HEMOSTASIS Flashcards

1
Q

smooth surface is not conducive to clot formation

has display membrane proteins (thrombomodulin) that inhibit clotting

store von willebrand factor in cytoplasmic alpha granules

A

intact endothelial cells

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2
Q

contain membrane proteins and extracellular matrix proteins (collagen) that normally do not contact blood

A

subendothelial cells

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3
Q

enucleated cells that are fragments of larger progenitor cells called megakaryocytes

production is primarily regulated by thrombopoietan and other growth factors

half life in the blood = 8-12days

A

platelets

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4
Q

vascular spasm/constriction
platelet plug formation

A

primary hemostasis

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5
Q

clot organization
blood coagulation

A

secondary hemostasis

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6
Q

fibrinolysis

A

tertiary hemostasis

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7
Q

reduces the flow of blood from the vessel rupture

A

vascular constriction

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8
Q

platelet adhesion
platelet secretion
platelet aggregation

A

formation of platelet plug

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9
Q

binding of platelet to non-platelet surface: sub endothelial collagen

plasma proteins required for normal platelet adhesion:
thrombin
fibronectin
VWF

A

platelet adhesion

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10
Q

primary ADP stimulates aggregation
Thromboxane A2
serotonin enhance vasoconstriction

A

platelet secretion

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11
Q

END RESULT: platelet plug

A

platelet aggregation

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12
Q

formation prothrombin activator in response to rupture of the vessel and damage

catalytic conversion of prothrombin to thrombin

thrombin acts as enzyme to convert fibrinogen into fibrin

A

clot formation

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13
Q

factors 3 and 4 roman numerals indicate inactive forms as they exist in the _____

A

plasma

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14
Q

proenzymes

________________ are each activated by proteolytic cleavage to become enzymatically active

A

factors 12,11, 9, 7, 10, 11

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15
Q

vitamin k dependent clotting factors

A

2, 7, 9, 10

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16
Q

co factors are non enzymatic proteins that are essential for the optimal activity of the enzymes of the clotting cascade

A

tissue factor (factor 3), factor 8, factor 4 are cofactors

17
Q

platelets contain 3 types of secretory granules which are

A

lysosome
alpha granules
delta granules

18
Q

__________________ are required for promotion and acceleration of almost all blood clotting reactions

except activation of 12 and 11 (intrinsic mechanism)

A

calcium ions

19
Q

physiologic inhibitors of coagulation

A

antithrombin 3
activated protein c and s
thrombomodulin
prostacyclin

20
Q

inactivates thrombin
attaches to thrombin 2a and inactivates it preventing thrombin from converting fibrinogen to fibrin

A

antithrombin 3

21
Q

inactivates antithrombin 3
binds to activated _________ factors

A

9a, 10a, 11a, 12a

22
Q

antithrombin 3 is enhanced and accelerated by presence of ____________ (either naturally released from basophils or given therapeutically as an anticoagulant)

23
Q

produced by liver

vitamin K dependent

inactivates factors 5 and 8

stimulates fibrinolysis

activated by thrombin 2a

24
Q

protein c inactivates factors ________

A

factors 5 and 8 inactivated by protein c

25
cofactor to protein c to enhance its ability to degrade factors 5 and 8 vitamin k dependent and produced by the liver
protein S
26
binds with thrombin thrombomodulin - thrombin complex activates protein c which inactivates factors 5 and 8
thrombomodulin
27
natural anticoagulants
heparin, anti thromboplastin
28
heparin comes from basophils and mast cells and potentiates effects of antithrombin 3 which inhibits factors ____________
9, 10, 11, 12 and thrombin (activated factor 3)
29
inhibits factor 3 (tissue factors - tissue thromboplastin)
antithromboplastin
30
________ is necessary for production of prothrombin, factor 7, 9, 10, & protein c
vitamin k
31
severe reduction in the number of platelets bleeding from small venules and capillaries
thrombocytopenia
32
widespread coagulation which leads to thrombosis in small blood vessels, increased fibrinolysis and depletion of coagulating factors which leads to generalized bleeding
disseminated intravascular coagulation
33
hemophilia which occurs in males transmitted by women (X chromosome) A: Factor 8 deficiency 85% B: Factor 9 deficiency
Hemophilia
34
hemophilia A is _______ deficiency
factor 8
35
hemophilia b is ________ deficiency
factor 9
36
abnormal blood clot develops in blood vesel
thrombus
37
freely floating blood clot
embolus