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Hundreds of tax deductions that could be filed and claimed go unaccounted for each year. Unfortunately, it is just because people do not realize that they can take them that they do not. Yet, there are many ways in which you can insure that you are getting the most from your filing status, your business and you personal situation. Getting the most out of your tax deductions is all about knowing what is available.e spore strip is aseptically removed from its protective envelope and placed in a tube of culture media. It is then incubated for 7 days. For each of the 7 days, the tube of culture media is inspected for cloudiness.

If the spores are live and have not been killed, cloudiness is noted in the culture media. If no cloudiness is noted in the culture media, then sterilization is confirmed.

The most common reason for the test to fail is not due to mechanical failure, but is actually due to operator error. If your autoclave has failed the spore test, this is a good time to review your sterilization procedures with your staff. Observe the technician who is responsible for sterilizing the hand pieces and/or instruments and look for the following problem areas:

• Is the autoclave being overloaded? Refer to the manufacturers specifications and make sure the technician is not putting in too many items at one time.

• Is the right temperature being achieved and maintained? Inadequate Temperature: Set the temperature control knob so that it reaches and maintains 270-degrees. Check on it periodically during the cycle to make sure this temperature is not fluctuating more than a couple of degrees.

• Is the right amount of pressure being reached and maintained? Inadequate Pressure: The chamber pressure should be maintaining approximately 30psi (or manufacturer specifications).

• Is the cycle being allowed to run for the right amount of time? Inadequate Time: The normal processing cycle varies somewhat by the autoclave manufacturer. Follow the manufactures guidelines. Shortening the cycle endangers everyone, so don’t.

• Improper packaging of instruments (follow manufacturers recommendations)

If any of the above shortcuts are being taken because the autoclave cannot keep up with your demand, it is time to either increase your inventory of handpieces and/or instr

al failure, but is actually due to operator error. If your autoclave has failed the spore test, this is a good time to review your sterilization procedures with your staff. Observe the technician who is responsible for sterilizing the hand pieces and/or instruments and look for the following problem areas:

• Is the autoclave being overloaded? Refer to the manufacturers specifications and make sure the technician is not putting in too many items at one time.

• Is the right temperature being achieved and maintained? Inadequate Temperature: Set the temperature control knob so that it reaches and maintains 270-degrees. Check on it periodically during the cycle to make sure this temperature is not fluctuating more than a couple of degrees.

• Is the right amount of pressure being reached and maintained? Inadequate Pressure: The chamber pressure should be maintaining approximately 30psi (or manufacturer specifications).

• Is the cycle being allowed to run for the right amount of time? Inadequate Time: The normal processing cycle varies somewhat by the autoclave manufacturer. Follow the manufactures guidelines. Shortening the cycle endangers everyone, so don’t.

• Improper packaging of instruments (follow manufacturers recommendations)

If any of the above shortcuts are being taken because the autoclave cannot keep up with your demand, it is time to either increase your inventory of handpieces and/or instr

temperature being achieved and maintained? Inadequate Temperature: Set the temperature control knob so that it reaches and maintains 270-degrees. Check on it periodically during the cycle to make sure this temperature is not fluctuating more than a couple of degrees.

• Is the right amount of pressure being reached and maintained? Inadequate Pressure: The chamber pressure should be maintaining approximately 30psi (or manufacturer specifications).

• Is the cycle being allowed to run for the right amount of time? Inadequate Time: The normal processing cycle varies somewhat by the autoclave manufacturer. Follow the manufactures guidelines. Shortening the cycle endangers everyone, so don’t.

• Improper packaging of instruments (follow manufacturers recommendations)

If any of the above shortcuts are being taken because the autoclave cannot keep up with your demand, it is time to either increase your inventory of handpieces and/or instr

allowed to run for the right amount of time? Inadequate Time: The normal processing cycle varies somewhat by the autoclave manufacturer. Follow the manufactures guidelines. Shortening the cycle endangers everyone, so don’t.

• Improper packaging of instruments (follow manufacturers recommendations)

If any of the above shortcuts are being taken because the autoclave cannot keep up with your demand, it is time to either increase your inventory of handpieces and/or instruments, or to get an autoclave that processes them faster A question I am frequently asked is If the Chemical Monitoring is Sufficient?

CHEMICAL MONITORING uses heat sensitive chemicals (not spores) to assess the physical conditions during the sterilization process. Chemical monitoring involves the use of indicators that change color when exposed to certain temperatures. Examples include autoclave tape, special markings on bags and pouches, and, chemical indicator strips, tabs or packets.

If a chemical indicator changes color, has sterilization taken place?

No... a chemical indicator only assesses the physical conditions (e.g., temperature) present during the cycle. When a sterilizer reaches the required temperature, it causes the chemical indicator to change color; however, it does not indicate how long the temperature was maintained.