Haematology Flashcards

1
Q

First line treatment of ITP?

A

Oral prednisolone

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2
Q

Most important factor to determine if cryoprecipitate should be given in bleeding?

A

A low fibrinogen level
Cryoprecipitate contains concentrated amounts of fibrinogen, factor VIII, and von Willebrand factor. It is primarily indicated for the treatment of hypofibrinogenaemia, which can occur in DIC

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3
Q

What is the typical blood picture of DIC?

A

DIC typical blood picture:
↓ platelets
↓ fibrinogen
↑ PT & APTT
↑ fibrinogen degradation products (D-dimer)

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4
Q

What sort of blood would you see in the blood film following DIC?

A

Schistocytes

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5
Q

When should COCP be stopped before an operation to mitigate VTE risk?

A

4 weeks before

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6
Q

How do you differentiate between haemophilia A and B?

A

normal factor VIIIc activity points to a diagnosis of haemophilia B (lack of factor IX)

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7
Q

How often should sickle cell patients receive the pneumococcal polysaccharide vaccine?

A

Every 5 years

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8
Q

How is iron overload prevented in someone receiving a lot of transfusions for beta-thalassemia?

A

iron chelation therapy (e.g. desferrioxamine) is important to prevent the complications of iron overload due to repeat transfusions

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9
Q

Thrombotic crises in sickle cell can be precipitated by what 3 things?

A

Infection, dehydration or deoxygenation

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10
Q

Provoked VTE treatment is usually 3 months except for?

A

If the patient has active cancer

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11
Q

Why do patients with hereditary spherocytosis often present with biliary colic?

A

HS -> chronic haemolysis -> increased bilirubin -> increased stone formation

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12
Q

Why does Bechets disease increase the risk of VTE

A

Vasculitis -> inflammation of vessels -> hypercoagulability -> VTE

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13
Q

What is associated with poor prognosis in lymphoma?

A

‘B’ symptoms in Hodgkin’s lymphoma are associated with a poor prognosis
weight loss > 10% in last 6 months
fever > 38ºC
night sweats
As well as increasing age, male sex

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14
Q

What type of blood product has the greatest risk of bacterial contamination when compared to other blood products?

A

Platelets; they have a shelf life of only five days from donation to reduce the risk of contamination.

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15
Q

Which blood products need to be irradiated for patients who are immunocompromised to reduce the risk of transfusion-associated graft vs host disease

A

This is only necessary for blood products containing lymphocytes, including whole blood and packed red cells but not plasma or cryoprecipitate.

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16
Q

What is used for prophylaxis for tumour lysis syndrome prior to chemotherapy? What is used as an alternative?

A

Allopurinol (either IV or oral), with Rasburicase as an alternative

17
Q

In someone with combined folate and B12 deficiency, what should be treated first?

A

The vitamin B12 deficiency must be treated first to avoid subacute combined degeneration of spinal cord
If folate is corrected before B12, the haematological symptoms may improve, masking the underlying B12 deficiency and allowing irreversible neurological complications, such as weakness, sensory loss, and unsteady gait, to progress.

18
Q

What is the blood transfusion for someone with ACS?

A

80 g/L

19
Q

Which antibiotic is used to help diagnose VWD and what result would it show if positive?

A

Ristocetin
In VWD, platelet agglutination is reduced or absent in response to ristocetin because:
vWF levels are decreased (quantitative deficiency in VWD types 1 and 3).
vWF function is defective (qualitative deficiency in VWD type 2).
Ristocetin should cause platelet aggregation and clot formation in normal blood