Week 5 Flashcards

(28 cards)

1
Q

What is haemostasis? And the 5 components?

A

The process that prevents blood loss following injury while maintaining blood circulation.

Blood vessels, platelets, coagulation factors, coagulation inhibitors, fibrinolysis.

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2
Q

Where are platelets formed? and types?

A

In the bone marrow from megakaryocytes.

Dense granules, α-granules, lysosomes.

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3
Q

What are the two main pathways in the coagulation cascade?

A

Extrinsic (Tissue Factor pathway) and Intrinsic (Contact Activation pathway).

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4
Q

What factor initiates the extrinsic pathway?

A

Tissue Factor (Factor III).

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5
Q

Name two natural anticoagulants in the body.

A

Antithrombin and Protein C.

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6
Q

What does Tissue Factor Pathway Inhibitor (TFPI) do?

A

It inhibits the initiation of the coagulation cascade.

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7
Q

What enzyme breaks down fibrin?

A

Plasmin.

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8
Q

What is the inactive precursor of plasmin?

A

Plasminogen.

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9
Q

What laboratory test detects fibrinolysis?

A

D-dimer test.

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10
Q

What does Prothrombin Time (PT) measure?

A

The extrinsic pathway of coagulation.

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11
Q

What does Thrombin Time (TT) measure?

A

The ability to convert fibrinogen to fibrin.

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12
Q

What are the three layers of blood vessels?

A

Tunica intima (inner), tunica media (middle), tunica externa (outer).

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13
Q

What happens to blood vessels immediately after an injury?

A

Vasoconstriction occurs to reduce blood flow and promote platelet activation

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14
Q

What molecule do endothelial cells release to promote vasoconstriction?

A

Endothelin (ET-1).

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15
Q

What is the primary function of platelets in haemostasis?

A

Forming the initial platelet plug during primary haemostasis

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16
Q

What is the role of fibrinogen in platelet aggregation?

A

It acts as a bridge between activated platelets by binding to GPIIb/IIIa receptors.

17
Q

What is the function of Factor II (Prothrombin)?

A

It is converted into thrombin, which converts fibrinogen into fibrin.

18
Q

Which factor stabilizes the fibrin clot?

A

Factor XIII (Fibrin-Stabilizing Factor).

19
Q

What is the role of calcium (Factor IV) in coagulation?

A

It allows coagulation factors to bind to phospholipid surfaces.

20
Q

What does Protein C do?

A

Inactivates Factors Va and VIIIa to slow coagulation.

21
Q

What is the function of Heparin Cofactor II?

A

It enhances thrombin inhibition.

22
Q

What is the International Normalized Ratio (INR) used for?

A

Standardizing Prothrombin Time (PT) results across laboratories.

23
Q

What does a fibrinogen assay measure?

A

The level of fibrinogen in plasma, important for clot formation.

24
Q

What is Haemophilia A caused by?

A

Deficiency of Factor VIII.

25
What is Haemophilia B also known as?
Christmas Disease (Factor IX deficiency).
26
What is Von Willebrand Disease?
A disorder caused by defective or deficient von Willebrand Factor, leading to impaired platelet adhesion.
27
What laboratory test is prolonged in Haemophilia A and B?
aPTT (Activated Partial Thromboplastin Time).
28
What is Disseminated Intravascular Coagulation (DIC)?
A condition where excessive clotting leads to simultaneous bleeding due to depletion of coagulation factors and platelets.