passmed clotting Flashcards

1
Q

Heparin Prevents activation factors of what 4 factors clot to 1972

A

2,9,10,11

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2
Q

warfarin affects what clotting factors

A

2,7,9,10

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3
Q

DIC affects what factors - 5 in total

A

1,2,5,8,11

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4
Q

liver disease affects what factors

A

1,2,5,7,9,10,11

Factor VIII is synthesised in the endothelial cells of the liver rather than the liver itself and therefore is less prone to the effects of hepatic dysfunction.

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5
Q

haemorrphial will present with what on APTT and PT and bleeding time compared to vWD and Vitamin k deficiency

all increased on APTT

APTT
APTT and bleeding
APTT and pT

A

Disorder APTT PT Bleeding time
Haemophilia Increased Normal Normal
von Willebrand’s disease Increased Normal Increased
Vitamin K deficiency Increased Increased Normal

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6
Q

what does haptoglobin do

A

mops up Hb

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7
Q

difference between APTT and PT

A

APTT (activated partial thromboplastin time) is a measure of the intrinsic and common clotting cascades (including clotting factors I, II, V, VIII, X). Note that this does not include factor IX, meaning that haemophilia B may not always have an abnormal APTT.

PT (prothrombin time) is a measure of the extrinsic and common pathways of the clotting cascade. Note that INR (international normalised ratio) which is commonly used for warfarin management is derived from PT. PT, therefore, is a measure of factors I, II, V, VII, X.

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8
Q

RF for PE ( blood, SOB , leg swelling and pain

A
General
increased risk with advancing age
obesity
family history of VTE
pregnancy (especially puerperium)
immobility
hospitalisation
anaesthesia
central venous catheter: femoral >> subclavian
Underlying conditions
malignancy
thrombophilia: e.g. Activated protein C resistance, protein C and S deficiency
heart failure
antiphospholipid syndrome
Behcet's
polycythaemia
nephrotic syndrome
sickle cell disease
paroxysmal nocturnal haemoglobinuria
hyperviscosity syndrome
homocystinuria
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