Summary & Overview
CPT 84106: Urine Porphobilinogen (PBG) Test
CPT code 84106 identifies a laboratory assay for porphobilinogen (PBG) in a urine specimen, a key diagnostic test in evaluating suspected porphyria and acute metabolic disorders. Nationally, accurate PBG testing supports timely diagnosis and management of conditions that can lead to serious neurological and systemic symptoms, making correct coding and lab reporting important for clinical workflows and billing compliance.
This analysis covers coverage and billing considerations among major national payers: Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise overview of what CPT code 84106 represents, typical sites of service, and the clinical context for ordering the test. The publication outlines common payer coverage themes, benchmark considerations, and coding guidance related to lab service lines. It also highlights where input data is unavailable and flags topics that may require payer-specific policy lookup.
Intended for coding professionals, lab managers, and health policy analysts, the content helps users understand the clinical purpose of the test, expectations for where it is performed, and which national payers are most relevant for coverage and reimbursement inquiries.
Billing Code Overview
CPT code 84106 describes a laboratory test performed by a lab analyst to detect porphobilinogen (PBG) in a urine specimen. The procedure assesses the presence of PBG, a biochemical marker used in the evaluation of suspected porphyrias and related metabolic disorders.
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Service type: Clinical laboratory test (qualitative or quantitative assay for PBG in urine)
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Typical site of service: Clinical laboratory or hospital laboratory, with specimen collection performed in outpatient clinics, inpatient settings, or ambulatory collection sites
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Clinical & Coding Specifications
Clinical Context
A 28-year-old adult presents to an urgent care clinic with episodic abdominal pain, nausea, vomiting, and new-onset dark urine. The clinician obtains a random urine specimen during the visit and orders testing for porphobilinogen to evaluate for acute intermittent porphyria during an acute symptomatic episode. The specimen is sent to the outpatient laboratory; the lab analyst performs a qualitative or quantitative assay to detect porphobilinogen in urine using a colorimetric or chromatographic method. Results are reported to the ordering clinician, who uses the result to guide further evaluation, urgent management, and possible referral to a metabolic or neurology specialist. Typical site of service is an outpatient clinic, urgent care, or hospital outpatient laboratory where specimens are collected and analyzed. The service type is a clinical laboratory procedure for biochemical diagnostic testing of urine for porphobilinogen, billed under 84106.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
26 | Professional component | Use when billing only the professional interpretation component separate from the technical laboratory processing, if applicable. |
TC |