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Probe construction varies between manufacturers, including differences in adhesives, acoustic lens materials and cable sheathing. Always consult the instructions for use (IFU) to ensure compatibility testing for the probe, the decontamination device and any pre-cleaning wipes used. Failure to do so may invalidate warranties and risk damage. The SoR Guidance provides some final reflection prompts to help hospitals establish best practice: l Are you satisfied that you and all your colleagues are familiar with the latest guidance on transducer decontamination?
l Have you checked that the processes used for every transducer meet both manufacturer and decontamination system guidance?
l Does everyone within your department/trust/ health board/company know how to use the decontamination unit(s)?
l What audit takes place to ensure that everyone is using the system(s) correctly?
l Do you regularly check the transducers and cables for damage?
l Have you ever had sticky yellow cables? If so, did you check the manufacturer guidance on which wipes to use to decontaminate the machine and cables?
l Are there any further training needs within your unit? If so, you can approach the supplier of the decontamination unit to get support.
Guidance is clearly recommending a move away from manual systems to automated devices, due to manual disinfection being variable in contact time, disinfectant concentration and technique. Automated units standardise these variables through validated cycles, controlled exposure to disinfectant and traceable records. This helps departments demonstrate compliance with infection prevention standards and regulatory expectations. Automated decontamination units represent a
significant advancement in infection prevention within ultrasound. Yet technology alone does not guarantee safety. Careful compatibility checks, correct product selection, meticulous handling, routine inspection and ongoing education are all essential. By embedding these principles into daily practice, departments can ensure decontamination processes remain effective, compliant and protective for patients and staff alike.
References 1. Things to consider with automated decontamination units - Society of Radiographers. Accessed at:
https://www.sor. org/news/cpd/cpd-shorts-things-to-consider- with-automatic-decon
2. Welsh HTM Decontamination of flexible endoscopes WHTM 01-06 Part F: Decontamination of Semi-Critical Ultrasound Probes; Semi-invasive and Non- invasive Ultrasound Probes - NHS Wales Shared Service Partnership. Accessed at: https://
nwssp.nhs.wales/ourservices/specialist- estates-services/specialist-estates-services- documents/whtms-library/whtm-01-06-part-f- decontamination-of-flexible-endoscopes/
Nanosonics UK Limited.
Ground Floor at The Forum, Unit C1 & C2, Hercules Business Park, Bird Hall Lane, Stockport, SK3 0UX, UK. T: +44 (0) 161 686 3030 E:
info@nanosonics.co.uk W:
www.nanosonics.co.uk
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