DENT 1103 Unit 4

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61 Terms

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Sequential steps for instrument processing

1. transport

2. cleaning (pre-cleaning)

3. packaging

4. sterilization

5. storage

6. delivery

7. quality assurance program

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Transport step for instrument processing

- contaminated instruments transported to processing area in a way that minimizes the risk of exposure to persons using proper PPE

Instruments are transported to --> contaminated area

- disposable items are disposed as contaminated waste

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Cleaning step for instrument processing

Removes as must bioburden as possible

- done with hands-free mechanical process (ultrasonic cleaner or instrument washer

If they cannot be cleaned immediately use holding solution

- thoroughly cleaning all visible contaminated before sterilization 

- hand scrubbing is the least desirable method

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Packaging step for instrument processing

- instruments packaged in contaminated area with chemical indicator placed inside packaging

- instruments are dry (using lint free cloth if wet)

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Sterilization step in instrument processing

- kills all microbes

- follow manufacturer's instructions 

- never overload sterilizer, place packages on edges in single layers or racks to increase circulation of steam around instruments

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Storage step for instrument processing

- store sterilized packages in clean dry environment 

- rotate so oldest sterilized dates be used first

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Delivery step for instrument processing

- deliver to point of use in a way that maintains sterility of instruments

- open package in front of client

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Quality assurance program for instrument processing

- includes training, record keeping, maintenance, and use of biologic indicators

- records of equipment maintenance checks, biological spore tests

- exposure incidents must be recorded 

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Ideal processing/ sterilization room

- centrally located and easy access from all client care areas

- dedicated only to instrument processing

- should not be part of common walkway (not have a door or window that opens to the outside)

- good air circulation

- air line ad vacuum line for flushing high-speed handpieces

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Workflow pattern for processing instrumnets

Should be processed in a single loop:

dirty --> clean --> sterile --> storage , without doubling back 

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Areas for processing isntrumnets

1. contaminated area

2, packaging area

3. sterilizing area

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Contaminated area

the initial receiving area

- instruments are held here for processing 

- cleaning done here before disinfection and sterilizing (use holding solution if can't be cleaned immediately)

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Items in contaminated area

utility gloves, counter space, sink, waste disposal container, holding solution, ultrasonic cleaner (use gown while in use), eye wash station

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Packaging area

arrange set ups & wrapping instruments before sterilizing, insert indicators in packaging

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Items in packaging area

lint free cloths, supplies for wrapping, indicator strips

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Sterilizing area

"clean" area where packages are sterilized and packs are stored and assembled on trays

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Items in sterilizing area

sterilizers, record keeping, fresh disposable supplies

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Equipment located in contaminated area

- holding solution

- pre cleaning instrument methods (items for hand scrubbing, ultrasonic cleaner)

- automated washer

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Holding solution use

used only if contaminated instruments can't be cleaned/processed immediately after procedure

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Holding solution function + aspects

- prevents drying of blood and debris on instruments 

- non-corrosive liquid (may use dishwasher detergent)

- container must be lid and labelled biohazard and chemical 

- changed at least twice daily or more frequently if cloudy

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Hand scrubbing

method of pre-cleaning instruments

- least desirable method requiring direct contact with contaminants

- goggles and gloves must be used

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Precautions for hand scrubbing

- clean only one or two instruments at a time (use long-handled brush)

- ensure you can see sharp ends when scrubbing

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Ultrasonic cleaner

method of pre-cleaning instruments

- uses ultrasonic sound waves that cause cavitation (bubbles) that when they burst by implosion, they remove debris from instruments

- instruments should be processed until they are visibly clean (10-15 mintues)

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Care for ultrasonic cleaner

- solution affects the function, must be discarded at least once a day: have an automatic drain eliminating contact to pour contaminated solution in sink

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Solution for ultrasonic cleaner

- always refer to manufacturer's instructions 

- some have antimicrobial activity preventing build-up of microbes but doesn't disinfect instruments

- do not use other chemicals like disinfectants which can fix blood and debris onto instruments 

- must be discarded at least once a day or sooner

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Automated washer

- the first place contaminated instruments go, like a dishwasher

- combination of very hot water and detergent to remove organic material

- classified as thermal disinfectors - machine has disinfecting cycle that subjects the instruments to a level of heat that kills most microorganisms 

- come out thoroughly dry, use lint free cloth if not

- instruments are then wrapped and sterilized

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Procedures performed in packaging area 

First load of the day: PCD with Biological monitoring

- packaging instruments 

- process indicators

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PCD

process challenge device

- used in the first load of the day for sterilizer placed in the hardest to each place indicated by manufacture

- contains class V indicator and biological indicator

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Biological monitoring

spore test - the only way to determine if sterilization has occurred and all bacteria and endospores have been killed

