Summary & Overview
CPT 80365: Oxycodone Detection and Quantification Assay
CPT code 80365 represents a lab-based assay to detect or measure oxycodone in a patient specimen. As oxycodone is a commonly prescribed synthetic opioid, assays that identify its presence or quantify levels support clinical decisions about pain management, opioid stewardship, and toxicology evaluation. Nationally, utilization of targeted opioid assays factors into outpatient and inpatient management of pain, pre-procedural screening, and suspected overdose or misuse assessments.
Key payers addressed in this analysis include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise overview of the code’s clinical purpose and typical sites of service, plus benchmarking context where available. The publication outlines common modifiers and payer coverage patterns, notes clinical scenarios where the assay is applied, and highlights coding relationships relevant to laboratory billing workflows.
This summary provides practical context for revenue cycle, laboratory management, and clinical teams seeking to understand how CPT code 80365 is used in practice, what payers commonly cover, and where this test fits within toxicology and therapeutic drug monitoring services. Data not available in the input.
Billing Code Overview
CPT code 80365 describes a laboratory assay in which the analyst measures the amount of or detects the presence of oxycodone, a synthetic opioid pain medication, in a patient specimen. This service is a toxicology/therapeutic drug monitoring assay focused specifically on oxycodone detection and quantification.
Service Type: Laboratory diagnostic test — drug of abuse/toxicology assay
Typical Site of Service: Clinical laboratory or hospital laboratory
Clinical & Coding Specifications
Clinical Context
A typical patient scenario involves a clinician ordering a urine or blood toxicology test to detect and/or quantify oxycodone in a patient who is receiving opioid therapy, presents with suspected overdose, reports inadequate pain control, or is being monitored for compliance in a controlled-substance agreement. The specimen is collected in an outpatient clinic, emergency department, inpatient hospital, or an independent clinical laboratory. The specimen is routed to the laboratory where a technologist performs an analytical assay (e.g., immunoassay screening followed by confirmatory testing such as gas chromatography–mass spectrometry or liquid chromatography–tandem mass spectrometry) to detect the presence and/or measure the concentration of oxycodone. Results are reported to the ordering provider and incorporated into the patient’s medical record to inform clinical decisions about analgesic management, safety, or diversion concerns.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
26 | Professional component | Use when billing only the professional component of laboratory testing separate from the technical component. |
90 | Reference (outside) laboratory | Use when the testing is performed by an outside/reference laboratory and billed by the ordering lab/provider. |