journal article Open Access Jul 25, 2024

Bayesian estimation of the prevalence of antimicrobial resistance: a mathematical modelling study

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Abstract
Abstract

Background
Estimates of the prevalence of antimicrobial resistance (AMR) underpin effective antimicrobial stewardship, infection prevention and control, and optimal deployment of antimicrobial agents. Typically, the prevalence of AMR is determined from real-world antimicrobial susceptibility data that are time delimited, sparse, and often biased, potentially resulting in harmful and wasteful decision-making. Frequentist methods are resource intensive because they rely on large datasets.


Objectives
To determine whether a Bayesian approach could present a more reliable and more resource-efficient way to estimate population prevalence of AMR than traditional frequentist methods.


Methods
Retrospectively collected, open-source, real-world pseudonymized healthcare data were used to develop a Bayesian approach for estimating the prevalence of AMR by combination with prior AMR information from a contextualized review of literature. Iterative random sampling and cross-validation were used to assess the predictive accuracy and potential resource efficiency of the Bayesian approach compared with a standard frequentist approach.


Results
Bayesian estimation of AMR prevalence made fewer extreme estimation errors than a frequentist estimation approach [n = 74 (6.4%) versus n = 136 (11.8%)] and required fewer observed antimicrobial susceptibility results per pathogen on average [mean = 28.8 (SD = 22.1) versus mean = 34.4 (SD = 30.1)] to avoid any extreme estimation errors in 50 iterations of the cross-validation. The Bayesian approach was maximally effective and efficient for drug–pathogen combinations where the actual prevalence of resistance was not close to 0% or 100%.


Conclusions
Bayesian estimation of the prevalence of AMR could provide a simple, resource-efficient approach to better inform population infection management where uncertainty about AMR prevalence is high.
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References
30
[1]
Naylor "Estimating the burden of antimicrobial resistance: a systematic literature review" Antimicrob Resist Infect Control (2018) 10.1186/s13756-018-0336-y
[2]
Tacconelli "Linking infection control to clinical management of infections to overcome antimicrobial resistance" J Hosp Infect (2021) 10.1016/j.jhin.2021.04.030
[3]
Rempel "Antimicrobial resistance surveillance systems: are potential biases taken into account?" Can J Infect Dis Med Microbiol (2011) 10.1155/2011/276017
[4]
van Leth "Unbiased antimicrobial resistance prevalence estimates through population-based surveillance" Clin Microbiol Infect (2023) 10.1016/j.cmi.2022.05.006
[5]
[6]
Cherny "Bayesian network modeling of patterns of antibiotic cross-resistance by bacterial sample source" Commun Med (Lond) (2023) 10.1038/s43856-023-00289-7
[7]
Roelofs (2019)
[8]
Johnson "MIMIC-IV (version 2.2)" (2023)
[9]
Johnson "MIMIC-IV, a freely accessible electronic health record dataset" Sci Data (2023) 10.1038/s41597-023-02136-9
[10]
PhysioBank, PhysioToolkit, and PhysioNet

Ary L. Goldberger, Luis A. N. Amaral, Leon Glass et al.

