spd unit 2 exam prct

0.0(0)
Studied by 9 people
call kaiCall Kai
learnLearn
examPractice Test
spaced repetitionSpaced Repetition
heart puzzleMatch
flashcardsFlashcards
GameKnowt Play
Card Sorting

1/85

encourage image

There's no tags or description

Looks like no tags are added yet.

86 Terms

1
New cards

This low-level disinfectant is incompatible with soap.

Quaternary ammonium compounds

2
New cards

When using qlutaraldehyde, technicians should always wear latex gloves for protection

False /

3
New cards

When using high-level disinfectants, it is important to remember they may be deactivated by

 

Organic matter

4
New cards

In an automated washer the key source of disinfection is 

Water temperature

5
New cards

The use of test strips to test the minimum effective concentration (MEC) in high-level disinfection solutions is required;

Each time the solution will be used

6
New cards

How are items that have undergone high-level disinfection (HLD) dried? 

With HEPA-filtered air

7
New cards

Iodophors are a member of this chemical family.

Halogens

8
New cards

These chemicals are used on animate (living tissue) to slow the growth of microorganisms 

Antiseptics

9
New cards

Phenolics are classified as 

Intermediate to low-level disinfectants

10
New cards

Which of the following are classified as high-level disinfectants?

Glutaraldehyde and ortho-phthalaldehydes

11
New cards

Micro grind or super cut scissors are usually identified with a black handle.

True

12
New cards

Stainless steel jaw needle holders last longer than tungsten carbide jaw needle holders.

False

13
New cards

Tissue forceps have teeth

 

True

14
New cards

An acceptable method for instrument identification is:

All the above

15
New cards

The part of a hemostat that locks and holds it in position is called the box lock.

False

16
New cards

Which solution can damage surgical instrumentation? 

Betadine

17
New cards

During instrument manufacture the process of passivation helps build a protective chromium oxide layer on each instrument’s surface.

True

18
New cards

The purpose of a suction style is to 

Unclog the suction during surgery

19
New cards

To properly test the sharpness of scissors four inches or less use

yellow test material

20
New cards

Kerrison/laminectomy rongeurs should be tested using 

an index card

21
New cards

The first step to inspect the insulation of a laparoscopic instrument is to

Check the collar at the distal tip

22
New cards

Loaner instruments should

Be decontaminated before use

23
New cards

Pneumatic cords are a cleaning concern because: 

They are dark in color, so soil is difficult to see

24
New cards

Information regarding cleaning processes for endoscopes should by provided by the:

Instrument manufacturer

25
New cards

Which of the following statements about endoscopes is true:

Flexible endoscopes are time-consuming to clean

26
New cards

Powered surgical instrument batteries should be charged per the manufacturer's instructions (IFU) 

Before sterilization

27
New cards

Robotic instruments: 

May have exposed cables

28
New cards

After use, loaner instrumentation must be decontaminated before it is shipped out.

True

29
New cards

Electronic testing of laparoscopic insulation should be done

In the clean assembly area prior to cleaning

30
New cards

Endoscope cameras:

Should be inspected for cuts, nicks or other damage to the cable.

31
New cards

The U.S. Food and Drug Administration classifies sterilization packaging as a

Class II Medical Device

32
New cards

Which of the following is NOT an acceptable sterilization packaging material?

Canvas

33
New cards

When arranging paper/plastic pouches in the sterilizer, the pouches should be arranged.

Paper-to-plastic

34
New cards

Some plastics including formulations of spun-bounded polyolefin are intended for use solely in these sterilization processes 

hydrogen peroxide (low temp).

35
New cards

When placing hinged instruments in an instrument tray

Unlock the handles and open the instruments

36
New cards

Which of the following packaging systems is required to be packaged twice and provides a second chance for sterile presentation? 

Sequential flat wrapper

37
New cards

How often should the insulation of electrosurgical instruments be tested for integrity?  

Every time the instrument is processed

38
New cards

Count sheets:

Provide a detailed list of tray contents

39
New cards

Which of the following cannot be used in an instrument set to protect delicate instruments? 

Plastic peel packs

40
New cards

This type of chemical indicator (CI) is also called a verification indicator and is a cycle-specific indicator. It is designed to react to all critical parameters of a sterilization cycle:

Type 6

41
New cards

The process by which instruments are steam sterilized for immediate use is called

immediate use steam sterilization

42
New cards

The best way to transport item that have been processed using immediate use steam sterilization at the point of use is 

Rigid container designed for IUSS

43
New cards

Before an item can be placed in a liquid chemical sterile processing system they must be 

Cleaned

44
New cards

Both the Association of periOperative Registered Nurses and The Joint Commission recommend that 

The use of immediate use steam sterilization be minimized or decreased.

