Haemostasis Flashcards

1
Q

What is primary haemostasis?

A

Formation of platelet plug

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2
Q

What is secondary haemostasis?

A

Formation of fibrin clot

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3
Q

How are platelets formed in bone?

A

marrow by ‘budding’ from megakaryocytes

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4
Q

Describe how endothelial wall damage lead to platelet adhesion?

A

endothelial wall damage exposes collagen
This causes Von Willebrand Factor and ther proteins to be released.
These factors/proteins have receptors for platelets, so platelets come and bind to them = platelet adhesion

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5
Q

How does platelet aggregation occur?

A

The platelets (which are now bound to the proteins at the site of endothelial damage) secrete chemicals

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6
Q

What are the 3 general causes of failure of platelet plug formation?

A
  1. Vascular cause
  2. Platelets
    - Reduced number (thrombocytopenia)
    - Reduced function
  3. Von Willebrand Factor
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7
Q

List some consequences of a failure of platelet plug formation.

A
Spontaneous Bruising and Purpura
Mucosal Bleeding, epistaxis, GI bleed, conjunctival bleed
Menorrhagia
Intracranial haemorrhage
Retinal haemorrhages
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8
Q

Screening test for primary haemostasis?

A

Platelet count (No simple screening tests for other components of primary haemostasis)

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9
Q

What converts fibrinogen to fibrin?

A

thrombin

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10
Q

What converts prothrombin to thrombin (what is prothrombinase)?

A

Factor Xa, and the protein cofactor, Factor Va

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11
Q

What are the 3 causes of failure of formation of a fibrin clot (secondary haemolysis)?

A
  1. Single clotting factor deficiency, usually hereditary
    eg Haemophilia
  2. Multiple clotting factor deficiencies, usually acquired e.g. Disseminated Intravascular Coagulation
  3. Increased fibrinolysis, usually part of complex coagulopathy
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12
Q

Fibronolysis converts what to what?

A

fibrin to fibrin degradation products (FDPs)

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13
Q

What is the enzyme in fibrinolysis?

A

plasmin

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14
Q

What converts plasminogen to plasmin?

A

Tissue plasminogen activator (TPA)

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15
Q

What is the characteristic sign of fibrin clot formation failure?

A

No characteristic clinical syndrome

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16
Q

What are the naturally occurring anticoagulants?

A

serine protease inhibitors

protein c and protein s

17
Q

What is thrombophilia?

A

Deficiency of naturally occuring anticoagulants, may be hereditary

18
Q

In thrombophilia, what is there an increased tendency to develop?

A

to develop venous thrombosis (deep vein thrombosis/pulmonary embolism)