Related Experiment Videos

[Peracetic acid: alternative to the sterilization of bronchofibroscopes]

J I Villate1, J Barrón, R Zalacaín

  • 1Servicio de Medicina Preventiva, Hospital de Cruces, Baracaldo, Vizcaya.

Insights

The Steris system effectively sterilizes fiberoptic bronchoscopes using peracetic acid, demonstrating no microbial growth post-treatment. Thorough pre-sterilization washing significantly enhances the system's disinfection efficacy.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Medical Device Sterilization

Background:

  • Fiberoptic bronchoscopes (FB) require effective sterilization to prevent healthcare-associated infections.
  • Cold sterilization methods are crucial for heat-sensitive medical instruments like FBs.

Purpose of the Study:

  • To evaluate the efficacy of the Steris system utilizing peracetic acid for cold sterilization of fiberoptic bronchoscopes.
  • To assess the impact of pre-sterilization washing on microbial decontamination.

Main Methods:

  • Fiberoptic bronchoscopes were intentionally contaminated with Pseudomonas aeruginosa, Acinetobacter baumanii, and Mycobacterium kansasi.
  • Samples were cultured after contamination, washing, and immediately/1 hour post-sterilization.
  • Chemical and biological indicators (Bacillus stearothermophilus spores) were used to validate the sterilization process.

Main Results:

  • No microbial growth was detected in any samples immediately or 1 hour after Steris system sterilization.
  • Pre-sterilization washing with enzyme soap was highly effective, yielding negative cultures in 14/24 samples and significantly reducing microbial load in others.
  • Chemical and biological tests confirmed the system's performance throughout 24 contaminations and 52 training cycles.

Conclusions:

  • The Steris system with peracetic acid is a viable and effective option for cold sterilization or high-level disinfection of fiberoptic bronchoscopes.
  • Appropriate pre-sterilization cleaning is critical for maximizing the effectiveness of disinfection and sterilization processes.
  • This study validates the Steris system's capability to eliminate challenging microorganisms from complex medical devices.

Related Concept Videos