, and hygiene between countries. | 122 | 35 | 243 | 22 | Are a minimal set of core indicators for infection, prevention, and control (IPC) within healthcare facilities in the country defined?108 |
| Social Determinants | Encompass the structural and contextual factors that shape AMR risk between countries, including educational level, climate change, pollution, conflict, nutrition, housing, finance status, demographic trends, technological environments, and individual characteristics. | 209 | 19 | 23 | 4 | What are the behavioural barriers, including structural barriers, to tackling AMR?32 | |
| Stewardship | Indicators that measure the comprehensiveness of efforts to reduce inappropriate antimicrobial use such as stewardship programmes and guidelines for antibiotic use, and consumption rates and sales of antibiotics | 468 | 80 | 297 | 31 | Report antimicrobial use for ATC class J01, A07AA, P01AB by AWaRe (Access, Watch, and Reserve) classification (relative use % of Access class antibiotics; relative use % of Watch class antibiotics; relative use % of Reserve class antibiotics)63. | |
| Community Awareness & Enabling Behaviors | Indicators designed to improve knowledge, shape attitudes, and foster practices that support responsible antimicrobial use. | 91 | 18 | 18 | 11 | What is the amount of funding mobilised for communication actions on AMR and antimicrobial stewardship per 1000 population?80 | |
| Workforce | Indicators referring to the development, education, and training of teams and individuals across the One Health sectors. | 77 | 22 | 63 | 10 | Does the country provide training and professional education on AMR to the agriculture (animal and plant), food production, food safety, and environment sectors?11 | |
| Access to Medicines & Health Services | To what extent the population experiences barriers when accessing healthcare services and essential medicines. | 70 | 20 | 48 | 11 | What is the unmet need for each of the following due to cost, distance, and waiting times? 1) Health care 2) Dental care 3) Prescribed medicines64. | |
| Research, Innovation, & Digital Technology | Assess whether there is investment in research to examine the drivers of AMR, effectiveness of interventions to mitigate AMR, and whether there are incentives in place that aim to foster innovation. | 28 | 16 | 22 | 6 | Amount of funding allocated for translational research and late-stage development of AMR medical countermeasures, including clinical trials for antimicrobials80. |
The total indicators extracted, and representative example indicators per subdomain. Some indicators and studies appear in multiple subdomains; subdomain sums may exceed the overall total.
Fig. 3. Indicators within 19 government framework subdomains for academic and grey literature.
Figure Notes: Some indicators and studies appear in multiple subdomains; subdomain sums may exceed the overall total. Access to Medicines & Health Services (Access); Community Awareness & Enabling Behaviours (Community Awareness); Research, Innovation, & Digital Technology (Research).
Domain: governance & leadership; subdomain 1: strategic vision
Strategic Vision refers to indicators relating to the adoption of a national long-term strategy informed by a situational analysis, with specific, measurable, achievable, relevant, and time-bound (SMART) aims for addressing AMR. Indicators also measure whether there is a high-level commitment to tackling AMR, e.g., AMR appears in political manifestos or on national risk registers. 88 indicators were extracted from 23 academic studies20–42; 25 from 12 grey literature sources11,13,15,17,43–50 (in particular, from Implementation of WOAH Standards: The Observatory Annual Report 2022)18.
Indicators include measurements of operational plan comprehensiveness34, zoonotic disease governance21, overall National Action Plan (NAP) design22, and specific NAP characteristics (e.g. shared leadership27,33, advocacy facilitators, functionality, preparedness and response to public health events, and incorporation of the primary healthcare sector)28. While some indicators measure whether countries have adopted a NAP21,32, and progress with NAP development29,30,45, most gauge whether specific elements are included, e.g. the implementation of a One Water stewardship framework36, antimicrobial use (AMU) reduction across One Health sectors41, the integration of long-term care facilities44, and sections dedicated to environmental, food and agricultural issues17,43,46. Certain indicators from the academic literature evaluate the level of political recognition and support that strategies and targets receive21,25,31.
Indicators also evaluate the degree to which NAPs incorporate international bodies’ priorities. This especially concerns alignment between NAPs and the GAP24,35,37,39,42, on infection prevention control (IPC), AMU and surveillance34, best practices26,38, support for IPC programmes13, and governance training programmes (e.g. provided by Medicines, Technologies, and Pharmaceutical Services (MTaPS)23. Other indicators consider the standards and criteria for implementation of targets40, the existence of a focal point or technical group to lead NAP implementation and monitoring and evaluation (M&E)11, and whether the setting of priorities is based on empirical evidence20.
Domain: governance & leadership; subdomain 2: participation
Participation refers to indicators that evaluate the extent to which the development, implementation, and M&E of national AMR strategies involve stakeholders, e.g., civil society, healthcare professionals, veterinarians, the food and pharmaceutical industries, and subject matter experts. Forty-seven indicators were extracted from 19 academic studies20,21,23,27,29,31–33,39,51–60; 11 from 7 grey literature sources15,18,49,61–64.
Indicators assess ‘participatory’, inclusive and consensus-oriented decision-making at the governmental and inter-governmental level21. They also evaluate stakeholders’ level of contribution and participation across One Health sectors52 and map the type of persons associated with AMR national-level policy-making20,54. Other indicators gauge how many stakeholder support activities involve non-state actors31, the participation of private-sector entities in AMR-related decision-making, and the safeguards against potential conflicts of interest62. Indicators consider participation in international AMR-related initiatives55, e.g. campaigns56, laboratory training programmes60, and surveillance data repositories15,29,32,57–60; and stakeholder participation in facilitating mechanisms, e.g. regional and national-level AMR meetings51 and joint programmes involving agricultural and veterinarian actors61,65.
Domain: governance & leadership; subdomain 3: coordination
Coordination refers to indicators that measure the comprehensiveness of mechanisms linking up One Health sectors, e.g. multisectoral committees. Thirty indicators were extracted from 14 academic studies21–30,52,53,66,67; 42 from 15 grey literature sources11,13–15,17,43,50,61,62,68–73.
Multiple indicators, both from the academic and grey literature, assess the extent to which national-level coordination includes all One Health sectors. Studies employ ordinal11,14,27,30, quantitative22, qualitative53, and multiple-choice72 metrics for overall assessments of One Health intersectoral coordination capacity. Other indicators record stakeholder contribution to coordinated initiatives11,43,52.
One Health initiatives are often included within NAPs29, in addition to collaborative research activities66. Other studies consider the level of coordination within sectors (e.g., between agricultural and veterinary stakeholders52 or intra-sectoral chains of command)61. For the human sector, indicators ordinally measure coordination between governments, NGOs and patient groups15; and institutional linkages between IPC and water, sanitation, and hygiene (WASH) programmes, patient associations, civil society bodies, and medical societies11,13,30,66.
Nationally and internationally, indicators also evaluate institutional alignment and collaboration, e.g. whether a country’s NAP is linked to or integrated with its other national strategies11,21; the extent to which national reference laboratories support the integration of peripheral laboratories across the veterinary and agricultural sector70; and how decision-making competences are shared between centralised levels of AMR governance62. Internationally, indicators measure integration of addressing AMR into other global agendas24–26, and countries’ collaboration with international research15 and programmes such as MTaPS23.
Several indicators assess national mechanisms for facilitating coordinated activity, e.g. whether countries have national, multisectoral coordinating committees17,26,28,53,71,72 and the extent to which local and national IPC monitoring, audit and feedback mechanisms are aligned13. Other indicators evaluate coordinating mechanisms, e.g. operational documents43, integrated laboratory data-sharing networks69, emergency logistics and supply chain management systems69, International Food Safety Authorities Network contact points72, and information-sharing processes for regulatory bodies43.
Domain: governance & leadership; subdomain 4: accountability
Accountability refers to indicators that assess whether responsibility is allocated to certain individuals or organisations to deliver the NAP’s objectives, and whether sanctions exist if any are unmet. Fifteen indicators were extracted from nine academic studies20–23,27,51,66,74,75; 7 from 5 grey literature documents11,13,61,76,77. In both sets of sources, indicators measure accountability at the national level through overall, quantitative scores21,22.
Indicators demonstrate the existence of relevant authorities to which responsibility for AMR-related initiatives can be allocated, e.g., focal persons acting as reference persons for AMR activities51, or focal working groups responsible for M&E and NAP implementation11. Other indicators map the role and scope of authorities and stakeholders, outlining mechanisms for delegating, accrediting, and authorising AMR-related responsibilities13,61. These mechanisms are evaluated according to their linkage to broader health system governance structures20, and their compliance with national-level policies and regulatory frameworks, concerning, e.g. food policy21. Lastly, indicators consider facilitating practices, e.g., institutional audits51; MTaPS-supported activities for entities addressing AMR23; the consistent and reliable reporting of information to national or international health authorities74,77.
Domain: governance & leadership; subdomain 5: transparency
Transparency encompasses indicators that measure the public availability and accessibility of NAPs, progress reports, funding information, and the extent to what degree do AMR policy development, implementation, and evaluation occur in an accessible and open environment. Six indicators were extracted from 6 academic studies21,22,27,75,78,79; 16 from 7 grey literature sources17,18,61–63,71,77. In both sets of sources, indicators measure AMR governance transparency through overall, quantitative scores21,22 and respondent awareness of AMR risks and response79.
Indicators consider whether information (e.g., NAPs21,75,78, progress reports, surveillance data17, funding allocations, a log of responsible entities75, audits of AMR treatment guidelines71, risk assessment outcomes)17 is published and accessible17,62,63. Other indicators assess whether stakeholders fulfil their obligations to facilitate transparency, either by sharing information77 or by consistently and punctually informing other AMR-related stakeholders about sector-specific developments and activities61.
Domain: governance & leadership; subdomain 6: sustainability
Sustainability encompasses the commitment of relevant stakeholders, the allocation of adequate budgets for present and future activities, and the consistency with which support is provided for AMR policy development, implementation and monitoring through the input of subject matter experts through technical advisory groups. Eighteen indicators were extracted from 9 academic studies21–23,26–28,31,34,80; 28 indicators from 14 grey literature sources11,13,15,17,43,44,46,61,69,72,80–83. Two studies measure sustainability through overall scores22, while another qualitatively assesses the overall sustainability of national veterinary laboratory systems61.
Indicators assess whether AMR activities are financially sustainable, e.g. ensuring accessibility of funds61; the appropriate costing of activities34; the identification, mobilisation, and diversification of funding15,26,34,43,72,80; the protection of allocated funds for operating budgets and resources13,28,81. Other indicators gauge AMR funding and investments’ level of government backing15,21,31,44,46,72. Lastly, indicators consider the existence of other, non-financial support that facilitates sustainable practices, e.g. advocacy mechanisms for International Health Regulation (IHR) implementation72; experts’ participation in a NAP implementation campaign28; MTaPS-supported activities for building technical capacity23; active Drug Safety Monitoring expert committees69.
Domain: governance & leadership; subdomain 7: equity
Equity refers to indicators that measure the extent to which AMR policy facilitates equitable access to antimicrobials or mitigates the impact of AMR on disadvantaged and vulnerable populations. Eleven indicators were extracted from three academic studies21,22,84; 18 from 3 grey literature sources11,72,85, in particular from the WHO guidance: addressing gender inequalities in national action plans on AMR85.
Indicators include geographic factors that impact access86, economic inequality and development measures21. Another measures the impact of a country’s poverty gap and public sanitation services on AMR84. Other indicators inquire whether national-level data are captured and categorised according to social stratifiers11,49,87. Grey-literature indicators assess if inclusion of vulnerable groups is promoted across all AMR-related national mechanisms49. Indicators also include retrospective reviews of services, policies, and education to identify and reduce gender biases or inequalities21,49,72.
Domain: action areas; subdomain 8: regulations & legislation
Regulations & Legislation covers legislation, incentives, and penalties in place for the containment of AMR. Seventy-four indicators were extracted from 10 academic studies21,22,34,66,88–93; and 54 from 14 grey literature sources11,15,17,44,46,48,49,61,62,69,71,72,77,85. Three studies generated 49 indicators18,66,88. Within the grey literature, over half came from WHO’s TrACSS11.
Many indicators focus on oversight of AMU and enforcement of guidelines, laws, and regulatory instruments. To regulate AMU, indicators consider whether legislative frameworks exist to prohibit or severely restrict highly critical antibiotics89 in animal health34,48,66,77,89. Indicators also include regulations for antibiotic use in human health, establishing whether over-the-counter (OTC) sales without prescription are banned71 and OTC prescriptions are written by legally authorised persons49,77,89. Other indicators focus on elements of antimicrobial supply legislation, e.g. controlling the marketing of pesticides; country-level coverage of drug regulations in the supply chain21,92. Indicators also consider the potential contribution of regulations that might reduce AMU91, e.g. taxing antibiotics for livestock use; restricting broad-spectrum antibiotics’ use in growth promotion15,90.
