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The burden of bacterial antimicrobial resistance in the WHO European region in 2019: a cross-country systematic analysis.

European Antimicrobial Resistance Collaborators (2022) The burden of bacterial antimicrobial resistance in the WHO European region in 2019: a cross-country systematic analysis. Lancet Public Health, 7 (11). e897-e913. ISSN 2468-2667 https://doi.org/10.1016/S2468-2667(22)00225-0
SGUL Authors: Moore, Catrin Elisabeth

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Abstract

BACKGROUND: Antimicrobial resistance (AMR) represents one of the most crucial threats to public health and modern health care. Previous studies have identified challenges with estimating the magnitude of the problem and its downstream effect on human health and mortality. To our knowledge, this study presents the most comprehensive set of regional and country-level estimates of AMR burden in the WHO European region to date. METHODS: We estimated deaths and disability-adjusted life-years attributable to and associated with AMR for 23 bacterial pathogens and 88 pathogen-drug combinations for the WHO European region and its countries in 2019. Our methodological approach consisted of five broad components: the number of deaths in which infection had a role, the proportion of infectious deaths attributable to a given infectious syndrome, the proportion of infectious syndrome deaths attributable to a given pathogen, the percentage of a given pathogen resistant to an antimicrobial drug of interest, and the excess risk of mortality (or duration of an infection) associated with this resistance. These components were then used to estimate the disease burden by using two counterfactual scenarios: deaths attributable to AMR (considering an alternative scenario where infections with resistant pathogens are replaced with susceptible ones) and deaths associated with AMR (considering an alternative scenario where drug-resistant infections would not occur at all). Data were solicited from a wide array of international stakeholders; these included research hospitals, surveillance networks, and infection databases maintained by private laboratories and medical technology companies. We generated 95% uncertainty intervals (UIs) for final estimates as the 25th and 975th ordered values across 1000 posterior draws, and models were cross-validated for out-of-sample predictive validity. FINDINGS: We estimated 541 000 deaths (95% UI 370 000-763 000) associated with bacterial AMR and 133 000 deaths (90 100-188 000) attributable to bacterial AMR in the whole WHO European region in 2019. The largest fatal burden of AMR in the region came from bloodstream infections, with 195 000 deaths (104 000-333 000) associated with resistance, followed by intra-abdominal infections (127 000 deaths [81 900-185 000]) and respiratory infections (120 000 deaths [94 500-154 000]). Seven leading pathogens were responsible for about 457 000 deaths associated with resistance in 53 countries of this region; these pathogens were, in descending order of mortality, Escherichia coli, Staphylococcus aureus, Klebsiella pneumoniae, Pseudomonas aeruginosa, Enterococcus faecium, Streptococcus pneumoniae, and Acinetobacter baumannii. Methicillin-resistant S aureus was shown to be the leading pathogen-drug combination in 27 countries for deaths attributable to AMR, while aminopenicillin-resistant E coli predominated in 47 countries for deaths associated with AMR. INTERPRETATION: The high levels of resistance for several important bacterial pathogens and pathogen-drug combinations, together with the high mortality rates associated with these pathogens, show that AMR is a serious threat to public health in the WHO European region. Our regional and cross-country analyses open the door for strategies that can be tailored to leading pathogen-drug combinations and the available resources in a specific location. These results underscore that the most effective way to tackle AMR in this region will require targeted efforts and investments in conjunction with continuous outcome-based research endeavours. FUNDING: Bill & Melinda Gates Foundation, Wellcome Trust, and Department of Health and Social Care using UK aid funding managed by the Fleming Fund.

Item Type: Article
Additional Information: Copyright © 2022 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license.
Keywords: Humans, Anti-Bacterial Agents, Methicillin-Resistant Staphylococcus aureus, Drug Resistance, Bacterial, Escherichia coli, World Health Organization, European Antimicrobial Resistance Collaborators, Humans, Escherichia coli, Anti-Bacterial Agents, Drug Resistance, Bacterial, World Health Organization, Methicillin-Resistant Staphylococcus aureus
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: Lancet Public Health
ISSN: 2468-2667
Language: eng
Dates:
DateEvent
2 November 2022Published
14 October 2022Published Online
24 August 2022Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
OPP1176062Bill and Melinda Gates Foundationhttp://dx.doi.org/10.13039/100000865
A126042Wellcome TrustUNSPECIFIED
R52354 CN001Department of Health and Social Carehttp://dx.doi.org/10.13039/501100000276
UEFISCDI PN-III-P4-ID-PCCF-2016-0084Romanian National Authority for Scientific Research and InnovationUNSPECIFIED
ID-585-CTR-42-PFE-2021Romanian Ministry of Research Innovation and DigitalizationUNSPECIFIED
CZ.02.2.69/0.0/0.0/18_053/0016952Research, Development and EducationUNSPECIFIED
CEECIND/01768/2021Fundação para a Ciência e a Tecnologiahttp://dx.doi.org/10.13039/501100001871
PN-III-P4-ID-PCCF-2016-0084Romanian National Authority for Scientific Research and InnovationUNSPECIFIED
CEECIND/00394/2017Fundação para a Ciência e a Tecnologiahttp://dx.doi.org/10.13039/501100001871
UID/DTP/04138/2019Fundação para a Ciência e a Tecnologiahttp://dx.doi.org/10.13039/501100001871
CENTRO-04-3559-FSE-000162Fundo Social EuropeuUNSPECIFIED
PubMed ID: 36244350
Web of Science ID: WOS:000928270600008
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/115343
Publisher's version: https://doi.org/10.1016/S2468-2667(22)00225-0

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