Blood Smear Flashcards

1
Q

:SPECIMEN OF CHOICE

A

ANTICOAGULANT-FREE BLOOD

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2
Q

• LAVENDER (PURPLE) - TOPPED TUBES
• Contain…

A

disodium or tripotassium ethylenediameteraccetic acid (EDTA)

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3
Q

• PREFERRED EDTA

A

LIQUID TRIPOTASSIUM (K3) EDTA

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4
Q

Time limit for blood smear preparation

• Made within____ of drawing the specimen
•_____= have unacceptable blood cell artifacts

A

4 hours

> 5 hours

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5
Q

ADVANTAGE using EDTA

A

• Multiple slides can be made
• Do not have to be prepared immediately
• Prevents platelets from clumping on the glass slides

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6
Q

The quality of these smears depends heavily on the…

A

source of collection and the handling of the specimen.

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7
Q

Why Anticoagulant-Free Blood?

A

• The absence of anticoagulants allows for optimal preservation of cellular morphology.

• It prevents artifacts that can be introduced by chemical additives.

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8
Q

Liquid Tripotassium (K3) EDTA is the preferred form of EDTA for hematological studies because it:

A

• Provides better anticoagulation.
• Reduces platelet clumping.
• Preserves cellular morphology.

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9
Q

is an in vitro phenomenon where platelets surround or adhere to neutrophils, forming clusters.

A

Platelet satellitosis

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10
Q

Platelet satellitosis

Causes…

A

Causes pseudothrombocytopenia in automated hematology analyzers.

• Platelet count appears falsely low (since platelets are not counted independently).

• White blood cell (WBC) count appears falsely high (pseudoleukocytosis) as the analyzer may count platelet-bound neutrophils as WBCs.

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11
Q

How to Eliminate Platelet Satellitosis?

A

• Recollect the specimen using sodium citrate tubes (light blue top).

• Mix blood in a 9:1 ratio (blood to sodium citrate).

Perform manual platelet count or peripheral smear review to confirm findings.

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12
Q

FINGER AND HEEL PUNCTURES

These are capillary blood collection methods, commonly used in:

A

• Neonates and infants (heel puncture).

• Adults when venous access is difficult (finger puncture).

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13
Q

FINGER AND HEEL PUNCTURES

Advantages

A

• Smears can be made immediately at the patient’s side, reducing processing delays.

• Useful for patients with difficult venous access.

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14
Q

FINGER AND HEEL PUNCTURES

Disadvantages

A

Platelet clumping: Capillary blood tends to have platelet aggregation, which can lead to inaccurate platelet counts.

Limited sample volume: Only a few slides can be made directly from skin puncture blood, limiting repeat testing.

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15
Q

Advantage and disadvantage sodium citrate tubes

A

Eliminates platelet satellitosis
Dilution effect requires correction

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16
Q

Dilution factor for sodium citrate

A

1.11

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17
Q

• Easiest to learn and perform.
• Most commonly used method in hematology laboratories.

A

Manual Wedge Technique

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18
Q

Manual blood smear

• Requires two clean glass slides (size L x W).

A

3 inches × 1 inch

19
Q

Uses a drop of blood approximately______

A

2–3 mm in diameter

20
Q

Spreader slide is positioned at a _____angle to ensure a smooth and even smear.

21
Q

IMPORTANT

The entire drop of blood must be__________ to prevent uneven distribution of cells.

A

picked up and spread evenly

22
Q

Types of Wedge Techniques
1. ________– The spreader slide pushes the blood forward.

  1. _________– The spreader slide pulls the blood backward.
A

Push-type wedge

Pull-type wedge

23
Q

Steps for Making a Blood Smear

A
  1. Clean the slides – Ensure both the base slide and spreader slide are clean and dry to prevent artifacts.
  2. Place an appropriate drop of blood (2–3 mm in diameter) near one end of the slide.
  3. Maintain a consistent 30–45° angle while spreading the blood using a second slide as the spreader.
  4. Move the spreader slide in a smooth, quick motion all the way to the end of the film.

