Hameostasis Flashcards

1
Q

What is it called when platelets are reduced in number?

A

Thrombocytopenia

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2
Q

List two causes of impaired thrombocyte production.

A

-Leukemia
-B12 deficiency

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3
Q

Give two examples of conditions where you will find accelerated thrombocyte clearance.

A

-Immune thrombocytopenia purpura (ITP)
-Disseminated intravascular coagulation (DIC)

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4
Q

Give a third reason you can find thrombocytopenia

A

Pooling and destruction in an enlarged spleen

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5
Q

Which 3 drugs commonly caused impaired thrombocyte function?

A

-Aspirin
-NSAIDs
-Clopidogrel

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6
Q

What does aspirin do?

A

Irriversibly blocks COX which leads to decreased production of thromboxane A2.

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7
Q

How does clopidogrel work?

A

Irreversibly blocks the ADP receptor P2Y12 on platelets.

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8
Q

What two functions does VWF have in haemostasis?

A

-Binding to collagen and capturing platelets
-Stabilising factor VIII

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9
Q

What is the inheritance pattern in VWF disease?

A

Is usually hereditary with autosomal inheritance pattern.

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10
Q

Which types of VW disease lead to deficiency of VWF?

A

Type 1 or 3

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11
Q

Which types of VWD lead to normal VWF production but with impaired function?

A

Type 2

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12
Q

What is the overall negative effect of a lack of VWF in haemostasis?

A

Inability to form the platelet plug

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13
Q

What are the clinical features pf disorders of primary haemostasis?

A

Immediate prolonged heavy bleeding.
Easy spontaneous bruising

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14
Q

What are petechiae and purpura caused by and which one does not blanch when pressure is applied?

A

They are caused by bleeding under the skin and purpura do no blanch when pressure is applied.

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15
Q

What is a common feature of thrombocytopenia?

A

Petechiae

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16
Q

In severe VWD what can the bleeding pattern resemble?

A

Haemophilia due to low FVIII

17
Q

What is the bleeding called when the ‘mark’ is greater than 10mm?

A

Ecchymosis

18
Q

What are the tests for disorders of primary haemostasis?

A

-Platelet count, platelet morphology
-PFA100
-Assays of VWF
-Clinical observation

19
Q

What treatment can you give in mild VWF disorders?

A

Desmopressin (DDAVP)

20
Q

What is haemophilia A caused by?

A

Factor VIII deficiency

21
Q

What is haemophilia B caused by

A

Factor IX deficiency

22
Q

What are the acquired causes of coagulation factor production deficiencies?

A

-Liver disease
-Anticoagulant drugs (Warfarin, DOACs)

23
Q

What is haemophilia?

A

inability to generate fibrin to stabilise the platelet plug

24
Q

What is the hallmark of haemophilia?

A

Haemarthrosis (spontaneous joint bleeding)

25
Q

What should be avoided in patients with haemophilia?

A

Intramuscular injections

26
Q

What is a common cause of a coagulation disorder which results in increased consumption and depletion of coagulation factors?

A

Disseminated intravascular coagulation

27
Q

Explain the differences in the bleeding patterns between Platelet/Vascular defects and coagulation defects

A

Platelet/Vascular:
-superficial bleeding into skin, mucosal membranes.
-Bleeding immediate after injury

Coagulation:
-Bleeding deep into tissues, muscles, joints
-Delayed, but severe bleeding after injury

28
Q

What does Prothrombin time measure?

A

the extrinsic pathway

29
Q

What does the activated partial thromboplastin time measure?

A

Measures the intrinsic pathway

30
Q

What drug treatment can be used in haemophilia A to mimic factor VIII?

A

Emicizumab

31
Q

What are the three contributary factors to thrombosis called?

A

Virchow’s triad:
-Blood, dominant in venous thrombosis
-Vessel wall, dominant in arterial thrombosis
-Blood flow, contributes to both arterial and venous thrombosis

32
Q

What term is used to refer to an increased risk of venous thrombosis?

A

Thrombophilia