Haemostasis and Thrombosis in Practice Flashcards

1
Q

How do you differentiate between haemophilia A and haemophilia B?

A

Measure factor VIII and IX levels

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2
Q

Which factor is lacking in haemophilia A?

A

Factor VIII

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3
Q

Which factor is lacking in haemophilia B?

A

Factor IX

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4
Q

How is haemophilia A inherited?

A

X-linked

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5
Q

What is the treatment for severe haemophilia A?

A

Recombinant factor VIII

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6
Q

What is the treatment for severe haemophilia B?

A

What are the complications of plasma derived factor VIII treatment?

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7
Q

What are the complications of plasma derived factor VIII treatment?

A

Hep A

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8
Q

Why do DDAVP and tranexamic acid not work in severe haemophila?

A

A base factor VIII level of around 3-5 is required

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9
Q

What is the main complication of treatment of severe haemophilia A with factor VIII concentrates?

A

Development of inhibitory antibodies so treatmetn will not work

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10
Q

What is the best treatment regimen for severe haemophilia A?

A

Aim to turn severe haemophilia to moderate - give a small amount of factor VIII every day

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11
Q

Thrombocytopenia presentation

A
Short history of of easy bruising and small red spots on her ankles
Petechiae
Menorrhagia
Epistaxis
Buccal bleeding
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12
Q

Possible causes of thrombocytopenia

A

AML
Aplastic anaemia
ITP

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13
Q

Does vitamin K cause thrombocytopenia?

A

No

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14
Q

What is the likely platelet count in a thrombocytopenic patient with spontaneous bruising and petechiae formation?

A

Reduced

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15
Q

Whcih underlying illnesses are associated with ITP?

A

HIV infection
SLE
Glandular fever

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16
Q

How does aspirin work?

A

Inhibits platelet function by inhibiting COX-1

17
Q

COX

A

Cyclo-oxygenase

18
Q

What can contribute to a VTE risk?

A

Factor V Leiden