Lecture 3a Flashcards

1
Q

What are the hemostatic system players?

A

Blood proteins (procoagulant and anticoagulant factors)
Platelet
Vessel wall

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2
Q

Where are the platelets concentrated in?

A

1/3 released from bone marrow or transfused are pooled in spleen

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3
Q

What are some of the platelet granules?

A

Denise granules
Alpha granules

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4
Q

What does thromboxane do?

A

Activate other platelets and increasing clotting

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5
Q

Where are von williebrand factors made and stored?

A

Endothelial cells and platelets

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6
Q

What is the principle of secondary hemostasis?

A

Clotting factors activate each other (cascade effects, circulates inactivated otherwise)
There are checks and balances

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7
Q

What does thrombin do?

A

It gives positive feedback to create more and more thrombin

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8
Q

What are the three essential steps for blood coagulation?

A

Prothrombin activator formed
Prothrombin to thrombin
Thrombin converts fibrinogen to fibrin

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9
Q

What kind of disease affect blood clotting?

A

Liver disease

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10
Q

What clotting factors for vitamin K?

A

Factors 2,7,9,10, protein C, protein S

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11
Q

How much stronger is the intrinsic pathway than the extrinsic pathway?

A

100x

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12
Q

What is the most abundant coagulation protein?

A

Fibrinogen

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13
Q

What are the anticoagulant plasma proteins?

A

Protein C + S
Anti-thrombin (III)
Tissue factory pathway inhibitor
Fibrinolysis

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14
Q

What does Anti-thrombin do?

A

Inactivates thrombin, 9a, 10a, 11a, 12a
Inhibition accelerate 1000x with heparin

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15
Q

What is fibrinoylysis?

A

The breakdown of fibrin

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16
Q

What do we order when we think someone has a blood clot?

A

D-dimer (if positive likely to have a clot)

17
Q

What is the function of tPA?

A

Converts of plasminogen to plasmin