2 - haemostasis Flashcards

1
Q

what are the components of normal haemostatic system?

A
  1. formation of platelet plug - primary haemostasis
  2. formation of fibrin clot - secondary haemostasis
  3. fibrinolysis
  4. anticoagulant defences
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2
Q

what happens in primary haemostasis?

A

= formation of platelet plug

endothelial wall damaged exposing collagen & releasing von willebrand factor & other proteins. platelets bind to collagen via ADP & VWF. platelets secrete thromboxane A2 etc so aggregation at site of injury. platelets stick together with glycoprotein IIb/IIIa.

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3
Q

what happens in secondary haemostasis?

A

= formation of fibrin clot

platelets have -ve charged phospholipids. they release ca2+ which sticks to surface. negatively charged coagulation factors attracted and stick on surface. tissue factor (tf) released which activated clotting factor VII, which activated V & X. they activate prothrombin (II) to thrombin (IIa). thrombin converts fibrinogen to fibrin

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4
Q

what does failure of forming platelet plug lead to?

A
  1. spontaneous bruising or purpura
  2. mucosal bleeding
  3. intracranial haemorrhage
  4. retinal haemorrhages
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5
Q

what screening test done for primary haemostasis?

A

platelet count

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6
Q

what happens in fibrinolysis?

A

plasminogen broken down to plasmin by tissue plasminogen activator (tPA). plasmin breaks down fibrin to fibrin degradation products

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7
Q

what are tests for fibrin clot formation?

A
  1. prothrombin time = put blood in tubes & spin in lab. add in phospholipid & tissue factor & calcium. you can measure how long takes for clot to form
  2. activated partial thromboplastin time = add in different thing which activate different factors, VIII & IX which make clotting factor V or X through different pathway
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8
Q

what are naturally occuring anticoagulants?

A
  1. serine protease inhibitors = antithrombin binds to thrombin & switches off
  2. protein C & S = switch of factor VIII and V
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9
Q

what is thrombophilia?

A

= deficiency of naturally occuring anticoagulants may be hereditary which causes increased tendency to develop venous thrombosis (DVT/PE)

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