Haemostatis and Bleeding Disorders Flashcards

(38 cards)

1
Q

define haemostasis

A

arrest of bleeding and maintenaince of vascular patency

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2
Q

what is the primary stage of haemostasis?

A

formation of platelet plug

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3
Q

what is the secondary stage of haemostasis?

A

formation of fibrin clot

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4
Q

what is the lifespan of platelets and why is this important with regards to surgery?

A

7-10 days, if someone on anti-platelets need to stop medication week before surgery to achieve normal homeostasis level

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5
Q

failure of the platelet pluf formation can be caused by what?

A

vascular

platelets

Von willebrand factor

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6
Q

what are vascular causes of failure to form the platelet plug?

A

hereditary i.e. marfans

aquired i.e. vasculitis (HS purpura)

inc in age (lack of collagen)

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7
Q

what are platlet casues of failure to form platelet plug?

A

thrombocytopenia (reduced number)

renal disease (reduced function)

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8
Q

failure of platelet plug formation can result in what?

A

spontaneous bruising and purpura

mucosal bleeding

intracranial haemorrhage

retinal haemorrhage

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9
Q

what are the three ‘stages’ of platelet plug formation?

A

initiation

propagation

amplification

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10
Q

TF and VIIa activate what?

A

V and Xa

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11
Q

V and Xa activate what?

A

prthrombin

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12
Q

prothrombin is converted to what during platelet plug formation?

A

thrombin

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13
Q

thrombin stimulates further relase of which factors?

A

VIII and IXa

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14
Q

VIII and IXa activate more of which other factors?

A

V and Xa

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15
Q

fibrin is broken down by what?

A

plasmin

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16
Q

what converts plasminogen to plasmin?

A

tissue plasminogen activator

17
Q

what is looked at in a coagulation screen?

A

prothrombin time

activated partial thromboplasmin time

FBC

18
Q

what is the prothrombin time measuring?

A

Tissue factor and VIIa

19
Q

what is the activated partial prothrombin time measuring?

20
Q

what is the FBC used to look at in a coagulation screen?

A

platelet count

21
Q

what is thrombophilia?

A

deficiency of naturally occuring anti-coagulants

22
Q

what is the commenest cause of primary haemostatic failure?

A

thrombocytopenia

23
Q

what can cause secondary haemostatic failure (fibrin clot)?

A

multiple or single clotting factor deficiences

24
Q

what can cause multiple clotting factor deficiencies?

A

liver failure

Vit K deficiency/warfarin therapy

DIC

25
why does a vit K deficiency affect clotting factors?
required to make 2,7,9,10
26
how can obstrucitve jaundice i.e. pancreatic cancer/gallstones cause a clotting factor deficiency?
need bile salts for absoprtion of Vit K- without vit K can't carboxylate 2,7,9,10
27
what can cause DIC?
sepsis obstetirc emergencies malignancy hypovolaemic shock
28
what is a single clotting factor deficiency?
hameophilia
29
which is more common haemophilia A or B?
A
30
which clotting factor is deficient in haemophilia A and in B?
A - factor VIII B- factor IX
31
what mode of inheritance is haemophilia?
X-linked
32
what occurs in someone with haemophilia?
recurrent haemarthroses, soft tissue bleeds prolonged bleeding after dental extractions/surgery
33
atypical picture of menorrhagia and easy bruising would suggest deficiency of what?
Von Willebrand Factor
34
where do people with haemophilia most commnly suffer haemarthroses?
ankle/knee- this is where you're most liekly to bump/twist
35
elevated PT time would indicate deficeincy in?
TF and VII
36
elevated APTT would indicate deficiency in?
VIII and IX
37
platelet adhesion at injury sites occut via what?
glycoprotein 1b and VWF
38
what is dipyridamole?
phosphodiesterase inhibitor- reduces cAMP production