Coagulation Flashcards
Method of coag
endothelial damage exposes procoag factors -> haemostatic response -> plt aggregation
What coag factors are prod by endothelial cells
PGI2, VWF, plasminogen activators, thrombomodulin
platelet adhesion
direct = Glp1a indirect = Glp1b and vwf
how to platelets attach to each other
Glp2b and Glp3a (fibronogen R)
what does plt adhesion cause
release of ADP and thromboxane A2 (-> aggregation)
arachidonic acid -> ____ (+via)
-> endoperoxidases (via COX)
what are endoperoxidases conv to
- > thromboxane A2 (stim agg)
- > PGI2 (inhib agg)
aspirin vs NSAIDS
aspirin - irrev inhib COX
NSAIDs - rev
actions of thrombin
activates F7, F8, F5, plt, F11, F13 (-> propogation)
catylises fibronogen -> fibrin
why is vit K important in coag
req as co-enz for lots of liver prod factors (2,7,9,10)
3 physiological anticoag
TFPI - stop F7-F7a (no initiation)
Prot c/Prot s - bind to thrombomodulin - stop 8->8a and 5->5a
antithrombin - stop prothrombin->thrombin and 10->10a
sympto of platelet disorders
petechiae, purpura, sml bruises, no haemoarthrosis
sympto of coag F disorders
bleeding in soft tissues (joints/muscles), large bruises
inheritance of haemophilia
X linked congen def of F8 (A) or F9 (B)
signs / sympto haemophilia
long APTT, normal PT, haemoarthrosis, soft tissue haematomas
inheritance of VWD
T1/2 = auto dom T3 = auto rec