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CLINICAL LAB SCIENEC

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CHAPTER 17: IMMUNOHEMATOLOGY (BLOOD BANKING) 419

This chapter provides a few routine tests performed in the routine blood banks.

The cross match, as mentioned earlier, is a rather long and cumbersome set of

tests, so the entire cross match will not be presented here. Medical laboratory

students enrolled in immunohematology classes usually learn both theory and

practice, and have the opportunity to perform an actual cross match.

Safety and Accuracy in Immunohematology

It should now be obvious to the astute clinical laboratory student that there is a

relationship between immunology/serology and immunohematology. Both areas

work on the premise of antibodies against antigens and require meticulous care

in providing accurate and timely results. However, in most routine procedures

in blood banking, the basic test are to discover RBC antigens by use of specific

antibody solutions obtained from persons with antibodies against various blood

groups. Efforts in this department are to obtain a safe supply of blood, test it

for communicable diseases, and ensure the patient has no antibodies against

the blood of the donor, which would cause a potentially life-threatening reaction.

The most atypical antibodies or alloantibodies (those from a donor) often

require a specialist in blood banking to determine the offending antibody.

In the Lab

BASIC IMMUNOHEMATOLOGY PROCEDURES

MANUAL IMMUNOHEMATOLOGY PROCEDURE #1

Preparation of 2% to 5% Cell Suspensions

Principle

A number of tests require red blood cell (RBC) suspensions and are performed in

test tubes. Other tests, such as blood grouping for identifying the ABO group, can be

performed either in test tubes or on glass microscope slides.

Red blood cells contain some plasma, which is rich in proteins. Surface proteins

may interfere with tests that use antisera against the antigens on the surface of the

RBCs. Therefore, the RBCs must be “washed” with normal saline (a salt solution

approximately equal to the salt concentration of a person’s blood plasma) to enhance

reactions in blood bank procedures.

To “wash” RBCs, several drops of RBCs are placed in glass test tubes (12 × 75 mm

tubes are preferable). Normal saline from a squeeze bottle is injected into the tube

containing the cells. Using a piece of plastic Parafilm, the top of the tube is covered

and the tube is then inverted several times to mix the cells and saline. The tube is

centrifuged, and the saline is removed, leaving a “button” of RBCs in the bottom.

This process is repeated two or three times, according to most blood bank basic

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