Friday, 19 April 2013

infection control guidelines for dentists

Sterilization
The sterilization section of the processing area should include the sterilizers and related supplies, with
adequate space for loading, unloading, and cool down. The area can also include incubators for
analyzing spore tests and enclosed storage for sterile items and disposable (single-use) items.
Manufacturer and local building code specifications will determine placement and room ventilation
requirements.
Sterilization Procedures. Heat-tolerant dental instruments usually are sterilized by 1) steam under
pressure (autoclaving), 2) dry heat, or 3) unsaturated chemical vapor. All sterilization should be
performed by using medical sterilization equipment cleared by FDA. The sterilization times, temperatures,
and other operating parameters recommended by the manufacturer of the equipment used, as well as
instructions for correct use of containers, wraps, and chemical or biological indicators, should always be
followed.
Items to be sterilized should be arranged to permit free circulation of the sterilizing agent (e.g., steam,
chemical vapor, or dry heat); manufacturer's instructions for loading the sterilizer should be followed.
Instrument packs should be allowed to dry inside the sterilizer chamber before removing and handling.
Packs should not be touched until they are cool and dry because hot packs act as wicks, absorbing
moisture, and hence, bacteria from hands. The ability of equipment to attain physical parameters
required to achieve sterilization should be monitored by mechanical, chemical, and biological indicators.
Sterilizers vary in their types of indicators and their ability to provide readings on the mechanical or
physical parameters of the sterilization process (e.g., time, temperature, and pressure). Consult with the
sterilizer manufacturer regarding selection and use of indicators.
Steam Sterilization.Among sterilization methods, steam sterilization, which is dependable and
economical, is the most widely used for wrapped and unwrapped critical and semicritical items that are
not sensitive to heat and moisture. Steam sterilization requires exposure of each item to direct steam
contact at a required temperature and pressure for a specified time needed to kill microorganisms. Two
basic types of steam sterilizers are the gravity displacement and the high-speed prevacuum sterilizer.
The majority of tabletop sterilizers used in a dental practice are gravity displacement sterilizers, although
prevacuum sterilizers are becoming more widely available. In gravity displacement sterilizers, steam is
admitted through steam lines, a steam generator, or self-generation of steam within the chamber.
Unsaturated air is forced out of the chamber through a vent in the chamber wall. Trapping of air is a
concern when using saturated steam under gravity displacement; errors in packaging items or
overloading the sterilizer chamber can result in cool air pockets and items not being sterilized.
Prevacuum sterilizers are fitted with a pump to create a vacuum in the chamber and ensure air removal
from the sterilizing chamber before the chamber is pressurized with steam. Relative to gravity
displacement, this procedure allows faster and more positive steam penetration throughout the entire
load. Prevacuum sterilizers should be tested periodically for adequate air removal, as recommended by
the manufacturer. Air not removed from the chamber will interfere with steam contact. If a sterilizer fails
the air removal test, it should not be used until inspected by sterilizer maintenance personnel and it
passes the test. Manufacturer's instructions, with specific details regarding operation and user
maintenance information, should be followed.
Unsaturated Chemical-Vapor Sterilization. Unsaturated chemical-vapor sterilization involves heating a
chemical solution of primarily alcohol with 0.23% formaldehyde in a closed pressurized chamber.
Unsaturated chemical vapor sterilization of carbon steel instruments (e.g., dental burs) causes less
corrosion than steam sterilization because of the low level of water present during the cycle. Instruments
should be dry before sterilizing. State and local authorities should be consulted for hazardous waste
disposal requirements for the sterilizing solution.
Dry-Heat Sterilization.Dry heat is used to sterilize materials that might be damaged by moist heat (e.g.,
burs and certain orthodontic instruments). Although dry heat has the advantages of low operating cost
and being noncorrosive, it is a prolonged process and the high temperatures required are not suitable for
certain patient-care items and devices.
Dry-heat sterilizers used in dentistry include static-air and forced-air types.
The static-air type is commonly called an oven-type sterilizer. Heating coils in the bottom or sides of the
unit cause hot air to rise inside the chamber through natural convection.
The forced-air type is also known as a rapid heat-transfer sterilizer. Heated air is circulated throughout
the chamber at a high velocity, permitting more rapid transfer of energy from the air to the instruments,
thereby reducing the time needed for sterilization.

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