Serology (Lect 2) Flashcards

(33 cards)

1
Q

T/F you use a population frequency chart for Ag and the % is frequency of presence or “incidence”

A

true

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2
Q

What is considered high incidence and low incidence?

A

High >90%
Low <10%

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3
Q

Briefly describe phenotype testing

A

to ID unknown Ag on RBC use Anti-Sera

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4
Q

Describe Abs briefly

A

person makes an Ab for an Ag they do NOT have on their RBCs
compatible blood is 100% population frequency of Ag
phenotype donor blood for Ag and look for negative Rxn

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5
Q

Whats the number one cause for transfusion rxns?

A

Data entry errors

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6
Q

Describe document control regulations

A

all results needed to be recordered as they are tested, even if they seem wrong
All data needs a second tech review
strict guidelines for how long documents need to be kept
all documents need to be legible and permanent

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7
Q

Describe sample lables

A

affixed lable bearing sufficient information for unique ID of Pt
2 unique ID’s
(ex date and time, collector, arm band..etc)

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8
Q

Describe sample integrity

A

EDTA preferred centrifuge to separate from plasma
NO GEL SEPARATOR
NO HEMOLYSIS
use enough volume

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9
Q

Describe pt Hx

A

ABO/rH
difficult blood typing
clinically sign Ab
adverse events to transfusion

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10
Q

Describe the 3-DAY RULE

A

samples should be retained for at least 7 days post transfusion
a sample should be obtained from pt within 3 days of scheduled transfusion

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11
Q

What are some reasons the 3-day rule should not be followed?

A

pt has been transfused in the preceding 3 mos w/ blood containing allogenic rbcs
pt has been pregnant preceding 3 mos
Hxt is uncertain

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12
Q

Describe quality control:
reagents

A

+/- controls need to be run daily
kit contents must not be mixed
manager must monitor QC once a month minimum

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13
Q

Describe equipment: critical equipment

A

directly involved in testing/storage of blood
temp needs to be monitored daily
must be maintained according to manufacturers guidlines

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14
Q

Describe QC daily
reagents. (ex I/A)
tests: (B/A)

A

before pt testing
reagents like IS/AHG
blood type/Ab screen

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15
Q

Describe qc Non-routine

A

run w/ pt testing
tests systems
reagents used for specific test
Phenotyping/ anti sera/ fetal screening

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16
Q

Describe BB reagents
; Ab colors

A

A blue
B yellow
D clear
G green (sometimes)

LONG OUTDATES

17
Q

Describe BB reagents RBC ags
screen/panel
reverce cells
outdates?

A

3% mix for tube testing
.8% mix for gel testing
screen/panel from one human donor who is 0 type
reverse cells can be from multiple donors
OUTDATES 3-5 WEEKS

18
Q

Describe handling of Ab and Ags

A

Ab - 2-10 deg, physical exam

Ag- 2-10deg physical exam

19
Q

Describe polycolonal

A

two different sources directed at same Ag multiple plasma cell courses to detect mutliple sites on same Ag

20
Q

Describe Monoclonal

A

Ab for specific Ag made from single plasma cell source to detect a single site on Ag

21
Q

Describe poly-specific

A

Ab mixture that detects multiple Ag or detects the Ag in different ways (IgG/IgM)
Anti-D/Anti-AHG

22
Q

Describe mono-specific

A

single Ab mixture to pick up single Ag
ABO/Ab

23
Q

T/F Polyclonal is mouse and monoclonal is rabbit

A

false
Monoclonal is mouse
Poly is rabbit

24
Q

Describe longevity

A

interaction based on Abs affinity and avidity
Affinity (binding)
Avidity (strength)

25
Describe the Agglutination chart
0-4+ do not give pts blood if not NEG Mix fields are pos/neg in the same tube, suspect reagent issues
26
Describe the immediate spin test what forms a lattice what type of test what brings sample together temp? plasma to cell ratio?
IgM abs form lattice w/o extra reagents Direct test centrifuge brings sample together Room temperature Plasma 2:1 cells 37 deg
27
Describe incubation of the immediate spin test what destorys RBCs why is _ more likely to bind?
compliment proteins attach and destry rbcs, IgG ab more liekly to bind to Ab in body temperature
28
Describe the Coombs test what forms a lattice requires removal of what inc at what
IgG ab forms lattice w/ addition of IgM anti-IgG reagent requries removal of unbound material for apporpriate rxn detection Incubate at body temp (inc ab binding)
29
T/F enhancements are added before the immediate spin to and before 37 deg incubation to reduce the zeta potential
false, enhancements added after the spin and before the incubation
30
What does LISS do
reduces zeta potential
31
What does ALb do
macromolecule decreases distance
32
What does PEG do
absorbs water
33
What does Polybrene do
binds and brings closer together