Summary & Overview
CPT 86829: HLA Antibody Solid Phase Immunoassay
CPT code 86829 covers a solid phase immunoassay on patient serum to detect antibodies to human leukocyte antigen (HLA), both Class I and Class II. This test is clinically important for transplant compatibility assessment, donor-recipient matching, and monitoring for sensitization that can affect graft outcomes. Nationally, HLA antibody testing is a critical component of transplant programs and immunogenetics laboratories that supports patient safety and organ allocation decisions.
Key payers included in this analysis are Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. The publication outlines what providers and laboratory managers need to know about coding, expected sites of service, and clinical context for use of 86829.
Readers will learn: a concise clinical description of the procedure, the typical site of service and laboratory setting, and the scope of payers addressed. This summary also highlights common operational contexts for the test (pre-transplant evaluation and post-transplant monitoring). Data not available in the input is noted where applicable; this publication does not provide payer-specific reimbursement rates, local coverage determinations, or ICD-10 guidances beyond noting that such details are not provided in the input.
Billing Code Overview
CPT code 86829 describes a solid phase immunoassay performed on patient serum to detect the presence or absence of antibodies to human leukocyte antigen (HLA), Class I or Class II. This laboratory service is a specialized immunologic test that assesses HLA antibody status, typically used in transplant evaluation, organ allocation, and monitoring for alloimmune sensitization.
Service Type: Laboratory — Immunology / Serology
Typical Site of Service: Clinical laboratory or hospital laboratory (outpatient or inpatient specimen processing)
Clinical & Coding Specifications
Clinical Context
A 48-year-old patient with end-stage renal disease is evaluated in the transplant clinic prior to a deceased-donor kidney transplant. The transplant team orders HLA antibody testing to identify pre-formed anti-human leukocyte antigen (HLA) Class I and Class II antibodies in the patient’s serum. A phlebotomy draw is performed; the specimen is delivered to the immunology laboratory. A laboratory analyst performs a solid phase immunoassay (single-antigen bead or panel-reactive antibody assay) to detect the presence or absence of HLA-specific antibodies. Results inform crossmatch decisions, organ allocation priority (calculated panel-reactive antibody), and post-transplant immunosuppressive planning. Typical workflow: specimen accessioning → serum separation → assay setup and incubation → instrument readout and interpretation → result reporting to the transplant team and electronic medical record. Typical site of service: hospital-based transplant center, hospital outpatient laboratory, or reference immunology laboratory.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
26 | Professional component | Use when billing only the professional interpretation/analysis portion, separate from the technical laboratory component. |
TC |