Summary & Overview
CPT 0018U: ThyraMIR microRNA Thyroid Cancer Risk Assay
CPT code 0018U identifies ThyraMIR, a Proprietary Laboratory Analyses (PLA) molecular diagnostic that analyzes 10 microRNA sequences from a thyroid fine needle aspirate (FNA) and applies an algorithm using patient data to report a positive or negative result for increased thyroid cancer risk. PLA codes matter nationally because they uniquely identify manufacturer- or laboratory-specific tests, enabling payers and providers to track utilization, coverage, and clinical adoption of proprietary diagnostics.
Key payers included in the national coverage context are Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find an overview of the clinical purpose of the assay, the typical service context, and what to expect in payer coverage discussions. The publication summarizes available benchmarks for utilization and reimbursement where reported, highlights policy and coding considerations relevant to PLA codes, and situates the test within thyroid nodule diagnostic workflows. It also outlines common billing modifiers and administrative items for operational planning.
Data not available in the input for associated taxonomies, specific ICD-10 mappings, related codes, and a detailed payer-by-payer coverage matrix.
Billing Code Overview
CPT code 0018U is a Proprietary Laboratory Analyses (PLA) code that describes ThyraMIR by Interpace Diagnostics. The test performs a gene analysis of 10 microRNA sequences from a thyroid fine needle aspirate (FNA) specimen and combines those laboratory results with patient data through an algorithm to report a positive or negative finding for increased thyroid cancer risk.
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Service type: Molecular diagnostic laboratory test with algorithmic interpretation
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Typical site of service: Clinical laboratory processing FNA specimens; results used in outpatient endocrine, cytology, or pathology settings
Clinical & Coding Specifications
Clinical Context
A typical patient is a 35–70-year-old adult presenting to an endocrinologist or otolaryngologist with a thyroid nodule identified on clinical exam or ultrasound. Ultrasound-guided fine needle aspiration (FNA) is performed and cytology returns an indeterminate result (for example, Bethesda category III: atypia of undetermined significance/follicular lesion of undetermined significance, or Bethesda IV: follicular neoplasm/suspicious for a follicular neoplasm). The treating clinician sends residual FNA material or a dedicated FNA specimen to a reference laboratory for molecular testing using the ThyraMIR assay (0018U).
The laboratory receives the FNA specimen, extracts RNA, measures expression of the panel of 10 microRNA sequences, and combines the molecular results with available clinical data through the proprietary algorithm to generate a report indicating increased or decreased risk of thyroid malignancy. The result is returned to the ordering provider, who integrates it with cytology, ultrasound features, patient risk factors, and patient preferences to inform management (surveillance versus diagnostic/therapeutic surgery). Typical sites of service are outpatient clinics, ambulatory surgery centers for the FNA procedure, and independent or hospital-based clinical reference laboratories for the 0018U assay. Billing is performed by the laboratory using the PLA code 0018U with appropriate specimen source and specimen collection documentation retained in the medical record.
Coding Specifications
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