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Official Description

Infectious agent antigen detection by immunoassay technique, (eg, enzyme immunoassay [EIA], enzyme-linked immunosorbent assay [ELISA], fluorescence immunoassay [FIA], immunochemiluminometric assay [IMCA]) qualitative or semiquantitative; hepatitis, delta agent

© Copyright 2026 American Medical Association. All rights reserved.

Common Language Description

The CPT® Code 87380 refers to a laboratory test designed to detect the presence of the hepatitis delta agent antigen in a blood sample using various immunoassay techniques. This test is crucial for identifying the hepatitis D virus (HDV), which is a defective RNA virus that can only replicate in the presence of the hepatitis B virus (HBV). The hepatitis delta agent is not structurally related to the hepatitis A, B, or C viruses, making it unique in its pathology. The presence of HDV can lead to severe liver complications, particularly in individuals who are already infected with HBV, potentially resulting in conditions such as fulminant acute hepatitis, cirrhosis, and hepatocellular carcinoma. To perform this test, a blood sample is collected and either placed in a fixative or sent fresh to a laboratory for analysis. The immunoassay techniques utilized in this test include enzyme immunoassay (EIA), enzyme-linked immunosorbent assay (ELISA), fluorescence immunoassay (FIA), and immunochemiluminometric assay (IMCA). Each of these methods employs specific mechanisms to detect the antigen. For instance, EIA and ELISA work by binding the antigen to a specific antibody and then adding a secondary enzyme-labeled antibody, which produces a color change or fluorescence detectable through colorimetric reading. FIA, on the other hand, uses a fluorescent compound to identify the binding of the detection antibody to the antigen, while IMCA relies on chemiluminescent substances to quantify the antigen-antibody complex through light emission. The test can yield qualitative or semi-quantitative results, providing essential information for the diagnosis and management of hepatitis D infections.

© Copyright 2026 Coding Ahead. All rights reserved.

1. Indications

The CPT® Code 87380 is indicated for the detection of the hepatitis delta agent antigen in patients who are suspected of having a hepatitis D virus infection. The following conditions may warrant the use of this test:

  • Hepatitis B Co-infection Patients who are already infected with hepatitis B virus (HBV) and exhibit symptoms of liver disease may require this test to determine the presence of the hepatitis delta agent, which can exacerbate their condition.
  • Acute Hepatitis Symptoms Individuals presenting with acute hepatitis symptoms, such as jaundice, fatigue, and abdominal pain, may be tested to identify the cause of their liver inflammation, including the possibility of HDV infection.
  • Chronic Hepatitis B Monitoring Patients with chronic hepatitis B may be monitored for the presence of the delta agent, as its detection can indicate a more severe disease progression and the need for more aggressive management.

2. Procedure

The procedure for conducting the test under CPT® Code 87380 involves several key steps to ensure accurate detection of the hepatitis delta agent antigen:

  • Step 1: Sample Collection A blood sample is obtained from the patient, typically through venipuncture. This sample is crucial for the subsequent analysis and must be handled with care to maintain its integrity.
  • Step 2: Sample Preparation The collected blood sample is either placed in a fixative to preserve the antigen or sent fresh to the laboratory for processing. Proper handling is essential to prevent degradation of the antigen.
  • Step 3: Immunoassay Technique Application The laboratory technician employs one of the immunoassay techniques—EIA, ELISA, FIA, or IMCA—to detect the hepatitis delta antigen. Each method involves specific reagents and procedures to bind the antigen to antibodies.
  • Step 4: Detection and Measurement After the binding process, a secondary enzyme-labeled antibody is added in EIA and ELISA methods, which produces a color change or fluorescence. In FIA, a fluorescent compound is used, while IMCA utilizes chemiluminescent substances. The resulting reaction is measured to determine the presence and quantity of the antigen.
  • Step 5: Result Interpretation The results are assessed qualitatively or semi-quantitatively based on the colorimetric readings or fluorescence emitted, providing critical information regarding the presence of the hepatitis delta agent in the sample.

3. Post-Procedure

After the completion of the test, the laboratory will analyze the results and report them to the requesting physician. It is important for healthcare providers to interpret the results in the context of the patient's clinical history and symptoms. If the hepatitis delta agent is detected, further evaluation and management may be necessary, particularly for patients with existing hepatitis B infection. Follow-up care may include additional testing, monitoring liver function, and discussing treatment options based on the severity of the disease. Patients should be informed about the significance of the results and any necessary lifestyle or medical adjustments that may be required.

Short Descr HEPATITIS DELTA AGENT AG IA
Medium Descr IAAD IA HEPATITIS DELTA ANTIGEN
Long Descr Infectious agent antigen detection by immunoassay technique (eg, enzyme immunoassay [EIA], enzyme-linked immunosorbent assay [ELISA], fluorescence immunoassay [FIA], immunochemiluminometric assay [IMCA]), qualitative or semiquantitative; hepatitis, delta agent
Status Code Statutory Exclusion (from MPFS, may be paid under other methodologies)
Global Days XXX - Global Concept Does Not Apply
PC/TC Indicator (26, TC) 9 - Not Applicable
Multiple Procedures (51) 9 - Concept does not apply.
Bilateral Surgery (50) 9 - Concept does not apply.
Physician Supervisions 09 - Concept does not apply.
Assistant Surgeon (80, 82) 9 - Concept does not apply.
Co-Surgeons (62) 9 - Concept does not apply.
Team Surgery (66) 9 - Concept does not apply.
Diagnostic Imaging Family 99 - Concept Does Not Apply
CLIA Waived (QW) No
APC Status Indicator Conditionally packaged laboratory tests
Type of Service (TOS) 5 - Diagnostic Laboratory
Berenson-Eggers TOS (BETOS) T1H - Lab tests - other (non-Medicare fee schedule)
MUE 1
CCS Clinical Classification 206 - Microscopic examination (bacterial smear, culture, toxicology)
90 Reference (outside) laboratory: when laboratory procedures are performed by a party other than the treating or reporting physician or other qualified health care professional, the procedure may be identified by adding modifier 90 to the usual procedure number.
Date
Action
Notes
2024-01-01 Changed Guideline information changed.
2022-01-01 Changed First appearance of change in codebook.
2022-01-01 Note Grammatical correction.
2021-01-01 Changed First appearance of change in CPT® Code Set.
2020-10-06 Changed Code changed.
2016-01-01 Changed Description Changed
2011-01-01 Changed Short description changed.
2007-01-01 Changed Code description changed.
1998-01-01 Added First appearance in code book in 1998.
Code
Description
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