AORN: sterilization process

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the byproducts are water and oxygen

H2O2 vapor

why is hot water not. used for cleaning

it can denature blood proteins

Reacts to two or more critical parameters; Placed inside the compatible sterilization package

multi parameter indicator

the amount of time a processed package is considered to be sterile

shelf life

what is packaged in a peel pouch

small, lightweight, low profile items

the oldest, safest, most economical and most commonly used sterilization method

steam sterilization

T or F: A chemical indicator is placed on the inside of the container

true

Which of the following are examples of aseptic practice? Select all that apply a. Use of single use items for one patient b. The sterilization of a reusable medical device for use in a clean procedure c. Use of a clean instrument for a vascular procedure d. RN circulator using clean gloves to pick up a used sponge

a. Use of single use items for one patient b. The sterilization of a reusable medical device for use in a clean procedure d. RN circulator using clean gloves to pick up a used sponge

the absence of infectious organisms

asepsis

what does an air pocket prevent pressurized steam from doing

contacting the instruments and sterilizing the trays or equipment

if a wet pack is placed on a sterile field, what is the entire field considered

contaminated

where must sterilized instruments, equipment and supplies be stored

controlled environment

what water temperature is used for cleaning

cool water

Which statement about biological indicators is FALSE? a. In the event of a positive BI result, the sterilizer is not used until the cause of the BI failure has been determined b. The BI used must be specific to the sterilization method c. A BI is run with each sterilization load that contains one or more implants d. A BI test for EO sterilization should be performed one a week

d. A BI test for EO sterilization should be performed one a week

What is the first step of instrument processing? a. Chemical disinfection b. Decontaminator cycle on washer sterilizer c. Soaking d. Cleaning

d. Cleaning

a slow burning process that causes the coagulation of proteins in microbial cells

dry heat

used on items resistant to moist heat sterilization

dry heat

T or F: Sharp and delicate instruments are placed inside a peel pack pouch to protect the tips

false

what must an individual perform after removing PPE

hand hygiene

what are often reasons for immediate use steam sterilization

lack of equipment and time constraints

what should NOT be packaged in a peel pouch

large, sharp or heavy items

what do sets weighing more than 25 pounds require

longer drying times

what is chemical sterilization also referred to as

low temperature sterilization

what follows manual cleaning

mechanical cleaning

a BI is run with each sterilization load that contained ____ implants

one or more

Reacts to one critical sterilization parameter; Placed inside the compatible sterilization package

single parameter indicator

Individual vials contain solutions that test for specific contaminants

solution vial test

Tests for the presence of air in steam sterilizing chambers

speciality indicator

the most common method of sterilization

steam

complete elimination or destruction of all forms of microbial life

sterility

T or F: The person who loaded the cart into the sterilizer is a part of the each loads documentation

true

combination of thermal and chemical actions for instrument cleaning

Washer disinfector/decontaminator

what is incubated for each BI that is run

a control BI

during surgery, what should the surfaces of instruments be wiped with

a sponge soaked in sterile water

6 required PPE

1. head cover 2. eye protection 3. mask 4. utility gown 5. fluid resistant gown 6. fluid resistant shoe covers

4 examples of chemical sterilization

1. hydrogen peroxide 2. per acetic acid 3. ethylene oxide 4. dry heat

5 aspects of sterilization cycle records

1. identification of items 2. load number 3. exposure parameters 4. operators identification 5. indicator results

10 steps to sterilization

1. point of use 2. transport to decontamination 3. cleaning 4. disinfection 5. verification of cleaning 6. inspection 7. instrument tray assembly 8. packaging 9. sterilization 10. storage

2 main types of steam sterilizers

1. pre vacuum 2 gravity displacement

6 classes of chemical indicators

1. process indicator 2. specialty indicators 3. single parameter indicator 4. multi parameter indicator 5. integrating indicators/ integrators 6. emulating indicator

4 causes of wet packs

1. sterilizer malfunction 2. storage conditions 3. incorrect loading 4. packaging errors

three physical parameters for steam sterilization

1. time 2. temperature 3. pressure

What is an appropriate action before transporting contaminated instruments from the point of use to the decontamination area? a. Keep instruments that can be disassembled in one piece b. Discard sharps into a sharps container c. Place a dry towel over instruments d. Place sharp instruments with delicate instruments

b. Discard sharps into a sharps container

What is NOT included in the record of each sterilization cycle? a. Physical, chemical and biological indicator results b. General description of the sterilization load c. Operators identification d. Exposure parameters for the sterilization method

b. General description of the sterilization load

Geobacillus stearothermophilus is a biological indicator used for ____ a. Ethylene oxide sterilizers b. Liquid peracetic acid sterilizer c. Dry heat sterilizers d. All of the above

b. Liquid peracetic acid sterilizer

Which step precedes the others? a. Disinfection b. Point of use cleaning c. Transport d. Packaging

b. Point of use cleaning

Which of the following PPE is necessary for health care workers in the decontamination area? Select all that apply a. N95 respirator b. Utility gloves c. Fluid resistant shoe covers d. Eye protection or a full face shield

b. Utility gloves c. Fluid resistant shoe covers d. Eye protection or a full face shield

