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This low-level disinfectant is incompatible with soap.
Quaternary ammonium compounds
When using qlutaraldehyde, technicians should always wear latex gloves for protection
False /
When using high-level disinfectants, it is important to remember they may be deactivated by
Organic matter
In an automated washer the key source of disinfection is
Water temperature
The use of test strips to test the minimum effective concentration (MEC) in high-level disinfection solutions is required;
Each time the solution will be used
How are items that have undergone high-level disinfection (HLD) dried?
With HEPA-filtered air
Iodophors are a member of this chemical family.
Halogens
These chemicals are used on animate (living tissue) to slow the growth of microorganisms
Antiseptics
Phenolics are classified as
Intermediate to low-level disinfectants
Which of the following are classified as high-level disinfectants?
Glutaraldehyde and ortho-phthalaldehydes
Micro grind or super cut scissors are usually identified with a black handle.
True
Stainless steel jaw needle holders last longer than tungsten carbide jaw needle holders.
False
Tissue forceps have teeth
True
An acceptable method for instrument identification is:
All the above
The part of a hemostat that locks and holds it in position is called the box lock.
False
Which solution can damage surgical instrumentation?
Betadine
During instrument manufacture the process of passivation helps build a protective chromium oxide layer on each instrument’s surface.
True
The purpose of a suction style is to
Unclog the suction during surgery
To properly test the sharpness of scissors four inches or less use
yellow test material
Kerrison/laminectomy rongeurs should be tested using
an index card
The first step to inspect the insulation of a laparoscopic instrument is to
Check the collar at the distal tip
Loaner instruments should
Be decontaminated before use
Pneumatic cords are a cleaning concern because:
They are dark in color, so soil is difficult to see
Information regarding cleaning processes for endoscopes should by provided by the:
Instrument manufacturer
Which of the following statements about endoscopes is true:
Flexible endoscopes are time-consuming to clean
Powered surgical instrument batteries should be charged per the manufacturer's instructions (IFU)
Before sterilization
Robotic instruments:
May have exposed cables
After use, loaner instrumentation must be decontaminated before it is shipped out.
True
Electronic testing of laparoscopic insulation should be done
In the clean assembly area prior to cleaning
Endoscope cameras:
Should be inspected for cuts, nicks or other damage to the cable.
The U.S. Food and Drug Administration classifies sterilization packaging as a
Class II Medical Device
Which of the following is NOT an acceptable sterilization packaging material?
Canvas
When arranging paper/plastic pouches in the sterilizer, the pouches should be arranged.
Paper-to-plastic
Some plastics including formulations of spun-bounded polyolefin are intended for use solely in these sterilization processes
hydrogen peroxide (low temp).
When placing hinged instruments in an instrument tray
Unlock the handles and open the instruments
Which of the following packaging systems is required to be packaged twice and provides a second chance for sterile presentation?
Sequential flat wrapper
How often should the insulation of electrosurgical instruments be tested for integrity?
Every time the instrument is processed
Count sheets:
Provide a detailed list of tray contents
Which of the following cannot be used in an instrument set to protect delicate instruments?
Plastic peel packs
This type of chemical indicator (CI) is also called a verification indicator and is a cycle-specific indicator. It is designed to react to all critical parameters of a sterilization cycle:
Type 6
The process by which instruments are steam sterilized for immediate use is called
immediate use steam sterilization
The best way to transport item that have been processed using immediate use steam sterilization at the point of use is
Rigid container designed for IUSS
Before an item can be placed in a liquid chemical sterile processing system they must be
Cleaned
Both the Association of periOperative Registered Nurses and The Joint Commission recommend that
The use of immediate use steam sterilization be minimized or decreased.
Items to be disinfected or sterilized at the point of use must be
Properly cleaned per Manufactureer’s Instructions for Use
Which of the following statements about immediate use steam sterilization is true?
It should be used only when there is not time to process items using the wrapped method
Implantable devices
should not be immediate use steam sterilization sterilized unless there is a tracking system in place to trace the item to a patient
What is the length of time after sterilization that an IUSS item can be used?
IUSS items must be used immediately
Immediate use steam sterilization documentation should include
All the above
When transporting items that have been immediate use steam sterilized, it is required that
They be transported in such a manner that reduces the potential for contamination
When loading a steam sterilizer, basins should be
Placed on edge
The higher the bioburden on an object
The more difficult it will be to sterilize
When combining load, hard goods should be placed on the top shelves to allow for more efficient removal of the condensate.
False
Which of the following does not affect sterilization?
How the user department tells the Sterile Processing (SP) staff to sterilize it.
The weakest part of a steam sterilizer is the
door
The most common reason for steam sterilization failure is
Lack of steam contact with contents of the load
The coolest place in a steam sterilizer is the
Drain
How frequently should a sterilizer’s strainer be removed and cleaned?
Daily
One of the most frequent causes of a clogged drain screen is
Tape
A sterilizer cart can be unloaded:
When an infrared device shows that the itmes have cooled to room temperature
Why is proper training for the safe and effective use of low-temperature sterilization important?
Chemicals used to sterilize instruments have toxic properties
Aeration instructions for a medical device can be found in/on the
Device manufacturer's IFU's
To ensure successful sterilization, the sterilizer chamber should not be:
Overloaded
When an items undergoes low-temperature sterilization, what is meant by the term "material compatibility"?
There should not be changes in the device's functionality
Information about a device's compatibility with a specific sterilization process can be obtained:
In the device's IFU
Which of the following items can be sterilized by H2O2?
Telescopes
What is a permissible exposure limit (PEL)?
The maximum amount of concentration of a chemical that a worker may be exposed to under Occupational Safety and Health Administration (OSHA) regulations
Which of the following sterilization methods can permeate throughout a wide range of materials to reach recessed areas?
Ethylene oxide (EO)
EO-sterilized items are aerated to remove residual:
EO
Permissible exposure levels (PELS) for low-temperature sterilization methods are established by the
Occupational Safety and Health Agency (OSHA)
Satellite storage areas
Follow the same guidelines used in SP storage
Endoscopes that have undergone high-level disinfection
(HLD) should be stored:
Completely dry
How should sterile packages be arranged and maintained to allow for stock rotation?
First in, first out
The sterile storage process begins
When the sterilizer door is opened
Sterile storage areas should have:
Positive airflow and at least four air exchanges per hour
Following liquid chemical sterilization (LCS), items intended to be used as critical devices may be stored for
No storage time; they should be used immediately
The shelving system of choice for the sterile storage area is:
Closed
Trays that overhang shelving
Can become contaminated
The type of shelving that leaves packaging the most vulnerable is
Open
The bottom shelf of any sterile storage system should be
Solid and 8 to 10 inches from the floor
Sterile trays should
All the above
Wrapped trays should not be stacked because
It can cause holes in the wrappers
Outside shipping containers
Should be removed prior to bringing items into the sterile storage area
How long can flexible endoscopes that have undergone
HLD or liquid chemical sterilization (LCS) be stored?
According to facility policy
It is important to identify devices that have undergone
HLD or LCS as patient-ready because doing so:
Distinguishes processed devices from non-processed devices
Requires employers to have an emergency action plan whenever another osha standard requires one
OSHA 29 CFR1910.38