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Asepsis
Absence of pathogenic microorganisms or disease
Bactericidal
A type of substance that kills bacteria and inhibits their growth and reproduction
Bioburden
Amount of organic debris on an object at any given time
Concurrent decontamination
Cleaning and decontaminating a spill or splatter on the floor while a surgical procedure is in progress
Contamination
Violation of the state of sterility
Cross Contamination
Contamination of a person, object, or environment by contact with contaminants from another source
Decontamination
Reduction of the microbial population on a surface
Disinfectant
Chemical agent that kills most microbes, but typically not spores
Event-related sterility
A package is considered sterile until opened or the integrity of packaging material is violated
Fomite
Inanimate object that harbors microorganisms, including dust, lint, droplets, and environmental surfaces
Fungicide
Agent that kills or destroys fungal organisms
HAI
Healthcare-associated infection; nosocomial infection
Indigenous microflora
Microorganisms that normally reside in body tissues (skin) or body systems
Infection
Invasion of the human body by microorganisms causing disease
Package integrity
The condition of packaging material remaining intact to prevent contamination
Pathogen
Any microbe capable of causing disease or infection
Sepsis
Infection
Spore
Resistant form of bacteria that forms a protective shell and remains dormant to survive adverse conditions
Sporicide
Agent that kills bacterial spores
Sterile
Item that has been rendered free of all living microorganisms
Sterile field
Specified area free of all microorganisms, including the incisional area and items around the patient
Sterile technique
Creating and maintaining a protected sterile field
Strike-through contamination
Occurs from the passage of fluid through a permeable sterile barrier
Surgically Clean
Mechanically cleaned and chemically disinfected but not sterile
Terminal disinfection
High-level disinfection process that renders items safe to handle before sterilization
Terminal sterilization
Mechanical dual decontamination and sterilization method that renders unwrapped items safe to handle prior to packaging
Transient microflora
Microorganisms that temporarily reside on body tissues or systems
Vector
Living carrier or host that transmits disease to another host
Virucide
Agent that destroys viruses
Wicking action
Absorption and spreading of a fluid through a porous or permeable material
Environmental Decontamination
Goal of minimizing microbial population counts in the OR environment to reduce the potential for SSIs for patients
Furniture
All furniture surfaces including legs, casters, and wheels are wiped down.
OR table
Table in the operating room thoroughly cleaned, including wheels.
Mattress pads
Pads removed and wiped down completely.
Patient positioning attachments
Attachments used during procedures are cleaned.
Equipment
Tables, stools, kick buckets, anesthesia machine, ESU, and suction unit cleaned and disinfected.
Horizontal surfaces
Cabinet shelves, doors, and handles are cleaned.
Disinfectant solution
Solution used to wet or flood the floor for cleaning.
Substerile rooms
Rooms for storage cleaned.
Stretchers
Equipment for patient transport cleaned.
Scrub sinks
Sinks requiring special cleaning due to heavy use.
Hallway floors
Floors cleaned similarly to OR floors.
Ceilings, walls, floors
Thorough cleaning inside and outside individual ORs.
Mounted lighting fixtures
Lighting fixtures in the OR cleaned.
Air vents and duct grills
Vacuumed to remove bacteria-containing dust.
Supply cabinets
Inside and outside surfaces, including shelves, are cleaned.
Sterile supply rooms
Rooms for storing sterile supplies are cleaned.
Housekeeping supply rooms
Rooms for storing housekeeping supplies are cleaned.
Dirty cases
Additional disinfection practices for cases involving patients with active COVID-19 infections.
Basin with sterile water
Used to soak and clean instruments within the sterile field.
Saline solution
Avoid using saline to prevent pitting and corrosion of instrument surfaces.
Enzymatic solution
Used to remove and destroy proteinaceous materials from instruments.
Lipolytic enzymatic cleaner
Removes fatty materials such as adipose tissue and bone marrow from instruments.
