Acquired Anaemias Flashcards

1
Q

Firstly define Anaemia

A

A haemoglobin below the normal range for Age/Sex/Ethnicity

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2
Q

What are the clinical features of anaemia

A
Think poor perfusion:
- Fatigue
- SOB
- Ankle Swelling
- Dizziness
- Chest Pain
Symptoms of the cause
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3
Q

What is your first test when suspecting anaemia?

A

A FBC

Tells you the haemoglobin and the MCV/MCH

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4
Q

How do we describe anaemias?

A

Morphologically based on MCH & MCV

1) Hypochromic, Microcytic
2) Normochromic, Normocytic
3) Macrocytic

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5
Q

FBC shows hypochromic, microcytic anaemia, what are the likely causes?

A

Most likely Fe-deficiency Anaemia, if you’re in any doubt do a serum Ferritin to check (should be low)

If Ferritin is fine then it may be a secondary anaemia or Thalassaemia

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6
Q

Fe-deficiency anaemia is not a diagnosis but must have a cause, what could cause it?

A

Malabsorption e.g. gastritis or coeliac

Blood loss e.g. GI or menorrhagia

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7
Q

What elements of a history/exam could suggest iron deficiency anaemia?

A

Evidence of bleeds e.g. dyspepsia, PR bleeding or menorrhagia
Diet (in kids/elderly)
Pregnancy (increases Fe need)

Koilonychia, atrophic tongue & angular stomatitis

Also do Abdo & rectal exam looking for the cause

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8
Q

What tests can we do if we get a case of Fe-deficiency anaemia?

A

Endoscopy & barium study can be done if there’s evidence of GI blood loss

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9
Q

How do you treat Fe-deficiency anaemia?

A

Oral Iron +/- transfusion

Treat the cause

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10
Q

Patient presents with a Normochromic, normocytic anaemia, how would you proceed?

A

Test their Reticulocyte count.
If it’s increased it means you’re losing RBCs and the marrow is compensating –> Blood loss of haemolysis

If its normal or low –> Secondary anaemia, marrow infiltration etc

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11
Q

So lets say this patient’s reticulocyte count is high and you suspect a haemolytic anaemia. What could cause that?

A

Autoimmune HA (Extravascular haemolysis)

Or an intravascular cause:

  • Mechanical e.g. art valve leaking
  • Severe inf
  • Pre-eclampsia, HUS or DIC
  • Drugs

Congenital causes e.g.:

  • G6PD deficiency
  • Hereditary Spherocytosis
  • Haemoglobinopathies e.g. Sickle cell
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12
Q

So we’ve done a FBC (normocytic/chromic) & a reticulocyte count (high).
How would we test a patient to see if they’re haemolysing?

A

Blood film = can see haemolysed cells
Serum Bilirubin = High
LDH = High
Serum Haptoglobin = low (eats up free haemoglobin)

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13
Q

How would we identify the cause of a haemolytic anaemia?

A

Coomb’s Test:
Detects Ab/complement on the red cell membrane so if +Ve suggests an immune source

Can also test urine for Haemosiderin & Urobilinogen

  • Haemosiderinuria in intravascular haemolysis
  • Extravascular haemolysis increases serum bilirubin –> high Urobilinogen
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14
Q

What can trigger an auto-immune haemolytic anaemia and how does coomb’s test help us with that?

A

Auto-antibodies from different triggers will agglutinate at different temperatures in coomb’s test so:

  • Warm temps = idiopathic, drugs or CLL
  • Cold Temps = CHAD, infection or lymphoma
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15
Q

How would we manage a haemolytic anaemia?

A

Support the marrow with Folic Acid
~Transfusion

Correct cause:

  • IV Abx if septic
  • Prosthetic valve replacement if leaky
  • Immunosuppression & treat trigger if immune

Can also remove the site of haemolysis i.e. spleen

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16
Q

Most secondary anaemias are Normochromic Normocytic, some are Hypochromic, microcytic. What causes them?

A

Something causes inflammation –> Increased hepcidin –> Decreased Fe absorption

Look for infection, inflammatory disorders and malignancy

17
Q

Ok so a FBC identifies a Macrocytic Anaemia, what would you do from there?

A

A blood film to test for Megaloblastic vs non-megaloblastic

18
Q

Megaloblastic anaemia? how would you proceed?

A

It’s probably a B12 or Folate Deficiency so do a B12/folate assay to identify which one

Also look out for neuro symptoms from Subacute Combined Degeneration of the cord in B12 deficiency

19
Q

What causes a B12 deficiency?

A

Gastric/ileal disease stopping absorption

More likely pernicious anaemia, an autoimmune attack on your gastric parietal cells/intrinsic factor

20
Q

What causes a folate deficiency?

A

Diet
Haemolysis
GI pathology e.g. Coeliac

21
Q

How do we treat a megaloblastic anaemia?

A

Oral Folate

B12 IM inj

22
Q

What could cause a non-megaloblastic Macrocytic anaemia?

A

Some problem with the marrow e.g. Myelodysplasia, Marrow infiltration or drugs:

  • Alcohol
  • MTX
  • Anti-retrovirals
  • Hydroxycarbamide
23
Q

What is haptoglobulin?

A

Protein which binds to hemoglobulin in blood plasma

24
Q

What is hepcidin

A

Hepcidin is a regulator of iron metabolism. Hepcidin inhibits iron transport by binding to the iron export channel ferroportin which is located on the basolateral surface of gut enterocytes and the plasma membrane of reticuloendothelial cells (macrophages).