Disinfection
Sterilization
Scopes
Cleaning and Decontamination
This and That
100

Remains on instruments and is made up of microorganisms and cellular tissue

What is biofilm or bioburden

100

Test systems containing viable microorganisms providing a defined resistance to a specific sterilization process

– Provides information on whether necessary conditions were met to kill a specified number of microorganisms for a given sterilization process, providing a level of confidence in the process

What is a biological indicator

100

What scopes require prior before they are sent to sterile processing

What is point of use cleaning

100

Identify three steps done in the OR room prior to transport to prepare instruments for processing (5)

1. Wipe Bioburden off as instruments are returned to scrubber

2. Open tips of instruments on stringers and remove disposable sharp objects

3.  Place delicate items in a separate area or on a towel to avoid damage

4. Use enzymatic product for pre treatment

5. Cover and place bio hazard sign on cart

100

The three categories of Spaulding's Classification

What is :  Critical, Semi Critical, Non Critical

200

High level disinfection kills most microorganisms with the exception of 

What are spores

200

The yellow dot indicates

Unsterile, not exposed to sterilization

200

1. What do scopes require before transport?

2. Recommendation for time that cleaning is performed after pre cleaning

1.  remove organic soil and biofilm with precleaning kits

2.  No more than one hour after pre cleaning

200

The instructions we follow when decontaminating or cleaning instruments

What are manufacturer's instructions for use (IFU)

200

First step of decontamination

What is wiping off bioburden from instruments returned to scrubber

300

Give an example of devices in OR using Spaulding's Classification

Critical

Semi Critical

Non Critical 

Critical:  Instruments, Implants, Sutures, Cardiac Catheters

Semi Critical:  Endoscope, cystoscopies, bronchoscopes, endocavity ultra sound probes

Non Critical:  Blood pressure cuffs. OR furniture and tables, Linen

300

The four principles of steam sterilization

What are steam, pressure, temperature, and time

300

Two actions to do if any evidence of contamination (water, wet spots, organic material) in the scope storage cabinet

Reprocess scope

Clean cabinet

300

The difference between Cleaning and Decontamination

Cleaning does not remove pathogenic microorganisms or make them safe to handle, use or discard

Decontamination removes pathogenic microorganisms and makes them safe to handle

300

Any instrument or device opened for a procedure, even if the procedure does not occur

What is contaminated

400

Concept that sterility is dependent upon: amount of handling, conditions during transport and storage, quality of packaging material , adherence to packaging manufacturers IFUs

What is event related sterility

400

The five steps of sterilization

1.Items are cleaned at point of use

2.Decontaminated

3.Inspected/Sterilized

4.Packaged

5.Stored in a controlled environment

400

Two reasons we do leak testing on scopes

To find

1.  Leaks in the endoscope.Openings in the scope that can let water and organic materials

2.  It reduces damage and repair costs and decreases the potential for patient infections or injury

400

Many facilities use this machine to clean and decontaminate instruments prior to sterilization

What is a washer sterilizer or mechanical washer

400

The steps to take if an unsterile tray is opened and on the sterile field (Name at least three)

•Immediately remove 

•Circulator notifies SPT staff

•Remove sterilizer from use. 

•Confirm what the failure was.

•Investigate cause of failure.

•Inform key people:  charge nurse, core, managers

•Completes a PASS report

•Root Cause Analysis

•Prevention of future failure events

500

Where instructions are found for a particular disinfecting solution

The level of disinfection required for reusable devices that enter the mucosa or an endocavity

1. MSDS
2. High Level Disinfection

500

Identify difference between Pre Vac and Gravity Displacement steam sterilizers

Gravity Displacement:  Steam enters from top and displaces lighter air out thru air vent

Pre Vac are high speed sterilizers similar to gravity except they are fitted with a vacuum pump (ejector) to insure air removal from sterilizing chamber and load before steam is admitted.Advantage is immediate, instantaneous steam penetration

500

Name five steps for processing a scope

1. Pre Clean

2.  Leak Test

3.  Clean

4.  High Level Disinfection

5.  Proper Storage

500

The steps of cleaning and decontamination that occur in decontam (name 3 of 5)

1. Verification all instruments are in fully opened position

2. Verification that multipart instruments are disassembled

3. All instruments are rinsed to remove foamss or gel

4.  Instruments are manually soaked in neutral ph enzymatic detergent following IFU

5.  Instruments are manually or mechanically cleaned:  ultrasonic washer, mechanical washers

500

Three types of sterile processing

What are:

•STEAM

Gravity

Pre-vacuum

•CHEMICAL

Sterrad

Ethylene oxide sterilization (EOS)

•HIGH LEVEL DISINFECTION

Combination of chemical solution and high heat

Medivator

  

M
e
n
u