- used in the first load of the day inside PCD and is done daily

- want a negative result: spores have been killed sterilization was successful

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Packaging instruments 

done to protect them from becoming contaminated after sterilization 

- materials: bags, paper wraps, indicator tape, monitoring strips

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Unpackaged sterilized instruments

prone to becoming contaminated

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Process indicators

Can be physical, chemical, and biological

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Physical monitoring

Looking at gauges and readings

- temperature recorded is for chamber not inside pack

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Chemical monitoring

Use heat-sensitive chemical that changes colour when exposed to certain conditions

- Process integrators 

- Process indicators

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Process integrators for chemical monitoring

Inside the instrument packages responding to combination of pressure, temperature and time

- assures sterilizing agent penetrated package

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Process indicators for chemical monitoring

Outside instrument packages, identifying if they've been exposed to certain temperature, not measuring duration or pressure

ex. tape and colour-change markings on packages

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Various forms of instrument sterilization

- Steam sterilization - autoclave

- Chemical vapour

- Dry heat

- Liquid chemical immersion

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Steam sterilizer autoclave

sterilize by steam under pressure - heating water to generate steam, producing moist heat that rapidly kills microorganisms: cool air is pushed out as steam fills chamber and pressure increases

- temperature: 121 decrees C

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Packaging for items inside steam sterilizer autoclave

- Packaging must be porous enough to allow penetration of steam

- Cannot use solid closed trays - limits penetration of heat 

- Use distilled water: tap water has minerals that can corrode 

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Advantages of steam autoclave sterilizer

- quick and reliable (cycle ranges from 3-30 minutes)

- allows for packages or wraps 

- steam penetrates fabrics and paper

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Disadvantages of steam autoclave sterilizer

- may rust and corrode items

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Chemical vapour (chemiclave)

- Chemicals used instead of water to create vapour for sterilizing 

- Paper packaged items only, no closed container (limits penetration of heat)

Not acceptable in Canada

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Advantages of chemical vapour

- does not rust, dull or corrode metal instruments 

- large range of items can be sterilized 

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Disadvantages of chemical vapour

- requires special solution increasing cost 

- fumes from vapour require good ventilation

- damages some plastics

- takes 20-40 minutes

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Dry heat sterilizing

- sterilization by conduction: direct contact with heat source
can be static air and forced air 

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Static air in dry heat sterilizing

Like an oven heating coil on bottom of chamber and hot air rises


heat transferred from static (non-moving) air to instrument in 1-2 hours

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Forced air for dry heat sterilizing

Circulates hot air throughout chamber at high velocity 

Rapid transfer of heat energy from air to instrument

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Advantages of dry heat sterilizing

- easy to use

- no rust or corrosion

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Disadvantages of dry heat sterilizing

- longer sterilization cycles and times 

- higher temperature than steam of chemical vapour 

- damages plastics, can burn fabric and paper 

- wrapping material must be heat resistant

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Liquid chemical immersion sterilants (cold soak)

sterilization by liquid chemical soaking - chemical must be EPA registered high level disinfectant/sterilant

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Advantages of liquid chemical immersion sterilants

May sterilize heat sensitive items - rubber dam frames, x-ray film holders

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Disadvantages of liquid chemical immersion sterilants

- instruments/items must be completely immersed for up to 10 hours

- impossible to determine diminished solution (limited use life)

- solution must be prepared daily

- creates toxic film

- items must be rinsed with sterilized water then packaged and dried with sterile globes and towel

- process cannot be verified with biological indicator

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Causes of failed sterilization of instruments

- inadequate instrument cleaning

- improper packaging

- improper loading of sterilizer

- improper timing/ temperature

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Dried blood remaining on instrument

fails to sterilize instruments because of inadequate instrument cleaning

- organisms insulated from sterilizing agent

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Excessive wrap

fails to sterilize instruments because of improper packaging

- prevents sterilizing agent from penetration

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Cloth wrap in chemical vapour sterilizer

fails to sterilize instruments because of improper packaging

- absorb chemical needed for sterilization

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Closed container in steam/chemical vapour

fails to sterilize instruments because of improper packaging 

- prevents direct contact with sterilizing agent

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Overloading packages

fails to sterilize instruments because of improper loading of sterilizer

- closes down penetration increasing time for heat to reach

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Packages too close together

fails to sterilize instruments because of improper loading of sterilizer

- prevents sterilizing agent from reaching all items

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Error in timing/ interrupted cycle

fails to sterilize instruments because of improper timing/ temperature

- inssufficient time to sterilize

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Proper handling and storage of sterilized instruments

- only handle cool dry packages from sterilizer 

- handle packages as few times as possible 

- packages that are torn or wet should be repackaged and reprocessed 

- avoid crushing, bending, or compression of packages

do not handle or remove wet packages