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Instrument Processing Room

Provided by the Organization for Safety and Asepsis Procedures

April 2009 Issue - Expires April 30th, 2012

Inside Dental Assisting

Abstract

The ultimate goal of instrument processing is to provide sterile instruments for the treatment of the next patient. Sterility must then be maintained until the instruments are used, and accomplishing this goal involves six major steps: transport and presoaking, cleaning, corrosion control and packaging, sterilizing, monitoring, and storage and transport. This article details instrument processing steps and reviews some of the problems that should be monitored to ensure sterility is maintained.

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Instrument processing is one of the most important patient safety aspects of the office infection control program. In order to maintain a high level of safety, it’s important to:

  • decide upon the specific instrument processing procedures to use
  • standardize and document them in written form as Standard Operating Procedures (SOPs), which are great for training new employees and temps, and evaluating procedures
  • perform them the same way every time
  • periodically evaluate the process
  • update the system if changes occur in products, equipment, or regulations/recommendations

The ultimate goal of instrument processing is to provide sterile instruments for treatment of the next patient. It’s not enough just to clean and sterilize the instruments. Sterility (see Glossary) needs to be maintained until the instruments are placed at chairside for the next patient. Accomplishing this goal involves six major steps: transport and presoaking, cleaning, corrosion control and packaging, sterilizing, monitoring, and storage and transport. The details of instrument processing have been described in several publications.1,2 Instrument processing steps are summarized here, and a listing of some pitfalls in the process are provided under Putting It All Together.

Transport and Presoaking

The goal here is to safely gather and transport the contaminated instruments to the processing room and prepare them for cleaning. The transport needs to occur fairly quickly so the operatory can be readied for the next patient. If thorough cleaning of the contaminated instruments will be delayed, place them in the cleaning detergent so they won’t dry and be more difficult to clean.

Cleaning

Removing as much bioburden (see Glossary) as possible from the instruments will facilitate the subsequent sterilization process. Allowing some bioburden to remain will challenge the sterilization process. The Centers for Disease Control and Prevention (CDC) recommends cleaning all items before sterilization, preferably using automated cleaning equipment (eg, ultrasonic cleaner, instrument washer, thermal disinfector). In everyday life in the office, an item is considered to be clean if it looks clean.

Corrosion Control and Packaging

Carbon steel items processed in a steam sterilizer will rust. This can be retarded by using rust-inhibitors, using stainless steel instruments, or using a dry heat or unsaturated chemical vapor sterilizer for these items. Packaging the instruments before placing them in a sterilizer will maintain the sterility of the instruments after removal from the sterilizers and during storage and transport to chairside for the next patient.

Sterilization

While proper cleaning will kill and remove most microbes from the instruments, they cannot be considered sterile. To achieve this they must be exposed to extreme physical conditions that have been shown to kill the most resistant microbes. In the dental office such conditions are achieved in gravity steam sterilizers, positive steam flush/pressure pulse sterilizers, vacuum steam sterilizers, dry heat sterilizers, or unsaturated chemical vapor sterilizers. Key points to help assure success are proper loading, operation and maintenance of the sterilizer. Heat sensitive reusable items can be cleaned and processed through a liquid sterilant at an exposure time that will achieve sterilization.

Monitoring

Sterilization monitoring determines if instruments have been exposed to physical conditions known to achieve the death of all microbes. The CDC recommends mechanical, chemical and biological monitoring (see Glossary). Mechanical and chemical monitoring yield immediate results used to determine if the instruments appear to be safe to use. Biological monitoring (spore-testing) provides the main guarantee of sterilization.

Storage and Transport

Use event-related storage (see Glossary) for sterilized instruments. Store sterilized instrument cassettes and packages in a low dust area and in a manner that will not tear the packaging or allow them to become wet causing wicking (see Glossary). Check each package or cassette before transporting to chairside. If packaging is torn, don’t use those instruments. Re-clean, re-package and re-sterilize them.

Communicating for Compliance

Communication is important in any business. In the dental office it involves expressing correct information to the boss, the rest of the staff, and to patients.

Employer

Evaluate instrument processing procedures in your office and inform the boss of:

  • any new sterilization supplies or equipment that might increase the efficiency and effectiveness of the procedures
  • any SOPs for instrument processing that need to be prepared or updated
  • any non-compliance problems in regard to the CDC recommendations or OSHA rules
  • results of the mechanical, chemical, and biological monitoring; and that these have been properly documented for future reference

Staff

Continue to communicate with other staff about all infection control procedures so that all will have a good understanding of what’s going on in the office. In regard to instrument processing, consider the following suggestions.

