Summary & Overview
CPT 0483U: Ciprofloxacin Susceptibility Test for Neisseria gonorrhoeae
CPT code 0483U is a Proprietary Laboratory Analyses (PLA) code for a molecular test that identifies a mutation in Neisseria gonorrhoeae conferring resistance to ciprofloxacin. As a PLA code, it applies to a single specific commercial test offered by MedArbor Diagnostics and SpeeDx Inc., and is used when oral, rectal, or vaginal swab specimens are analyzed to determine ciprofloxacin susceptibility. This code matters nationally as antimicrobial resistance in Neisseria gonorrhoeae is a public health concern and targeted susceptibility testing can inform treatment selection and stewardship efforts.
Key payers covered in this analysis include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise overview of the clinical purpose of the test, typical service setting, and the payer landscape considered. The publication provides benchmarks where available, notes on coverage patterns, and clinical context about specimen types and the molecular target of the assay. Data not available in the input is noted where applicable. The content is intended for clinicians, coding and billing professionals, and policy analysts seeking a clear national summary of CPT code 0483U and its role in diagnostic testing for ciprofloxacin resistance in gonococcal infections.
Billing Code Overview
CPT code 0483U is a Proprietary Laboratory Analyses (PLA) code for Ciprofloxacin Susceptibility of Neisseria gonorrhoeae performed by MedArbor Diagnostics and SpeeDx Inc. The test detects a specific mutation in Neisseria gonorrhoeae that indicates resistance to the antibiotic ciprofloxacin.
Service type: Diagnostic molecular susceptibility testing
Typical site of service: Clinical laboratory or reference laboratory
Clinical & Coding Specifications
Clinical Context
A 27-year-old sexually active patient presents to a sexual health clinic with symptoms of urethral discharge and dysuria after unprotected intercourse. A clinician collects an oral, rectal, and vaginal swab based on reported exposure sites and clinical exam. Rapid molecular testing for Neisseria gonorrhoeae is positive, and the clinician orders a targeted proprietary assay to determine ciprofloxacin susceptibility by detecting a specific resistance-associated mutation in N. gonorrhoeae. The specimen is sent to MedArbor Diagnostics / SpeeDx Inc. for the proprietary test reported by 0483U. Results guide epidemiologic surveillance and, where permitted by local treatment guidance, targeted antibiotic selection when ciprofloxacin susceptibility is confirmed.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
00 | Default billing indicator (no modifier) | Use when no other modifier applies and the service is furnished as usual. |
22 | Increased procedural services | Use when work required is substantially greater than typically required for this test (document justification).
52 | Reduced services | Use when the test is partially reduced or not fully performed (document reason).