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R1R2

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Everything posted by R1R2

  1. have your lab director talk to the pathologist, His is not a tech call. THis is why your lab director gets paid the big bucks.
  2. Clarifying question - Is it Friday afternoon or Monday morning?
  3. I have seen this so many times and have always come to the conclusion that it was a mislabeled sample. Let us know what you find.
  4. I see that you are not in the US. In US, ABO typing is considered non waived, high complexity testing. All those that do the test will need documented training, followed by competency assessment as well as documentation of education, i.e., diploma or transcripts. Do you have similar requirements in Brazil?
  5. Agree with AMcCord. Can't and don't want to imagine nursing personnel performing this test.
  6. I read a journal article a while back that looked at the detrimental effects to blood if left out at RT for different amounts of time and then but back in the fridge. They did this multiple times to each unit of blood. The result of their study was that the 30 minute rule, if there ever was one, could be changed to the 1 hour rule. I thought that was really interesting. Anyway, we take the temp of every red cell returned. If OK we put it back into inventory. The LIS will prompt for integrity/appearance acceptability and return temp.
  7. what the heck does that mean?
  8. I agree with David and would not bother with the expense of AABB accreditation.
  9. I was being facetious. I haven't seen a bleeding time in decades.
  10. What's a bleeding time?
  11. Not all major ABO incompatibility transfusions result in death. I recently read somewhere that a few percentage (can't remember the exact number) up to 30% are fatal. In my career I have seen one not fatal and one fatal,.
  12. I only do one comparison semiannually.
  13. I think it develops with experience. Our older peers said the same thing about us.
  14. so, is the employee still around?
  15. PERHAPS weak D was included because a positive weak D would alert you to a possible false positive fetal screen.
  16. "CFR 606.100(c) "All records pertinent to a lot or unit were not reviewed before the release or distribution of a lot or unit of final product". The inspector asserts that testing review must be performed prior to releasing products and since supervisory review is typically performed each morning, any products that were released throughout the day (or night) would not have had their associated testing reviewed prior to release. " I don't think any of our responses helped you with this FDA observation, did they?
  17. In my house, the cake would not make it to the next day.
  18. Agree with TreeMoss. I would check your FDA paperwork and make sure it is correct. I took over a transfusion service and they had registered even though they did not need to register. I changed that right quick.
  19. I know that FDA can visit any hospital but curious as to why they visited you if you only thaw plasma? Do you have an LIS or do you record results on logs?
  20. Was this in reference to daily QC perhaps?
  21. I would think that the freshest irradiated or unirradiated unit you have on hand would be suitable for a baby in a true emergency. A full unit could be issued and tranfusionist would use what they needed and discard. This plan should be discussed with all involved before it happens to make sure everyone is OK with this. Perhaps a procedure should be written as well.
  22. we purchase pooled cryo from the blood center. no more pooling
  23. There is no requirement that the info is read back to a person at time of issue.
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