Summary & Overview
CPT 87902: Hepatitis C Genotype by Nucleic Acid, Technical Component
CPT code 87902 represents the technical laboratory component of a molecular diagnostic assay to determine the specific genotype of hepatitis C virus (HCV) from a patient specimen. Nationally, genotype determination guides clinical management of HCV, influences antiviral selection, and supports public health surveillance, making accurate billing and coding for this test important for clinical workflows and laboratory reimbursement.
This analysis covers major national payers including Aetna, Blue Cross Blue Shield, Cigna, UnitedHealthcare, and Medicare. Readers will find a concise overview of clinical context for HCV genotyping, typical sites where the service is performed, commonly applied billing modifiers, and what to expect in payer coverage approaches. The publication summarizes available benchmarks and policy considerations, highlights coding definitions and service characterization, and notes where input data are unavailable.
Intended for laboratory managers, medical coders, and health policy analysts, the content clarifies the role of CPT code 87902 in laboratory billing for HCV genotype testing and outlines the practical implications for billing workflows and payer interactions at a national level.
Billing Code Overview
CPT code 87902 describes a laboratory procedure in which a lab analyst performs the technical component of a nucleic acid test to determine the specific genotype of a specimen containing hepatitis C virus. This service is a molecular diagnostic assay focused on identifying viral genotype by analyzing nucleic acid from a patient specimen.
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Service type: Laboratory molecular diagnostic testing (technical component)
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Typical site of service: Clinical laboratory or hospital laboratory performing molecular virology testing
Data not available in the input for payers beyond those listed elsewhere, associated taxonomies, ICD-10 diagnoses, and related codes.
Clinical & Coding Specifications
Clinical Context
A 48-year-old patient with known chronic hepatitis C infection presents for genotype testing to guide antiviral therapy selection. The clinician collects a peripheral blood specimen (serum or plasma) which is sent to the molecular diagnostics laboratory. The laboratory analyst performs nucleic acid-based testing to determine the hepatitis C virus (HCV) genotype and subgenotype using validated molecular methods (for example, RT-PCR with sequencing or genotype-specific probes). Results are reported to the ordering provider and entered into the electronic medical record to inform direct-acting antiviral regimen choice and duration. Typical site of service is an independent clinical laboratory, hospital outpatient laboratory, or reference laboratory performing specialized molecular diagnostics.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
26 | Professional component | Use when billing only the professional (interpretation) component separate from the technical component. |
TC | Technical component | Use when billing only the technical component (laboratory testing, equipment, reagents). |