Probe disinfection is critical in protecting patient and hospital staff:

1. There are risks associated with not doing proper probe reprocessing. For example, up to 7% of ultrasound probes were found to be contaminated with human papillomavirus (HPV) after disinfection with low level wipes.^1,2,3
2. Spaulding Classification is a widely used framework that specifies medical device reprocessing requirements based on the intended use.

1. The probe disinfection landscape in Europe is changing. A 2016 European Society of Radiology (ESR) study found a wide range of practices across Europe, with a need to raise awareness among practitioners of the importance of infection prevention and control measures.

Based on that, the ESR issued a best practice recommendation in November 2017:

• High level disinfection of probes is mandatory for endocavitary ultrasound and all interventions.
• Automated systems offer standardized and reproducible decontamination processes, helping to avoid operator-associated errors or variations.
• Dedicated transducer covers should be used for endocavitary ultrasound and all interventions.
• Sterile gel should be used for endocavitary ultrasound and all interventions.

Some countries have already started to develop their own regulations further:

• In 2017, Ireland and Scotland made high level disinfection mandatory between examinations.⁴
• In 2019 the French Ministry of Health published data sheets about endocavity probe reprocessing for healthcare professionals.⁵
• Other countries recommend strongly the same practices.⁶

1. Casalegno JS, Le Bail Carval K, Eibach D, Valdeyron ML, Lamblin G, Jacquemoud H, et al. High risk HPV contamination of endocavity vaginal ultrasound probes: an underestimated route of nosocomial infection? PloS one. 2012;7(10):e48137
2. Ma ST, Yeung AC, Chan PK, Graham CA. Transvaginal ultrasound probe contamination by the human papillomavirus in the emergency department. Emergency medicine journal. 2013;30(6):472–5
3. M’Zali F, Bounizra C, Leroy S, Mekki Y, Quentin-Noury C, Kann M. Persistence of Microbial Contamination on Transvaginal Ultrasound Probes despite Low-Level Disinfection Procedure. PloS one. 2014;9(4):e93368.
4. https://hpspubsrepo.blob.core.windows.net/hps-website/nss/1937/documents/1_RES-183-1-v1.pdf (IIrish HSE Guidance for Decontamination of Semi‐critical Ultrasound Probes QPSD-GL-028-1- 2017) Health Service Executive (HSE) Quality Improvement Division (2017). HSE Guidance for Decontamination of Semi‐critical Ultrasound Probes; Semi‐invasive and Non‐invasive Ultrasound Probes. Document: QPSD-GL-028-1
5. https://solidarites-sante.gouv.fr/soins-et-maladies/qualite-des-soins-et-pratiques/securite/article/prevention-des-risques-d-infection-associes-a-l-utilisation-des-sondes-d
6. Werkgroep Infectie Preventie (2017). Reiniging, desinfectie en sterilisatie van medische hulpmiddelen voor hergebruik niet-kritisch, semi-kritisch of kritisch gebruik: 56.
   Direzione Sanitaria AUSL Pescara (2009). Linee Guida per la “Corretta gestione di Procedure Assistenziali e Igienico-Sanitarie in Setting di Cura Ospedalieri e Territoriali”: 88.
   Kommission für Krankenhaushygiene und Infektionsprävention (KRINKO), and Bundesinstitut für Arzneimittel und Medizinprodukte (BfArM), (2012). Anforderungen an die Hygiene bei der Aufbereitung von Medizinprodukten. Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz: 66.
   Society and College of Radiographers and British Medical Ultrasound Society (2017). «Guidelines For Professional Ultrasound Practice.» 127.
   Welsh Health Technical Memorandum (WHTM) (2014). WHTM 01-06 - Decontamination of flexible endoscopes Part C: Operational management, NHS Wales Shared Services Partnership – Specialist Estates Services: 74

Ultrasound probe disinfection can be done in several ways:

Please check the probe manufacturer’s specifications to ensure the probe and disinfectant are compatible: www.gehealthcare.com/transducers

Learn more about probe disinfection in our e-book.

GE Healthcare recommends in its user manual the following about cleaning and disinfection of ultrasound probes.

“Adequate cleaning and disinfection between patient cases are necessary to prevent disease transmission. All probes must be thoroughly cleaned prior to disinfection. The level of disinfection required is based on patient contact.”

• Probes that contact mucosal or non-intact skin require cleaning followed by high-level disinfection by either soaking or use of an automated system such as TD100®.
• Probes that contact intact skin require cleaning followed by intermediate-level disinfection (wipe or spray).

UMONIUM^38® Neutralis Tissues by Laboratoire Huckert’s International are ultrasound disinfection wipes, totally safe for operators, patients, environment and material¹, that help you achieve a high-level disinfection² of surface and endocavitary probes. With these wipes, you can disinfect the entire probe including the handle, the cable and the connector but also the probe environment.

These wipes have a bactericidal, mycobactericidal, fungicidal and sporicidal activity validated under the strictest conditions (closest to operating conditions) and comply with all European standards³.

UMONIUM^38® Neutralis Tissues have an excellent performance before disinfection and proven effectiveness against biofilms formation.

They are fully adapted for sensitive environments such as AR and IVF establishments, since they are safe up to embryo cells level and gametes⁴. It is a product adapted to gynecology environment.

Thanks to a neutral PH (PH = 7), UMONIUM^38® Neutralis Tissues are non-corrosive and have multi-material compatibility.

They are an economical and ready-to-use solution. The reprocessing workflow is simple, two wipes are required: one for cleaning and one for disinfection. Each wipe can treat 3 m² of surface. The shelf life is 3 years after opening the box.

It is an eco-friendly product and the wipes are made of wood-pulp.

How to reprocess your probe with UMONIUM38® Neutralis Tissues?

 

How to disinfect surface probes with Neutralis Tissues?

 

How to disinfect endocavitary probes with Neutralis Tissues?

1. EN16615, EN14561, EN14562, EN14563, EN13727, EN13624, EN14476, EN14348
2. Achieved by following the recommended reprocessing workflow
3. Bactericidal, Mycobactericidal, Fungicidal, Sporicidal validated in 5 seconds according to the American Standard ASTM2967-15
4. Tests Mouse Embryo Assay (MEA) and Human Sperm Survival Assay (HSSA)