Blood Coagulation Pathways Quiz

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Questions and Answers

Which factor initiates the intrinsic pathway of blood coagulation?

  • Activation of factor VII.
  • Contact of blood with injured endothelial collagen tissue. (correct)
  • Conversion of fibrinogen to fibrin.
  • Release of tissue factor.

What is the primary function of thrombin in the common coagulation pathway?

  • To convert prothrombin to fibrinogen.
  • To activate factor X to Xa.
  • To release tissue factor from damaged tissue.
  • To convert fibrinogen to fibrin. (correct)

The extrinsic pathway of coagulation is initiated by which of these?

  • Conversion of factor IX to IXa.
  • Contact of blood with collagen.
  • Release of tissue factor from damaged tissues. (correct)
  • Activation of factor XI.

What role does factor XIIIa play in the formation of a blood clot?

<p>It stabilizes the fibrin clot. (A)</p> Signup and view all the answers

In both the intrinsic and extrinsic pathways, what factor is ultimately directly activated to convert prothrombin into thrombin?

<p>Factor Xa (B)</p> Signup and view all the answers

Which term refers to a reduction in platelet count?

<p>Thrombocytopenia (B)</p> Signup and view all the answers

What is the primary event during the initial moments of primary hemostasis?

<p>Platelet adhesion to collagen (B)</p> Signup and view all the answers

What does the term 'hemostasis' most accurately describe?

<p>The arrest of bleeding by the body's own mechanisms (A)</p> Signup and view all the answers

In the coagulation process, what is the final substance produced from the conversion of fibrinogen?

<p>Fibrin threads (B)</p> Signup and view all the answers

Which of the following is NOT a condition associated with thrombocytosis?

<p>Acute infections (D)</p> Signup and view all the answers

Which factor is also known as the antihemophilic factor?

<p>Factor VIII (D)</p> Signup and view all the answers

What is the role of tissue factor in secondary hemostasis?

<p>Initiates the extrinsic pathway (B)</p> Signup and view all the answers

In which stage of hemostasis would "bleeding time" be measured?

<p>Primary hemostasis (A)</p> Signup and view all the answers

Which disorder is specifically linked to a structural or functional abnormality of platelets?

<p>Glanzmann thrombasthenia (D)</p> Signup and view all the answers

Which one of the following is NOT a procoagulant, also known as a clotting factor?

<p>Histamine (C)</p> Signup and view all the answers

Which vitamin is essential for the synthesis of prothrombin and other clotting factors?

<p>Vitamin K (B)</p> Signup and view all the answers

What is the primary function of von Willebrand factor (vWF)?

<p>To act as a carrier protein for factor VIII and aid in platelet adhesion (D)</p> Signup and view all the answers

A patient experiences bleeding that continues for 12 minutes after a small cut. What is most likely affected according to the content?

<p>Their bleeding time only (C)</p> Signup and view all the answers

Which of the following best describes hemophilia?

<p>An X-linked congenital disorder leading to deficient clotting factors (D)</p> Signup and view all the answers

Which is a naturally occurring anticoagulant that helps prevent blood clotting within blood vessels?

<p>Heparin (D)</p> Signup and view all the answers

A patient's blood does not have A or B antigens. According to the information, what ABO blood group are they?

<p>Group O (B)</p> Signup and view all the answers

A patient has blood type B. What antibodies are present in their plasma?

<p>Anti-A (A)</p> Signup and view all the answers

A researcher is using a substance to prevent clotting when drawing blood for in vitro tests. Which substance is likely being used?

<p>EDTA (C)</p> Signup and view all the answers

Flashcards

Thrombocytopenia

A decrease in the number of platelets in the blood, leading to a condition called thrombocytopenic purpura.

Thrombocytosis

An increase in the number of platelets in the blood. This can occur due to a variety of reasons.

Glanzmann thrombasthenia

A rare inherited bleeding disorder caused by defects in platelet structure or function.

Coagulation

The process by which soluble fibrinogen in the blood is converted into fibrin threads, forming a clot.

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Primary Hemostasis

The initial phase of hemostasis where platelets adhere to exposed collagen and form a temporary plug at the site of injury.

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Secondary Hemostasis

The second phase of hemostasis where a fibrin network is laid down to strengthen the platelet plug, forming a definitive clot.

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Intrinsic Pathway

The pathway of coagulation triggered by factors within the blood itself.

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Extrinsic Pathway

The pathway of coagulation triggered by the release of tissue factor from injured tissues.

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Common Pathway

The final common pathway of coagulation where both the intrinsic and extrinsic pathways converge.

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Hemostasis

The process by which bleeding is stopped through a series of physiological processes.

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Fibrin

A protein that forms thread-like structures to trap blood cells and platelets, creating a stable clot.

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What is von Willebrand factor (vWF)?

A large glycoprotein synthesized by endothelial cells and platelets that acts as a carrier protein for factor VIII and helps platelets adhere to injured vessels.

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What is Clotting Time?

The time from the start of bleeding until the formation of a firm clot, typically lasting between 2-10 minutes.

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What are anticoagulants?

Substances that prevent blood clotting. They can be natural or synthetic.

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What is Hemophilia?

A congenital bleeding disorder caused by a deficiency in either factor VIII (Hemophilia A) or factor IX (Hemophilia B). Minor injuries can lead to prolonged bleeding.

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What is coagulation?

The process by which soluble fibrinogen in the blood is converted into fibrin threads, forming a clot.

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What is Bleeding Time?

The time from the start of bleeding until the formation of a platelet plug, usually lasting within 2-8 minutes.

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What is the liver's role in coagulation?

Liver plays a critical role in the production of several clotting factors, including prothrombin, proconvertin, fibrinogen, factors V, VII, IX, X, and antihemophilic globulin. Liver failure can lead to severe coagulation disorders.

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What is the role of Vitamin K in coagulation?

Vitamin K is essential for the synthesis of prothrombin and other clotting factors. Deficiency in Vitamin K can lead to increased bleeding.

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