• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/41

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

41 Cards in this Set

  • Front
  • Back
What is the definition of primary hemostasis?
PLATELETS
Immediate response to vascular injury
Endothelial cells and underlying CT
What is secondary hemostasis?
Blood proteins, procoagulants
Anticoagulants, fibrinolytic agents
COAGULATION
What is the pathway of primary hemostasis?
Platelet adhesion via vWF--> platelet shape change --> granule release (ADP, TXA2) --> Recruitment of more platelets --> Aggregation (hemostatic plug)
What is the prothrombic effect of endothelium?
Endothelium causes vasoconstriction
What do a granules contain?
P-selectin - adhesion molecule
Fibrinogen, fibronectin, factors 5 + 8
Growth factors PDGF, TGF-B
What do dense granules contain?
Products for metabolism/recruitment, ADP, serotonin, epi, calcium
What happens when platelets degranulate after shape change?
Release ADP, Ca
What are the 3 aggregation mediators?
ADP
TxA2
Thrombin
What does thrombin bind to, and what does it cause?
Thrombin binds to PAR on platelets --> causes more secretion of ADP
What is the pathology of von Willebrand Disease?
Deficiency of vWF
What is the pathology of Bernard-Soulier syndrome?
Large platelets and small platelet count
Defective primary hemostasis
What is Glansmann thrombasthenia?
Hereditary defect of Gp11b111a, doesn't allow binding of platelets
What is the mechanism of action of Clopidogrel?
ADP receptor inhibitor, used to prevent thrombosis
What is the mechanism of action of Aspirin and NSAIDS?
Blocks COX action on AA
Prevent production of TxA2
What is thrombocytopenia?
Decreased platelet numbers from decreased production in marrow or from increased peripheral destruction
What does prostacyclin do?
Vasodilation
Inhibits platelet aggregation
OPPOSITE OF TXA
What is the source of prostacyclin?
Endothelial cells
What does thromboxane do?
Vasoconstriction
Stimulates platelet aggregation
What is the source of thromboxane?
Platelet
What does nitric oxide do, and what is it's source?
Vasodilation, inhibits platelet aggregation
Source: endothelial cells
What does thrombin do in regards to secondary hemostasis?
Proteolyzes fibrinogen to fibrin
What does fibrin do in regards to secondary hemostasis?
Fibrin polymerizes into insoluble gel that encases platelets to form definitive secondary hemostatic plaque
What factor number is fibrinogen?
I
What factor number is prothrombin?
II
What factor number is factor s?
V
What 5 factors are vitamin K dependent?
7, 9, 10, 11, Protein C
Which intrinsic and extrinsic factors contribute to prothrombin?
Intrinsic --> factor 12
Extrinsin --> tissue factor + factor 7
What is the intrinsic pathway of factors?
12 --> 11 --> 9 --> 8
What is the extrinsic pathway of factors?
7
What is the common pathway of factors?
10 --> 5 --> 2
What does PT (prothrombin time) measure?
Time to clot = 12-14"
Monitors coumadin
Factor deficiencies of 7, 10, 5, 2 or 1 will show prolonged PT
Increases from deficiencies in extrinsic or common
What does PTT (partial thromboplastin time) measure?
Monitors heparin
Time to clot = ~40"
Increases from deficiencies in intrinsic or common
Factors 12, 11, 9, 8, 10, 5, 2, 1
What are the 2 most common hereditary clotting deficiencies?
Factor 8 and vWF deficiencies
What does coumadin/warfarin do?
Vitamin K antagonist
Common tx for pt's prone to thrombi
What are the clinical features of Hemophilia A and B?
Spontaneous hemorrhage, easy bruising, hemorrhage into joints, prone to CNS hemorrhage
What lab value is elevated with Hemophila A and B?
PTT
What lab values are elevated with DIC?
PT and PTT
What lab values are prolonged in Vit K deficiency?
Acute deficiency - PT prolonged
Chronic deficiency - PTT prolonged
What are clinical features of bleeding from defective primary hemostasis?
Thrombocytopenia, vWF disease, scurvy
Petichiae, ecchymosis, Gums/GI/GU bleeds
What are clinical features of bleeding from defective secondary hemostasis?
Factor deficiency, liver disease, acquired inhibitors
Hematomas, joints, mm, CNS, retroperitoneum
What are the anti-thrombic effects of endothelium?
Intact endothelium resists thrombosis
Physicall inhibits platelet adhesion
PTI2, NO, ADPase = vasodilation + platelet aggregation inhibition