AI Clotting Lecture Flashcards
What is hemostasis?
Normal hemostasis is a balance between clot generation, thrombus formation, and regulatory mechanisms that inhibit uncontrolled thrombogenesis.
What are the goals of hemostasis?
- To limit blood loss from vascular injury
- To maintain intravascular blood flow
- To 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.
What occurs during secondary hemostasis?
Clotting factors are activated, stabilizing the 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.
Name two anti-clotting mechanisms of endothelial cells.
- Negatively charged to repel platelets
- Produce platelet inhibitors such as prostacyclin and nitric oxide
What is the lifespan of platelets?
8-12 days.
What are the three phases of platelet alteration upon endothelial damage?
- Adhesion
- Activation
- Aggregation
What is the function of alpha granules in platelets?
They contain fibrinogen, factors V & VIII, von Willebrand factor, platelet-derived growth factor, and more.
What does the term ‘tenase complex’ refer to?
A crucial enzymatic complex in blood coagulation that catalyzes the activation of factor X (FX) to its active form, factor Xa (FXa).
True or False: The intrinsic pathway plays a major role in the initiation of hemostasis.
False. It plays a minor role and is more of an amplification system.
What is the prothrombinase complex?
Factor Xa binds with Va to rapidly convert prothrombin (II) into thrombin (IIa).
What activates the common pathway in coagulation?
Factor Xa initiates the common pathway.
What is the role of thrombin in coagulation?
Thrombin converts fibrinogen (I) to fibrin (Ia), forming a mesh that stabilizes the clot.
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 a deficiency in von Willebrand factor, causing defective platelet adhesion/aggregation.
What are the laboratory findings typically associated with Hemophilia?
- Normal PT
- Normal platelets
- Prolonged PTT
What is the primary source of coagulation factors in the body?
The liver.
What is traumatic coagulopathy?
Acute coagulopathy seen in trauma patients, often related to activated protein C decreasing thrombin generation.
What is Factor V Leiden mutation?
A mutation that leads to activated protein C resistance, present in 5% of the Caucasian population.
What is Antiphospholipid Syndrome?
An autoimmune disorder characterized by antibodies against phospholipid-binding proteins in the coagulation system, leading to recurrent thrombosis.
Fill in the blank: The most significant cause of intraoperative bleeding is ______.
[anticoagulant medications]
What is the role of DDAVP in von Willebrand’s Disease?
It increases von Willebrand factor levels.