Serology (Lect 2) Flashcards

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
Q

Describe the Agglutination chart

A

0-4+ do not give pts blood if not NEG
Mix fields are pos/neg in the same tube, suspect reagent issues

26
Q

Describe the immediate spin test
what forms a lattice
what type of test
what brings sample together
temp?
plasma to cell ratio?

A

IgM abs form lattice w/o extra reagents
Direct test
centrifuge brings sample together
Room temperature
Plasma 2:1 cells
37 deg

27
Q

Describe incubation of the immediate spin test
what destorys RBCs
why is _ more likely to bind?

A

compliment proteins attach and destry rbcs, IgG ab more liekly to bind to Ab in body temperature

28
Q

Describe the Coombs test
what forms a lattice
requires removal of what
inc at what

A

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
Q

T/F enhancements are added before the immediate spin to and before 37 deg incubation to reduce the zeta potential

A

false, enhancements added after the spin and before the incubation

30
Q

What does LISS do

A

reduces zeta potential

31
Q

What does ALb do

A

macromolecule decreases distance

32
Q

What does PEG do

A

absorbs water

33
Q

What does Polybrene do

A

binds and brings closer together