5-PRETRANSFUSION LAB Flashcards

(42 cards)

1
Q

Which test uses reagent red blood cells in hypotonic buffered saline combined with recipient serum or plasma to detect antigen-antibody interaction

A

Antibody screen

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2
Q

Which temperature is used for incubation in antibody screen gel technology

A

37 degrees Celsius

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3
Q

Which reagent in the antibody screen gel card contains polyspecific AHG

A

LISS/Coombs

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4
Q

Which step involves identifying microtubes with donor or patient information in antibody screen

A

Identify microtubes

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5
Q

Which step involves removing aluminum foil from microtubes in antibody screen

A

Remove aluminum foil

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6
Q

Which volume of test cell reagent is pipetted into microtubes in antibody screen

A

50 microliters

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7
Q

Which volume of donor or patient plasma or serum is added to microtubes in antibody screen

A

25 microliters

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8
Q

Which incubation time is used in antibody screen gel technology

A

15 minutes

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9
Q

Which centrifugation time is used in antibody screen gel technology

A

10 minutes

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10
Q

Which result in antibody screen shows agglutinated cells forming a red line or dispersed agglutinates

A

Positive

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11
Q

Which result in antibody screen shows compact button of cells at the bottom of microtube

A

Negative

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12
Q

Which result in antibody screen shows a layer of positive cells at the top and button of negative cells

A

Mixed field

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13
Q

Which test is the final check of ABO compatibility between donor and recipient

A

Crossmatching

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14
Q

Which test detects antibodies in patient serum that react with donor red blood cells not detected in antibody screening

A

Crossmatching

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15
Q

What does a serologic crossmatch consist of

A

Mixing recipient plasma with donor red cells

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16
Q

What does a nonreactive serologic crossmatch indicate

A

Donor unit is compatible and safe for transfusion

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17
Q

Which phase of crossmatch involves mixing patient serum with donor red cells and immediate centrifugation

A

Phase I Saline/Immediate Spin

18
Q

Which temperature and incubation time is used in Phase II of crossmatch

A

37 degrees Celsius for 10 minutes

19
Q

What reagent is added in Phase II of crossmatch

20
Q

What is done after incubation in Phase II of crossmatch

A

Centrifuge and examine for hemolysis and agglutination

21
Q

What is the purpose of Phase III Direct Coombs/Anti-Human Globulin phase

A

Detect antibodies bound to red cells

22
Q

What reagent is added in Phase III of crossmatch

A

Anti-human globulin serum

23
Q

How many times are cells washed in Phase III of crossmatch

A

At least 3 times

24
Q

What indicates incompatibility in Phase III of crossmatch

A

Reactivity or hemolysis at any phase

25
What should be done if test results are visually negative in Phase III
Examine under microscope
26
Who should check test results in crossmatch
Second medical technologist
27
Which test is useful for identifying patients with auto-antibodies
Autocontrol
28
Which condition may make finding a compatible blood unit difficult
Presence of auto-antibodies
29
What is the direct Coombs test used for
Detection of in vivo coating of red blood cells with globulins
30
Which specimen is used in the direct Coombs test
Washed red blood cells from patient or donor
31
Which reagent is used in the direct Coombs test
Antiglobulin reagent
32
Which disease is diagnosed using the direct Coombs test
Hemolytic disease of the newborn
33
Which disease is diagnosed using the direct Coombs test
Autoimmune hemolytic anemia
34
Which investigations are performed using the direct Coombs test
Red blood cell sensitization caused by drugs + Transfusion reactions
35
What are the post-analytical procedures in pretransfusion testing
Labeling of unit with product and patient identification + Generation of compatibility report
36
What information is included on the blood unit label
Product details + Patient identification information
37
Which report accompanies the blood product
Compatibility report
38
When must donor units be labeled
At time of issue
39
What must be confirmed by the transfusionist at bedside
Recipient identification + Donor unit information
40
When can blood components not be issued
Until all discrepancies are resolved
41
What must be inspected before issuing blood components
Hemolysis + Clots
42
What is done if an adverse event related to transfusion occurs
Investigated according to policy