PBL 2: Sharon Phillips Flashcards

1
Q

What are the routine coagulation tests?

A
  • prothrombin time assess extrinsic pathways
  • activated partial prothrombin time assess intrinsic pathways
  • bleeding time assess platelet function
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2
Q

How is the bleeding test done?

A

Scalpel blade is used to make a shallow incision on underside of forearm superficially
Time measured from when incision made and bleeding stopped
Should be 3-10 minutes for normal adult

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3
Q

What is INR?

A

Compensates for different manufactures giving slightly different results
Derived from Prothrombin Time
Standard Value
Should be 0.8-1.2

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4
Q

How do you test Prothrombin Time?

A

Mix tissue factor (3) and calcium with delcalcified, platelet poor plasma

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5
Q

How do you test activated partial prothrombin time?

A

Addition of contact activator (kaolin) and phospholipids

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6
Q

How do you test thrombin time?

A

Test for deficiency in fibrinogen/thrombin inhibition

Add thrombin to platelet poor plasma and measure to time taken for blood clot to form

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7
Q

What suggests that she has Von Willebrand’s disease?

A

Factor VIII levels are low so haemophilia A or VWD
Factor IX levels normal so not Haemophilia B
Prolonged bleeding time
Low VWF factor so VWD

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8
Q

What is the function of VWF?

A

Forms bridge between collagen and platelet in platelet adherence to form a platelet plug

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9
Q

Why is factor VIII low?

A

Factor 8 bound to VWF and VWF prevents it from proteolysing

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10
Q

What are the types of VWD

A
  • type 1: VWF production reduced, most common, mild to moderate
  • type 2: protein present but reduced/defective
  • type 3: total absent protein
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11
Q

What are the symptoms of VWD?

A
Excessive bleeding
Bruising
Frequent nosebleeds
Menorrhagia
Heavy menstruation
OR asymptomatic, only notice when have an injury
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12
Q

What is the treatment for VWD?

A

Not always necessary
Prior to surgery/dental work intravenous desmopressin acetate to increase VWF levels stimulating coagulation (nasal inhaler for mild cases)
Intravenous factor VIII which is rich in VWF

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13
Q

What should VWD sufferers avoid?

A

Avoid damage to liver as cirrhosis interferes with its ability to produce proteins and coagulation factors - alcohol intake, binge drinking avoid

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14
Q

What is the inheritance of VWD compared to haemophilia?

A

Autosomal dominant - VWD (individual is female and mother also affected not likely to be X linked not haemophilia)
Haemophillia ix X linked

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15
Q

What can desmopressin cause?

A

Hyponatremia

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16
Q

What is the function of antithrombin?

A

Inhibits thrombin, Xa, VII, IX and XI
SERPIN - serine protease inhibitor
- increased activity in presence of heparin

17
Q

What is the function of protein C and S?

A

Vitamin K dependent glycoproteins

  • synthesised in the liver
  • protein C: serine protease inactivates Va and VIIIa
  • protein S is cofactor for activated protein C