Manual Platelet Count (direct method) Flashcards

(41 cards)

1
Q

Often hard to differentiate from bacteria and debris

[platelet are difficult to count due of this]

A

Small size

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2
Q

Affinity for adhering to glass.

[platelet are difficult to count due of this]

A

Adhesiveness

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3
Q

Tendency to clump together.

[platelet are difficult to count due of this]

A

Aggregation

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4
Q

Normal platelet size ranges from:

A

2 - 4 µm

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5
Q

The primary function of platelets is:

A

Blood coagulation

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6
Q

The normal platelet count range is:

A

150, 000 - 400, 000/ uL

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7
Q

Whole blood is diluted with REES - ECKER DILUTING FLUID which makes platelets readily visible under the bright-field microscope.

A

Principle of Direct Platelet count

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8
Q

Diluting fluid commonly used in the direct method.

A

Rees - Ecker solution

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9
Q

Anticoagulant of choice for platelet counts is:

A

EDTA

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10
Q

The reference MANUAL PLATELET COUNT method.

A

Brecher - Cronkite

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11
Q

Brecher-Cronkite method uses:

[microscope]

A

Phase contrast microscope

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12
Q

Dilution factor for direct platelet count.

A

200

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13
Q

Platelets are counted in what area of the hemocytometer.

A

Central large square

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14
Q

Red (large square)

[are]

A

1mm²

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15
Q

Green (WBC square)

[area]

A

0.0625 mm²

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16
Q

Brecher - Cronkite Method

[diluting fluid]

A

1% ammonium oxalate

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17
Q

Yellow (RBC square)

[area]

18
Q

Blue (smaller RBC square)

[area]

19
Q

If low counts: Used WBC pipet

[dilution]

20
Q

If low counts: Used RBC pipet

[dilution]

21
Q

Prevents platelet clumping.

[tocantin’s method]

A

Neutral formalin

22
Q

Depth of the counting chamber.

23
Q

Prevents platelet clumping

A

Neutral formalin

24
Q

[3] Important parameters fo calculating the platelet counts:

A
  1. average number of platelets per square millimeter
  2. dilution factor
  3. volume of diluted blood counted.
25
Platelet counts below normal indicate:
Thrombocytopenia
26
Platelet count above normal indicate:
Thrombocytosis
27
To allow platelets to settle, hematocytometer is kept covered for?
10 - 15 minutes
28
Platelet counts from both chambers should differ by no more than:
10%
29
BACTERIA and DEBRIS can be mistaken for platelets because they are?
Refractile
30
Platelet aggregation in plasma.
Platelet satellitosis
31
[2] Equipment used: [brecher - cronkite method]
1. Hematocytometer 2. Thoma pipet
32
Microscope: [brecher - cronkite method]
Phase contrast microscope
33
Diluting fluid: [brecher - cronkite method]
1% ammonium oxalate
34
Microscope: [tocantin's method]
Light microscope
35
Diluting fluid: [tocantin's method]
Rees and Ecker
36
[7] Methods for Direct Platelet Count:
1. Brecher - Cronkite 2. Tocantin's 3. Guy and Leake's 4. Nygard's 5. Walker and Sweeney's 6. Van allens 7. Unopette (calibrated)
37
If 5 RBC squares are counted area should be
0.20mm²
38
If 25 RBC squares (central large square) are counted area should be
1 mm²
39
[4] Platelet counts BELOW NORMAL indicate thrombocytopenia and are found associated with: [APAI]
1. Aplastic anemia 2. Pernicious anemia 3. Acute leukemia 4. Idiopathic thrombocytopenia purpura
40
[4] Platelet count ABOVE NORMAL indicate thrombocytosis and are found associated with: [PHCA]
1. Polycythemia vera 2. Hemolytic anemia 3. Chronic Myeloproliferative Disorders 4. After splenectomy
41