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A series of questions and answers related to sterilization and disinfection practices, primarily focusing on central service departments in healthcare facilities. It covers various aspects of sterilization methods, equipment maintenance, infection control, and regulatory standards. The content is structured as a quiz, providing a quick review of key concepts and best practices in sterile processing. It is useful for technicians and healthcare professionals involved in sterile processing, offering a concise overview of essential knowledge in the field. Questions on sterilization techniques, equipment maintenance, and safety protocols, making it a valuable resource for quick reference and exam preparation. It also touches on the importance of quality control and adherence to standards in maintaining a sterile environment.
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ANS Cavita- tion
electrical cords ANS whenever the equipment is cleaned
dry heat sterilization
cleaning process. ANS False. They should all be cleaned manually.
ANS FDA food and drug admin- istration
ANS intermediate to low level disinfectants
ANS Below 43 C (110 F)
ANS must be labeled with a copy of the original manufacturer's label or a generic label that identifies hazard warnings and directions
ANS arteries
sociated infection. ANS Approximately 10%
ANS spirillum
ANS Square-fold and envelope-fold
ANS True
movement of products ANS From soiled areas to clean processing areas within central service
disinfected ANS At the beginning and end of each shift.
ANS an oxidizing agent
ANS Use an active air removal system
microorganisms ANS antiseptics
allow air removal, steam penetration and facilitate drying
ANS The inventory system that uses two identical carts to facilitate Supply replenishment is called the.
ANS In- strument
times appears on sinks and equipment ANS descaler
ANS Surgical fixation
ANS rod shaped bacteria
called ANS polymerization
serves as the foundation of a professional development plan ANS career ladder
current. ANS Ohm
control of infections and related outcomes. ANS APIC
ANS gastroscope
ANS Bufferd Iodine
ANS Class |
ANS True
conduct for your profession are called ANS ethical behavior
temperature ANS mesophiles
ANS improper cleaning
ANS iron and silicates
inner ear
steam from chamber but doesn't dry device completely ANS Drying phase of steam sterilization
load that was run at an exposure temperature of 320 degrees •F ANS 2 hours
ANS Dry steam
intended for use solely in these sterilization processes ANS low temperature
into body cells takes place ANS small intestines
cloudy
ANS decreases the likelihood of mineral scale deposits
a used in a sterilizaiton system that processes immersible instruments for immediate use ANS Paracetic Acid (PA)
satisfy factors that measure the strength and quality of nursing care viewed as one of the highest achievement a hospital can obtain
ANS Magnet status
True or False ANS False
ANS To cut out
ANS Geobacillus stearothermophilus
be positioned. ANS On the top of the basins
tically raise or lower the body temperature ANS hypothermia unit
department head ANS director
ANS should not be flash sterilized
of ANS 100%
provided by ANS the instrument manufacturer
ANS Class ll Medical Device
sterilization process and provide a direct measure of lethality are called ANS Bi- ological test
object is called ANS D-value
ANS the mechanical convection sterilizer
placed on edge
should not be placed inside of wrapped sets or containers
ANS can be counted as an asset on the facility's balance sheet
ANS Par-level system
facility ANS consignment
ANS re- turned immediately to the biomedical department
ical devices that have contributed to patient injury and/or death to the manufacturer and the FDA. ANS
instruments. ANS meet CDC and OSHA requirements
tion? ANS radio frequency identification tags (RFID)
for cleaning? ANS Deionization
Semi-critical devices.
ANS it is called a negative test
daily
they have no protective wrapping
cessing systems should ANS
ANS NFPA (national fire protection association)
ANS who
standards and ensuring their integrity ANS ANSI
ANS sterilization
provided by ANS the instrument manufacturer
run, read, record, retain
sterilant, the time required to achieve sterilization is longer than the time required to achieve high level disinfection ANS
cannot be chipped or scratched ANS False
ANS means half
ANS Do not come apart for cleaning, have mechanical/electrical components in the proximal end of the instrument, and are heavier than standard laparoscopic instruments
mental activities by outlining ANS minimal levels of quality and safety
ANS False
ANS removed from the con- tainer and lid and cleaned separately
achieve disinfection is called ANS Wet contact time
ANS During scheduled soiled pick up rounds, by staff from user departments, and in case carts
ANS should be decontaminated at least daily
in healthcare because ANS Cycles are fast and inexpensive
ANS Package integrity, an expiration date and deals and filters to be sure they are intact (all of above).
ANS Tape
neutral detergent or enzyme. ANS True
above) ANS disposable instruments should be used during the case. Heat-sensi- tive items should not be used as they will probably be destroyed during cleaning. And if reusable items are used guidelines suggest disposing of the items contam- inated with high-risk tissue.
ANS Basin sets should be placed on edge/tilted, sold containers should be placed so air can get out, there should be visible space between packs (do all of the above)
house and for items purchased sterile. ANS True
process should be ANS
ANS Between 68 and 73 degrees Fahrenheit
ANS water temper- ature
ANS Heavier instruments should be placed on the bottom of the tray
medical device being sterilized. ANS True
be monitored using chemical, physical and biological monitors. ANS True
soil. ANS Gross. Pg 125
ANS Used to remove cement
ANS a medical procedure that allows doctors to visually examine the rectum and the lower part of the colon (the sigmoid colon) using a thin, flexible tube with a camera and light. It's used to screen for colorectal cancer, diagnose symptoms like bleeding or pain, and to remove polyps.