Summary & Overview
CPT 0210U: BioPlex 2200 RPR Quantitative Syphilis Antibody Assay
CPT code 0210U denotes a Proprietary Laboratory Analyses (PLA) test: the BioPlex 2200 RPR Assay – Quantitative by Bio–Rad Laboratories, which quantifies syphilis-related antibody levels in blood. As a PLA code, 0210U uniquely identifies a single manufacturer’s assay rather than a class of tests, aiding clarity in billing and utilization tracking. Nationally, PLA codes like 0210U matter because they affect lab billing specificity, payer coverage decisions, and public health surveillance of infectious disease testing.
Key payers discussed include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. The publication provides a consolidated view of coverage considerations and how 0210U appears across major commercial and federal payers. Readers will find benchmarks and context on clinical use, typical sites of service, and how PLA coding shapes reimbursement workflows. The analysis outlines clinical context—quantitative serologic assessment for syphilis—and operational implications for laboratories and billing teams, including typical specimen type and service setting.
The report does not provide state-specific guidance. Data not available in the input is noted where relevant. The content is intended to inform payers, laboratory administrators, policy analysts, and billing professionals about the role and implications of CPT code 0210U in national lab testing and payment landscapes.
Billing Code Overview
CPT code 0210U is a Proprietary Laboratory Analyses (PLA) code that describes a single, manufacturer-specific laboratory test: the BioPlex 2200 RPR Assay – Quantitative by Bio–Rad Laboratories. The test measures the level of syphilis-related antibodies in a patient specimen, typically using a blood sample.
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Service type: Quantitative serologic testing for syphilis antibodies (proprietary laboratory assay)
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Typical site of service: Clinical or reference laboratory processing blood specimens
Clinical & Coding Specifications
Clinical Context
A 28-year-old sexually active patient presents to an outpatient clinic with concerns about possible syphilis exposure after a partner tested positive. The clinician documents history of recent unprotected sexual contact and orders serologic testing. A blood specimen is collected via venipuncture and sent to the laboratory for treponemal and non-treponemal testing. The laboratory performs the BioPlex 2200 RPR Assay – Quantitative (0210U) to evaluate the level of non-treponemal syphilis-related antibodies. Results are returned to the ordering clinician and used alongside treponemal test results, clinical exam, and sexual history to determine diagnosis, staging, and need for treatment or follow-up testing.
Common workflow steps:
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Clinician encounter and documentation of exposure risk and symptoms.
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Order placed for syphilis serology including quantitative non-treponemal testing (
0210U). -
Phlebotomy in clinic or specimen collected at facility; specimen labeled and shipped to laboratory.
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Laboratory performs the BioPlex 2200 RPR Quantitative assay and generates the quantitative antibody level.
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Laboratory report, including interpretive reference ranges and specimen processing (
TCand26considerations), is transmitted to the ordering clinician. -
Clinician reviews combined serology results, documents interpretation, and communicates diagnosis and follow-up plan to the patient.