Coagulation Flashcards

(40 cards)

1
Q

What is physiological hemostasis

A

Repair of everyday wear and tear, happening all the time

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2
Q

What is pathological hemostasis

A

-Clotting in the absence of hemorrhage
-Excessive clotting
-Clotting in the wrong location

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3
Q

What are the basic components that maintain hemostasis

A

Vessels
Platelets
Coagulation factors
Inhibitors

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4
Q

What are the steps of hemostasis

A

Vasoconstriction
Platelet Activation
Coagulation cascade
Antithrombotic control

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5
Q

Vasoconstriction -

A

VERY fast, neurogenic
Vessel spasm

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6
Q

What are platelets filled with

A

Alpha and dense granules

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7
Q

What is in alpha granules

A

Adhesion molecules and GFs

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8
Q

What is in dense granules

A

Activators, cofactors, some GFs

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9
Q

What important things live under the endothelial layer of the vessel

A

von Willebrand factor
collagen

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10
Q

Who produces vWF

A

Endothelial cells, platelets, megakaryocytes

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11
Q

Where is vWF stored

A

Weibel palade bodies

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12
Q

What does vWF bind to

A

Glycoprotein IIb/IIIa on the platelet

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13
Q

What are the steps involved in making the platelet plug

A

Adhesion
Shape change
Secretion
Aggregation

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14
Q

What happens during adhesion

A

Platelets bump into exposed vWF –> weak attachments
Roll along vessel wall and encounter collagen –>
Integrin forms stronger attachments

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15
Q

What happens during shape change

A

Collagen and thrombin (and platelet-activating factor and ADP) activate platelets
Platelets change shape
More stable plug is formed

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16
Q

What happens during secretion

A

Platelets dump all their granules
Platelet plug activates other platelets as they pass

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17
Q

What happens during aggregation

A

Platelets flip phosphatidyl serine to the outside of their membrane (now negatively charged)
Fibrinogen bridges form between platelets

18
Q

Why is it important for the platelets membranes to have a negative charge

A

Helps with the coagulation cascade

19
Q

What is the goal of secondary hemostasis

A

To have fibrin (glue) form around the platelet plug to create a good seal

20
Q

Which coag factors are made in the liver

A

II, VII, IX, X, XII, XIII

21
Q

Which coag factors need to be carboxylated

A

II, VII, IX, X

22
Q

What are the three pathways in the coag cascade

A

Intrinsic
Extrinsic
Common

23
Q

What molecules are involved in the extrinsic pathway

A

Tissue factor (III), VII

24
Q

What sets off the extrinsic pathway

A

Trauma that exposes TF to blood

25
What molecules are involved in the common pathway
X, V, II (thrombin)
26
What molecules are involved in the intrinsic pathway
XII, XI, IX, VIII
27
What sets off the intrinsic pathway?
Damage to endothelial cell
28
What activates the common pathway
TF + VII and/or VIII
29
Which pathway is the main activator of the cascade
Extrinsic
30
Draw the coagulation cascade
31
What test is used to test the intrinsic pathway
aPTT Activated partial thromboplastin time
32
What test is used to test the extrinsic pathway
PT Partial thromboplastin
33
What test is used to test the common pathway
aPTT and PT - remember the cascade is like a Y
34
What factors are hemophiliacs lacking
IX and/or VIII
35
What factors will be impacted by a vit K deficiency
II, VII, IX, X
36
Why do we care about vitamin K
Coag factors need to be modified in order to be active, the enzyme that drives the redox cycle needs vit K in order to work
37
What does thrombin do
Cleaves fibrinogen --> fibrin Activates platelets Mediates vascular permeability Activates a fibrinolysis inhibitor
38
What is the ultimate goal of hemostasis
To return normal blood flow following an injury
39
Do animals that have hypocalcemia have a hard time clotting
NO. Coag needs very little Ca. To not have enough Ca to not clot you would already be dead
40
Do animals lacking factors XI and XII clinically bleed
No