Lecture 2 Flashcards

1
Q

Why do we still need to look at blood films?

A

validate numeric data generated by the hematology analyzer

add valuable info that only a trained human can provide

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2
Q

List 6 things that need to be validated in the blood film?

A
RBC quantity (RBC count, HCT, Hgb)
RBC indices (MCV, MCHC, RDW)
WBC count 
WBC differential
Platelet count
Platelet indices
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3
Q

What 4 things can you add that only a trained human eye can provide?

A

RBC morphology (clues to cause of anemia)
WBC morphology ( shows whether or not there is inflammatory response or neoplasia)
platelet morphology
infectious diseases

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4
Q

What 4 things are important in a blood film preparation?

A
  1. Anticoagulated blood (EDTA tube)
    - invert tube at least 8 times before making smear
  2. Fill tube to appropriate line
  3. Prepare the film asap after collection
  4. rapidly dry films to prevent air drying artifact (DO NOT heat fix)
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5
Q

2 blood film smear techniques

A

Push film

Coverslip

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6
Q

What is the name of the stain used for the fixative?

A

Diff Quik stain

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7
Q

how long do you leave the smear in the fixative?

A

at least 2 min won’t hurt it to stay longer

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8
Q

What stain is used for detecting reticulocytes and Heinz bodies?

A

New methylene blue

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9
Q

Can you use tap water to rinse the slide

A

yes if it is the right pH/ if not need to use distilled

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10
Q

true/ False

You need to wash with water in between stains

A

False - just let it drip on paper towel in between stains

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11
Q

What results in a refractile artifact or moth eaten appearance?

A

Water artifact

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12
Q

What does refractile artifact mean?

A

As you focus up and down on the cell the artifact flashes; in one plane of focus it may appear dark while in another one it may appear bright

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13
Q

What is water artifact often mistaken for?

A

Red blood cell inclusion ie. parasite

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14
Q

What 3 things can you evaluate from the blood smear grossly?

A

if the smear was appropriately made
if the animal is anemic
if there is autoagglutination

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15
Q

What part of the blood film is too thick to evaluate?

A

base

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16
Q

What part of the blood film do you look at to see platelets or parasites ie. big things?

A

the feathered edge

clumped platelets, large cells, microfilaria, leukocyte inclusions

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17
Q

What part of the blood film is used to evaluate and count RBC and WBC’s?

A

the “counting area”

18
Q

What is seen in the feathered edge?

A

Clumped platelets
large cells
Microfilaria
Leukocyte inclusions

19
Q

What part of the smear do you evaluate first on low power?

A

feather edge to check for platelet clumps and microfilaria

20
Q

IF analyzer says you have a low platelet count (thrombocytopenia) what should you do?

A

go to the feathered edge to see if there is platelet clumping

21
Q

what do the RBC’s look like in the feathered edge?

A

completely flattened and lack central pallor, look like spherocytes. Abnormal shapes are difficult to recognize in this area

22
Q

What is evaluated in the monolayer on the blood smear?

A

Estimate platelet number
Estimate leukocyte number and differential count
Morphologic evaluation of all the cells
Data validation

23
Q

What happens when you place a coverslip on the blood smear?

A

Big things will appear on the periphery of the coverslip

24
Q

Where is the monolayer located on the blood smear?

A

one 10x field behind the feathered edge

25
Q

Why is the monolayer the optimal area for examination of cells

A

it dries quickly
cells are spread out and not disrupted
RBC’s are separated with little overlapping
WBC’s are also uniformly distributed

26
Q

What do you evaluate on the blood smear on low power?

A

Confirm cell counts
Determine the predominant WBC
Look for big things: platelet clumps, abnormal cells, microfilaria

27
Q

What WBC cell should be predominate in dogs, cats, and horses?

A

neutrophils

28
Q

What WBC will be predominant in birds and reptiles?

A

lymphocytes

29
Q

What animal species usually have clumped platelets?

A

cats

30
Q

What are clumps of WBC’s referred to as?

A

Leukergy

31
Q

What do you evaluate under high power on the blood film?

A

WBC number and morphology
RBC arrangement, size, shape, color, and inclusions, and validate numeric data
platelet number and morphology

32
Q

True/ False

It is okay to accept a low platelet count from an automated analyzer w/o confirming it on the blood film

A

FALSE! - there may be platelet clumping

33
Q

What is the bare minimum of platelets in dogs and cats?

A

7-10 per 100x field

34
Q

How do you estimate platelets counts?

A

determine average # of platelets per 100x field and multiply by 20,000/microliter

35
Q

What do large platelets suggest?

A

increased marrow production of platelets

normal for felids and Cavalier King Charles Spaniels

36
Q

True/False

the analyzer will still count large platelets

A

False

37
Q

How do you estimate the number of leukocytes in the smear?

A

Take the average # of leukocytes per 100x field after evaluating 10 fields and multiply by 10,000

38
Q

What 3 things do you do when evaluating platelets on the smear?

A

Evaluate number of platelets per 100x field (should be at least 7-10)
Estimate platelet count
Check for large platelets

39
Q

What 3 things do you do when evaluating leukocytes on the smear?

A
  • Estimate leukocyte number per microliter
  • Do a differential leukocyte count on 50x or 100x (look at 200 WBC’s and tabulate the type)
  • Evaluate leukocyte morphology on 50x and 100x
40
Q

What do you evaluate neutrophils for?

A

left shifting and toxicity

41
Q

What do you evaluate lymphocytes and monocytes for?

A

Reactivity (will have more cytoplasm)