Introduction to Haemostasis Flashcards

1
Q

What is haemostasis?

A

The arrest of bleeding and the maintenance of vascular patency

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2
Q

What are requirements of haemostasis?

A

Permanent state of readiness
Prompt response
Localised response
Protection against unwanted thrombosis

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3
Q

What are components of normal haemostatic systems?

A

Formation of platelet plug (primary haemostasis)
Formation of fibrin clot (secondary haemostasis)
Fibrinolysis
Anticoagulant defenses

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4
Q

How are platelets formed?

A

Formed in bone marrow by budding from megakaryocytes

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5
Q

How long do platelets live for?

A

7-10 days

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6
Q

Endothelial (vessel wall) damage exposes and does what?

A

Exposes collagen and releases von willebrand factor (VWF) and other proteins to which platelets have receptors -> platelet adhesion at site of injury

Then there is secretion of various chemicals from platelets that lead to aggregation of platelets at site of injury

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7
Q

What are causes of failure of platelet plug formation?

A

Vascular
Platelets - reduced number (thrombocytopenia); reduced function
Von Willebrand factor

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8
Q

What are consequences of failure of platelet plug formation?

A

Spontaneous bruising and purpura
Mucosal bleeding - epistaxis, GI, conjunctival, menorrhagia
Intracranial haemorrhage
Retinal haemorrhages

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9
Q

What are screening tests for primary haemostasis?

A

Platelet count

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10
Q

Describe how the formation of fibrin clot happens

A
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11
Q

What are causes of failure of fibrin clot formation?

A

Single clotting factor deficiency (usually hereditary e.g. haemophilia)

Multiple clotting factor deficiencies (usually acquired e.g. DIC)

Increased fibrinolysis (usually part of complex coagulopathy)

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12
Q

Draw out how fibrinolysis occurs

A
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13
Q

What are consequences of failure of fibrin clot formation?

A

No characteristic clinical syndrome
May be combined primary / secondary haemostatic failure
Pattern of bleeding depends on single or multiple abnormalities, and the clotting factors involved

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14
Q

What screening tests can we do for fibrin clot formation?

A

PT time
Activated partial thromboplastin time (APTT)

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15
Q

What questions are important to ask in bleeding disorders?

A

History - bleeding / bruising
Duration (?life -long)
Previous surgery / dental extractions

Drug history
FH
Examination

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16
Q

What are naturally occurring anticoagulants?

A

Serine protease inhibitors (anti-thrombin)
Protein C and protein S

17
Q

Draw how serine protease inhibitors (anti-thrombin) cause anticoagulation

A
18
Q

Draw how protein C and protein S cause anticoagulation

A
19
Q

What is thrombophilia?

A

Deficiency of naturally occurring anticoagulants may be hereditary

Increased tendency to develop venous thrombosis (DVT / PE)