DFields

Using the PEG method for warm autoadsorption is so much easier and faster than first treating the cells with WARM (ZZAP)--is there a true risk of missing an underlying alloantibody? Are others out there using the PEG adsorption method (for auto and/or alloadsorptions?)

Depending on the training level of your staff, using a control routinely is an option so there is no chance to "forget" to go back and run one.

Please tell us what type label you use for the syringe aliquot--so that it still fits in the pump and has all required info.

Of those sites doing cultures, does everyone do both aerobic and anaerobic? Recently I had read article(s) that both are required but is this true?