Medicine - Haematology Flashcards

1
Q

What tests should you order when querying IDA in a sick vs healthy patient?

A

No illness: Ferritin

Illness: TIBC, TF, iron

Why? Ferritin is an acute phase protein

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2
Q

What markers will be raised in iron deficiency anaemia?

A

LDH, haptoglobins, uBR

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3
Q

Differentiate the class of immunoglobulin associated with warm vs cold AIHA?

A

Warm: IgG

Cold: IgM

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4
Q

How is warm AIHA managed?

A

Steroids, splenectomy

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5
Q

Recall some causes of warm AIHA

A

Lymphoma
CLL
Drug allergy
SLE

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6
Q

Recall some causes of cold AIHA

A

Myclopasma pneumoniae
EBV
CMV

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7
Q

What abnormality would be seen on blood film in warm AIHA?

A

Spherocytes

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8
Q

What test is used to identify paroxysmal nocturnal haemoglobinuria?

A

Ham’s test

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9
Q

If warm AIHA and hereditory spherocytosis both have spherocytes, what test can be used to differentiate them?

A

Coomb’s/DAT test
Positive in AIHA
Neg in HS

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10
Q

Recall 3 possible causes of MAHA

A

HUS
TTP
Adenocarcinoma

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11
Q

Recall 3 electrolyte abnormalities seen in tumour lysis syndrome

A

Hyperkalaemia
Hyperphosphataemia
Hypocalcaemia

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12
Q

How should tumour lysis syndrome be managed?

A

Allopurinol
IV if high risk
PO if low risk

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13
Q

What Hb level indicates packed RBC transfusion?

A

No ACS: <70g/L

ACS: <80g/L

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14
Q

Recall 4 contraindications for platelet transfusion

A

Chronic BM failure
Heparin-induced thrombocytopaenia
ITP
TTP

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15
Q

Which inherited thrombophilia increases the relative risk of DVT the most?

A

Antithrombin III deficiency

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16
Q

What is the prevalence of Factor V Leiden?

17
Q

What is the most common inherited bleeding disorder?

A

Von Willebrand

18
Q

What is the aetiology (broadly) of heparin-induced thrombocytopaenia?

A

Antibodies form against heparin and platelet factor 4 –> platelet activation via various mechanisms –> PROTHROMBOTIC state (even though it’s a thrombocytopaenia)

19
Q

Which blood group antigens are most likely to cause a delayed transfusion reaction?

A

Duffy

Kidd

20
Q

What % of the population are Rh pos?

21
Q

What sort of transfusion reaction does Rhesus incompatability cause?

A

Delayed haemolytic

22
Q

Recall the storage conditions for RBCs, platelets and FFP

A

RBCs: 4C for 35 days
Platelets: 22C for 7 days
FFP: frozen

23
Q

How long does FFP need to thaw?

A

20-30 mins

24
Q

How long can RBCs be out of the fridge?

25
Most of the heritable haem disease information
is in the path decks
26
Recall the parameters of each class of blood loss (depending on % volume lost)
Type 1: 0-15% lost, HR <100, BP normal, cap refill normal Type 2: 15-30% lost, tachycardic, BP normal, cap refil >2s Type 3: 30-40% lost, + tachycardic, BP reduced, cap refil >2s Type 4: >40% lost, ++ tachycardic, BP reduced, cap refil undetectable, anuric
27
What investigation is required to confirm the diagnosis of ITP?
Blood film
28
What is the risk of replacing folate without B12 in a patient who is both B12 and folate deficient?
Subacute combined degeneration of the cord
29
What are the 4 key electrolyte derangements in tumour lysis syndrome?
Hyperkalaemia, hyperuricaemia, hyperphosphataemia, | Hypocalcaemia
30
How should tumour lysis syndrome be managed?
Rasburicase (allopurinol = prophylaxis)
31
What sort of cancer does pernicious anaemia predispose to?
Gastric carcinoma
32
What is the mechanism of action of dabigatran?
Dirent thrombin inhibitor
33
What does irradiation do to red cells?
Reduces the number of T lymphocytes to reduce the risk of GvHD in people who've received lots of blood transfusions
34
What are the 2 main constituents of cryoprecipitate?
Factor VIII and fibrinogen
35
What is the first line treatment of ITP?
Oral prednisolone