Several indicators evaluate the existence and adequacy of legislation for safe wastewater treatment and disposal. TrACSS, for example, inquires whether national legislation is in place and enforceable for preventing environmental antibiotic contamination11,88. Indicators also quantify antibiotic residue according to environmental protection criteria49. Other indicators gauge regulation concerning the detection and prevention of substandard and falsified medical products in human49 and animal health61,62. Finally, certain indicators assess other forms of legal or regulatory instruments, e.g. nutrition guidelines21, legislation for AMR surveillance17,80, transnational transport of food, goods, animals and people11, IHR implementation72, and contextual factors including rule of law and corruption21.
Domain: action areas; subdomain 9: prevention & control
Prevention and control refer to IPC programmes, biosecurity mechanisms, access to clean water and sanitation, and hygiene. 122 indicators were extracted from 33 academic studies21,22,24,26,28,30,32,36,40,51,53,55,57,60,66,74,80,84,86,90,93–105; 243 from 21 grey literature studies11–13,15,18,43,44,46,49,61,68,69,71,77,83,106–112, including 100-plus from IPCAT213.
Indicators for WASH include the proportion of the population with basic or safely managed drinking water and sanitation facilities; access to hygiene installations in communities and healthcare facilities; hand hygiene infrastructure; waste management services; environmental cleaning protocols; and WASH adherence21,84. Human health IPC indicators cover the existence of national IPC programmes11; focal points108; budgets44; updated and implemented national and facility-level guidelines13,108; adaptation and implementation of multimodal strategies such as the States Parties Self-Assessment Annual Report12; integrated monitoring and audit frameworks linked to AMR and WASH surveillance, microbiological support for healthcare-associated infection (HAI) surveillance, clear reporting lines, timely feedback mechanisms13; defined surveillance objectives and benchmarking69; capacity assessments such as Joint External Evaluation (JEE) IPC scores26,55; and institutional policies and training for IPC personnel13. Animal health indicators include farm biosecurity measures90; livestock density and diversity metrics21; animal–human contact rates95; inspection and hygiene practices along the farm-to-fork food chain21; good manufacturing practices30; manure management21; traceability and movement control, zoning and compartmentalisation61; preparedness plans for containment of resistant pathogens68; vaccination strategies for zoonoses61,68; vector control measures69; and monitoring of antibiotic residues and environmental discharges11,49. Policy and planning indicators encompass the percentage of NAPs addressing WASH98; environmental contamination, inclusion of One Health environment sector scorecards, the existence of national strategic plans for HAI and AMR surveillance that are aligned with IHR12,36,98; vaccination coverage metrics for key pathogens68; AMU reduction interventions on farms71; and stakeholder perceptions of biosecurity improvements13.
We observed crossover between indicators for IPC and other domains, including Coordination, Feedback Mechanisms, and Accountability. Multi-domain indicators include presence of IPC M&E plans for NAPs13,108; consistency and quality of surveillance platform data, national platforms for IPC data-sharing, feedback mechanism for IPC scores, and clarity on responsible entities for IPC performance monitoring13; cross-sector linkage of IPC with AMR, WASH, and environmental programmes, regular audits and guideline reviews99; training programmes for IPC professionals13; outbreak preparedness and response capacity68; and health outcome monitoring, e.g., HAI incidence40, Clostridioides difficile infections surveillance, sepsis critical care admissions, and measures of population-level intervention impact on infection rates57.
Domain: action areas; subdomain 10: social determinants
Social determinants encompass the structural and contextual factors that shape AMR risk within different populations across countries, including educational level, climate change, pollution, conflict, nutrition, housing, financial status, demographic trends, technological environments, and individual characteristics such as gender, age, and ethnicity. A total of 209 indicators were extracted from 19 academic studies21,32,36,42,84,86,91,92,94–96,98,101,102,113–117, with over half of the indicators coming from one study21; 23 from 4 grey literature studies69,77,109,110, including 15 from the Joint Monitoring Programme for Water Supply, Sanitation and Hygiene (JMP)110.
Indicators for WASH appeared in both IPC and Social Determinants21,94–96,98. Economic and financial indicators comprise GNI per capita, GDP, public social and education expenditure, unemployment, labour force participation, income inequality, and measures of political stability, corruption perception, and rule of law21,94,96. Demographic indicators cover urbanisation rates, age distribution, gender and ethnic composition, population growth, migration or refugee ratios, and population density or proximity to water bodies, all of which affect transmission dynamics and healthcare demands21,77,96,110,113. Nutrition and food security metrics such as undernourishment prevalence, stunting in children, anaemia among women of reproductive age, dietary energy and protein supply adequacy, food price indices, and food insecurity ratios highlight vulnerability to infection and influence AMU in agriculture and human health21.
Many environmental indicators were grouped within the Social Determinants subdomain (89). These include climate indicators, e.g. average temperature and precipitation, air quality, CO2 and greenhouse gas emissions, climate risk indices, water stress and renewable water resources, land use factors, pollution scores, and indicators of ecosystem health, all of which affect pathogen emergence, spread, and AMR selection pressures21,94,96. Housing and living conditions, e.g., quality of housing, overcrowding, and access to electricity, influence infection risk and healthcare-seeking behaviour110. Technological and infrastructure indicators include internet penetration, mobile subscriptions, logistics performance, transport accessibility, electricity access, and technology adoption rates, which shape health communication, surveillance capacity, and distribution of medical and veterinary interventions21,96. Conflict and governance contexts are captured by political stability, violence and conflict indices, proportions of refugees and internally displaced people, justice system metrics (unsentenced detainees, property rights, press freedom), and governance indicators (public spending, affordability of justice), reflecting how crises and instability disrupt health services, surveillance, and stewardship efforts21.
Domain: action areas; subdomain 11: stewardship
Stewardship refers both to indicators that measure the comprehensiveness of efforts to reduce inappropriate AMU, such as stewardship programmes and guidelines for antibiotic use in human, animal, and environmental (aquaculture) health, and consumption rates and sales of antibiotics. A total of 468 indicators were extracted from 78 academic studies21,22,24,26,30,32,34,36,40,41,51,53,55,56,60,65,66,79,80,86,90–95,97,100,101,103,105,113,114,116,118–160; 297 from 31 grey literature studies11,14,18,44,46,48,49,63,68,69,71,77,83,107,109,161–170, with 163 indicators originating from the 9th Annual Report on Antimicrobial Agents Intended for Use in Animals (ANIMUSE)48.
Key indicators for Stewardship assess whether NAPs include One Health stewardship frameworks, guidelines, and dedicated governance structures (e.g., antimicrobial stewardship (AMS) committees, AMS focal points, drug and therapeutics committees, auditing and feedback mechanisms)28,36,103,129,147. Human-sector consumption metrics encompass defined daily dose (DDD) and DDD/1000/day (DID) in hospital and community settings, stratified by antibiotic class, access, watch, reserve (AWaRe) categories, age groups, syndromes, and seasonal or regional variation63,86,94,101,103,125,127,128,130,143,155,164. Additional indicators include antibiotic treatment courses per country population,103, percentage of hospitals in the country with early switch/discharge protocols97, prescribing rates per consultation or population103, percentage of prescriptions aligned with guidelines146, and metrics of outpatient vs. inpatient antibiotic use130.
Animal-sector indicators cover antimicrobial consumption68,165, antimicrobial consumption by Antimicrobial Expert Group (AMEG) categorisation170, treatment incidence per flock or per production round100,128,150, proportions of classes used121, routes of administration171, traceability of medicated feed119, classification of veterinary antimicrobials per WOAH/WHO importance lists18,119, targets for AMU reduction168, and projections of future consumption139,140. Environmental stewardship indicators include monitoring and reduction of antibiotic discharges97,143, biosecurity practices to optimise AMU11 and minimisation of antimicrobial pesticide use11,14,71. Broader metrics capture national monitoring systems for sales/use in human and animal sectors11,77, adoption of AWaRe classification in essential medicines lists28,79,103,136,151, capacity for AMU monitoring30, interaction of livestock antibiotic consumption with GDP113, and perceived contributions or achievable reductions in sector-specific AMU90. Surveillance and evaluation indicators include variation in antibiotic use (DDD/1000/day), trends in consumption rates and costs (EUR/DDD), benchmarking of antibiotic use, and correlation analyses over time90,127,131. Stewardship implementation metrics also cover rapid diagnostic test availability, feedback on prescriptions, AMS resource presence, training and behaviour-change methodologies, audit and quality improvement activities, integration of AMS into facility accreditation, and feedback loops for prescribers103,142,147.
Domain: action areas; subdomain 12: community awareness & enabling behaviours
Community awareness and enabling behaviours encompass indicators designed to improve knowledge, shape attitudes, and foster practices that support responsible AMU, including the comprehensiveness and consistency of public awareness campaigns, including educational programmes at school. Ninety-one indicators were extracted from 18 academic studies21,22,24,27,28,30,31,40,51,56,66,91,104,117,138,147,172,173, with 38 indicators originating from a single study31; 18 across 11 grey literature studies11,15,17,43,49,62,71,77,111,164,168.
Indicators focused on educational metrics (e.g., students’ participation rates in prudent antibiotic use campaigns and the core concepts of curriculum used11,173). Others measured public awareness campaign output (e.g. counts of education activities, and the variety of materials produced24,31). Knowledge and attitude assessments are reflected in government- or survey-derived awareness and understanding scores, personal and political knowledge, attitude, and practice scores, perceived awareness of interconnected issues (climate change, food security, AMR), and perception of priority areas for action24,56,117,172. Indicators also track engagement in national and international campaigns and the existence of formal communication strategies12,30,147.
Behavioural change metrics include self-reported antibiotic use patterns, public perception of benefits and worries about AMR, and adoption of recommended practices such as obtaining antibiotics by prescription12,49,111. Capacity-building indicators assess countries’ ability to raise AMR awareness, measured by Global One Health Index (GOHI)-AMR improved awareness and understanding scores and the presence of incentives to promote and monitor public engagement21,138. Finally, stakeholder mapping and community engagement metrics gauge the number of identified and engaged actors, jointly developed risk communication activities, and the proportion of activities adopted by communities12.
Domain: action areas; subdomain 13: workforce
Workforce encompasses indicators referring to the development, education, and training of teams and individuals across the One Health sectors. Indicators in this subdomain include staffing and the existence of an overarching, coherent workforce strategy. A total of 77 indicators were extracted from 22 academic studies21,22,27,28,30–32,40,53,60,66,90,91,95,99,102,115,119,133,141,174,175; 63 from 10 grey literature studies11–13,15,17,43,49,69,77,108, with over half originating from IPCAT213.
Academic measures include participation in laboratory training and national training modules, the existence of pre-service and in-service pharmacovigilance curricula, and mandatory IPC training for healthcare workers99,104. Other staffing-level indicators capture the proportion of the employed population working in agriculture or animal husbandry, ratios of IPC personnel, and estimated numbers of pharmacists and technicians per country32,95,115. Some indicators measure competency and preparedness via stakeholder knowledge, perceptions, and practices toward AMS90,174,175; education quality is also tracked11,21,31. Performance analyses such as correlations between hospital transmission rates and numbers of healthcare workers or practising nurses per 100,000 population that highlight the impact of staffing levels on infection control are also included141. National assessment tools such as GOHI education scores benchmark country progress in workforce development and continuous professional education23,45,69. These indicators further track the number of professionals trained in joint risk assessment and the integration of AMR content into medical and veterinary curricula13,43,49. Lastly, indicators encompass IHR workforce readiness during public health emergencies12.
Domain: action areas; subdomain 14: access to medicines & health services
Access to Medicines & Healthcare Services captures the extent to which the population experiences barriers when accessing healthcare services and essential medicines. Seventy indicators were extracted from 19 academic studies21,51,84,86,92,96,101,103,115,120,134,141,176–182; 48 from 11 grey literature studies11,15,44,49,61,64,72,83,106,112,167. The majority of grey literature indicators (38) were from Universal Health Coverage (UHC) Watch64. Academic indicators include both financial metrics and utilisation measures.
Financial metrics include total health expenditure as a percentage of GDP, the ratio of public to private health spending, out-of-pocket payments as a share of national income, and cost estimates per infection13,76. Utilisation measures here include the proportion of children with cough or fever who visit formal versus informal healthcare providers and the estimated cumulative number of facility visits before age five120. Service capacity within this subdomain is gauged by hospital bed density, ICU and IMCU beds per 100,000 inhabitants, hospital admissions per year, numbers of registered medicine outlets, and days antibiotics are out of stock51,84,86,134,179,180. Essential medicines access is tracked via the count of countries approving the WHO essential medicines list ‘Access’, ‘Forgotten’, and pediatric formulations, while GOHI scores assess domestic health expenditure, health service coverage, and UHC service indices for infectious diseases21,182. Grey literature indicators complement these with measures of financial protection, e.g., households facing catastrophic or impoverishing health spending by consumption quintile; unmet need for healthcare and dental care due to cost, distance, or waiting time; and system resilience metrics (e.g., public spending on health as a share of government and GDP, occupancy rates of acute-care beds, and veterinary service strength)64. Trusted and utilised health services under this subdomain are gauged by outpatient contact rates and the continuity of essential health services12.
