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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 B surface antigen (HBsAg), quantitative

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Common Language Description

Quantitative hepatitis B surface antigen (HBsAg) testing is a laboratory procedure that measures the concentration of hepatitis B surface antigen in a patient's blood. This antigen is a protein produced by the hepatitis B virus (HBV) and is an important marker for diagnosing and monitoring hepatitis B infection. The test is performed using various immunoassay techniques, including enzyme immunoassay (EIA), enzyme-linked immunosorbent assay (ELISA), fluorescence immunoassay (FIA), and immunochemiluminometric assay (IMCA). The quantitative aspect of the test provides valuable information regarding the viral load, which is crucial for assessing the effectiveness of treatment in patients with chronic hepatitis B. By determining the amount of HBsAg present, healthcare providers can evaluate a patient's response to antiviral therapies, such as peginterferon alfa-2a, and make informed decisions about continuing, adjusting, or discontinuing treatment based on the likelihood of achieving a virological response. This test is typically utilized for patients who have already been diagnosed with hepatitis B, allowing for ongoing management of their condition.

© Copyright 2026 Coding Ahead. All rights reserved.

1. Indications

Quantitative hepatitis B surface antigen (HBsAg) testing is indicated for patients who have a confirmed diagnosis of hepatitis B infection. The test is particularly useful in the following scenarios:

  • Monitoring Treatment Response This test helps assess how well a patient is responding to antiviral therapy for chronic hepatitis B infection.
  • Evaluating Relapse It is used to determine if there is a relapse in patients undergoing prolonged antiviral therapy.
  • Guiding Treatment Decisions The results can inform decisions about whether to continue current treatment, switch to another antiviral medication, or discontinue treatment to avoid unnecessary side effects.

2. Procedure

The procedure for conducting quantitative hepatitis B surface antigen (HBsAg) testing involves several key steps:

  • Sample Collection A blood sample is drawn from the patient, typically from a vein in the arm. This sample is essential for the subsequent testing process.
  • Sample Preparation The collected blood is processed in the laboratory to separate the serum, which contains the HBsAg. This step is crucial for accurate measurement.
  • Immunoassay Technique The serum is then subjected to an immunoassay technique, such as immunochemiluminometric assay (IMCA), to detect and quantify the presence of HBsAg. This technique utilizes specific antibodies that bind to the HBsAg, allowing for its measurement.
  • Result Interpretation After the assay is completed, the results are analyzed to determine the concentration of HBsAg in the serum. These results are then reported to the healthcare provider for further evaluation.

3. Post-Procedure

After the quantitative hepatitis B surface antigen (HBsAg) testing procedure, patients may not require any specific post-procedure care. However, it is important for healthcare providers to discuss the results with the patient, as these results can significantly impact treatment decisions. Patients should be informed about the implications of their HBsAg levels, including the potential need for adjustments in their antiviral therapy. Additionally, healthcare providers may recommend follow-up testing, such as HBV DNA viral load measurements, to further assess the patient's condition and treatment response.

Short Descr HEPATITIS B SURFACE AG QUAN
Medium Descr HEPATITIS B SURFACE ANTIGEN QUANTITATIVE
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 B surface antigen (HBsAg), quantitative
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) none
MUE 1
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.
26 Professional component: certain procedures are a combination of a physician or other qualified health care professional component and a technical component. when the physician or other qualified health care professional component is reported separately, the service may be identified by adding modifier 26 to the usual procedure number.
GA Waiver of liability statement issued as required by payer policy, individual case
GY Item or service statutorily excluded, does not meet the definition of any medicare benefit or, for non-medicare insurers, is not a contract benefit
GZ Item or service expected to be denied as not reasonable and necessary
Date
Action
Notes
2023-01-01 Added Code added.
Code
Description
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