Overview of Decontamination Process Flashcards

1
Q

What are the reasons for cleaning and disinfecting instruments before sterilisation?

A

Legal requirement

Preserve function- biological matter can clog instruments

To remove biological contamination-
-> minimises the spread of infection/cross-contamination (could lead to mis-diagnosis)

So that it is safe to inspect

-> this allows steam to clean devices properly

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2
Q

What are the requirements of the container for transporting used instruments?

A

 Durable
 Leak proof
 Rigid sided
 Colour coded/clearly marked
 Tight-fitting lid

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3
Q

What daily tests should be carried out for AWD?

A

Check spray arms rotate and are not blocked

Check filter/strainer for debris and contamination from instruments

Check door seal for damage and cleanliness

Check chemical and water level- replenish

Verify condition of load carrier

Record disinfection temp of first cycle

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4
Q

How should AWD be loaded (this should be established at validation)?

A

No overlapping of instruments

Do no overload machine

Assemblies should be disassembled

Restorative materials should be removed beforehand

Forceps should be open at hinge and positioned so they will remain open

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5
Q

What are the stages of AWD cycle?

A

Flush
Wash
Rinse
Disinfection
Drying

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6
Q

What is the function of using an illuminated magnifier when inspecting instruments?

A

Can verify if AWD was successful

Can identify if contamination still present

Can verify functionality of instruments
-> if damaged can be sent for repair

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7
Q

What happens if contamination is still present on instruments that have been through AWD?

A

They are manually cleaned and processed through ultrasonic
-> removes dried-in or gross contaminants

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8
Q

What are the recommendations for manual cleaning?

A

Water should be <35

pH neutral or enzymatic detergent is used
-> amount depends on volume of water
-> Follow manufacturers instructions

Use long handled soft bristled brush

Use separate sinks for washing and rinsing

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9
Q

What are the 2 methods of manual cleaning?

A

Immersion

Non-immerion
-> required for handpieces as they should not be immersed

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10
Q

What is used following manual cleaning?

A

Ultrasonic bath

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11
Q

What are the recommendations when using ultrasonic bath?

A

Fill to required level

Degas before use

Load as for AWD

*do not process handpieces using this

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11
Q

What are the recommendations when using ultrasonic bath?

A

Fill to required level

Degas before use

Load as for AWD

*do not process handpieces using this

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12
Q

Why are instruments reprocessed through AWD following manual/ultrasonic cleaning?

A

Disinfection stage makes it safe for staff to handle and inspect

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13
Q

What temperature and pressure banding are achieved by sterilisers? (type N, S, B)

A

134-137 degrees for minimum hold time of 3 mins

Pressure equivalent gauge (from atmospheric) 2.05 – 2.35 bar
-> required to reach temperature

Pressure equivalent absolute (from absolute zero) 3.05 – 3.35 bar

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14
Q

What additional tests are needed for Type B sterilisers?

A

Bowie dick- steam penetration
-> daily

Air leakage test- weekly

Air Detector function test- weekly

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15
Q

How does a steriliser work?

A

Purified water is introduced into chamber and heated
-> when it boils and turns to steam pressure in chamber increases

16
Q

What is a type N steriliser known as?

A

Gravity displacement

17
Q

What can be processed by type N steriliser?

A

Rigid steel instruments

Cannot process wrapped, channelled or lumened instruments

18
Q

What is a type B steriliser known as and why?

A

Vacuum capable or porous load
-> active air removal in initial stage creates vacuum in chamber
-> this means no air in chamber allowing steam to flow in from generator

19
Q

What happens in type B steriliser when sterilisation is finished?

A

Machine draws another vacuum for drying
-> Allows water to vaporise at Lower temp

20
Q

What can be processed by type B steriliser?

A

Wrapped (ensure no damage to these), channelled and lumened instruments

Porous loads- cotton swabs

21
Q

What is different about instruments processed by type N and type B?

A

Type B- wrapped instruments, sterile at point of use

Type N- sterilised only, should be wrapped as soon as possible

22
Q

How should wrapped instruments be stored?

A

Environmentally controlled atmosphere free of moisture and contaminants

23
Q

What are the safety considerations when decontaminating instruments?

A

Are instruments being transported correctly

Are we wearing PPE

Are items being disposed of in correct waste stream

Are single use items managed correctly

Are we storing sterilised items correctly

24
Q

What are the considerations regarding staff in an LDU?

A

Do staff understand key stages of process

Are staff trained to use equipment

Have staff been supplied with PPE

Do staff know how to work safely
-> are they aware of dangers

25
Q

What are the considerations regarding records of decontamination process?

A

 Do we have training records for all staff on
all equipment and processes
 Do we have machine printouts and cycle data
 Are our validation and testing records up to date
 Are we maintaining a maintenance register for our equipment
 Are we recording faults and failures

26
Q

What are the considerations regarding compliance with standards when carrying out decontamination?

A

Are we following the correct and most
up to date guidance (SHTM 01 – 01):

 Can the equipment consistently achieve the set-points (temperature, chemical, pressure, time)
 Has it been produced in line with the relevant standards (MDR)
 Does my test partner comply with the guidance (SHTM 01 -01)
 Do they test my equipment in-line with the required standards (BS EN)

27
Q

Sinners Circle:

A

Time

Chemical

Energy

Temperature

Water