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Disinfection
Process destroying most microorganisms but not reliably destroying bacterial spores.
Low-Level Disinfection (LLD)
Process destroying vegetative bacteria, some fungi, and viruses, but not spores.
Intermediate-Level Disinfection (ILD)
Process destroying vegetative bacteria, mycobacteria, most viruses, and fungi, but not spores.
High-Level Disinfection (HLD)
Process destroying all microorganisms except large numbers of bacterial spores.
Spaulding Classification
System classifying medical devices based on infection risk: critical, semicritical, noncritical.
Contact Time
The length of time a disinfectant must remain wet on a surface.
Disinfectant
A chemical agent used on inanimate objects to destroy microorganisms.
Disinfection limitation
It is used to eliminate many microorganisms, but does not reliably destroy bacterial spores.
Factors in disinfection effectiveness
Proper cleaning, correct concentration, and contact time.
Disinfection selection basis
It is selected based on the Spaulding classification of the device.
Why clean before disinfection?
Soil shields microorganisms from the disinfectant and can deactivate the chemical.
Low-level disinfection use
Commonly used for noncritical patient-care items.
High-level disinfection target
Destroys all microorganisms except large numbers of bacterial spores.
ILD vs. HLD difference
HLD kills all vegetative microorganisms and mycobacteria; ILD does not reliably kill mycobacteria.
Disinfectant instructions
Manufacturer's instructions must be followed to ensure they are used safely and effectively.
PPE in disinfection
Required to protect workers from chemical exposure.
Why is contact time critical?
Insufficient contact time prevents the chemical from killing the targeted microorganisms.
Improper disinfection risk
Can increase the risk of healthcare-associated infections (HAIs).
Stainless Steel
An alloy of iron, chromium, and other elements highly resistant to corrosion.
Martensitic Stainless Steel
Hardened, magnetic stainless steel used for sharp cutting instruments.
Ringed Instrument
An instrument with finger rings for gripping and manipulating, like scissors.
Box Lock
The hinge point or joint where two halves of a surgical instrument meet.
Ratchet
The locking mechanism on ringed instruments that holds them closed.
Passivation
Chemical process applying a protective chromium oxide layer to prevent corrosion.
Surgical instrument classification
Commonly classified based on their design or function.
Major instrument categories
Cutting, clamping, retracting, and grasping/holding instruments.
Why identify instruments correctly?
Ensures correct assembly, proper function, and prevents delays during surgery.
Instrument locking mechanism
The ratchet allows a ringed instrument to lock into place.
Instrument joint area
The box lock is the joint area where two halves meet.
Instrument inspection areas
Instrument jaws, tips, and blades must be inspected for damage and cleanliness.
Effect of damaged instruments
Can cause tissue trauma, procedural delays, or fail to function properly.
Surgical instrument handling
Should be handled carefully to prevent damage and misalignment.
Box lock processing position
Instruments with box locks should be processed in the open position.
Purpose of testing instruments
To ensure they function properly and are safe for surgical use.
Central Service role in safety
Ensures clean, sterile, and fully functional instruments reach the patient.
Microorganism
A microscopic organism, such as a bacterium, virus, or fungus.
Spore
A highly resistant, dormant structure formed by some bacteria to survive harsh conditions.
Binary fission
The primary method of asexual reproduction in bacteria.
Biofilm
A colony of microorganisms protected by an extracellular matrix that resists cleaning.
Decontamination area
The physical area where contaminated items are received, sorted, and cleaned.
Cavitation
The process in ultrasonic cleaners where low-pressure bubbles implode to dislodge soil.
Impingement
The physical force of spraying water to mechanically knock soil off instruments.
Protease enzyme
An enzymatic cleaner specifically effective against protein-based soils like blood.
Lipase enzyme
An enzymatic cleaner specifically effective against fat-based soils.
Toxic Anterior Segment Syndrome (TASS)
Acute eye inflammation caused by chemical or detergent residues on ophthalmic instruments.
Central Service (CS) / Sterile Processing Department (SPD)
The department that receives, decontaminates, packages, sterilizes, and distributes medical devices.
PPE
Personal Protective Equipment; specialized clothing or equipment worn to protect against hazards.
IFU
Instructions for Use; manufacturer's mandatory guidelines for processing medical devices.
Standard Precautions
Infection prevention practices treating all human blood and bodily fluids as infectious.
Healthcare-Associated Infection (HAI)
An infection acquired by a patient during the course of receiving healthcare.
Sterile Processing Workflow
A strict one-way flow moving from decontamination to preparation, sterilization, and storage.
Decontamination vs. cleaning
Cleaning is physical soil removal; decontamination makes an item safe to handle without PPE.
Gross soil
Visible tissue, blood, bone, or other body fluids left on surgical instruments.
Sharps
Devices or objects with corners, edges, or projections capable of cutting or piercing.
Turnover
The cycle time between the completion of one procedure and preparation for the next.
Goals of point-of-use treatment
To prevent soil drying, prolong instrument life, reduce biofilm, and protect transport technicians.
Surgical Site Infection (SSI)
An infection that occurs after surgery in the part of the body where the surgery took place.
Chain of Infection
A series of six linked steps required for an infection to develop and spread.
Asepsis
The absence of microorganisms that cause disease.
Biocidal
An activity or chemical agent that is capable of killing living organisms, especially microorganisms.
Fomite
An inanimate object that can harbor and transmit infectious agents.
Pathogen
A microorganism capable of causing disease.
Six elements of the chain of infection
Causative agent, reservoir, portal of exit, mode of transmission, portal of entry, and susceptible host.
Three primary routes of transmission
Contact, droplet, and airborne.
Medical vs. Surgical Asepsis
Medical asepsis (clean technique) limits pathogens; surgical asepsis (sterile technique) completely eliminates all microorganisms.
Standard
A recommended guideline or benchmark established by consensus or professional organizations.
Best Practice
A method or technique consistently shown to produce superior results compared to other means.
HIPAA
Health Insurance Portability and Accountability Act; federal law protecting the privacy of patient health information.
Three categories of FDA recall
Class I (high risk of death/injury), Class II (temporary/reversible risk), Class III (low risk).
Bowie-Dick Test
A test used to detect air leaks and inadequate air removal in dynamic-air-removal steam sterilizers.
Biological Indicator (BI)
A sterilization monitoring device containing viable spores used to demonstrate that sterilization conditions were met.
Chemical Indicator (CI)
A device used to monitor one or more sterilization parameters through a physical or chemical change.
Geobacillus stearothermophilus
The spore-forming microorganism used to biologically monitor steam and hydrogen peroxide gas plasma sterilizers.
Ethylene Oxide (EtO) target spore
Bacillus atrophaeus is the spore used to biologically monitor EtO sterilization.
Three parameters of steam sterilization
Saturated steam, temperature, and exposure time.
Superheated steam
Dry steam that has been heated to a temperature higher than its boiling point.
Wet pack cause
Inadequate drying time, incorrect loading, or poor steam quality.
Sterile storage temperature
Should be maintained between 68°F and 75°F.
Sterile storage humidity
Should not exceed 70% relative humidity.
Sterile storage air exchanges
A minimum of 4 air exchanges per hour under positive pressure.
Event-related sterility
Concept that sterile packages remain sterile until an event causes them to become contaminated.
Water quality in CS
Essential to prevent instrument staining, corrosion, scaling, and pyrogen reactions.
Deionised water
Water that has had all minerals removed through an ion exchange process.
Reverse Osmosis (RO)
A water purification process using a semipermeable membrane to remove impurities.