REVIEW QUESTIONS Flashcards

(42 cards)

1
Q

Bleeding Time is used to evaluate the activity of:

A

Platelets

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2
Q

Which of the following test results is normal in a patient with classic von Willebrand’s disease?

A

Platelet count

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3
Q

No bleeding is observed in deficiency of which of the following factors?

A

XII

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4
Q

Hemolytic Uremic syndrome is associated with:

A

E.coli

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5
Q

Coagulation Factors affected by Coumarin Drugs:

A

II, VII, IX, X

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6
Q

Thrombotic thrombocytopenic purpura is characterized by:

A

Increase platelet aggregation

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7
Q

A protein that plays a vital role in both coagulation and platelet aggregation:

A

I

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8
Q

The defect characterizing Gray’s Syndrome:

A

Alpha Granule

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9
Q

Factor XIII is activated by which factor?

A

IIa

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10
Q

Factor V is a cofactor to factor X to activate factor II

A

True

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11
Q

What clotting factors are inhibited by Protein S

A

V and VIII

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12
Q

What is the second phase of secondary hemostasis?

A

Activation of Factor X

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13
Q

Several hours after birth, a baby boy develops petechiae and a hemorrhagic diathesis. Platelet count is 8,000/uL. What is likely the explanation?

A

Isoimmune Neonatal Thrombocytopenia

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14
Q

When performing platelet aggregation studies, which is most likely associated with Bernard Soulier Syndrome?

A

Normal to Epinephrine, Decreased to Ristocetin

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15
Q

Which of the following is a characteristics of acute idiopathic thrombocytopenic purpura?

A

Spontaneous remission within a few weeks

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16
Q

Factor XIII is a serine protease

A

False

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17
Q

Which of the following inhibitors inhibit Factor IIa?

A

Both; Protein C and Antithrombin III

18
Q

Which of the following is correct regarding acquired thrombotic thrombocytopenic purpura?

A

Autoimmune Disease

19
Q

TAFI target protein:

20
Q

Which step requires calcium?

A

Factor XIII activation

21
Q

Giant platelet is associated with which condition:

A

Bernard Soulier Syndrome

22
Q

Platelet abnormality will affect both bleeding time and clotting time

23
Q

Which of the following is associated with post transfusion purpura?

A

Immune mediated thrombocytopenia/Alloantibodies

24
Q

Thiazide diuretics results to:

A

Decreased Platelet Production

25
Which of the following Factors is used only in the Extrinsic Coagulation Pathway?
VII
26
Hereditary hemorrhagic telangectasia is a disorder of
Connective Tissue
27
Which of the following coagulation factors is considered to be labile?
V
28
What role does vitamin K play in the Prothrombin group?
Carboxylates the factors to allow calcium binding
29
Factor I deficiency will affect APTT and PT
True
30
Aspirin prevents platelet aggregation by inhibiting the action of which enzyme?
Cyclooxygenase
31
Which statement regarding protein C is correct?
Activity is enhanced by Protein S
32
Thrombocytopenia may be associated with
Hypersplenism
33
The APTT is sensitive to a deficiency of which clotting factor?
None
34
Which of the following factors will activate factor XI?
Hageman Factor
35
Lumi-aggregation measures:
Aggregation and ATP release
36
APTT is used to?
Both; Monitor heparin therapy and evaluate the common pathway
37
Neurologic findings may be commonly associated with which of the following disorders?
TTP
38
True of TTP and DIC:
APTT prolonged in DIC
39
Which of the following tests is most likely to be abnormal in patients taking Aspirin?
Bleeding Time
40
Platelet aggregation response for Glannzmann's Thrombasthenia
Normal to Ristocetin, Decreased to Epinephrine
40
Thrombin-Trombomodulin complex is necessary for the activation of:
Protein C
41
Scott syndrome will affect which of the following?
Secondary Hemostasis