Exposure to World Health Organization's AWaRe antibiotics and isolation of multidrug resistant bacteria: a systematic review and meta-analysis.

AWaRe framework Antibiotic exposure Antibiotic stewardship Critical priority pathogens High-priority pathogens Multidrug resistant organisms Resistance selection

Journal

Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases
ISSN: 1469-0691
Titre abrégé: Clin Microbiol Infect
Pays: England
ID NLM: 9516420

Informations de publication

Date de publication:
Sep 2022
Historique:
received: 25 01 2022
revised: 10 03 2022
accepted: 12 03 2022
pubmed: 28 3 2022
medline: 20 9 2022
entrez: 27 3 2022
Statut: ppublish

Résumé

Antibiotic use drives antibiotic resistance. To systematically review the literature and estimate associations between prior exposure to antibiotics across World Health Organization's (WHO) AWaRe categories (Access, Watch, Reserve) and isolation of critical and high-priority multidrug resistant organisms (MDROs) on the WHO priority pathogen list. Embase, Ovid Medline, Scopus, Cochrane Database of Systematic Reviews, Cochrane Central Register of Controlled Trials, and ClinicalTrials.gov (from inception to 20/08/2020). Case-control, cohort, or experimental studies that assessed the risk of infection/colonization with MDROs. Inpatients or outpatients of any age and sex. Prior exposure to antibiotics that could be categorized into the AWaRe framework. Tailored design-specific checklists applied to each included study. For each antibiotic/class, crude odds ratios (ORs) were pooled through random-effects meta-analyses, both overall and by MDRO. Heterogeneity was examined. We identified 349 eligible studies. All were observational, prone to bias due to design and lack of adjustment for confounding, and not primarily designed to compare associations across AWaRe categories. We found statistically significant associations between prior exposure to almost all antibiotics/classes across AWaRe categories and colonization/infection with any MDRO. We observed higher ORs for Watch and Reserve antibiotics than with Access antibiotics. First generation cephalosporins (Access) had the least association with any MDRO colonization/infection (58 studies; OR = 1.2 [95% CI: 1.0-1.4]), whereas strongest associations were estimated for linezolid (Reserve) (22 studies; OR = 2.6 [95% CI: 2.1-3.1]), followed by carbapenems (Watch) (237 studies; OR = 2.3 [95% CI: 2.1-2.5]). There was high heterogeneity for all antibiotic/MDRO associations. Optimising use of Access antibiotics is likely to reduce the selection of MDROs and global antibiotic resistance. Despite data limitations, our study offers a strong rationale for further adoption of AWaRe as an important tool to improve antibiotic use globally.

Sections du résumé

BACKGROUND BACKGROUND
Antibiotic use drives antibiotic resistance.
OBJECTIVES OBJECTIVE
To systematically review the literature and estimate associations between prior exposure to antibiotics across World Health Organization's (WHO) AWaRe categories (Access, Watch, Reserve) and isolation of critical and high-priority multidrug resistant organisms (MDROs) on the WHO priority pathogen list.
DATA SOURCES METHODS
Embase, Ovid Medline, Scopus, Cochrane Database of Systematic Reviews, Cochrane Central Register of Controlled Trials, and ClinicalTrials.gov (from inception to 20/08/2020).
STUDY ELIGIBILITY CRITERIA METHODS
Case-control, cohort, or experimental studies that assessed the risk of infection/colonization with MDROs.
PARTICIPANTS METHODS
Inpatients or outpatients of any age and sex.
INTERVENTIONS METHODS
Prior exposure to antibiotics that could be categorized into the AWaRe framework.
DATA ANALYSIS METHODS
Tailored design-specific checklists applied to each included study. For each antibiotic/class, crude odds ratios (ORs) were pooled through random-effects meta-analyses, both overall and by MDRO. Heterogeneity was examined.
RESULTS RESULTS
We identified 349 eligible studies. All were observational, prone to bias due to design and lack of adjustment for confounding, and not primarily designed to compare associations across AWaRe categories. We found statistically significant associations between prior exposure to almost all antibiotics/classes across AWaRe categories and colonization/infection with any MDRO. We observed higher ORs for Watch and Reserve antibiotics than with Access antibiotics. First generation cephalosporins (Access) had the least association with any MDRO colonization/infection (58 studies; OR = 1.2 [95% CI: 1.0-1.4]), whereas strongest associations were estimated for linezolid (Reserve) (22 studies; OR = 2.6 [95% CI: 2.1-3.1]), followed by carbapenems (Watch) (237 studies; OR = 2.3 [95% CI: 2.1-2.5]). There was high heterogeneity for all antibiotic/MDRO associations.
CONCLUSIONS CONCLUSIONS
Optimising use of Access antibiotics is likely to reduce the selection of MDROs and global antibiotic resistance. Despite data limitations, our study offers a strong rationale for further adoption of AWaRe as an important tool to improve antibiotic use globally.

Identifiants

pubmed: 35339675
pii: S1198-743X(22)00153-7
doi: 10.1016/j.cmi.2022.03.014
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Carbapenems 0
Cephalosporins 0
Electrolytes 0
Linezolid ISQ9I6J12J

Types de publication

Journal Article Meta-Analysis Review Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1193-1202

Subventions

Organisme : World Health Organization
ID : 001
Pays : International

Informations de copyright

Copyright © 2022 The Author(s). Published by Elsevier Ltd.. All rights reserved.

Auteurs

Giorgia Sulis (G)

Department of Epidemiology, Biostatistics and Occupational Health, School of Population and Global Health, McGill University, Montreal, Canada.

Sena Sayood (S)

Division of Infectious Diseases, Washington University School of Medicine in St. Louis, MO, USA.

Shashi Katukoori (S)

Division of Hospital Medicine, University of Alabama Medical School, Birmingham, AL, USA.

Neha Bollam (N)

University of North Carolina, Chapel Hill, NC, USA.

Ige George (I)

Division of Infectious Diseases, Washington University School of Medicine in St. Louis, MO, USA.

Lauren H Yaeger (LH)

Bernard Becker Medical Library, Washington University School of Medicine in St. Louis, MO, USA.

Miguel A Chavez (MA)

Division of Infectious Diseases, Washington University School of Medicine in St. Louis, MO, USA.

Emmanuel Tetteh (E)

Division of Infectious Diseases, Washington University School of Medicine in St. Louis, MO, USA.

Sindhu Yarrabelli (S)

Samraksha Healthcare, Warangal, Telangana, India.

Celine Pulcini (C)

Infectious Diseases Department, Université de Lorraine, CHRU-Nancy and APEMAC, Université de Lorraine, Nancy, France.

Stephan Harbarth (S)

Infection Control Programme, Geneva University Hospitals and Faculty of Medicine, Geneva, Switzerland.

Dominik Mertz (D)

Division of Infectious Diseases, Department of Medicine, McMaster University, Hamilton, Ontario, Canada.

Mike Sharland (M)

Paediatric Infectious Diseases Research Group, Institute of Infection and Immunity, St George's University London, London, UK.

Lorenzo Moja (L)

Secretariat of the Model List of Essential Medicines, Department of Essential Health Products and Standards, World Health Organization, Geneva, Switzerland.

Benedikt Huttner (B)

Secretariat of the Model List of Essential Medicines, Department of Essential Health Products and Standards, World Health Organization, Geneva, Switzerland.

Sumanth Gandra (S)

Division of Infectious Diseases, Washington University School of Medicine in St. Louis, MO, USA. Electronic address: gandras@wustl.edu.

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Classifications MeSH