Case 11 - Anaemia Flashcards

1
Q

Development of RBC and the corresponding anaemia film?

A

Materials needed to make the nucleus - folate, B12
Materials needed to make Hb - iron

The nucleus is made and then extruded from the cell - the high concentration of Hb in the cell determines when this happens
If the nucleus is ready, the cell will undergo divisions
Therefore anything that slows down Hb production > more divisions, so microcytic hypochromic anaemia
Anything that slows down the nuclear development, leads to fewer divisions, so macrocytic normochromic anaemia

The patient may not produce Hb properly in teh first place too - e.g. renal disease

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2
Q

How is iron absorbed?

A

Ferroportin decreases the amount of hepcidin there is
Hepcidin releases iron from macrophages and enterocytes so there is more for metabolism

Transferrin saturation, high IL-6 concentration (increases in chronic disease) all increase ferroportin

Low transferrin saturation and hypoxia decrease ferroportin

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3
Q

How is B12 absorbed?

A

Transcobalamin binds to B12 to resist the acidity of the stomach, gets broken apart by pancreatic proteases
Intrinsic factor is able to bind B12
Cubulin receptors in terminal ileum take up complex

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4
Q

How is folate transported?

A

Folate is stored in RBC with roughly 3 months worth of supply
Dietary folate polyglutamates are converted to monoglutamates
In high folate states they are absorbed through simple diffusion
In low folate states, they are transported by a carrier

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5
Q

Signs and symptoms of anaemia?

A
Pale
Clammy
Chest pain
Cold hands and feet
Headache
Dizzy
Light-headedness
Fatigue
Weakness
Arhrythmia
SOB
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6
Q

What blood tests can be done for anaemia?

A

FBC - Hb
MCV - size of cells
MCH - tells you conc of Hb ie. hypochromic/normochromic
MCHC - tells you mean Hb conc - increase is an indicator of microspherocytosis
Blood film and microscopy to assess shape of the cells and whether it is a haemolytic anaemia
Inner paler patch should be less than a third of the diameter of the cell

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7
Q

What are causes of normocytic normochromic anaemia?

A

Blood loss
Anaemia of chronic disease
Anaemia of renal failure (EPO deficiency)

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8
Q

What are symptoms of normocytic normochromic anaemia?

A
Tachycardia
Pale 
Clammy
Loss of consciousness
Hypotension
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9
Q

What is the treatment of normocytic normochromic anaemia?

A

Replace blood with transfusions and clotting factors to prevent coagulopathies - if there’s no response too fluids, cross match and transfuse

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10
Q

What are causes of microcytic hypochromic anaemia?

A
Thalasseamias
Iron deficiency
Chronic inflammation (IL-6)

Iron deficiency could be dietary, malabsorption or due to blood loss somewhere in the GIT for example, may also be due to menorrhagia
Important to ask about diet, but rare to get iron deficiency anaemia on the basis of diet, so should question about other blood loss

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11
Q

How can thalassaemias be categorised?

A

Beta thalassaemia trait (minor) - where only one beta globin is abnormal. Increased HbA2

Beta thalassaemia major - where 2 beta globins are abnormal. No HbA, only HbF

Alpha thalassaemia - anywhere from 1-4 genes affected

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12
Q

What are symptoms of microcytic hypochromic anaemia?

A

Headache
Brittle nails
Hair loss
Koilinichya

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13
Q

Management of iron deficiency anaemia?

A

Can do iron transfusions if very severe
Iron supplements are available in tablets and liquid form (100-200mg a day)
Will give constipation, stomach upset and potentially dark stool
Increase vitamin C intake to help absorption
Can take up to 6 months for the iron levels to come back normal

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14
Q

Management of thalassaemia?

A

Transfusion-based management
Iron chelation gets rid of excess iron
Can have stem cell transplant

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15
Q

Causes of macrocytic normochromic anaemia?

A

Folate and B12 deficiency
Also alcohol, pregnancy, hypoxia, hypothyroidism

Could be dietary, malabsorption (crohn’s), intrinsic factor deficiency, increased requirement, increased turnover or due to alcohol (folate)

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16
Q

Symptoms of macrocytic normochromic anaemia?

A

Mild jaundice
Neuropathy
Angular cheilitis

17
Q

Treatment of B12 deficiency anaemia?

A

Have to give injection of hydroxycobalamin, as oral intake cannot be absorbed if there is a problem with intrnsic factor or absorption
Every couple of days initially, then every 2-3 months

18
Q

Treatment of folate deficiency anaemia?

A

Increase dietary supplementation
Then, use supplements if not helping, give concurrently with B12
Alone it exacerbates neuropathies

19
Q

What are the types of haemolytic anaemias?

A

Congenital:

  • Hereditary spherocytosis
  • Sickle cell/thalassaemias
  • Glucose-6-phosphate deficiency

Acquired:

  • Autoimmune haemolytic anaemia
  • Drugs, infections, toxins
  • Copper defiency
20
Q

What are the investigations done in haemolytic anaemias?

A

FBC:
-Reticulocytes increased in haemolytic
-Hb and haematocrit low
MCV

Blood film - size and shape of the RBC

Bilirubin and LDH will rise

Coombs testing:

  • Indirect antiglobulin testing - tests for blood compatibility for transfusion. Positive result means the bloods will be incompatible
  • Direct antiglobulin testing - tests for antibody causing AIHA
21
Q

What is hereditary spherocytosis?

A

Where there is loss of the biconcave shape of the RBC - large central area of pallor
Inherited autosomal dominant
Treat with folic acid and splenectomy
Investigate with EMA-binding

22
Q

What is glucose-6-phosphate deficiency?

A

Key enzyme in energy development is missing
Usually protects against oxidative stress
X-linked genetic disease, with lyonization

23
Q

What is acquired haemolytic anaemia (AIHA)?

A

Think of this when presenting with anaemia and jaundice
Can be warm (IgG) or cold (IgE)
Unconjugated hyperbilirubinaemia

24
Q

What is warm AIHA?

A

Secondary to rheumatological condition
Lymphonma
Drugs
Leukaemia

Treat with steroids and ensure no underlying disease

25
Q

What is cold AIHA?

A

Due to UC
EBV
Mycoplasma pneumonia

Treat the underlying disease to cure the anaemia

26
Q

What is the haemoglobinopathy in sickle cell anaemia?

A

Normal HbA= 2 alpha and 2 beta
HbA2= 2 alpha and 2 delta
HbF= 2 alpha and 2 gamma

Where there is beta globin variant inherited in an autosomal recessive manner - need 2 copies of the variant
Leads to sickling of the RBC and can be exteremly painful

27
Q

Prevention of sickle cell crises

A

Screen everyone at birth with heel-prick test
Prophylactic penicillin
Parents shown how to palpate spleen

To prevent crises:

  • Keep well hydrated
  • Keep warm
  • Eat well
  • Take folic acid and penicillin
  • Pneumococcal immunisations
  • Hydroxyurea can prevent chest and pain crises
28
Q

Management of sickle cell

A

Transfusions
Stem cell transplant
Operation plans

29
Q

Complications of sickle cell

A

The sickle cells gather and bind with platelets to form clots

Pain crises (bone)
Chest crises
Abdominal
Stroke

Give opioids and fluids