Laboratory Safety and Quality Assessment Flashcards

1
Q

Safety Procedure Manuals is mandated by:

A

Centers for Disease Control and Prevention (CDC)
Occupational Safety and Health Administration (OSHA)

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2
Q

The Safety Procedure Manuals are updated _____ by the laboratory director

A

Annually

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3
Q

The Safety Procedure Manuals are updated annually by the _____

A

Laboratory Director

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4
Q

The _____ provides the guidelines for writing the procedures and policies in the Safety Procedure Manuals

A

Clinical and Laboratory Standards Institute (CLSI)

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5
Q

List down the Infectious Agents

A

Bacteria
Fungi
Parasites
Viruses

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6
Q

List down the Reservoir

A

Humans
Animals
Insects
Fomites
Blood/Body Fluids

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7
Q

List down the Portal of Exit

A

Nose
Mouth
Mucous Membrane
Specimen Collection

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8
Q

List down the Means of Transmission

A

Droplet
Airborne
Contact
Vector
Vehicle

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9
Q

List down the Portal of Entry

A

Nose
Mouth
Mucous Membranes
Skin
Unsterile Equipment

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10
Q

List down the Susceptible Host

A

Patients
Elderly
Newborns
Immunocompromised
Health-care Workers

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11
Q

How to break the link for the Reservoir?

A

Disinfection
Hand Hygiene

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12
Q

How to break the link for the Portal of Exit?

A

Sealed biohazardous waste containers
Sealed specimen containers
Hand Hygiene
Standard Precautions

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13
Q

How to break the link for the Means of Transmission?

A

Hand Hygiene
Standard Precautions
PPE
Patient Isolation

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14
Q

How to break the link for the Portal of Entry?

A

Hand Hygiene
Standard Precautions
PPE
Sterile Equipment

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15
Q

How to break the link for the Susceptible Host?

A

Immunizations
Patient Isolation
Nursery Precautions
Healthy Lifestyle

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16
Q

States that all patients are considered to be possible carriers of bloodborne pathogens

A

Universal Precautions (UP)

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17
Q

Universal Precaution guideline recommends _____ and _____

A

Wearing gloves
Wearing face shields

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18
Q

The CDC excluded _____ and _____ not visibly contaminated by blood from UP

A

Urine
Body Fluids

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19
Q

Major disadvantage of BSI guidelines

A

Do not recommend handwashing after removing gloves

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20
Q

In _____, the CDC and the Healthcare Infection Control Practices Advisory Committee (HICPAC) combined the major features of UP and BSI Guidelines and called the new Guidelines Standard Precautions.

A

1996

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21
Q

In 1996, the _____ and _____ combined the major features of UP and BSI Guidelines and called the new Guidelines Standard Precautions.

A

CDC
HICPAC

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22
Q

In 1996, the CDC and the Healthcare Infection Control Practices Advisory Committee (HICPAC) combined the major features of_____ and _____ and called the new Guidelines Standard Precautions.

A

UP
BSI

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23
Q

In 1996, the CDC and the Healthcare Infection Control Practices Advisory Committee (HICPAC) combined the major features of UP and BSI Guidelines and called the new Guidelines _____.

A

Standard Precautions

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24
Q

Standard Precautions are as follows:

