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 4 requirements of haemostasis?

A

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

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3
Q

What are the 4 components of a normal haemostatic system?

A
  1. Formation of platelet plug
  2. Formation of fibrin clot
  3. Fibrinolysis
  4. Anticoagulant defences
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4
Q

How are platelets formed in the bone marrow?

A

By ‘budding’ from megakaryocytes

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5
Q

How long is the average platelets lifespan?

A

7-10 days

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6
Q

What is released as a result of exposed collagen due to endothelial damage?

A

Von Willebrand factor

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7
Q

What occurs by platelets at the site of injury?

A

Adhesion

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8
Q

Name some consequences of failure of platelet plug formation?

A

Spontaneous bruising and purpura
Mucosal bleeding
Intracranial haemorrhage
Retinal haemorrhages

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9
Q

Name 3 reasons for the failure of fibrin clot formation?

A

Single clotting factor deficiency
Multiple clotting factor deficiencies
Increased fibrinolysis

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10
Q

Name 3 reasons for failure of platelet plug formation?

A

Vascular reasons
Platelets - reduced number/function
Von Willebrand factor failure

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11
Q

What converts prothrombin to thrombin?

A

Clotting factors V and Xa

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12
Q

What does tissue factor (TF) do?

What is this called?

A

Activate clotting factor VIIa

Initiation

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13
Q

What two actions does thrombin have?

A

It converts fibrinogen to fibrin and activates clotting factors VIII and IXa

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14
Q

What does clotting factors XIII and IX do?

A

Activate clotting factors V and Xa

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15
Q

What does clotting factors V and Xa do?

A

Convert prothrombin to thrombin

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16
Q

What are the three stages in the formation of a fibrin clot?

A

Initiation
Propagation
Amplification

17
Q

What occurs in fibrinolysis?

A

Fibrin is broken down into FDPs (fibrin degradation products)

18
Q

What causes the breakdown of fibrin to FDPs?

19
Q

How is plasmin formed?

A

Plasminogen is converted to plasmin by tPA (tissue plasminogen activator)

20
Q

What are the most common site(s) of bleed in haemophilia patients?

A

Lower limb (hinge) joints - ankles and knees
Elbows can also be affected

21
Q

What two screening tests are use in fibrin clot formation investigation?

A

Prothrombin time (PT)
Activated partial thromboplastin time (aPTT)

22
Q

What is added to a patient in prothrombin time investigations?

A

Phospholipid
Tissue factor
Calcium

23
Q

What does prothrombin time depend on?

A

The amount / efficiency of clotting factor VIIa

24
Q

What is the extrinsic fibrin clot formation pathway?

A

Tissue factor pathway (prothrombin time)

25
What is the intrinsic fibrin clot formation pathway?
The factor VIII / IXa pathway (activated partial thromboplastin time)
26
Name three types of naturally occurring anticoagulants?
Serine protease inhibitors (anti-thrombin) Protein C and protein S
27
What is 'primary haemostasis'?
Formation of a platelet plug
28
What is 'secondary haemostasis'?
Formation of a fibrin clot
29
What is involved in platelet plug formation?
Platelets and Von Willebrand factor
30
What does thrombin activate to cause a positive feedback loop?
Clotting factor IXa
31
Where are coagulation factors synthesised?
In hepatocytes
32
What can cause a reduced production of coagulation factors?
Liver failure