Domain: action areas; subdomain 15: research, innovation & digital technology
Research, Innovation & Digital Technology includes indicators that assess whether there is investment in research to examine the drivers of AMR and the effectiveness of interventions to mitigate AMR. This subdomain includes indicators that measure whether incentives exist, in the public and private sectors, that aim to foster innovation with respect to the development of diagnostics and treatments for AMR. Twenty-eight indicators were extracted from 14 academic studies21,22,27,31,34,36,51,53,60,66,80,93,183,184; 22 from 6 grey literature studies15,49,62,69,77,112.
In the case of AMR-related research, different academic studies generated AMR research scores through assessment of countries’ commitment to research and development (R&D) through the development of novel agents, presence of a research budget, and reference to R&D within the NAP. These scores were variously presented (e.g. quantitative22, qualitative53, ordinal, and binary measures)27,34. Certain indicators evaluate the provenance15,80, and amount80, of funding made available for AMR-related research while others assess the type (e.g. push incentives15) and scope of this funding68,82. Studies also consider the adequacy of AMR-related research by measuring the national number of researchers in the AMR field21, the number of publications affiliated with a given country31,51, whether these publications address issues such as irrational AMU183, and whether relevant scientific or professional conferences are held31. The grey literature in particular focuses on structural factors related to AMR research, e.g. the extent to which national research agendas are informed by global AMR agendas and tailored to national needs49 and the degree to which capacity building for the implementation of such research is the product of the collaboration between academia, the private sector, and civil society49.
Domain: monitoring & evaluation; subdomain 16: surveillance & laboratory
Surveillance & Laboratory encompasses indicators that assess the comprehensiveness of surveillance programmes and the capacity and quality of laboratory systems across all sectors. A total of 941 indicators were extracted from 115 academic studies21,22,26,27,29,30,40,51,53,55,57–60,65,74,80,84,87,91,92,94–96,99,101–105,113,121,124–126,132–134,138,141,144,145,147,148,153,154,160,176–180,185–243; 486 from 29 grey literature studies11–15,17,18,43,44,46,47,49,61,63,69–71,73,77,106,107,109,112,161–165,244. Over half of the grey literature indicators were from the WHO Global AMR and Use Surveillance System (GLASS)63 (207) and IPCAT 213 (111).
Academic indicators related to surveillance21,74,99,138,153, the representativeness and coverage of surveillance platforms104, prioritised pathogens or infections214, data completeness and consistency, standardised case definitions104, sampling schemes53,216, data collection intervals193,230, data verification and validation processes27,102,190, and the establishment and integration of surveillance across One Health sectors21. Measures of laboratory capacity and quality span assessments of infrastructure and operations (e.g., availability of national reference laboratories, continuity of services, referral pathways, sample transport)21,53,74, diagnostic methods and techniques (e.g., culture, antimicrobial susceptibility testing (AST) for bacteria and fungi, molecular/genomic testing, pathogen-specific assays)86, standardisation of procedures (e.g., adherence to Clinical and Laboratory Standards Institute and European Committee on Antimicrobial Susceptibility Testing guidelines, participation in external quality assurance/proficiency testing schemes)53,57,224,233, data management, and analysis capabilities (e.g., electronic reporting platforms, and interoperability)92,113,153,197,214,234. Many indicators quantify network attributes such as the number and distribution of surveillance sites194,202,217,235, coverage of sentinel sites or industry monitoring systems58,104, integration of peripheral and reference labs53,74, and the establishment of national coordinating centres or integrated surveillance strategies21,138. Quality-related indicators include completeness and timeliness of AST data, frequency and methods of data analysis and dissemination, and metrics on external quality assurance participation27,53,197.
Surveillance output indicators encompass pathogen-specific resistance rates and incidence densities134,194,223,232, bloodstream infection incidence by age, sex, and clinical setting104,187,202,205, genotype prevalence and molecular epidemiology (e.g., sequence types, resistance genes, virulence determinants)203,206, environmental surveillance metrics (e.g., antimicrobial resistance gene (ARG) abundance in water, wastewater, food chain)21,30,228, and outcome measures (e.g. deaths and disability-adjusted life years (DALYs) attributable to AMR)103,104,205. Further indicators capture temporal trends201,206,235, correlations between resistance prevalence and antimicrobial consumption96,141, blood culture positivity rates218, and burden estimates163. Grey-literature indicators emphasise the establishment of integrated AMR surveillance systems11,69,70, laboratory network robustness11,12,17,70,77, essential diagnostics lists11,69, external quality assessment implementation11,73, AST capacity for critical pathogens11,13, and reporting to GLASS63. Additional measures assess the presence of sustainable specimen referral and transport systems, biosafety/biosecurity frameworks, laboratory quality management systems, tiered diagnostic network implementation, and early warning surveillance protocols12,69.
Domain: monitoring & evaluation; subdomain 17: reporting
Reporting refers to mechanisms for communicating progress and data on the national AMR strategy to stakeholders, including annual progress reports and formal submissions to international and regional AMR surveillance initiatives. Fifty-six indicators were extracted from 18 academic studies22,27,29,34,53,66,67,75,78,99,104,128,135,153,190,194,197,204; 85 from 12 grey literature studies11,13,15,18,43,45,48,63,71,77,107,244, with 39 indicators originating from ANIMUSE48.
Indicators grouped under Reporting address the existence of governance structures or processes for sharing AMR and AMU data with global and regional databases and regulatory bodies (e.g., evidence of protocols for submission to GLASS, Central Asian and European Surveillance of Antimicrobial Resistance network (CAESAR), European Centre of Disease Control (ECDC), European AMR Surveillance Network (EARS-Net), WHO reports, WOAH AMU/AMR databases, European Food Safety Authority (EFSA), European Surveillance of Veterinary Antimicrobial Consumption (ESVAC))67,78. Animal health indicators cover registration and reporting of antimicrobial products, submission of AMU and residue data, and integration within One Health reporting frameworks, bacteria–drug combinations, and core data elements11,18,48,53,77,128. Laboratory reporting measures include counts of culture-positive/negative results, proportions of commonly reported pathogens, and frequency of AST result submission197,204. Grey-literature indicators emphasise reporting NAP status updates11,15,44,49, annual animal-sector AMU reports to WOAH11,18,61, participation in GLASS15,45,63,71,77, and the establishment of clear reporting pathways for AMR and AMU information13.
Domain: monitoring & evaluation; subdomain 18: feedback mechanisms
Feedback mechanisms refer to indicators that capture the existence and quality of processes for relaying surveillance data and performance information to regional, organisational, and individual stakeholders. Sixteen indicators were extracted from 6 academic studies21,22,53,59,80,104; 50 from 13 grey literature studies11,13,17,43,44,49,61,69–71,77,81,108.
Indicators sought to measure scoping themes from national performance to regional- and hospital-level IPC and stewardship. Sector-specific feedback processes include the establishment of national platforms for sharing pathogen-specific data13,104. Multisector coordination indicators examine whether data analysed are used for policy advocacy and resource allocation, whether data reviews occur, and whether AMU and AMR surveillance data inform decision-making and policy11,13,69,71. Metrics of zoonotic events (infection transmission between animal and human species) include the proportion of events evaluated with timeliness metrics or decision tools, joint investigations, and activities implemented based on joint risk assessments43. Key indicators examine the documented use of surveillance data for decision-making, inclusion of monitoring mechanisms in NAPs, and governance responsiveness scores11,21.
Monitoring and audit frameworks are evaluated for integration of IPC indicators within national systems, tools for systematic data collection (e.g., WHO hand hygiene self-assessment), alignment of national and local monitoring activities, linkage with WASH monitoring, regular collection of IPC monitoring and audit data, facility-level self- or peer- evaluation against standards, and dissemination of monitoring results to drive improvement13,43. Laboratory feedback is measured by participation in external quality assurance/proficiency testing schemes and whether alternate bodies perform equivalent functions70. Indicators also assess whether treatment guidelines undergo regular audit, review, and dissemination, and whether collected data guide action and guideline updates49,71. Other indicators measure whether surveillance results are systematically distributed to field actors via organised channels17. Indicators also gauge whether veterinary laboratory quality management systems and risk-analysis capacity routinely inform risk management and communication61. Finally, the presence of national bodies that review surveillance findings and translate them into recommendations and implemented actions captures the end-to-end feedback process77.
Several IPC-related indicators were jointly grouped as feedback mechanism indicators, including the existence of strategic plans for monitoring and feedback, schedules for guideline review, national systems for monitoring adherence with periodic audits, and timely feedback reports to stakeholders on HAI trends, outbreak control, and multidrug-resistant pathogen occurrences13,43.
Domain: monitoring & evaluation; subdomain 19: effectiveness
Effectiveness indicators examine whether structured mechanisms exist at the national level to evaluate if policies or interventions achieve their intended health and economic outcomes. Nineteen indicators were extracted from nine academic studies20–22,27,28,34,36,91,133; 17 from 8 grey literature studies11,13,18,77,109,110,165,245.
Indicators include metrics, e.g., M&E plan quality by country, aggregate M&E scores, and national evaluation frameworks for IPC and AMR strategies13,22,34. Governance effectiveness and efficiency are measured via global governance indices; food safety evaluation scores capture the impact of interventions in related sectors across countries21,22. Perception-based metrics include respondents’ satisfaction with the functioning of AMR multisector coordination committees and perceived impact from policy measures28,91. Outcome indicators quantify health and economic burdens attributable to AMR, e.g. loss of life expectancy, excess health expenditure, reduced labour participation and productivity due to AMR and broader risk indices245. Burden-of-disease measures such as DALYs attributed to AMR serve to assess the ultimate impact of interventions77. Certain indicators also attempt to measure the cost-effectiveness of policies through comparisons between intervention costs and observed reductions in AMR-related morbidity, mortality, or economic losses13,245.
Discussion
Our scoping review offers a comprehensive, cross‑sectoral inventory of AMR indicators, drawing from quantitative and qualitative sources across the One Health sectors. By systematically cataloguing over 3000 indicators from academic and grey literature, we fill a critical gap in the AMR evidence landscape and provide a foundation for harmonised, One Health-oriented monitoring.
Our findings demonstrate the structural imbalance in indicator development, with limited coverage of Accountability, Transparency, and Equity subdomains, despite their central importance to the Governance & Leadership domain. Strengthening measurement within these areas is essential for effective policy governance, to ensure AMR strategies are properly developed, then implemented, evaluated, and iteratively improved. The paucity of equity-focused indicators is particularly concerning, given recognition that the burden of AMR falls disproportionately on marginalised, disadvantaged populations246. This imbalance extends across One Health sectors: far more indicators are available for human than for animal and environmental health (Supplementary Fig. 1). This lack likely contributes to animal and environmental health’s underrepresentation in national AMR agendas, weakening the multisectoral coordination required for effective AMR control. These findings suggest two priority actions for international organisations such as the Quadripartite and partners: first, develop standardised indicators for underrepresented domains—particularly Accountability, Equity, and Transparency; second, develop indicators for the animal and environmental health sectors comparable to those for human health.
Our work has several limitations. First, we focused our attention on collating existing qualitative and quantitative indicators, but a critical appraisal of the indicators identified fell outside the remit of this review. Further work is planned to use these indicators as input for a consensus process to develop an index that will benchmark national performance in responding to AMR. Second, the comparative, cross‑country inclusion criteria that we used necessarily deprioritised subnational and local indicators, e.g. regional biosecurity protocols and community‑level stewardship initiatives. However, many regional indicators may be relevant to a given country’s specific context, though deemed irrelevant to comparing cross-national performance. Third, restricting our inclusion criteria to studies published between 2014 and 2024 may have excluded earlier efforts to measure national AMR response. However, we deemed studies published pre-2014 as less policy-relevant as they precede the publication of the GAP on AMR. Fourth, our initial focus on English-language publications, subsequently supplemented by non-English studies, may have introduced bias: non-English literature may emphasise different aspects of AMR policy. Fifth, the academic evidence base disproportionately reflects European and high-income country contexts, with 37% of included studies situated in Europe and only 11% in the WHO African Region. This may mean we have captured indicators predominantly from countries with more developed surveillance systems, as these are more likely to report findings publicly, and that the resulting indicator set reflects structural biases in the literature rather than a balanced global perspective. This should be considered when interpreting the indicators and the planned One Health AMR Accountability Index.
