DAT, IAT, Elution, Crossmatch Flashcards

1
Q

mono AHG

A

anti-IgG

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2
Q

poly AHG

A

anti-IgG and anti-C3d

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3
Q

polyspecific AHG pro

A

more sensitive (things below detectable limit)

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4
Q

poly AHG con

A

less specific

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5
Q

mono AHG pro

A

more specific

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6
Q

mono AHG con

A

less sensitive - misses Jka antibodies

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7
Q

DAT

A

polyspecific

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8
Q

IAT

A

detect antibody in patient serum

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9
Q

DAT

A

directly test RBC’s for antibody or complement that has already been formed

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10
Q

if DAT +

A

can cause HDFN, DHTR, autoimmune hemolytic anemia

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11
Q

reticuloendothelial system

A

macrophages in spleen and liver regularly remove and destroy old, damaged RBC’s

AND foreign cells

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12
Q

antiglobulin test false negatives

A

-insufficient washing
-AHG not added immediately after washing
-loss of AHG reactivity
-improper centrifugation
-improper cell suspension

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13
Q

antiglobulin test false POSITIVES

A

-complement fixes at room temp
-collected from line contaminated with dextrose
-cold autoantibody
-contaminates that look like clumping
-fibrin strands
-spinning cells too long

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14
Q

most false positives can be observing specimen and cell suspension

A

without AHG

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15
Q

DAT limitations

A

DAT can be negative if there is complete destruction of RBC’s in an immune hemolytic process (ABO incompatibility)

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16
Q

all healthy RBC’s have a small amount

A

of bound antibody and complement

17
Q

reasons for positive for DAT

A

HDFN, HTR, autoimmune/ drug induced hemolytic anemia

18
Q

follow up for + DAT

A

check patient’s history (recent transfusion, new drug)
-DAT but with IgG or C3d
-elution and antibody ID
-RBC phenotyping on patient or transfused unit

19
Q

elution

A

release, concentrate and purify antibodies bound to RBC’s (end with freed antibody)

20
Q

elution tech

A

temp dependent– IgG
WASH and resuspend cells in saline or saline and albumin

alter pH
acid elution
organic solvents

21
Q

elution 45

A

gentle method, RBC’s remain intact

22
Q

elution 56

A

total elution, allows for antibody ID

23
Q

most critical step of elution

A

initial wash; remove unbound immunoglobulins

24
Q

elution control

A

last wash supernatant should be saved and testing in parallel with elute to detect presence of unbound antibody

LAST WASH should be nonreactive otherwise invalid

25
Q

cord blood testing

A

done on infants of mothers who are group O or D-

26
Q

crossmatching

A

RBC unit should be tested with compatibilty with recipient plasma

27
Q

plasma units should be selected for compatibility but

A

require no crossmatch

28
Q

plasma cross match with patient cells

A

minor crossmatch

29
Q

if a patient has no history of antibody and a negative screen they

A

only need IS crossmatch

30
Q

if patient has antibody history or positive screen

A

FULL AHG crossmatch