Haemostasis Flashcards

1
Q

what is haemostasis?

A

the arrest of bleeding and the maintenance of vascular patency

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2
Q

what is primary haemostasis?

A

formation of a platelet plug

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3
Q

what is secondary haemostasis?

A

formation of the fibrin clot

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4
Q

when does fibrinolysis occur?

A

when haemostasis is secure

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5
Q

where are platelets formed and how?

A

bone marrow

budding off from megakaryocytes

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6
Q

what is the average life span of a platelet?

A

7-10 days

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7
Q

what do platelets bind to in damaged endothelium?

A

collagen

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8
Q

what is a reduced number of platelets called?

A

thrombocytopenia

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9
Q

what is a common cause of reduced platelet function?

A

taking anti-platelet medications

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10
Q

how can problems with primary haemostasis present?

A

spontaneous bruising
mucosal bleeding
retinal haemorrhages

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11
Q

what is the screening test to assess primary haemostasis?

A

platelet count - part of a FBC

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12
Q

what does TF/VIIa do?

A

activates V/XA

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13
Q

what does V/Xa do?

A

converts prothrombin to thrombin

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14
Q

what does thrombin do?

A

converts fibrinogen to fibrin

activates VIII/IXa

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15
Q

what does VIII/IXa do?

A

activates V/Xa

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16
Q

what are the two possible groups of causes of a problem with secondary haemostasis?

A

single clotting factor deficiencies

multiple clotting factor deficiencies

17
Q

name a cause of a single clotting factor deficiency

A

haemophilia

18
Q

what clotting factor is deficient in haemophilia A?

A

VIII

19
Q

what clotting factor is deficient in haemophilia B?

A

IX

20
Q

name a potential cause of a multiple clotting factor deficiency

A

DIC

21
Q

what is fibrinolysis?

A

the breakdown of the fibrin clot

22
Q

what breaks down fibrin?

A

plasmin

23
Q

what is the plasmin precursor?

A

plasminogen

24
Q

what converts plasminogen to plasmin?

A

tissue plasminogen activator (TPA)

25
Q

what is the breakdown product of fibrin?

A

fibrin degradation products (FDPs)

26
Q

what are cross-linked FDPs called?

A

D-dimers

27
Q

what are the two screening tests for secondary haemostasis?

A
prothrombin time (PT) 
activated partial thromboplastin time (APTT)
28
Q

what test measures the intrinsic pathway in secondary haemostasis?

A

PT

29
Q

what test measures the extrinsic pathway in secondary haemostasis?

A

APTT

30
Q

name three naturally occurring anticoagulants

A

anti thrombin
protein C
protein S

31
Q

what is thrombophilia?

A

a deficiency of naturally occurring anticoagulants

32
Q

what does thrombophilia increase the risk of?

A

venous thrombosis

33
Q

what is the role of VWF?

A

helps hold platelets to each other and to collagen

34
Q

what clotting factor may be deficient if there is an isolated prolonged PT?

A

factor VII

35
Q

what coagulation screen result should be monitored when on warfarin?

A

INR - based on PT

36
Q

what coagulation screen result should be observed when on heparin?

A

APTT