New Standards in Endoscope Reprocessing

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The latest recommendations highlight the importance of meticulous manual cleaning, inspection of internal channels and investing in specialty storage cabinets.


Best practices in the high-level disinfection of flexible endoscopes must be prioritized after every one of the estimated 15 million colonoscopies performed each year in the U.S., says James Collins, BS, RN, CNOR, endoscopy accreditation nurse for the Digestive Disease & Surgical Institute at the Cleveland Clinic. He’s one of seven co-authors of the latest multisociety guideline on reprocessing flexible GI endoscope and accessories, which was published in January 2021.

Last March, the Association for the Advancement of Medical Instrumentation (AAMI) released the updated ANSI/AAMI ST91:2021/ standard for the reprocessing of flexible and semi-rigid endoscopes. Some of the key revisions and additions involve factors related to decontamination sinks; training competency and certification; HVAC and water quality monitoring; leak testing; broadened cleaning and inspection steps; heightened focused on endoscope drying; and revised storage requirements. “Drying and storage has become one of the elements being looked at more closely, due to the fact that wet endoscopes are a hazard for bacterial growth,” says Mr. Collins. “We know more about biofilms and how they work, and the effects they have on wet scopes that aren’t dried properly.”

Randall Rentschler, RN, BA, CNOR, CSSM, TNS, perioperative service director at Artesia (N.M.) General Hospital, says the latest revisions will require “sweeping changes” to many GI suites and their budgets. His hospital included. Mr. Rentschler is already working through implementing the changes, including requirements related to installing forced-air drying cabinets, which he notes is an expensive upgrade. “The expectation is to have drying cabinets with integrated adapters that connect to flexible scopes and force HEPA-filtered air through their channels,” he explains. “Also, the scope cabinet can no longer be kept in rooms where procedures are performed. There needs to be a separated area for scope storage, and facilities must maintain separation between clean and dirty workflows.”

Mr. Rentschler points to other key updates to AAMI’s standard: automated endoscope reprocessors (AERs) must be six feet from the manual cleaning sink; a three-tank sink for separate leak testing, manual cleaning and rinsing of scopes prior to placement in AERs; use of borescopes to visually inspect a scope’s lumens for damage or dampness; and confirming a scope is dry before hanging it in a storage cabinet.

Frank Edward Myers III, MA, CIC, FAPIC, director of infection prevention and clinical epidemiology at UC San Diego Health, supports the updated standard. “It’s a good upgrade from where we were,” he says. “I’m excited about beginning to assess drying cabinets. We know there are many AERs on the market that haven’t been adequately drying internal channels of scopes.”

I’ve always believed reprocessing techs are the heart of the GI unit.
— James Collins, BS, RN, CNOR

Mr. Meyers welcomes the push for three-bay sinks. “There are many facilities still trying to reprocess scopes in a one-bay sink, which is an invitation for cross contamination,” he says. He’s also excited to continue advancing the use of borescopes as part of the cleaning process. “We ask our techs to clean the channels of scopes,” he says, “but we’re asking them to clean without being able to see inside.”

Focus on the Fundamentals of Endoscope Care
STANDARD STEPS
DRY TIME Flexible endoscopes must be hung vertically in specialized cabinets that circulate HEPA-filtered air to prevent moisture from remaining on surfaces or in channels.

From point-of-use treatment to the drying and storage phase, there are eight essential elements involved in the cleaning and high-level disinfecting of flexible endoscopes, according to James Collins, BS, RN, CNOR, endoscopy accreditation nurse for the Digestive Disease & Surgical Institute at the Cleveland Clinic. 

1. At the point of use in the procedure room, the exterior of the endoscope is wiped, and the channels are purged of any fluids or blockages. This process should take approximately five minutes to complete.

2. During transport from the procedural room, the scope should be secured in a covered container that is properly labeled with the time the point-of-use treatment was done. With some devices, if reprocessing is not started within 60 minutes of the point-of-use treatment, additional  reprocessing steps are required. 

3. In the reprocessing area, a nurse or reprocessing tech must conduct both a leak test and pre-inspection of the endoscope. 

4. The internal channels of the endoscope are manually cleaned using a brush that is both the correct length and diameter. The scope’s exterior is then wiped down, preferably with a lint-free cloth, using fresh detergent that is mixed to the scope manufacturer’s set dilution. Techs must take note of the correct water temperature. 

5. Following brushing and flushing, the endoscope is rinsed to remove detergents and residual chemicals. The scope is also inspected a second time. 

6. Before loading the scope into the automated endoscope reprocessor (AER), the tech must set the unit with the correct disinfectant exposure time, which can range from 27 minutes to 30 minutes. 

7. At the end of the AER cycle, the endoscope is removed and again inspected, both to ensure the integrity of the device and that the channels are dry. Some facilities might elect to do additional air purging. 

8. After ensuring the endoscope is dried, or in the process of being dried, the instrument is tagged that is has been processed and is ready for patient use. The scope is then placed into a storage cabinet that sends HEPA-filtered air through its channels.

For Mr. Collins, handwashing is an added and unequivocal ninth step. “Hand hygiene must be effectively carried out,” he says.     

Rose Quinn

Mr. Meyers believes GI professionals who advocate for the safety of patients will back the changes. “That is not to say there aren’t challenges involved in making them happen,” he says. “Many accrediting bodies have adopted these practice changes and that posed a challenge for some facilities because of the capital expenses involved.” While there is always a little resistance when finances are involved, he says, “Overall, everyone understands the importance of these process improvements.”

While strict adherence to standard but constantly evolving evidence-based steps in a flexible endoscope reprocessing program is essential to reducing cross-contamination risks, Mr. Collins believes any infection prevention program is only as effective as the individuals who back, teach and implement it.

“First and foremost, we have to start with education and training,” he says. “We need to ensure that our reprocessing staffs are keenly aware of the correct instructions for use to properly process the endoscopes they have in their inventory, and that they have support of facility leadership.”

In his training, Mr. Collins stresses the importance of each step in the cleaning and high-level disinfecting process, and that every step deserves equal attention. “If there is a failure anywhere in those steps, then chances are there won’t be a good outcome,” he says. “There are no shortcuts in endoscope reprocessing and sometimes steps need to be repeated.” 

Mr. Collins acknowledges that being part of an endoscope reprocessing team is a stressful job, and not always a rewarding one. “That’s why we need to build these individuals up and ensure they feel like they’re a valued team member,” he says. “I’ve always believed reprocessing techs are the heart of the GI unit because procedures can’t be performed without a clean scope.” OSM

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