Bleeding Flashcards

1
Q

Describe primary haemostasis?

A
  • platelet formation
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2
Q

Describe secondary haemostasis?

A
  • fibrin clot formation
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3
Q

What are the 4 processes of normal bleeding

A
  • primary haemostasis
  • secondary haemostasis
  • fibrinolysis
  • anticoagulant defences
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4
Q

Vascular reasons for a failure of platelet plug formation

A
  • collagen defect

- hence-schonlein purpura

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5
Q

platelet defects that can cause failure of platelet formation

A
  • reduced number
  • reduced function
  • marrow problems
  • increased destruction
  • defects
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6
Q

What may give rise to a pancytopenia?

A
  • marrow failure
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7
Q

Increased destruction of platelets may be due to what?

A
  • coagulopathy
  • autoimmune
  • hypersplenism
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8
Q

Explain hereditary von willerbrand factor deficiency?

A
  • reduced von willerband expression
  • bleeding tendency
  • autosomal dominant
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9
Q

Secondary haemostasis failure can either be due to ___ or ___

A
  • multiple clotting deficiencies

- single clotting deficiency

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10
Q

Vitamin K is responsible for what clotting factor formation

A
  • factor II, VII, IX, X
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11
Q

What are the clotting results in multiple clotting factor deficiencies?

A
  • increased PT

- Increased APTT

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12
Q

Single clotting deficiency may be due to what?

A
  • haemophilia
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13
Q

What are causes of vitamin K deficiency?

A
  • poor dietary intake
  • malabsorption
  • obstructive jaundice
  • vitamin K antagonists (warfarin)
  • haemorrhagic disease of the newborn
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14
Q

What causes disseminated Intravascular coagulation

A
  • excessive and inappropriate activation of the haemostatic system
  • clotting factor consumption
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15
Q

blood results in disseminated intravascular coagulaiton

A
  • raised d dimers
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16
Q

causes of disseminated intravascular coagulation

A
  • sepsis
  • obstetric emergencies
  • malignancy
  • hypovolaemic shocck
17
Q

Treatment of disseminated intravascular coagulation

A
  • treat underlying cause

- replacement therapy of platelet, plasma and fibrinogen

18
Q

What is haemophilia

A
  • hereditary single disorders

- x linked

19
Q

what is the most common type of haemophilia?

A
  • haemophilia A
20
Q

Haemophilia A is due to what deficiency?

A
  • factor VIII
21
Q

Haemophilia B Is due to what deficiency

A
  • Factor IX deficiency
22
Q

What are the blood results in haemophilia?

A
  • isolated elevated APTT
23
Q

Clinical features of haemophilia?

A
  • recurrent haemarthrosis

- recurrent soft tissue bleeds

24
Q

Management of haemophilia?

A
  • clotting factor replacement
25
Q

What factors make the intrinsic pathway

A

XII
XI
IX (Haemophilia B, Vitamin k)
VIII (Haemophilia A)

26
Q

What factors make the common pathway?

A

X
V
II (thrombin)
I (Fibrin)

27
Q

How is the intrinsic pathway measured?

A
  • APTT
28
Q

How is the extrinsic pathway measured?

A
  • PT
29
Q

What are the clotting factors in the extrinsic pathway?

A

TF (III)

VII (Vitamin K involved in)