irshadaad

If there is any reference about expiry of thawed FFP pooled (open system). If pooled(open system) and stored at 1-6C what will be the expiry, if close system pooled stored at room temp or 1-6 above all if there is any reference about pooling of FFP after thawing

Nice

I just answered this question. My Score FAIL

For rbc ,it may be a risk ,for plts how much of quntity of rbc can be there which may be problem for RES of the infant but FFP whats the fun of considering RH when there are no rbcs and D is not found on plt and wbc...hope it helps

what about diffrential adsorption....elimnate anti -D remains your anti E and Anti -C ,if still its hard then adsorb any of these two ....hope it helps

whats the composition of modified LISS

welcome this forum is indeed a great treasure for blood bankers

i want know composition of modified LISS

Does it change to 24 hrs same like washed cells...do you have any referance pls

we are some times re centrifuging sagm added blood unit to remove its sagm+plasma content in order convert it into a prbc for neonatal use.......does this removal change the expiry date to 24 hours.... i got cofused with a statement from circular of information 2009...regarding this...please help me to it .

some times we get screening negative but on running penal we find some of the cells are reactive i guess these things do help to rule out nature of the antibody

why not to go for an antigen profile of the pt. and try to rule out later what possible antibody can play....

Hey guys wish you all ....happy new year...

we are re using left over tubes in the diamed cards and as i remember we did not see any trouble in re using the liss-coombs and nacl cards and normalyy we leave the cards @ room temp.im thinking now to have a survey of the finding...this is something nice been taken into account.....

this is what happens every where in the places which are called HOSPITALs and health centres....nurses and doctors consider lab.workers E>Ts......but its funny

nowa days multiple lines can be attached to the pt thru central line so what is surprising in it to release multi components in emergency situations...even in india componant theraphy has started long back...i did my diploma in pgi chandhigarh in 1982...we were doing componant fractionation that time and same we did when started working as blood bank technologists in sheri kashmir institute of medical sceinces soura srinagar kashmir....

its not satisfying me to write Rh phenotype as CDE/cde or cde/cde when ........ /..d.. is not existing can you help me please

yes it seems reasonable thank you guys

i ve a quiry.....we had a pt with anti E and anti Lea previosly,but now Lea is not visible on doing the penal ,shall we still give bloo NEGATIVE FOR Lea ....THANKS

welcome, this is the place where blood bankers can feed their apetite for knowledge and refresh it

i think it is partial D

some people bother only about how much monetory benifit will they gain they dont bother for refresh their knowledge, RR1 is very right....we dont need to be shy in this forum to ask or to comment this how we can learn from each other. im so delighted and benifited since i have joined here..i feel it quenches my thirst...cose in my setup i dont have access to new additions of books and other materials....so this has come to me as a blessing....and i thank malcolm personaly the way he is keeping this site alive with his contributions

i think they should give o

you can use transfer bags in a closed sytem ,so you will not waist the blood even if or will not use you can recieve it back and keep it unto its normal expiry

we also supply for exchange transfusion for sicklers ,units which are sickle neg and the Rh pheno and K compromising rbcs after they will remove a unit or so from the pt no ffp...in special situations only the physician will request for a desired Hct