  • Inform the staff of any new procedures, supplies or equipment that are being used for instrument processing.
  • Inform the staff of any problems with instrument processing, such as sterilization failures and finding used needles or syringes on trays brought to the instrument processing room.
  • Make sure everyone in the office knows how to read chemical indicators in and on instrument packages and what to do if one shows a failure.
  • Solicit recommendations for improvements in all the instrument processing steps including the safe transport of instruments to/from various office sites.
  • Continually reinforce the careful handling of contaminated instruments and other sharps.
  • Make sure everyone in the office knows how to handle instrument processing and other infection control questions from patients.

Patients

Some patients will be curious about what’s been done to the instruments that will be used on them. Here are some examples of what can be said about the instruments. We take your safety very seriously in this office. We:

  • carefully clean the instruments.
  • package them to protect them.
  • run them through a sterilizer at high temperatures.
  • test the sterilizers.
  • check the packages to make sure the instruments stay sterile until we unwrap them.

Putting It All Together

Avoiding the pitfalls of instrument processing will help ensure the desired end result of always having safe instruments for all patients. Consider the following pitfalls in instrument processing.

Pitfall: Intermingling of contaminated and sterile items. Results in using nonsterile instruments on patient.

  • Separate the instrument processing room from the treatment rooms to keep chances of cross-contamination low.
  • Place several signs marked “CONTAMINATED” in the instrument processing room at sites where uncleaned, cleaned, and cleaned and packaged instruments are located. Remember, nothing is considered sterile unless it has been properly cleaned, packaged AND processed through a sterilizer. Use of signs may seem simplistic, but they can really help on busy days; when temps, the doctor or sales reps may enter the processing room; and to alert housekeeping staff during their nightly cleaning.
  • Place signs marked “STERILE” at sites used for packages after they have been removed from the sterilizer.
  • Use chemical indicators (that are visible from the outside) on all packages. These will change color after processing through a properly functioning sterilizer differentiating them from packages that have not been processed through a sterilizer.

Pitfall: Dangerous handling of chemical solutions and sharp contaminated instruments. Results in injuries and potential exposure to pathogens or irritating chemicals

  • Dispose of used needles and scalpels in sharps containers at chairside to avoid a second handling in the instrument processing room.
  • Use instrument cassettes to reduce the direct handling of contaminated sharp instruments.
  • Wear heavy duty gloves if gathering up loose contaminated instruments at chairside.
  • Transport contaminated instruments to the instrument processing room in containers that allow visibility of their contents. This prevents the dangerous act of reaching blindly into a container of sharp instruments.
  • Besides the heavy duty gloves, wear masks and protective eyeglasses and clothing to prevent direct contact with contaminated items and cleaning chemicals.
  • Always use a basket or cassette rack in ultrasonic cleaners to avoid contact with the contaminated used solution when removing the processed instruments from the chamber.
  • Avoid routinely hand-scrubbing instruments. It’s too dangerous.
  • Avoid splashing when handling liquid detergents, rinsing instruments and when emptying used cleaning solution into the sink.
  • Handle instrument packages carefully and as few times as possible to avoid puncturing your hands or tearing the packaging.

Pitfall: Inadequate cleaning. Results in bioburden remaining on the instruments which can interfere with sterilization.

  • Avoid over-loading any cleaning device. Use only one or two layers of loose instruments in the ultrasonic cleaning basket. Follow the manufacturer’s directions for loading instrument washers.
  • Use a cleaning solution designed for use with dental/medical instruments. Other types of detergents may damage the instruments.
  • Fill the ultrasonic cleaner tank to about an inch from the top to assure proper cleaning throughout the chamber.
  • Make sure all instruments are submerged in the ultrasonic cleaning solution.
  • If uneven cleaning is suspected in a part of the ultrasonic tank, dip a wide piece of aluminum foil to the bottom of the tank, “zap” it for 30–60 seconds and check to see if the dents are evenly distributed over the entire submerged part. If not, a transducer may be faulty.
  • Check instruments after the cleaning process. If they are visibly clean, proceed (and consider reducing the cleaning time to be as efficient as possible). If not, check the cleaning equipment and the procedures used.
  • Rinse ultrasonically cleaned instruments/cassettes well to remove the residual cleaning solution that does contain microbes.

Pitfall: Improper packaging. Results in interference with the sterilization process or allows recontamination of the instruments after sterilization.

  • Use packaging materials that have been cleared by the FDA (Food and Drug Administration) so packaging will not be damaged during sterilization and instruments will maintain sterility after sterilization (eg, sterilization wrap, paper/plastic peel pouches, nylon plastic tubing, and certain paper bags).
  • Avoid using paper bags for heavy or sharp instruments for they may protrude through the bag.
  • Avoid using closed containers in steam or unsaturated chemical vapor sterilizers; a closed container will keep the sterilizing agent from directly contacting the surface of the items to be sterilized.
  • Avoid using paper/plastic peel pouches in a dry heat sterilizer for the plastic may separate from the paper.
  • Some blue or green sterilization wrap contains plastic material that may melt in a dry heat sterilizer.
  • Avoid using staples to seal packages. Use “autoclave” tape or heat-seal nylon plastic tubing.
  • Instrument cassettes do need to be wrapped or placed in large paper/plastic pouches.

