
SMILLER
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Everything posted by SMILLER
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PPID in the OR
I believe we do this during the time-out, before any wrist bands are covered up. Scott
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FDA Guidance - PLT Bacterial testing
It appears from the literature that these types of systems irreversibly inactivate RNA and DNA. Whether the FDA will approve it as equivalent to irradiation to inactivate WBCs is the question. I have not found anything that specifically mentions this. Scott
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Temperature of blood/coolers upon receipt
Can you get a copy of the policy from your supplier that they use to validate their shipping containers? Type up a letter for your pathologist to approve explaining it and give that to your Quality people. Then if they want something more, ask them to show you the regulatory standard they are worried about. Scott
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Cold agglutinin procedure
Back in the last century, I believe that cold agglutination titres were used to differentiate "atypical" pneumonia (Mycoplasma pneumoniae) from other causes. Not so much to do with blood banking. Scott
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FDA Guidance - PLT Bacterial testing
There is a savings there then for our chemo patients. I wonder if somehow the FDA would go so far as to say the primary culture at the blood center could be skipped? Scott
- Derivative Tag Requirements
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FDA Guidance - PLT Bacterial testing
Not being familiar with the method, I was wondering if it is unnecessary to irradiate pathogen-reduced platelets? Also, apparently the FDA does not approve of it's use on pooled platelets. Why is that? Thanks, Scott
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Temperature of blood/coolers upon receipt
Glancing at the AABB Standards (31st ed), they only state that incoming products shall be "inspected, tested as necessary" before use. In our case, we log the temp as "acceptable" for RBC products received from our supplier if they arrive on wet ice. (and labels are legible, units not leaking, etc.) Likewise, for FFP, on dry ice, and so on. This is written into our procedure for checking in blood products. I do not believe we have ever had to "validate" coolers sent from our blood supplier, although we have to do this with our own coolers used for transport. Not sure about CAP or FDA regs, they may be more strict. Scott
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Hemolysed samples for pretransfusion testing?
Except once you have a post- specimen during a possible reaction situation, you cannot go back in time to redraw the original hemolyzed specimen to do a visual comparison. But like Malcolm pointed out, this is a minor part of the workup anyway compared to other tests (first and foremost, the post- DAT!) Scott
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whole-blood transfusion
That particular recent thread has a lot of information on it. Interesting points of view and references to several papers. Notably, Dr.Neil Blumberg has some pretty persuasive rhetoric for whole blood use in trauma situations. However, like you, I wonder at the practicality of such a system compared with our current practices. Scott
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Hemolysed samples for pretransfusion testing?
Oh, I agree Malcolm. And we do accept slightly or even moderately hemolyzed samples in our lab, depending on the test. My point was, in the case of a possible transfusion reaction, when one has to document pre- and post- appearance of the plasma, it is completely pointless if the pre- specimen is hemolyzed to begin with. Anyway, this thread seems to be more concerned with automated ananlyzer requirements regarding hemolysis. I have found a few papers online, but it seems like they are only verifying that analyzers only begin have problems with at least moderate amounts of hemolysis. Not being experienced at all with what Byfaith is working with, I would guess that if the manufacturer doesn't have a problem with lesser hemolysis, they may be nothing to worry about. Scott
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Hemolysed samples for pretransfusion testing?
OK. But for a possible hemolytic transfusion reaction, do you not have to compare plasma pre- and post-transfusion? We do (maybe its not required?) If the pre-transfusion specimen starts out hemolyzed, it's not going to matter that your automated analyzer completes it's testing-- the comparison in the case of a workup would be useless. And I would agree with those who say it is generally bad lab practice to test hemolyzed specimens for any test. It indicates that there was a rough draw and the quality of the specimen is questionable for many analytes. Scott
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Hemolysed samples for pretransfusion testing?
We are still doing it the old fashioned way -- manual gel -- but if the plasma is so dark that you cannot tell the difference between it and significant hemolysis (thinking possible transfusion reaction comparison), I would think you would want to have it redrawn. We let sight hemolysis pass with a comment added to the specimen when it's checked in. Not sure but I would think that would be around 50 mg/dl or less. For an automated platform, can you not consult specimen requirements from the manual? Scott
- Auto-anti-D?
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Auto-anti-D?
Interesting. One question Malcolm, up until reading this report from our reference lab (most of which could be written in Greek and I would not understand it less) I had never heard of the DAU partials. I saw in one paper that the DAU-0 is thought to be the "primordial" example of this particular clade (if you want to call it that), and that DAU-1 through 5 are further variants on that. This seems to go against the current distribution of the various DAUs (D - African Observed), where DAU-0 is found in Europeans, and all of the others are found in Africans. Would this mean that the DAUs started in Europe and then somehow spread to Africa where they further differentiated? It seem backwards somehow. Thanks, Scott
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Nursing Order
Truth is important, but the appropriateness of such a statement should be measured by its usefulness. Scott
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Auto-anti-D?
Results of our reference lab testing on this patient makes him out to be a partial-D, specifically DAU-0. (Nothing about an anti-LW, which is where I was going.) They note that "patients with a partial RHD*DAU0 allele have not been reported to make anti-D, therefor, this patient's reported anti-D is most likely autoimmune." The Genotype is: RHD*DAU0-ce(48C) / RHD*03N.01-ceS. Also they found that the patient is homozygous for the "Duffy null promoter FY*02N.01-67c SNP". Whatever that is. The report seems very comprehensive with lots of information, including references. Scott
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Programmed transfusion at predefined frequencies
There is a catch-22 there for the clinicians when they think an otherwise stable patient needs a transfusion If you think the patient needs blood, just one unit should be adequate; and if only one unit is ordered, why transfuse at all? In general, we require a recent Hgb before routine transfusions. Scott
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Low vs High Triggers
Any study that challenges the status quo should be met with caution (but NOT with derision I think!) This is an admittedly only a pilot study that, like others before it, suggests more robust studies need to be done. I think it is interesting though because it is from a different standpoint -- that of a vascular specialist or a perfusionist. Scott
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Nursing Order
Similar to David, above. When a unit is ordered, it is ordered for transfusion. We have exceptions for OR, atypical antibody patients, and things like massive transfusion protocols. Scott
- Programmed transfusion at predefined frequencies
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Programmed transfusion at predefined frequencies
I believe the point of the post-transfusion H&H in this discussion is more to avoid giving another (perhaps) unnecessary unit. I think the consensus is that for a Hgb to stabilize fully, you want to look at it at 24 hrs. However, the H&H done an hour or even a half hour after a transfusion finishes is going to be close enough to make clinical decisions like whether to transfuse another unit. Scott
- Low vs High Triggers
- Programmed transfusion at predefined frequencies
- Theranos