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Posts posted by MAGNUM
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I also have a policy in my policy and procedures stating the same and also stating that the blood bank is not responsible, but the medical director is available for consultation.
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I do have a disclaimer for the cell saver because an outside company operates the unit during procedures, and I have never been questioned about the cell saver by CAP or JC,
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You are most definitively preaching to the choir.
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It's because cardboard boxes or shipping containers can carry dirt and other contaminants and introduce them to new environments.
Also, nasty vermin such as roaches love cardboard.
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I actually pulled the package insert for our panoscreen cells from Immucor, and on page 2 the insert actually says add plasma, then cells and mix. The the next line says add potentiator, the step to do the immediate spin is no longer present. I would never have noticed this if not for this blog. There is a note that if desired the immediate spin can be performed. I do believe that I will be having a discussion with my Director and Medical Director so that I can change the procedure because if it is not needed (which in my humble opinion it is not necessary) then we need to get rid of the steps.
scott
- Malcolm Needs, SbbPerson and AMcCord
- 3
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We stop the transfusion and initiate the transfusion reaction procedure. And until the workup is complete (minus any micro), the patient is unable to receive any other products. Normally it is just something with the donor plasma and Benadryl should cover and propholactically thereafter prior to transfusion. Normally the physicians order Tylenol before the transfusions, so adding Benadryl is not an issue.
- L.C.H. and Kelly Guenthner
- 2
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I use the temp-chek, if they are issued in a cooler, otherwise 15 minutes.
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yes, all of the above
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On 2/21/2021 at 9:56 AM, John C. Staley said:
I had always found it difficult to convince nurses that we were working with a person/patient and not a room/bed! This became even more difficult after all the privacy rules and regulations came about. It was almost as if they were terrified to say a patient's name aloud!
I have even gone so far as to tell the nurse taking care of the patient that when they learned the patient's name and not the room number to give me a call back and we will discuss the patient at that time.
- Sonya Martinez, John C. Staley, mrmic and 3 others
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We send our KB's to another hospital in our division and get nice 2-4 hr turn around time. They use flow. We started using them because the local ARC does not perform KB's, and with only 6 or 7 a year we couldn't justify the cost for performing them inhouse.
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I have wondered that myself, it just suddenly appeared when we bought our new hematrax printer.
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1 hour ago, Neil Blumberg said:
No one knows for sure, but very fresh blood (<7 days storage) is totally unnecessary in terms of proven benefit and may actually be more dangerous, for reasons that are largely unknown.
Is there a reference for the non use of very fresh blood?
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1 hour ago, jayinsat said:
When the FDA issued the EUA on August 23, 2020, we started stocking convalescent plasma in house from our supplier. We fill the orders once they come in. Before that, it was a pain.
Are you able to make a stock order with ARC for, say, 5 O's, 5 A's, and 2 B's? Our supplier prefers it that way here in South Texas.
ARC does not allow stock supplies of the COVID plasma.
On the somewhat same note, how do you take care of your AB patients when the blood center cannot or will not supply AB convalescent plasma?
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We too use ARC. The pack slips have the order number on them so that you can match up the order numbers. When we get orders for the convalescent plasma, we order the plasma and on the order printout, we note the patient name, then once the plasma arrives, we match up the pack list with the order printout. In the meantime, we keep all the orders and their respective printouts on our metallic white board, that is basically the only way that we have found to somewhat keep abreast of the orders.
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I marked it down as N/A since it has to do with AMR's and such. At least that is my thinking. During our CAP inspection in September, my inspector didn't give it a second thought.
- David Saikin and AMcCord
- 2
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As of yet, we have been unable to migrate BCTA into the OR. But our division is looking to force the issue and put it in the OR regardless.
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I use Meditech and do not have any paper. As to histories, we look up each patient history when we get specimens on the patient. Normally on Monday, Wednesday, and Friday, I download a copy of patient histories onto a DVD in case of Ransom Ware Attacks. The file is downloaded and saved as a Word file that is accessible from any PC.
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I am not aware of a free PDF download of the TM. I guess you will have to purchase the TM.
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TS FOR PACKED CELLS, PLT COUNT FOR PLATELETS, PT/PTT FOR FFP, AND FIBRINOGEN FOR CRYO. THAT ALL TYPICALLY GOES OUT THE WINDOW WHEN IT COMES TO TRAUMAS AND MTP'S.
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Issueing a full unit for approximately 30 ml and discarding the rest is such a waste. Surely there is some other alternative.
LIS downtime validation
in Transfusion Services
Posted
Usually the only reason that we do any testing after a downtime is if the LIS has been updated, and then it is not heavily involved since I have done all the testing pre downtime.