Common Tests for primary hemostasis Flashcards

1
Q

Reasons platelets are hard to count

A

Adhere to foreign surfaces, easily disintegrate, hard to differentiate from debris, unevenly distributed due to clumping

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Normal platelet count (general)

A

150 to 450 x 10^9/L

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Platelet count decrease after 65 years

A

122 to 350 x 10^9/L in men, 140 to 379 x 10^9/L in women

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Platelet count < 100,000/µL

A

Most common cause of clinically important bleeding

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Phase-contrast microscope method reference

A

Described by Brecher and Cronkite

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

EDTA whole blood dilution for phase-contrast

A

1:100 with 1% ammonium oxalate to lyse RBCs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Platelets counted in phase-contrast method

A

25 small squares of central large square (1 mm²) in hemocytometer

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Verification of manual thrombocyte count

A

Estimate on Wright-stained PBS made from same specimen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Alternate method to count platelets

A

Light microscope, but harder to visualize platelets

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Reference method for platelet count

A

Phase-contrast microscope method by Brecher and Cronkite

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Dilution for phase-contrast method

A

1:100 with 1% ammonium oxalate (lyses nonnucleated RBCs)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Area for platelet count in hemocytometer

A

25 small squares of the central large square (1 mm²)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Accuracy verification for manual count

A

Estimate on Wright-stained PBS from the same specimen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Alternate method for platelet visualization

A

Light microscope (more difficult to visualize platelets)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Platelet characteristics under phase-contrast microscopy

A

Diameter: 2-4 µm, Shape: round/oval, Color: light purple sheen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Background feature often seen in phase-contrast microscopy

A

Ghost erythrocytes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Counting area for platelets in hemocytometer

A

25 small squares of the central large square (1 mm²)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Acceptable difference in counts between sides of hemocytometer

A

< 10% difference

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Action for uneven platelet distribution

A

Repeat the procedure if > 10% difference

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Anticoagulant used for phase-contrast platelet count

A

1% ammonium oxalate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Purpose of placing charged hemocytometer in a moist chamber

A

Allows platelets to settle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

Components of a moist chamber

A

Damp filter paper in a Petri dish, applicator stick as support

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Incubation time for platelets in the moist chamber

A

15 minutes

24
Q

Formula for percentage difference

A

[(V1 - V2) / (V1 + V2 ) x 100]

25
General formula for manual cell counts (average of platelet count should be counted on two sides)
PLT count (cells/µL) = (cells counted x dilution factor) / (area (mm²) x depth (0.1))
26
Examine the thin area where
a few RBCs slightly overlap under oil immersion.
27
Normal platelet count per 100x field on a wedge smear
Approximately 7 to 21 platelets.
28
Platelet estimation formula
Average platelets/OIF x 20,000 = estimated platelet count (µL).
29
Adjusted platelet estimation formula
(Average platelets per field x total RBC count) / 200 RBCs per field.
30
Topic
Details
31
200 in adjusted formula represents
Average RBCs per oil immersion field in the optimal assessment area.
32
Platelet estimate of 0 to 49,000/µL; qualitative report
marked decrease
33
Platelet estimate of 50,000 to 99,000/µL; qualitative report
moderate decrease
34
Platelet estimate of 100,000 to 149,000/µL; qualitative report
slight decrease
35
Platelet estimate of 150,000 to 199,000/µL; qualitative report
low normal
36
Platelet estimate of 200,000 to 400,000/µL; qualitative report
normal
37
Platelet estimate of 401,000 to 599,000/µL; qualitative report
slight increase
38
Platelet estimate of 600,000 to 800,000/µL; qualitative report
moderate increase
39
Platelet estimate above 800,000/µL; qualitative report
marked increase
40
Designed to test platelet-rich plasma (PRP)
light-transmittance (optical) platelet aggregometry
41
Centrifuge requirement for PRP
50 x g for 30 minutes
42
PRP specimen storage
18 to 24°C until test
43
PRP aggregometry initiation
No less than 30 minutes, within 4 hours
44
Minimum whole blood volume needed for adequate PRP
9 to 12 mL
45
Light-transmittance aggregometry is unreliable when whole-blood platelet count is
< 100,000/µL
46
PRP amount with a platelet count of
200,000 to 300,000/µL
47
Aggregating reagents ACE
ADP, Collagen, Epinephrine/adrenaline
48
Normal response to ACE
BSS and vWF disease
49
Abnormal response to ACE
Glanzmann's thrombasthenia
50
Ristocetin normal response
Glanzmann's thrombasthenia
51
Ristocetin abnormal response
BSS and vWF
52
Measures platelet aggregation and ATP release (from dense granules)
Platelet lumiaggregometry
53
Specimen for platelet lumiaggregometry
Whole blood diluted with saline
54
Reagent for platelet lumiaggregometry
Luciferin-luciferase
55
Source of luciferin-luciferase
Firefly