Addenda:
Addenda:
A colleague has a question regarding controls for EDTA/glycine-acid (EGA) treatment of direct antiglobulin test (DAT) positive red blood cells. Currently they treat a Fy(a+b+), S+s+ cell along with the patient's red cells to show that the EGA treatment has not denatured these antigens. When calling some reference laboratories about their use of this reagent, none of them are doing using such a control practice. In addition, the manufacturer's instructions state that EGA treating the positive control cells can be omitted if the laboratory has previously confirmed that the relevant antigens are not destroyed by the treatment. They report having shown that these antigens are not denatured by the QC that they have done. Could a review of this QC be sufficient to stop EGA treating the positive control even if in the future different reagent red cells will be used as the control cells?
In response to the above question, the Scientific Director of a large immunohematology reference laboratory comments that the manufacturer's instructions should always be followed.
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