Hemostasis Flashcards

(39 cards)

1
Q

What is Plasminogen?

A

A precursor to plasmin found in blood and tissue fluid.

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2
Q

What is Plasmin?

A

An enzyme that breaks down fibrin in blood clots.

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3
Q

What is Fibrin?

A

A protein that forms the meshwork of a blood clot.

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4
Q

What are Plasminogen activators?

A

Substances that convert plasminogen to plasmin.

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5
Q

Name two types of Plasminogen activators.

A
  • t-PA
  • u-PA
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6
Q

What are anti-activators?

A

Substances that inhibit the activity of plasminogen activators.

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7
Q

What are PAI-1 & PAI-2?

A

Plasminogen Activator Inhibitors that regulate fibrinolysis.

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8
Q

What is D-Dimer?

A

A fibrin degradation product used as a marker for clot formation and breakdown.

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9
Q

What does FDP stand for?

A

Fibrin Degradation Products.

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10
Q

What is the Coagulation Cascade?

A

A sequence of events leading to blood clot formation.

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11
Q

What is the initiation phase of coagulation?

A

The phase where tissue factor binds and activates factor VII.

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12
Q

What is the Extrinsic factor tenase?

A

The complex of VIIa, TF, phospholipid, and calcium that cleaves factor X.

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13
Q

What role does Xa play in thrombin generation?

A

Generates a small amount of thrombin by cleaving prothrombin.

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14
Q

What occurs during the amplification phase?

A

Small amounts of thrombin activate factors V, VIII, and XI.

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15
Q

What is the Prothrombinase complex?

A

A complex that generates large amounts of thrombin by cleaving prothrombin.

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16
Q

What does thrombin do?

A

Cleaves fibrinogen to fibrin and activates factor XIII.

17
Q

What are coagulation factors?

A

Glycoproteins produced by the liver that participate in coagulation.

18
Q

List the names of coagulation factors I through XIII.

A
  • I: Fibrinogen
  • II: Prothrombin
  • III: Thromboplastin
  • IV: Calcium ion
  • V: Labile factor
  • VII: Proconvertin/Stable factor
  • VIII: Anti-Haemophilic factor
  • IX: Christmas factor
  • X: Stuart-Prower factor
  • XI: Plasma thromboplastin antecedent (PTA)
  • XII: Hageman (contact) factor
  • XIII: Fibrin stabilizing factor
19
Q

What is the role of platelets?

A

Primary defense against bleeding and formation of a hemostatic plug.

20
Q

What initiates platelet aggregation?

A

ADP released from platelets upon adherence.

21
Q

What is the difference between primary and secondary aggregation?

A

Primary aggregation is reversible; secondary aggregation is irreversible.

22
Q

What are natural anticoagulants?

A

Proteins that inhibit coagulation, including antithrombin III and proteins C and S.

23
Q

What is the action of antithrombin III?

A

Inactivates thrombin and enhances its action with heparin.

24
Q

What is the function of activated protein C (APC)?

A

Destroys factors VIIIa and Va, preventing further thrombin generation.

25
What does haemostasis refer to?
The physiological mechanisms that keep blood fluid and limit blood loss.
26
What are the four components of the haemostatic system?
* Vascular component * Platelet component * Coagulation component * Fibrinolytic component
27
What is the reference range for PT?
12-16 seconds.
28
What is the reference range for PTTK/APTT?
35-45 seconds.
29
What is the reference range for TCT?
10-14 seconds.
30
What is the reference range for WBCT?
3-11 minutes.
31
What is the reference range for bleeding time (BT)?
2-7 minutes.
32
Fill in the blank: The primary haemostatic plug is formed by ______.
[platelet aggregation]
33
True or False: Fibrinolysis is the process that prevents blood clot formation.
False
34
What triggers platelet activation?
Endothelial damage.
35
What is the morphology of resting platelets?
Smooth and discoid.
36
What happens to platelets upon activation?
They become round and sticky, forming a hemostatic plug.
37
What are the three stages of haemostasis?
* Primary Haemostasis * Secondary Haemostasis * Tertiary Haemostasis
38
What is tertiary haemostasis?
The gradual dissolution of the stable plug by fibrinolysis.
39
What is hemostasis
Haemostasis is complex web of interactions comprising arrest of haemorrhage from the site of vascular injury through the: Formation of the primary haemaostatic (platelet) plug, ●Generation of fibrin-meshwork around the platelet plug by the coagulation cascade and ●Clot dissolution (fibrinolysis) after tissue healing is complete.