Guidelines for Reprocessing Ultrasound Transducers: 2026

Q3 Medicine
Nathan Peters, Marija Juraja, Nicola Isles, Ellen Woodcock, Elissa Kennedy-Smith, Cartan Costello, Jo McCann, Karen Mizia
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引用次数: 0

Abstract

Introduction

Ultrasound equipment is recognised as a potential source of harmful microorganisms which could lead to clinical infection. This highlights the importance of standardised infection prevention and control strategies for ultrasound practice across Australia and New Zealand. This revised guideline supersedes the similarly named 2017 guideline and was collaboratively developed by the Australasian Society for Ultrasound in Medicine (ASUM) and the Australasian College for Infection Prevention and Control (ACIPC).

Methods

A multidisciplinary working group was assembled consisting of ultrasound practitioners from varying specialty areas and infection control specialists. The guideline recommendations were informed by a review of relevant literature, national and international standards, and current Australian and New Zealand regulatory requirements. A catalyst for the revision of these guidelines was the release of the Australian Standard AS5369:2023—Reprocessing of reusable medical devices and other devices in health and non-health related facilities. Consensus was achieved through structured discussions and iterative drafting including wider stakeholder feedback.

Results

Recommendations for transducer reprocessing were based on the invasiveness of the ultrasound transducer as well as the type of human tissue it contacted during use. Particular attention is also given to the safe use of ultrasound gel, transducer covers, as well as broader considerations of standard and transmission-based precautions, including the use of aseptic technique.

Conclusion

Implementation of this guideline by ultrasound clinicians and their facilities will reduce the risk of transmission of potentially harmful microorganisms and ensure infection prevention and control practices across Australia and New Zealand are aligned with accepted national standards.

Impact Statement

This guideline outlines the Australian and New Zealand standard for infection prevention and control as it relates to ultrasound practice. This 2026 revision supersedes the similarly named 2017 guideline and was collaboratively developed by the Australasian Society for Ultrasound in Medicine (ASUM) and the Australasian College for Infection Prevention and Control (ACIPC). The multidisciplinary working group used published literature, national and international standards, and relevant regulatory requirements in formulating the recommendations. This guideline should be used by clinicians and facilities using ultrasound to reduce the transmission of potentially harmful microorganisms and improve patient care.

Abstract Image

超声换能器再处理指南:2026
超声设备被认为是可能导致临床感染的有害微生物的潜在来源。这突出了标准化感染预防和控制策略在澳大利亚和新西兰超声实践的重要性。修订后的指南取代了同名的2017年指南,由澳大利亚超声医学学会(ASUM)和澳大利亚感染预防与控制学院(ACIPC)合作制定。方法由不同专业领域的超声医师和感染控制专家组成多学科工作组。指南建议是通过对相关文献、国家和国际标准以及当前澳大利亚和新西兰监管要求的审查得出的。修订这些指南的催化剂是澳大利亚标准as5369:2023的发布——卫生和非卫生相关设施中可重复使用的医疗器械和其他器械的再处理。通过有组织的讨论和反复起草,包括更广泛的利益攸关方反馈,达成了共识。结果基于超声换能器的侵入性及其在使用过程中接触的人体组织类型,提出了换能器再处理的建议。还特别注意超声凝胶、换能器盖的安全使用,以及对标准和基于传输的预防措施的更广泛考虑,包括无菌技术的使用。超声临床医生及其设施实施本指南将降低潜在有害微生物传播的风险,并确保澳大利亚和新西兰的感染预防和控制实践与公认的国家标准保持一致。影响声明本指南概述了澳大利亚和新西兰的感染预防和控制标准,因为它与超声实践有关。这项2026年修订取代了类似名称的2017年指南,由澳大利亚超声医学学会(ASUM)和澳大利亚感染预防与控制学院(ACIPC)合作制定。多学科工作组在制定建议时参考了已发表的文献、国家和国际标准以及相关的监管要求。临床医生和使用超声的机构应使用本指南,以减少潜在有害微生物的传播并改善患者护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Australasian Journal of Ultrasound in Medicine
Australasian Journal of Ultrasound in Medicine Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
1.90
自引率
0.00%
发文量
40
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