Chapter 6 (MICR) Flashcards

1
Q

which of the following is not a biological hazard?
a) bacteria
b) microbial toxins
c) infectious material (blood, body fluid, cell lines)
d) prions
e) they are all biological hazards

A

they are all hazards

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2
Q

who is responsible for the administration and enforcement of the human pathogens and toxins act and regulations?
a) federal minister of health
b) provincial minister of health
c) municipal minister of health
d) none of the above

A

a) federal minister of health

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3
Q

what does the scope of the human pathogens and toxins act and regulations include?
a) human pathogens
b) terrestrial animal pathogens
c) prescribed list of microbial pathogens
d) all of the above

A

d) all of the above

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4
Q

T/F the purpose of the legislation (HPTAR) is to establish a safety and security regime to protect the health and safety of the public against the risks posed by human and animal pathogens and toxins

A

true

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5
Q

Which of the following is responsible for notification, reporting, and incident investigation regarding laboratory incidents?
a) OHIP
b) CMLTO
c) PHAC
d) CSMLS

A

c) PHAC

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6
Q

which of the following is not used when classifying risk groups?
a) pathogenicity
b) virulence
c) risk of spread
d) availability of effective treatment
e) infectious dose

A

e) infectious dose

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7
Q

what are the risk groups and what are their risks to individuals and the community?

A

risk group 1: low individual risk, low community risk
risk group 2: moderate individual, low community risk
risk group 3: high individual risk, low community risk
risk group 4: high individual risk, high community risk

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8
Q

T/F the risk group and containment level are generally the same

A

T (risk group 2 = containment level 2)

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9
Q

what is the exception to the rule where risk group is generally the same as containment level?
a) HIV and MTBC are Risk Group 2 but must be handled at CL3
b) HIV and MTBC are Risk Group 3 but can be handled at CL2
c) HIV and HPV are Risk Group 3 but can be handled at CL2
d) HPV and MTBC are Risk Group 2 but must be handled at CL3

A

b) HIV and MTBC are risk group 3 but can be handled at CL2

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10
Q

containment levels describe?

A

the minimum physical features and operational practices needed for the safe handling and storage of biohazards within an identified area

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11
Q

which of the following would not be a physical containment requirement?
a) containment barrier (non openable windows)
b) access (doors are accesible to anyone)
c) surface and finished (cleanable and non-absorbent)
d) air handling (minimize spread of infectious aerosols)

A

b) access because the doors should be lockable to keep track of who has access and at what times

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12
Q

T/F the majority of clinical and diagnostic laboratories are likely to handle and store risk group 2 material at containment level 2

A

true!

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13
Q

containment level 1 achieves biosafety by:
a) use of GMLP, basic physical contamination design such as handwashing sinks
b) GMLP, administrative controls, procedures for PPE, primary containment devices like BSC
c) stringint facility design, engineering controls (HEPA filters), specialized biosafety equipment
d) none of the above

A

a) use of GMLP, basic physical contamination design such as handwashing sinks

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14
Q

containment level 2 achieves biosafety by:
a) use of GMLP, basic physical contamination design such as handwashing sinks
b) GMLP, administrative controls, procedures for PPE, primary containment devices like BSC
c) stringint facility design, engineering controls (HEPA filters), specialized biosafety equipment
d) none of the above

A

b) GMLP, administrative controls, procedures for PPE, primary containment devices like BSC

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15
Q

containment level 3 achieves biosafety by:
a) use of GMLP, basic physical contamination design such as handwashing sinks
b) GMLP, administrative controls, procedures for PPE, primary containment devices like BSC
c) stringint facility design, engineering controls (HEPA filters), specialized biosafety equipment
d) none of the above

A

c) stringint facility design, engineering controls (HEPA filters), specialized biosafety equipment

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16
Q

which of the following is not part of the links in the chain of transmission?
a) portal of entry + exit
b) infectious dose
c) susceptible host
d) mode of transmission

A

b) infectious dose

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17
Q

T/F an infectious agent is a disease-causing organism or pathogen, often a virus or a bacterium

A

true

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18
Q

which of the following is not a type of reservoir?
a) person
b) animal
c) environmental component (soil, water)
d) all of the above

A

d) all of the above

19
Q

which of the following is not considered a portal of exit?
a) blood
b) saliva
c) feces
d) strand of hair

A

d) strand of hair

20
Q

T/F direct transmission requires close association with the infected host, as well as physical contact

A

F, physical contact is not required

21
Q

T/F indirect transmission requires a vector such as animal or insect

A

true

22
Q

which of the following is not portal of entry?
a) penetration
b) inhalation
c) ingestion
d) reception

A

d) reception

23
Q

which of the following would not be a susceptible host?
a) pregnant woman
b) medical status such as cancer
c) taking immunosuppresant medications
d) being in your 30’s

A

d) being in your 30’s

24
Q

what are the chains of transmission?