5. Apply even, gentle pressure to the spreader slide to avoid ridges or waves.

  1. Ensure the smear has a feathered edge with a gradual transition from thick to thin.
  2. Allow the smear to air-dry completely before staining —do not blow on it or use artificial heat.
  3. Use the correct staining procedure (e.g., Wright-Giemsa stain) to ensure accurate cell visualization.
  4. Label the slide properly with patient identification details.
24
Q

Smear too thin or too long

A

Drop of blood too small
Spreader slide at too low an angle
Improper speed in making smear

25
Smear too thick or too short
Drop of blood too large Spreader slide at too high an angle Improper speed in making smear
26
Ridges or waves in smear
Uneven pressure on spreader slide Hesitation in pushing spreader slide
27
Holes in smear
Slides not clean Uneven or dirty edge of spreader slide
28
Uneven cell distribution
Uneven pressure during spread of blood Delay in spreading blood Uneven or dirty edge of spreader slide
29
Artifacts or unusual cell morphology
Smear dried too slowly Smear not fixed within one hour after preparation High humidity
30
Features of a well-made wedge PBF 1. The film is _______the length of the slide 2. The film is_____ shaped, very slightly rounded at the feather edge, not____ shaped 3. The______ are visible 4. The film is smooth without_____ 5. When the slide is held up to the light the thin portion (feather edge) of the film has a "_____" appearance. 6. The whole drop of blood is picked up and spread.
two-thirds to three-fourths finger; bullet lateral edges of the film irregularities, hole, or streaks. rainbow
31
is a crucial step in preparing peripheral blood films (PBFs) because it ***enhances the visibility of blood cells and allows for the evaluation of their morphology.*** The most commonly used stains belong to the _________group, particularly_____(2)
Staining Romanowsky stain Wright stain and Wright-Giemsa stain.
32
• Used for staining (2). • _______– contains both acidic and basic dyes, allowing different cell structures to be stained distinctly.
Romanowsky Stains (Wright Stain and Wright-Giemsa Stain) peripheral blood films and bone marrow smears Polychrome stain
33
Purpose: • Enhances contrast between different cellular components. • Allows proper evaluation of RBC, WBC, and platelet morphology.
Staining
34
Fixative: • _______– fixes cells to the slide, preventing washing away during staining.
Methanol
35
• Faster and easier than traditional Romanowsky stains.
Quick Stains (Modified Wright or Wright-Giemsa Stain)
36
Advantages of quick stain
• Rapid processing. • Cost-effective and convenient for routine laboratory use.
37
Quick stain • The entire staining process takes about______ • ________is used as a buffer to maintain proper staining pH.
1 minute. Aged distilled water
38
Staining MANUAL TECHNIQUE • Performed over a… • Stains:_____ before use or poured from the bottle through a filter onto the slide.
sink or pan with a staining rack filtered
39
Manual staining technique • IMPORTANT: • Flood the slides completely • Stain should remain on the slide at least______ • Equal amount of_____ is added •_________ = MIXING IS CORRECT (indicator)
1 to 3 minutes buffer Metallic sheen (or green "scum")
40
Slides that are too pink may be due to:
• Stain time too short • Wash time too long • pH of stain or buffer too acidic
41
Slides that are too blue may be due to:
• Overstaining • Wash time or buffering time too short • pH of stain or buffer too alkaline
42
FEATURES OF A WELL-STAINED PERIPHERAL BLOOD FILM • Best results are obtained….
on fresh slides
43
FEATURES OF A WELL-STAINED PERIPHERAL BLOOD FILM RBC - appear________ WBC: Nuclei should be______ • Neutrophil - Cytoplasm should be______ with _______ granules • Eosinophil - _______granules
orange to salmon pink purple to blue pink to tan with violet or lilac granules bright orange refractile