The accumulation of bacteria and other biological elements

bioburden

the amount of microbial contamination on an instrument

bioburden

The accumulation of bacteria and other biological elements creates a tight adhesion to the instruments surface

biofilm

a coating of biological organisms and material tightly adhered to the surface of an instrument

biofilm

used to monitor the efficacy of the sterilizer

biological indicator

designed to detect any residual air that has been not removed during the mechanical air removal step

bowie dick test

What type of monitor is an external strip or tape? a. Physical b. Ultrasonic c. Chemical d. Biological

c. Chemical

sound waves that create vacuums that remove debris from crevices

cavitation

what type of action are cleaning solutions

chemical action

devices that test sterilization equipment or monitor the presence or attainment of one or more sterilization parameters

chemical indicators

if an item cannot tolerate high heat and moisture from steam, what are they processed through

chemical sterilization

the removal of organic and inorganic soil from equipment and instruments and the first step in the decontamination process

cleaning

what does cool water prevent

coagulation of blood on instruments

Which statement about completely submerging an instrument into the cleaning solution is TRUE? a. It increases the potential of contamination to the worker b. It increases the risk of splashes and sprays to the worker c. It reduces the need for instrument disassembly d. It reduces the risk of chemical and contaminant aerosolization

d. It reduces the risk of chemical and contaminant aerosolization

Which of the following statements about sterilization packages is TRUE? a. Large items can be peel packed as long as it fits into the pouch b. Write information on the porous side of the peel pack c. It is important to allow for billowing or gaping of the sterilization wrap d. Sterilization wraps can be reusable, woven materials or single use nonwoven materials

d. Sterilization wraps can be reusable, woven materials or single use nonwoven materials

if the IFUs for the device, sterilizer or packaging conflict or are vague, what should you follow

device manufactures IFU

when should a biological indicator test be run

each day the sterilizer is used

Reacts to all critical parameters for specified sterilization cycles

emulating indicator

is shelf life event or time related

event

verify that the package has been exposed to the sterilization process

external chemical indicators

T or F: All sterilized items should be cooled for 30 minutes before being handled

false

T or F: An items sterility is based on how long it is on the shelf

false

T or F: Cupped instruments are placed with the cup portion up

false

T or F: If one wet pack is found on a sterilization load, all packages are considered to be wet packs

false

T or F: Instruments are to be closed when placing them on a stringer

false

Designed to react to all critical elements over a range of sterilization cycles

integrating indicators/integrators

verify that one or more of the conditions required for sterilization have been met

internal chemical indicators

an item must be fully immersible to undergo this process

per acetic acid

a paper or digital readout that records the time the sterilizer reached the chosen cycles temperature, pressure and content exposure time

physical parameters

what is used in steam sterilization

pressurized, saturated steam

External indicator that distinguishes between processed and non processed items

process indicator

the complete elimination or destruction of all forms of microbial life

sterilization

what does a negative biological indicator indicate

sterilization conditions were met

Individual swabs or strips test for specific contaminants: protein, blood or carbohydrates

swab or strip test

what does biofilm inhibit

the ability of cleaning solutions and disinfectants to effectively decontaminate the instrument

what type of action is water temperature

thermal action

why is steam completely exhausted from the chamber

to avoid condensation

T or F: Documentation is necessary for each sterilization cycle

true

T or F: Instruments must be completely dry before instrument tray assembly and sterilization

true

T or F: Tray weight should be evenly distributed

true

is wet pack sterile or unsterile

unsterile

reusable, woven materials or single use, non woven material that are specific to the sterilization method and cycle; ensures that the instrument or set is completely covered and does not allow for gapping or billowing

wraps

Which of the following CIs are placed on the outside of a package or container? a. Class 1: process indicator b. Class 2: specialty indicator c. Class 3: single parameter indicator d. Class 4: multi parameter indicator

a. Class 1: process indicator

Which of the following is NOT done when assembling an instrument tray? a. Instruments are damp when placed in a container or wrapped b. Instruments are counted as they are placed in a tray c. Instruments are opened when being placed on a stringer d. Instruments are placed with heavier instruments on the bottom

a. Instruments are damp when placed in a container or wrapped

Inspection and testing evaluates an instrument for ____. Select all that apply a. Integrity of cables and cords b. Sharpness c. Cleanliness d. Alignment

a. Integrity of cables and cords b. Sharpness c. Cleanliness d. Alignment

Which of the following cleaning and decontamination tests reports on blood, protein and carbohydrates? a. Specific strips or swabs b. Specific solution vials c. ATP test d. All of the above

a. Specific strips or swabs

methods by which microbial contamination is prevented

aseptic technique

Which IFU is followed if there is conflicting or vague information about the sterilization of an item? a. Sterilizer manufacturers IFU b. Device manufacturers IFU c. Packaging manufacturers IFU d. Assembly manufacturers IFU

b. Device manufacturers IFU

aeration is a critical step

ethylene oxide

Tests for ATP, which is present in all organic material

ATP test

absence of pathogenic microorganisms

asepsis

what must an instrument set not weigh more than

25 pounds

cooling times for trays

30 minutes to 2 hours


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