2 - haemostasis Flashcards
what are the components of normal haemostatic system?
- formation of platelet plug - primary haemostasis
- formation of fibrin clot - secondary haemostasis
- fibrinolysis
- anticoagulant defences
what happens in primary haemostasis?
= 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.
what happens in secondary haemostasis?
= 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
what does failure of forming platelet plug lead to?
- spontaneous bruising or purpura
- mucosal bleeding
- intracranial haemorrhage
- retinal haemorrhages
what screening test done for primary haemostasis?
platelet count
what happens in fibrinolysis?
plasminogen broken down to plasmin by tissue plasminogen activator (tPA). plasmin breaks down fibrin to fibrin degradation products
what are tests for fibrin clot formation?
- 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
- activated partial thromboplastin time = add in different thing which activate different factors, VIII & IX which make clotting factor V or X through different pathway
what are naturally occuring anticoagulants?
- serine protease inhibitors = antithrombin binds to thrombin & switches off
- protein C & S = switch of factor VIII and V
what is thrombophilia?
= deficiency of naturally occuring anticoagulants may be hereditary which causes increased tendency to develop venous thrombosis (DVT/PE)