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Challenging the Sterrad 100NX sterilizer with different carrier materials and wrappings under experimental "clean"
Magda Diab-Elschahawi1, Alexander Blacky, Nicole Bachhofner
1Clinical Institute of Hospital Hygiene, Vienna General Hospital, Medical University of Vienna, Waehringer Guertel 18-20, Vienna, Austria. magda.diab-elschahawi@meduniwien.ac.at
Background:
Sterrad sterilizers have been developed for the sterilization of thermolabile materials. The aim of the present study was to challenge the efficacy of this low-temperature hydrogen peroxide-based sterilization system with different carrier materials and wrappings under experimental "clean" and "dirty" conditions.
Methods:
We tested the sporocidal effect of the Sterrad 100NX sterilizer (Advanced Sterilization Products, Irvine, CA) on the carrier materials titanium, polyethylene, and polyurethane with single versus 3 wrappings of inoculated carriers. To simulate insufficient cleaning or crystalline residues, carriers were charged with spore inocula containing organic and inorganic burdens.
Results:
Our qualitative results show that irrespective of the number of wrappings in the "clean" condition, sterilization by the Sterrad 100NX was equally effective on all 3 carrier materials, reaching a log-10 reduction rate of ≥ 6 under standard half-cycle conditions. Any additional organic or inorganic challenge significantly impaired the sterilization outcome.
Conclusion:
Results of our current study emphasize the utmost importance of thorough and reliable cleaning of medical devices before being exposed to a subsequent hydrogen peroxide sterilization process. Any institution using this sterilization technology should have a well-established and validated cleaning process and enforce a rigorous quality assurance program for all steps of the presterilization processing of medical devices.
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