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CLS 3311 Advanced Clinical Immunohematology

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CLS 3311

Advanced Clinical

Immunohematology



Compatibility (Pretransfusion)

Testing

Pretransfusion Testing

• Purpose: To select blood components that

will not cause harm to the recipient and will

have acceptable survival when transfused.



• When performed properly, pretransfusion

tests will confirm ABO compatibility

between the component and the recipient

and will detect most clinically

significant unexpected antibodies.

Pretransfusion Testing

Donor Basic Testing (processing):

• ABO Grouping: Forward and Reverse

• Rh typing: Complete with Weak D

• IAT: Antibody screen

• Transmissible disease testing: HIV, HTLV, HCV,

HBV and RPR

Recipient Basic Testing:

• ABO Grouping: Forward and Reverse

• Rh typing: Only Immediate is REQUIRED. Exception

is for neonates and women of child bearing age.

• IAT & Panel: Antibody Screen and Identification

Pretransfusion Testing

The Actual Crossmatch (X-m)

• Test DONOR CELLS with RECIPIENT SERUM

• May include I.S., 37oC, & AHG Phase (extended X-M)

• OR may just be Immediate Spin phase only to

confirm ABO compatibility of Recipient and Donor

• OR may be Computer Crossmatch !!

PURPOSE

• Detect Patient Antibodies that can react with

DONOR Cells

AABB Requirements for

Pretransfusion Testing

1. Positive identification of recipient and recipient sample

2. ABO group and Rh typing of recipient and donor blood.

3. Red cell antibody detection tests for clinically significant

antibodies using recipients serum or plasma.

4. Comparison of current findings of recipients sample with

record of previous patient results.

5. Selection of components of ABO group and Rh type

appropriate for the recipient.

6. Performance of a serologic or computer crossmatch.

7. Labeling of products with the recipients identifying

information.

Steps In Pre-transfusion Testing

Review available RECIPIENT Records

• Previous ABO & Rh and any PRIOR indication of

Unexpected antibodies

• For any Prior Adverse Reactions to transfusion

Donor Unit Id and ABO/Rh

• Confirm donor unit # with the collecting facilities

records, and confirm by retesting donor ABO/Rh

• Confirm match between donor unit ABO/Rh and the

patient ABO/Rh

Steps In Pre-transfusion Testing

Correct Identification of:

1. Recipient by confirming patient identity from

identification bracelet ON PATIENT

2. Recipient Sample by clear identification/

labeling on the recipient sample

– FULL patient name & unique hospital #,

– Name of requesting physician,

– Date and time of collection, & phlebotomist’s

initials

– Information clearly written on both the request form

and the sample itself

Steps In Pre-transfusion Testing

Collecting Patient Sample

• Sample must NOT be hemolyzed -

– Unless the patient is doing the hemolyzing

– Why?

• Can use serum or plasma

– Plasma prevents detection of complement dependent

antibodies and…

– Fibrin clots, which may form, can be mistaken for

agglutination

• If sample must be drawn from IV line:

– Infusion should be stopped for 5-10 minutes and the first 10

ml’s of sample discarded. Why?

Steps In Pre-transfusion Testing

Selection of Appropriate Donor Unit(s)

• ABO & Rh compatible

• Donor unit expiration date.

• Correct component preparation for the patient needs

such as thawing plasma, etc.

Accurate Testing & Recording Of

• Donor results: Computer data entry

• Recipient results: Computer data entry

• Do we ever make data entry errors in the laboratory?

Steps In Pre-transfusion Testing



AT THE TIME OF TRANSFUSION

Accurate Identification Of:

• Recipient pre-transfusion records

– Retrieve the correct patient’s records

• Correct donor unit is retrieved & released

• The correct recipient is identified on

unit/ward prior to initiating the component’s

infusion

Steps In Pre-transfusion Testing

• Recipient sample & Donor segment should be

stored at 1 to 6oC for minimum of seven days

• Transfusion should occur within 72 hours of

sample collection & testing

– Patients transfused or pregnant within the last 3

months, may be developing a clinically significant

antibody at a detectable level

– If sample used is > 72 hrs. post collection, a

clinically significant antibody may have formed and

will be missed. Only a new serum sample will pick

up the antibody.

Pre-transfusion Testing Procedures



TYPE & SCREEN

• Consists of ABO, Rh, IAT

• Ordered most often for Pre-Surgical Patient with:

– No abnormalities in ABO Grouping, Rh Typing

– No unexpected Ab’s detected with IAT

– No patient records of unexpected Ab’s or problems with

prior transfusions

• Patient ABO, Rh, & IAT are performed but no units

are crossmatched or reserved for the patient.

