Coagulation Flashcards

1
Q

List 4 main characteristics of ideal coagulants

A

Should require less monitoring.
Fixed dosing.
Oral administration is preferred. Predictable PK. Broad therapeutic window

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2
Q

Which factors are affected by which anticoagulants

A

Factor Xa, IIa - Low molecular weight heparins
Direct thrombin inhibitors - IIa
Direct Factor Xa inhibitors - Xa

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3
Q

Give the mechanism of action of heparin

A

Binds to inactive antithrombin III. Activation of AT-III, which binds to Factor Xa and binds to Thrombin and BLOCKS its effect.

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4
Q

What does aPTT stand for

A

Activated Partial Thromboplastin Time

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5
Q

List a major adverse effect of heparin use

A

Bleeding (Epistaxis, Haematuria, Vaginal Bleeding)
Mild transient thrombocytopenia

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6
Q

Give a stepwise approach of reversal of heparin effects

A

STOP heparin, Identify source of bleeding, administer protamine sulphate (antidote)
Closely monitor aPTT

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7
Q

List 3 examples of LMWH

A

Enoxaparin, Dalteparin, Fondaparinux

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8
Q

What is the effect of chain length on activity

A

The longer the chain length, the more likely the drug will inhibit both the thrombin and the factor Xa activity

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9
Q

What is Virchow’s triad of thrombosis

A

Venous stasis, Hypercoagulability, Blood vessel wall injury

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10
Q

What are signs and symptoms of DVT and PE

A

Unilateral, chest pain, dyspnea, hemoptysis, cyanosis

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11
Q

Catergorise bleeding disorders

A

Primary: Idiopathic thrombocytopaenia purpura
von Willebrand disease
Secondary: Haemophilia, Liver Disease, Vitamin K deficiency

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12
Q

3 signs of haemophilia

A

Ecchymosis, Haematomas, GIT bleeding

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13
Q

Describe the phases of haemostasis

A

There is cell injury, then Von Willebrand factor is expressed. Then there is the GPIIb/IIIa + Fibrinogen mesh, which leads to inital clot formation and primary clot formation. Then Fibrinogen forms into fibrin (From Factor XIIIa). From fibrin, a stable clot is formed and then there is clot stabilisation

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14
Q

Describe the process of platelet plug formation.

A

1) Vasospasm. 2) Platelet adhesion 3) Platelet activation. 4) Platelet aggregation.

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15
Q

What is the function of ADP in platelet plug formation?

A

ADP binds to P2Y12 receptors on the platelet. This increases intracellular Calcium, which increases expression of GP2B3A receptors and increases Thromboxane A2 production.

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16
Q

Where does Von Willebrand factor bind on the platelet and what is its function?

A

GP1B and it causes platelet adhesion.

17
Q

Describe secondary haemostasis

A

Intrinsic pathway:Extrinsic pathway (Damaged vessel wall)
XII –> XIIa
XI –> XIa
IX–> IXa + VIII Factor VIIa + Tissue factor/Factor III
X –> Xa + V
Prothrombin –> Thrombin
Fibrinogen –> Fibrin
XIII –> XIIIa –> Stable fibrin clot