Hospital outbreak sustained by Klebsiella pneumoniae sequence type 147 co-producing NDM-1 and OXA-48, Rome, Italy,

Valerio Capitani1, Mariateresa Ceparano1, Annalisa Rosso1

  • 1Department of Public Health and Infectious Diseases, Sapienza University of Rome, Rome, Italy.

Insights

An outbreak of carbapenemase-producing Klebsiella pneumoniae in Rome was contained using infection control measures. Genomic surveillance and rapid diagnostics are crucial for managing multidrug-resistant organism spread in hospitals.

Area of Science:

  • Clinical microbiology
  • Infectious disease epidemiology
  • Genomic surveillance

Background:

  • Carbapenemase-producing Klebsiella pneumoniae (CRKP) poses a significant threat in healthcare settings.
  • Outbreaks of CRKP require rapid and effective infection prevention and control (IPC) strategies.
  • Co-production of NDM-1 and OXA-48 carbapenemases represents a challenging multidrug-resistant organism (MDRO).

Purpose of the Study:

  • To describe an outbreak of CRKP in a tertiary care hospital in Rome.
  • To evaluate the effectiveness of IPC measures in containing the outbreak.
  • To highlight the role of genomic surveillance in understanding CRKP dissemination.

Main Methods:

  • Retrospective analysis of a CRKP outbreak spanning February-March 2025.
  • Implementation and assessment of IPC measures: patient cohorting, environmental cleaning, contact surveillance.
  • Rapid molecular typing (NanoTyping) and whole genome sequencing (WGS) for strain characterization and phylogenetic analysis.
  • Environmental sampling for pathogen detection.

Main Results:

  • Ten patients in critical care units were colonized or infected with NDM-1 and OXA-48 co-producing K. pneumoniae.
  • Nine infections were hospital-acquired, detected via rectal swab screening.
  • IPC measures contained initial transmission, but spread to other wards occurred.
  • Genomic analysis confirmed clonal spread of the high-risk ST147 clone, with evidence of regional dissemination.
  • A single contaminated environmental surface was identified.

Conclusions:

  • Rapid implementation of IPC measures is vital but challenging in intensive care settings.
  • Genomic surveillance combined with rapid diagnostics is essential for real-time outbreak response.
  • Enhanced screening, routine surveillance, and rigorous IPC protocols are critical for preventing MDRO spread in healthcare facilities.

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