Understanding AAMI TIR99 – Guidance on Ultrasound Probe Processing
Upcoming Virtual Courses
Expert Insights
Understanding AAMI TIR99:2024 – Ultrasound Probe Processing Guidance (May 2024)
May 20 to May 20, 2024
Overview
This training program is designed to equip healthcare professionals with the knowledge and skills necessary to ensure the safe and effective processing of dilators, transesophageal and ultrasound probes, in accordance with the guidelines set forth by the Association for the Advancement of Medical Instrumentation (AAMI) Technical Information Report (TIR) 99.
In today's healthcare environment, the proper sterilization and reprocessing of reusable medical devices are of paramount importance to prevent infections and ensure patient safety. AAMI TIR99:2024 provides essential guidance on the best practices, protocols, and quality control measures specific to the processing of probes and dilators.
By the end of this training, healthcare professionals will be better equipped to implement best practices, reduce the risk of infections, and enhance patient safety through the proper processing of medical probes and dilators in accordance with AAMI TIR99:2024. This program is essential for anyone involved in the reprocessing of these devices and aims to contribute to the overall improvement of healthcare quality and safety.
This virtual instructor led training is not a substitution for the publication product, so we recommend purchasing the technical information report in conjunction.
What to expect
Over the course of (2) hours, the attendee will be able to:
- Understand the key principles and recommendations outlined in AAMI TIR99 for the reprocessing of medical probes and dilators.
- Apply the step-by-step processes for cleaning, disinfection, and sterilization of probes and dilators, including the selection of appropriate cleaning agents and equipment, in a practical healthcare setting.
- Implement quality control measures, documentation practices, and tracking systems to ensure the integrity and effectiveness of reprocessing procedures for medical probes and dilators, contributing to improved patient safety and compliance with regulatory standards.
Who Should Attend?
Sterile Processing, Nursing, Infection Preventionist, and Healthcare Technology Management (HTM) professionals that oversee or involved in the proper processing of dilators, transesophageal, and ultrasound probes.
Virtual Training Information
Speakers
Garland-Rhea Grisby, CFER, CSPDT
Endoscope Service Manager
Kaiser Permanente Medical Center
Mindy Benedict
Director, Infection Prevention & Control
Olympus Corporation of America
Certification in Infection Control, The Certification Board of Infection Control & Epidemiology, Inc. (CBIC®)
ASGE’s Recognized Industry Associate (ARIA), The American Society for Gastrointestinal Endoscopy
Certified Flexible Endoscope Reprocessor (CFER), The Certification Board for Sterile Processing and Distribution, Inc. (CBSPD)