Pre-transfusion Testing

Procedures

Supplying blood for the

‘type & screen’ surgical patient

• Conservative Approach involves pulling the

patient sample and the appropriate donor unit

segments and doing an Extended Crossmatch

with IS, 37 and AHG phases.

• Moderate approach involves pulling the patient

sample and the appropriate donor unit segments

and performing an Abbreviated crossmatch

such as an Immediate Spin Crossmatch only.

Pre-transfusion Testing

Procedures

Liberal Approach: Computer Crossmatch

• Every keystroke in the computer system must be

validated.

• Donor Identification, ABO/Rh, IAT results entered

• Recipient Identification, ABO/Rh, IAT results entered

– Two different individuals must do the ABO (Rh) on the

same recipient specimen

– OR the same individual performs the ABO on 2

different collections of the same recipient

Pre-transfusion Testing

Procedures

Computer Crossmatch continued

• The test results are entered into a computer

that then selects the most appropriate Donor

unit in terms of ABO, Rh, & expiration

date for that recipient.

• Computer system contains logic to detect

and alert user of any discrepancies

between the recipient and donor.

• ‘Tube’ crossmatch is NOT performed.

Pre-transfusion Testing

Procedures

Extended Crossmatch

• Is to be Performed on Recipients with:

1. Unexpected antibodies

2. Prior records of unexpected antibodies OR

3. Problems with transfusion, ABO and/or Rh

• The Antibody(s) should be identified

prior to transfusion, if possible

– Some may not be possible to identify, such as auto

antibodies.

Pre-transfusion Testing Procedures

Special Circumstances

Extreme Emergency

• No time for even ABO and Rh testing

• Initially, the unit of choice is Gr O Rh Negative

• The Attending Physician must understand that a

sample must be obtained from the patient as

quickly as possible. Physician must sign waiver

omitting pre transfusion testing. Specimen

of choice is pretransfusion, if possible.

• If recipient is Rh Pos then the he/she can be

quickly switched to Rh Pos blood

Extreme Emergency

• The physician must sign a Release Form before you

release uncrossmatched blood for transfusion.

• This release indicates that the clinical condition

warrants the risks of transfusion in the absence

of knowing about the ABO, Rh, & IAT

• In cases where units are released without knowing the

Recipient’s ABO & Rh, the established protocol for

compatibility testing must be performed on the

Recipient & Donor units after the fact.

– Even if the units have already been transfused OR even if the

Recipient Dies. All work must be completed.

– All patient records must be complete.

Pre-transfusion Testing Procedures

Special Circumstances

Extreme Emergency Continued

• IF recipient is Rh Neg but has NO evidence of

anti-D, is male or beyond child bearing age, then

it may be more efficient to give Rh Pos blood

• If a recipient is hemorrhaging heavily, you will

end up replacing his blood volume more than

once

• If it is determined that giving Rh Pos units to an

Rh Neg patient is appropriate, the attending

Physician must be informed and consent

must be obtained in advance.

Pre-transfusion Testing Procedures

Special Circumstances

• Transfusing NON - ABO Group Specific Blood

– when the Recipient must be transfused the attending

Physician must be informed and agree.

• If group specific blood becomes available

and the choice is to switch to ABO group

specific blood, you MUST:

– Test for the presence of anti-A and/or anti-B in the

patient’s serum before returning to ABO group

specific blood

– If the Recipient doesn’t reverse group appropriately,

they should be given Gr O packed cells

Pre-transfusion Testing Procedures

Special Circumstances



Intrauterine & Infant Transfusions

• Blood must be compatible with MATERNAL

antibodies that are capable of crossing the placenta.

Crossmatch with Mom’s serum, if possible.

• If the ABO & Rh of the fetus or infant is known, then

group & type specific blood can be given

– if no fetomaternal incompatibility has been detected

• If the ABO & Rh are unknown, O Neg can be given

Pre-transfusion Testing Procedures

Special Circumstances

Massive Transfusion

• Replacement approximating or exceeding the

patients blood volume within a 24-hour period.

• If the patient has no unexpected Ab’s,

pretransfusion testing can be ELIMINATED

• If the patient has an unexpected antibody, the

units must be antigen typed, with commercial

antisera, for the corresponding antigen and

antigen negative blood must be transfused.



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