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Following information required: Age Anamnesis Physical examination Inspection of blood smear Above will make diagnosis likely in 95 % of patient
Physical examination :
Pallor ( not detectable unless Hb < 8 gr%) Jaundice ( Icterus ) Petechie, brusing Hepatomegaly Splenomegaly Significant lymphadenopaty
Haemoglobin Estimate :
Done on machine: ( do not trust unless machine standardized ) Machine requires : calibration and standardazation Costly automated machines are not essential for accurate haemoglobin measurements
Normocytic,normochromic anaemia::
Investigatios: - Aplasia : all cell lines depressed - Leukemia,lymphoma : usually changes in 2-3 cell lines ( RBC, WC, Thromb ) - Chronic inflamation ( infections, arthritis): clinical supportive evidence + marked rouleax on blood film. - Chronic liver, renal disease : clinical supprtive evidence. - Haemolys : regenerative RBC cahnges ( polychromasia +++ ) without leukocyte, pletelet abnormalitiies on film
Acute Haemorrhage
When should blood tranfusion be given ? How much blood ? For how long ? BLOOD TRANFUSION THERAPY: Never curative form of treatment May be life saving ( until definitive treatment succesful ) Carries potentially grave risks ( disease transmission, sensitization, etc ) Is contraindicated unless essential for life support When given,must be in appropiate amounts ( single unit transfusins are not rational )