Uensbe Flashcards

(28 cards)

1
Q

Anticoagulant or Procoagulant

tPA (tissue plasminogen activator) =

A

Anti-coagulant (promotes fibrinolysis)

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2
Q

Anticoagulant or Procoagulant

Thrombomodulin =

A

Anti-coagulant (activates protein C, which inactivates factors Va and VIIIa)

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3
Q

Anticoagulant or Procoagulant

Anti-coagulant (activates protein C, which inactivates factors Va and VIIIa)

A

Thrombomodulin

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4
Q

Anticoagulant or Procoagulant

TAFI (Thrombin-Activatable Fibrinolysis Inhibitor) =

A

Pro-coagulant (inhibits fibrinolysis)

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5
Q

Anticoagulant or Procoagulant

PAI (Plasminogen Activator Inhibitor) =

A

Pro-coagulant (inhibits tPA and uPA, blocking fibrinolysis)

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6
Q

Anticoagulant or Procoagulant

Fibrinogen =

A

Pro-coagulant (precursor to fibrin, essential for clot formation)

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7
Q

Other name

I

A

Fibrinogen

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8
Q

Other name

II

A

Prothrombin

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9
Q

Other name

III

A

Tissue Factor (TF) / Thromboplastin

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10
Q

Other name

IV

A

Calcium ions (Ca²⁺)

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11
Q

Other name

VIII

A

Anti-hemophilic Factor A

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12
Q

Other name

IX

A

Christmas Factor / Anti-hemophilic B

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13
Q

Other name

X

A

Stuart-Prower Factor

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14
Q

Other name

XI

A

Plasma Thromboplastin Antecedent (PTA)

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15
Q

Other name

XII

A

Hageman Factor

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16
Q

Other name

XIII

A

Fibrin-Stabilizing Factor

17
Q

Other name

V

VII

A

Labile Factor

Stable Factor

18
Q

Other name

Prekallikrein
_________

A

Fletcher Factor

19
Q

Other name

HMWK

A

Fitzgerald Factor

20
Q

Vitamin K–dependent;

inactivates Factors Va and VIIIa (with Protein S)

21
Q

Also called Christmas Factor; part of intrinsic pathway

22
Q

Factor I; converted by thrombin to fibrin, forms the clot mesh

23
Q

Product of fibrin degradation;

indicates recent clot formation and breakdown

24
Q

Bleeding Time (BT)
Clotting Time (CT)

Thrombomodulin (↑ activity)

Activates Protein C → anticoagulant effect

A

Normal
Increased

25
Bleeding Time (BT) Clotting Time (CT) Vitamin K Deficiency Affects factors II, VII, IX, X (↓ synthesis)
Normal Increased
26
Bleeding Time (BT) Clotting Time (CT) Glanzmann Thrombasthenia Platelet aggregation defect (GpIIb/IIIa)
Increased Normal
27
Bleeding Time (BT) Clotting Time (CT) Protein C Excess/Activation Inactivates Va and VIIIa → anticoagulation
Normal Increased
28
Bleeding Time (BT) Clotting Time (CT) Von Willebrand Disease Defective platelet adhesion + ↓ FVIII stability
Increased Normal or Increased