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36 Cards in this Set

  • Front
  • Back
what are three steps of platelets
adhesion, activation, aggregation
primary hemostasis
platelet plug
secondary hemostasis
fibrin clot
adhesion membrane receptor
glycoprotein Ib/IX;

on platelet.... binds to vWF
how are platelets activated
secrete alpha granules...... activates gp IIa/IIIb receptor .... phospholipid reorganization..... shape change from rounded to flat for more SA ..... contraction
what is the common pathway
x -> Xa
what starts the intrinsic pathway
Kal and factor XII
what does thrombin do
fibrinogen to fibrin
what is an example of SERPIN
antithrombin .... in presence of heparin ..... can bind with thrombin and prevent it from activating fibrin
Protein C
with protein S it inactivates cofactors
what starts the extrinsic pathway
factor VII
what does plasmin do
part of fibrin feedback pathway

plasminogen will bind with tPA and form plasmin ...... break up fibrin clot
Prothrombin Time PT
measures extrinsic pathway

often a measure of oral anti coagulant
Partial Thromboblastin Time
measure of intrinsic pathway
normal platelet count
150,000- 400,000
mixing study
mixes patient plasma with normal plasma
mixing study corrects
deficiency
mixing study doesn't correct
inhibitor.... factor specific or lupus anticoagulant type
primary hemostasis disorders
mucocutaneous bleeding

prolonged bleeding time.... low platelet count
secondary hemostasis
soft tissue bleeding

elevated PT, PTT, and TT
regulatory disorders of hemostatsis
soft tissue bleeding

normal lab tests
what is dominant clinical manifastation of vW syndrom
mucocutaneous bleeding
vW syndrome
autosomal dominant

BT/PFA-100 is increased
hemophelia A
sex linked
soft tissue bleeding
usually start in early childhood
classifications of hemophelia A
<1% VIII
1-5%
>5%
symptomes of hemophilia A
intercranial bleeding
intermuscular hemotoma
bleeding into other tissues
hemophelia B
sex linked
factor IX
when does spontaneous bleeding happen
platelet count less than 20,000
acute ITP
viral prodrom common
sudden onset
severe
frequent remission
chronic
adult
female
gradual onset
moderate
infrequent remission
what happens in ITP
autoantibodies are directed at platelet membrane

increased IgG bound to platelet surface leads to increased sequestering
what are common targets of ITP
glycoprotein IIa/IIIb and Ib/IX
Thrombotic Thrombocytopenic Purpura
TTP
intravascular platelet activation .....forms platelet rich micro thrombi throughout circulation
DIC elevates
thrombin and plasmin
what are two end products of DIC
microvascular thrombosis/ hemmorhage
heparin therepy can treat DIC
FALSE