Building on the inventory compiled in the current study, we plan to use these indicators to build a novel One-Health AMR Accountability Index to measure national performance in addressing AMR247. Our next step involves screening the indicators identified for inclusion in a Delphi survey. Indicators will be formally screened and prioritised based on feasibility, data availability, and subdomain balancing. Indicators will be removed if the overall theme is duplicated or collinearity is identified. After indicator refinement, we will undertake a multi-stage consensus process with international AMR experts to select and weight indicators for inclusion into a unified AMR Accountability Index. The One Health AMR Accountability Index will be piloted in different international regions to reflect regional differences and different country income classifications.
As a separate exercise, we have created a human-health-focused AMR Accountability Index in conjunction with WHO Europe, anchored in the Roadmap on Antimicrobial Resistance for the WHO European Region 2023–2030. This index will provide composite indicators that cover the Roadmap’s five action areas and six enablers spanning both multisectoral and human health domains. Currently, the human-health-focused AMR Accountability Index is undergoing a piloting process in six WHO European region Member States to ensure the Index reflects structural differences and country contexts. Ultimately, One Health AMR Accountability Index seeks to fill a current gap in global AMR policy efforts by benchmarking national performance, identifying countries requiring technical support, and tracking global progress toward AMR containment goals.
Methods
Literature review
A scoping approach was employed to review and synthesise existing literature to identify and consolidate quantitative and qualitative measures used to assess and compare national performance in addressing AMR. This review encompassed academic and grey literature searches. The academic literature search was conducted between 26 November 2024, and March 2025. Three electronic databases, Medline, EMBASE, and Global Health, were systematically searched to capture peer-reviewed articles in English from 2014 through 2024. This was supplemented by an additional search using the same search terms for non-English studies in January 2025. Where necessary, non-English studies were translated using Google Translate to assess eligibility and extract relevant data. The starting year of 2014 was chosen to coincide with the release of key global policy instruments (e.g., the World Health Assembly resolution that paved the way for the 2015 WHO GAP on AMR), ensuring that pivotal developments in AMR policy and measurement were captured. In parallel with the academic literature search, a thorough grey literature review was undertaken to capture indicators that might not appear in peer-reviewed journals. Grey literature was identified through Google Scholar and targeted searches of major international organisations. Our methods are further outlined within a previously published PROSPERO protocol (CRD42024625477)248.
Academic literature search terms
The search strategy combined terms related to antimicrobials (e.g., “antibiotic*,” “antimicrobial*,” “antifungal*,” “antiinfective*”), resistance (e.g., “resistance,” “resistant”), and policy or performance measures (e.g., “performance,” “benchmark,” “indicator*,” “evaluation,” “governance,” “framework,” “policy,” “rate*”). Further terms specifying national and governmental contexts (e.g., “national,” “country,” “government*”) were included. Boolean operators (AND, OR) were used to generate comprehensive results while minimising irrelevant studies.
Grey literature search details
For Google Scholar, we screened the first 300 results sorted by relevance for each search string. The 300-result cap was used to balance sensitivity and feasibility, as relevance markedly declines beyond this range in Google Scholar indexing1. Second, relevant websites of major multilateral organisations involved in AMR policy, such as the World Health Organization (WHO)2, the World Organisation for Animal Health (WOAH)3, the Food and Agriculture Organization (FAO)4, the United Nations Environment Programme (UNEP)5, the Organisation for Economic Co-operation and Development (OECD)6, and the World Bank7, were examined to identify policy documents, reports, and white papers listing or discussing AMR indicators. Additionally, websites of prominent think tanks and professional societies (e.g., the Centre for Global Development, the Alliance for Reducing Microbial Resistance, and the European Society of Clinical Microbiology and Infectious Diseases) were searched for relevant non-peer-reviewed materials. The full list of all grey literature sources with links is listed in Supplemental Table 1. All grey literature records were screened and extracted by two reviewers (BH and EO) manually using the same inclusion criteria and data charting procedures applied to the academic literature. All identified documents were saved in a shared repository, and duplicates were removed.
Inclusion and exclusion criteria
Inclusion criteria were deliberately broad to capture any cross-country comparison of AMR policy or performance that presented either quantitative or qualitative indicators. Inclusion criteria included any article using indicators to measure national performance in addressing AMR. Exclusion criteria included: 1) Wrong study outcome (articles relevant to antivirals, tuberculosis, or vaccines). Tuberculosis was excluded on the basis that TB-specific AMR operates within a largely separate policy, surveillance, and programmatic infrastructure with dedicated international frameworks and accountability structures, and its inclusion risked conflating two distinct policy domains; 2) wrong study design (systematic reviews that identify individual studies in multiple countries focused on developing understanding of AMR, systematic reviews, organisational or regional-level studies of prevalence of AMR or AMU, cost-effectiveness studies, or editorials or conference abstracts); and 3) wrong study comparator (articles measuring regional, organisational, or individual performance and articles used to measure performance in one country in isolation). As the primary purpose of this review was to identify indicators suitable for cross-national benchmarking, single-country studies may reflect idiosyncratic national priorities or data systems that cannot be meaningfully standardised or compared across diverse country contexts.
Two reviewers (US, SR) screened titles and abstracts for relevance, each working separately to apply inclusion and exclusion criteria independently. Any discrepancies were resolved through iterative discussions or by consulting a third reviewer (MA) if consensus could not be reached. Studies that met inclusion criteria at the abstract level were retained for full-text review, after which the same reviewers independently confirmed eligibility with discrepancies again resolved through iterative discussions or by consulting a third reviewer (MA) if consensus could not be reached. Cohen’s Kappa was reported to assess inter-rater reliability for both title and abstract screening as well as full text screening.
Data extraction and thematic synthesis
All peer-reviewed articles and grey literature documents included were collated into a database. Basic bibliographic information (author(s), publication date, title) and details about the identified indicators (description, measurement approach, data sources used, and One Health domain coverage, which included animal health, environmental health, human health, and multisectoral coordination) were recorded for each. Indicators with sectoral overlap were categorised across animal health, environmental health, and human health, depending on the nature of the indicator. For example, indicators relating to meat production, livestock, or animal products were captured under animal health, while indicators relating to food safety, foodborne disease, or human dietary exposure were captured under human health. Indicators relating to soil contamination, agricultural runoff, or AMR in environmental systems were captured under environmental health. If an indicator had multiple metrics or definitions, each variant was noted separately to ensure a comprehensive initial pool of potential measures.
A narrative thematic synthesis was then performed. We employed a framework-based approach, adapting existing frameworks (Roadmap on Antimicrobial Resistance for the WHO European Region 2023–20306 and Anderson et al.16) to identify relevant domains a priori. We then inductively refined these categories based on the indicators identified. We merged these frameworks to identify 19 AMR subdomain groups under three domains: Governance & Leadership, Action Areas, and Monitoring & Evaluation (Fig. 4).
Fig. 4. Thematic synthesis of AMR policy domains.
Authors’ creation.
Indicator screening and coding
Indicators were excluded if not considered cross-national measures of performance in AMR response, were duplicates (i.e., were identical or had near-identical constructs and measures); not specific to AMR. Four reviewers (US, VK, BH, and SR) independently conducted initial indicator exclusions; two reviewers (MA and EO) evaluated their accuracy and consistency.
Two reviewers coded each indicator according to the framework’s policy domains (Fig. 4); MA and EO reviewed the coding to ensure concordance in approach. Indicators were then examined within each thematic category to highlight commonalities and identify overlap. Finalised extracted indicators must: (1) measure national performance in addressing AMR in two or more countries; (2) be quantitative or qualitative within the scope of AMR; (3) measure performance in any sector across the One Health spectrum; (4) be relevant to AMR.
Supplementary information
Acknowledgements
This study was funded by the Novo Nordisk Foundation (Grant no. NNF24SA0099921). The funder played no role in study design, data collection, analysis and interpretation of data, or the writing of this manuscript. M.A. is supported by the NIHR as a clinical lecturer. The authors thank Judith Barrett Johnston for professional editing services and Dimitra Vyzantiadou for the creation of the graphic for Fig. 1.
Author contributions
E.O., M.A., and E.M. participated in conceiving the study, literature search, analysis, interpretation of the data, writing and critical revision of the manuscript for important intellectual content. U.S. and V.K. participated in the literature search, analysis, interpretation of the data, writing and critical revision of the manuscript for important intellectual content. B.H. and S.R. participated in the literature search and critical revision of the manuscript for important intellectual content. D.L., K.K., and E.M. participated in interpreting results and providing critical revisions. All authors read and approved the final manuscript.
Data availability
All data generated or analysed during this study are included in this published article and its supplementary information files.
Competing interests
The authors declare no competing interests.
Footnotes
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary information
The online version contains supplementary material available at 10.1038/s44259-026-00213-8.
References
- 1.Naghavi, M. et al. Global burden of bacterial antimicrobial resistance 1990–2021: a systematic analysis with forecasts to 2050. Lancet404, 1199–1226 (2024). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Global Leaders Group on Antimicrobial Resistance. Towards specific commitments and action in the response to antimicrobial resistancehttps://www.amrleaders.org/about-us/what-we-do/glg-report (2024).
- 3.World Health Organization. European Strategic Action Plan on Antibiotic Resistance (WHO Regional Office for Europe, 2011).
- 4.European Commission. Action Plan Against the Rising Threats from Antimicrobial Resistance (European Commission, 2011).
- 5.Health Emergency Preparedness and Response Authority. UNGA Political Declaration: A global commitment to combat antimicrobial resistance (AMR) (European Commission, 2024).
- 6.World Health Organization. Roadmap on antimicrobial resistance for the WHO European Region 2023–2030 (WHO Regional Office for Europe, 2023).
- 7.Tejpar, S., Rogers Van Katwyk, S., Wilson, L. & Hoffman, S. J. Taking stock of global commitments on antimicrobial resistance. BMJ Glob. Health7, e008159 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.European Commission. A European One Health Action Plan against Antimicrobial Resistance (AMR) (European Commission, 2017).
- 9.Mendelson, M. et al. Ensuring progress on sustainable access to effective antibiotics at the 2024 UN General Assembly: a target-based approach. Lancet403, 2551–2564 (2024). [DOI] [PubMed] [Google Scholar]
- 10.Chatterjee, A. et al. Quantifying drivers of antibiotic resistance in humans: a systematic review. Lancet Infect. Dis.18, e368–e378 (2018). [DOI] [PubMed] [Google Scholar]
- 11.World Health Organization. Tracking AMR Country Self-assessment Survey - TrACSS (World Health Organization, 2025).
- 12.World Health Organization. IHR (2005) States Parties self-assessment annual reporting tool 2nd ed. (World Health Organization, 2021).
- 13.World Health Organization. Instructions for the national infection prevention and control assessment tool 2 (IPCAT 2) (World Health Organization, 2017).
- 14.World Health Organization. Joint External Evaluation Tool: International Health Regulations (2005) 3rd ed. (World Health Organization, 2022).
- 15.Global Coalition on Aging & Infectious Diseases Society of America. 2024 AMR Preparedness Index Progress Report (Global Coalition on Aging, 2024).
- 16.Anderson, M., Schulze, K., Cassini, A., Plachouras, D. & Mossialos, E. A governance framework for development and assessment of national action plans on antimicrobial resistance. Lancet Infect. Dis.19, e371–e384 (2019). [DOI] [PubMed]
- 17.LLatornico, F., Keck, N., Treilles, M. & Kabali, E. FAO Assessment Tool for Laboratories and AMR Surveillance Systems (ATLASS) for the food and agriculture sectors (Food and Agriculture Organization of the United Nations, 2018).
- 18.World Organisation for Animal Health. Implementation of WOAH Standards: The Observatory Annual Report. https://www.woah.org/en/what-we-do/standards/observatory/implementation-of-standards-the-observatory-monitoring-report/ (2022).
