Haemostasis CC Flashcards

1
Q

What is Haemophilia A?

A

X linked recessive

Decreased factor 8

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2
Q

Complications of haemophilia A

A
Severe bleeding (Eg during dental extraction, post op etc..)
GI bleeding
Haematuria
recurrent haemarthroses
Muscle haematomas
Intracranial bleeding
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3
Q

What is the treatment for heamophilia A

A

Recombinant Factor 8 or DDAVP (Releases stores of factor 8)

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4
Q

What 3 lab abnormalities would you see with Haemophilia A

A

Increased: Activated Partial Thromboplastin Time (APTT)
Increased APTT ratio (Increased clotting time)
Decreased Factor 8 level

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5
Q

Another name for haemophilia B?

A

Christmas Disease

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6
Q

What is Haemophilia B?

A

Decreased or no factor 9

Clinically v similar to haemophilia A so need specific lab tests

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7
Q

What is vonWillebrand factor used for in the body?

A

Assists platelet plug formation by attracting platelets to site of damage and stabilises Factor 8 by preventing it from premature destruction

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8
Q

Name four symptoms of of vonWillebrands Disease

A

Heaving bleeding
Bruising
Heavy periods
Prolonged bleeding after trauma

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9
Q

Lab findings of vonWillebrands Disease (6)

A
Decreased Hb (Due to bleeding)
Microcytic anaemia (Decreased iron due to losing too much iron)
Increased APTT (Longer time to clot)
Decreaased factor 8
Decreased vWb factor antigen
Decreased vWb collagen binding activity
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10
Q

What is Immune thrombocytic purpura?

A

Increased removal of platelets due to autoantibodies against the growth proteins found on platelets

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11
Q

Symptoms of Immune thrombocytic purpura

A

Easy/excessive bruising
bleeding (eg from gums, nose)
Petechiae

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12
Q

Lab abnormalities of Immune thrombocytic purpura

A

Decreased platelet count

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13
Q

What is thrombophilus

A

Increased risk of thrombus formation

Acquired or congenital

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14
Q

Describe what the type 1 and type 2 thrombophilias are

A

Type 1- Deficiency in natural anticoagulents

Type 2- Overactivity of coagulation factors (The more mild of the two)

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15
Q

What is Disseminated Intravascular Coagulation?

A

Pathological activation of coagulation

You get lots of microthrombi forming

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16
Q

What can trigger Disseminated Intravascular Coagulation

A

Cancer, burns, infection (Gram negative sepsis), massive haemorrhage

17
Q

What would the lab results show for Disseminated Intravascular Coagulation

A

Raised: Prothrombin time, International normalised ratio (Ratio of patients prothrombin time to normal mean prothrombin time), APTT
Increased fibrin degradation products (Eg. D dimers)
Decreased fibrinogen

On blood screen, due to the clots causing haemolysis, you will see red blood cell fragments