trophon EPR High Level Disinfection for Ultrasound Probes

Simply smarter ultrasound probe disinfection in 7 minutes

Simply smarter ultrasound probe disinfection in 7 minutes

trophon® EPR is a high level disinfection system that is fast and simple. Disinfection takes place in an automated, closed system and uses a vaporized hydrogen peroxide solution.
 

The compact design means it can be located at the point of care, helping to improve patient workflow, while the fully enclosed system helps protect both patients and staff by limiting exposure to harmful disinfectant chemicals. As a point of care solution, it can help reduce the need to transport probes between the ultrasound suite and separate cleaning rooms.

A new study shows trophon® EPR is the first high level disinfection system for ultrasound probes that is effective against high-risk, cancer causing strains of Human Papilloma Virus⁽¹⁾.


Appropriate reprocessing of ultrasound probes between patients is critical to reduce the risk of HPV transmission. Recent research shows disinfectants commonly used on ultrasound probes do not kill natural, infectious high-risk HPV(2).
 

Given the prevalence of HPV, the potential for HPV transmission in the healthcare setting and the virus's links to cancer, these research developments are of concern.





1. Meyers, C., et al., Efficacy of a high-level disinfectant system against high-risk human papilloma virus. Presented at SHEA 2015.

2. Meyers, J., et al., Susceptibility of a high-risk human papillomavirus type 16 to clinical disinfectants. J Antimicrob Chemother, 2014.

Guided recommend the high-level disinfection of semi-critical devices. Click on the link below to review.

AORN: Association of periOperative Registered Nurses

Controlling infections has never been more important. More and more, healthcare-acquired infections (HAIs) are a major challenge for healthcare organizations. Consider these facts:

• 1 in 25 patients will acquire an infection during a hospital stay1.
   

• HAIs cost the U.S. up to $147 billion annually in direct and indirect costs2.
   

• Up to 70% of HAIs are preventable using existing infection prevention practices3.
   

• Of the 1.7 million people infected in U.S. hospitals, 98,987 die⁴ As a result, there are more efforts around controlling and preventing HAIs than ever before-and the disinfection of ultrasound transducers can play a critical part in that.
   

• 12.9% of transducers are contaminated with pathogenic bacteria following routine disinfection5.
   

• Up to 7.5% of transvaginal ultrasound transducers were found to have HPV DNA, a known cause of cervical cancer, after low-level disinfection with wipes6.
   

• Up to 9% of barrier sheaths and condoms leak7.
   

• One of the Top 5 non-compliance findings by The Joint Commission is reducing the risk of infections associated with medical devices or equipment8.

1. Electronically accessed. https://www.cdc.gov/nchs/data/nvsr/nvsr61/nvsr61_04.pdf

2. Marchetti, A. and Rossiter, R. (2013). J Med Econ 2013 Dec;16(12):1399-404.

3. Scott RD. Atlanta: Centers for Disease Control and Prevention (2009).

4. Klevens, M et al., Estimating Health Care-Associated Infections and Deaths in U.S. Hospitals,. Public Health Rep. 122: 160-66, 2007 (2002 Data).

5. Leroy SJ. Hosp Infect 2013 83(2):99-106.

6. Ma S et al. Emerg Med J. 2013 30(6):472-5.

7. Vickery K et al. J Inf Pub Health 2013; in press.

8. Electronically accessed: thejointcommission.org. May 2014. Issue Two. Improperly sterilized or high-level disinfected equipment.

Comprehensive training and product support material is available to help you install and use your trophon EPR system.
 

Training can be completed online. You'll be asked to watch a 15 minute video followed by a questionnaire. Upon successful completion of the questionnaire you will be able to download and print your certification to operate your trophon EPR.
 

Click here for training, certification and support information.

Ordering trophon EPR accessories and supplies is easy.
 

Phone: 866-281-7545
 

Fax: 877-279-6990
 

Email: gehcaccessorysales@ge.com
 

Online: gehealthcare.com/accessories

Sonex-HL™
The small sealed cartridges that contain a proprietary aqueous solution of 35% Hydrogen Peroxide are 80 mL each which is enough for up to 40 exams (up to 240 exams per box). Product cannot ship air. (6 cartridges / box; approximately 240 cycles)

trophon Chemical Indicators
trophon In-Process Chemical indicators are used by healthcare providers to confirm that Minimum Effective Concentration of disinfectant is delivered by the trophon EPR system. (300/box; 1" / 26 mm)

Clean Ultrasound Probe Covers
Decrease risk of recontamination after high-level disinfection. Custom-designed for ultrasound probes, these covers protect the entire probe, including the handle. (100/box)

trophon Printer and trophon Connect
The printer records each HLD cycle and generates an adhesive label detailing the results of each disinfection cycle for documentation and traceability. This allows the probe and the HLD cycle date and time to be linked with the patient and the procedure.
 

trophon Printer Paper / Labels
Labels are used with trophon Printer to help address the audit trail often required by hospitals and clinics to track and adhere to infection control guidelines. Labels can be placed in a manual log to reduce the potential for incomplete or inaccurate documentation. The labels are direct thermal, adhesive, and high quality with a seven year print stability. (1 roll - 900 prints)
 

The trophon Connect software application provides a traceability solution for trophon EPR High Level Disinfection (HLD) system. It enables download of a detailed HLD report at the click of a button. It is designed to help the user meet audit and accreditation requirements.

1. As informações contidas neste material são apresentadas de forma geral, embora se pretenda que não haja dados imprecisos, pode haver diferentes interpretações a esse respeito; Essas informações podem ser restritas em seu país. As configurações e recursos finais do produto podem ser diferentes daqueles mostrados na foto/vídeo;
   
   
2. Os produtos e tecnologias mencionados neste material estão sujeitos à regulamentação do governo e podem não estar disponíveis em todas as localidades. Seu embarque e efetiva comercialização só poderão ocorrer após a aprovação do regulador. Os produtos e tecnologias podem estar com nome fantasia distinto do aprovado, sendo que sua comercialização ocorrerá sob o nome registrado. A GE HealthCare reserva-se o direito de fazer alterações nas especificações e recursos mostrados neste documento ou de descontinuar o produto descrito a qualquer momento, sem aviso ou obrigação. Entre em contato com seu representante GE HealthCare para obter as informações mais atualizadas.
   
   
3. O cliente e/ou fornecedor de cuidados de saúde tem a responsabilidade exclusiva de utilizar o seu próprio julgamento médico e profissional independente na tomada de decisões clínicas, médicas ou financeiras. Nada neste material deve ser utilizado para diagnosticar ou tratar uma doença ou condição de saúde.