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Antimicrobial susceptibility to last-resort antibiotics in carbapenemase-producing bacteria from Ukrainian patients

  • Nelianne J. Verkaik
  • , the participating laboratories, on behalf of the SWAB Working Group Surveillance of Antimicrobial Resistance
  • Erasmus University Rotterdam
  • National Institute of Public Health and the Environment
  • ADRZ Medisch Centrum
  • Amphia Hospital
  • Amsterdam UMC
  • Certe
  • Diakonessenhuis Utrecht
  • ETZ Elisabeth
  • Haga Ziekenhuis
  • Haaglanden Medisch Centrum
  • IJsselland Ziekenhuis
  • Isala Clinics
  • Jeroen Bosch Ziekenhuis
  • Regional Laboratory of Microbiology Twente Achterhoek
  • Maastricht University
  • North West Hospital Group
  • Radboud University Nijmegen
  • Laboratory of Public Health Haarlem
  • Ziekenhuis St Jansdal
  • Utrecht University
  • University of Groningen

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Since March 2022, an increase was observed in multidrug-resistant microorganisms (MDRO), associated with the hospital transfer of Ukrainian patients. The goal was to collect phenotypic susceptibility data and assess clinical implications. Carbapenemase-producing Enterobacterales (CPE, n = 96), Pseudomonas aeruginosa (CPPA, n = 20), and carbapenem-resistant Acinetobacter baumannii-calcoaceticus (CRAB, n = 6) from Ukrainian patients were obtained from March to December 2022 from the Dutch MDRO surveillance. Antimicrobial susceptibility testing was performed using broth microdilution (BMD) when available, fosfomycin agar dilution, disk diffusion (DD) for cefiderocol, and diverse gradient strips. All isolates were sequenced with Illumina next-generation sequencing. For meropenem, aminoglycosides, ceftazidime-avibactam, ceftolozane-tazobactam, and imipenem-relebactam, susceptibility rates were low (0%-30%), due to the high number of blaNDM-positive isolates (79/122; 65%). For cefiderocol, results depended on reading with or without microcolonies, applying EUCAST or CLSI breakpoints, and whether DD or BMD was used; e.g., for Klebsiella pneumoniae, 30%-97% were susceptible. For colistin, 103/111 (93%) non-intrinsically resistant CPE/CPPA/ CRAB isolates were susceptible. For most CPE, a low minimal inhibitory concentration (MIC) of <0.5 mg/L was measured for tigecycline and ceftazidime-avibactam-aztreonam. For CPPA, cefiderocol tested susceptible in 65%-100% of isolates. For CRAB, ampicillin-sulbactam MICs were ≥128 mg/L; for sulbactam-durlobactam, 1-2 mg/L. Admission in a Ukrainian hospital in the last year was a risk factor for MDRO, and majority were screening isolates (79%). There is extensive phenotypic resistance to last-resort antibiotics in MDRO from Ukrainian patients. Interpretation of cefiderocol susceptibility results depends on several variables. When treating patients recently admitted in Ukraine, suspected for Gram-negative bacterial infection, this should be taken into consideration. IMPORTANCE Since March 2022, multidrug-resistant microorganisms associated with Ukrainian patients have been detected in national surveillance systems of several European countries. We studied the phenotypic antimicrobial susceptibility to last-resort antibiotics of multidrug-resistant microorganisms from Ukrainian patients in the Netherlands and assessed clinical implications. Our research revealed that there was extensive phenotypic resistance to last-resort antibiotics. Healthcare professionals should be aware of multidrug-resistant microorganisms when treating patients recently admitted in Ukraine, suspected for Gram-negative bacterial infection.

Original languageEnglish
Article numbere0114224
JournalMicrobiology spectrum
Volume12
Issue number11
DOIs
Publication statusPublished - 1 Nov 2024

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Acinetobacter baumannii
  • Pseudomonas aeruginosa
  • Ukraine
  • War
  • antimicrobial susceptibility testing
  • carbapenemase-producing Enterobacterales
  • cefiderocol
  • ceftazidime-avibactam
  • ceftolozane-tazobactam
  • imipenem-relebactam
  • multidrug-resistant microorganisms

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