Compatibility Testing Flashcards

1
Q

Testing of the Donor sample

A
  • ABO grouping
  • Rhgrouping
  • weak D, Du
  • TTI’s
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2
Q

Identify what type of blood typing:
- Sample Red Cells and Typing sera
- Sample Antigen detected

A

Forward typing

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2
Q

Testing for the Patient sample

A
  • ABO grouping
  • Rh grouping
  • Unexpected antibodies
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2
Q

Identify what type of blood typing:
- Sample serum/plasma and Known Red Cells
- sample antibody detected

A

Reverse typing

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3
Q

More sensitive method when it comes to blood typing

A

tube method

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4
Q

Detect as many clinically significant antibodies, minimize detection of nuisance antibodies, and prompt delivery of blood to patient

A

Antibody screening

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4
Q

Determines ABO and Rh grouping of both patient and donor
blood

A

ABO Grouping

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5
Q

Reactive at 37°C and/or in the AHG test and known to cause transfusion reaction or unacceptably short
survival of transfused red cells

A

clinically significant antibodies

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6
Q

Antibody Screening is performed using selected _______ red cells that are known to
carry optimal representation of important blood group
antigens.

A

group O

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7
Q

Phase 1 of Antibody Screening

A

Immediate spin

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8
Q

May be omitted but it may also give additional information as to whether the reaction is due to an IgM antibody instead of IgG or complement
activation.

A

Immediate spin

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9
Q

Usually considered “nuisance” antibodies

A

IgM antibodies

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10
Q

In performing Immediate Spin, 3 tubes are needed that contains

A
  • Recipient serum plus saline suspension Screening Cell I
  • Screening Cell II, and
  • Recipient’s own cells for the auto control
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11
Q

Phase 2 of Antibody Screening

A

37C Incubation

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12
Q

This phase is required since IgG clinically-significant antibodies are warm-acting antibodies

A

37C phase

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13
Q

37C Incubation can be added with enhancement media such as

A

LISSor albumin

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14
Q

Composed of NaCl, glycine and phosphate buffer along sodium preservative.

A

LISS or Low Ionic Strength Solution

15
Q

This solution
speeds up antigen-antibody reaction but unfortunately enhances “nuisance” antibodies, so add after immediate spin
step

A

LISS or Low Ionic Strength Solution

16
Q

This is added to 37C incubation to lower zeta potential so cells can agglutinate without Coombs step and may detect Rh antibodies

17
Q

Whether adding an enhancement media or not we must do _______, but we do not need to read at this step. We-can proceed directly to Coombs (AHG or AGT) phase.

A

37C incubation

18
Q

Phase 3 of Antibody Screening

A

Coombs phase (AHG or AGT)

19
Q

This phase is required since a number of these clinically significant antibodies may only show up at
this phase

A

Coombs phase (AHG or AGT)

20
Q

Adding this in Phase 3 to all negative results to confirm negative reactions

A

Coombs Control Cells

21
Q

Always Potentially Clinically Significant antibodies

A
  • ABO
  • Rh
  • Duffy
  • Kell
  • SsU
  • Kidd
22
Sometimes clinically significant antibodies
- Lea - Lutheran (Lu a, Lu b) - MN - Cartwright (Yta) - P1
23
Rarely clinically significant antibodies
- Leb - Xga - Chido/Rodgers (Ch a/Rga) - HTLA - Sda
24
Note: Crossmatching **is only a part** of compatibility testing
25
Mixing the patient’s serum with donor’s red cells
Major Crossmatching
26
Mixing patient’s red cells with donor’s plasma
Minor Crossmatching
27
Completely eliminated from most blood banks –antibody screening beforehand
Minor crossmatching
28
Methods of Major Crossmatch Tests
- Intermediate Spin Crossmatch - Antiglobulin Crossmatch - Antiglobulin Crossmatch
29
Mixing patient’s serum with donor’s red cells and centrifuge immediately
Intermediate Spin Crossmatch
30
Using this eliminate some false-positive reactions, improving sensitivity
EDTA
30
False Reaction in Intermediate Spin Crossmatch is seen in:
1. presence of other immediate spin-reactive antibodies (e.g. autoanti-I) 2. patients with hyperimmune ABO antibodies 3. procedure not performed correctly (delay in centrifugation, reading) 4. Infant specimen
31
Begins in the same manner as the immediate spin crossmatch, continues to a 37°C incubation, and finishes with an anti-globulin test
Antiglobulin Crossmatch
32
Methods used to enhance antigen-antibody reactions:
- Albumin - Low ionic strength sol’n (LISS) or Polyethylene glycol (PEG)
33
Added before incubation, this enhances reactivity of some antibodies
Albumin
34
May be added in place of albumin, facilitate complexing of antigens and antibodies
LISS or PEG
35
Rapid and sensitive crossmatch technique. Used in detecting ABO incompatibility accompanied by negative antibody screening on the patient.
Polybrene (P-AHG)
36
Not required, however, in large volume transfusion, _________ using patient red cells and donor plasma is sufficient
immediate spin crossmatch