A
  1. infectious agent
  2. reservoir
  3. portal of exit
  4. mode of transmission
  5. portal of entry
  6. susceptible host
25
Q

A BSC must be used for procedures involving open vessels of biohazards that:
a) may produce infectious aerosols
b) involves high concentrations
c) involves large volumes
d) all of the above

A

d) all of the above

26
Q

which of the following route of exposure is the least understood and most underestimated?
a) skin contact
b) injection
c) inhalation
e) none, they are all equally understood

A

c) inhalation

27
Q

T/F aerosols are suspensiosn of liquid particles in air that may gain access to the respiratory system

A

F, solid and liquid particles

28
Q

respiratory exposure to airborne infectious agents is dependent on:
a) type of infectious agent
b) concentration of infectious agent
c) persistence of aerosol
d) length of exposure time
e) all of the above

A

e) all of the above

29
Q

T/F the CSMLS deems the N95 respirator as the minimum level of protection for MLTs that may be exposed to airborne infectious agents

A

True

30
Q

which of the following is false regarding decontamination?
a) process by which materials and surfaces are rendered safe to handle and reasonably free of microorganisms, toxins, or prions
b) can be accomplished only through disinfection only
c) can be done via autoclaves, filtration, boiling or incineration
d) all of the above is true

A

b) can be done via disinfection, inactivation or sterilization!

31
Q

T/F sterilization is a process that completelt eliminates all living microorganisms including bacterial spores

A

true

32
Q

the effective operating temperature for steam autoclaves is usually
a) 100C
b) 150C
c) 121C
d) 131C

A

c) 121C

33
Q

unsatisfactory decontamination by autoclaves is commonly attributed to:
a) insufficient temperature
b) inadequte cycle time
c) incomplete penetration of steam
d) all of the above

A

d) all of the above

34
Q

the recommended test microorganisms generally used as biological indicators are:
a) geobacillus stearothermophilus and staphylococcus aureus
b) geobacillus stearothermophilus and bacillus atrophaeus
c) bacillus atrophaeus and staphylococcus aureus
d) you can use any microorganism as a biological indicator

A

b) geobacillus stearothermophilus and bacillus atrophaeus

35
Q

_______ is used for sterilizers that use steam, hydroxen peroxise gas plasma or peracetic acid, and ______ is used for sterilizers that use dry heat or ethylene oxide

A

geobacillus stearothermophilus; bacillus atrophaeus

36
Q

list the advantages and disadvantages to biological indicators

A

A: very specific to temperature and time
D: test material must be incubated for 24-48hrs before result, not always easy to store until results received

37
Q

steam, temperature and time-dependent chemical integrators include:
a) sealed glass tubes containing chemical that changes colour when exposed to proper conditons
b) paper strips impregnated w/ chemical that changes colout when proper conditions met
c) tube within a foil and paper strip which contains blue wax that migrats along tube when proper materials met
d) all of the above

A

d) all of the above

38
Q

what is a chemical integrator?

A

system that responds to change in one or more predefined process variables with a chemical or physical change

39
Q

disinfection can be defined as:
a) completely eliminates all living microorganisms including bacterial spores
b) eliminates most forms of living microorganisms, but not all
c) removes living microorganisms from surfaces
d) none of the above

A

b) eliminates most forms of living microorganisms, but not all

40
Q

a 1:10 dilution can be used for _______, while a 1:100 dilution can be used for _____

A

spill control; wipe down of surfaces or equipment

41
Q

which of the following is not a susceptible bacteria?
a) fungal spores
b) gram negative bacteria
c) mycobacteria
d) enveloped viruses
e) gram positive bacteria

A

c) mycobacteria -> its resistant

42
Q

which of the following is extremely resistant?
a) protozoal oocysts
b) bacterial endospores
c) prions
d) mycoplasms
e) non-enveloped virus

A

c) prions

43
Q
A