KEY CLOTTING DISORDERS Flashcards

1
Q

Most common cause of inherited haemophilia?

A

Von Willebrand’s disease.

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2
Q

Platelet disorders are typically characterised by what?

A

Easy bruising + spontaneous bleeding from small vessels.

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3
Q

Coagulation disorders are typically characterised by what?

A

Bleeding after injury or surgery.

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4
Q

The APTT test is a reflection of which clotting pathway?

A

The intrinsic pathway.

**Reflects intrinsic pathway and therefore function of platelets.

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5
Q

Vitamin K is needed to synthesis which clotting factors?

A

II, VII, IX and X.

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6
Q

Common presenting complaints of Von Willebrand disease?

A

Epistaxis
Easy bruising
Menorrhagia
Bleeding after minor trauma or surgery (e.g. tooth extraction).

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7
Q

Most common inheritance pattern of Von Willebrand disease?

A

Autosomal dominant.

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8
Q

Clotting profile (PT + APTT) results in Von Willebrand disease?

A

Prolonged APTT + PT.

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9
Q

Other blood results seen in Von Willebrand disease?

A

Reduced VIII and reduced Von Willebrand factor.

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10
Q

Deficiency in haemophilia A?

A

Factor VIII.

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11
Q

Deficiency in haemophilia B?

A

Factor IX.

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12
Q

Haemophilia inheritance pattern?

A

X-linked recessive.

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13
Q

Feature of severe haemophilia?

A

Spontaneous bleeding into joints.

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14
Q

Presentation of haemophilia in neonates?

A

Intracranial haemorrhage, haematomas + prolonged bleeding after circumcision.

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15
Q

Clotting profile in haemophilia?

A

APTT prolonged.

PT normal.

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16
Q

Most common inherited thrombophilia?

A

Activated protein C resistance (Factor V Leiden).

17
Q

What does thrombocytopenia mean?

A

Low levels of platelets.

18
Q

DIC arises due to what?

A

Systemic activation of coagulation, often as part of an inflammatory response.

19
Q

PT test assesses which clotting pathway?

A

Extrinsic and common pathways.

20
Q

Most common presenting complaints in Von Willebrand disease?

A

Menorrhagia, post-op bleeding, epistaxis.

21
Q

Most likely cause of bleeding + thrombosis in a young woman?

A

Anti-phospholipid 2 syndrome.

22
Q

Most common inherited thrombophilia?

A

Factor V Leiden.

23
Q

How long on LMWH in provoked VTE?

A

3 months.

24
Q

How long on LMWH for unprovoked VTE?

A

6 months.

25
Q

Treatment for anti-phospholipid syndrome in pregnancy?

A

Aspirin + LMWH.

26
Q

Management in a minor allergic reaction to a blood transfusion?

A

Stop transfusion temporarily and give anti-histamine.

27
Q

Management of anaphylaxis caused by a blood transfusion?

A

Terminate transfusion + give IM adrenaline.

28
Q

Blood clotting results in haemophilia?

A

Prolonged APTT.

PT, bleeding time and thrombin time all normal.

29
Q

Transfusions of packed red cells can cause what electrolyte abnormality?

A

Hyperkalaemia.

30
Q

Most common cause of isolated thrombocytopenia?

A

ITP.

31
Q

Grossly elevated APTT?

A

Haemophilia (B)

32
Q

Universal donor of FFP?

A

AB negative

33
Q

Pentad of symptoms and signs suggesting TTP?

A
Fever
Neurological signs
Thrombocytopenia
Haemolytic anaemia
Renal failure