coagulation Flashcards

(54 cards)

1
Q

what are the key mediators of endothelial damage ?

A

endothelins - cause vasocontriction

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2
Q

what are the active forms of coagulation factors called ?

A

serine proteases

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3
Q

what is the centre of the coagulation cascade ?

A

activation of factor 10 into factor 10 a

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4
Q

what happens after the activation of factor 10 ?

A

changes prothrombin 2 to thrombin 2a

then thrombin converts fibrinogen into fibrin

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5
Q

what are the factor 5a inhibitors drugs and what is the end result ?

A

apixaban
rivaroxaban
they inhibit thrombin formation

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6
Q

what is the end result associated with inhibiting factor 2 a ?

A

decreased fibrin formation

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7
Q

what activates factor 10 3amatan ?

A

tissue factor , which is found in sub endothelial cells , so only released when endothelial damage happens

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8
Q

after the activation of tissue factor what happens ?

A

tissue factor activates factor 7 to make it 7a
then 7a activates 10 a

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9
Q

how does thrombin make more thrombin ?

A

positive feedback factor 9a men el a5er can activate factor 10 to restart the whole clotting cascade

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10
Q

what are the clotting factors deficiencies with hemophilia ?

A

hemophilia A : def factor 8
hemophilia B : def factor 9
Hemophilia C : def factor 11

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11
Q

where is factor 8 produced ?

A

in the endothelial cells

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12
Q

what is the association between factor 8 and von willebrand disease?

A

inactive form of factor 8 is bound to VWF to increase its plasma half life

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13
Q

what co factors are needed for the activation of factor 10 ?

A

phospholipid and calcium

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14
Q

what are the two multicomplement pathways associated with the activation of factor 10 ?

A

TF:VII a
IXa: VIIIa

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15
Q

what is the function of factor 13 ?

A

crosslinks fibrin

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16
Q

what happens if there is a defeciency in factor 13 ?

A

inadequate clot formation

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17
Q

what does factor 13 need to work ?

A

calcium as a co factor

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18
Q

what is factor 13 activated by ?

A

thrombin 2a formation

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19
Q

what is the other name for factor 12 ?

A

also called factor hageman

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20
Q

what is the function of factor 12 ?

A

activates factor 11

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21
Q

what activates factor 12 ?

A

contact with negative charges like silica

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22
Q

what is the function of the PTT test ?

A

tests the intrinsic pathway

23
Q

what are the main 2 pathways that fibrin can be made ?

A

either by the tissue factor pathway
or by the factor 12 pathway

24
Q

what is the difference between the intrinsic and the extrinsic pathway ?

A

the one that starts with tissue factor is the extrinsic pathway
the one that starts with factor 12 is the intrinsic pathway

25
how is the intrinsic pathway tested vs the extrinsic pathway ?
intrinsic is tested with the PTT the extrinsic is tested by the PT where we add TF to the plasma
26
what are the requirements for the activation of the intirinsic pathway ?
kinins , which circulate s inactive kininogens
27
what is the purpose of the kinins ?
these are the connections between inflammation and coagulation through factor 12
28
what is the most important factor of the kinin system ?
bradykinin
29
what are the clinical associations with bradykinin ?
bradykinin aslan is a vasodilator , that is degraded by ACE , which raises the levels of bradykinin which may lead to angioedema
30
what are the cases that are contraindicated with ACE use ?
hereditary angioedema ( C1 inhibitor defeciency )
31
which of the factors is associated with the formation of kinins ?
factor 12
32
what are the 2 co factors needed in order to activate factor 12 to make bradykinins ?
1- activated factor 12 converts prekallikrein to kallikrein 2- kallikren converts HMWK to bradykinin
33
what are the effects of prekallikren deficiency ?
results in prolonged PTT but no bleeding problems because of the low significance of it as a clotting factor
34
what are the natural inhibitors of the coagulating system ?
antithrombin 3 protein C and S tissue factor pathway inhibitor
35
what does antithrombin 3 inhibit ?
factor 2 , 7 , 9, 10 , 11 , 12
36
what does a deficiency of these natural anticoagulants cause ?
hypercoaguable state
37
what does protein C inhibit ?
factor 5a and factor 8a
38
what is protein C activated by ?
thrombomodulin which is found on endothelial cells , so endothelial cells produce a good amount of protein C
39
what is the co factor for the function of protein C ?
protein S
40
what does tissue factor pathway inhibitor inhibit ?
inactivates 10 a
41
what is the clinical relevance of TFPI ?
the plasma levels of it are increased with heparin administration
42
what helps break down a clot when it is made ?
plasminogen and plasmin they break down fibrin
43
what are the natrual plasminogen activators ?
these are chemicals that help activate plasminogen in oder to increase the breakdown of fibrin and clots tPA and urokinase
44
what are the clinical uses of the plasminogen activators ?
tPa and urokinase are used to breakdown clots in MI and stroke streptokinase is used
45
once plasmin breaks down the fibrin what are the end products ?
1- fibrin degradation products 2- d dimer
46
what does the presence of d dimer in the plasma mean ?
that means that there is a breakdown of clots in the blood by plasminogen
47
what is an elevated d dimer used for ?
to diagnose DVT and PE
48
what is primary fibrinolysis ?
overactivity of plasmin where there is a rise in FDP with a normal d dimer level
49
what effect does plasmin have on the clotting factors ?
can deplete them
50
what are the diseases associated with primary fibrinolysis ?
prostate cancer - due to an increase in urokinase cirrohsis - loss of antiplasmin from the liver
51
what is the difference in lab values between hyperfibrinolysis and clot breakdown ?
hyperfibrinolysis - FDPs with normal D dimer levels clot breakdown - increase in both FDPs and d dimer
52
what are the vitamin k dependant factors ?
2 , 7 , 9 , 10 , protein C and S
53
what is the MOA of warfarin ?
vitamin K antagonist
54
what are the key acute phase reactants ?
fibrinogen ferritin CRP