PP: Haemostasis Flashcards

1
Q

Define haemostasis.

A

A process which causes bleeding to stop, meaning to keep blood within a damaged blood vessel.

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2
Q

Describe the principles of normal haemostasis.

A
  • Prevents bleeding

- Prevents unnecessary coagulation and allows blood to flow

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3
Q

Describe the critical steps in the clotting cascade.

A

Prothrombin—>thrombin

Firbrinogen—> fibrin

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4
Q

Explain the tests in a coagulation screen.

A

APPT measures the activity of the intrinsic pathway. Therefore, prolonged APPT is seen in patients with a deficiency in intrinsic clotting factors e.g. (XII, XI, IX & VIII)

PT measures the activity of the extrinsic pathway. Therefore, prolonged PT is seen in patients with a deficiency in extrinsic clotting factors e.g. VII

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5
Q

Describe the common causes of thrombocytopenia.

A
  • Patients without a spleen
  • Aspirins
  • Pregnancy
  • Cancer
  • Alcohol abuse
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6
Q

Explain the differences
between thrombocytopenia caused by marrow failure and thrombocytopenia
caused by peripheral destruction.

A

??

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7
Q

Explain the mode of inheritance of haemophilia A.

A

X-linked

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8
Q

Explain the mode of inheritance of von-Willebrand disease.

A

Autosomal dominant

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9
Q

Explain the basic clinical and laboratory abnormalities

of patients with haemophilia A.

A
  • Lack of factor 8

- Bleeding into muscles and joints

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10
Q

Explain the basic clinical and laboratory abnormalities

of patients with von-Willebrand disease.

A
  • Abnormal platelet adhesion to vessel wall
  • Reduced VWF which carries FVIII so this too can be low
  • Skin an mucous membrane bleeding
  • Prolonged bleeding after trauma
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11
Q

Explain the causes of disseminated intravascular

coagulation.

A
  • Cancer, especially certain types of leukemia
  • Infection in the blood, especially by bacteria or fungus
  • Liver disease
  • Pregnancy complications (such as placenta that is left behind)
  • Massive tissue injury
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12
Q

How do you diagnose DIC?

A
  • Platelet count.
  • Global clotting times (aPTT and PT)
  • One or two clotting factors and inhibitors (eg, antithrombin)
  • Assay for D-dimer or FDPs.
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13
Q

How do you treat DIC?

A
  • Plasma transfusions to replace blood clotting factors if a large amount of bleeding is occurring.
  • Blood thinner medicine (heparin) to prevent blood clotting if a large amount of clotting is occurring.
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14
Q

What is Von Willebrand factor?

A

Involved in platelet adhesion to the vessel wall, platelet aggregation and also carries FVIII

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15
Q

What is thrombocytopenia?

A

Thrombocytopenia is a condition in which you have a low blood platelet count.

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16
Q

What cell produces platelets in the bone marrow?

A

Megakaryocytes

17
Q

What is the normal life span of a platelet?

A

7-10 days

18
Q

What structure do platelets adhere to?

A

Collagen when underling tissues are exposed

19
Q

Name some mediating factors of clotting.

A
  • Glycoprotein complexes
  • VWF
  • Fibrinogen
  • Collagen
  • ADP
  • Thrombin
  • Thromboxanw/arachidonic acid
20
Q

What is fibrinolysis?

A

Break down of a thrombus

21
Q

Name 3 natural anti coagulants.

A
  • Protein C
  • Protein S
  • Anti-thrombin