Table B: Standard Recommendations for Flash Sterilization
Table B: Standard Recommendations for Flash Sterilization
CHARACTERISTICS OF ITEM(S) TO BE STERILIZED
GRAVITY
VACCUME
Nonporous
Non-Lumened
3 minutes @270°F (132°C) with no weight restrictions, load size restrictions, or density restrictions
Instruments must be properly decontaminated.
3 minutes @270°F with no weight restrictions, load size restrictions, or density restrictions. Instruments must be properly decontaminated
Porous
Lumened
Mixed Loads
10 minutes @270°F with no weight restrictions, load size restrictions, or density restrictions. Instruments must be properly decontaminated
4 minutes @270°F with no weight restrictions, load size restrictions, or density restrictions. Instruments must be properly decontaminated
Complex Instrumentation
Power Instrumentation
Special Substances
Please see Table D. Comply with manufacturers recommendations. Observe not only the sterilization parameters, but also adhere to drying recommendations and cool down protocols to prevent instrument damage. Never immerse, wrap in a moist towel, or run a hot power instrument in an attempt to cool it down. This will lead to premature ware to motor and bearings.
Generally a much shorter cycle. Please see Table D. Comply with manufacturers recommendations. Observe not only the sterilization parameters, but also adhere to drying recommendations and cool down protocols to prevent instrument damage. Never immerse, wrap in a moist towel, or run a hot power instrument in an attempt to cool it down. This will lead to premature ware of motor and bearings.
Implants
Not Recommended. If necessary, use a 10 minute cycle @ 270° F. You must run a biological indicator with the implant and report any adverse readings to the surgeon and infection control.
Not Recommended. If necessary, use a 4 minute cycle @ 270° F. You must run a biological indicator with the implant and report any adverse readings to the surgeon and infection control.
Record Keeping for Flash Sterilization.
Document the following for each cycle
1. The patients name or hospital ID
2. The load contents
3. The type and identification # of the autoclave
4. The parameters of the cycle used:
a. Cycle type: Gravity or Vacuum
b. Exposure time
c. Temperatures
5. The date and time of the cycle
6. Results of any internal chemical or biological indicators.
Document the following for each cycle
1. The patients name or hospital ID
2. The load contents
3. The type and identification # of the autoclave
4. The parameters of the cycle used:
a. Cycle type: Gravity or Vacuum
b. Exposure time
c. Temperatures
5. The date and time of the cycle
6. Results of any internal chemical or biological indicators.
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