Haematology Flashcards

1
Q

Transfusion of PRBCs can significantly alter which electrolytes:

A

Hyperkalaemia

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2
Q

Lymphoma or leukemia patient that started chemotherapy now has AKI, hyperkalaemia, hyperphosphatemia and hypocalcaemia, diagnosis and management:

A

Tumout lysis syndrome. Allopurinol or rasburicase

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3
Q

Cough, dyspnoea, fever, pulmonary infiltrates on CXR, history of anaemia, jaundice, and severe pain when cold, diagnosis:

A

Sickle cell disease with acute chest syndrome

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4
Q

Patient taking COCP is due for a surgery, advice:

A

Stop taking COCP 4 weeks before surgeries.

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5
Q

Cryoprecipitate contents and indications:

A

Factor VIII, XIII, fibrinogen and von Willebrand factor. Indications include massive haemorrhage and uncontrolled bleeding due to haemophilia

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6
Q

Hodgkin’s lymphoma: signs of poor prognosis:

A

B-symptoms, increasing age, male sex, stage IV disease and lymphocyte depleted subtype

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7
Q

Reversal agent for dabigatran:

A

Idarucizumab

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8
Q

Beta thalassaemia major treatment:

A

Transfusions and iron chelation with desferrioxamine

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9
Q

The transfusion threshold for patients with ACS is:

A

80 g/L

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10
Q

Philadelphia chromosome, leukocytosis, basophilia, eosinophilia, thromocytopenia, anaemia, no blast cells, diagnosis and treatment:

A

Chronic myeloid leukaemia, imatinib (tyrosine kinase inhibitor)

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11
Q

Haemarthroses, haematoma, prolonged APTT:

A

Haemophilia B

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12
Q

Acute haemolytic reaction during transfusion symptoms:

A

Fever, abdominal pain, hypotension

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13
Q

Common causes of abdominal pain in hereditary spherocytosis:

A

Gallstones, splenomegaly

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14
Q

Elder with anaemia, massive splenomegaly, weight loss, night sweats, tear drop cells on film, diagnosis:

A

Myelofibrosis

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15
Q

Anaemia with vitamin B12 and folate deficiencies, treatment:

A

1 mg cyanocobalamin IM injections three times a week, treat B12 deficiency first to avoid subacute combined degeneration of spinal cord

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16
Q

Hypercalcaemia, renal impairment, anaemia, bleeding, bone pain (back), infections, rouleaux formation on film, diagnosis:

A

Multiple Myeloma

17
Q

Unprovoked venous thromboembolism and family history, most common cause:

A

Factor V Leiden (Activated protein C resistance)

18
Q

Causes of massive splenomegaly

A

myelofibrosis
chronic myeloid leukaemia
visceral leishmaniasis (kala-azar)
malaria
Gaucher’s syndrome

19
Q

Blood results in sickle cell disease:

A

Low haemoglobin; normal MCV; and raised reticulocytes

20
Q
A