Haemoglobin
Too few cells
1)Reduced production
- haematinic/nutritonal deficiency
- alcohol, drugs, toxins
- liver (TPO), renal (EPO)
- bone marrow problem
2)Increased destruction/loss
- Blood loss - anaemia
- sepsis, viruses
- immune-mediated - autoimmune, drug-related
- hypersplenism
- fragmentation syndromes
Microcytic anaemia
MCV | Serum iron | serum Ferritin | Transferrin saturation | |
Iron deficiency anaemia | low | low | VERY LOW | low |
anaemia of chronic disease | normal or low | low | normal or high | normal or low |
Iron deficiency and chronic disease | low | low | normal or low | low |
Thalassaemia | very low or low | normal | normal or high | normal or high |
Macrocytic anaemia - causes
1. B12/Folate deficiency
2. Liver disease/ alcoholism
3. Reticulocytosis due to haemolysis or haematinic repletion
4. Severe hypothyroidism
5. drugs affecting DNA synthesis e.g. hydroxyurea, methotrexate, azathioprine
6. Haematological condition: MDS, myeloma, aplastic anaemia
Refer Haem after going through 1-5
Features of haemolysis
CBE:
1. Macrocytic anaemia
2. Reticulocytosis/polychromasia
3. Fragmented red cells (schistocytes) or spherocytes
Biochemistry:
1. high LDH
2. high bilirubin (unconjugated)
3. low haptoglobin
Haemolytic anaemia - inherited causes
Thalassaemia, sickle cell disease, G6PD, hereditary spherocytosis
- Blood film features
- family history
- Previous blood tests
Haemolytic anaemia - acquired causes
- immune - DAT "Coombs" test positive - mainly spherocytes
- idiopathic - frontline-treatment steroids (like ITP)
- may be related to lymphoproliferative disease
- non-immune - mainly schistocytes
- fragmentation syndrome - DIC, TTP, preeclampsia/HELLP
- severe infections (meningococcus, clostridia, malaria)
- severe liver disease (spur cell anaemia)
- valve haemolysis
Normocytic anaemia
- bleeding
- Causes of microcytic and macrocytic anaemia
- Anaemia of renal disease
- Anaemia of chronic disease/inflammation
- Anaemia of malignancy
- bone marrow problem
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