automated analyzers (wk 11 study questions) Flashcards

1
Q

3 benefits to the practice for using automated analyzers

A

Reduced labor costs
More complete information
Improved data reliability

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2
Q

Which of the automated cell counts are least accurate, RBC, WBC or Platelet?

A

platelet

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3
Q

Polycythemia

A

Increased number of RBCs; Accompanied by increased PCV and hemoglobin concentration

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4
Q

Anemia

A

Decrease in the oxygen-carrying capacity of the blood

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5
Q

three categories of analyzers

A

Impedance
Laser Flow Cytometry
Quantitative Buffy Coat Analysis System

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6
Q

Why should the CVT run regular quality control measures on the analyzer?

A

to ensure accuracy

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7
Q

Explain how impedance is used to count cells and how the machine can tell
an RBC from a WBC using this method

A

 Passage of electric current across two electrodes separated by a glass tube with a small opening or aperture
 Electrolyte fluid conducts the current.
 Counting by moving a specific volume of cells in the electrolyte solution through the aperture by use of a vacuum or positive pressure
 Cells are poor conductors and impede the flow of the current
 Change in current is a function of cell size

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8
Q

disadvantages to using the impedance analyzer

A

Variation of cell size
Morphologic abnormalities not noted
Platelet clumping inaccuracies
Nucleated RBC inaccuracies

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9
Q

Quantitative Buffy Coat analysis system and its limitations

A

-Uses differential centrifugation and staining to estimate cells
-Uses specialized microhematocrit tube.
-Gives hematocrit value and estimates WBC and platelet concentrations
Limitation:
-Groups granulocytes and agranulocytes
-Left shift and Lymphopenia may go undetected
-Provides only estimates

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10
Q

Laser-based flow cytometer

A

Uses focused laser beams to evaluate the size and density; Cells scatter light differently

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11
Q

When would manual cell counts be performed?

A

avian and exotic practices

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12
Q

three advantages for running a CBC using the automated analyzer

A

-Faster than manual counts
-No operator bias
-More reproducible: counts more cells than manual
-Little training needed

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13
Q

disadvantages of running a CBC on the automated analyzer

A

-Clots, large platelets, and Nucleated RBCs can cause errors
-Can not pick up diagnostic changes in cell morphology

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14
Q

When should a blood smear be made and examined for a patient sample?

A

Recommended for all CBCs but definitely for sick patients

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15
Q

hematology analyzers

A

Impedance method:
-Cells pass through a charged aperture, disrupting the current
-Each interruption is counted
-The length of the interruption is proportional to cell size
-Chemical lysing agents are also used to help differentiate the cells

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16
Q

What are the graphs called that are shown on the results screen?

A

histogram

17
Q

Dot plot

A

A visual representation of the CBC

18
Q

What does the size and shape of the cloud on a dot plot tell us?

A

an indication of whether the cells of one type (i.e. the RBCs) are all similar in size or abnormally varied

19
Q

What would the RBC dot plot look like if the patient was anemic?

A

very small

20
Q

What would the WBC dot plot look like if the patient had neutrophilia?

A

larger

21
Q

What can the dot plot tell you about abnormal cell morphology?

A

size only

22
Q

doublets

A

Two discreet red blood cells that are in close proximity to one another when they are examined by the laser beam; mapped as one event but counted as two cells

23
Q

RBC fragments

A

-Portions of red blood cell membranes from broken cells
-Particles have a similar size to platelets but refract light differently and are therefore located to the left of the platelet population
-Colored pink

24
Q

uRBC

A

Unlysed RBC (colored orange)

25
Q

qualiBeads in the Lasercyte

A

Each CBC5R tube contains a known quantity of standard-sized particles called
QualiBeads. Quality assurance check for each individual run. If too few or too many QualiBeads, the sample run will be flagged

26
Q

Explain how to load the Lasercyte to run a sample

A

3 mL tube
invert 8 times
remix sample prior to testing
place CBC5R tube in slot 2
place sample in slot 1
close lid and run

27
Q

Platelet clumping can cause an error in the RBC count. Do you think the RBC
count will be too low or too high?

A

too high-recognized as RBC
therefore increased RBC count

28
Q

Platelet clumping will also cause an error in the platelet count. Will it be too low
or too high?

A

Too low as platelets will not be counted