Pulling the plug on a pseudomonas outbreak: ancillary equipment as vectors of infection

J B Veater1, C Jones-Manning2, J Mellon3

  • 1Clinical Microbiology, University Hospitals of Leicester NHS Trust, Leicester, UK.

PubMed
Abstract

Insights

Contaminated irrigation plugs, not endoscopes, caused a Pseudomonas aeruginosa outbreak during cystoscopy. This highlights the risk of ancillary equipment in infection transmission and the need for updated reprocessing guidelines.

Area of Science:

  • Infection Control
  • Microbiology
  • Medical Device Reprocessing

Background:

  • Flexible endoscopes are known infection vectors, but ancillary equipment like irrigation plugs are often overlooked.
  • Irrigation plugs used in flexible endoscopy pose a potential risk for pathogen transmission.
  • This study investigates a specific outbreak linked to contaminated cystoscopy irrigation plugs.

Purpose of the Study:

  • To report a cystoscopy-associated outbreak of Pseudomonas aeruginosa infections.
  • To identify the source of infection, focusing on ancillary endoscopic equipment.
  • To evaluate the role of irrigation plugs in healthcare-associated infections.

Main Methods:

  • Review of laboratory, clinical, and decontamination unit records.
  • Audits of the decontamination unit and assessment of cystoscopes and irrigation plugs for contamination.
  • Variable nucleotide tandem repeat (VNTR) typing of Pseudomonas aeruginosa isolates to confirm outbreak linkage.

Main Results:

  • Pseudomonas aeruginosa strains were isolated from irrigation plugs, but not from flexible cystoscopes.
  • Fifteen confirmed infections, including bacteraemia and urinary tract infections, were identified.
  • Reprocessing failures, potentially due to non-dismantling of plugs and incompatible manufacturer instructions, were implicated.

Conclusions:

  • Ancillary endoscopic equipment can be significant vectors for infection outbreaks.
  • Outbreak investigations should meticulously consider all associated equipment.
  • Manufacturers' reprocessing instructions for ancillary devices require careful review for compatibility with clinical practice.

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