Strive to Standardize
By: Outpatient Surgery Editors
Published: 12/3/2024
Proper high-level disinfection demands consistent training, clear policies and a keen eye toward all potential dangers.
Most experts believe high-level disinfection (HLD) activities should be standardized but not centralized. “Centralization of disinfecting activities — especially with scopes — is not a good idea,” says Casey Czarnowski, BA, CRCST, CSPDT, CIS, CER, a sterile processing educator and consultant. “When you’re processing flexible endoscopes, this activity should start near the point of use of the scope.”
Power of policy
To standardize correctly, staff must be trained in a consistent fashion on anything that involves HLD. Most importantly, this means writing policy that covers how to clean, disinfect, dry and store a flexible endoscope. Then, conduct annual competency assessments with all staff who work with the scopes to make sure everybody is doing the same thing, consistently, no matter which step they play in the process.
“You could certainly centralize these operations, but to do it right, in my view, you’d have to buy a system that includes an entire range of products, including rigid trays, covers, liners and carts, which is a significant capital expense,” says Mr. Czarnowski. “And then you must train everyone who participates in every step of the process in how to use it. That’s why I think a decentralized concept for treating these instruments near where they are used is often the best way to go.”
That concept emphasizes the cleaning that should take place before instruments are high-level disinfected and how it impacts the HLD process. “Flushing that scope at the point of use with a bedside kit with detergent, a sponge, a syringe and a basin is a critical step in the subsequent high-level disinfection of that instrument and is incredibly important,” says Mr. Czarnowski.
Transporting fragile and expensive flexible scopes, explains Mr. Czarnowski, is not easy to do without damaging them. Always keeping them near where they are used reduces the likelihood that you’ll damage them during transport or storage. Hanging the scopes near their point of use is also helpful, because immediately placing them into a nearby drying cabinet reduces the amount of time the scope was wet inside after reprocessing, which decreases the potential for formation of biofilm. The drying and storage components of the process that take place after HLD are important. “We can’t be storing these devices in a basic office filing cabinet, which I’ve seen done,” says Mr. Czarnowski. “It must be a dedicated and IFU-provided cabinet, ideally with an active drying component, not something you bought at your local big-box hardware store.”
The Association of periOperative Registered Nurses (AORN) updated its Guideline for Manual High-Level Disinfection (HLD) this year. The updates further clarify what perioperative nurses should do to keep the manual HLD process for endoscopes and other reusable semi-critical devices consistent, efficient and safe for patients, while avoiding injuries from high-level disinfectants to patients and personnel. Included in AORN’s new and revised recommendations:
• Precleaning and transport. Perform point-of-use treatment on the device immediately after use and swiftly transport it to the decontamination area to maintain workflow efficiency.
• Enhanced communication with sterile processing staff. During handoffs with decontamination staff, clearly communicate details about what occurred with the device during and after the case, including exposure to a large amount of contaminants such as blood or difficult-to-clean products such as simethicone or radiographic medium; the pretreatment performed and its completion time; whether the device was kept moist until pretreatment; any specific conditions of the instrument to note; the presence of any reusable accessories with the device; and patient identification.
• Inspection. Visually inspect the device’s accessible internal channels using a clean borescope before HLD to identify otherwise-undetectable damage or debris.
• Verification. Conduct objective tests to confirm performance of manual cleaning before HLD at established intervals. Recommended tests include ATP, protein, carbohydrate and hemoglobin.
• Rinsing after HLD. The manufacturer’s IFU may recommend a large volume of fresh rinse water to facilitate removal of chemical residues. The basin used for this should be large enough to contain the volume of rinse water recommended in the IFU. Changing the rinse water after each use can help prevent contamination of the item after processing.
• Drying. Dry the device in accordance with the manufacturer IFU for at least 10 minutes after HLD before it goes into storage, as residual moisture on device surfaces facilitates microbial growth and biofilm formation. All accessible device channels should be dried in accordance with the IFU with pressure-regulated instrument air or high-efficiency particulate air (HEPA)-filtered air to prevent introducing contaminants that may be present in lower-quality air.
• Ergonomics. The sterile processing area should feature ergonomic elements that reduce staff discomfort, such as work surfaces and sinks at comfortable heights, space to perform cleaning with sufficient lighting for the task, and a comfortable room temperature with minimal noise.
• Personal protective equipment. Personnel performing manual HLD should wear PPE that corresponds with their degree of anticipated exposure. Because cleaning and processing devices during HLD creates splashing, staff should wear PPE with as much fluid resistance as possible for their safety. Recommended PPE includes fluid-resistant surgical masks, gowns and shoe covers or boots; face shields or eye protection such as goggles; gloves recommended by the glove and disinfectant manufacturers for use with high-level disinfectants; and respirators and aprons as recommended on the chemical safety data sheet.
AORN’s Manual High-Level Disinfection Guideline Update 2024 webinar covers it all. The on-demand webinar is free to AORN members and $11 for non-members. Visit osmag.net/AORNHLD to access it.
—Outpatient Surgery Editors
Prepared for chemical spills?
The patient safety element inherent in proper high-level disinfection is clear, but staff safety is also a critical aspect that SPD leaders must never lose sight of.
“When working with high-level disinfectants, we encounter a variety of chemicals requiring careful management to ensure safety,” says David Jagrosse, CRCST, CHL, president of David Jagrosse Consulting in Daytona Beach, Fla., and past president of the Healthcare Sterile Processing Association. “A crucial part of this process is having Safety Data Sheets (SDSs) readily available as part of your Hazard Communication Program (HazCom) or Chemical Safety Program.”
The safety sheets to which Mr. Jagrosse refers provide vital information on chemical exposure limits and spill-response protocols and must be accessible to all staff. The SDSs cover a lot of ground, all of which is critical information for facilities and their SPD staff. Mr. Jagrosse says Section 6 and its information about adequate spill-response preparation is especially important for HLD. “This section provides detailed guidance on handling chemical spills, including specific cleanup materials and procedures,” he says.
There are several key considerations facilities must factor into their spill-response preparation plan. Mr. Jagrosse stresses the importance of paying close attention to details such as the materials that a spill kit contains. “For example, if you store eight gallons of a chemical, your spill kit should be able to address a spill of equal volume,” he says. “Beware of off-the-shelf kits that may only cover minor spills, and check expiration dates on kit components regularly. HLD chemicals often require a deactivation and subsequent product to remove and dispose of the materials.” OSM