Summary & Overview
CPT 86807: HLA Antibody Screening for Transplant Compatibility
CPT code 86807 represents an immunogenetic laboratory screening that quantifies the percent reactive antibody in a transplant recipient's serum against potential donor human leukocyte antigens (HLA). This test is a key pre-transplant compatibility assessment used to identify recipients at elevated risk of donor-specific immune reactions and potential graft rejection. Nationally, HLA antibody screening influences transplant candidacy decisions, organ allocation considerations, and perioperative planning for immunosuppression.
Key payers covered in the discussion include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. The publication provides a concise overview of clinical context and billing characteristics for CPT code 86807, plus practical benchmarking points relevant to laboratory and transplant programs.
Readers will learn what CPT code 86807 denotes clinically, where the service is typically performed, and which major payers are relevant for coverage considerations. The article summarizes available benchmarks and policy-relevant points in a national context and highlights areas where data was not provided. Data not available in the input is clearly noted; the focus remains on clarifying the clinical purpose and billing identity of the code for administrators, laboratory directors, and revenue cycle staff.
Billing Code Overview
CPT code 86807 describes a laboratory screening that measures the percent reactive antibody in a transplant recipient's serum against potential donor human leukocyte antigens (HLA). This screening assesses the likelihood of transplant incompatibility by evaluating sequential recipient samples for HLA reactivity.
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Service type: Immunogenetic laboratory testing (HLA antibody screening)
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Typical site of service: Clinical laboratory or hospital-based immunology/transplant laboratory
Clinical & Coding Specifications
Clinical Context
A 52-year-old patient with end-stage renal disease is evaluated for a living-related kidney transplant. The transplant center orders antibody screening to assess the presence and percent reactivity of recipient anti-HLA antibodies to potential donor antigens. The clinical workflow begins with the transplant coordinator sending recipient serum samples to the histocompatibility/immunogenetics laboratory. A lab analyst performs sequential serum screening using complement-dependent or solid-phase assays to determine percent reactive antibody (PRA) and to identify specific donor HLA incompatibilities. Results are reported to the transplant physician and surgical team to guide donor selection, crossmatch planning, desensitization strategy, and perioperative immunosuppression. Typical sites of service include hospital-based transplant immunology laboratories, independent reference immunology labs, and tertiary care transplant centers.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
26 | Professional component | Use when billing only the physician/interpretive portion of a laboratory service, if applicable for consultative review of HLA results. |
TC | Technical component |