Disorders of haemostasis Flashcards

1
Q

Primary or Secondary? Acquired FVIII deficiency

A

Secondary

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2
Q

Primary or Secondary? Decompensated cirrhosis of the liver?

A

Secondary

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3
Q

Primary or Secondary? DIC

A

BOTH!

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4
Q

Primary or Secondary? ITP (immune thrombocytopenic purpura)

A

Primary

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5
Q

Primary or Secondary? Heparin treatment

A

Secondary

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6
Q

Primary or Secondary? Thrombo-asthenia

A

Primary

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7
Q

Primary or Secondary? Haemophilia

A

Secondary

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8
Q

Primary or Secondary? Vitamin K deficiency

A

Secondary

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9
Q

Primary or Secondary? Von Willebrand’s Disease

A

Primary

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10
Q

Primary or Secondary? Warfarin treatment

A

Secondary

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11
Q

Features of acquired FVIII deficiency

A

Antibodies against FVIII
PT and platelet count normal
APTT prolongued

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12
Q

Features of DIC

A

SIRS, sepsis leading to DIC:

Prolongued everything, low fibrinogen

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13
Q

Features of ITP

A
Purpura
Mucousal bleeding
Antibodies against platelets...
Low platelet count
Normal PT, APTT, TT, fibrinogen, but prolonged bleeding time
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14
Q

Features of heparin treatment

A

Increase APTT (therapeutic levels 1.5-2.5 times normal APTT)

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15
Q

Features of thrombo-asthenia

A

Inherited disorder of platelets - specifically GPIIb-IIIa

Prevents binding of platelets to each other (normally GPIIb-IIIa binds with vWF and fibrinogen)

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16
Q

Features of Haemophilia A

A

Factor VIII deficiency

Prolonged APTT - reduced FVIII

17
Q

Features of Haemophilia B

A

Factor IX deficiency

Prolonged APTT - reduced FIX

18
Q

Features of Vitamin K deficiency

A

Vit K dependant factors: II, VII, IX, X

19
Q

Features of vW disease

A

Defective vW factor
- Quantitative (most common)
- Qualitative
Prolonged bleeding time and APTT

20
Q

Features of Warfarin treatment

A

Prolonged PT

Overdose - prolonged APTT