Rh-fan Posted February 26, 2013 Share Posted February 26, 2013 In the Netherlands we have to repeat a antibody screening/identification after 72 hours, to see if there is new antibody formation.How is that in other countries, dou you also repeat the ruling out after 72 hours or after 48 hours?Peter Link to comment Share on other sites More sharing options...
Malcolm Needs ☆ Posted February 26, 2013 Share Posted February 26, 2013 (edited) In the UK, BCSH Guidelines also state 72 hours. Edited February 26, 2013 by Malcolm Needs Spelling - first one for a long time - no, first one that I've NOTICED for a long time.....and then I forgot to correct it the first time! Hey **!!!!!!!!! Link to comment Share on other sites More sharing options...
Deny Morlino Posted February 26, 2013 Share Posted February 26, 2013 72 here Link to comment Share on other sites More sharing options...
Joanne P. Scannell Posted February 26, 2013 Share Posted February 26, 2013 AABB changed 72 hours to 3 days many years ago.Date of draw being Day 0.This way, the specimen expires at midnight ... just like everything else. Link to comment Share on other sites More sharing options...
Rh-fan Posted February 26, 2013 Author Share Posted February 26, 2013 AABB changed 72 hours to 3 days many years ago.Date of draw being Day 0.This way, the specimen expires at midnight ... just like everything else.So that can be up to 96 hours or is that not a good interpretation. If you draw the sample at 4 in the morning (at day 0) you can transfuse till day 3 at 24:00. That is 92 hours.Is this correct? Link to comment Share on other sites More sharing options...
mollyredone Posted February 26, 2013 Share Posted February 26, 2013 Our computer is set at 84 hours. Link to comment Share on other sites More sharing options...
Joanne P. Scannell Posted February 26, 2013 Share Posted February 26, 2013 Yes.00:01 Jan 1 will expire on 23:59 Jan 4.AABB 5.13.3.2 Link to comment Share on other sites More sharing options...
Dr. Pepper Posted February 26, 2013 Share Posted February 26, 2013 So that can be up to 96 hours or is that not a good interpretation. If you draw the sample at 4 in the morning (at day 0) you can transfuse till day 3 at 24:00. That is 92 hours.Is this correct?Correct. Depending on when the specimen was drawn on day 0, your timeframe will be between 72 and 96 hours. Link to comment Share on other sites More sharing options...
Dansket Posted February 26, 2013 Share Posted February 26, 2013 So that can be up to 96 hours or is that not a good interpretation. If you draw the sample at 4 in the morning (at day 0) you can transfuse till day 3 at 24:00. That is 92 hours.Is this correct?That is correct, we have been doing this for years. It makes sense, otherwise, if you specify specimen outdate to the level of precision of hours, you have to monitor for expired specimens on an hourly basis. Typically (with exceptions), we release blood from crossmatch on the morning of the 3rd day after specimen collection. Link to comment Share on other sites More sharing options...
SMILLER Posted February 26, 2013 Share Posted February 26, 2013 Same as Joanne, above. The screen "expires" at midnight on the third day after the specimen was drawn. Of course, we extend usually will extend specimen outdates beyond three days if the patient has not been pregnant/transfused in the last 3 mos.Scott Link to comment Share on other sites More sharing options...
Malcolm Needs ☆ Posted February 26, 2013 Share Posted February 26, 2013 If we get sent a specimen without a time on it (almost, but not quite universal), we put it into our computer as 00.01, so that it will outdate after 72 hours whatever the real time was. Mind you, having said that, it is very unusual that we are asked to cross-match a second time on the same sample (usually, we are asked to cross-match the first time before we even receive the sample). Link to comment Share on other sites More sharing options...
Rh-fan Posted February 27, 2013 Author Share Posted February 27, 2013 Thank you all for this information,I am writing an abstract/case report about a patient who had made an anti Jkb after 72 hours and 4 days later had made an anti S (beside the anti E and anti Fya that were known already). And I was interested in the time in other labs.Peter Link to comment Share on other sites More sharing options...
carolyn swickard Posted February 27, 2013 Share Posted February 27, 2013 Thank you all for this information,I am writing an abstract/case report about a patient who had made an anti Jkb after 72 hours and 4 days later had made an anti S (beside the anti E and anti Fya that were known already). And I was interested in the time in other labs.PeterYikes! Nasty surprise! Good luck in the future on this pt - should be about done with new antibodies by now. Link to comment Share on other sites More sharing options...
Rh-fan Posted February 28, 2013 Author Share Posted February 28, 2013 The patient has made all 'normal' allo antibodies and now has made a pan-reactive antibodies that needs 4 absorptions.I hope that this is an auto antibody and not a allo against a HFA.Peter Link to comment Share on other sites More sharing options...
EDibble Posted March 3, 2013 Share Posted March 3, 2013 Thank you all for this information,I am writing an abstract/case report about a patient who had made an anti Jkb after 72 hours and 4 days later had made an anti S (beside the anti E and anti Fya that were known already). And I was interested in the time in other labs.PeterAgreed, that is quite a "responder" you have there! Link to comment Share on other sites More sharing options...
rebeccarjthomas Posted March 5, 2013 Share Posted March 5, 2013 INteresting. I worked for a long time at a facility where we repeated adsorption studies on patients with WAA every two weeks - recommending as compatible or more compatible than ac during the intervening time. However, we had a patient that developed a new antibody (anti-Kell) within one week post adsorption study. So at that time, we revised our policyon repeat adsorption studies to repeating once every seven days. Of course, one policy just like one technic serve as our best, thoughtfully considered practice - but exceptions happen - like your patient. Wow, did you just get a phenotype and start giving this patient phenotypically matched units? Link to comment Share on other sites More sharing options...
Rh-fan Posted March 6, 2013 Author Share Posted March 6, 2013 There was no pre transfusion typing but we performed genotyping.Peter Link to comment Share on other sites More sharing options...
Desoki Posted March 7, 2013 Share Posted March 7, 2013 Also in our country Saudi arabia repeat every 72h Link to comment Share on other sites More sharing options...
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