Whole Blood & Apheresis Collection of BC intendent for Transfusion Flashcards
Blood centers are required to obtain donors’ written acknowledgement of the following elements:
1) donor provided & reviewed info regarding the risks & hazards of specific donation procedure
2) donor has reviewed the educational material regarding relevant transfusion-transmitted infections.
3) A sample of the donor’s blood is tested for specified transfusion-transmitted pathogens
4) if the donation is determined to be unsuitable or is deferred from donation, the donor’s record will identify the donor as ineligible to donate and will be notified of the basis of the deferral and period of deferral
5) the donor has the opportunity to ask questions and withdraw from the donation procedure
Informed consent for plateletpheresis
must be performed before first donation and annually thereafter
Informed consent for plasmapheresis
must be performed before first donation and annually thereafter unless more than 6 months elapse between plasmapheresis collections
Adverse donor reactions - broad categories
1) Needle-related injuries (bruise/hematoma, local nerve injury, arterial puncture)
2) Systemic Reactions (vasovagal reactions, citrate reactions)
Local nerve injuries
relatively uncommon
inevitable due to anatomic variation of close assoc. nerves & veins
c/o sensory changes away from phlebotomy site (forearm, wrist, hand, upper arm, or shoulder)
usually transient, followed by full recovery (7% may take 3-9 months) severe cases –> neurologist
Vasovagal reactions
Dizziness, sweating, nausea, vomiting, weakness, apprehension, pallor, hypotension & bradycardia –> may progress to syncope, convulsions, loss of bladder/bowel function
*** distinguished from orthostatic BP changes by LOW PULSE RATE
severe reactions or prolonged recovery times may need short-term observation or IVF admin in ER
Risk factors for vasovagal reactions
young age, low estimated blood volume (<3.5 L), fear and first-time donation status
Therapeutic phlebotomy
d/o: hemochromatosis, polycythemia vera & other conditions associated with erythrocytosis such as testosterone supplementation
generally units rom therapeutic donors intended for allogeneic transfusion must be labeled with disease or condition requiring therapeutic phlebotomy.
This can be waived (labeling and frequency requirements) with FDA variance - hereditary hemochromatosis or individual with erythrocytosis from testosterone therapy
Goal for therapeutic phlebotomy
titrate hematocrit of patient attempting to maintain levels
males: <=52%
females: <=48%
WB collection time
Average time for 500 mL is less than 10 min
Draw time longer than 15-20 min may not be suitable for collecting platelets or plasma for transfusions, as determined by blood center policy
Expiration dates for WB
ACD, CPD, CP2D = 21 days at 1-6 C
CPDA-1 = 35 days
Platelet prep from WB
WB should be not cooled less than 20 C
Must be separated within 8 hours of collection
Expiration of components prepared with open system
RBCs (stored at 1-6C): 24 hours
WB, RBCs & plts (stored at rm temp): 4 hours
Thawed cryo & plasma: 4 hours