- 19.Anderson, M., Kluge, H. H. P., Wong, D. L. F., Butler, R. & Mossialos, E. Promoting sustainable national action to tackle antimicrobial resistance: a proposal to develop an antimicrobial resistance accountability index. Lancet Microbe5, e304–e311 (2024). [DOI] [PubMed]
- 20.Birgand, G. et al. Comparison of governance approaches for the control of antimicrobial resistance: Analysis of three European countries. Antimicrob. Resist. Infect. Control7, 28 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Zhang, Q. et al. How far has the globe gone in achieving One Health? Current evidence and policy implications based on global One Health index. Sci. One Health3, 100064 (2024). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Patel, J. et al. Measuring the global response to antimicrobial resistance, 2020-21: a systematic governance analysis of 114 countries. Lancet Infect. Dis.23, 706–718 (2023). [DOI] [PubMed] [Google Scholar]
- 23.Joshi, M. P. et al. Strengthening multisectoral coordination on antimicrobial resistance: a landscape analysis of efforts in 11 countries. J. Pharm. Policy Pract.14, 27 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Chua, A. Q., Verma, M., Hsu, L. Y. & Legido-Quigley, H. An analysis of national action plans on antimicrobial resistance in Southeast Asia using a governance framework approach. Lancet Reg. Health West. Pac.7, 100084 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Vogeler, C. S. & Parth, A.-M. An elephant in the room? Explaining agenda-setting in antimicrobial resistance policies in 30 European countries. Soc. Sci. Med.356, 117164 (2024). [DOI] [PubMed] [Google Scholar]
- 26.Joshi, M. P. et al. Moving from assessments to implementation: promising practices for strengthening multisectoral antimicrobial resistance containment capacity. J. Globe Health Rep.5, 7 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.TTegegne H. A. et al. OH-EpiCap: a semi-quantitative tool for the evaluation of One Health epidemiological surveillance capacities and capabilities. medRxiv10.1101/2023.01.04.23284159 (2023). [DOI] [PMC free article] [PubMed]
- 28.Yahaya, A. A. et al. Perspectives on the Regional Strategy for Implementation of National Action Plans on Antimicrobial Resistance in the WHO African Region. Antibiotics13, 202 (2024). [DOI] [PMC free article] [PubMed]
- 29.Okolie, O. J., Igwe, U., Ismail, S. U., Ighodalo, U. L. & Adukwu, E. C. Systematic review of surveillance systems for AMR in Africa. J. Antimicrob. Chemother.78, 31EP–51EP (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Sabbatucci, M. et al. Tracking progress on antimicrobial resistance by the quadripartite country self-assessment survey (TrACSS) in G7 countries, 2017-2023: opportunities and gaps. Pharmacol. Res.204, 107188 (2024). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Earnshaw, S. et al. European antibiotic awareness day: a five-year perspective of Europe-wide actions to promote prudent use of antibiotics. Eurosurveillance19, 20928 (2014). [DOI] [PubMed] [Google Scholar]
- 32.Kamere, N. et al. Scoping review of national antimicrobial stewardship activities in eight African countries and adaptable recommendations. Antibiotics11, 1149 (2022). [DOI] [PMC free article] [PubMed]
- 33.Carelli, D. E., Mitsouli, E. T., Ogne, J. B. & Pierre, J. The best laid plans? international governance perspectives in AMR national action plans in Europe. Eur. J. Public Health33, 682–686 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Samuel, F., Orubu, E., Sutradhar, I., Zaman, M. H. & Wirtz, V. J. Benchmarking national action plans on antimicrobial resistance in eight selected LMICs: Focus on the veterinary sector strategies. J. Glob. Health10, 020414 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Iwu, C. D. & Patrick, S. M. An insight into the implementation of the global action plan on antimicrobial resistance in the WHO African region: a roadmap for action. Int. J. Antimicrob. Agents58, 106411 (2021). [DOI] [PubMed] [Google Scholar]
- 36.Kaiser, R. A., Taing, L. & Bhatia, H. Antimicrobial resistance and environmental health: a water stewardship framework for global and national action. Antibiotics11, 1014 (2022). [DOI] [PMC free article] [PubMed]
- 37.Carelli, D. E., Ogne, J. B. & Pierre, J. Coming of age: governance challenges in updated AMR national action plans in the EU. Eur. J. Public Health34, 885–889 (2024). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Rubin, O. & Munkholm, L. Isomorphic dynamics in national action plans on antimicrobial resistance. Public Adm. Dev.42, 142–153 (2021). [DOI] [PubMed] [Google Scholar]
- 39.Avello, P. et al. National action plans on antimicrobial resistance in Latin America: an analysis via a governance framework. Health policy Plan.39, 188–197 (2024). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Bravo, G. et al. SPiNCAR: A systematic model to evaluate and guide actions for tackling AMR. PloS ONE17, e0265010 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.D’Atri, F. et al. Targets for the reduction of antibiotic use in humans in the Transatlantic Taskforce on Antimicrobial Resistance (TATFAR) partner countries. Eurosurveillance24, 1800339 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Munkholm, L. & Rubin, O. The global governance of antimicrobial resistance: a cross-country study of alignment between the global action plan and national action plans. Globaliz. Health16, 109 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Food and Agriculture Organization of the United Nations, World Health Organization & World Organisation for Animal Health. Monitoring and Evaluation for Effective Management of Zoonotic Diseases - An operational tool of the Tripartite Zoonoses Guide (World Health Organization, 2024).
- 44.Organisation for Economic Co-operation and Development. Embracing a One Health Framework to Fight Antimicrobial Resistance (OECD Publishing, 2023).
- 45.United Nations General Assembly. Political declaration of the high-level meeting on antimicrobial resistance (United Nations, 2024).
- 46.Global Leaders Group on Antimicrobial Resistance. Priorities of the Global Leaders Group on AMR (Global Leaders Group, 2023).
- 47.World Health Organization. Surveillance of health care-associated infections at national and facility levels - Practical handbook (World Health Organization, 2024).
- 48.World Organisation for Animal Health. Annual Report on Antimicrobial Agents Intended for Use in Animalshttps://www.woah.org/app/uploads/2024/05/woah-amu-report-2024-final.pdf (World Organisation for Animal Health, 2024).
- 49.World Health Organization. People-centred approach to addressing antimicrobial resistance in human health: WHO core package of interventions to support national action plans (World Health Organization, 2023).
- 50.Food and Agriculture Organization of the United Nations. Food and Agriculture Organization of the United Nations. https://www.fao.org/home/en (2026).
- 51.Joshi, M. P. et al. Multidisciplinary and multisectoral coalitions as catalysts for action against antimicrobial resistance: Implementation experiences at national and regional levels. Glob. Public Health13, 1781–1795 (2018). [DOI] [PubMed] [Google Scholar]
- 52.Willemsen, A., Reid, S. & Assefa, Y. A review of national action plans on antimicrobial resistance: strengths and weaknesses. Antimicrob. Resist. Infect. Control11, 90 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 53.Ferdinand, A. S. et al. Development of a cross-sectoral antimicrobial resistance capability assessment framework. BMJ Glob. Health9, e014282 (2024). [DOI] [PMC free article] [PubMed]
- 54.Chan, O. S. K. et al. Antimicrobial resistance policy protagonists and processes—a qualitative study of policy advocacy and implementation. Antibiotics11, 1029 (2022). [DOI] [PMC free article] [PubMed]
- 55.Elton, L. et al. Antimicrobial resistance preparedness in sub-Saharan African countries. Antimicrob. Resist. Infect. Control9, 145 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 56.Bajalan, A. et al. Awareness regarding antimicrobial resistance and confidence to prescribe antibiotics in dentistry: a cross-continental student survey. Antimicrob. Resist. Infect. Control11, 158 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 57.Viprey, V. F. et al. European survey on the current surveillance practices, management guidelines, treatment pathways and heterogeneity of testing of Clostridioides difficile, 2018-2019: results from the Combatting Bacterial Resistance in Europe CDI (COMBACTE. J. Hosp. Infect.131, 213–220 (2023). [DOI] [PubMed] [Google Scholar]
- 58.Rahbe, E., Kovacevic, A., Opatowski, L. & Leclerc, Q. J. Investigating the feasibility and potential of combining industry AMR monitoring systems: a comparison with WHO GLASS. medRxiv10.1101/2024.03.27.24303768 (2024). [DOI] [PMC free article] [PubMed]
- 59.Pallett, S. J. et al. National action plans for antimicrobial resistance and variations in surveillance data platforms. Bull. World Health Organ.101, 501–512F (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 60.Cole, M. J. et al. The European response to control and manage multi- and extensively drug-resistant Neisseria gonorrhoeae. Eurosurveillance27, 2100482 (2022). [DOI] [PMC free article] [PubMed]
- 61.World Organisation for Animal Health. Evaluation of the Performance of Veterinary Services PVS Tool – Terrestrial 2019 (World Organisation for Animal Health, 2023).
- 62.Food and Agriculture Organization of the United Nations. Methodology to Analyse AMR-Relevant Legislation in the Food and Agriculture Sector - Guidance Document for Regulators (Food and Agriculture Organization of the United Nations, 2020).
- 63.World Health Organization. Global Antimicrobial Resistance and Use Surveillance System (GLASS) (World Health Organization, 2023).
- 64.World Health Organization Barcelona Office for Health Systems Financing. UHC Watch (World Health Organization, 2024).
- 65.Kinoshita, T., Tokumasu, H., Tanaka, S., Kramer, A. & Kawakami, K. Policy implementation for methicillin-resistant Staphylococcus aureus in seven European countries: a comparative analysis from 1999 to 2015. J. Mark. Access Health Policy5, 1351293 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 66.Balkhy, H. H. et al. The strategic plan for combating antimicrobial resistance in Gulf Cooperation Council States. J. Infect. Public Health9, 375–385 (2016). [DOI] [PubMed] [Google Scholar]
- 67.Mesa Varona, O. et al. Monitoring antimicrobial resistance and drug usage in the human and livestock sector and foodborne antimicrobial resistance in six European countries. Infect. Drug Resist.13, 957–993 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 68.Center for Global Development. The Commitment to Development Index (Center for Global Development, 2023).
- 69.World Health Organization. WHO benchmarks for strengthening health emergency capacities (World Health Organization, 2023).
- 70.Food and Agriculture Organization of the United Nations. The International FAO Antimicrobial Resistance Monitoring (InFARM) system: Manual for implementation – Annex 3 (Food and Agriculture Organization of the United Nations, 2024).
- 71.World Health Organization. WHO implementation handbook for national action plans on antimicrobial resistance: guidance for the human health sector (World Health Organization, 2022).
- 72.World Health Organization. International Health Regulations (2005): State Party Self-Assessment Annual Reporting Tool (World Health Organization, 2021).
- 73.World Health Organization. Central Asian and European Surveillance of Antimicrobial Resistance – External quality assessment results 2020 (World Health Organization, 2022).
- 74.Albiger, B., Glasner, C., Struelens, M. J., Grundmann, H. & Monnet, D. L. Carbapenemase-producing Enterobacteriaceae in Europe: assessment by national experts from 38 countries, May 2015. Eurosurveillance20, 21300 (2015). [DOI] [PubMed] [Google Scholar]
- 75.Harant, A. Assessing transparency and accountability of national action plans on antimicrobial resistance in 15 African countries. Antimicrob. Resist. Infect. Control11, 15 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 76.World Health Organization Eastern Mediterranean Region. Operational approach to antimicrobial stewardship in the WHO Eastern Mediterranean Region (World Health Organization, 2024).
- 77.World Health Organization, World Organisation for Animal Health & Food and Agriculture Organization of the United Nations. Monitoring and evaluation of the global action plan on antimicrobial resistance (World Health Organization, 2019).
- 78.Charani, E. et al. An analysis of existing national action plans for antimicrobial resistance-gaps and opportunities in strategies optimising antibiotic use in human populations. Lancet Glob. Health11, e466–e474 (2023). [DOI] [PubMed] [Google Scholar]
- 79.Gahimbare, L. et al. Monitoring progress on Antimicrobial Resistance (AMR) response in the World Health Organization African region: insights from the Tracking AMR Country Self-Assessment Survey (TrACSS) 2021 results for the human health sector. J. Public Health Afr.14, 2392 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 80.European Health and Digital Executive Agency, Intellera Consulting & Tetra Tech International Development. Study on the Design of a Monitoring Framework of the EU One Health Action Plans against AMR and Council Recommendation on Stepping up EU Actions to Combat Antimicrobial Resistance in a One Health Approach. https://op.europa.eu/en/publication-detail/-/publication/e872ae01-e50d-11ef-bc1c-01aa75ed71a1 (European Health and Digital Executive Agency, 2024).
- 81.World Bank & Food and Agriculture Organization of the United Nations. From reacting to preventing pandemics: Building Animal Health and Wildlife Systems for One Health in East Asia and Pacific (World Bank, 2022).
- 82.Alliance for Reducing Microbial Resistance & G7 Research Group. G7 Compliance Report on Antimicrobial Resistance, 2021–2023 (Alliance for Reducing Microbial Resistance, 2024).
- 83.Council of the European Union. Council Recommendation on stepping up EU actions to combat antimicrobial resistance in a One Health approach (Council of the European Union, 2023).
- 84.Alsan, M. et al. Out-of-pocket health expenditures and antimicrobial resistance in low-income and middle-income countries: an economic analysis. Lancet Infect. Dis.15, 1203–1210 (2015). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 85.World Health Organization. Addressing gender inequalities in national action plans on antimicrobial resistance – Guidance to complement the people-centred approach (World Health Organization, 2024).
