Pathophys of Hemostasis Flashcards

1
Q

What is primary hemostasis?

A

Step 1-vasoconstriciton: direct injury resulting in recruitment of chemical messenger from endothelial cells and platelets.
(Chemical Messengers: Thromboxane A2, serotonin, endothelin I–MOST potent vasoconstrictor)

Step 2-platelet plug formation, VonWillebrand factor is released, platelets are activated by vWF, platelet proteins on platelets bind to fibrinogen causing platelets to adhere.
–lasts 12-24 hrs

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2
Q

What are some outer membrane proteins on thrombocytes?

A

-glycoproteins: GPIIb/IIIa binds fibrinogen to platelets.

  • glycosaminoglycans
  • coagulation proteins
  • no nucleus
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3
Q

Lifespan of platelets?

  • platelets contain what?
  • what regulates the production of thrombocytes?
  • where are platelets produced?
  • what do activated and non-activated platelets look like?
A
  • lifepsan 8-12days
  • serotonin, calcium, ADP, PDGF (platelet dereived growth factor), thromboxane A2
  • Thrombopoietin from liver, kidney, smooth muscle, and bone marrow.
  • look like potato chips in inactivated state and like spikey balls in the activated
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4
Q

What activates the platelets?

A

vonwillibrand factor

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5
Q

Describe the steps of platelet aggregation?

A
  1. A tissue injury
  2. B vWF released from endothelial cells at site of injury, recruits platelets.
  3. platelet adhesion to vWF on endothelial wall.
  4. ) vWF activates platelet and causing shape change.
  5. ) once shape change, platelet release granules recruiting more platelets
  6. ) aggregation (hemostatic plug) (collagenous)
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6
Q

Platelet plug formation defective if?

A
  • low platelets
  • decreased vWF
  • medications inhibiting platelets (ASA, clopidrogel)
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7
Q

What is Secondary Hemostasis ?

A
  • coagulation

* activated by either a defect in vessel endothelium or disruption in vessel wall

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8
Q

How is the intrinsic pathway activated?

A

-initially exposed collagen in the vessel activates factor XII (Hageman Factor)

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9
Q

what element is essential for the clotting cascade?

A

CALCIUM, for both intrinsic and extrinsic

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10
Q

What factor starts the extrinsic pathway?

A

tissue factor (factor III)

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11
Q

What activates tissue factor?

A

inflammatory cytokines, cell injury, and vessel injury (bleeding into the tissue)

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12
Q

What starts the common pathway?

What ends the pathway?

A

starts with factor X, goes through prothrombin, thrombin, and figrinogen, and ends with the formation of fibrin

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13
Q

How long does it take to complete clot formation?

A

3-6 minutes

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14
Q

What is clot retraction?

A

Platelets contract and draw the edges of the blood vessel closer together

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15
Q

What is necessary to remove clots as the blood vessels heal? When does this occur?

A

fibrinolysis is necessary to remove clots.

occurs within 2 days of clot formation and continues until the clot is fully dissolved.

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16
Q

What is plasmins function?

What leads to the formation of plasmin?

A
  • digests firbin in the clot to break it up.

- the formation of plasmin is dependent on the activation of plasminogen by tPA, XIIa, and thrombin from plasminogen.

17
Q

Where do tPA and urokinase come from? What causes their release?

A
  • liver, plasma, and enodthelium

- release stimulated by vasoactive drugs, venous occlusion, increased body temp, and exercise.

18
Q

What regulatory mechanisms limit clot growth?

A

-removal of clotting factors with dilution (simple circulation)

  • Inhibit activated clotting factors with:
  • -antithrombin III (inactivates II and X)
  • -Protein C (inactivates V and VII)
  • -Protein S (accelerates the action protein C)
  • -Heparin (inactivates II and ATIII)
19
Q

What are some nutritional deficiences and liver failure that can alter the ability to control hemostasis?

A
  • Ca 2+ helps activate multiple clotting factors throughout the entire coagulation cascade
  • Vit K is required fro synthesis of clotting factors II, VII, IX, and X, protein C, and prothrombin
  • most of clotting factors are synthesized in the liver. Liver failure would be bad.