Best Practices for Sterilization in Dental Settings

Key points

  • Instrument reprocessing requires a series of steps to assure that contaminated patient-care items are safe for reuse.
  • All procedures must be performed correctly and in the proper sequence every time.

Recommendations

CDC provides recommendations for the sterilization process in the Guideline for Disinfection and Sterilization in Healthcare Facilities (2008) as well as on page 21–25 and 42–44 of the Guidelines for Infection Control in Dental Health-Care Settings — 2003 and in the Summary of Infection Prevention in Dental Settings: Basic Expectations for Safe Care.

CDC recommends that dental health care personnel be familiar with the recommended practices for reprocessing patient-care items. Always follow manufacturer's validated Instructions for Use when reprocessing items.

Instrument classification

Patient-care items are categorized depending on the potential risk for transmission of infection.

Critical‎ items penetrate soft tissue or bone. These items have the highest risk of transmitting infections and should always be heat sterilized.

Semicritical items touch mucous membranes, like the inside of the cheeks or the gums. These items have a lower risk of transmission than critical items. Most semicritical items can (and therefore should) be heat sterilized. If they cannot tolerate heat sterilization, they should be processed using a high-level disinfectant. ‎

Noncritical items only contact unbroken skin. These items have the lowest risk of transmission. In most cases, noncritical items can ‎be cleaned and, if visibly soiled, low-level disinfected.

Safety practices

  • Before final disinfection or sterilization, always treat instruments as though they are contaminated.
  • Handle contaminated instruments carefully.
  • Minimize handling of loose contaminated instruments during transport.
  • Carry instruments in a covered container that is puncture-resistant and leak-proof.
  • Wear appropriate personal protective equipment when handling and reprocessing contaminated items or equipment.
  • Wear a face mask, eye protection or face shield, and a gown or jacket to protect against splashes.

Cleaning

Cleaning is the basic first step in all decontamination processes. Cleaning removes debris and organic contamination from instruments. Blood, saliva, and other contamination can cause the disinfection or sterilization process to fail if it is not removed.

Debris can be removed from an instrument in several ways. Dental health care personnel may scrub the instrument manually with a surfactant or detergent and water. Dental health care personnel may also use automated equipment (e.g., ultrasonic cleaner, washer-disinfector) and chemical agents. Using automated equipment can be more efficient and safer than manually cleaning contaminated instruments.

If manual cleaning is performed:

  • Use work practice controls to reduce the chance of injury from sharp objects.
  • Never reach into trays or containers holding sharp instruments that cannot be seen, such as a sink of soapy water.
  • Use a long-handled brush to keep the scrubbing hand away from sharp instruments.
  • Wear puncture-resistant, heavy-duty utility gloves.

After cleaning, instruments should be rinsed with water to remove chemical or detergent residue. Take care to minimize splashing.

Packaging

After cleaning, instruments should be allowed to dry thoroughly before they are packaged, wrapped or otherwise contained. Wet instruments can compromise the packaging material's integrity and ability to maintain sterility. Once dry, instruments should be inspected and then wrapped, packaged, or placed into container systems before heat sterilization. Packaging materials allow for penetration of the sterilization agent and maintain sterility of the processed item after sterilization.

Dental health care personnel should follow the manufacturer's instructions for packaging patient-care items. This includes following instructions for the item being sterilized, the packaging, and any sterilization equipment being used.

Unwrapped Sterilization‎

Unwrapped sterilization, sometimes called flash sterilization, is not a viable method of sterilization to be used on a routine basis and is not consistent with CDC recommendations. Flash sterilization should not be used for reasons of convenience, as an alternative to buying additional instrument sets, or to save time.

More information is available in the Guideline for Disinfection and Sterilization in Healthcare Facilities (2008) and the Guidelines for Infection Control in Dental Health-Care Settings - 2003.

Labeling

Before placing packaged instruments in the sterilizer, at a minimum, include the following information on the label:

  • Sterilizer used
  • Cycle or load number
  • Date of sterilization
  • Expiration date, if applicable

This information helps dental health care personnel retrieve items in the event of an instrument processing or sterilization failure.

Sterilization process

The majority of patient-care items in dentistry are heat-tolerant and therefore should be heat sterilized.

Follow the manufacturer's recommendations for sterilization times, temperatures, and other operating parameters for all equipment and supplies used during reprocessing. This includes correct use of containers, wraps, and chemical or biological indicators.

If the manufacturer's instructions for use are not clear, contact the manufacturer for assistance.

Keep Reading‎

For detailed information on the different types of sterilization methods, please see pages 22–24 of the Guidelines for Infection Prevention and Control in Dental Settings — 2003.

Storage

Ideally, sterile instruments and supplies should be stored in covered or closed cabinets. They should not be stored under sinks or in other places where they might become wet.

Storage practices for wrapped sterilized instruments can be either date- or event-related. For date-related shelf-life practices, sterilized packages are expiration-dated and used on a "first in, first out" basis. Event-related shelf-life practices recognize that the product should remain sterile indefinitely, unless an event causes it to become contaminated (such as torn or wet packaging).

Dental health care personnel should inspect packaging of sterilized instruments before opening and use to ensure the material has not been compromised (wet, torn, or punctured) during storage. If a package has been compromised, the contents should be reprocessed—that is, cleaned, packaged, and heat-sterilized again—before patient use.

Unwrapped Instruments‎

Once instruments are unwrapped, are handled with nonsterile gloves (such as nitrile or latex patient examination gloves), or are placed into or on non-sterile containers, instrument sterility cannot be guaranteed. Storage, even temporary, of unwrapped semicritical instruments is discouraged because it permits exposure to dust, airborne organisms, and other unnecessary contamination before use on a patient.

Special considerations

The use of heat-sensitive semicritical items that must be processed with liquid chemical germicides is discouraged. Heat-tolerant or disposable alternatives are available for the majority of such items.

If heat-sensitive instruments must be used, they can be sterilized or high-level disinfected by soaking them in a liquid chemical germicide cleared by FDA as sterilants.

However, these powerful chemicals are highly toxic and manufacturer instructions—for example, regarding dilution, immersion time, temperature, and disposal—and safety precautions for using chemical sterilants or high-level disinfectants must be followed precisely.

Education and training

This video, from CDC's Foundations: Building the Safest Dental Visit training, describes the workflow pattern for a sterilization area that ensures devices and instruments clearly flow from high-contamination areas to clean and sterile areas.

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