Detergent solutions
Cidezyme is an enzymatic cleaner for removing organic debris from surgical instruments.
Enzymatic foam
Sprayed over instruments to aid in breaking down proteinaceous debris.
Case cart system
Efficient method for transporting surgical equipment, supplies, and instruments.
Chelation
Process of binding minerals in the solution to prevent deposits on instrument surfaces.
Emulsification
Action of dispersing two liquids not capable of being mixed to break down organic soil.
Ultrasonic cleaning
Some solutions are specifically for use in ultrasonic cleaners to enhance wetting ability.
Manual cleaning
Detergent solutions used for manual cleaning, creating friction to remove soil and bioburden.
Washer-decontaminator
Liquid solution available in different pH levels for cleaning surgical instruments.
Moderate-pH product
Low-level alkaline product that may be combined with surfactants and chelating agents, safe for use on stainless steel instruments but could harm the chromium oxide layer.
High-pH product
Effective for removing heavy soil, but can be corrosive to stainless steel and requires neutralization with a rinse to prevent damage.
Three-sink arrangement
Manual cleaning setup involving a wash sink with detergent, intermediate rinse with distilled water, and final rinse with distilled water.
Rigid Endoscopes
Type of endoscope requiring thorough cleaning of channels, holes, and joints to remove blood and debris.
Flexible Endoscopes
Type of endoscope that must undergo immediate pre-cleaning after use to prevent microbial biofilm formation.
Ultrasonic cleaner
Utilizes cavitation with high-frequency sound waves to dislodge particles from instruments, not suitable for narrow channels.
Washer-disinfector (WD)
Machine for cleaning instruments that may require manual or automatic detergent addition, followed by rinse, wash, sterilization, lubrication, and drying phases.
Central Sterile Processing Department (CSPD)
Ensures adherence to AAMI standards, monitors cycle parameters, tests for residual soil, and oversees personnel competencies for consistent practices.
Creutzfeldt-Jakob Disease (CJD)
A rare, fatal neurodegenerative disorder caused by abnormal prion proteins, requiring special handling and reprocessing of contaminated instruments.
Prions
Resistant to typical sterilization methods
Iatrogenic transmission
No cases reported since 1976
Central nervous system (CNS)
Involves surgical procedures potentially transmitting prions
Corneal grafts
Potential transmission source for prions
Steam sterilization
Method used after soaking instruments in sodium hypochlorite or sodium hydroxide
CDC and WHO guidelines
Established for handling instruments potentially contaminated with prions
Lubrication
Process of lubricating instruments before sterilization
Nonwoven materials
Single-use wrappers for sterilization, fluid-resistant but not impervious
Woven textiles
Reusable materials like linen or muslin for sterilization wrappers
Sterilization packaging criteria
Includes ease of opening, strength, barrier efficiency, and material safety
Peel packs and pouches
Used for sterilizing surgical instruments in healthcare facilities
Instruments pouches
Positioned to ensure proper sterilant penetration, with sharp edges protected by sterilant-permeable covers.
Double peel-packing
Used for heavy or complex items, focusing on air removal and sterilant access.
Rigid instrument containers
Reusable, made of materials like anodized aluminum, stainless steel, or plastic, providing secure containment during sterilization.
Sterilization recommendations for rigid containers
Include sterilization below absorbent items, extended drying phase, and pre-vacuum sterilization for better air removal.
Key principles for wrapper packaging
Include size restrictions, double thickness for bacterial protection, and inspection for holes, tears, and seal integrity.
Instrument sets density
Should not be overly dense to ensure sterilant penetration and drying, generally accepted weight limit is 25 pounds.
Preparation of Instrument and Basin Sets
Involves inspection, reassembly, and preparation steps to ensure proper sterilization and functionality.
Steam Sterilization
Utilizes moist heat in the form of saturated steam under pressure within an enclosed environment to destroy all microorganisms.
Critical Steam Sterilization Parameters
Include time, contact, temperature, moisture, and pressure to ensure effective sterilization.