Hemostasis Flashcards
primary hemostasis involves
platelet plug formation
secondary hemostasis involves
blood coagulation
tertiary hemostasis involves
dissolution of fibrin clot
platelet glycoprotein that binds to collagen
GPIa
platelet glycoprotein that binds to Von willebrand factor
GPIb
fibrinogen binds to which platelet glycoprotein
GPIIb/GPIIIa
defective GPIb results in
Bernard-Soulier syndrome
prevent degradation of factor VIII
Vw factor
granule contents that activate other platelets and promote aggregation
Calcium and ADP
platelet aggregation is mainly facilitated by
fibrinogen
defective GPIIb/GPIIIa leads to
thrombasenia of Glanzmann and Naegeli (cannot form platelet plug)
conversion of fibrinogen to fibrin requires
thrombin
in the extrinsic pathway, factor VII is activated by
tissue factor
in the extrinsic pathway, factor X is activated by
tissue factor + factor VIIa + Calcium + platelet phospholipids
in the intrinsic pathway, factor IX is activated by
factor XIa
in the intrinsic pathway, factor X is activated by
factor IXa + factor VIIIa + Calcium + PL
what makes up prothrombinase complex
factor Xa + factor Va + Calcium + PL
converts prothrombin to thrombin
prothrombinase complex
coverts soft clot to hard clot
factor XIIIa
pathway activated by crush injury
extrinsic
intrinsic pathway defect will have increase in which lab time
APTT
extrinsic pathway defect will have increase in which lab time
Prothrombin time (INR)
Vitamin K dependent clotting factors
II, VII, IX, X, proteins C & S
Vit K is coenzyme for what
y-Carboxylase