Approach To Thrombosis Flashcards
(35 cards)
What are the social correlates related to thrombotic disorders?
Traffic, road users, organization, regulatory mechanisms
These factors can influence the prevalence and management of thrombotic disorders.
What is the main goal of haemostasis?
To stop bleeding and to do so only at the site of injury
This involves a balance between pro-coagulant and anticoagulant mechanisms.
What does Virchow’s triad consist of?
Three components: stasis, hypercoagulability, endothelial injury
These factors contribute to the risk of thrombosis.
What are the two main processes of haemostasis?
- Primary haemostasis
- Secondary haemostasis
Primary involves vasoconstriction and platelet plug formation; secondary involves coagulation factors.
What is the role of platelets in primary haemostasis?
Formation of a platelet plug
This is the first physiological response to blood vessel injury.
What is the purpose of secondary haemostasis?
To stabilize and reinforce the weak platelet plug and convert fibrinogen to fibrin
This prevents further blood loss from the injury site.
Name two key components involved in the coagulation pathways.
- Tissue factor (TF)
- Calcium
These components are essential for the activation of coagulation factors.
What are the main steps in the cell-based model of haemostasis?
- Initiation
- Amplification
- Propagation
These steps describe how coagulation factors are activated to form fibrin.
What are promoters of fibrinolysis?
- Plasmin
- Tissue plasminogen activator (tPA)
These substances help dissolve clots and restore blood flow.
What are inhibitors of fibrinolysis?
- Antiplasmin
- Plasminogen activator inhibitor-1 (PAI-1)
These substances prevent excessive clot breakdown.
What factors can contribute to acquired risk factors for thrombosis?
- Age
- Pregnancy
- Trauma
- Surgery
- Immobility
- Malignancy
These factors can increase the risk of thrombotic events.
What is thrombotic thrombocytopenic purpura (TTP)?
A condition characterized by renal failure, hemolytic anemia, and thrombocytopenia
Treatment includes fresh frozen plasma and plasma exchange.
What is a common inherited thrombophilia condition?
Factor V Leiden
This condition increases the risk of thrombosis and is prevalent in Caucasian populations.
Fill in the blank: The process of _______ stabilizes and reinforces the clot formed during primary haemostasis.
Secondary haemostasis
This involves the conversion of fibrinogen to fibrin.
True or False: Antithrombin deficiency is an autosomal dominant condition.
True
This condition significantly increases the risk of thrombosis.
What are the two physiological responses involved in primary haemostasis?
- Local vasoconstriction
- Platelet plug formation
These responses occur immediately after vascular injury.
What is the function of the vascular endothelium in haemostasis?
- Anticoagulant properties
- Procoagulant properties
It regulates the balance between bleeding and clotting.
What does a thrombophilia screen test for?
Deficiencies or abnormalities in coagulation factors
This helps identify the underlying causes of thrombotic events.
What are the three main components of Virchow’s triad?
- Stasis
- Endothelial injury
- Hypercoagulability
These factors contribute to thrombosis risk.
What is Factor V Leiden?
Commonest genetic risk factor for thrombosis, present in 5% of Caucasian population, rare in black and Asian populations. Causes activated protein C resistance, increasing risk by 7%.
Factor V Leiden is a mutation that affects the clotting process, leading to increased risk of venous thromboembolism.
What is the Prothrombin 20210 mutation?
G20210A mutation on chromosome 11, increases risk of thrombosis by 3%.
This mutation leads to elevated levels of prothrombin, a clotting factor, which can contribute to venous clots.
What is the prevalence of Protein C deficiency?
Prevalence is 0.2-0.3%, inherited in an autosomal dominant manner, located on chromosome 2, and increases thrombosis risk by 10-15%.
Protein C plays a crucial role in regulating blood coagulation.
What is Protein S deficiency?
An autosomal dominant condition located on chromosome 3, liver and vitamin K dependent, increasing thrombosis risk by 2%.
Protein S is a cofactor for Protein C, and its deficiency can lead to increased clot formation.
What are common investigations for thrombosis diagnosis?
Doppler ultrasound scan, venogram.
These imaging techniques help visualize clots in veins, particularly in the legs.