Decontamination Flashcards

(27 cards)

1
Q

what is a user with regards to decontamination

A

the person designated by the executive manager to be responsible for the management of the process

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2
Q

what is an operator with regards to decontamination

A

the person with the authority to operate decontamination equipment in processing of medical devices

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3
Q

what is a competent person with regards to decontamination

A

a chartered engineer responsible for drawing up a written scheme of examination for the system

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4
Q

what is an authorising engineer (decontamination) AE(D)

A

a person assigned to advise on decontamination procedures, WDs, sterilisers and associated sterilisation processes

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5
Q

what is an authorised person (decontamination) AP(D)

A

has technical knowledge and appointed by the NHS in charge of practical implementation and operation of procedures relating to engineering aspects of decon equipment

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6
Q

what is a competent person (decontamination) CP(D)

A

person designated by AP(D) to carry out maintenance, validation and periodic testing of decontamination equipment

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7
Q

how long should decontamination records be kept

A

for the lifetime of the equipment plus 25 years afterwards

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8
Q

why do devices have to be processed through a WD first

A

to remove soiling, allowing steam to penetrate the devices

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9
Q

what are the stages of WD

A

prewash - removes difficult gross contamination
wash - mechanical and chemical processes loosen and break up contamination
rinse - removes detergent
thermal disinfection - temperature raised and held at pre-set disinfection temperature (90-95 degrees for 1 minute)
drying - purges the load and chamber with filtrated heated air to remove moisture

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10
Q

what are the daily tests for the WD

A

remove and clean strainers and filters
check spray arms and nozzles freely rotate
check nozzles are not blocked
check detergent levels
check door seal
verify condition of load carrier
record disinfection temp of first cycle
ACT

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11
Q

what are the weekly tests for WD

A

daily tests AND
protein residue test

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12
Q

what is the automatic control test for WD

A

shows the operating cycle functions properly and the disinfection temperature/ time are within the original specification

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13
Q

what are the quarterly tests for WD - carried out by CP(D)

A

weekly tests AND
check safe operation of doors and door interlocks
check mechanical alignment of all load carriers
automatic control test
cleaning efficacy test
chemical dosing
verification of calibration
thermometric tests

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14
Q

what are the types of sterilisers

A

type N - air removal, non-vacuum no suitable for instruments with a lumen
type B - vacuum
type S - specific load types

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15
Q

what are the sterilisation parameters for saturated steam in a 134 degrees cycle

A

134 minimum temperature
137 maximum temperature
minimum holding time 3 minutes

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16
Q

what are daily tests of steam sterilisers

A

bowie and dick or helix test - checks steam penetration (type B and S only)
clean door seal with clean, damp non-linting cloth
check chamber and shelves for debris
fill reservoir with water

17
Q

what are weekly tests for steam sterilisers

A

daily tests AND
safety checks - door seal and interlocks
automatic control test
air leakage test

17
Q

instruments should be transported in a box that is:

A

tight lidded
leak proof
rigid
colour coordinated

18
Q

how should a WD be loaded

A

no overlapping instruments
hinge instruments open at hinge
assembles disassembled
do not overload machine

19
Q

what should you do before an Ultrasonic bath is used

A

run degas cycle

20
Q

what values are required for adequate sterilisation

A

134-137 degrees for minimum hold time 3 mins
atmospheric pressure 2.05 to 2.35 bar or absolute 3.05 to 3.35 bar

21
Q

what are the spaulding classifications

A

critical - devices entering sterile tissue and must be sterilised
semi-critical - devices only in contact with intact mucous membranes and no penetration - sterilised but high level disinfection also accepted
non-critical - devices in contact with skin only - cleaned/ disinfected

22
Q

what is the sinner cycle and what are the four aspects

A

factors that affect the cleaning cycle
time, temp, chemicals, energy

23
Q

why must records be kept in decon

A

for audit purposes
verify compliance
diagnostic tool for faults
medicolegal record if pt has complaint/ infection

24
what is the chain of infection
infectious agent reservoir mode of transmission portal of entry susceptible host portal of exit
25
what are the stages of decontamination cycle
acquisition cleaning disinfection inspection packaging sterilisation transport storage use transport
26
if you find instruments on top of the steriliser how could you check they have already been processed
should be positioned not overlapping if they have been through steriliser check for recent print outs check for colour change of packaged instruments if unsure start from BEGINNING (AWD) and then sterilise