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Meta-Analysis
. 2023 Mar;29(3):302-309.
doi: 10.1016/j.cmi.2022.12.006. Epub 2022 Dec 9.

Antibiotic resistance associated with the COVID-19 pandemic: a systematic review and meta-analysis

Affiliations
Meta-Analysis

Antibiotic resistance associated with the COVID-19 pandemic: a systematic review and meta-analysis

Bradley J Langford et al. Clin Microbiol Infect. 2023 Mar.

Abstract

Background: COVID-19 and antimicrobial resistance (AMR) are two intersecting global public health crises.

Objective: We aimed to describe the impact of the COVID-19 pandemic on AMR across health care settings.

Data source: A search was conducted in December 2021 in WHO COVID-19 Research Database with forward citation searching up to June 2022.

Study eligibility: Studies evaluating the impact of COVID-19 on AMR in any population were included and influencing factors were extracted. Reporting of enhanced infection prevention and control and/or antimicrobial stewardship programs was noted.

Methods: Pooling was done separately for Gram-negative and Gram-positive organisms. Random-effects meta-analysis was performed.

Results: Of 6036 studies screened, 28 were included and 23 provided sufficient data for meta-analysis. The majority of studies focused on hospital settings (n = 25, 89%). The COVID-19 pandemic was not associated with a change in the incidence density (incidence rate ratio 0.99, 95% CI: 0.67-1.47) or proportion (risk ratio 0.91, 95% CI: 0.55-1.49) of methicillin-resistant Staphylococcus aureus or vancomycin-resistant enterococci cases. A non-statistically significant increase was noted for resistant Gram-negative organisms (i.e. extended-spectrum beta-lactamase, carbapenem-resistant Enterobacterales, carbapenem or multi-drug resistant or carbapenem-resistant Pseudomonas aeruginosa or Acinetobacter baumannii, incidence rate ratio 1.64, 95% CI: 0.92-2.92; risk ratio 1.08, 95% CI: 0.91-1.29). The absence of reported enhanced infection prevention and control and/or antimicrobial stewardship programs initiatives was associated with an increase in gram-negative AMR (risk ratio 1.11, 95% CI: 1.03-1.20). However, a test for subgroup differences showed no statistically significant difference between the presence and absence of these initiatives (p 0.40).

Conclusion: The COVID-19 pandemic may have hastened the emergence and transmission of AMR, particularly for Gram-negative organisms in hospital settings. But there is considerable heterogeneity in both the AMR metrics used and the rate of resistance reported across studies. These findings reinforce the need for strengthened infection prevention, antimicrobial stewardship, and AMR surveillance in the context of the COVID-19 pandemic.

Keywords: Antibiotic resistance; Antimicrobial resistance; Antimicrobial stewardship; COVID-19; Infection; Prevention and control.

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Figures

Image 1
Graphical abstract
Fig. 1
Fig. 1
Preferred Reporting Items for Systematic Reviews and Meta-Analyses flow diagram.
Fig. 2
Fig. 2
COVID-19 pandemic and Gram-positive antimicrobial resistance incidence rate ratio.a aAll included studies reported infection prevention and control/antimicrobial stewardship program initiatives.
Fig. 3
Fig. 3
COVID-19 pandemic and Gram-positive antimicrobial resistance risk ratio and reported presence vs. absence of infection prevention and control/antimicrobial stewardship programs.a aRepresents proportions of patients (e.g. visits) or organisms in which antimicrobial resistance was identified.
Fig. 4
Fig. 4
COVID-19 pandemic and Gram-negative antimicrobial resistance incidence rate ratio.a aAll included studies reported infection prevention and control/ASP initiatives.
Fig. 5
Fig. 5
COVID-19 pandemic and Gram-negative antimicrobial resistance risk ratio and reported presence vs. absence of infection prevention and control/antimicrobial stewardship programs.∗ ∗Represents proportions of patients (e.g. visits) or organisms in which antimicrobial resistance was identified.

References

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