Sterilization destroys all microorganisms on the surface of stuff or in
a fluid to prevent disease transmission when using that item.
Steam
sterilization is moist heat in the form of saturated steam under pressure,
which is the most widely used and the most dependable method for sterilization.
Steam sterilization is nontoxic, inexpensive, rapidly microbicidal, sporicidal,
rapidly heats and penetrates fabrics. However, steam sterilization has some deleterious effects on
some materials, such as corrosion and combustion of lubricants associated with
dental handpieces.
The basic principle of steam sterilization is to
expose each item to steam with direct contact at the required temperature and
pressure for the specific time. Thus, there are four parameters of steam
sterilization: steam, pressure, temperature, and time. The ideal steam for
sterilization is dry saturated steam and entrained water. Pressure is the main
aid for obtaining the high temperature necessary to quickly kill microorganism.
Specific temperature must be obtained to ensure the microbicidal activity. Two
common steam-sterilizing temperatures are 121°C and 132°C. These temperatures
must be maintained for a minimum period to kill microorganisms. Generally, the
sterilization times at constant temperature vary depending on the type of item
and the sterilizer type.
There are two basic types of steam sterilizer
autoclaves, the gravity displacement autoclave and the high-speed prevacuum
sterilizer. The minimum exposure time for sterilization of wrapped healthcare
supplies are 30 minutes at 121°C in a gravity displacement sterilizer or 4
minutes at 132°C in a prevacuum sterilizer.
For the gravity displacement, steam comes out at the top or the side of the sterilizing chamber. Since the steam is lighter than air, it forces air out the bottom of the chamber through the drain vent. The gravity displacement autoclaves are primarily used to sterilize laboratory media, water, pharmaceutical products, regulated medical waste, and nonporous articles whose surfaces have direct steam contact.
The high-speed prevacuum sterilizers are similar to the gravity displacement sterilizers, except they has vacuum pump to remove the air from the sterilizing chamber and load before the steam is admitted. The advantage of using prevacuum sterilizer is that it is nearly instantaneous for the steam to penetrate into porous loads.
For the gravity displacement, steam comes out at the top or the side of the sterilizing chamber. Since the steam is lighter than air, it forces air out the bottom of the chamber through the drain vent. The gravity displacement autoclaves are primarily used to sterilize laboratory media, water, pharmaceutical products, regulated medical waste, and nonporous articles whose surfaces have direct steam contact.
The high-speed prevacuum sterilizers are similar to the gravity displacement sterilizers, except they has vacuum pump to remove the air from the sterilizing chamber and load before the steam is admitted. The advantage of using prevacuum sterilizer is that it is nearly instantaneous for the steam to penetrate into porous loads.
Moist heat destroys microorganism by irreversible
coagulation and denaturation of enzymes and structural proteins. The presence
of moisture significantly affects the coagulation temperature of protein and
the temperature at which microorganisms are destroyed.
Steam sterilization should be used to sterilize all
possible critical and semicritical items those are heat and moisture resistant.
Furthermore, steam sterilizers also are used in healthcare facilities to
decontaminate microbiological waste and sharps containers but sterilizer these
items with gravity displacement sterilizer require additional exposure time.
Flash sterilization is a type of steam sterilization use to sterilize an
unwrapped object at 132°C for 3 minutes at 27-28 lbs. of pressure in a gravity displacement
sterilizer. Flash sterilization usually uses for cleaning patient-care items
that cannot be wrapped, sterilized, and stored before use. It can also uses for
sterilizing an item that does not have enough time to sterilize by package
method. However, flash sterilization is not recommended for implantable devices
because the potential for serious infections.
Ethylene oxide (ETO), as a low-temperature sterilant, has been used
process for sterilizing temperature- and moisture-sensitive medical devices and
supplies in health care establishment. There are two types of ethylene oxide
sterilizers, mixed gas and 100% ethylene oxide. Ethylene oxide sterilizers
combined ethylene oxide with a chlorofluorocarbon (CFC) stabilizing agent.
However, there are several disadvantages about chlorofluorocarbon. It has
scientific evidence linking it to destruction of the earth’s ozone layer. Fortunately, there are alternative
technologies to ethylene oxide with chlorofluorocarbon that be cleared by the
FDA for medical equipment include 100% ethylene oxide; ethylene oxide with a
different stabilizing gas, such as carbon dioxide or
hydrochlorofluorocarbons (HCFC) ; submersion in peracetic acid; hydrogen
peroxide gas plasma; and ozone.
Hydrogen peroxide (H₂O₂) gas plasma is a new sterilization technology by producing free radicals within a plasma field that are able to interact with essential cell components and thereby disrupt the metabolism of microorganism. Hydrogen peroxide gas is used to sterilize materials and devices that cannot tolerate high temperatures and humidity, such as plastics, electrical devices, and corrosion- susceptible metal alloys. This method has been compatible with most medical devices and material tested.
After these items are cleaned, dried, and inspected, they must be wrapped or placed in rigid containers and should be arranged instrument trays before sterilization.
