Comparison of Low‐Level to High‐Level Disinfection in Eliminating Microorganisms From Ultrasound Transducers Used on Skin: A Noninferiority Randomized Controlled Trial

Author:

Peters Nathan123ORCID,Williamson Frances24ORCID,Bauer Michelle J.5ORCID,Llewellyn Stacey6ORCID,Snelling Peter J.278ORCID,Marsh Nicole9101112ORCID,Harris Patrick N. A.513ORCID,Stewart Adam G.513ORCID,Rickard Claire M.910111214ORCID

Affiliation:

1. Department of Anaesthesia and Perioperative Medicine Royal Brisbane and Women's Hospital Brisbane Australia

2. School of Medicine University of Queensland Brisbane Queensland Australia

3. Department of Surgery University of Melbourne Melbourne Australia

4. Emergency and Trauma Centre Royal Brisbane and Women's Hospital Brisbane Australia

5. University of Queensland Centre for Clinical Research University of Queensland Brisbane Australia

6. Statistics Unit QIMR Berghofer Medical Research Institute Brisbane Australia

7. Emergency Department Gold Coast University Hospital Southport Australia

8. School of Medicine and Dentistry Griffith University Southport Australia

9. School of Nursing and Midwifery Griffith University Brisbane Australia

10. Nursing and Midwifery Research Centre Royal Brisbane and Women's Hospital Brisbane Australia

11. Alliance for Vascular Access Teaching and Research Group Griffith University Brisbane Australia

12. School of Nursing, Midwifery and Social Work University of Queensland Brisbane Australia

13. Central Microbiology Pathology Queensland Brisbane Australia

14. Herston Infectious Diseases Institute Metro North Hospitals and Health Service Brisbane Australia

Abstract

IntroductionThere is a lack of international consensus as to whether high‐ or low‐level disinfection (HLD or LLD) is required for ultrasound (US) transducers used during percutaneous procedures. This study compared the effectiveness of LLD to HLD on US transducers contaminated with microorganisms from skin.MethodsTwo identical linear US transducers repeatedly underwent either LLD or HLD during the study. Randomization determined which of these transducers was applied to left and right forearms of each participant. Swabs taken from transducers before and after reprocessing were plated then incubated for 4–5 days, after which colony forming units (CFU) were counted and identified. The primary hypothesis was the difference in the proportion of US transducers having no CFUs remaining after LLD and HLD would be less than or equal to the noninferiority margin of −5%.ResultsOf the 654 recruited participants 73% (n = 478) had microbial growth from both transducers applied to their left and right forearms before reprocessing. These were included in the paired noninferiority statistical analysis where, after disinfection, all CFUs were eliminated in 100% (95% CI: 99.4–100.0%) of HLD transducer samples (n = 478) and 99.0% (95% CI: 97.6–99.7%) of LLD transducer samples (n = 473). The paired difference in the proportion of transducers having all CFUs eliminated between LLD and HLD was −1.0% (95% CI: −2.4 to −0.2%, P‐value <.001).ConclusionsDisinfection with LLD is noninferior to HLD when microorganisms from skin have contaminated the transducer. Therefore, using LLD for US transducers involved in percutaneous procedures would present no higher infection risk compared with HLD.

Funder

Australasian Society for Ultrasound in Medicine

Publisher

Wiley

Subject

Radiology, Nuclear Medicine and imaging,Radiological and Ultrasound Technology

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