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The U.S. Food and Drug Administration (FDA) presents…”Duodenoscope Sampling & Culturing”

The availability of voluntary, standardized protocols that were developed for duodenoscope surveillance sampling and culturing was announced on Feb. 26, 2018 by the U.S. Food and Drug Administration (FDA), the Centers for Disease Control and Prevention (CDC) and the American Society for Microbiology (ASM), along with other endoscope culturing experts. Hospitals and health care facilities that utilize duodenoscopes can, in addition to meticulously following manufacturer reprocessing instructions, take these additional steps to further reduce the risk of infection and increase the safety of these medical devices. These protocols are an update to the Interim Duodenoscope Surveillance Protocol released by CDC in March 2015.

Duodenoscopes are flexible, lighted tubes that are used to treat patients undergoing endoscopic retrograde cholangiopancreatography (ECRP). More than 500,000 ERCPs are performed each year in the United States. Duodenoscopes undergo a multi-step cleaning and high-level disinfection procedure called reprocessing so that they can be reused between patients. However, the complex design of duodenoscopes makes it difficult to remove contaminants compared to other types of endoscopes.  If not thoroughly cleaned and disinfected, tissue or fluid from one patient can remain in a duodenoscope when it is used on a subsequent patient. In rare cases, this can lead to patient-to-patient infection.

Presenters:

The FDA, CDC, ASM and other endoscope culturing experts will review the voluntary duodenoscope surveillance sampling and culturing protocols, which can be leveraged by facilities to help monitor the quality of their reprocessing procedures. During the webinar, participants will also have an opportunity to ask questions about these voluntary protocols. No registration is required to participate in the webinar.

Target Audience: Health Care Facilities

Following the conference, a transcript, audio recording and slides will be available at:  https://www.fda.gov/MedicalDevices/NewsEvents/WorkshopsConferences/ucm411063.htm

Questions: Contact the Division of Industry and Consumer Education (DICE) in the Center for Devices and Radiological Health (CDRH) at 1-800-638-2014, 301-796-7100 or dice@fda.hhs.gov

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NOTE: The FDA does not provide Continuing Education (CEU) or Certificates of Attendance for webinar participation.