10 Questions
What is the main reason for ensuring that items are cleaned and disinfected according to the manufacturer's Instructions for Use (IFU)?
To prevent patient harm
Why should preparation and packing zones check for holes in wrappers and disposable filters?
To prevent damage to the sterilized items
What should be done if an instrument, wrapper, or filter falls on the floor?
Reclean the instrument, discard wrapper/filter
Why is it essential to use FDA-approved wrappers and containers for sterilization?
To comply with regulatory standards
What can happen if sterilizer carts are improperly loaded?
Damage to the sterilized items
Why is it crucial to check instruments for functionality, cleanliness, alignment, assembly, and sharpness?
To prevent patient harm
What should be ensured when loading the sterilizer carts?
Avoiding overloading the cart
Why is it necessary to follow count sheets even with extensive experience?
To avoid missing essential supplies
What could happen if the sterilizer parameters are not set properly for the load contents?
Risk of wet or nonsterile loads
Why should one never use an instrument that has fallen on the floor?
It may cause harm to patients or staff
Learn about Continuous Quality Improvement (CQI) in the context of instrument processing, involving input from various stakeholders like decontamination staff, processing employees, clinicians, and physician personnel. Discover how CQI can help in improving work processes.
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