HSPA Chapters 9 & 10 Reading Guide

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Last updated 6:51 PM on 6/26/26
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84 Terms

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Disinfection

Process destroying most microorganisms but not reliably destroying bacterial spores.

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Low-Level Disinfection (LLD)

Process destroying vegetative bacteria, some fungi, and viruses, but not spores.

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Intermediate-Level Disinfection (ILD)

Process destroying vegetative bacteria, mycobacteria, most viruses, and fungi, but not spores.

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High-Level Disinfection (HLD)

Process destroying all microorganisms except large numbers of bacterial spores.

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Spaulding Classification

System classifying medical devices based on infection risk: critical, semicritical, noncritical.

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Contact Time

The length of time a disinfectant must remain wet on a surface.

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Disinfectant

A chemical agent used on inanimate objects to destroy microorganisms.

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Disinfection limitation

It is used to eliminate many microorganisms, but does not reliably destroy bacterial spores.

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Factors in disinfection effectiveness

Proper cleaning, correct concentration, and contact time.

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Disinfection selection basis

It is selected based on the Spaulding classification of the device.

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Why clean before disinfection?

Soil shields microorganisms from the disinfectant and can deactivate the chemical.

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Low-level disinfection use

Commonly used for noncritical patient-care items.

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High-level disinfection target

Destroys all microorganisms except large numbers of bacterial spores.

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ILD vs. HLD difference

HLD kills all vegetative microorganisms and mycobacteria; ILD does not reliably kill mycobacteria.

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Disinfectant instructions

Manufacturer's instructions must be followed to ensure they are used safely and effectively.

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PPE in disinfection

Required to protect workers from chemical exposure.

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Why is contact time critical?

Insufficient contact time prevents the chemical from killing the targeted microorganisms.

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Improper disinfection risk

Can increase the risk of healthcare-associated infections (HAIs).

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Stainless Steel

An alloy of iron, chromium, and other elements highly resistant to corrosion.

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Martensitic Stainless Steel

Hardened, magnetic stainless steel used for sharp cutting instruments.

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Ringed Instrument

An instrument with finger rings for gripping and manipulating, like scissors.

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Box Lock

The hinge point or joint where two halves of a surgical instrument meet.

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Ratchet

The locking mechanism on ringed instruments that holds them closed.

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Passivation

Chemical process applying a protective chromium oxide layer to prevent corrosion.

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Surgical instrument classification

Commonly classified based on their design or function.

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Major instrument categories

Cutting, clamping, retracting, and grasping/holding instruments.

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Why identify instruments correctly?

Ensures correct assembly, proper function, and prevents delays during surgery.

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Instrument locking mechanism

The ratchet allows a ringed instrument to lock into place.

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Instrument joint area

The box lock is the joint area where two halves meet.

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Instrument inspection areas

Instrument jaws, tips, and blades must be inspected for damage and cleanliness.

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Effect of damaged instruments

Can cause tissue trauma, procedural delays, or fail to function properly.

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Surgical instrument handling

Should be handled carefully to prevent damage and misalignment.

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Box lock processing position

Instruments with box locks should be processed in the open position.

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Purpose of testing instruments

To ensure they function properly and are safe for surgical use.

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Central Service role in safety

Ensures clean, sterile, and fully functional instruments reach the patient.

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Microorganism

A microscopic organism, such as a bacterium, virus, or fungus.

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Spore

A highly resistant, dormant structure formed by some bacteria to survive harsh conditions.

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Binary fission

The primary method of asexual reproduction in bacteria.

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Biofilm

A colony of microorganisms protected by an extracellular matrix that resists cleaning.

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Decontamination area

The physical area where contaminated items are received, sorted, and cleaned.

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Cavitation

The process in ultrasonic cleaners where low-pressure bubbles implode to dislodge soil.

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Impingement

The physical force of spraying water to mechanically knock soil off instruments.

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Protease enzyme

An enzymatic cleaner specifically effective against protein-based soils like blood.

