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Fya and Fyb frequencies
66% & 83%
Jka and Jkb frequencies
77% & 73%
K and k frequencies
9% & 91%
D antigen frequency
85%
CEce frequencies
70%, 30%, 80%, 98%
Le(a) and Le(b) frequencies
22% & 72%
MN frequencies
78% & 72%
Ss frequencies
55% & 89%
ABO frequencies
O = 45
A = 40
B = 11
AB = 4
Lele sese Hh AO antigens and secretions
Ags: H, A, Le(a)
secretions: Le(a)
Lele Sese Hh AO antigens and secretions
Ags: H, A, Le(b)
secretions: H, A, Le(a), Le(b)
lele Sese, Hh antigens and frequencies
Ags: H
secretions: H
which Abs show dosage?
duffy, kidd, MNSs, CEce
which Abs are destroyed by enzymes?
duffy, MN
which Ags are not well developed at birth?
lewis, P1, I
how does Kell react to enzymes?
no effect
what neutralizes Lewis Abs?
saliva and Lewis substance
what neutralizes P1?
hydatid cyst fluid and saliva
what neutralizes I/i?
plasma, milk, amniotic fluid
what neutralizes Sda?
pooled urine
causes of weak/missing antibody (rvs)
elderly, NB, immunosuppressed (leukemia, hypogammaglobulinemia, BMT, immundef)
cause of weak/missing antigen (fwd)
subgroup of A/B, disease (leukemia), BMT
how to resolve weak/missing antibody/antigen
incubate RT 30min
incubate 4C 30 min
adsorption/elution
cause of extra rxn in rvs
subgroup of A, cold allo, cold auto
how to resolve an extra rxn in the rvs
run O cells, A2 cells, AC
AC pos = cold auto = autoadsorption or REST
O and A2 pos = cold allo = ABID, repeat rvs typing using Ag negative A and B cells
A2 pos = Anti A1 = type pt cells with anti A1 lectin
what causes rouleaux?
MM, waldenstrom’s, plasma expander dextrose, wharton’s jelly, inc FIB
how to resolve rouleaux interference in ABO typing?
fwd: wash cells
rvs: saline replace
causes of pos IS XM
wrong ABO typing
allo ab
auto ab
causes of pos extended XM
new allo ab
alloab to low incidence
warm reactive auto
donor pos DAT
acute HTR
within 15 min
ABO mismatch
SS: fever, chills, low BP, hgburia/hematuria, burning at infusion site, back/flank pain, dyspnea
delayed HTR
2-8 days
previous antibody
SS: dec HH, inc bili, fever, dark urine, pos IAT post transfusion
febrile TR
1-2 hrs
cytokines OR Ab to WBC
prevent via leukocyte reduced components
SS: 1-2 C inc, shaking, chills, nausea, vomiting
bacterial TR
rbc = during transfusion
plt = 3 hrs
y. enterocolitica, e. coli, pseudomonas, c. freundii
prevent by visually checking unit
SS: sudden fever inc 2C, abd cramps, diarrhea, DIC, shock, renal failure, vascular shock
TRALI
1-6hrs
donor Abs to pt wbcs (HLA)
SS: fever, hypoxemia, low BP, pulm edema, dyspnea
TACO
1-6hrs
volume overload
SS: high BP, pulm edema, dyspnea
anaphylactic TR
immediate
Anti IgA in IgA def pts
prevent by checking IgA levels, washing rbcs or giving plt/plasma from IgA def donor
SS: low BP, resp distress, abd cramps, vomit, diarrhea, rash, no pain/fever
allergic TR
IgE Abs to soluble Ag in donor plasma
treat with antihistamine
SS: hives, itching, diffuse rash
GVHD
30 days
viable transfused lymphs attack pt tissue
prevent by irradiating unit
SS: skin rash first, fever, diarrhea, hepatomegaly
ZZAP
dissociate IgG from red cells and inc red cell absorptivity to autoab
DTT: cleaves IgM disulfide bonds
enzymes: remove An from rbc
make kell null cells
chloroquine diphosphate
separate IgG from red cells for phenotyping
thiol reagents
cleave IgM to distinguish from IgG
cleaves disulfide bonds
DTT, 2-ME, AET
whole blood QC
min hct 33%
leukocyte reduced rbc QC
hgb: 43g
hct 65-75%
less than 0.8% hemolysis
washed rbcs
24 hr storage
hgb 43g
hct 65-75%
less than 0.8% hemolysis
frozen rbc QC
volume > 185ml
hgb 36g
hct 65-75%
RDP
5 - 7 days
75% units >5.5 x 10^10
pH > 6
SDP
24-48 hrs
75% > 3.0 x 10^11
pH > 6.0
thawed plasma
5 days
FFP QC
F VIII > 70%
all coag factors
cryo QC
150 mg FIB
80 IU F VIII
expected increases for plts
RDP: 5-10k
SDP: 20-60k
quality system
organizational structure, procedures, processes, and resources needed to implement quality management
quality assurance
planned, systematic activities implemented within the quality system to provide confidence that requirements for quality will be fulfilled
quality control
operational techniques and activities used to fulfill the requirements for quality
policy
a very broad view of what is expected
if a pt needs blood, they will need and TS sample sent to BB
process
the steps that occur to get the type and screen sample from the pt thru testing by the BB (flowcharts)
procedure
provides directions to completing each step in the process. these are called SOPs in the lab. the SOP for ABO typing would describe how to determine the type, part of the larger TS process