10.16.18 Hemostasis and Thrombosis Flashcards

1
Q

What are the 2-fold mechanisms underlying the arrest of bleeding?

A
  1. Vasoconstriction

2. Formation of hemostatic plug

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2
Q

Arrest of bleeding following vascular injury

A

Hemostasis

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3
Q

What type of interactions is hemostasis dependent upon?

A
  1. Platelet adhesion/aggregation
  2. Endothelial cell function
  3. Blood coagulation system
  4. Clot lysis (fibrnolysis)
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4
Q

What are the aspect of normal vessels that suppress hemostasis

A
  1. Prostacyclin
  2. Heparan sulfate
  3. Tissue factor pathway inhibitor
  4. Nitric oxide
  5. Thrombomodulin
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5
Q

What are platelets formed from?

What does a normal platelet count lie between?

A

Cytoplasm of bone marrow megakaryocyte

150-450

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6
Q

What is sequence of events leading to blood clotting?

A
  1. Vasoconstriction
  2. Platelet aggregation
  3. Coagulation
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7
Q

What are the consequences of uncontrolled hemostasis?

A
  1. Bleeding (hemorrhage)

2. Thrombosis (venous or arterial)

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8
Q

Interacts in a highly ordered sequence of specific plasma proteins that convert soluble fibrinogen to insoluble fibrin in order to stabilize the primary hemostatic plug

A

Blood Coagulation System

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9
Q

What are the zymogens/active enzymes in secondary hemostasis?

Cofactors?

Non-protein cofactors?

A

2,7,9,10 (Vit K dep); 11,12, 13 (Vit K indep)

5,7, TF, vWF- Cofactors

Ca, PL surfaces (non-protein cofactors)

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10
Q

What factor is activated by thrombin and cross-links/stabilizes fibrin?

A

Factor 13

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11
Q

What are the key factors that start and control hemostasis?

A

Factor 7 and 8 (shortest half life/plasma amounts)

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12
Q

What do activated platelets release to recruit more platelets and promote aggregation

A

Granule contents (ADP, TxA2)

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13
Q

integrin receptor; adheres to fibrinogen, enhances aggregation and stabilizes thrombus

A

Platelet glycoprotein IIb/IIIa

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14
Q

What is released by endothelial cells to inhibit further platelet aggregation?

A

Prostacyclin and nitric oxide

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15
Q

What stage of hemostasis are platelets and blood coagulation proteins involved in?

A

Platelets- primary

BCP- secondary

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16
Q

In what pathways is thrombin involved in?

A

Coagulation and anticoagulation

17
Q

What coagulation factor does the common pathway begin with and what protease activates it?

A

Factor 10 activated by F7a/TF

18
Q

How does thrombin form fibrin monomer?

A

Cleaves 2 small activation peptides from fibrinogen

19
Q

the degradation product of cross-linked fibrin; reflects ongoing activation of the hemostatic system

minimal levels in health individual

A

D-Dimer

20
Q

Elevated D-dimer is useful for using in which clinical interpretations?

A
  1. Evaluation of thrombus formation
  2. Ruling out DVT
  3. Monitoring anticoagulative treatment
  4. Disseminated intravascular coagulation (DIC)
21
Q

In what ways can you turn off clotting?

A
  1. Tissue Factor Pathway inhibitor
  2. Coagulation protease inhibitor
  3. Protein C System
  4. Fibrinolysis
22
Q

Stimulates activation of protein C by thrombin

A

Thrombomodulin