- 86.Browne, A. J. et al. Global antibiotic consumption and usage in humans, 2000-18: a spatial modelling study. Lancet Planet. Health5, e893–e904 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 87.Medland, N. A. et al. Surveillance systems to monitor antimicrobial resistance in Neisseria gonorrhoeae: a global, systematic review, 1 January 2012 to 27 September 2020. Eurosurveillance27, 2100917 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 88.Weets, C. M. & Katz, R. Global approaches to tackling antimicrobial resistance: a comprehensive analysis of water, sanitation and hygiene policies. BMJ Glob. Health9, e014224 (2024). [DOI] [PMC free article] [PubMed]
- 89.Luthman, O., Robb, D. H. F., Henriksson, P. J. G., Jorgensen, P. S. & Troell, M. Global overview of national regulations for antibiotic use in aquaculture production. Aquac. Int.32, 9253–9270 (2024). [Google Scholar]
- 90.Postma, M. et al. Opinions of veterinarians on antimicrobial use in farm animals in Flanders and the Netherlands. Vet. Rec.179, 68 (2016). [DOI] [PubMed] [Google Scholar]
- 91.Visschers, V. H. M. et al. Perceptions of antimicrobial usage, antimicrobial resistance and policy measures to reduce antimicrobial usage in convenient samples of Belgian, French, German, Swedish and Swiss pig farmers. Prev. Vet. Med.119, 10–20 (2015). [DOI] [PubMed] [Google Scholar]
- 92.Ahmad, R., Zhu, N. J., Leather, A. J. M., Holmes, A. & Ferlie, E. Strengthening strategic management approaches to address antimicrobial resistance in global human health: a scoping review. BMJ Glob. Health4, e001730 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 93.Jensen, C. S. While we are waiting for the Superbug: constitutional asymmetry and EU governmental policies to combat antimicrobial resistance. J. Common Mark. Stud.58, 1361–1376 (2020). [Google Scholar]
- 94.Booth, A. & Wester, A. L. A multivariable analysis of the contribution of socioeconomic and environmental factors to blood culture Escherichia Coli resistant to fluoroquinolones in high- and middle-income countries. BMC Public Health22, 354 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 95.Opatowski, L., Opatowski, M., Vong, S. & Temime, L. A one-health quantitative model to assess the risk of antibiotic resistance acquisition in asian populations: impact of exposure through food, water, livestock and humans. Risk Anal.41, 1427–1446 (2021). [DOI] [PubMed] [Google Scholar]
- 96.Collignon, P., Beggs, J. J., Walsh, T. R., Sumanth Gandra, S. G. & Ramanan Laxminarayan, R. L. Anthropological and socioeconomic factors contributing to global antimicrobial resistance: a univariate and multivariable analysis. Lancet Planet. Health2, e398 (2018). [DOI] [PubMed] [Google Scholar]
- 97.Eckmann, C. et al. Antibiotic treatment patterns across Europe in patients with complicated skin and soft-tissue infections due to meticillin-resistant Staphylococcus aureus: a plea for implementation of early switch and early discharge criteria. Int. J. Antimicrob. Agents44, 56–64 (2014). [DOI] [PubMed] [Google Scholar]
- 98.Munkholm, L., Rubin, O., Baekkeskov, E. & Humboldt-Dachroeden, S. Attention to the Tripartite’s one health measures in national action plans on antimicrobial resistance. J. Public Health Policy42, 236–248 (2021). [DOI] [PubMed] [Google Scholar]
- 99.Leong, M., Picton, R., Wratten, M., Mahe, A. & Zimmerman, P.-A. Baseline evaluation of the World Health Organization (WHO) infection prevention and control (IPC) core components in Pacific Island Countries and Territories (PICTs). Antimicrob. Resist. Infect. control13, 108 (2024). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 100.Caekebeke, N. et al. Comparing farm biosecurity and antimicrobial use in high-antimicrobial-consuming broiler and pig farms in the Belgian-Dutch border region. Front. Vet. Sci.7, 558455 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 101.Ardakani, Z. et al. Evaluating the contribution of antimicrobial use in farmed animals to global antimicrobial resistance in humans. One Health17, 100600 (2023). [DOI] [PMC free article] [PubMed]
- 102.Chiang, C.-H. et al. Healthcare-associated infections in intensive care units in Taiwan, South Korea, and Japan: recent trends based on national surveillance reports. Antimicrob. Resist. Infect. Control7, 129 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 103.Funiciello, E. et al. Identifying AWaRe indicators for appropriate antibiotic use: a narrative review. J. Antimicrob. Chemother.79, 3063–3077 (2024). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 104.Takaya, S. et al. Surveillance systems for healthcare-associated infection in high and upper-middle income countries: a scoping review. J. Infect. Chemother.26, 429–437 (2020). [DOI] [PubMed] [Google Scholar]
- 105.Carmo, L. P. et al. Veterinary expert opinion on potential drivers and opportunities for changing antimicrobial usage practices in livestock in Denmark, Portugal, and Switzerland. Front. Vet. Sci.5, 29 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 106.United Nations Department of Economic and Social Affairs. Global indicator framework for the Sustainable Development Goals and targets of the 2030 Agenda for Sustainable Development (United Nations, 2024).
- 107.European Centre for Disease Prevention and Control et al. Point prevalence survey of healthcare-associated infections and antimicrobial use in European long-term care facilities (European Centre for Disease Prevention and Control, 2014).
- 108.World Health Organization. Assessment tool of the minimum requirements for infection prevention and control programmes at the national level (World Health Organization, 2021).
- 109.Vivideconomics. The costs and risks of AMR water pollution (Vivideconomics, 2020).
- 110.World Health Organization & United Nations International Children’s Emergency Fund. WHO/UNICEF Joint Monitoring Programme for Water Supply, Sanitation and Hygiene (JMP) (World Health Organization, 2023).
- 111.World Health Organization. Worldwide country situation analysis: response to antimicrobial resistance (World Health Organization, 2015).
- 112.World Health Organization. Monitoring framework for the WHO Strategic and operational priorities to address drug-resistant bacterial infections in the human health sector, 2025–2035 (World Health Organization, 2024).
- 113.Mendelsohn, E. et al. Global patterns and correlates in the emergence of antimicrobial resistance in humans. Proc. Biol. Sci.290, 20231085 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 114.Zavaleta, E. et al. Antibiotic consumption in primary care in Costa Rica and Italy: a retrospective cross-country analysis. Cureus15, e41414 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 115.Collignon, P., Athukorala, P.-C., Senanayake, S. & Khan, F. Antimicrobial resistance: the major contribution of poor governance and corruption to this growing problem. PloS ONE10, e0116746 (2015). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 116.Holloway, K. A., Rosella, L. & Henry, D. The impact of WHO essential medicines policies on inappropriate use of antibiotics. PloS ONE11, e0152020 (2016). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 117.Naing, S., van Wijk, M., Vila, J. & Balleste-Delpierre, C. Understanding antimicrobial resistance from the perspective of public policy: a multinational knowledge, attitude, and perception survey to determine global awareness (Antibiotics, 2021). [DOI] [PMC free article] [PubMed]
- 118.Padget, M. et al. A community survey of antibiotic consumption among children in Madagascar and Senegal: the importance of healthcare access and care quality. J. Antimicrob. Chemother.72, 564–573 (2017). [DOI] [PubMed] [Google Scholar]
- 119.Caipo, M., Gatica, M., de, L. A., Rojas, H. & Del Barrio, L. A qualitative approach for a situation analysis of AMR risks in the food animal production sector. Front. Vet. Sci.10, 1045276 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 120.Fink, G., D’Acremont, V., Leslie, H. H. & Cohen, J. Antibiotic exposure among children younger than 5 years in low-income and middle-income countries: a cross-sectional study of nationally representative facility-based and household-based surveys. Lancet Infect. Dis.20, 179–187 (2020). [DOI] [PubMed] [Google Scholar]
- 121.van Bijnen, E. M. E. et al. Antibiotic exposure and other risk factors for antimicrobial resistance in nasal commensal staphylococcus aureus: an ecological study in 8 European Countries. PloS One10, e0135094 (2015). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 122.Andersson, K., van Driel, M., Hedin, K., Hollingworth, S. & Merlo, G. Antibiotic use in Australian and Swedish primary care: a cross-country comparison. Scand. J. Prim. Health Care40, 95–103 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 123.Robertson, J. et al. Antimicrobial medicines consumption in eastern europeand central asia - an updated cross-national study and assessment of quantitative metrics for policy action. Front. Pharmacol.9, 1156 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 124.Ceccarelli, D. et al. Antimicrobial resistance prevalence in commensal Escherichia coli from broilers, fattening turkeys, fattening pigs and veal calves in European countries and association with antimicrobial usage at country level. J. Med. Microbiol.69, 537EP–547EP (2020). [DOI] [PubMed] [Google Scholar]
- 125.Gladstone, B. P. et al. Antimicrobial resistance rates in gram-positive bacteria do not drive glycopeptides use. PloS ONE12, e0181358 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 126.Tomic, T. et al. Antimicrobial utilization and resistance in Pseudomonas aeruginosa using segmented regression analysis: a comparative study between Serbia and eight European Countries. Int. J. Clin. Pharm.45, 989–998 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 127.Horvat, O. et al. Are there striking differences in outpatient use of antibiotics between South Backa District, Serbia, and Some Scandinavian Countries? Front. Public Health6, 91 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 128.Joosten, P. et al. Assigning Defined Daily/Course Doses for Antimicrobials in Turkeys to Enable a Cross-Country Quantification and Comparison of Antimicrobial Use (Antibiotics, 2021). [DOI] [PMC free article] [PubMed]
- 129.Suzuki, H. G., Dewez, J. E., Nijman, R. G. & Yeung, S. Clinical practice guidelines for acute otitis media in children: a systematic review and appraisal of European national guidelines. BMJ Open10, e035343 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 130.Scholle, O., Rasmussen, L., Reilev, M., Viebrock, J. & Haug, U. Comparative analysis of outpatient antibiotic prescribing in early life: a population-based study across birth cohorts in Denmark and Germany. Infect. Dis. Ther.13, 299–312 (2024). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 131.Carmo, L. P. et al. Comparison of antimicrobial consumption patterns in the swiss and danish cattle and swine production (2007-2013). Front. Vet. Sci.4, 26 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 132.Chantziaras, I., Boyen, F., Callens, B. & Dewulf, J. Correlation between veterinary antimicrobial use and antimicrobial resistance in food-producing animals: a report on seven countries. J. Antimicrob. Chemother.69, 827–834 (2014). [DOI] [PubMed] [Google Scholar]
- 133.van Dorst, P. W. M. et al. Cost-effectiveness of test-and-treat strategies to reduce the antibiotic prescription rate for acute febrile illness in primary healthcare clinics in Africa. Appl. Health Econ. Health policy22, 701–715 (2024). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 134.Hesstvedt, L. et al. Differences in epidemiology of candidaemia in the Nordic countries - what is to blame? Mycoses60, 11–19 (2017). [DOI] [PubMed] [Google Scholar]
- 135.Babu Rajendran, N. et al. EPI-Net One Health reporting guideline for antimicrobial consumption and resistance surveillance data: a Delphi approach. Lancet Reg. Health Eur.26, 100563 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 136.Jackson, C. et al. Estimating global trends in total and childhood antibiotic consumption, 2011-2015. BMJ Glob. Health4, e001241 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 137.Van Boeckel, T. P. et al. Global antibiotic consumption 2000 to 2010: an analysis of national pharmaceutical sales data. Lancet Infect. Dis.14, 742–750 (2014). [DOI] [PubMed] [Google Scholar]
- 138.Zhou, N. et al. Global antimicrobial resistance: a system-wide comprehensive investigation using the Global One Health Index. Infect. Dis. Poverty11, 92 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 139.Schar, D., Klein, E. Y., Laxminarayan, R., Gilbert, M. & Van Boeckel, T. P. Global trends in antimicrobial use in aquaculture. Sci. Rep.10, 21878 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 140.Mulchandani, R., Wang, Y., Gilbert, M. & Van Boeckel, T. P. Global trends in antimicrobial use in food-producing animals: 2020 to 2030. PLOS Glob. Public Health3, e0001305 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 141.Kachalov, V. N. et al. Identifying the drivers of multidrug-resistant Klebsiella pneumoniae at a European level. PLoS Comput. Biol.17, e1008446 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 142.Wang, S., Pulcini, C., Rabaud, C., Boivin, J.-M. & Birge, J. Inventory of antibiotic stewardship programs in general practice in France and abroad. Med. Mal. Infect.45, 111–123 (2015). [DOI] [PubMed] [Google Scholar]
- 143.Rubinic, I. et al. Measuring hospital antibiotic consumption in EU/EEA countries: comparison of different metrics, 2017 to 2021. Euro Surveill.29, 2300433 (2024). [DOI] [PMC free article] [PubMed]
- 144.Pontinen, A. K. et al. Modulation of multidrug-resistant clone success in Escherichia coli populations: a longitudinal, multi-country, genomic and antibiotic usage cohort study. Lancet Microbe5, e142–e150 (2024). [DOI] [PubMed] [Google Scholar]
