Haemostasis Flashcards

1
Q

what are the requirements of haemostasis

A

permanent state of readiness
prompt response
localised response
protection against unwanted thrombus

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2
Q

what are the components of a normal haemostatic system

A

formation of platelet plug (primary Haemostasis)
formation of fibrin clot (secondary Haemostasis)
fibrinolysis
anticoagulant defences

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3
Q

from which cells do platelets arise

A

megakaryocytes

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4
Q

what is the average lifespan of a platelet

A

7-10 days

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5
Q

what causes platelet adhesion

A

damage to endothelial surface (vessel wall) exposes collagen and VW factor which have platelet receptors

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6
Q

what causes platelet aggregation

A

secretion of chemical by platelets

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7
Q

what are the consequences of failure of platelet plug formation

A

spontaneous bruising and purport
mucosal bleeding (epistaxes, GI, conjunctival, menorrhagia)
intracranial haemorrhage
retinal haemorrhages

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8
Q

what screening tests can be done for assessment of primary Haemostasis

A

platelet count

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9
Q

which factors are involved in the extrinsic coagulation pathway

A

tissue factor and VII

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10
Q

which factors are involved in the intrinsic pathway

A

VIII and IX

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11
Q

which factors are involved in the common pathway

A

V and X
prothrombin
fibrinogen

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12
Q

what are the causes of failure of fibrin clot formation

A

single clotting factor deficiency
multiple clotting factor deficiency
increased fibrinolysis

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13
Q

what causes fibrinolysis

A

plasminogen is converted to plasmin in the presence of tissue plasminogen activator
plasmin breaks down fibrin to fibrin degradation products

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14
Q

what screening tests are available for secondary Haemostasis

A

prothrombin time

activated partial thromboplastin time

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15
Q

which pathway does prothrombin time measure

A

extrinsic

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16
Q

which pathway does the APTT measure

A

intrinsic

17
Q

what is the action of anti-thrombin

A

inhibits thrombin, and the intrinsic, extrinsic and common pathways

18
Q

what is the action of protein C and protein S

A

in the presence of thrombin bound to thrombomodulin, they inhibit the intrinsic and common pathways (factors V, X, VIII, IX)