Hydrogen peroxide (H₂O₂) gas plasma is a new sterilization technology by producing free radicals within a plasma field that are able to interact with essential cell components and thereby disrupt the metabolism of microorganism. Hydrogen peroxide gas is used to sterilize materials and devices that cannot tolerate high temperatures and humidity, such as plastics, electrical devices, and corrosion- susceptible metal alloys. This method has been compatible with most medical devices and material tested.
After these items are cleaned, dried, and inspected, they must be wrapped or placed in rigid containers and should be arranged instrument trays before sterilization.
The guidelines mention that hinged instruments should be
opened; items with removable parts should be disassembled unless the device
manufacturer provide specific instructions; complex instruments should be
prepared and sterilized according to device manufacturer’s instructions;
devices with concave surfaces should be positioned to help water drain; heavy
items should be positioned not to damage brittle items; and the weight of the
instrument set should be based on the design and density of the instruments and
the distribution of metal mass. Further, there are several methods to maintain
sterility of surgical instruments, including rigid containers, peel-open
pouches, roll stock or reels and sterilization wraps. The packaging
material must allow penetration of the sterilant, provide protection against
contact contamination during handling, provide an effective barrier to
microbial penetration, and maintain the sterility of the processed item after
sterilization. The key points of ideal sterilizeation
wrap are successful barrier, penetrability, aeration, ease of use,
drapeability, flexibility, puncture resistance, tear strength, toxicity, odor,
waste disposal, linting, cost, and transparency.
The loading procedures must be able for free circulation of steam around each item. Furthermore, there are several important basic principles for loading a sterilizer, such as allow for proper sterilant circulation; perforated trays should be placed so the tray is parallel to the shelf; non perforated containers should be placed on their edge; small items should be loosely placed in wire baskets; and peel packs should be placed on edge in perforated or mesh bottom racks or baskets.
The loading procedures must be able for free circulation of steam around each item. Furthermore, there are several important basic principles for loading a sterilizer, such as allow for proper sterilant circulation; perforated trays should be placed so the tray is parallel to the shelf; non perforated containers should be placed on their edge; small items should be loosely placed in wire baskets; and peel packs should be placed on edge in perforated or mesh bottom racks or baskets.
The wrapped surgical trays remained sterile for varying
periods depending on the type of material used to wrap the trays. Safe storage
time for sterile packs depend on the porosity of the wrapper and storage
conditions. For example, heat-sealed, plastic peel-down pouches and wrapped
packs sealed in 3-mil polyethylene overwrap can be sterile for as long as 9
months after sterilization. In addition, items wrapped in double-thickness
muslin comprising four layers can remain sterile for at least 30 days.
All of the
sterilization procedure should be evaluated the sterilizing conditions and
indirectly the microbiologic status of the processed items by using a
combination of mechanical, chemical, and biological indicators. The mechanical monitors include temperature record chart and
pressure gauge for daily assessment. The mechanical monitors for ethylene oxide
include computer printouts, gauges that provide time, temperature, and pressure
records. Chemical indicators are convenient, inexpensive, and indicate that the
item has been exposed to the sterilization process. Chemical indicator should
be used in conjunction with biological indicators, but should not replace them
because only a biological indicator consisting can measure the microbial
killing power of the sterilization process by resistant spores. Chemical
indicators are attached to each pack to show that the package has been
processed through a sterilization cycle, but these indicators do not prove
sterilization has been achieved. Chemical indicators usually are heat-or
chemical-sensitive inks, which will change color when one or more sterilization
parameters present. Biological indicators measure the sterilization process
directly by using the most resistant microorganisms, not checking the physical
and chemical conditions. If a sterilizer is used frequently, using biological
indicators everyday allow earlier discover equipment malfunctions or procedural
errors, which can minimizes the extent of patient surveillance and product
recall needed in the event of a positive biological indicator.
After the
sterilization process, medical and surgical devices should be stored with
aseptic technique in order to prevent contamination. Sterile supplies should be
stored far enough from the floor, the ceiling, and the outside walls to allow
for adequate air circulation, ease of cleaning, and compliance with local fire
codes. Also, medical and surgical supplies should not be stored in location
where they can become wet, such as under sinks. Moisture brings microorganisms
from the air and surfaces. The ideal storage is closed or covered cabinet but
open shelving can also be used for storage.
In dental clinic, not only the disinfection and sterilization of the dental
instruments are important but also clinic environment’s hygiene is a great
point to make sure of. In order to keep the hygiene of the clinic in a best
condition, regular cleaning is very important. No matter what before or after
using the clinic we have to clean and do some simple disinfection. We have few
but necessary steps to do.
1. Spray some of disinfectant or high concentration
alcohol on the paper towel.
2. Wipe the surface of whole dental chair and both
handle and control desk. (Changing different napkin paper in different parts of
is necessary.)
3. Using a bucket of diluted detergent to clean the tube
of the dental chair by step on the foot controller to let the tube suck the detergent
in the machine.
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