Other Flashcards
(63 cards)
What are the goals of hemostasis?
- To limit blood loss from vascular injury
- Maintain intravascular blood flow
- Promote revascularization after thrombosis
What are the two stages of hemostasis?
- Primary Hemostasis
- Secondary Hemostasis
What occurs during Primary Hemostasis?
Immediate platelet deposition at the endovascular injury site.
Leading to initial platelet plug formation and only adequate for minor injury
What occurs during Secondary Hemostasis?
Clotting factors are activated, leading to a stabilized clot formed and secured with crosslinked fibrin.
What role do vascular endothelial cells play in hemostasis?
They have antiplatelet, anticoagulant, and fibrolytic effects to inhibit clot formation.
What are some anti-clotting mechanisms of endothelial cells?
- Negatively charged to repel platelets
- Produce platelet inhibitors such as prostacyclin and nitric oxide
- Excrete adenosine diphosphatase
- Increase protein C, an anticoagulant
- Produce Tissue Factor Pathway Inhibitor (TFPI)
- Synthesize tissue plasminogen activator (t-PA)
What is the lifespan of platelets?
8-12 days.
What are the two types of storage granules in platelets?
- Alpha granules
- Dense bodies
What do alpha granules contain?
- Fibrinogen
- Factors V & VIII
- von Willebrand factor
- Platelet-derived growth factor
What do dense bodies contain?
- ADP
- ATP
- Calcium
- Serotonin
- Histamine
- Epinephrine
What are the three phases of platelet alteration upon ECM exposure?
- Adhesion
- Activation
- Aggregation
What initiates the Extrinsic Pathway?
Endothelial injury exposing tissue factor (TF) to the plasma.
What complex does TF form with to activate factor X?
TF forms an active complex with factor VIIa (TF/VIIa complex).
What is the role of factor Xa in the hemostatic process?
Factor Xa begins the final common pathway.
What is the main function of the Intrinsic Pathway?
It amplifies thrombin generation initiated by the extrinsic pathway.
What activates factor XII in the Intrinsic Pathway?
Contact with a negatively charged surface.
What does the Common Pathway involve?
Factor X becomes Xa and binds with Va to form the prothrombinase complex.
What does thrombin do?
Converts fibrinogen (I) to fibrin (Ia) and stabilizes the clot.
What is Fibrinolysis?
The process where endovascular TPA & urokinase convert plasminogen to plasmin, breaking down clots.
What are the four major coagulation counter-mechanisms?
- Fibrinolysis
- Tissue factor pathway inhibitor (TFPI)
- Protein C system
- Serine Protease Inhibitors (SERPINs)
What is Von Willebrand’s Disease?
The most common inherited bleeding disorder, characterized by deficiency in von Willebrand factor.
What is Hemophilia A?
Factor 8 (VIII) deficiency occurring in 1 in 5,000 individuals.
What is the primary cause of drug-induced bleeding?
Anticoagulant medications.
What is the significance of liver disease in hemostasis?
It leads to impaired synthesis of coagulation factors and platelet dysfunction.