Pitfall: Improper sterilization. Prevents the instruments from becoming sterile.

  • Use deionized or distilled water rather than tap water in steam sterilizers to avoid “water spotting” on the instruments.
  • Use FDA-cleared sterilizers and follow the manufacturer’s directions for operation and maintenance. Boiling water, bead “sterilizers,” hot oil baths, cooking ovens and toaster ovens are not considered as sterilizing systems.
  • Load the sterilizer chamber with a single layer of packages or cassettes or place them on their edges to assure adequate exposure to the sterilizing agent. Most sterilizers have racks that properly position packages.
  • Avoid handling wet packages. Dry them inside the sterilizer chamber or sterilizer cassette before removing them. This prevents wicking and reduces the chance of tearing the packaging materials upon handling.
  • Plan for obtaining a back-up sterilizer when the primary sterilizer fails.

Pitfall: Improper storage. Results in recontamination of the previously sterilized instruments.

  • Avoid the following “events” for they may damage the packaging material.
    • excessive handling
    • handling wet packages
    • sliding wrapped cassettes onto shelves
    • getting the packages wet which causes wicking
    • stacking them so those on and near the bottom become compressed
  • Check the integrity of packages before they are distributed to chairside.

Pitfall: Improper or infrequent sterilization monitoring. Results in erroneous reading of the sterilization indicators, prolongs identification of sterilization failures and may allow non-sterile instruments to be used on patients.

  • Use sterilization indicators as instructed by their manufacturers or by the sterilization monitoring service being used.
  • Use spore-test indicators before their expiration dates.
  • Place spore-tests inside of packages that are in the center of the load or wherever the sterilizer manufacturer indicates.
  • If mechanical, chemical or biological monitoring indicates a failure, stop using that sterilizer until the problem is identified and corrected.
  • Perform extra spore-testing when there are changes in sterilization equipment, personnel, supplies, and procedures or if there is a question about the sterility of a certain package or container.

Questions about sterilizing and handling instruments?

See “Resources” and read the CDC recommendations on sterilization of patient-care items3 and the Occupational Safety and Health Administration’s (OSHA) bloodborne pathogens standard in regard to prevention of sharps injuries.4

Glossary

Bioburden:

The mixture of microbes, body fluids and dental materials on instruments used in patients’ mouths.

Biological monitoring:

The use of biological indicators (ie, spore strips or spore vials containing live bacterial spores) to test the use and functioning of sterilizers––also known as spore testing. CDC recommends routine biological monitoring weekly. It should also be performed at other times when procedures, personnel, supplies or equipment changes.

Chemical monitoring:

The use of chemical indicators (ie, inks or other chemicals that change color or form when exposed to certain levels of heat or other physical conditions) to test the use and functioning of sterilizers. CDC recommends placing a chemical indicator inside of every package, and if it can’t be seen from the outside, another one is to be placed on the outside of every package.

Event-related storage:

This means that the sterilized instrument cassettes or packages can be used if no event has occurred during storage and transport that has compromised the packaging material.

Mechanical monitoring:

The documentation of readings (eg, time, temperature, and pressure) from sterilizer gauges and readouts to determine the use and functioning of sterilizers. CDC recommends mechanical monitoring of every load.

Spore testing:

The use of highly resistant bacterial spores (biological indicators) to test the use and functioning of sterilizers.

Sterility:

The absence of live microbes.

Wicking:

The drawing through of microbes from the surface to the inside of wet paper.

Practice Tips

There are several things that can be done to help ensure success and enhance safety when handling or processing contaminated instruments.

  • Avoid two-handed sharpening of contaminated scalers at chairside by supplying multiple scalers with each patient set-up. Clean, sterilize and then sharpen instruments using a sterilized stone. Sterilizing sharp instruments in a dry heat sterilizer may help reduce dulling.
  • A sterilized sharpening stone also can be taped to a countertop so that one-handed sharpening could be performed when necessary. Use instrument sharpening plastic test sticks to assess instrument sharpness as needed. If using a mechanical instrument sharpening device, follow the manufacturer’s directions for sterilization.
  • Handpieces need to be cleaned before being sterilized. The outside can be wiped or brushed with alcohol or water depending upon the manufacturer’s directions. Handpieces that need to be lubricated before sterilization also need to be purged after lubrication (“blownout” with compressed air) to remove the excess lubricant. This purging can cause the airborne spread of contaminants from inside the handpiece. Lubricate and purge the handpiece into a vacuum line or into a device capable of containing the contaminated spray.
  • Avoid using cloth as the outer sterilization wrap for it is not a good barrier to microbes and it can absorb too much steam or chemicals inside the sterilizers.
  • If it is absolutely necessary to hand-scrub the instruments, use a long-handled brush, heavy duty gloves, mask, protective eyewear and protective clothing. To avoid contaminated splatter, hand-brush the instruments while they are submerged. For safety, clean just one instrument at a time.