- 145.McDonnell, L. et al. National disparities in the relationship between antimicrobial resistance and antimicrobial consumption in Europe: an observational study in 29 countries. J. Antimicrob. Chemother.72, 3199–3204 (2017). [DOI] [PubMed] [Google Scholar]
- 146.Thompson, W. et al. Patterns of dental antibiotic prescribing in 2017: Australia, England, United States, and British Columbia (Canada). Infect. Control Hosp. Epidemiol.43, 191–198 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 147.Kerr, F. et al. Practical Pharmacist-Led Interventions to Improve Antimicrobial Stewardship in Ghana, Tanzania, Uganda and Zambia (Pharmacy, 2021). [DOI] [PMC free article] [PubMed]
- 148.Cong, W. et al. Prevalence of antibiotic prescribing in COVID-19 patients in China and other low- and middle-income countries during the pandemic (December 2019-March 2021): a systematic review and meta-analysis. J. Antimicrobial Chemother.78, 2787EP–2794EP (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 149.Bijnen, E. et al. Primary care treatment guidelines for skin infections in Europe: congruence with antimicrobial resistance found in commensal Staphylococcus aureus in the community (BMC Family Practice, 2014). [DOI] [PMC free article] [PubMed]
- 150.Joosten, P. et al. Quantitative and qualitative analysis of antimicrobial usage at farm and flock level on 181 broiler farms in nine European countries. J. Antimicrob. Chemother.74, 798–806 (2019). [DOI] [PubMed] [Google Scholar]
- 151.Wieters, I. et al. Reported antibiotic use among patients in the multicenter ANDEMIA infectious diseases surveillance study in sub-saharan Africa. Antimicrob. Resist. Infect. control13, 9 (2024). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 152.Ferrer, P. et al. Sales of macrolides, lincosamides, streptogramins, and amoxicillin/clavulanate in the in- and outpatient setting in 10 European countries, 2007-2010. SpringerPlus4, 612 (2015). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 153.Galia, L. et al. Surveillance of Antifungal Resistance in Candidemia Fails to Inform Antifungal Stewardship in European Countries (Journal of Fungi, 2022). [DOI] [PMC free article] [PubMed]
- 154.Klein, E. Y., Tseng, K. K., Pant, S. & Laxminarayan, R. Tracking global trends in the effectiveness of antibiotic therapy using the Drug Resistance Index. BMJ Glob. Health4, e001315 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 155.Benko, R. et al. Trends in the hospital-sector consumption of the WHO AWaRe Reserve group antibiotics in EU/EEA countries and the United Kingdom, 2010 to 2018 (Eurosurveillance, 2022). [DOI] [PMC free article] [PubMed]
- 156.Hillerton, J. E., Irvine, C. R., Bryan, M. A., Scott, D. & Merchant, S. C. Use of antimicrobials for animals in New Zealand, and in comparison with other countries. N. Z. Vet. J.65, 71–77 (2017). [DOI] [PubMed] [Google Scholar]
- 157.Hsia, Y. et al. Use of the WHO Access, Watch, and Reserve classification to define patterns of hospital antibiotic use (AWaRe): an analysis of paediatric survey data from 56 countries. Lancet Glob. Health7, e861–e871 (2019). [DOI] [PubMed] [Google Scholar]
- 158.Moura P. et al. Users’ perception of the OH-EpiCap evaluation tool based on its application to nine national antimicrobial resistance surveillance systems. medRxiv10.1101/2023.03.15.23287323 (2023). [DOI] [PMC free article] [PubMed]
- 159.Sanchez, M. L. et al. Variability in the community consumption of antibiotics: a problem in Europe, Spain and Asturias. Le. Infez. Med.27, 134–140 (2019). [PubMed] [Google Scholar]
- 160.Hagedoorn, N. N. et al. Variation in antibiotic prescription rates in febrile children presenting to emergency departments across Europe (MOFICHE): a multicentre observational study. PLoS Med.17, e1003208 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 161.European Food Safety Authority. Antimicrobial consumption and resistance in bacteria from humans and food-producing animals (European Food Safety Authority, 2024). [DOI] [PMC free article] [PubMed]
- 162.European Centre for Disease Prevention and Control. Antimicrobial resistance in the EU/EEA (EARS-Net) - (Annual Epidemiological Report 2023, 2024).
- 163.Anderson, M. et al. Averting the AMR crisis - what are the avenues for policy action for countries in Europe? Eur. Obs. Health Syst. Policies (2019). [PubMed]
- 164.One Health Trust. ResistanceMap. One Health Trusthttps://resistancemap.onehealthtrust.org/ (2025).
- 165.European Centre for Disease Prevention and Control, European Food Safety Authority & European Medicines Agency. Third joint inter-agency report on integrated analysis of consumption of antimicrobial agents and occurrence of antimicrobial resistance in bacteria from humans and food-producing animals in the EU/EEA. EFSA J.19, e06712 (2021). [DOI] [PMC free article] [PubMed]
- 166.World Health Organization. Antimicrobial stewardship programmes in health-care facilities in low- and middle-income countries: a WHO practical toolkit. World Health Organization. https://www.who.int/publications/i/item/9789241515481 (2019). [DOI] [PMC free article] [PubMed]
- 167.Anderson, M., Panteli, D. & Mossialos, E. How can the EU support sustainable innovation and access to effective antibiotics? Policy Brief, No. 51https://www.ncbi.nlm.nih.gov/books/NBK594073/ (2023). [PubMed]
- 168.Sultanate of Oman Ministry of Health & Sultanate of Oman Ministry of Agriculture, Fisheries Wealth and Water Resources. Report of the Third High-Level Ministerial Conference on Antimicrobial Resistance (2022).
- 169.Eurostat. Consumption of antibiotics in the community and hospital sectors - defined daily doses (DDD) per day. Eurostat Database (sdg_03_70)https://ec.europa.eu/eurostat/databrowser/view/sdg_03_70/default/table (2025).
- 170.European Medicines Agency Science Medicines Health. Guideline on the reporting of antimicrobial sales and use in animals at the EU level – denominators and indicators. EMA/CVMP/882931/2022 (2023).
- 171.Robertson, J. et al. Antimicrobial medicines consumption in Eastern Europe and Central Asia – an updated cross-national study and assessment of quantitative metrics for policy action. Front. Pharmacol.9, 1156 (2019). [DOI] [PMC free article] [PubMed]
- 172.Farrell, S. et al. A multinational survey of companion animal veterinary clinicians: How can antimicrobial stewardship guidelines be optimised for the target stakeholder? Vet. J.303, 106045 (2024). [DOI] [PubMed]
- 173.OOgunnigbo, O. et al. Exploring the antimicrobial stewardship educational needs of healthcare students and the potential of an antimicrobial prescribing app as an educational tool in selected African countries. Antibiotics11, 832 (2022). [DOI] [PMC free article] [PubMed]
- 174.Bedekelabou, A. P., Oyetola, D. W., Coulibaly, Z. L., Akinsola, O. & Bada-Alambedji, R. First assessment of the knowledge, attitudes, and practices of health actors in Togo and Ivory Coast in regard to antibiotic resistance. Int. J. One Health8, 108–123 (2022). [Google Scholar]
- 175.Dyar, O. J., Lund, M., Lindsjo, C., Stalsby Lundborg, C. & Pulcini, C. Preparedness to prescribe antibiotics responsibly: a comparison between final year medical students in France and Sweden. Eur. J. Clin. Microbiol. Infect. Dis.38, 711–717 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 176.Serra-Burriel, M., Campillo-Artero, C., Agodi, A., Barchitta, M. & Lopez-Casasnovas, G. Association between antibiotic resistance in intensive care unit (ICU)-acquired infections and excess resource utilization: evidence from Spain, Italy, and Portugal. Infect. Control Hosp. Epidemiol.43, 1360–1367 (2022). [DOI] [PubMed] [Google Scholar]
- 177.Carrara, E. et al. Clinical management of severe infections caused by carbapenem-resistant gram-negative bacteria: a worldwide cross-sectional survey addressing the use of antibiotic combinations. Clin. Microbiol. Infect.28, 66–72 (2022). [DOI] [PubMed] [Google Scholar]
- 178.Balasubramanian, R., Van Boeckel, T. P., Carmeli, Y., Cosgrove, S. & Laxminarayan, R. Global incidence in hospital-associated infections resistant to antibiotics: an analysis of point prevalence surveys from 99 countries. PLoS Med.20, e1004178 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 179.Allel, K. et al. The impact of inpatient bloodstream infections caused by antibiotic-resistant bacteria in low- and middle-income countries: a systematic review and meta-analysis. PLoS Med.20, e1004199 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 180.Li, G. et al. Towards understanding global patterns of antimicrobial use and resistance in neonatal sepsis: insights from the NeoAMR network. Arch. Dis. Child.105, 26–31 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 181.Monedero-Recuero, I., Gegia, M., Wares, D. F., Chadha, S. S. & Mirzayev, F. Situational analysis of 10 countries with a high burden of drug-resistant tuberculosis 2 years post-UNHLM declaration: progress and setbacks in a changing landscape. Int. J. Infect. Dis.108, 557–567 (2021). [DOI] [PubMed] [Google Scholar]
- 182.Tebano, G. et al. Essential and forgotten antibiotics: an inventory in low- and middle-income countries. Int. J. Antimicrob. Agents54, 273–282 (2019). [DOI] [PubMed] [Google Scholar]
- 183.Sweileh, W. M. Global research publications on irrational use of antimicrobials: call for more research to contain antimicrobial resistance. Global. Health17, 94 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 184.Outterson, K., Orubu, E. S. F., Rex, J., Ardal, C. & Zaman, M. H. Patient access in 14 high-income countries to new antibacterials approved by the US Food and Drug Administration, European medicines agency, Japanese pharmaceuticals and medical devices agency, or health Canada, 2010-2020. Clin. Infect. Dis.74, 1183–1190 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 185.Stedt, J. et al. Antibiotic resistance patterns in Escherichia coli from gulls in nine European countries. Infect. Ecol. Epidemiol.4, 23203 (2014). [DOI] [PMC free article] [PubMed]
- 186.Yang, D. et al. Antimicrobial resistance genes aph(3’)-III, erm(B), sul2 and tet(W) abundance in animal faeces, meat, production environments and human faeces in Europe. J. Antimicrob. Chemother.77, 1883–1893 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 187.Waterlow, N. R., Cooper, B. S., Robotham, J. V. & Knight, G. M. Antimicrobial resistance prevalence in bloodstream infection in 29 European countries by age and sex: an observational study. PLoS Med.21, e1004301 (2024). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 188.Kariuki, S., Kering, K., Wairimu, C., Onsare, R. & Mbae, C. Antimicrobial resistance rates and surveillance in sub-Saharan Africa: where are we now? Infect. Drug Resist.15, 3589–3609 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 189.Veloo, A. C. M. et al. Antimicrobial susceptibility profiles of anaerobic bacteria, isolated from human clinical specimens, within different European and surrounding countries. A joint ESGAI study. Anaerobe61, 102111 (2020). [DOI] [PubMed] [Google Scholar]
- 190.Holm, M. et al. Capturing data on antimicrobial resistance patterns and trends in use in regions of Asia (CAPTURA). Clin. Infect. Dis.77, S500–S506 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 191.Dossouvi, K. M. & Ametepe, A. S. Carbapenem resistance in animal-environment-food from africa: a systematic review, recommendations and perspectives. Infect. Drug Resist.17, 1699–1728 (2024). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 192.Wang, M. et al. Clinical outcomes and bacterial characteristics of carbapenem-resistant Klebsiella pneumoniae complex among patients from different global regions (CRACKLE-2): a prospective, multicentre, cohort study. Lancet Infect. Dis.22, 401–412 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 193.Mizuno, S. et al. Comparison of national strategies to reduce meticillin-resistant Staphylococcus aureus infections in Japan and England. J. Hosp. Infect.100, 280–298 (2018). [DOI] [PubMed] [Google Scholar]
- 194.Rahbe, E., Watier, L., Guillemot, D., Glaser, P. & Opatowski, L. Determinants of worldwide antibiotic resistance dynamics across drug-bacterium pairs: a multivariable spatial-temporal analysis using ATLAS. Lancet Planet. Health7, e547–e557 (2023). [DOI] [PubMed] [Google Scholar]
- 195.Sebastian, S. et al. Different microbial and resistance patterns in primary total knee arthroplasty infections - a report on 283 patients from Lithuania and Sweden. BMC Musculoskelet. Disord.22, 800 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 196.Kenyon, C. R., De Baetselier, I. & Crucitti, T. Does gonorrhoea screening intensity play a role in the early selection of antimicrobial resistance in men who have sex with men (MSM)? a comparative study of Belgium and the United Kingdom. F1000Research7, 569 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 197.Poudyal, N. et al. Effective stakeholder engagement for collation, analysis and expansion of antimicrobial resistance (AMR) data: a CAPTURA experience. Clin. Infect. Dis.77, S519–S527 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 198.GRAM Typhoid Collaborators. Estimating the subnational prevalence of antimicrobial resistant Salmonella enterica serovars Typhi and Paratyphi A infections in 75 endemic countries, 1990–2019: a modelling study. Lancet. Glob. Health12, e406–e418 (2024). [DOI] [PMC free article] [PubMed]
- 199.De Jong, A. et al. European-wide antimicrobial resistance monitoring in commensal Escherichia coli isolated from healthy food animals between 2004 and 2018. J. Antimicrob. Chemother.77, 3301–3311 (2022). [DOI] [PubMed] [Google Scholar]
- 200.Handley, B. L. et al. Evaluating the yaws diagnostic gap: a survey to determine the capacity of and barriers to improving diagnostics in all yaws-endemic countries. medRxiv10.1101/2022.05.30.22275669 (2022).
