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Questions and Answers
What is a decontamination room?
What is a decontamination room?
Where soiled items are received and cleaned
What is the purpose of the prep and packaging area?
What is the purpose of the prep and packaging area?
Where cleaned items are inspected, assembled, and packaged
What occurs in the high level disinfectant room?
What occurs in the high level disinfectant room?
Where items are high-level disinfected before going to prep and packaging area
What happens in the sterilization area?
What happens in the sterilization area?
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What is the sterile storage area?
What is the sterile storage area?
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What is the function of the dispatch area?
What is the function of the dispatch area?
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What does IFU stand for?
What does IFU stand for?
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IFU's are in alignment with recommendations from ____ standards.
IFU's are in alignment with recommendations from ____ standards.
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What does PPE stand for?
What does PPE stand for?
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What is the workflow in sterile processing?
What is the workflow in sterile processing?
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Instruments should always go in a ___ to ___ order.
Instruments should always go in a ___ to ___ order.
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When leaving decontamination, you must leave all PPE behind.
When leaving decontamination, you must leave all PPE behind.
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What does CBSD stand for?
What does CBSD stand for?
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What does HIPAA stand for?
What does HIPAA stand for?
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What is a regulation?
What is a regulation?
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What is a standard?
What is a standard?
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CSPD rules follow ______ standards.
CSPD rules follow ______ standards.
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What does AAMI stand for?
What does AAMI stand for?
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What standards does AAMI have?
What standards does AAMI have?
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What does CDC stand for?
What does CDC stand for?
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What are recommended practices?
What are recommended practices?
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What does AORN stand for?
What does AORN stand for?
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What does EPA stand for?
What does EPA stand for?
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What does the EPA do?
What does the EPA do?
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What does FDA stand for?
What does FDA stand for?
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What does the FDA regulate?
What does the FDA regulate?
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The FDA regulates single-use devices.
The FDA regulates single-use devices.
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The FDA does not regulate the reprocessing of open but unused devices or pacemakers or hemodialysis.
The FDA does not regulate the reprocessing of open but unused devices or pacemakers or hemodialysis.
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What is the medical device reporting regulation?
What is the medical device reporting regulation?
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What does OSHA stand for?
What does OSHA stand for?
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What does OSHA regulate?
What does OSHA regulate?
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What is an SDS?
What is an SDS?
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What does NFPA stand for?
What does NFPA stand for?
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What does a blue diamond indicate on the fire diamond?
What does a blue diamond indicate on the fire diamond?
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What does a red diamond indicate on the fire diamond?
What does a red diamond indicate on the fire diamond?
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What does a yellow diamond indicate on the fire diamond?
What does a yellow diamond indicate on the fire diamond?
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What does a white diamond indicate on the fire diamond?
What does a white diamond indicate on the fire diamond?
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What does JC stand for?
What does JC stand for?
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How does Spalding's classification rank items?
How does Spalding's classification rank items?
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High level disinfection can kill spores.
High level disinfection can kill spores.
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Spores can only be killed by sterilization.
Spores can only be killed by sterilization.
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Should you always sterilize loaner instruments?
Should you always sterilize loaner instruments?
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What is a Class A fire?
What is a Class A fire?
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What is a Class B fire?
What is a Class B fire?
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What is a Class C fire?
What is a Class C fire?
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What is a Class D fire?
What is a Class D fire?
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What is a Class E fire?
What is a Class E fire?
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What is the fire triangle?
What is the fire triangle?
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What does PASS stand for?
What does PASS stand for?
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What does RACE stand for?
What does RACE stand for?
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Study Notes
Sterile Processing Basics
- Decontamination Room: The initial area where soiled items are cleaned.
- Prep and Packaging Area: Where cleaned items are inspected, assembled, and packaged for use.
- High Level Disinfectant Room: Dedicated space for high-level disinfection of items before they move to preparation and packaging.
- Sterilization Area: The zone where terminal sterilization of instruments occurs.
- Sterile Storage Area: Storage for sterile items until they are needed for procedures.
- Dispatch Area: The location where instruments are dispensed for use.
- IFU: Stands for Instructions for Use; essential for proper handling of medical instruments.
- IFU Alignment: IFUs must align with OSHA (Occupational Safety and Health Administration) standards.
- PPE: Refers to Personal Protective Equipment, vital for safe handling of materials.
- Workflow Components: Key steps include decontamination, prep and package, sterilization, sterile storage, and distribution.
- Instrument Handling: Items should always be organized from dirty to clean.
- PPE Protocol: All PPE must be left behind when exiting the decontamination area for safety.
Standards and Regulations
- CBSD: The Certification Board for Sterile Processing and Distribution, involved in maintaining standards.
- HIPAA: The Health Insurance Portability and Accountability Act, focusing on patient data protection.
- Regulation Definition: Laws that govern practices within the sterile processing domain.
- Standard Definition: Established norms guiding sterile practices.
- CSPD Standards: Follow AAMI (Association for the Advancement of Medical Instrumentation) standards for safety and efficiency.
- AAMI Standards: Cover essential areas such as decontamination, sterilization processes, and indicators for sterilization.
Health and Safety Organizations
- CDC: Centers for Disease Control and Prevention, provides guidelines to prevent health hazards.
- Recommended Practices: Based on scientific data and expert opinion, ensure safe and effective procedures.
- AORN: Association of Operating Room Nurses, focuses on nursing standards and practices in surgery.
- EPA: Environmental Protection Agency, regulates environmental disinfectants and manages waste from sterilization processes.
- FDA: Food and Drug Administration, oversees regulation of drugs, medical devices, and asserts control over single-use devices.
Fire and Safety Protocols
- SDS: Safety Data Sheet; crucial for understanding the risks associated with chemicals used in sterile processing.
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NFPA Fire Diamonds:
- Blue Diamond: Indicates health hazard.
- Red Diamond: Indicates flammability risk.
- Yellow Diamond: Denotes instability hazard.
- White Diamond: Provides special hazard information.
- Joint Commission (JC): Oversees compliance with health care regulations.
Disinfection and Sterilization
- Spalding's Classification: Ranks instruments as critical, semi-critical, or noncritical based on risk of infection.
- High-Level Disinfection Limitation: Cannot kill spores; sterilization is required for spore elimination.
- Loaner Instrument Policy: Always sterilize loaner instruments before use for patient safety.
Fire Safety Classifications
- Class A Fire: Involves ordinary combustible materials (wood, paper).
- Class B Fire: Involves flammable liquids (gasoline, oils).
- Class C Fire: Involves electrical equipment and materials.
- Class D Fire: Involves combustible metals (magnesium, sodium).
- Class E Fire: Involves kitchen fires from oils and fats.
Emergency Procedures
- Fire Triangle Components: Ignition source, oxygen, and fuel are necessary for a fire.
- PASS Acronym: For extinguisher use—Pull, Aim, Squeeze, Sweep.
- RACE Acronym: Emergency response steps—Rescue, Alarm, Contain, Extinguish.
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Description
Test your knowledge on the basics of sterile processing with these flashcards. Chapter 1 covers essential terms such as decontamination, prep and packaging, high level disinfectant areas, and sterilization zones. Ideal for students and professionals in the healthcare field.