Around the World

Infectious Diseases Declining Worldwide

The World Health Statistics 2008 report is now available at http://www.who.int/whosis/whostat/2008/en/index.html. A key conclusion in the report is that the global burden of disease is shifting from infectious diseases to noncommunicable diseases, with chronic conditions such as heart disease and stroke now being the chief causes of death globally. WHO states that “the shifting health trends indicate that leading infectious diseases - diarrhea, HIV, tuberculosis, neonatal infections and malaria - will become less important causes of death globally over the next 20 years”. It’s not clear at this time if this change is due to fewer infectious disease deaths or more noncommunicable disease deaths.

Traveler’s Guides

The World Health Organization (WHO) indicates that more than 800 million international journeys were made in 2007. Global travel exposes many people to changes in altitude, humidity, disease agents, and temperature - all of which can lead to ill-health. Many health risks can be minimized by precautions taken before, during and after travel. WHO’s 2008 edition of International Travel and Health is now available. Chapters can be downloaded at: http://www.who.int/ith/chapters/en/index.html. The CDC has a very interesting website that provides travelers with health information about numerous worldwide destinations. Check it out at http://wwwn.cdc.gov/travel/destinationList.aspx. OSAP offers the Traveler’s Guide to Safe Dental Care which is available in English, Spanish and Portuguese at http://www.osap.org/displaycommon.cfm?an=1&subarticlenbr=55.

OSAP thanks the following companies that help to underwrite each issue of this special series of Infection Control In Practice.

A-dec—a-dec.com

Air Techniques—airtechniques.com

A.R. Medicom—medicom.com

Biotrol International—biotrol.com

ConFirm Monitoring Systems—confirmmonitoring.com

Crosstex International—crosstex.com

DentalEZ Group—dentalez.com

Dentsply—professional.dentsply.com

DUX Dental—duxdental.com

Harry J. Bosworth—bosworth.com

Henry Schein, Inc—henryschein.com

Hu-Friedy—hu-friedy.com

KaVo America—kavousa.com

Micro-Scientific—opticide.com

Midmark—midmark.com

Miele—miele.com

Nitram—nitramdental.com

North Bay/Bioscience, LLC—nbbs.com

Palmero Health Care—palmerohealth.com

Patterson Dental—pattersondental.com

SciCan—scican.com

Septodont—septodontusa.com

SmartPractice—smartpractice.com

Sultan Healthcare—sultanhealthcare.com

Total Care/Pinnacle/Metrex—kerrtotalcare.com

Q & A

Question:

Why package instruments before sterilization? Won’t the packaging material just interfere with the sterilizing process?

Answer:

If instruments are not packaged before sterilization they will become recontaminated (through contact with dust, spatter, aerosols, contaminated surfaces, hands, and moisture) when they are removed from the sterilizer and before they are delivered to the next patient. In addition, the bacterial spores used in spore testing of sterilizers are killed when they are placed inside wrapped cassettes or instrument pouches. The sterilizer cycles used for packaged instruments do operate for longer times than those for unwrapped items to ensure proper sterilization.

Resources

1. Miller, CH and Palenik, CJ: Instrument processing. In Infection Control and Management of Hazardous Materials for the Dental Team, St Louis, 3rd ed. 2005, Elsevier-Mosby, p. 191-249.

2. Bednarsh, H and Cuny, E. Instrument sterilization in dentistry. Accessed June 2008 at: http://www.rdhmag.com/display_article/290536/56/ARTCL/none/none/Instrument-Sterilization-in-Dentistry/.

3. CDC. Infection control guidelines for dental health-care settings - 2003. Accessed June, 2008 at: http://www.cdc.gov/mmwr/preview/mmwrhtml/rr5217a1.htm.

4. OSHA. Bloodborne pathogens standard. Accessed June 2008 at: http://www.osha.gov/pls/oshaweb/owadisp.show_document?p_table=STANDARDS&p_id=10051.

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Learning Objectives:

After reading this article, the reader should be able to:

  • locate detailed information on instrument processing and related CDC recommendations and OSHA rules.
  • list and understand the steps for instrument processing.
  • describe the rationale for each instrument processing step.
  • identify and correct pitfalls in instrument processing.

Disclosures:

The author reports no conflicts of interest associated with this work.

Queries for the author may be directed to jromano@aegiscomm.com.