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Definition
Anemia - insufficient Hb to carry out O2 requirement
to tissues.
WHO definition : Hb conc. 11 gm %
For developing countries : cut off level suggested is
10 gm %
- WHO technical report Series no. 405, Geneva 1968
Centre for disease control, MMWR 1989;38:400-4
WHO Classification of Anaemia
Palpitation Weakness
Dizziness
Clinical Features
Pallor of skin
And m/m
Soft ejection
systolic
murmur Edema
Signs
Platynychia
Tachycardia Koilonychia
Glossitis
Stomatitis
Causes of Anemia
Microcytic
Hypochromic Macrocytic
Normocytic,
normochromic
Hemorrhage or blood Hemoglobinopathies, (SS,
loss SC, CC)
Hereditary Spherocytosis
Unstable hemoglobins
Autoimmune hemolytic
Infections anemia
Chronic disease Some enzymatic
deficiencies
Normal Levels
Hb 13.5 – 14 gm %
Transferrin saturation 25 – 50 %
S. Ferritin level 30 μg / Lit
Red Cell protoporphyrin 30 μg / dL
MCV 76 – 100 fL
MCH 27 – 33 pg
MCHC 33.37 gm / dL
PCV 32 – 40 %
Laboratory Evaluation
Initial Testing:
Blood
Oral Iron Parenteral transfusion
Human Recombinant
Injectable Iron Erythropoietin
Macrocytic Anemia
2 Categories
Megaloblastic:
• Almost always caused by
B12/folate deficiency
• Megaloblastic features.
Non-megaloblastic:
• Alcoholism
Hemolytic Anemia
Inherited:
Acquired:
Diagnosis
• Hemoglobinemia/hemoglobinuria (when
hemolysis is intravascular, or so brisk
extravascularly that macrophages
cannot keep up)
• Reticulocytosis
• Indirect hyperbilirubinemia
• Increased LDH
• Decreased haptoglobin
• Direct antiglobulin test (DAT)
Hemoglobinopathies
Hb estimations
Peripheral smear
sed MCV
sed MCH
HbA2 ( 22)
Sickle Cell Disease
Structural Hb variant
Exists in homo & heterozygous forms
Under hypoxic conditions, HbS
polymerizes, gels or crystallizes.
hemolysis of cells, &
thrombosis of vessels in
various organs
In long standing cases,
multiple organ damage.
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