Chapter 13,14,15 (1-100)
問題一覧
1
EO!
2
EO!
3
relative humidity!
4
It compromises patient safety!
5
PEL!
6
Proper cleaning, decontamination, sterilization using the correct cycle, and aseptic transfer to the point of use!
7
circulate warm air through the chamber to remove residuals from instruments!
8
Cotton towels!
9
The supervisor should be notified and the sterilization load should not be released!
10
The FDA!
11
1 ppm TWA!
12
Oxidation of key cellular components!
13
Physical, chemical, and biological monitors!
14
It's effective against a wide range of pathogens!
15
To control the flow of air and condensate!
16
Residual!
17
Avoiding overloading to ensure all surfaces are reached!
18
H2O2 gas plasma!
19
Physical, chemical, and biological monitors!
20
At levels greater than 1 ppm time-weighted average!
21
To remove EO residual gases from instruments and packaging!
22
Lack of contact between steam and the entire surface of the device being sterilized!
23
To understand when and how to safely use the low temperature sterilization methods that are available!
24
They can lead to failure of the sterilization process!
25
They offer the best protection for the sterile instruments!
26
To reflect a shift in process from an unwrapped container to a sealed contained device for greater protection from contamination!
27
To allow for proper steam penetration and condensate drainage!
28
uses 100 % cartridges and classified as carcinogen by OSHA!
29
Geobacillus stearothermophilus!
30
It offers safety relative to ETO and rapid cycle times!
31
They should be positioned so air can exit and steam can enter!
32
OSHA!
33
All the answers satisfy effectiveness!
34
Low-temperature!
35
SFPP!
36
The steam cannot penetrate into all areas!
37
Insulation!
38
Flash Sterilization!
39
Chamber drain!
40
TWA!
41
is required each day but recommended for every cycle run!
42
High Level Disinfection (HLD) or Sterilization!
43
Digital!
44
In selected clinical situations in a controlled manner, and when there is no time to process the items using the preferred wrapped method!
45
To ensure they are clean and functional!
46
Transport in a manner that reduces the potential for contamination!
47
To sterilize items for immediate delivery to the procedure room when there is no time to send them to the central sterile department!
48
Gravity and Dynamic Air Removal!
49
75 minutes!
50
97 to 100 percent!
51
SDS!
52
Air is displaced through the drain!
53
The probability of a viable microorganism being present on a product's unit after sterilization!
54
Steam!
55
alkylation!
56
Sterilization cycle printouts, biological and chemical indicator results!
57
Pressure!
58
Patient identification record!
59
Immediate-Use Steam Sterilization!
60
Door!
61
To sterilize instruments and medical devices in their final containers, allowing them to be stored till usage!
62
Leaves chemical residues!
63
EO cartridges should not necessarily be stored in a liquid storage cabinet!
64
Time-Weighted Average!
65
It is the process when a medical device is processed immediately before use and/or close to the patient care area!
66
It is exhausted through a discharge line!
67
In an area designed to clean instruments!
68
Terminal Sterilization!
69
Paper, plastic, and Tyvek-filled pouches!
70
non-cellulose items!
71
Regular intervals for review and update of their knowledge!
72
Conditioning, Exposure, Exhaust, and possibly Drying!
73
Cellulose materials!
74
ranges from 59% - 95%!
75
They should be located in a well-ventilated area with a room air exchange rate of at least 10 changes per hour!
76
Operating rooms or surgical suites, labor and delivery units, and procedure areas!
77
Exchange cart system!
78
When the sterilizer door is opened!
79
Should be removed prior to bringing items into the sterile storage area!
80
Case cart!
81
cross-functional team!
82
Attitude!
83
The product manufacturer!
84
Action level (AL)!
85
anticipating possible interview questions!
86
Telescopes!
87
Door!
88
In a rigid container designed for IUSS!
89
They cannot be stored!
90
OSHA!
91
Device manufacturer’s IFU!
92
In the device’s IFU!
93
Understand how the sterilizer operates!
94
More difficult it will be to sterilize!
95
EO!
96
The process by which surgical instruments and medical devices are sterilized in their final containers, allowing them to be stored until needed!
97
Daily!
98
IUSS items must be used immediately!
99
Moisture!
100
Tape!
