iLearning Recorded Webinar

Infection Prevention:

Mitigating Cross Contamination During Processing Medical Devices
and Flexible Endoscopes

Overview

General

Cross contamination is a process by which bacteria or other microorganisms are unintentionally transferred from one object to another, with harmful effect,  especially because of unsanitary handling procedures. This module will provide information enabling the learner to identify practice gaps that could lead to cross contamination during processing of medical devices and flexible endoscopes. Strategies to mitigate identified practice gaps and engage staff members to maintain situational awareness for cross contamination during work practices will be discussed. The participants will be able to identify potential cross contamination opportunities during workflow processes while cleaning and handling medical devices and flexible endoscopes

Target Audience

This CNE activity is intended primarily for RNs with a responsibility for or an interest in endoscope processing and ensuring safe patient care in the endoscopy suite. The presentation will also be of interest to allied healthcare personnel and MDs involved in endoscopy.

 

Learner Objectives

Upon completion of this presentation, participants will be able to:

  1. Review society and regulatory guidance for mitigating cross contamination in the Gastroenterology workplace.
  2. Identify spaces in the GI Suite and reprocessing workplace where cross contamination frequently occurs.
  3. Discuss strategies for mitigating cross contamination
Teaching Methodology

Participants will complete the recorded webinar learning activity. They will view the presentation, then register to complete the evaluation and take the post-test on the website. They will submit the documentation as directed. A bibliographic reference is included for those wishing additional information.

Contact Hours

Upon successful completion of the entire online program and submission of required documentation, participants will be granted 1 contact hour. No partial credit will be granted

Accreditation

Provider approved by the California Board of Registered Nursing, Provider Number 08747, the District of Columbia Board of Nursing, Provider Number 50-574, the Florida Board of Registered Nursing, Provider Number 50-574 and the Georgia Board of Nursing, Provider Number 50-574.

According to the criteria of the American Board of Certification for Gastroenterology Nurses (ABCGN), contact hours earned in this activity are considered GI Specific for the purpose of recertification through the ABCGN.

This program has been pre-approved by the Certification Board for Sterile Processing and Distribution (CBSPD).

This program has been approved by the International Association of Healthcare Central Service Material Management (IAHCSMM).

This program is acceptable for surgical technologist recertification by the National Center for Competency Testing.

Disclosures

Successful completion: Participants must complete the entire program, register, achieve a score of 80% on the post-test and submit required documentation.

  1. Conflict of interest: Planners disclose no conflict of interest. The speakers disclose salary or honorarium from the commercial support entity; they have signed a statement agreeing to present material fairly and without bias.
  2. Commercial company support: Fees are underwritten by education funding provided by Cantel Medical.
  3. Non-commercial company support: None.
  4. Alternative/Complementary therapy: None.
Certificate Issue / Replacement

Participants successfully completing the activity and submitting required documentation will be permitted to print a certificate of completion. Participants are advised to retain the certificate for eight years following activity completion.

Replacement of misplaced certificate is available from Educational Dimensions. There is a fee for this service. Request a replacement by contacting us.

Guide to Study

Detailed instructions for completing this eLearning activity

The following steps will assist you in your successful completion of this eLearning Activity.

  1. Read the content or view the recorded presentation. If you want contact hours at the completion of studying the eLearning material, you will be required to register, complete an evaluation and take a post-test prior to printing your Certificate of Completion. We urge you to complete the eLearning activity once you have started. However, if you do need to come back later, you can sign in with your email and eLearning ID.
  2. First Time Visitors will be asked to register using an email address as your User Name. Make a note which email address you have used. Then you will create an eLearning ID using a combination of at least 6-10 letters or numbers. Please make a note of your eLearning ID and if for some reason you forget, you may request that your eLearning ID be sent to you. The web site is secured by Trustwave.
  3. Return Visitors: If you have registered already you do not need to register again. Just Sign In using your email and eLearning ID.
  4. Evaluation Form: Once you have registered or signed in you will be asked to complete an evaluation form and submit it. This is required to obtain the Certificate of Completion.
  5. Post-test: A post-test, based on the content of the eLearning activity, will need to be taken. A passing score of 80% is required. This is required to obtain the Certificate of Completion.
  6. Printing Your Certificate of Completion: Once you have successfully passed the post-test you will be able to print your Certificate of Completion. You will be given an opportunity to verify the information that will be printed on your certificate. Please make sure your printer is ready to print. You will not have access to the certificate page on later visits unless you contact us. Once you choose to print the Certificate of Completion, it will not be possible to make corrections. To obtain a corrected certificate you will need to contact Educational Dimensions. Fees may apply.
  7. Browser recommendations: We require using an up-to-date browser with JavaScript enabled. You must enable cookies from this site in order to access the secure areas.
  8. If you encounter any technical problems during this eLearning activity, please contact us.

Recorded Webinar Video

Suggested Readings

AAMI. (2020). PPE regulations, specifications & standards. Retrieved from https://www.aami.org/news-resources/covid-19-updates/coronavirus-resources-for-the-field. ​

AORN, Guideline for a Safe Environment of Care, Part 1. (2017) Recommendation IX.g . Denver, CO: Association of Perioperative Registered Nurses.

Carter, E. J., Pouch, S. M., & Larson, E. L. (2014). Common infection control practices in the emergency department: A literature review. American Journal of Infection Control, 42(9), 957-962. doi: 10.1016/j-ajic.2014.01.026

CDC Infection Control Environmental Infection Control Guidelines Background I. Regulated Medical Waste  Guidelines for Environmental Infection Control in Health-Care Facilities (2003)  Categories of Medical Waste:

https://www.cdc.gov/infectioncontrol/guidelines/environmental/background/medical-waste.html.

Kenters, N., Huijskens, E. G. W., Meier, C., & Voss, A. (2015). Infectious diseases linked to cross-contamination of flexible endoscopes. Endoscope International Open, 3(4), E259-E265. doi: 10.1055/s-0034-1392099

Loudon, H. (2015). Infection prevention: The essentials of cleaning and disinfection for safer practice. Professional Nurse Today, 19(4), 28-33.

Lowman, W., Venter, L., & Scribante, J. (2013). Bacterial contamination of re-usable laryngoscope blades during the course of daily anaesthetic practice. South African Medical Jouranl, 103(6), 286-289. doi: 10.7196/SAMJ.6385

Nandy, P., Young, M., Haugen, S. P., Katzenmeyer-Pleuss, K.Gordon, E. A., Retta, S. M., Wood, S. C., & Lucas, A. D. (2017). Evaluation of one-way valves used in medical devices for prevention of cross-contamination. American Jouranl of Infection Control 45(7), 793-798. doi: 10.1016/j.ajic.2017.02.015

Ong, S.W.X., Tan, Y.K., Chia, P.Y., Lee, T.H., Ng, O.T., Wong, MSY, Marimuthu, K. (2020) Air, surface environmental, and personal protective equipment contamination by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) from a symptomatic patient.  Journal of the American Medical Association, epub ahead of print 4 March 2020.

Sttanton, M. (2019). 3-Zone Sterile Processing: Harness the productivity and value in this modern workflow. Retrieved from https://www.hpnonline.com/continuing-education/article/21110980/3zone-sterile-processing. IAHCSMM, Self-Study Series.

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