Decon sciences Flashcards

1
Q

lifecycle of re-usable surgical instruments

A

cleaning
disinfection
inspection
packaging
sterilisation
transport
use
storage
transport

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2
Q

What is a critical device?

A

a device that penetrates soft tissue, makes contact with bone and enters or contacts the bloodstream or normally sterile tissue

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3
Q

How should a critical device be processed?

A

device must be cleaned then sterilised

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4
Q

give examples of critical devices

A

surgical and biopsy instruments
forceps

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5
Q

what is a semi critical device?

A

a device that comes into contact with non-intact skin or mucous membrane, but does not penetrate soft tissue or make contact with the bloodstream, bone or normally sterile tissue

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6
Q

how should a semi-critical device be processed?

A

the device must be cleaned and subject to high-level disinfection

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7
Q

give an example of semi-critical devices

A

dental mirror
anaesthetic syringes

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8
Q

what is a non-critical device?

A

a device that only comes into contact with the skin and intact mucous membrane

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9
Q

how should a non-critical device be processed?

A

cleaning followed by low level disinfection

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10
Q

give an example of a non-critical device

A

chair light handle

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11
Q

Why must instruments be cleaned as the first stage? (5 reasons)

A

functionality of instrumentation
minimise spread of contamination
prevent failed procedures
achieves steam contact
it is a legal requirement

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12
Q

What is the recommended cleaning method for dental instruments?

A

a washer disinfector

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13
Q

what is the secondary (back up) method for cleaning dental instruments

A

ultrasonic bath

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14
Q

What are the 3 types of sterilisers?

A

type B = vacuum
type N = non vacuum
type S (used for specialised pieces of equipment)

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15
Q

What are the 2 manual cleaning methods?

A

immersion
non-immersion

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16
Q

indications for carrying out manual cleaning

A

recommended by manufacturers instructions
no other alternative
automated process of the ultrasonic or washer-disinfector has failed to remove contamination

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17
Q

what are the 5 stages of an AWD? what does each stage do

A

flush/prewash
- removes gross contamination
main wash
- supplemented by detergent to more efficiently remove biological matter
rinse
- removes any remaining biological or chemical residue prior to disinfection
thermal disinfection
- actively kills micro-organisms with the use of heated water
drying
- removes moisture from surface of instruments through use of hot air

18
Q

Time and temperature of the thermal disinfection stage

A

90-95 degrees for minimum of 1 minute

19
Q

daily checks required for Washer-disinfector

A

check that the spray arms spin freely without obstruction
check the spray jets are not blocked
make sure that there is no debris on the filter
check the condition of the door seal
- wipe clean if necessary
ensure there is an adequate amount of chemical in the reservoir
record the disinfection temperature of the first cycle every day

20
Q

Why is steam used for sterilisation?

A

steam carries a massive amount of energy
it is a non-toxic component in the sterilisation process
for certain applications it can be recondensed and used again
the main ingredient is water = readily available
no waste product except water

21
Q

what are the 4 types of purified water

A

reverse osmosis
de-ionised
distilled
sterile

22
Q

How does a type n steriliser work?

A

machine heats water in the chamber
as it turns to steam it passively forces the air from the chamber

23
Q

disadvantages of a type n steriliser

A

process can leave pockets of air within chamber
- not entirely sufficient
not favourable for a high quality sterilisation process
cannot processed wrapped, channelled or lumened instruments
instruments processed this way are sterilised - NOT sterile at the point of use

24
Q

type N steriliser - required temperature, pressure and time

A

134-137 degrees Celsius
2.05-2.35 bar gauge
minimum stage hold time of 3 minutes

25
how does a type B steriliser work?
all air removed fro chamber chamber filled with steam - as air has been removed first, a vacuum has been created steam rushes into chamber effectively contacting all surfaces - has the capability to penetrate wrappings of instruments and sterilise the inside of the instruments
26
type B steriliser required temperature, pressure and time
must achieve 134-137 degrees C at 2,05-2.35 bar gauge (3.05-3.35 absolute pressure) for at least 3 minutes
27
daily checks for a steriliser include:
checking door seals are intact and free from debris - clean if necessary verify chamber is free from damage, debris, contamination or instruments from previous cycle fill and drain feed water reservoir each day drain the used water reservoir each day
28
specific type B steriliser daily test
steam penetration test Bowie dick test pack OR helix
29
specific type b steriliser weekly tests
an air leakage test an air detector function test (both tests are machine cycles)
30
what are the elements of the sinner circle?
energy time temperature chemicals
31
what pressure is used in a washer disinfector?
1-1.5 bar (2 - 2.5 bar absolute)
32
guidance for decontamination is called...
SHTM - Scottish health technical memorandum
33
how long do decontamination records need to be stored for?
25 years
34
top 5 causes of dental handpiece faults
incorrect or inadequate lubrication poor or inadequate cleaning, including incorrect processing incorrect instrument usage damaged or oversized bur fitted incorrect compressor settings and lack of maintenance
35
Washer disinfector loading requirements
the available load carrier furniture must be used clip trays must be used and positioned correctly no overlapping or shadowing of equipment hinged instruments much be opened at the hinge all assemblies should be disassembled beforehand
36
What is used to inspect instruments after the WD cycle?
an illuminated magnifier
37
SHTM 01-05 part A
Management - rationale - definitions - documentation and traceability - relevant legislation
38
SHTM 01-05 Part B
decontamination equipment and test methods
39
SHTM 01-05 part C
process - provides practical guidance on the whole instrument decontamination process - has been written in collaboration with SDCEP
40
government legislation regarding decontamination
medicines and medical devices act 2021 medical device regulations 2002 health and safety at work act 1974 consumer protector act 1987 pressure safety regulations 2000 control of substances hazardous to health (COSHH) 2002