Lecture 6: Haemostasis Flashcards

1
Q

Name two vascular disorders

A

Vascular bleeding

Hereditary haemorrhagic telangiectasia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Give inherited and acquired causes of vascular bleeding

A

Inherited:

  • Hereditary haemorrhagic telangiectasia
  • Ehlers-Danlos syndrome

Acquired:

  • Scurvy
  • Steroids
  • Senile
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Name the disorder of low platelets

A

Thrombocytopaenia

Normal range 150-400x10^9/L

Symptoms when platelets <10

Epistaxis, GI bleeds, menorrhagia, bruising

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Inherited causes of thrombocytopenia

A

Rare

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Acquired causes of thrombocytopenia

A

ITP, drug-related, DIC

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Name inherited and acquired disorders of platelet function

A

Inherited:
- Many rare diagnoses e.g. Glanzmann’s

Acquired:
- Drugs e.g. aspirin, NSAIDs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Name inherited and acquired disorders of coagulation

A

Inherited:
- Inherited haemophilia

Acquired:

  • Non-inherited causes of haemophilia (liver disease, DIC)
  • Anti-coagulant drugs
  • Vitamin K deficiency
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What causes haemophilia A and what causes haemophilia B?

A

A - 8
B - 9

Both x-linked conditions affecting males only

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What are the clinical features of haemophilia?

A

Spontaneous bleeding into joints and muscle

Unexpected post-op bleeding

Chronic debilitating joint disease

Major haematoma

Haemarthritis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is APTT?

A

Assess the intrinsic pathway

Tests factors VIII, IX, XI XII

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is PT?

A

Assesses the extrinsic pathway

Tests factors II, V, VII, X

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What would the APTT and PT be for haemophilia?

A

APTT - prolonged

PT - normal

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is von willebrand disease?

A

Autosomal dominant

vWF - large multimeric protein that carries factor VIII in the blood

vWF also binds platelets to endothelial collagen

vWD = deficiency of vWF and FVIII in plasma

Mucocutaneous, nosebleeds, menorrhagia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What would the APTT and PT be for vWD?

A
APTT - prolonged 
PT - normal
Also
Low vWF level 
Low FVIII
Prolonged bleeding time 
Defective platelet function 

Treatment with desmopressin, anti-fibrinolytic and plasma products

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What would the APTT and PT be for meningococcal DIC?

A
PT - prolonged 
APTT - prolonged
TT - prolonged 
Also
Low fibrinogen, low platelets, raised D-dimers
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What conditions are treated with Heparin?

A

MIs, PEs, DVTs

17
Q

What conditions are treated with Warfarin?

A

PEs, DVTs, AF, prosthetic valves

18
Q

Name two DOACs

A

Dabigatron - direct thrombin inhibitor

Rivaroxaban - factor Xa inhibitor

19
Q

What factors require vitamin K for synthesis?

A

II, VII, IX, X

Vitamin K is required for gamma-carboxylation

20
Q

What causes vitamin K deficiency?

A

Malabsorption of vitamin K

Biliary obstruction

Haemorrhagic of the newborn