Chapter 7 pt 2 Flashcards

disinfection, decontamination, sterilization

1
Q

disinfection

A

microorganisms on inanimate surfaces are destroyed

reduces 99% of pathogens in room

not including spores

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2
Q

antisepsis

A

most but not all microorganism on animate surfaces are destroyed

surgical scrub, surgical site

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3
Q

antiseptic

A

surgically clean animate surfaces

cannot fully kill everything

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4
Q

sterilization

A

destruct all microorganisms + spores on inanimate surfaces

anything used on wound needs to be sterile, even if they don’t come in direct contact (basin)

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5
Q

CDC/ FDA system does what (classification of pt care items)

A

rates degree of risk for infection
- how item will be used
- where items will be used

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6
Q

classification of patient care items

A

indicates appropriate method of disinfection/ sterilization to be used

  • critical (sterilisation)
  • semi- critical (high level disinfect)
  • non- critical (low level disinfect)
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7
Q

critical items

A

invasive/ vascular access
high potential for SSI
- monitors/ probes/ vascular or urinary/ implantable

STERILIZED!!!

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8
Q

semi critical items

A

mucous membrane or non intact skin within mucous
- natural orifices

lesser risk of infection
- laryngoscopes, endoscopes, resp eq

at minimum, high level disinfectant

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9
Q

non critical items

A

pt intact skin or clean equipment
least risk for SSI
- bp cuff

low level disinfectant

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10
Q

disinfection principles

A

safety when utilizing disinfecting agents
- never mix solutions
- use PPE when handling
- ventilated storage areas
- throw out expired solutions
- use for intended purpose

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11
Q

what do cleaning agents do

A

physically removing blood, body fluids bioburden

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12
Q

disinfecting agents

A

destroy pathogenic microorganisms by direct exposure to agents

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13
Q

3 levels of disinfection

A

high level - all microorganisms (not spores + prions)
intermediate level - most microorganisms + TB
low level - kills some virus, most bacteria
- ineffective against spores prions and TB

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14
Q

sterilizing agents

A

destroy all microorganism (spores but not prions)
- steam (most common) + chemical agents

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15
Q

disinfectant efficiency factors

A

concentration level of disinfectant
- high concentration increases level of disinfect

bioburden

contact time - contact with all surfaces, disassemble multiple part items

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16
Q

disinfection efficiency factors

A

selection based on item + classification
- critical, semi, non

manufactures recommendations - temp+ PH

exposure time
- 20- 30 minutes (high)
- 10- 15 minutes ( intermediate)

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17
Q

disinfectant compounds

A

high level:
- cidex aka glutaraldehyde
- household bleach aka sodium hypochlorite

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18
Q

intermediate or low level disinfectant compounds

A

phenol (carbonic acid)
alcohol

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19
Q

environmental decontamination

A

design is conductive to minimizing microbial counts
- washable floors and walls
- easily cleaned furniture
- prevent cross contamination

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20
Q

decontamination of the operating suite pre op

A

prior to first procedure
clean all surfaces especially horizontal ones
damp dusting:
- begin with the highest surface you can reach
remove mattress pads
clean fluids from floor
clean cabinet doors

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21
Q

decontamination of the operating suite inter op

A

basin with sterile water available
instruments not easily cleaned kept in basin
instruments with lumen periodically flushed
wet lap on mayo to wash instruments in between use

never use saline!!

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22
Q

turnover steps

A

clean
damp dusting
soak instruments no saline
mop
wash hands
clean up case cart

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23
Q

routine schedule for OR surfaces to clean

A

scrub sink, cabinets, floors, walls, ceiling

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24
Q

concurrent cleaning

A

by circulator
ASAP after cases

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25
Q

reusable linen

A

handle as little as possible
leakproof biohazard bags
not rinsed or sorted on OR
wear appropriate PPE

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26
Q

decontamination practices prior to first procedure

A

damp dust
disinfectant solution
horizontal surface, highest

remove pads on OR table
move OR table to mop under floor
cabinet doors

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27
Q

decontamination practices intraop

A

soak clean instruments no saline
periodically flush lumen

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28
Q

what to do for sharps in turnover

A

STSR responsibility
puncture proof sharps container
- no overflow

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29
Q

endoscopic to open case

A

order in which things are opened is CRITICAL for flow of surgery

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30
Q

things you HAVE to have in case cart

A

blade
bovie
suction tip
lap songe

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31
Q

phrase for instruments needed in every case

A

start, control, and stop the bleeding

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32
Q

who recommends that the OR be cleaned between procedures

A

CDC

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33
Q

weekly cleaning routine

A

literally everything

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34
Q

what do do with a dirty case (infection/ disease)

A

last case of day
clean with phenolic detergent
cleaned with 70% alcohol
rubber/ plastic tubing replaced

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35
Q

instrument cleaning cycle

A

operating room (in use)
decontamination
assembly + sterilize
sterile storage

repeat

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36
Q

decomtam room

A

filtered exhaust to outside
negative pressure
seperate from clean room

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37
Q

how much humidity + temp in decontamination

A

64-70 degrees
35- 72%

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38
Q

how many air exchanges in decontamination

A

10 time/ hr

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39
Q

cleaning instruments

A

soak
proteolytic- gets blood

40
Q

decontamination room purpose

A

remove physical debris

41
Q

what kind of water does decontamination room use

A

neutral pH to not damage

42
Q

cleaning solutions used in decontamination room

A

-chelation - prevents spots
-enzymatic - break down tissue
-emulsification - disperse 2 liquids that can’t mix
-solubilization - increases dissolvablty

