WBC Counts Flashcards

(25 cards)

1
Q

Machine count

A
  1. Expensive
  2. Rapid
  3. Precise (+/- 2%)
  4. Repeatable
  5. Anyone can run a machine
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2
Q

Hemocytometer

A

Special grid slide
1. Cheap
2. Slow
3. Laborious
4. Moderately precise (+/- 10%)
5. Math
6. Learning curve

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3
Q

Manual Count

A

Regular glass slide
1. Slow
2. Moderately precise (+/- 5-15%)
3. Repeatable if consistent operator
4. Learning curve
5. Average WBC on 10x/4

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4
Q

What is a ‘gate’ in a machine count?

A

A ‘normal range’ for a cell, each machine has a slightly different gate depending on the person programming.

Clouds inside a gate should be ‘clean’

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5
Q

Should you examine scatterplot or smear first?

A

Scatterplot

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6
Q

Do you need to do a smear evaluation even if the clouds are clean?

A

Yes, machines can’t see clumping and rbc morphologies (ie. acanthocytes, schiztocytes, keratocytes)

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7
Q

Steps when performing a smear evaluation

A
  1. 20x: rapid scan of smear from top to bottom
  2. 50x
  3. 100x: go to monolayer
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8
Q

Why should you look at a blood smear at 20x?

A
  1. Assess for WBC clumping
  2. Estimate WBC count to compare to machine
  3. Easier to find leukocytes present in low numbers
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9
Q

Left shift

A

the shifting of a population of cells towards immaturity

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10
Q

The circulating pool is called to tissues via ___________

A

chemotaxis

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11
Q

The marginating pool can de-marginate in ______________

A

seconds to minutes

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12
Q

The storage pool can be called in ____________

A

minutes to hours

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13
Q

The three types of left shifts

A
  1. Regenerative
  2. Transitional
  3. Degenerative
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14
Q

Regenerative left shift

A
  1. increased seg neutrophils in blood (neutrophilia)
  2. bone marrow expanded to meet demand
  3. active inflammation
  4. Prognosis: good
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15
Q

Transitional left shift

A
  1. segmented neutrophils WRI
  2. active inflammation
  3. Prognosis: monitor
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16
Q

Degenerative left shift

A
  1. segmented neutrophils decreased (neutropenia)
  2. inflammation overwhelming BM
  3. Prognosis: guarded to critical
17
Q

Toxicity

A

results of rapid maturation of neutrophil that leads to morphologic defects (ie. lacy cytoplasm, foamy cytoplasm, dohle bodies)

18
Q

How long does it take for neutrophils to be produced?

A

Normally 3-5 days. Can be sped up to 2-4 days in need.

19
Q

dohle bodies

A

chucks of rough ER that has a bunch of polysomes (blue appearance)

20
Q

Two important leukograms

A
  1. Stress/Glucocorticoid Leukogram
  2. Physiologic/Excitement Leukogram
21
Q

Stress Leukogram

A

Due to an increase in glucocorticoid. It causes
1. Neutrophilia (demargination of NEU)
2. Monocytosis (demargination of monocytes)
3. Eosinopenia (marrow sequestration of EOS)
4. Lymphopenia* (lympholysis/apoptosis)
5. Hyperglycemia that is still below 200 mg/dL*

22
Q

Difference between marginating pool size of dogs and cats

A

Dogs: Marginating pool is the same size as circulating pool
Cats: Marginating pool is twice the size as circulating pool

23
Q

Excitement Leukogram

A

Due to epinephrine/catecholamines. It causes:
1. Neutrophilia (demargination)
2. Monocytosis (demargination)
3. Eosinopenia (marrow sequestration)
4. Lymphocytosis* (redistribution from lymphoid tissues)
5. Hyperglycemia that is >200 mg/dL +/- glucosuria

24
Q

Acute inflammation

A
  1. Usage of circulating, marginating, and storage pool
  2. Expansion of granulopoiesis
  3. Mobilization of monocytes
25
Chronic Inflammatoin
1. BM expands to meet demand 2. Monocyte pool expands