PERIPHERAL BLOOD SMEAR Flashcards

1
Q

Blood smears should be made within__ hours after collection of EDTA blood

A

3

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2
Q

Correction for pseudothrombocytopenia

A

Recollect blood specimen using 3.2% sodium citrate

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3
Q

Platelets adhere on the surface of WBCs

A

Platelet satellitosis

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4
Q

Correction for pseudothrombocytopenia

A

Recollect blood specimen using 3.2% sodium citrate

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5
Q

Platelets form large clumps

A

EDTA-induced platelet clumping

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6
Q

Correction for pseudoleukocytosis

A

Recollect blood specimen using 3.2% sodium citrate

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7
Q

Conversion factor for correction when recollecting with 3.2% sodium citrate

A

1.1

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8
Q

Best for evaluation of blood cell morphology

A

Anticoagulant-free blood

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9
Q

Methods of blood film preparation:

A

Two-glass slide method
Coverslip technique
Automated methods

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10
Q

Most frequently used method in blood film preparation

A

Two-glass slide method (manual wedge technique)

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11
Q

Angle between the 2 slides in manual wedge technique

A

30 to 45 degrees

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12
Q

Too high angle equals

A

Thicker smear

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13
Q

Size of the drop of blood in manual wedge technique

A

2-3 mm

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14
Q

Distance of the drop from the margin

A

1 cm

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15
Q

Larger drop of blood equals

A

Thicker smear

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16
Q

Faster speed of the spreader equals

A

Thicker smear

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17
Q

If too high hematocrit

A

Angle should be lowered as low as 25 degrees

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18
Q

If too low hematocrit

A

Angle should be raised

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19
Q

Scanning methods

A

Longitudinal (tail to head)
Battlement (back and forth serpentine)

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20
Q

Characteristis of an ideal blood smear

A

Gradual transition from thick to thin area
2/3 to 3/4 the length of the film slide
Fingershaped
Visible lateral edges
Without irregularities, holes, or streaks
Feather edge has a rainbow appearance
Whole drop of blood is picked up and spread

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21
Q

Coverslip techniques:

A

Glass slide-coverslip method (Beacom’s method)
Two-coverslip method (Ehrlich’s method)

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22
Q

Coverslip technique is sometimes used for making what

A

Bone marrow aspirate smears

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23
Q

Only advantage of using the coversli technique

A

Excellent WBC distribution

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24
Q

Automated methods in making smears:

A

CellaVision HemaPrep
Centrifugal (Spinner) type
Coulter LH
Sysmex SP-10

25
No power source necessary, portable, and semi-automated preparation of two blood films
CellaVision HemaPrep
26
Uses approx. 0.2 mL of well-mixed anticoagulated blood
Centrifugal (Spinner) type
27
Slide makers and stainers
Coulter LH and Sysmex SP-10
28
Purpose of blood smear staining
Evaluation of cellular morphology
29
Important solutions for blood smear staining:
Fixative: methanol Stain: Wright or Wright-Giemsa Buffer: 0.05M sodium phosphate or aged distilled water
30
Defined as a stain which contains methylene blue and a halogenated fluorescein dye
Romanowsky-type stain
31
Basic stain that colors the nucleus and some cytoplasmic structures a blue or purple color
Methylene blue
32
An acidic stain that colors some cytoplasmic structures an orange-red color
Eosin
33
Examples of Romanowsky-type stains
Wright Giemsa May-Grunwald
34
Techniques of staining:
Manual Automated Quick
35
RBC appearance in well-stained smear
Orange to salmon-pink
36
WBC nuclei in well-stained smear
Purple to blue
37
Neutrophil cytoplasm in well-stained smear
Pink to tan with violet to lilac granules
38
Eosinophil granules in a well-stained smear
Bright-orange
39
When RBCs are gray or blue; WBCs are too dark; and eosinophil granules appear gray, what are usually the causes
Stain/buffer is too alkaline/basic Inadequate rinsing Heparinized blood was used
40
When RBCs are too pale or red and WBCs are barely visible, the usual causes would be
Stain/buffer is too acidic Underbuffering Over-rinsing
41
Blood film bluer than normal
Patient has increased blood proteins
42
Grainy appearance
RBC agglutination
43
Holes all over the film
Patient has increased lipid levels
44
Blue specks out at the feather edge
Markedly increased WBC counts and platelet counts
45
10x objective
LPO
46
40x objective
HPO
47
100x or 50x
OIO
48
Detect snowplow effect which will make the blood smear unacceptable
LPO
49
Assess overall film quality and distribution of cells
LPO
50
Locate rare abnormal WBCs
LPO
51
Detect fibrin strands, rouleaux formation, and unexpected parasites
LPO
52
Used to estimate total WBC count
HPO
53
Multiplication factor for WBC count counted using 40x high-dry objective
2000
54
Multiplication factor for WBC count counted using 50x oil immersion objective
3000
55
Used to examine the nuclear details of the WBC
OIO
56
Used for the tabulation of the actual WBC differential and estimation of platelet count
OIO
57
Multiplication factor used for the estimation of the platelet count
20, 000
58
Formula used for the estimation of platelet count of anemic patients
Average number of platelets per field x total RBC count / 200 RBCs per field
59
Storage of blood smear slides
At least 7 days before proper disposal