Take Better Care of Your Endoscopes

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These tools and tests enhance reprocessing practices and reduce cross-contamination risks.


Healthcare facilities continue to face challenges in performing safe and effective endoscope reprocessing. Is it any wonder? The complex design of endoscopes makes the devices difficult to clean, reprocessing techs must follow complicated and lengthy reprocessing directions while working in tight spaces with inadequate equipment and feel rushed or lack confidence to complete all of the reprocessing steps.

National organizations recommend visual inspection and cleaning verification of endoscopes after manual cleaning and before high-level disinfection or sterilization. Inspection and verification usually rely on your reprocessing techs abilities to identify defects and interpret spot-test results, which can sometimes lead to human error. The human factors of cleaning endoscopes get a boost by using the following technologies during routine reprocessing.

1. Borescopes

The channels of a scope, especially the biopsy/suction channel, can be damaged by the graspers or snares that are passed through during procedures. These defects can become traps for debris and cannot be seen with the naked eye. The dilemma of not being able to see inside the channel of a device that was made for visualizing channels within the human body is rather ironic.

Borescopes, a relatively new visual inspection technology in device reprocessing, can be used to identify damage or debris along the inside of an endoscope's channels. A borescope is basically a flexible scope used to see inside a flexible scope. There are a few different models on the market today, with varying lengths, image quality and price points. They're not outrageously expensive ($1,000 to $3,000), so purchasing one for your department should not be a barrier to performing this work.

You can run into trouble if your reprocessing team is not trained or educated to use a borescope and interpret what they're seeing. You should work with the borescope manufacturer to provide an in-service and training materials. Instructions and visual aids should be posted and available where the inspection takes place. If this is a new process for your department, ask your endoscope manufacturer to secure loaner equipment or expedite repairs. When implementing new testing or verification programs, it's common to discover problems with a high percentage of the fleet of devices.

2. Automated leak testers

Leak testing is important because it's used to identify areas of the scope that are damaged. Identifying leaks can prevent additional damage caused by fluid invasion during subsequent reprocessing and, most importantly, prevent fluid harbored in damaged areas from cross-contaminating patients.

Scopes that fail leak tests can have damage that was difficult to spot, or damage to an internal component that cannot be seen at all. For example, the control body contains delicate O-rings that can be disturbed, without any signs of external damage like cracks, if the scope is dropped or mishandled.

Unfortunately, leak testing is one of the most misunderstood and frequently missed steps in endoscope reprocessing. Manual dry or wet tests are common methods for leak testing, but there are several critical steps that need to be completed in order to perform them correctly.

  • Manual leak test. The scope is pressurized and manipulated while the tech observes a pressure gauge, looking for changes in pressure.
  • Wet test. The scope is pressurized and submerged in a sink of clean water. A tech manipulates the scope and looks for bubbles exiting the scope.

Both dry and wet leak tests rely on the attention and interpretation of the person performing the work. Sometimes, defects are missed. An automated leak tester can help simplify the process to make sure it's done correctly and consistently.

There are several models of automatic leak testers available. They can be expensive ($3,000 to $5,000), but the cost benefit is easily justified. Automated leak testing technology is more sensitive and consistent than using an un-aided eye to watch a pressure gauge during a dry test or searching for bubbles during a wet test.

Damage to scopes can also be caught early using an automated tester, so repairs and the costs associated with them should be relatively small, compared with damage that has to be obvious enough to catch during manual testing. Catching defects early also lowers cross-contamination risks.

3. Cleaning verification

HOLE IN NONE Automated leak testers take the human element out of identifying damaged scopes in which residual water can harbor.   |  Pamela Bevelhymer, RN, BSN, CNOR

There are several different types of tests available for verifying the effective cleaning of endoscopes, each of which use different methods to measure the presence of protein, hemoglobin, carbohydrates or adenosine triphosphate (ATP).

ATP is an organic chemical that provides energy for many different processes in cells. It's also a substrate for enzymes and is an important part of RNA synthesis. The presence of ATP, above a certain threshold, is an indicator that potentially pathogenic material still remains in the scope.

There are many options available for performing cleaning verification. Some kits may test for one or more of protein, hemoglobin and carbohydrates. This test is usually performed by flushing sterile water through a channel or swabbing a surface of a scope with a test strip to determine the presence of organic material.

ATP kits include collection materials and a bioluminescence reader, which measures the amount of ATP present using relative light units (RLUs). Cleaning verification tests are usually set to read as pass/fail, although some ATP tests report the results in RLUs, which should be clarified for a threshold of pass/fail by the manufacturer. It's important to note that after manual cleaning and before high-level disinfection, there may be some organic material present. The cleaning verification tests determine whether the amount of organic material has been reduced enough to make high-level disinfection effective and render the endoscope safe for patient use.

There is a wide variance of cost among the different tests available. Work with your infection preventionist to determine which test, or combination of tests, would be best for your facility; it's important to investigate which form of testing can be done correctly and consistently, with results that are easy to interpret. You should also develop policies and procedures for managing scopes that have failed a single cleaning verification test and those that fail multiple tests. These scopes may be damaged and harboring debris that is impossible to remove. They must be cleaned and disinfected, according to the OEM instructions or repair company's policy, and sent in for fixing.

Safer scopes

Implementing new equipment and tools to help your reprocessing techs effectively clean endoscopes is an important step toward improving patient safety. Before starting any new process, perform a risk assessment with a multi-disciplinary team, and review it routinely. It's important to define on which scopes and how frequently you'll perform enhanced reprocessing protocols.

Any cleaning verification program or enhancement to leak testing should be added to your existing reprocessing steps and done in accordance to manufacturers' instructions for use. Develop a detailed plan, including staff education, for incorporating these tools and tests into your endoscope reprocessing practices. Communicate the plan clearly to the reprocessing team, and record the results of the tests and channel inspections to identify trends and gaps. Combining all of these elements will strengthen your endoscope reprocessing program and promote safe patient care. OSM

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