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BETA v.3.0

2025 CPT code 86829

Qualitative assessment of the presence or absence of antibody(ies) to HLA Class I or Class II HLA antigens using solid phase assays (e.g., microspheres or beads, ELISA, Flow cytometry).

Report only once per class of HLA antibody tested (I or II). If both classes are tested, use 86828. Do not report specimen collection separately.

Modifiers may be applicable in certain situations (e.g., 59 for a distinct procedural service, 90 for reference lab, 91 for repeat testing).

Medical necessity is established when the test is performed for appropriate clinical indications, such as pre-transplant evaluation, assessment of transfusion risks, or evaluation of pregnancy complications.

The lab analyst performs the technical steps to identify the presence or absence of HLA Class I or HLA Class II antibodies in patient serum using an immunoassay method that involves a solid substrate such as antigen–coated beads or test wells. The lab analyst evaluates the antibody/antigen reaction using a special instrument and process such as flow cytometry or enzyme–linked immunosorbent assay, called ELISA, and reports a qualitative result.

IMPORTANT:If testing for both HLA Class I and Class II antibodies, use 86828. Do not report flow cytometry method codes 8818488189 in addition to this code.

In simple words: This test checks if you have antibodies against certain proteins (HLA) found on your cells. These antibodies can be important for things like organ transplants.

The laboratory analyst performs a solid phase immunoassay using patient serum to determine the presence or absence of antibodies to human leukocyte antigen (HLA), Class I or Class II antigens.The analyst mixes the serum with beads or wells coated with HLA Class I or Class II HLA antigens in the presence of a marker (e.g., a fluorescent immunoglobulin) that will become visible if there is an antibody/antigen reaction. The reaction is evaluated using an instrument and process such as flow cytometry or ELISA, and a qualitative result is reported. (If solid phase testing is performed to assess presence or absence of antibody to both HLA classes, use 86828).

Example 1: A patient is being evaluated for a kidney transplant and needs to be screened for HLA antibodies to assess compatibility with potential donors., A patient has had multiple blood transfusions and needs to be tested for the presence of HLA antibodies, which can complicate future transfusions., A pregnant woman is being tested for HLA antibodies to assess the risk of complications related to fetal-maternal incompatibility.

Medical record documentation should include the reason for the test, relevant clinical history (e.g., prior transplants, transfusions, pregnancies), and the interpretation of the test results.

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