Summary & Overview
CPT 87906: HIV-1 Genotype by Nucleic Acid (Non-RT/Protease Regions)
CPT code 87906 covers technical laboratory genotyping of HIV‑1 by nucleic acid methods for genomic regions other than reverse transcriptase and protease (for example, integrase or fusion genes). These targeted molecular assays support clinical decision‑making for antiretroviral resistance surveillance, epidemiologic characterization, and specialized patient management. Nationally, access to and coverage of such advanced genotyping tests affect infectious disease care pathways, public health reporting, and specialized laboratory workflows.
Key payers included in the analysis are Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise overview of the clinical context and typical sites of service, a summary of common modifiers and billing considerations, and an outline of where this service fits within laboratory molecular diagnostics. The publication also highlights benchmarking points and policy or coding updates where available. Data not available in the input is identified explicitly to avoid assumptions.
Billing Code Overview
CPT code 87906 describes a laboratory technical procedure in which a lab analyst performs nucleic acid analysis to determine the genotype of an HIV‑1 virus for regions other than the reverse transcriptase and protease regions (for example, the integrase gene or fusion gene). This is a specialized molecular diagnostic test focused on sequencing or genotyping non‑RT/non‑protease regions of HIV‑1 to inform virologic characterization.
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Service type: Molecular diagnostic laboratory test (technical component)
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Typical site of service: Clinical laboratory or hospital laboratory performing molecular virology testing
Clinical & Coding Specifications
Clinical Context
A 42-year-old person with known HIV-1 infection presents for evaluation following suboptimal viral suppression on current antiretroviral therapy. The treating infectious disease clinician orders genotypic resistance testing focused on the HIV-1 integrase gene to detect mutations that confer resistance to integrase strand transfer inhibitors. A blood specimen (plasma) is collected in the outpatient infusion clinic or ambulatory lab and sent to a molecular diagnostics laboratory. The laboratory analyst performs nucleic acid extraction, sequencing or targeted genotyping of regions other than reverse transcriptase and protease (for example, the integrase gene), interprets the technical assay results, and reports detected resistance-associated substitutions to the ordering clinician. Typical site of service includes outpatient ambulatory clinics, hospital outpatient departments, and reference molecular laboratories. Typical workflow steps: specimen collection → specimen accessioning and nucleic acid extraction → amplification/sequencing or targeted assay of integrase/fusion regions → bioinformatic analysis and quality control → technical result reporting to the laboratory information system (with or without separate professional interpretation by a clinical molecular pathologist).
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
26 | Professional component | When billing only the physician/clinical interpretation portion if separated from the laboratory technical component. |