45
New cards

Items to be disinfected or sterilized  at the point of use must be 

Properly cleaned per Manufactureer’s Instructions for Use

46
New cards

Which of the following statements about immediate use steam sterilization is true?

It should be used only when there is not time to process items using the wrapped method

47
New cards

Implantable devices 

should not be immediate use steam sterilization sterilized unless there is a tracking system in place to trace the item to a patient

48
New cards

What is the length of time after sterilization that an IUSS item can be used?

IUSS items must be used immediately

49
New cards

Immediate use steam sterilization documentation should include

All the above

50
New cards

When transporting items that have been immediate use steam sterilized, it is required that

They be transported in such a manner that reduces the potential for contamination

51
New cards

When loading a steam sterilizer, basins should be 

Placed on edge

52
New cards

The higher the bioburden on an object

The more difficult it will be to sterilize

53
New cards

When combining load, hard goods should be placed on the top shelves to allow for more efficient removal  of the condensate.

False

54
New cards

Which of the following does not affect sterilization? 

How the user department tells the Sterile Processing (SP) staff to sterilize it.

55
New cards

The weakest part of a steam sterilizer is the 

door

56
New cards

The most common reason for steam sterilization failure is 

Lack of steam contact with contents of the load

57
New cards

The coolest place in a steam sterilizer is the 

Drain

58
New cards

How frequently should a sterilizer’s strainer be removed and cleaned?

Daily

59
New cards

One of the most frequent causes of a clogged drain screen is 

Tape

60
New cards

A sterilizer cart can be unloaded:

When an infrared device shows that the itmes have cooled to room temperature

61
New cards

Why is proper training for the safe and effective use of low-temperature sterilization important? 

Chemicals used to sterilize instruments have toxic properties

62
New cards

Aeration instructions for a medical device can be found in/on the

Device manufacturer's IFU's

63
New cards

To ensure successful sterilization, the sterilizer chamber should not be:

Overloaded

64
New cards

When an items undergoes low-temperature sterilization, what is meant by the term "material compatibility"?

There should not be changes in the device's functionality

65
New cards

Information about a device's compatibility with a specific sterilization process can be obtained:

In the device's IFU

66
New cards

Which of the following items can be sterilized by H2O2? 

Telescopes

67
New cards

What is a permissible exposure limit (PEL)?

The maximum amount of concentration of a chemical that a worker may be exposed to under Occupational Safety and Health Administration (OSHA) regulations

68
New cards

Which of the following sterilization methods can permeate throughout a wide range of materials to reach recessed areas? 

Ethylene oxide (EO)

69
New cards

EO-sterilized items are aerated to remove residual:

EO

70
New cards

Permissible exposure levels (PELS) for low-temperature sterilization methods are established by the 

Occupational Safety and Health Agency (OSHA)

71
New cards

Satellite storage areas

Follow the same guidelines used in SP storage

72
New cards

Endoscopes that have undergone high-level disinfection
(HLD) should be stored:

Completely dry

73
New cards

How should sterile packages be arranged and maintained to allow for stock rotation?

First in, first out

74
New cards

The sterile storage process begins

When the sterilizer door is opened

75
New cards

Sterile storage areas should have:

Positive airflow and at least four air exchanges per hour

76
New cards

Following liquid chemical sterilization (LCS), items intended to be used as critical devices may be stored for

No storage time; they should be used immediately

77
New cards

The shelving system of choice for the sterile storage area is:

Closed

78
New cards

Trays that overhang shelving

Can become contaminated

79
New cards

The type of shelving that leaves packaging the most vulnerable is

Open

80
New cards

The bottom shelf of any sterile storage system should be

Solid and 8 to 10 inches from the floor

81
New cards

Sterile trays should

All the above

82
New cards

Wrapped trays should not be stacked because

It can cause holes in the wrappers

83
New cards

Outside shipping containers

Should be removed prior to bringing items into the sterile storage area

84
New cards

How long can flexible endoscopes that have undergone
HLD or liquid chemical sterilization (LCS) be stored?

According to facility policy

85
New cards

It is important to identify devices that have undergone
HLD or LCS as patient-ready because doing so:

Distinguishes processed devices from non-processed devices

86
New cards

Requires employers to have an emergency action plan whenever another osha standard requires one

OSHA 29 CFR1910.38