PATH: Hemostasis and Thrombosis Flashcards

1
Q

What is the function of hemostasis?

A

To maintain blood in the vascular system fluid and free of clots , yet allow rapid activation of clotting if necessary

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is thrombosis?

A

A pathologic extension of hemostasis in which there is inappropriate activation of the hemostatic system

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are the anti-thrombotic properties of endothelium?

A

Anti-platelet effects (barrier function, ADP breakdown, NO, prostacyclin), anti-coagulant properties, and fibrinolytic properties (t-PA)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What are the pro-thrombotic properties of endothelium?

A

Synthesis of von Willebrand Factor, procoagulant (synthesize tissue fator activating extrinsic coag. pathway, and expresses binding sites for activated clotting factors IX and X), and anti-fibrolytic (PAI)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What kind of granules do platelets contain?

A

Alpha granules and electron dense bodies

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are 3 functions of activated platelets in hemostasis?

A

Adhesion to ECM (vWF), secretion/ release, aggreagation causing generation of ADP, thrombin and TXA2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What occurs during primary hemostasis?

A

Vasoconstriction, exposure of blood elements to collagen, release of tissue factors that activate coagulation cascade and formation of a hemostatic plug at the SOI

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is the effect of TXA2?

A

Causes vasoconstriction which lowers blood flow to the area allowing more platelets to filter out and become attracted to other platelets. This allows for the formation of the primary hemostatic plug

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

How do platelets bind to vWF?

A

Gp1b receptors

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

How are platelets bound to one another in a hemostatic plug?

A

Connected through fibrinogen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What converts Fibrinogen to fibrin and what effect does this have?

A

Thrombin converts fibrinogen to fibrin which is a much stronger molecule

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What are the effects of thrombin in generating hemostasis?

A

Increase neutrophil adhesion, activate monocytes, lymphocytes, and endothelium, converts fibrinogen to fibrin and increases platelet aggregation and stimulation which causes thromboxane A2 release

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What are the initiators of the intrinsic and extrinsic coagulation pathways?

A

Extrinsic by tissue factor and intrinsic by Factor XII or Hageman Factor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is the ultimate goal of the coagulation pathways?

A

Activation of Factor II to IIa (thrombin)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What products are released by the endothelium that block the coagulation cascade?

A

Thrombomodulin and t-PA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

How does plasmin act?

A

Acts on fibrin to make fibrin degradation products

17
Q

What is a thrombus?

A

A solid mass or plug formed from blood elements found at the site of formation

18
Q

What is an embolus?

A

Detached intravascular solid, liquid, or gaseous mass found at a site different from its origin

19
Q

What is Virchow’s Triad?

A

The three major factors that favor thrombosis: vascular lesions (endothelial injury), decreased flow (stasis), and hypercoagulability

20
Q

What is the cellular driver and mediator of arterial thrombosis? Venous? Which is more common?

A

Arterial- platelet driven/mediated; Venous- RBC; Arterial more common

21
Q

What is activated protein C resistance?

A

Factor V deficiency where heterozygotes are 3-10 times more likely to develop thromboses, and homozygotes have a 50 fold increased risk

22
Q

What are the possible fates of a thrombus?

A

Propagation, Embolization, Dissolution, or Organization (recanalization)