- 201.Guzman-Blanco, M., Labarca, J. A., Villegas, M. V. & Gotuzzo, E. Extended spectrum beta-lactamase producers among nosocomial Enterobacteriaceae in Latin America. Braz. J. Infect. Dis.18, 421–433 (2014). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 202.Freeman, J. et al. Five-year Pan-European, longitudinal surveillance of Clostridium difficile ribotype prevalence and antimicrobial resistance: the extended ClosER study. Eur. J. Clin. Microbiol. Infect. Dis.39, 169–177 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 203.Kakooza, F. et al. Genomic surveillance and antimicrobial resistance determinants in Neisseria gonorrhoeae isolates from Uganda, Malawi and South Africa, 2015-20. J. Antimicrob. Chemother.78, 1982–1991 (2023). [DOI] [PubMed] [Google Scholar]
- 204.Tornimbene, B. et al. Global antimicrobial resistance and use surveillance system on the African continent: early implementation 2017–2019. Afr. J. Lab. Med.11, 1594 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 205.GBD 2021 Antimicrobial Resistance Collaborators. Global burden of bacterial antimicrobial resistance 1990–2021: a systematic analysis with forecasts to 2050. Lancet404, 1199–1226 (2024). [DOI] [PMC free article] [PubMed]
- 206.Carey, M. E. et al. Global diversity and antimicrobial resistance of typhoid fever pathogens: insights from a meta-analysis of 13,000 Salmonella Typhi genomes. eLife12, e85861 (2023). [DOI] [PMC free article] [PubMed]
- 207.Hou, J. et al. Global trend of antimicrobial resistance in common bacterial pathogens in response to antibiotic consumption. J. Hazard. Mater.442, 130042 (2023). [DOI] [PubMed] [Google Scholar]
- 208.Karlowsky, J. A. et al. In vitro activity of ceftazidime-avibactam against clinical isolates of Enterobacteriaceae and Pseudomonas aeruginosa collected in Asia-Pacific countries: results from the INFORM global surveillance progr. Antimicrob. Agents Chemother.62, e02569 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 209.Karlowsky, J. A. et al. In vitro activity of ceftazidime-avibactam against clinical isolates of Enterobacteriaceae and Pseudomonas aeruginosa collected in Latin American countries: results from the INFORM global surveillance pro. Antimicrob. Agents Chemother.63, e01814 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 210.Karlowsky, J. A. et al. In vitro activity of imipenem/relebactam against non-MorganellaceaeEnterobacterales and Pseudomonas aeruginosa in Latin America: SMART 2018–2020. Braz. J. Infect. Dis.27, 102766 (2023). [DOI] [PMC free article] [PubMed]
- 211.Karlowsky, J. A. et al. In vitro activity of imipenem/relebactam against piperacillin/tazobactam-resistant and meropenem-resistant non-Morganellaceae Enterobacterales and Pseudomonas aeruginosa collected from patients with lower respiratory tract infections: SMART 2018–2020. JAC-Antimicrob. Resist.5, dlad059 (2023). [DOI] [PMC free article] [PubMed]
- 212.Rutz, J. et al. Individual and institutional predisposing factors of MRSA surgical site infection and outcomes—a retrospective case-control-study in 14 European high-volume surgical centres. JAC-Antimicrob. Resist.6, dlad142 (2024). [DOI] [PMC free article] [PubMed]
- 213.Kinross, P. et al. Livestock-associated meticillin-resistant Staphylococcus aureus (MRSA) among human MRSA isolates, European Union/European Economic Area countries, 2013. Eurosurveillance22, 00696 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 214.Babu Rajendran, N. et al. Mandatory surveillance and outbreaks reporting of the WHO priority pathogens for research & discovery of new antibiotics in European countries. Clin. Microbiol. Infect.26, 943.e1–943.e6 (2020). [DOI] [PubMed] [Google Scholar]
- 215.Baede, V. O. et al. Markers of epidemiological success of methicillin-resistant Staphylococcus aureus isolates in European populations. Clin. Microbiol. Infect.29, 1166–1173 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 216.Beeton, M. L. et al. Mycoplasma pneumoniae infections, 11 countries in Europe and Israel, 2011 to 2016. Eurosurveillance25, 1900112 (2020). [DOI] [PMC free article] [PubMed]
- 217.Dyson, Z. A. et al. Pathogen diversity and antimicrobial resistance transmission of Salmonella enterica serovars Typhi and Paratyphi A in Bangladesh, Nepal, and Malawi: a genomic epidemiological study. Lancet Microbe5, 100841 (2024). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 218.Barkume, C. et al. Phase I of the surveillance for enteric fever in Asia Project (SEAP): an overview and lessons learned. J. Infect. Dis.218, S188–S194 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 219.Tosas Auguet, O. et al. Population-level faecal metagenomic profiling as a tool to predict antimicrobial resistance in Enterobacterales isolates causing invasive infections: an exploratory study across Cambodia, Kenya, and the UK. EClinicalMedicine36, 100914 (2021). [DOI] [PMC free article] [PubMed]
- 220.Stefaniak, K., Kiedrzynski, M., Korzeniewska, E., Kiedrzynska, E. & Harnisz, M. Preliminary insights on carbapenem resistance in Enterobacteriaceae in high-income and low-/middle-income countries. Sci. Total Environ.957, 177593 (2024). [DOI] [PubMed] [Google Scholar]
- 221.Savoldi, A., Carrara, E., Graham, D. Y., Conti, M. & Tacconelli, E. Prevalence of antibiotic resistance in Helicobacter pylori: a systematic review and meta-analysis in World Health Organization regions. Gastroenterology155, 1372–e17 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 222.Argimon, S. et al. Rapid genomic characterization and global surveillance of Klebsiella using pathogenwatch. Clin. Infect. Dis.73, S325–S335 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 223.Criscuolo, N. G., Pires, J., Zhao, C. & Van Boeckel, T. P. resistancebank.org, an open-access repository for surveys of antimicrobial resistance in animals. Sci. Data8, 189 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 224.Torumkuney, D. et al. Results from the survey of antibiotic resistance (SOAR) 2014-16 in Bulgaria, Romania, Serbia and Croatia. J. Antimicrob. Chemother.73, v2–v13 (2018). [DOI] [PubMed] [Google Scholar]
- 225.Malik, H. et al. Review of antibiotic use and resistance in food animal production in WHO South-East Asia Region. J. Infect. Public Health16, 172–182 (2023). [DOI] [PubMed] [Google Scholar]
- 226.Yang, D. et al. Risk factors for the abundance of antimicrobial resistance genes aph(3’)-III, erm(B), sul2 and tet(W) in pig and broiler faeces in nine European countries. J. Antimicrob. Chemother.77, 969–978 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 227.Jarlier, V. et al. Strong correlation between the rates of intrinsically antibiotic-resistant species and the rates of acquired resistance in Gram-negative species causing bacteraemia, EU/EEA, 2016. Eurosurveillance24, 1800538 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 228.Huijbers, P. M. C., Larsson, D. G. J. & Flach, C.-F. Surveillance of antibiotic resistant Escherichia coli in human populations through urban wastewater in ten European countries. Environ. Pollut.261, 114200 (2020). [DOI] [PubMed]
- 229.Piovani, D., Figlioli, G., Nikolopoulos, G. K. & Bonovas, S. The global burden of enteric fever, 2017–2021: a systematic analysis from the global burden of disease study 2021. EClinicalMedicine77, 102883 (2024). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 230.Odoj, K. et al. Tracking candidemia trends and antifungal resistance patterns across Europe: an in-depth analysis of surveillance systems and surveillance studies. J. Fungi10, 685 (2024). [DOI] [PMC free article] [PubMed]
- 231.Al-Saleh, A., Shahid, M., Farid, E. & Bindayna, K. Trends in methicillin-resistant Staphylococcus aureus in the Gulf Cooperation Council countries: antibiotic resistance, virulence factors and emerging strains. East. Mediterr. Health J.28, 434–443 (2022). [DOI] [PubMed] [Google Scholar]
- 232.Rossolini, G. M., Bochenska, M., Fumagalli, L. & Dowzicky, M. Trends of major antimicrobial resistance phenotypes in enterobacterales and gram-negative non-fermenters from ATLAS and EARS-net surveillance systems: Italian vs. European and global data, 2008-2018. Diagn. Microbiol. Infect. Dis.101, 115512 (2021). [DOI] [PubMed] [Google Scholar]
- 233.Eyre, D. W. et al. WGS to predict antibiotic MICs for Neisseria gonorrhoeae. J. Antimicrob. Chemother.72, 1937–1947 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 234.Unemo, M. et al. WHO global antimicrobial resistance surveillance for Neisseria gonorrhoeae 2017-18: a retrospective observational study. Lancet Microbe2, e627–e636 (2021). [DOI] [PubMed] [Google Scholar]
- 235.Rahbe E., Watier L., Guillemot D., Glaser P., & Opatowski L. Worldwide antibiotic resistance dynamics: how different is it from one drug-bug pair to another? medRxiv10.1101/2022.02.09.22270726 (2022).
- 236.Maugeri, A., Barchitta, M., Magnano San Lio, R. & Agodi, A. Socioeconomic and governance factors disentangle the relationship between temperature and antimicrobial resistance: a 10-year ecological analysis of European countries. Antibiotics12, 861 (2023). [DOI] [PMC free article] [PubMed]
- 237.Petrovski, K. R. et al. Susceptibility to antimicrobials of mastitis-causing Staphylococcus aureus, Streptococcus uberis and Str. dysgalactiae from New Zealand and the USA as assessed by the disk diffusion test. Aust. Vet. J.93, 227–233 (2015). [DOI] [PubMed] [Google Scholar]
- 238.George, C. R. R. et al. Systematic review and survey of Neisseria gonorrhoeae ceftriaxone and azithromycin susceptibility data in the Asia Pacific, 2011 to 2016. PloS ONE14, e0213312 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 239.Himanshu et al. Systematic surveillance and meta-analysis of antimicrobial resistance and food sources from China and the USA. Antibiotics11, 1471 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 240.Arieti, F. et al. The antimicrobial resistance travel tool, an interactive evidence-based educational tool to limit antimicrobial resistance spread. J. Travel Med.29, taac045 (2022). [DOI] [PMC free article] [PubMed]
- 241.Anonymous The burden of bacterial antimicrobial resistance in the WHO African region in 2019: a cross-country systematic analysis. Lancet Glob. health12, e201–e216 (2024). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 242.Aguilar, G. R. et al. The burden of antimicrobial resistance in the Americas in 2019: a cross-country systematic analysis. Lancet Reg. Health Am.25, 100561 (2023). [DOI] [PMC free article] [PubMed]
- 243.Cole, M. J. et al. The European gonococcal antimicrobial surveillance programme (Euro-GASP) appropriately reflects the antimicrobial resistance situation for Neisseria gonorrhoeae in the European Union/European Economic Area. BMC Infect. Dis.19, 1040 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 244.World Health Organization. Antimicrobial resistance: global report on surveillance (WHO, 2014).
- 245.Food and Agriculture Organization of the United Nations. Annex to the GLG Report: Towards specific commitments and action in response to antimicrobial resistance (FAO, 2024).
- 246.Anderson, M. et al. The Socioeconomic Drivers and Impacts of Antimicrobial Resistance(AMR):implications for Policy and Research. https://eurohealthobservatory.who.int/publications/i/the-socioeconomic-drivers-and-impacts-of-antimicrobial-resistance-(amr)-implications-for-policy-and-research (2024). [PubMed]
- 247.Anderson, M., Kluge, H. H. P., Lo Fo Wong, D., Butler, R. & Mossialos, E. Promoting sustainable national action to tackle antimicrobial resistance: a proposal to develop an antimicrobial resistance accountability index. Lancet Microbe5, 100997 (2024). [DOI] [PubMed] [Google Scholar]
- 248.Anderson M., Mossialos E., Shafaque U., Ranganathan S. A systematic review and critical appraisal of indicators to comparatively measure national performance in addressing antimicrobial resistance (AMR). PROSPERO 2024 CRD42024625477. https://www.crd.york.ac.uk/PROSPERO/view/CRD42024625477 (2024).
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Data Availability Statement
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