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BETA v.3.0

2025 CPT code 86834

Antibody to human leukocyte antigens (HLA), solid phase assays (eg, microspheres or beads, ELISA, Flow cytometry); semi-quantitative panel (eg, titer), HLA Class I

Immunology analytes/procedures not specified in 86015-86835 and not in the Chemistry subsection (82009-84830) may be reported using the unlisted immunology procedure code 86849.

Modifiers may be applicable. Modifier 90 is used if the test is performed by a reference (outside) laboratory. Modifier 91 is used for repeat testing.

Medical necessity for this test is determined by the patient's clinical condition and the need to assess HLA antibody levels for transplantation or other medical reasons.

The lab analyst performs the technical steps to quantify the level of specific HLA Class I antibodies in patient serum. Clinicians may order this test to evaluate the level of specific HLA Class I antibodies present in patient serum, often to determine if the antibody level is decreasing following desensitization treatment to help the patient avoid rejecting a transplant.

IMPORTANT:Do not report flow cytometry method codes 8818488189 in addition to this code. Distinguish this code from 86830 for the HLA Class I antibody phenotype panel method and 86832 for qualitative high definition HLA Class I antibody specificity test.

In simple words: This test measures the level of antibodies against specific HLA Class I antigens in your blood.HLA antigens are proteins found on the surface of your cells, and these antibodies can be important in transplantation, as they might cause your body to reject a transplanted organ.

The lab analyst performs a solid phase immunoassay using patient serum to quantify the level of specific antibodies to specific Class I human leukocyte antigens, or HLA. The lab analyst performs the technical steps to quantify the level of specific HLA Class I antibodies in patient serum using an immunoassay method that involves a solid substrate such as beads coated with a specific HLA Class I antigen. The lab analyst performs the test with several serum dilutions by mixing each dilution with beads covered with specific HLA Class I antigens in the presence of a marker that will become visible if there is an antibody/antigen reaction, such as a fluorescent immunoglobulin. 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 evaluates the result for each serum dilution to quantify the amount of antibody present.

Example 1: A patient is awaiting a kidney transplant and has previously developed antibodies against some HLA antigens. This test is performed to monitor the level of these antibodies after desensitization therapy., A patient has experienced a previous transplant rejection. This test is used to quantify the levels of specific HLA Class I antibodies to aid in determining the cause of rejection and guide future transplant attempts., A patient is undergoing evaluation for a bone marrow transplant. This test helps assess the risk of graft-versus-host disease by identifying the presence and level of HLA antibodies.

Medical record documentation should include the reason for the test, the patient's relevant medical history (including prior transplants, transfusions, and pregnancies), and the interpretation of the test results.

** Some payers may pay separately for specimen collection (e.g., 36415 for venipuncture).

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