2. Basic techniques and prinicples Flashcards

(47 cards)

1
Q

1667

A

first recorded animal to human blood transfusion by Jean-Baptiste Denis

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2
Q

1818

A

first human to human blood transfusion by James Blundell

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3
Q

1900

A

ABO system was identified by Karl Landsteiner

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4
Q

1908

A

Reuben Ottenburg first described the use of the crossmatch

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5
Q

1910

A

William Moss wrote first procedures for BB testing

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6
Q

1941

A

Charles Drew helped establish National Blood Donor Service (WWII)

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7
Q

AABB publishes…

A

Standards for Blood Banks and Transfusion Services

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8
Q

rules for reading tubes (6)

A

Standardized light and mirror (optical aid)
Remove no more than 3 tubes at a time
Observe for hemolysis before shaking (clear red background)
Shake tubes to create “swirling” action
Grade when cell button is completely resuspended/breaks off
Reaction grades ≠ interpretations

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9
Q

M+

A

microscopic agglutination

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10
Q

2+mf

A

mixed field agglutination

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11
Q

principle of DAT

A

Detection of in vivo sensitization of RBCs with IgG and/or complement

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12
Q

Part of HTR, HDFN and AIHA investigation

A

DAT

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13
Q

DAT procedure

A

Patient cells are washed, treated with polyspecific AHG, and spun

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14
Q

if DAT is +…

A

perform a monospecific DAT to determine if cells are sensitized with IgG or complement

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15
Q

requires QC with checkcells

A

any procedure involving AHG
(DAT)

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16
Q

principle of IAT

A

Detection of in vitro sensitization of RBCs with IgG

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17
Q

Part of ABS (antibody screen), XSM (crossmatch), Ag typing, and titering

A

IAT

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18
Q

with PEG in IAT, you must use…

A

anti-IgG AHG

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19
Q

IAT procedure

A

Patient plasma is added to screen cells I, II and III and incubated at 37° for 15 minutes

then washed, treated with AHG

20
Q

AGT false positives (8)

A

Improper specimen
Autoagglutinable cells
Polyagglutinable cells
Bacterial contamination
Overcentrifugation
Overreading
Preservative-dependant Ab
DAT + cells used for IAT (will always be +)

21
Q

AGT false negatives (7)

A

Inadequate washing
AHG reagent or serum not added
AHG reagent deteriorated
Inadequate incubation
Weak or heavy cell suspension
Under or overcentrifugation
Poor reading technique

22
Q

method of choice for ID of Ab after DAT+

23
Q

acid elution procedure

A

Ab-sensitized RBC in vivo + eluting solution (mix/spin) →

free Ab in acidic supernatant + buffering solution (mix/spin) →

free Ab in neutral supernatant

24
Q

ensures that Ab in acid elution is from RBC and not free Ab

A

test with 4th washing

25
used for forward ABO typing
Anti-A Anti-B
26
used for Rh typing
Anti-D
27
Checks for auto/polyagglutinable cells after A+/B+ result
monoclonal control
28
used for reverse ABO typing
A1 and B cells
29
used for detecting unexpected Ab
screen cells (I, II, III)
30
used to detect IgG-sensitized RBCs
AHG
31
pretransfusion tests (6)
Type & screen Crossmatch DAT Elution Ab panel Ag typing
32
informational tests (5)
ABO/Rh type Prenatal screen & type Cord blood testing DAT only Ab titer
33
clinically significant BG systems (7)
ABO Rh Duffy Kell Kidd Ss Lub
34
**clinically insignificant BG systems (4)**
MN Lewis Lua P1
35
antithetical alleles
antigens represent different forms of a gene produced from the same locus
36
6-digit number assigned to each BG antigen
ISBT notation
37
carbohydrate based BG (5)
ABO, Lewis, P, Ii, MNS
38
protein based BG (4)
Rh, Kidd, Duffy, Lutheran
39
both carbohydrate and protein BG
Kell
40
BG enhanced by proteolytic enzymes (6)
Rh, Kidd, Lewis, P, Fy:3, Ii
41
BG destroyed by proteolytic enzymes (2)
Duffy, MN
42
BG unaffected by proteolytic enzymes (3)
Kell, SsU, Lutheran
43
IgM BGs (5)
ABO, Lewis, P1, Mn, Lua
44
IgG BGs (6)
Rh, Kell, Duffy, Kidd, SsU, Lub
45
**BG usually able to bind complement (3)**
ABO, Kidd, Lewis
46
BG that rarely bind complement (5)
Duffy, P1, Ss, Lutheran, Kell
47
BG that usually don't bind complement (1)
Rh