We have never seen RBC or WBC fragments on a slide after vortexing EDTA samples. The RBC and WBC counts do not decrease between the runs before and after vortexing and are well within what you would expect between replicate runs on the same sample. Whether the technique seems logical or not is an opinion. Until an opinion is tested, it is only an opinion, not a fact. I was surprised to discover that vortexing does not damage the cells, but the results were clear. Try it for yourself if you want proof. It isn't hard to test it out. Take some CBCs that you have just finished with, and vortex them for about a minute on the highest setting. Then immediately rerun the tube. Compare your WBC, RBC, and PLT counts before and after the vortexing. We found no significant difference. We do exempt hem-onc patients from this practice, even though we found no differences there either, I think it was just to make the pathologist feel better. I will say it usually only works on patients who have no other major issues, but the collection was less than optimal resulting in a small amount of platelet agglutination, but no apparent clot. Just enough to cause the analzyer to flag for platelet clumping. It's not a magic trick, it won't clear up EDTA platelet clumping, and if it doesn't work, you can always recollect anyway.