Lecture 7 Flashcards

1
Q

Blood Bank sample requirements

A

patient’s full name and unique identity number
Writing must be legible and indelible
Date of collection
Sample must be collected within 3 days of scheduled transfusion
initials or signature of the person who collected the sample

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2
Q

Hemolyzed samples

A

cannot be used for testing
hemolysis caused by activation of complement by antigen-antibody complexes will be masked

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3
Q

To avoid contamination blood

A

samples should not be taken from intravenous tubing lines

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4
Q

ABO Grouping

A

the most critical pretransfusion serologic test
Tube tests offer greater sensitivity

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5
Q

Group I Discrepancy

A

occur between forward and reverse groupings owing to weak or missing antibodies
most common discrepancy

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6
Q

Group I Discrepancy: reason

A

depressed antibody production
Newborn/elderly
Leukemia (CLL)
Lymphoma
Immunosuppresive drugs

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7
Q

Resolution of Group I Discrepancies

A

enhance the reverse group reaction
incubating the patient serum with reagent A1 and B cells at room temperature(25ºC) for approximately 15 to 30 minutes

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8
Q

What if Group 1 resolution doesn’t work?

A

serum-cell mixture can be incubated at 4ºC for 15 to 30 minutes

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9
Q

Group II Discrepancies

A

Occurs between forward and reverse groupings owing to weak or missing antigens

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10
Q

Group II Discrepancies: Causes

A

Subgroups of A and/or Subgroups of B being present
Leukemias
Hodgkin’s disease
Acquired B” Phenomena
Antibodies to low incidence antigens

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11
Q

Group II resolution: Possible weak subgroup of A

A

Test cells with anti-A,B reagent
Test with Anti-A1 lectin
May require genotype testing to confirm

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12
Q

Group II resolution: Possible acquired B

A

Treating red cell with acetic anhydride re-acetylates the surface molecules

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13
Q

Group III Discrepancies

A

Occurs due to protein or plasma abnormalities

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14
Q

Group III discrepancies: Causes

A

Elevated globulin levels like:
Waldenstroms macroglobulinemia
Multiple Myeloma
Hodgkin’s disease
Rouleaux due to elevated Fibrinogen
Wharton Jelly

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15
Q

Group III discrepancies: Resolution

A

Cells must be washed to alleviate problem

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16
Q

Group IV discrepancies

A

Polyagglutination-spontaneous RBC Agglutination
Bacterial contamination

17
Q

Warm autoantibodies

A

Presence of warm autoimmune antibodies. Most common
reactive at 37o C

18
Q

Cold autoantibodies

A

anti-I and anti-H and anti-IH
Benign cold reacting autoantibodies are present in all normal human sera

19
Q

Resolution to Group IV Discrepancies

A

If the poly agglutination is suspected, lectin studies should be performed

20
Q

Potent Cold Autoantibodies

A

○ cause spontaneous agglutination, causing positive Coomb’s test (DAT)
resolved by incubating red cells at 37C for a short period of time

21
Q

Warm Antibodies

A

When expected of causing a false positive reaction in the forward grouping the cells can be treated to a gentle heat elution at 45C for the cells to be reliably typed

22
Q

Unexpected ABO isoantibodies

A

react at room temperature with the corresponding antigen present on the reagent cells
A2 and A2B individuals: produceanti-A1, or A1
A1B: produce anti-H

23
Q

Unexpected Alloantibodies

A

may cause a discrepancy in the reverse grouping
In this situation- a panel should be performed with the patient’s serum

24
Q

Cis-AB

A

inheritance of both AB genes from one parent carried on one chromosome and the O gene inherited from the other parent
results in the offspring inheriting three ABO genes

25
Q

Rh Grouping

A

performed using anti-D blood grouping serum
Rh Controls must be run alongside, to avoid incorrect designation of Rh-negative patients as Rh-positive

26
Q

If the Rh-control is positive?

A

Rh grouping test is invalid and must be rerun
DAT should be performed to determine whether autoantibodies is responsible for the positive Rh control

27
Q

If Rh group of the recipient cannot be established and transfusion is essential

A

Rh-negative blood should be given

28
Q

Antibody Screen

A

The patient’s serum or plasma must be tested for unexpected antibodies

29
Q

Antibody Screen offers several advantages over direct crossmatch testing

A

group O red cells that are known to carry optimal representation of important blood group antigens
Testing can be performed well in advance of the anticipated transfusion

30
Q

Antibodies regarded as always being potentially clinically significant

A

ABO, Rh, Kell, Duffy, Kidd, SsU

31
Q

Antibodies that may sometimes be clinically significant

A

Lewis (Lea), MN, P,1 Lutheran (Lua, Lub), Cartwright (Yta)

32
Q

Rarely seen antibodies that are clinically significant

A

Leb, Chido/Rogers (Cha/Rga), York (Yka), Sda, Xga

33
Q

Crossmatch Testing

A

testing of the patient’s serum with the donor cells
“compatibility test”

34
Q

Two main functions for performing the crossmatch

A

a final check of ABO compatibility between donor and patient
may detect the presence of an antibody in the patient’s serum that will react with antigens on the donor RBCs that was not detected in the antibody screening

35
Q

Crossmatch Testing: Results

A

A jagged or firm button edge is indicative of a positive reaction = incompatible
smooth swirling of free cells off the RBC button indicates a negative reaction = compatible

36
Q

Whenever the crossmatch test result is positive

A

results of the autocontrol and antibody screening test should be reviewed

37
Q

Causes of positive results in the serologic crossmatch

A

Incorrect ABO grouping of the patient or donor
Resolution - Repeat testing