Bleeding Disorders Flashcards

1
Q

What are causes of Peripheral Platelet Destruction?

A

Coagulopathy - Disseminated intravascular coagulation
Autoimmune - Immune thrombocytopenic Purpura (ITP)
Hypersplenism

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

What vascular abnormalities can cause platelet problems?

A

Vasculitis

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

What are other causes of acquired platelet dysfunction?

A

Drugs - Aspirin + NSAIDs

Renal failure

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

Describe Von Willebrand Factor deficiency?

A

Acquired or Hereditary
Autosomal dominant
Common
Variable severity

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

Name a type of multiple clotting factor deficiencies?

A

Disseminated Intravascular Coagulation (DIC)

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

Name a single clotting factor deficiency?

A

Haemophilia

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

What multiple factor deficiencies can cause bleeding issues?

A

Liver failure
Vit K deficiency, warfarin therapy
Complex coagulopathy - (DIC)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Where are all coagulation factors synthesised?

A

In hepatocytes

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

What factors does vit K carboxylate?

A

Factors II, VII, IX & X

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

How is Vit K sourced?

A

Diet
Intestinal synthesis
Absorbed in upper intestine
Required bile salts for absorption

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

What are causes for Vit K deficiency? (5)

A
Poor dietary intake
Malabsorption
Obstructive jaundice
Vit K antagonists (warfarin)
Haemorrhagic disease of the newborn
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Describe Disseminated Intravascular Coagulation (DIC)?

A

Excessive and inappropriate activation of the haemostatic system - Primary, Secondary, Fibrinolysis
Microvascular thrombus formation - end organ failure
Clotting factor consumption - bruising, purpura and generalised bleeding

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

Describe Fibrinolysis?

A

Fibrinogen becomes fibrin
Plasminogen becomes plasmin
Plasmin converts fibrin into FDPs (Fibrin Degradation Products) e.g. D-Dimers

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

What are causes of DIC?

A

Sepsis
Obstetric emergencies
Malignancy
Hypovalaemic shock

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

How do you treat DIC?

A
Treat underlying cause
Replacement therapy:
- Platelet transfusion
- Plasma transfusion
- Fibrinogen replacement
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Describe Haemophilia

A

X-linked hereditary

Abnormally prolonged bleeding recurs episodically

17
Q

What causes Haemophila A?

A

Factor VIII deficiency

18
Q

What causes Haemophila B?

A

Factor IX deficiency

19
Q

What are clinical features of severe haemophilia?

A

Recurrent haemarthroses
Recurrent soft tissue bleeds - bruising in toddlers
Prolonged bleeding after dental extractions, surgery and invasive procedures

20
Q

What is seen in single factor deficiency?

A

Isolated prolonged APTT

21
Q

What else can haemophilia cause?

A

Joint problems

Arthropathy (caused by multiple events of bleeding into the joint, fusion occurs)

22
Q

What else can prolong the APTT?

A

Heparin therapy