W3 specimen prep Flashcards
what do MLAs do to prepare specimens?
allow time to clot. Centrifugation. separating serum or plasma from cells and or making an aliquot to share specimens
what does a centrifuge do/what is it needed for?
separate plasma or serum from formed elements (cells-rbc,wbc)
its important to note all samples must be capped in order to -prevent spills -prevent the development of aerosols -possible evaporation -possible exogenous contamination of specimen
specimens received in ice water
are centrifuged in a 4 degrees refrigerated centrifuge and these would be something like ammonia or lactate
RPM
revolutions per minute
RCF
relative centrifugal force and this can be converted into rpm because the speed and time could change related to the diameter
serum samples and the centrifuge
gold or red, SST
NEED TIME TO CLOT BEFORE CENTRIFUGE- if clotting incomplete fibrin left in serum may cause problems with instrument
Plain red- 30-60 minutes
sst-30 minutes
clot activator tubes- usually used for stat and have enzyme at the bottom that forms thrombin only needs 5-15 minutes.
always set a timer
-* set serum tubes for 10 minutes 1000-1300 RCF *for gel and non gel tubes – this creates complete separation of serum from cells
plasma samples and centrifuge
-contain anticoagulant- don’t need to sit
10 minutes 1000-1300 ref
-blue tops (sodium citrate) also centrifuged-plasma not taken off -15 minutes at 1500 rcf
microtainer tubes and centrifuge
same clotting times for serum -placed in small ones adapter still need to be balanced
gel tubes-90 seconds 6000-15000 rcf
non-gel-3 minutes 2000 rcf
whole blood and centrifuge
edta lab are actually never centrifuged and can be delivered to hem
why do we need to centrifuge specimens right away
there is 25 more potassium in rbc than serum delay= movement of potassium into plasma or serum and this messes up some tests especially if its for calcium, also rbc start to metabolize glucose in blood
- should be spun before 2 hours
- left out of fridge for 8
failure of migration of gel
- do not re-spin
1. aliquot serum or plasma into new labelled tube
2. spin aliquot (there will be a button or a couple of rbc at bottom)
3. aliquot cell free serum or plasma into a new labelled aliquot tube and use that one
- do not re-spin
what to do if there are fibrin strands and what does this mean
usually it means you centrifuged the specimen to early and you need to transfer the serum to an aliquot tube and respin
rubber stopper removal
never recap-you can get them mixed up, use new caps or usually use parafilm
what is on an aliquot tube?
same patient demographics-name, dob, phn
- accession number
- tests to be done
- type of specimen(pst plasma, Nacit plasma)
- volume
- usually lis reprint label, if not you would write it out.
- make sure only the tests that is required to be run on the aliquot remains on the label– cross out the other tests
Aliquot technique
- determine number of aliquot tubes and volume of specimen required (if two tests are done chem then one tube required but if ones in hem and one is in hem then two tubes required)
- label aliquot tubes –**place in rack behind appropriate specimen tube
- check patient and testing information on label to aliquot label —work left to right from lowest accession number to highest
- remove stopper, hold both tubes in left hand and check labels again
- ransfer fluid using a pipette
- cover both tubes immediately with parafilm or new cap
- check labels again hem