Secondary Haemostasis Issues Flashcards

1
Q

What is DIC?

A

Excessive/inappropriate activation of the haemostatic system

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2
Q

Give examples of when DIC occurs

A
Major trauma
ABO incompatibility reactions
Cancers
Septic shock
Ischaemia
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3
Q

Describe the pathogenesis of DIC

A
TF released from damaged tissue
Activates coag cascade
Multiple thrombus formation
Causes ischaemia
More TF release
cycle continues
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4
Q

How does DIC present?

A

Shock
Bleeding from mouth, nose and venopuncture sites
Ecchymoses
Evidence on thrombosis

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5
Q

What does coag screen show in DIC?

A

PT, APTT, TT all prolonged

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6
Q

What does FBC show in DIC?

A

Thrombocytopenia

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7
Q

d-Dimer is high in DIC

true/false

A

True

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8
Q

How is DIC treated?

A

Replace what is lost: Platelets or FFP and fibrinogen

Consider heparin if critically ill and not bleeding

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9
Q

What is vitamin K needed for?

A

Gamma-carboxylation of glutamic acid residues on factors II, VII, IX, X on proteins C and S

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10
Q

Why do caog factors need carboxylated to work?

A

Adds negative COOH group so that positive Ca2+ sticks to the coag factor
Platelets stick to this

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11
Q

What is vitamin K?

A

Fat soluble vitamin

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12
Q

What does vitamin K need to be absorbed?

A

Bile salts

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13
Q

How does vitamin K def present?

A

GI bleed
Cerebral bleed
Bruising
Haematuria

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14
Q

What may lead to inadequate stores of vit K?

A
Abx 
Bleeding disorders (haemorrhagic disease of the newborn)
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15
Q

What may leads to malabsorption of vit K?

A

Obstructive jaundice

Crohns

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16
Q

Which drugs may cause def of Vit K?

A

Abx

OAC

17
Q

What does coag screen show in vit K def?

A

PT and APTT prolongation

18
Q

What is the management of vit K?

A

IV vit K1

phytomenadione

19
Q

How may cholestasis lead to vit K def?

A

Lack of bile salts causing malabsorption of vit K

20
Q

How is haemophilia inherited?

A

X linked

21
Q

Which factor is defective in haemophilia A?

A

VIII

22
Q

Which factor is affected in haemophilia B?

A

IX

23
Q

What are “target joints”?

A
Mostly ankle or knee
Movement leads to bleed 
Fibrin cant be made to stop bleed
Iron causes joint irritation
Neovascularisation occurs - but these are fragile and break
Cycle continues
24
Q

<1 IU/dL of factor VIII indicates…

A

Severe haemophilia

25
Q

1-5 IU/dL of factor VIII indicates…

A

Moderate haemophilia

26
Q

> 5 IU/dL of factor VIII indicates…

A

Mild haemophilia

27
Q

Describe bleeding in moderate haemophilia

A

Prolonged bleed following injury

28
Q

Describe bleeding severe haemophilia

A

Target joints

Bleed spontaneously

29
Q

Describe bleeding mild haemophilia

A

Prolonged bleeding after surgery

30
Q

Describe coag screen in haemophilia A

A

Normal PT

Prolonged APTT

31
Q

How is mild haemophilia A treated?

A

Vasopressin IV/subcut

Or factor VIII IV every 2 days

32
Q

How is haemophilia B treated?

A

Factor IX given every 2 weeks

33
Q

What is the goal of drug therapy in haemophilia?

A

To keep factor levels above 2%