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Lipase enzyme

An enzymatic cleaner specifically effective against fat-based soils.

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Toxic Anterior Segment Syndrome (TASS)

Acute eye inflammation caused by chemical or detergent residues on ophthalmic instruments.

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Central Service (CS) / Sterile Processing Department (SPD)

The department that receives, decontaminates, packages, sterilizes, and distributes medical devices.

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PPE

Personal Protective Equipment; specialized clothing or equipment worn to protect against hazards.

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IFU

Instructions for Use; manufacturer's mandatory guidelines for processing medical devices.

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Standard Precautions

Infection prevention practices treating all human blood and bodily fluids as infectious.

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Healthcare-Associated Infection (HAI)

An infection acquired by a patient during the course of receiving healthcare.

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Sterile Processing Workflow

A strict one-way flow moving from decontamination to preparation, sterilization, and storage.

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Decontamination vs. cleaning

Cleaning is physical soil removal; decontamination makes an item safe to handle without PPE.

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Gross soil

Visible tissue, blood, bone, or other body fluids left on surgical instruments.

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Sharps

Devices or objects with corners, edges, or projections capable of cutting or piercing.

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Turnover

The cycle time between the completion of one procedure and preparation for the next.

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Goals of point-of-use treatment

To prevent soil drying, prolong instrument life, reduce biofilm, and protect transport technicians.

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Surgical Site Infection (SSI)

An infection that occurs after surgery in the part of the body where the surgery took place.

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Chain of Infection

A series of six linked steps required for an infection to develop and spread.

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Asepsis

The absence of microorganisms that cause disease.

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Biocidal

An activity or chemical agent that is capable of killing living organisms, especially microorganisms.

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Fomite

An inanimate object that can harbor and transmit infectious agents.

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Pathogen

A microorganism capable of causing disease.

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Six elements of the chain of infection

Causative agent, reservoir, portal of exit, mode of transmission, portal of entry, and susceptible host.

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Three primary routes of transmission

Contact, droplet, and airborne.

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Medical vs. Surgical Asepsis

Medical asepsis (clean technique) limits pathogens; surgical asepsis (sterile technique) completely eliminates all microorganisms.

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Standard

A recommended guideline or benchmark established by consensus or professional organizations.

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Best Practice

A method or technique consistently shown to produce superior results compared to other means.

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HIPAA

Health Insurance Portability and Accountability Act; federal law protecting the privacy of patient health information.

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Three categories of FDA recall

Class I (high risk of death/injury), Class II (temporary/reversible risk), Class III (low risk).

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Bowie-Dick Test

A test used to detect air leaks and inadequate air removal in dynamic-air-removal steam sterilizers.

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Biological Indicator (BI)

A sterilization monitoring device containing viable spores used to demonstrate that sterilization conditions were met.

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Chemical Indicator (CI)

A device used to monitor one or more sterilization parameters through a physical or chemical change.

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Geobacillus stearothermophilus

The spore-forming microorganism used to biologically monitor steam and hydrogen peroxide gas plasma sterilizers.

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Ethylene Oxide (EtO) target spore

Bacillus atrophaeus is the spore used to biologically monitor EtO sterilization.

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Three parameters of steam sterilization

Saturated steam, temperature, and exposure time.

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Superheated steam

Dry steam that has been heated to a temperature higher than its boiling point.

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Wet pack cause

Inadequate drying time, incorrect loading, or poor steam quality.

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Sterile storage temperature

Should be maintained between 68°F and 75°F.

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Sterile storage humidity

Should not exceed 70% relative humidity.

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Sterile storage air exchanges

A minimum of 4 air exchanges per hour under positive pressure.

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Event-related sterility

Concept that sterile packages remain sterile until an event causes them to become contaminated.

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Water quality in CS

Essential to prevent instrument staining, corrosion, scaling, and pyrogen reactions.

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Deionised water

Water that has had all minerals removed through an ion exchange process.

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Reverse Osmosis (RO)

A water purification process using a semipermeable membrane to remove impurities.