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Chapter 5 - Decontamination of airway equipment

from Section 1 - Basic science

Published online by Cambridge University Press:  10 January 2011

Ian Calder
Affiliation:
National Hospital for Neurology and Royal London Hospital
Adrian Pearce
Affiliation:
Guy's and St Thomas' Hospital, London
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Summary

Cross-infection may occur through reusable airway devices. The infective agent for transmissable spongiform encephalopathies (TSE) transmission is an abnormal prion protein. No prion-specific nucleic acid is involved in disease transmission, and abnormal prion-protein infectivity is not controlled by standard decontamination procedures of standard autoclaving or cold chemical sterilisation. A guideline on infection control within anaesthesia was published by the Association of Anaesthetists of Great Britain and Ireland (AAGBI) in 2008 and provides valuable advice. There are three possible options for airway equipment, single use equipment, steam sterilisation or cold chemical sterilisation. Single use equipment eliminates the risk of cross-infection between patients through the airway device and is the preferred option. Repeated cycles of heat sterilisation will produce loss of transmitted light in rigid laryngoscope bundles. Cold chemical sterilisation is appropriate for devices which are not single use and are thermally sensitive. Automated disinfectors should be used for fibrescopes.
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Publisher: Cambridge University Press
Print publication year: 2010

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