Chapter 1-5
Chapter 1-5
Jelani Davis · 100問 · 1年前Chapter 1-5
Chapter 1-5
100問 • 1年前Chapter 6-9
Chapter 6-9
Jelani Davis · 90問 · 1年前Chapter 6-9
Chapter 6-9
90問 • 1年前Chapter 18
Chapter 18
Jelani Davis · 20問 · 1年前Chapter 18
Chapter 18
20問 • 1年前Chapter 19
Chapter 19
Jelani Davis · 45問 · 1年前Chapter 19
Chapter 19
45問 • 1年前Chapter 10,11,12
Chapter 10,11,12
Jelani Davis · 80問 · 1年前Chapter 10,11,12
Chapter 10,11,12
80問 • 1年前Chapter 20
Chapter 20
Jelani Davis · 45問 · 1年前Chapter 20
Chapter 20
45問 • 1年前問題一覧
1
EO!
2
EO!
3
relative humidity!
4
It compromises patient safety!
5
PEL!
6
Proper cleaning, decontamination, sterilization using the correct cycle, and aseptic transfer to the point of use!
7
circulate warm air through the chamber to remove residuals from instruments!
8
Cotton towels!
9
The supervisor should be notified and the sterilization load should not be released!
10
The FDA!
11
1 ppm TWA!
12
Oxidation of key cellular components!
13
Physical, chemical, and biological monitors!
14
It's effective against a wide range of pathogens!
15
To control the flow of air and condensate!
16
Residual!
17
Avoiding overloading to ensure all surfaces are reached!
18
H2O2 gas plasma!
19
Physical, chemical, and biological monitors!
20
At levels greater than 1 ppm time-weighted average!
21
To remove EO residual gases from instruments and packaging!
22
Lack of contact between steam and the entire surface of the device being sterilized!
23
To understand when and how to safely use the low temperature sterilization methods that are available!
24
They can lead to failure of the sterilization process!
25
They offer the best protection for the sterile instruments!
26
To reflect a shift in process from an unwrapped container to a sealed contained device for greater protection from contamination!
27
To allow for proper steam penetration and condensate drainage!
28
uses 100 % cartridges and classified as carcinogen by OSHA!
29
Geobacillus stearothermophilus!
30
It offers safety relative to ETO and rapid cycle times!
31
They should be positioned so air can exit and steam can enter!
32
OSHA!
33
All the answers satisfy effectiveness!
34
Low-temperature!
35
SFPP!
36
The steam cannot penetrate into all areas!
37
Insulation!
38
Flash Sterilization!
39
Chamber drain!
40
TWA!
41
is required each day but recommended for every cycle run!
42
High Level Disinfection (HLD) or Sterilization!
43
Digital!
44
In selected clinical situations in a controlled manner, and when there is no time to process the items using the preferred wrapped method!
45
To ensure they are clean and functional!
46
Transport in a manner that reduces the potential for contamination!
47
To sterilize items for immediate delivery to the procedure room when there is no time to send them to the central sterile department!
48
Gravity and Dynamic Air Removal!
49
75 minutes!
50
97 to 100 percent!
51
SDS!
52
Air is displaced through the drain!
53
The probability of a viable microorganism being present on a product's unit after sterilization!
54
Steam!
55
alkylation!
56
Sterilization cycle printouts, biological and chemical indicator results!
57
Pressure!
58
Patient identification record!
59
Immediate-Use Steam Sterilization!
60
Door!
61
To sterilize instruments and medical devices in their final containers, allowing them to be stored till usage!
62
Leaves chemical residues!
63
EO cartridges should not necessarily be stored in a liquid storage cabinet!
64
Time-Weighted Average!
65
It is the process when a medical device is processed immediately before use and/or close to the patient care area!
66
It is exhausted through a discharge line!
67
In an area designed to clean instruments!
68
Terminal Sterilization!
69
Paper, plastic, and Tyvek-filled pouches!
70
non-cellulose items!
71
Regular intervals for review and update of their knowledge!
72
Conditioning, Exposure, Exhaust, and possibly Drying!
73
Cellulose materials!
74
ranges from 59% - 95%!
75
They should be located in a well-ventilated area with a room air exchange rate of at least 10 changes per hour!
76
Operating rooms or surgical suites, labor and delivery units, and procedure areas!
77
Exchange cart system!
78
When the sterilizer door is opened!
79
Should be removed prior to bringing items into the sterile storage area!
80
Case cart!
81
cross-functional team!
82
Attitude!
83
The product manufacturer!
84
Action level (AL)!
85
anticipating possible interview questions!
86
Telescopes!
87
Door!
88
In a rigid container designed for IUSS!
89
They cannot be stored!
90
OSHA!
91
Device manufacturer’s IFU!
92
In the device’s IFU!
93
Understand how the sterilizer operates!
94
More difficult it will be to sterilize!
95
EO!
96
The process by which surgical instruments and medical devices are sterilized in their final containers, allowing them to be stored until needed!
97
Daily!
98
IUSS items must be used immediately!
99
Moisture!
100
Tape!