5-29 GOUELI Coag Biochem Flashcards

1
Q

What is a normal platelet count?

A

150,000 – 450,000 platelets/uL

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2
Q

Define hemostasis?

A

Physiological blood clotting in response to injury.

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3
Q

Define Thrombosis?

A

Pathologic blood clotting

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4
Q

Define Hemorrhage?

A

Pathologic bleeding

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5
Q

What is the overview, big picture of how hemostasis works?

A

1) Vasoconstriction in response to injury
2) Platelet plug (Primary Hemostasis)
3) Fibrin plug (clot) (Secondary Hemostasis)
4) Clot dissolves (Anti-coagulants / fibrinolytics)

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6
Q

What are the 3 fundamental mechanisms in PRIMARY HEMOSTASIS?

A

Adhesion – platelets adhere to exposed collagen
Aggregation
Secretion (of platelet granule contents)

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7
Q

What coagulation factor does vWF stablilize?

A

Factor VIII

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8
Q

What does GP Ib bind?

A

vWF

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9
Q

What does GP VI bind?

A

Collagen

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10
Q

What does GP IIa-IIIb bind?

A

Other platelets via vWF/fibrinogen

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11
Q

What is ADP’s role in platelet aggregation?

A

ADP released from platelet granules -> binds platelet ADP-receptors -> activates platelets -> unmasks Gp IIb-IIIa

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12
Q

What is Plavix?

A

ADP-receptor antagonist -> ↓clot formation

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13
Q

If you admit someone for MI, what must you put them on?

A

Aspirin. Otherwise it’s malpractice

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14
Q

What is secondary hemostasis? What are the broad steps involved?

A

Secondary Hemostasis is formation of the FIBRIN PLUG (clot)
2 pathways (INTRINSIC, and EXTRINSIC) converge to common path
OVERARCHING GOAL is producing fibrin!

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15
Q

What is the “additional substance” necessary for the extrinsic pathway?

A

Tissue factor

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16
Q

Where does Tissue Factor come from?

A

Not plasma

Surface protein expressed on endothelial cells exposed to cytokines

17
Q

Where do the clotting factors (eg Factor VIII, Factor IX) come from?

A

Synthesized by liver (as zymogens)

18
Q

What is the role of phospholipids in the activation of zymogens?

A

Surface of activated platelets kinda flip.
This surface provides an area where zymogens can be enzymatically
cleaved to form activated factors (eg Factor VIIIa)

19
Q

Will a patient with Factor XII deficiency have any symptoms? Why?

A

No b/c that part of the pathway can be activated by many things, including thrombin

20
Q

What does heparin do?

A

Activates ATIII

21
Q

What anticoagulant does Coumadin also antagonize? What are the implications?

A

Protein C and S activity also decreases from Coumadin.
Thus, admin of Coumadin to patient INITALLY causes HYPERcoag!
Thus, we BRIDGE W/HEPARIN