Circulation 2000 10.1161/01.cir.101.23.e215
[11]
Jenkins "Trends in antibacterial resistance among Streptococcus pneumoniae isolated in the USA: update from PROTEKT US Years 1–4" Ann Clin Microbiol Antimicrob (2008) 10.1186/1476-0711-7-1
[12]
Diekema "Twenty-year trends in antimicrobial susceptibilities among Staphylococcus aureus from the SENTRY antimicrobial surveillance program" Open Forum Infect Dis (2019) 10.1093/ofid/ofy270
[13]
Mutnick "Geographic variations and trends in antimicrobial resistance among Enterococcus faecalis and Enterococcus faecium in the SENTRY Antimicrobial Surveillance Program (1997–2000)" Diagn Microbiol Infect Dis (2003) 10.1016/s0732-8893(03)00012-9
[14]
Al-Hasan "Antimicrobial resistance trends of Escherichia coli bloodstream isolates: a population-based study, 1998–2007" J Antimicrob Chemother (2009) 10.1093/jac/dkp162
[15]
Dunne "A multicenter analysis of trends in resistance in urinary Enterobacterales isolates from ambulatory patients in the United States: 2011–2020" BMC Infect Dis (2022) 10.1186/s12879-022-07167-y
[16]
Gentry "Trends in susceptibility rates and extended-spectrum β-lactamase production of Klebsiella pneumoniae in bloodstream infections across the United States Veterans Affairs healthcare system" Microb Drug Resist (2015) 10.1089/mdr.2014.0287
[17]
Mathai "Epidemiology and frequency of resistance among pathogens causing urinary tract infections in 1,510 hospitalized patients: a report from the SENTRY Antimicrobial Surveillance Program (North America)" Diagn Microbiol Infect Dis (2001) 10.1016/s0732-8893(01)00254-1
[18]
Sader "Antimicrobial susceptibility of pseudomonas aeruginosa to ceftazidime-avibactam, ceftolozane-tazobactam, piperacillin-tazobactam, and meropenem stratified by U.S. census divisions: results from the 2017 INFORM program" Antimicrob Agents Chemother (2018) 10.1128/aac.01587-18
[19]
Sanchez "Klebsiella pneumoniae antimicrobial drug resistance, United States, 1998–2010" Emerg Infect Dis (2013) 10.3201/eid1901.120310
[20]
Sanchez "Antibiotic resistance among urinary isolates from female outpatients in the United States in 2003 and 2012" Antimicrob Agents Chemother (2016) 10.1128/aac.02897-15
[21]
Begier "Epidemiology of invasive Escherichia coli infection and antibiotic resistance status among patients treated in US hospitals: 2009-2016" Clin Infect Dis (2021) 10.1093/cid/ciab005
[22]
Sader "Antimicrobial susceptibility of Enterobacteriaceae and Pseudomonas aeruginosa isolates from United States medical centers stratified by infection type: results from the international network for optimal resistance monitoring (INFORM) surveillance program, 2015–2016" Diagn Microbiol Infect Dis (2018) 10.1016/j.diagmicrobio.2018.04.012
[23]
Sader "Antimicrobial susceptibility of Gram-negative bacteria from intensive care unit and non-intensive care unit patients from United States hospitals (2018–2020)" Diagn Microbiol Infect Dis (2022) 10.1016/j.diagmicrobio.2021.115557
[24]
Castanheira "Prevalence of carbapenemase genes among carbapenem-nonsusceptible Enterobacterales collected in US hospitals in a five-year period and activity of ceftazidime/avibactam and comparator agents" JAC Antimicrob Resist (2022) 10.1093/jacamr/dlac098
[25]
MacDougall "Hospital and community fluoroquinolone use and resistance in Staphylococcus aureus and Escherichia coli in 17 US hospitals" Clin Infect Dis (2005) 10.1086/432056
[26]
Metcalf "Short-read whole genome sequencing for determination of antimicrobial resistance mechanisms and capsular serotypes of current invasive Streptococcus agalactiae recovered in the USA" Clin Microbiol Infect (2017) 10.1016/j.cmi.2017.02.021
[27]
Critchley "The burden of antimicrobial resistance among urinary tract isolates of Escherichia coli in the United States in 2017" PLoS One (2019) 10.1371/journal.pone.0220265
[28]
Mojica "Population structure, molecular epidemiology, and β-lactamase diversity among Stenotrophomonas maltophilia isolates in the United States" mBio (2019) 10.1128/mbio.00405-19
[29]
EUCAST "New S, I and R definitions" (2019)
[30]
CLSI (2023)
Metrics
2
Citations
30
References
Details
Published
Jul 25, 2024
Vol/Issue
79(9)
Pages
2317-2326
License
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Authors
Funding
Wellcome Trust Award: 226691/Z/22/Z
Cite This Article
Alex Howard, Peter L Green, Anoop Velluva, et al. (2024). Bayesian estimation of the prevalence of antimicrobial resistance: a mathematical modelling study. Journal of Antimicrobial Chemotherapy, 79(9), 2317-2326. https://doi.org/10.1093/jac/dkae230
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