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For RBCs, just like WBCs, we need to assess the basics: o quantity of RBCs. o quality of the RBCs o RBC turnover rate Quantity o Sufficient RBCs, and what's the total hemoglobin? (Hgb, HCT) Quality of the RBCs o Are they beat up? (RDW) o Are they small or large? (MCV) o Their hemoglobin content? (MCH, MCHC) o Do they contain funky stuff? (abnormal hemoglobin, malaria, etc.) Turnover rate and bone marrow capacity to make RBCs (retic count).
RDW is an expression of the homogeneity of the RBC population size. (Roll the cursor over the image.)
A large RDW says there's a wide variation in the RBC diameters within the test pool. It doesn't say the cells are large or small, rather that the population is not homogenous. Younger cells are larger (reticulocytes). Older, and generally beat up, RBCs are smaller
Truthfully, these calculated values aren't all that helpful. o They tend to parallel the MCV o Abnormalities reflect RBC cellular problems.
Microcytic anemias
General features of microcytic anemias Small, hypochromic (poorly colored) RBCs Wide RDW, small MCV, low MCH and MCHC. Iron deficiency (poor diet or bad absorption). Chronic blood loss. Inherited defects of RBC structure (hereditary spherocytosis).
Macrocytic anemias
Large pale cells Large MCV and RDW (cursor). Low MCH and MCHC. Folic acid and B12 deficiencies. Hypersegmented PMNs
It's not as easy as "Just give me the numbers. I'm the Doc, I'll figure it out." The values have to fit the clinical situation.
Simple, no platelets. Now to help your patient, all you have to do is figure why.
Sources of error
The biggest source of error is not matching the results with clinical situation. Not just for the CBC, this one'll get you for everything. Clerical errors. o Right name (?), bar code (?) o Did the results go in the wrong chart? o Can you really read that FAXed copy? Sampling errors. o With a clotted sample, nothing is valid. (If you draw the blood in a syringe and then try injecting it into the anti-coagulated tube, it'll clot every time, even if it doesn't look it.) o Did you draw the sample above an IV line? Is it diluted with fluid?
If the tubes aren't kept rocking right up until the moment the aliquot is sent into the machine, the cells will settle out and the aliquot won't be representative. (You know, did the aliquot come from the cell rich end of the tube?) Errors of judgment. o Is the problem with the quality of the cellular elements? o Is the problem with the quantity of the cellular elements?