CRCST · Cleaning, Decontamination and Disinfection · 6 min read
Point-of-Use Treatment, Soiled Transport and Sorting
- Explain the purpose, methods, and precautions associated with point-of-use treatment for surgical instrumentation.
- Describe safe transport procedures and containment requirements for contaminated medical devices traveling to the decontamination area.
- Identify proper sorting, inspection, and handling techniques for various device categories in decontamination based on manufacturer instructions for use and facility policy.
The Critical Role of Point-of-Use Treatment
Point-of-use treatment should occur during a procedure as needed and immediately afterward to prevent soil from drying; thorough cleaning follows in decontamination. The central goal of point-of-use treatment is to prevent blood, bodily fluids, and gross soil from drying on medical devices. Dried blood and organic debris become significantly more difficult to clean and remove compared to moist soil. If soil is allowed to dry, subsequent decontamination becomes harder and slower, and any residual soil left behind will compromise subsequent disinfection or sterilization. Point-of-use treatment supports thorough cleaning in decontamination, which is vital because effective sterilization cannot be assured if soil remains.
Prompt care also prevents biological complications on the surfaces of instruments. Microorganisms can begin adhering to soiled instruments very quickly after a procedure ends. Rapid point-of-use treatment and cleaning help prevent the development of a biofilm. A biofilm is a community of microorganisms enclosed in a self-produced matrix, which makes the microbes much more difficult to remove and significantly less susceptible to disinfectants. Preventing this matrix from forming protects both the instruments and future patients.
Clinical personnel carry out point-of-use treatment by removing gross soil with a water-moistened sponge or cloth in accordance with the device manufacturer's instructions for use (IFU) and facility policy. Instrument lumens should also be flushed when and as directed by the device IFU and facility policy. To keep soil moist during transit, clinical staff may apply a device-compatible point-of-use spray, foam, or gel. When permitted by the device IFU and facility policy, covering instruments with a water-dampened towel is another acceptable method. However, saline must never be used for routine point-of-use moistening or cleaning because its chloride content corrodes metal instruments.
While point-of-use treatment is an essential preliminary step, technicians must remember that it maintains moisture and removes gross debris but does not replace the decontamination process. Furthermore, liquid soaking solutions must not be used to transport soiled items due to the serious risk of liquid spills and splashes to personnel along the transport path.
Common mistakes
- Using saline at the point of use to keep instruments moist, which exposes metal surfaces to chloride and causes severe pitting and corrosion.
- Submerging power equipment, such as drills and saws, during cleaning when the manufacturer's instructions for use do not specifically permit immersion.
- Attempting to pick up an undiscarded surgical sharp in a soiled tray using gloved hands instead of utilizing a mechanical tool like forceps.
- Treating single-use medical devices as routine reusable inventory without meeting applicable regulatory requirements and facility policy.
Key points
- Point-of-use treatment occurs during a procedure as needed and immediately afterward to prevent blood and soil from drying and to help inhibit biofilm development.
- Point-of-use treatment involves gross soil removal, lumen flushing, and moistening with water, approved sprays, foams, or gels, but never saline or liquid soaking transport baths.
- Contaminated devices must travel promptly in closed, leak-proof, puncture-resistant carts or containers bearing biohazard labels or red coloring along designated low-exposure routes.
- Users must dispose of single-use sharps at the point of use; any sharps found later in decontamination must be retrieved using mechanical forceps and reported.
- Decontamination sorting separates items by immersion capability, lumen presence, ultrasonic compatibility, and delicate handling needs in accordance with the device IFU.
- Post-cleaning visual inspection, with magnification when required by the device IFU or facility policy, checks for remaining soil, damage, and corrosion; an unclean device must be recleaned before packaging.
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