43
Q

characteristics of 1st sink for manual cleaning

A

lukewarm, pH neutral, enzymatic cleaner

use soft brush
ratchets + box locks
change solution frequently

44
Q

process of manual cleaning

A

clean with sink, 2nd sink used to rinse, dried for spots

45
Q

mechanical cleaning

A

eliminates manual cleaning process
3 types of equipment
prepare instruments

46
Q

3 types of cleaning equipments

A

washer - sterilizer
washer - decontaminator
ultrasonic cleaner

47
Q

washer disinfector phases

A

hands off processing
1 pre rinse
2 cleaning: detergent solution
3 final ringe: 185 degrees
4 dry: using high temp

48
Q

washer sterilizer

A

requires manual cleaning
- bakes on bioburden
requires proper arrangement
neutral pH
instruments safe to handle

49
Q

washer sterilizer phases

A

prerinse
injects detergent
fill total emergence
wash- agitation
post rinse
steam sterilization - 270 degrees
milking
drying

50
Q

ultra sonic cleaner

A

removes small particles in hard to get places

used last usually

51
Q

how the ultra sonic cleaner works

A

high sound waves convert to bubbles,
bubbles get too big, unstable, implode- pulls particles off instrument to surface of solution

52
Q

special care instruments

A

follow manufacture instruction
flush lumen with hydrogen peroxide

53
Q

cleaning power instruments

A

do not submerge
h20 only, never alcohol
- causes drying/ cracking
lukewarm water
oiling may be necessary
- run 30- 60 seconds

54
Q

cleaning rigid endoscopes

A

soaked in enzymatic solution
stored dry
avoid denting

55
Q

definition of sterility

A

absence of all living microbes, including spores

no grey area
tissues are sterile

56
Q

what are instruments checked for

A

function and integrity, prepared f or sterilization

57
Q

where do you check function of instruments

58
Q

FDA + cosmetic act requirements for instrument packing and wrapping

A

packing material maintain sterility until use

opened easily, prevent contamination

sterilizing agent must be able to each all surfaces of the item

59
Q

4 option of packing materials

A

woven
non woven
pouch packing (peel pack)
rigid instrument container

60
Q

what are woven textiles made up

A

cotton, or cotton blend
reusable

61
Q

woven textile ply

A

single ply (wrap x2), or double ply (x1)

towel may be placed in between instruments and wraps to assist with moisture absorption

62
Q

thread count range

A

140- 288 tc

higher thread count, lower bacteria penetration

63
Q

non wovan wrap characteristics

A

single use
made of plastic synthetic fibers
stored laid out flat

64
Q

paper wrap characteristics

A

single use
extreme memory, not flexible
easily penetrated by steam

65
Q

what is tyvek- plastic packaging used for

A

EtO and sterrad
- steam will melt material and damage contents

66
Q

what is the most common type of pouch packaging

A

paper- plastic

at least 2mm- not flimsy

67
Q

what is paper plastic packing used with

A

steam and EtO

68
Q

why is correct size important for paper plastic packs

A

too big- compromise sterility
too small- can tear, difficult to remove air

69
Q

what is the order to put when double pouch packing paper plastic

A

paper to paper, plastic to plastic

70
Q

what do we use to protect the tips with paper plastic pouching

A

commercial tip protector or foam sleeves ( no latex)

71
Q

when do you label paper plastic pouching

A

prior to sterilization on plastic only

71
Q

where on basket do you put paper plastic pouching

A

placed on edge in perforated basket
all in the same direction

72
Q

rigid instrument container characteristics

A

reusable: metal or plastic
stackable + easily storable
locking lids - chemical indicator
assure sterility, can’t be torn

73
Q

what is used to return contaminated items to CSPD

A

rigid instrument containers

74
Q

sterilization recommendations for rigid inst pans

A

placed on shelves (in autoclave) beneath absorbable items

75
Q

in what conditions are woven fabrics stored

A

68-73 degrees
30-60% humidity
2 hours to rehydrate

76
Q

what is AAMI max muslin wrap

A

12x12x20
- not exceed 12 lbs

77
Q

how are linens packed in general packing

A

linens packed loose
-allows steam to penetrate
double wrap
- single ply x2

78
Q

what is the max weight for instrument pans and who sets it

A

25 lbs
AAMI and ANSI

79
Q

how large does the instrument set have to be

A

large enough to have 6” below on 4 sides of table or stand

80
Q

how thick are instrument pan dust covers

A

2-3 mm thick
- clearly marked if sterile

81
Q

steps of preparation of instrument sets and basin sets

A

inspect
reassemble
preparation

82
Q

inspection process of scissors/ trocars

A

look for cracks or scratches

83
Q

inspection process of ratchets

A

ensure they don’t spring

84
Q

inspection process for clamps

A

make sure they stay locked
jaws align

85
Q

what do we need to ensure for preparation when reassembling

A

sterilant contacts all surfaces
item will be protected until use
items weight is evenly distributed in packaging

86
Q

preparation regulations of large loose instrument

A

minimal movement
heavier on bottom
may use a towel to separate layers

87
Q

preparation regulations of basins

A

nested with towel between**
no more than 7lbs
fold is down during sterilization
***

88
Q

preparation regulation for light handles

A

down for drainage

89
Q

preparation regulation for trays

A

contain all instruments for procedure

autoclaved flat to allow steam/air removed via perforations

90
Q

two kinds of folds for preparation

A

envelope
- small trays+ individual items
square fold (parallel folding)
- large trays

91
Q

what does a Label provide

A

content
quality assurance
inventory control
rotation of stock

92
Q

what do you label before sterilizing

A

everything

93
Q

labeling options

A

permanent marker
label gun
bad code scanning labels

94
Q

Julian date

A

of calendar days
no year needed due to event related sterility

ex: 1- 365