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MaryPDX last won the day on January 31

MaryPDX had the most liked content!

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  1. I just answered this question. My Score PASS  
  2. We've been doing it for over 15 years (from the time we had Ortho's gel cards). Whatever validation was recorded, it's from eons ago and I wasn't involved with that one. I would imagine it was similar to the validation done with the DAT method in gel cards (from my other post in that section)
  3. MaryPDX


    Yes it correlated very well. As far as the Grifols DC card (DAT card), I've heard early 2018, but I haven't seen anything yet from FDA that it's licensed.
  4. MaryPDX


    Yes. We have 2 Erytras, so T&S, ABID, xm (AHG ones, not IS), unit retypes...
  5. We use Immucor cells in Grifols gel cards and they work fine. (we use them for additional rule outs when necessary, not the first line of the ABID.)
  6. MaryPDX


    Did a total of 20 tests (combination of QC and patients). Ran the C3 test manually (tube method, which was our standard SOP), and in the buffer gel cards. Results of testing using both methods were recorded on paper for the Pathologist, Manager and our Technical Coordinator to view. They all had to sign off on the new method before the procedure was updated. Procedure of buffer gel card method: 1. Bring your reagents, QC and patients to room temperature. 2. Make a 0.8% red cell suspension (of QC and patients.) 3. For QC, you will need a POS, NEG and a control well (pos control cells only in the control well). 4. For patients you will need 2 wells, one that you will add red cells and reagent to, other patient cells only. The reason for the red cell + buffer only wells is to ensure that no spontaneous agglutination is happening. 5. Add 50ul of red cells to wells 6. Add 25ul of anti-C3 reagent to reagent wells only (DO NOT add reagent to buffer only control wells) 7. Incubate 5 min. RT 8. Spin in appropriate gel centrifuge. 9. Record results. Just an FYI, before you turn your findings in, make a copy of the paperwork, just in case someone loses it. (speaking from experience here). Hope this helps. Mary
  7. MaryPDX

    Crossmatch Billing

    We bill for all crossmatches performed.
  8. MaryPDX

    Ordering Emerg Blood

    Here they order EMERRGENCY blood in EPIC, which prompts the pager to go off. If they order a massive transfusion, the LIFT team also get activated (dedicated people that will run the products from here to where patient is located. Floors still call us to give us a heads up that they are placing the order.
  9. MaryPDX

    Billing for liquid plasma

    We use P9059
  10. Our facility hasn't started CD47 yet, but anticipate that may happen in 2018. I've been dredging through the internet to find anything, which is how I found the NY blood center pdf. Besides the use of Immucors Gamma-clone IgG antisera (for antibody screens), I haven't seen anything mentioned on how to avoid it. I was thinking along the line of using Platelets (which have cd47 on them) to remove the antibody, but have seen nothing regarding if anyone has tried this. The search continues....
  11. http://nybloodcenter.org/media/filer_public/2017/10/04/2017aabbpostervelliquetteserological_observationsfinalcp246.pdf Apparently, weakly pos to negative DATs are common. Because the antibody covers cd47, the body sees the lack of cd47 and targets the cell for destruction.
  12. MaryPDX

    HU5F9-G4: anti-CD47

    Here's a little something I found useful: http://nybloodcenter.org/media/filer_public/2017/10/04/2017aabbpostervelliquetteserological_observationsfinalcp246.pdf For screens, I would avoid any phase except the IAT one to minimize the carryover. Our facility hasn't started any trials of this drug yet, so I haven't had a chance to try this (or try using gel in a neutral card with Immucor Gammaclone IgG). My suspicion is that gel won't work, but I still want to give it a shot.
  13. MaryPDX

    Antigen Tested Units

    We do it this way also.
  14. MaryPDX

    Blood Bank staff

    Blood Bank dedicated staff on Days, generalists on evenings and nights.
  15. MaryPDX

    Screen pos, xmatch neg?

    Looks like an interfering substance to me. Have you tried rinsing your screening cells with diluent (1x is usually sufficient), re-suspending those cells in diluent, then re-testing in gel to see if the reactions go away?

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