Haematology Flashcards

1
Q

Features of an anaphylactic reaction to blood transfusion (e.g. FFP, cyroprecipitate and platelets) and how should it be treated?

A

Features of anaphylactic shock (acute wheeze and hypotension in absence of fever) with acute onset.
Immediately treated with IM adrenaline and transfusion terminated.

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2
Q

Most common cause of an isolated thrombocytopenia?

A

Immune (idiopathic) thrombocytopenic purpura (ITP)

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3
Q

Most common inherited bleeding disorder?

A

Von Willebrand’s disease

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4
Q

What type of cells are seen on the blood film of G6PD deficiency?

A

Heinz bodies mainly
Bite and blister cells also sometimes.

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5
Q

What organism is the most common cause of neutropenic sepsis?

A

Coagulase negative, gram positive bacteria such as Staphylococcus epidermis

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6
Q

Most common form of non-hodgkin/any lymphoma in the UK?

A

Diffuse large B cell lymphoma

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7
Q

What type of drugs can cause haemolytic anaemia (i.e. haemolysis) in people with G6PD deficiency?

A

Anti-malarials (e.g. primaquine)
Ciprofloxacin
Sulph group drugs

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8
Q

How would you differentiate Haemophillia and Von Willebrand’s disease?

A

Bleeding time is prolonged in VW while normal in haemophillia.
(APTT is prolonged in both though)

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9
Q

What is the empirical antibiotic choice for neutropenic sepsis?

A

Piperacillin with tazobactam (Tazocin)

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10
Q

Common feature of graft versus host disease in a pt with recent hx of allogenic bone marrow transplant?

A

Painful maculopapular rash (often neck palms and sole)

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11
Q

What is Burkitt lymphoma associated with? Appearance on blood film?

A

Epstein barr virus- pt gets sever throat pain if contracted in adulthood .
Starry sky appearance

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12
Q

What do thymomas present as?

A

Anterior mediastinal mass and symptoms of myasthenia gravis (fatiguability)

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13
Q

Blood film associated with myelofibrosis?

A

Tear drop poikilocytes

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14
Q

Deficiency in which immunoglobulin increases the risk of anaphylactic blood transfusion reactions?

A

IgA defeciency

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15
Q

What can chronic lymphocytic leukaemia (CLL) transform into, making pts suddenly unwell?

A

High-grade (non-hodgkin’s) lymphoma (Richter’s transformation)

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16
Q

If a patient with suspected DVT post-op has renal impairment, what is the most appropriate management for this pt?

A

LMWH followed by warfarin for 3 months

17
Q

What is the tranfusion threshold for patients with ACS? And without ACS?

A

With acs-80 g/L
Without acs- 70 g/L

18
Q

What type of crisis in sickle cell disease is associated with a sudden drop in haemoglobin?

A

Aplastic crisis (sudden drop of haemoglobin w/low reticulocyte count)

19
Q

What is given to pts with polycythaemia vera to reduce the risk of thrombotic events?

A

Aspirin

20
Q

What medications increased risk of VTE?

A
  • Combined oral contraceptive pill
  • Hormone replacement therapy
  • Raloxifene and tamoxifen
  • Antipsychotics (especially olanzapine)

selective estrogen receptor modulators (SERMs) used in breast cancer

21
Q

What drugs cause haemolysis in patients with G6PD deficiency?

A
  • Anti-malarials- primaquine
  • Ciprofloxacin
  • Sulph group drugs- sulphonamides, sulphasalazine, sulfonylureas
22
Q
A