Summary & Overview
CPT 80332: Detection of One or Two Serotonergic Antidepressants
CPT code 80332 represents a laboratory assay that detects or measures one or two serotonergic antidepressants in a patient specimen. This code covers targeted toxicology/therapeutic drug monitoring for psychiatric medications that influence serotonin, and it matters nationally because such testing supports medication management, safety monitoring, and forensic or compliance evaluations across outpatient and inpatient settings. Payers commonly involved in coverage considerations include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare.
Readers will find an overview of clinical context and use cases for 80332, how the service is typically delivered in clinical laboratories, and the implications for billing and claims submission. The publication includes benchmarking and coverage considerations for major national payers listed above, summaries of common modifiers and claim components, and guidance on coding specificity for single versus dual-analyte assays. It also outlines the typical sites of service and the role of these assays in psychiatric medication management and safety monitoring. Data not available in the input is noted where applicable.
Billing Code Overview
CPT code 80332 describes a laboratory test in which a lab analyst measures the amount of or detects the presence of one or two serotonergic antidepressants in a patient specimen. This service is a therapeutic drug monitoring / toxicology assay focused on commonly used psychiatric medications that act on serotonin pathways.
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Service type: Laboratory testing for drug detection/quantification
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Typical site of service: Clinical laboratory or hospital laboratory; specimens collected in outpatient clinics, inpatient settings, or other collection sites as appropriate
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Clinical & Coding Specifications
Clinical Context
A 34-year-old adult patient receiving care in an outpatient psychiatric clinic presents for therapeutic drug monitoring after initiating or adjusting therapy with a selective serotonin reuptake inhibitor (SSRI) or serotonin–norepinephrine reuptake inhibitor (SNRI). The prescriber requests quantitative/qualitative laboratory testing to detect the presence or measure the concentration of one or two serotonergic antidepressants in serum or plasma to assess adherence, potential toxicity, drug interactions, or unexpected lack of therapeutic effect. The specimen is collected in the clinic or an outpatient phlebotomy draw station, labeled, and sent to a clinical laboratory. The laboratory performs the assay using immunoassay or mass spectrometry methods, documents results in the electronic medical record, and reports levels to the ordering clinician who integrates findings with clinical assessment and medication history.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
26 | Professional component | Use when billing only the professional interpretation component of a split pathology/lab service, if applicable under local policies. |
90 | Reference (outside) laboratory | Use when testing is performed by an outside independent reference lab and the billing provider is the ordering/principal lab. |