A
  1. Hand Hygiene
  2. Gloves
  3. Mouth, Nose, and Eye Protection
  4. Gown
  5. Patient Care Equipment
  6. Environmental Control
  7. Linen
  8. Occupational Health and Blood-borne Pathogens
  9. Patient Placement
  10. Respiratory Hygiene/Cough Etiquette
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25
PPE used in the laboratory includes:
Gloves Fluid-resistant Gowns Eye and Face Shields Plexiglas Countertop Shields
26
Wearing gloves is not a substitute for _____
Hand Hygiene
27
Wearing _____ is not a substitute for hand hygiene.
Gloves
28
Hand hygiene includes _____ and _____
Hand Washing Using Alcohol Based Antiseptic Cleaners
29
All biologic waste, except _____, must be placed in appropriate containers labeled with the biohazard symbol
Urine
30
Empty urine containers can be discarded as _____
Non-biologically Hazardous Waste
31
Urine may be discarded by _____
Pouring it into a laboratory sink under a Plexiglas Countertop Shield
32
Disinfection of the sink using a _____ or _____ dilution of sodium hypochlorite should be performed daily.
1:5 or 1:10
33
Disinfection of the sink using a 1:5 or 1:10 dilution of _____ should be performed daily.
Sodium hypochlorite
34
Disinfection of the sink using a 1:5 or 1:10 dilution of sodium hypochlorite should be performed _____.
Daily
35
Sharp objects in the laboratory includes:
Needles Lancets Broken Glassware
36
All sharp objects must be disposed in _____, _____ with the biohazard symbol
Puncture-resistant Leak-proof
37
True or False Every chemical in the workplace should be presumed hazardous.
True
38
For chemical spills and exposures, when a skin contact occurs, the best first aid is to _____ then _____
Flush the area with large amounts of water for at least 15 minutes Seek medical attention
39
Hazardous chemicals should be labeled with a description of their particular hazard, such as:
Poisonous Corrosive Flammable Explosive Teratogenic Carcinogenic
40
The _____ requires that all employees have a right to know about all chemical hazards present in their workplace.
OSHA Federal Hazard Communication Standard
41
The information about chemical hazards present in their workplace of an employee is provided in the form of _____ on file in the workplace
Material Safety Data Sheets (MSDSs)
42
Information contained in an MSDS includes the following:
1. Physical and chemical characteristics 2. Fire and explosion potential 3. Reactivity potential 4. Health hazards and emergency first aid procedures 5. Methods for safe handling and disposal 6. Primary routes of entry 7. Exposure limits and carcinogenic potential
43
Refers to the overall process of guaranteeing quality patient care and is regulated throughout the total testing system.
Quality Assessment
44
Refers to all of the laboratory’s policies, processes, procedures, and resources needed to achieve quality testing.
Quality System
45
Quality assessment program includes not only testing controls, referred to as quality control (QC), but also encompasses:
Preexamination Variables Examination Variables Postexamination Variables
46
A variable that occur before the actual testing
Preexamination Variables
47
These variables are the processes that directly affect the testing of specimens.
Examination Variables
48
True or False Reagent strips must be refrigerated, and must be recapped immediately after removing each strip.
False Reagent strips must be NEVER be refrigerated, and must be recapped immediately after removing each strip.
49
Frequently encountered instruments in the laboratory:
Refractometers Osmometers Automated Reagent Strip Readers Automated Microscopy Instruments
50
Common equipment in the laboratory:
Refrigerators Centrifuges Microscopes Water Baths
51
Temperatures of refrigerators and water baths should be taken _____ and recorded
Daily
52
The calibration of cetrifuges must be done _____ and the appropriate relative centrifugal force for each setting is recorded
Every 3 months
53
Centrifuges are routinely disinfected on a _____
Weekly basis
54
Refers to the materials, procedures, and techniques that monitor the accuracy, precision, and reliability of a laboratory test.
Quality Control
55
Quality Control refers to the _____, _____, and _____ that monitor the accuracy, precision, and reliability of a laboratory test.
Materials Procedures Techniques
56
Quality Control refers to the materials, procedures, and techniques that monitor the _____, _____, and _____ of a laboratory test.
Accuracy Precision Reliability
57
_____ are performed to ensure that acceptable standards are met during the process of patient testing.
QC Procedures
58
Used to verify the accuracy and precision of a test and are exposed to the same conditions as the patient samples.
External Quality Control
59
The ability to maintain both precision and accuracy.
Reliability
60
Reliability is the ability to maintain both _____ and _____
Precision Accuracy
61
Consists of internal monitoring systems built in to the test system
Internal Quality Control
62
Internal Quality Control is also called _____
Internal or Procedural Controls
63
Uses a mechanical or electrical device in place of a liquid QC specimen
Electronic Controls
64
Can be internal or an external component inserted into a point of care (POC) instrument.
Electronic Controls
65
Verifies the functional ability of a testing device but it does not verify the integrity of the testing supplies.
Electronic Controls
66
True or False Electronic Controls verifies the functional ability of a testing device and verify the integrity of the testing supplies.
False Electronic Controls verifies the functional ability of a testing device BUT IT DOES NOT verify the integrity of the testing supplies.
67
The testing of unknown samples received from an outside agency, and provides unbiased validation of the quality of patient test results.
Proficiency Testing (External Quality Assessment)
68
The _____ mandates comparison testing for laboratory accreditation.
Clinical Laboratory Improvement Amendments (CLIA)
69
Are processes that affect the reporting of results and correct interpretation of data
Postexamination Variables