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marvy1

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Posts posted by marvy1

  1. I use large saline (2L) bags from dialysis and add a small amount of yellow food color. For fake blood, I got a powdered fake blood that I made a concentrate from and then add a small amount to the 2L bags. I then use smaller bags (300mL) and spike the large 2L bags with the smaller bags to make the individual components.

  2. We are going to RFP this coming year for some new automated analyzers. We did a quick look this spring at what is out there. I am surprised no one is speaking about the Biorad analyzers:  newly released IH 500, IH1000 (Gel based) and Tango Infinity (4th generation solid phase analyzer) along with stand alone  Gel readers and centrifuges. Although we are not sure which direction we are heading, I think they are certainly worth mentioning.

  3. RN responsibility to look in computer to see if blood product is available

    If avail they enter "order" to release product which creates printout (in duplicate) in Transfusion Dept

    We issue products based on this printout and send 1 cc of product release paperwork with product. We make a phone call to # appearing of paperwork letting RN staff know product was sent

    RN staff is responsible to return this product release paperwork to Transfusion which lets us know product was picked up at tube station. IVIG and neonate syringes not sent by tube

  4. We have seen Anti-D being ruled out when there is also an Anti-E or Anti-C present. We now test Rh neg patients by Gel if they are shown to have Anti-E or Anti-C by Echo. But usually our Anti-Ds show up ok on Echo.As for the weak reactivity vs Anti-D reagent on Echo, we do see a 1+ or 2+ lower reactivity of the Anti-D vs tube. At one point, we had even weaker reactivity on one of our Echos with the Anti-D reagent (we have 2 of them) and Immucor replaced the camera and reactivity increased. I also know "tweaking" the belt on the strip carrier arm can also change reactivity

  5. Tightening or loosening the belt on the strip carrier can optimize the strength of the reverse cells. On the Echo I have found the strengths to normally be at least 1 grade less than tube strength. With regards to Gel vs Echo, I have found approx equal number of clinically signficant antibodies on either method that were not found on the other method (We use both Gel and solid phase methods)

  6. We get a lot of patients reacting like this. Attribute reactivity on the Echo to an autoantibody. Do need notice cold autos coming up that much, so assume it is a warm (Echo supposedly on reacts with IgG). I'm guessing if you do tube DAT it might be microscopically positive for IgG? If saline IAT  tube reactivity is negative we issue blood that is compatible by that method, especially if the patient was not recently transfused. I find autoantibodies love solid phase method.

  7. We have 2 echos for our primary testing. As well, we use Gel, PEG and SIAT for secondary methods. We get samples referred to us from other hospitals who almost exclusively use Gel. We notice that the referring hospitals have pos screens by gel and that we identify various antibodies by gel (E, K, S) that are either completely missed by Echo (Neg screen/ Neg panel) or only found on the Echo by panel testing (Neg screen/pos panel). I have brought examples of these to Immucor tech support and they did not really give me a good reason as to why this is happening. Will continue to bring examples to them to see if they continue to give me the same responses.

  8. We got in green coolers from Tegrant (Thermosafe). They do require a bit of duct tape at the seams after a few years of use and they are a bit heavy. However, I validated them to hold 1-10 C for 6 days.

  9. The latest I heard on genotyping mom's blood for fetal Rh typing was that it is not avail in the US due to licensing issues. Maybe that has changed since Puget Sound is doing it (or are they sending samples to Europe for testing?)

  10. We tested the shockwatch in parallel with our existing SafeTVue 10. At first they seem to compare ok, but then as a little time went on, we noticed that several units (maybe 1 in 5) which never left the fridge remained ok according the the SafeTVue10 but changed color on the shockwatch. We felt confident the temp of the units never actually rose.

  11. A Group and Screen (by Echo method) is automatically added to any product order. If we performed a manual Group and manual (by tube/Gel etc) antibody screen, we will NP the Echo Group and Screen result sometimes. We typically do this if we have a patient using a lot of product. If we don't, every order will create a new specimen since the software will be looking for the Group and Screen result and not find any since the Group and Screen was done by tube method using different test codes.

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