Week 2 - Haemostasis and protein metabolism/disorders Flashcards

1
Q

What is Haemophilia?

A

hereditary bleeding disorders caused by lack of clotting factors

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2
Q

What is Haemophilia A?

A

most common type (83%)

due to a deficiency of factor VIII

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3
Q

What is Haemophilia B?

A

results from a deficiency of factor IX

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4
Q

What is Haemophilia C?

A

mild type

caused by a deficiency of factor XI

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5
Q

How is Haemophilia treated?

A

blood transfusions

injection of missing factors

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6
Q

What does Activated partial thromboplastin time (APTT) test?

A

Disorders associated with intrinsic pathway

Monitor heparin therapy

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7
Q

What does Prothrombin time test?

A

Disorders associated with extrinsic pathway

monitor oral anticoagulant therapy with warfarin, hepatic disease, vitamin K malabsorption

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8
Q

What does Plasma thrombin time test?

A

Measures time for a fibrin clot to form when thrombin is added to plasma
Measures availability of fibrinogen
Acute leukaemia, lymphoma or poor nutrition

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9
Q

What does Plasma fibrinogen test?

A

Measures fibrinogen levels

May be decreased in certain congenital deficiencies

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10
Q

What are the main features of healthy blood vessel?

A
  • a functional endothelium
  • does not initiate or support platelet adhesion or blood coagulation
  • endothelium produces NO and PGI2 to inhibit platelet adhesion and promote vasodilation
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11
Q

What is DVT?

A
  • decreased flow rate of the blood,
  • damage to the blood vessel wall and
  • an increased tendency of the blood to clot (hypercoagulability)
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12
Q

How is DVT assessed biochemically?

A

Blood D-dimer levels are elevated due to increased fibrin turnover

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