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#1
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Daily fluctuation in RBCs / HGB
Hi guys,
My HGB drops around 27-28 points or so in 2 weeks, so I've always assumed it drops about 2 points a day. I've always wondered if it ever went up but since I only get a CBC once every 2 weeks, I would never know. So yesterday I had my regular CBC and today right before my transfusion I had another one (this was ordered by the dr, they've never done this before, I told the nurse they should be putting blood IN! LOL) Anyway, here's the results: Fri: HGB 93, WBC 1.3, Neut 0.8, Plat 88 Sat: HGB 96, WBC 1.8, Neut 1, Plat 95 And my $64,000 question is - how much does HGB fluctuate on a daily basis? I mean, I sort of want to have a party (better results - and in my red cells!) but I don't want to party like it's 1999 if my results are due to something stupid like dehydration or a natural flux. Theoretically, my HGB should have been 91 today. Thanks, Deb |
#2
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There is always a "lab error" of about a point (0.5 each way?) or 10 for you. At least that is what I'm always told. I worked most of my career in accounting and always have trouble with internalizing this concept.
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Dallas, Texas - Age 81 - Pure Red Cell Aplasia began March 2005 - Tried IVIG - Then cyclosporine and prednisone. Then Danazol, was added. Then only Danazol . HG reached 16.3 March 2015. Taken off all meds. Facebook PRCA group https://www.facebook.com/groups/PureRedCellAplasia/ |
#3
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My Hgb drop experience...
Over the years, when hospitalized, the Lab techs would do my Hgb 2 to3 times a day around the units transfused. Of course YMMV but the average "bump" would be 10 to 12 points (g/L) depending on the actual volume in the bag. The drop for me is 1 point per day, and that has been the same with me for the last four years.
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Ric: Low-risk MDS (blasts <4%); 4 cycles Revlimid no positive response; PRBC transfusion dependent; so far, 392'units' over 8 3/4 years; BMB #4 (15/04/01) shows evolution to AML (blasts 20-30%) 47,XY,del(5) (q22q35),+21[24][cp24]/46,XY(1). |
#4
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Wow Triumphe - I'm with you. 5 points either way sounds horrendously inaccurate to the point of why bother testing.
riccd2001 - I had the CBC before the tfx. I usually estimate 10 points per 200 ml, and then work out what my HGB should be afterwards based on volume. I get counts done every 2 weeks and the HGB always drops, usually around 27 points. It also used to drop every time when I had weekly counts done. It would be interesting (but real inconvenient) to get daily counts. Do you get monthly transfusions, or 1 unit every 2 weeks? I've never seen my count go up much, so I am hoping it is not lab error, but I realize it could be. What about the WBCs, from 1.3 to 1.8 is almost a 40% difference in one day. I think WBCs and platelets probably fluctuate more than RBCs, and I didn't do anything that would have caused dehydration in 24 hrs. Probably never know. Hope it happens again though! LOL. Deb |
#5
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I did a quick Google search and came up with this. There were other results, but I did not check them.
http://www.masimo.com/pdf/SpHb/LAB5447A.pdf
__________________
Dallas, Texas - Age 81 - Pure Red Cell Aplasia began March 2005 - Tried IVIG - Then cyclosporine and prednisone. Then Danazol, was added. Then only Danazol . HG reached 16.3 March 2015. Taken off all meds. Facebook PRCA group https://www.facebook.com/groups/PureRedCellAplasia/ |
#6
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Oh well - so much for keeping track of counts!
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#7
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I agree about the margin of error. When Ken checked in for his second ATG, his initial CBC showed his Hgb at 7.7. I had been charting his counts all along, and even though his Plts and RBCs were in free-fall at that point, I had a pretty good feeling for how quickly they were falling, and that represented a much faster drop than I'd been seeing. I managed to talk them into retesting just the Hgb, and the second count (an hour later) came back as 8.2. That's quite a difference.
Monitoring the counts over time gives you a good feel for the general direction things are going, but it's important not to get hung up on a single number.
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-Lisa, husband Ken age 60 dx SAA 7/04, dx hypo MDS 1/06 w/finding of trisomy 8; 2 ATGs, partial remission, still using cyclosporine |
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