Anaemia Flashcards

(39 cards)

1
Q

What are the 4 mechanisms of anaemia?

A

reduced production of red cells/haemoglobin by the bone marrow

reduced survival of red cells in the circulation (haemolysis).

loss of blood from the body

pooling of red cells in a very large spleen.

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2
Q

What are the three classifications of anaemia? (size)

A

Microcytic
Normocytic
Macrocytic

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3
Q

What are reticulocytes?

A

Early red cells

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4
Q

What is ferritin?

A

Cellular store of iron

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5
Q

What is a classic form of microcytic anaemia?

A

Iron deficiency

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6
Q

What is ESR (process)?

A

Rate at which red cells fall in test tube

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7
Q

What does ESR stand for?

A

Erythrocyte sedimentation rate

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8
Q

Why do rouleaux develop?

A

Increased number of plasma proteins with positive charge
Attract red cells
Stacking of coins

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9
Q

What is anaemia of chronic disease?

A

Characterised by pattern of low-normal transferrin
No obvious cause except that the patient is ill
Diagnosis by exclusion

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10
Q

What is the issues with measuring

A

Not very sensitive measure of iron stores

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11
Q

What causes low MCV?

A

Iron deficiency
Alpha/Beta Thalassemia
Anaemia of chronic disease

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12
Q

What laboratory tests can be conducted to diagnose microcytic anaemia?

A

Iron screening

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13
Q

What comprises an iron screening

A
Ferritin
Serum iron
Transferrin
Transferrin saturation
Hb electrophoresis
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14
Q

What question should you ask in iron defficency?

A
Heavy menstrual blood loss
Menopausal and bleeding?
Diet - vegan/vegetarian
GI symptoms: dysphagia
Weight loss
Medication e.g. NSAIDS, asprin
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15
Q

What are features of iron deficiency anaemia?

A

Glossitis
Angular stomatitis
Koilonychia

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16
Q

She reports weight loss, what investigations should you carry out?

A

Investigation for blood in the stool
GI investigations
Coeliac antibody testing

17
Q

What is haemolysis?

A

Breakdown of red blood cells

Shortened lifespan

18
Q

What are causes of inherited haemolytic anaemia?

A

Membrane abnormalities
Abnormal Hb
Metabolic pathways

19
Q

Why is MCV raised in haemolytic anaemia?

A

Reticulocytes are larger

20
Q

What are heinz bodies?

A

Precipitated oxidised haemoglobin

21
Q

What is the cause of haemolytic anaemia on this case?

A

G6PD deficiency

22
Q

What are those with a G6PD deficiency told to do?

A

Avoid oxidant drugs
Don’t eat broad beans
Avoid naphthalene
Be aware that haemolysis can result from infection

23
Q

What is LDH?

A

Is an intracellular enzyme that is leaked into the plasma when cells breakdown

24
Q

What are spherocytes?

A

Smaller RBC’s with loss of central pallor

25
What are the two types of haemolytic anaemia?
Inherited | Acquired (normal red cells but environment becomes toxic to the cell)
26
What are the two types of acquired haemolytic anaemia?
Non-immune | Immune mediated
27
What test do you do to look for auto-antibodies?
Direct antiglobulin test | DAT
28
How does DAT work?
Add rabbit antibody that is directed against human immunoglobulin Binds human immunoglobulin together
29
What is AIHA?
Auto immune haemolytic anaemia
30
What causes hereditary spherocytosis?
Due to inherited defect in red cell membrane
31
What are polychromatic macrocytes?
Blue, large cells Due to the presence of ribosomes they pick up blue dye Young cells
32
What is treatment for hereditary spherocytosis?
Folic acid | Splenectomy
33
What is meant by inappropriately normal reticulocytes?
When Hb is so low you would expect reticulocytosis to compenstae
34
What is a neutrophil with many lobes known as?
hyper-segmented neutrophil
35
Why do you always have to check B12 and folic acid blood test?
Present exactly the same on blood films | Need to do both to differentiate
36
What is megaloblastic change?
Nucleocytoplasmic dissociation
37
What can cause megaloblastic change?
Drugs Folate antagonists e.g. methotrexate BM cancer
38
What does B12 require to be absorbed?
Intrinsic factor
39
What is pernicious anaemia?
Destroy cells in stomach | Cannot absorb B12