Hemostasis Flashcards

1
Q

primary hemostasis involves

A

platelet plug formation

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2
Q

secondary hemostasis involves

A

blood coagulation

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3
Q

tertiary hemostasis involves

A

dissolution of fibrin clot

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4
Q

platelet glycoprotein that binds to collagen

A

GPIa

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5
Q

platelet glycoprotein that binds to Von willebrand factor

A

GPIb

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6
Q

fibrinogen binds to which platelet glycoprotein

A

GPIIb/GPIIIa

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7
Q

defective GPIb results in

A

Bernard-Soulier syndrome

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8
Q

prevent degradation of factor VIII

A

Vw factor

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9
Q

granule contents that activate other platelets and promote aggregation

A

Calcium and ADP

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10
Q

platelet aggregation is mainly facilitated by

A

fibrinogen

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11
Q

defective GPIIb/GPIIIa leads to

A

thrombasenia of Glanzmann and Naegeli (cannot form platelet plug)

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12
Q

conversion of fibrinogen to fibrin requires

A

thrombin

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13
Q

in the extrinsic pathway, factor VII is activated by

A

tissue factor

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14
Q

in the extrinsic pathway, factor X is activated by

A

tissue factor + factor VIIa + Calcium + platelet phospholipids

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15
Q

in the intrinsic pathway, factor IX is activated by

A

factor XIa

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16
Q

in the intrinsic pathway, factor X is activated by

A

factor IXa + factor VIIIa + Calcium + PL

17
Q

what makes up prothrombinase complex

A

factor Xa + factor Va + Calcium + PL

18
Q

converts prothrombin to thrombin

A

prothrombinase complex

19
Q

coverts soft clot to hard clot

A

factor XIIIa

20
Q

pathway activated by crush injury

21
Q

intrinsic pathway defect will have increase in which lab time

22
Q

extrinsic pathway defect will have increase in which lab time

A

Prothrombin time (INR)

23
Q

Vitamin K dependent clotting factors

A

II, VII, IX, X, proteins C & S

24
Q

Vit K is coenzyme for what

A

y-Carboxylase

25
sensitive test for Vitamin K deficiency
Prothrombin time (INR)
26
drug that activates plasminogen into plasmin
streptokinase or TPA
27
breaks down fibrin into fibrin degradation products
plasmin
28
binds to and inhibits factor X and thrombin
anti-thrombin III
29
activates anti-thrombin III
heparin | Blocks factor 2 & 10
30
block epoxide reductase in liver to prevent regeneration of activated Vit K
warfarin
31
deficient in Hemophilia A
factor VIII
32
deficient in Hemophilia B
factor IX
33
inheritance of hemophilia
x linked recessive
34
test to determine effectiveness of platelet plug formation
bleeding time
35
low platelet count is called
thrombocytopenia
36
disorder with increased clotting time and increased APTT
hemophilia
37
Increased in VW disease
Aptt, bleeding time
38
protein C & S inactivates factors
5 and 8