Summary & Overview
CPT 0043U: TBRF Borrelia ImmunoBlot IgM Test
CPT code 0043U identifies a proprietary immunoblot serology test marketed by IGeneX Inc. that detects IgM antibodies to four recombinant Borrelia protein groups associated with Tick–Borne Relapsing Fever (TBRF). As a PLA code, 0043U is specific to a single manufacturer's assay and signals unique clinical and contracting considerations for payers, providers, and laboratories. Nationally, specialized serologic assays for tick-borne infections are significant due to growing clinician demand for targeted diagnostics in complex cases of suspected Lyme disease and relapsing fever.
Key payers in this analysis include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise account of what 0043U represents, typical settings where the test is performed, and the scope of coverage considerations tied to proprietary laboratory assays. The publication summarizes benchmark topics relevant to this code, including coding classification as a PLA, implications for laboratory billing and test ordering workflows, and the clinical context for IgM-based Borrelia testing. Where input data is missing, the report notes those gaps as "Data not available in the input."
Billing Code Overview
CPT code 0043U is a Proprietary Laboratory Analyses (PLA) code for the Tick–Borne Relapsing Fever (TBRF) Borrelia ImmunoBlot IgM test developed by IGeneX Inc. The test detects IgM antibodies to four recombinant protein groups of Borrelia, the tick-borne bacteria associated with Lyme disease and relapsing fever.
Service Type: Laboratory diagnostic testing (proprietary immunoblot serology)
Typical Site of Service: Clinical laboratory or specialized reference laboratory
Data not available in the input.
Clinical & Coding Specifications
Clinical Context
A 34-year-old patient presents to an infectious disease clinic with several weeks of intermittent fevers, recurrent headaches, fatigue, and a history of recent tick exposure while hiking in an endemic area. The clinician suspects tick-borne relapsing fever (TBRF) or another Borrelia-related infection and orders a specialized serologic test to detect early immune response. The specimen (serum) is collected in the outpatient laboratory or clinic phlebotomy area and sent to IGeneX Inc. for the proprietary Tick–Borne Relapsing Fever Borrelia ImmunoBlot IgM assay (0043U). Results are reviewed by the ordering clinician; a positive IgM immunoblot supports recent or acute infection and informs further management, public health reporting if applicable, and possible confirmatory testing or treatment decisions. Typical sites of service include outpatient clinic, outpatient laboratory, urgent care, and reference laboratory processing.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
00 | Default — no modifier | Use when no special circumstances apply to the billed service. |
11 | Professional component |