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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; Chlamydia trachomatis

© Copyright 2026 American Medical Association. All rights reserved.

Common Language Description

The CPT® Code 87320 refers to the detection of the infectious agent Chlamydia trachomatis through various immunoassay techniques. This procedure involves testing a specimen for the presence of antigens associated with Chlamydia trachomatis, a bacterium responsible for a common sexually transmitted infection (STI). The testing methods utilized in this code include enzyme immunoassay (EIA), enzyme-linked immunosorbent assay (ELISA), fluorescence immunoassay (FIA), and immunochemiluminometric assay (IMCA). These techniques are designed to identify the presence of specific antigens in a sample, which can be obtained from cervical, urethral, or rectal swabs. Chlamydia trachomatis infections often go unnoticed as they frequently do not present any symptoms, particularly in women, which can lead to serious long-term health issues such as infertility due to damage to the reproductive tract. In men, while symptoms may include burning and itching sensations in the urethra, they are less likely to experience reproductive complications. The immunoassay techniques employed in this procedure are sensitive and capable of detecting even minute quantities of the antigen. For instance, EIA and ELISA work by binding the antigen to a specific antibody and then using a secondary enzyme-labeled antibody to produce a color change or fluorescence, indicating the presence of the antigen. Similarly, FIA utilizes a fluorescent compound to detect the binding of the antibody to the antigen, while IMCA employs chemiluminescent substances to quantify the antigen-antibody complex through light emission. This comprehensive approach to testing is crucial for the timely diagnosis and management of Chlamydia trachomatis infections.

© Copyright 2026 Coding Ahead. All rights reserved.

1. Indications

The procedure associated with CPT® Code 87320 is indicated for the detection of Chlamydia trachomatis in patients who may be at risk for this sexually transmitted infection. The following conditions and symptoms warrant the use of this immunoassay technique:

  • Asymptomatic Screening Individuals who are asymptomatic but are at risk for Chlamydia trachomatis infection, particularly sexually active women under 25 years of age and men who have sex with men.
  • Symptomatic Patients Patients presenting with symptoms such as abnormal vaginal discharge, pelvic pain, or urethral discharge, which may suggest a Chlamydia infection.
  • Contact Tracing Individuals who have had sexual contact with a confirmed case of Chlamydia trachomatis infection.
  • Follow-Up Testing Patients who have been previously treated for Chlamydia trachomatis to confirm the resolution of the infection.

2. Procedure

The procedure for CPT® Code 87320 involves several key steps to ensure accurate detection of Chlamydia trachomatis antigens. The following procedural steps are outlined:

  • Step 1: Specimen Collection A specimen is collected from the patient, which may include a cervical, urethral, or rectal swab. The choice of specimen type depends on the patient's symptoms and risk factors. Proper collection techniques are essential to obtain a viable sample for testing.
  • Step 2: Sample Preparation The collected specimen is prepared for analysis. This may involve the addition of specific reagents that facilitate the binding of the Chlamydia trachomatis antigens to the antibodies used in the immunoassay.
  • Step 3: Immunoassay Technique Application The prepared sample undergoes testing using one of the immunoassay techniques: EIA, ELISA, FIA, or IMCA. Each method employs specific antibodies that bind to the Chlamydia antigens present in the sample. The choice of technique may depend on laboratory capabilities and the required sensitivity of the test.
  • Step 4: Detection and Interpretation After the immunoassay is performed, the results are analyzed. For EIA and ELISA, a color change or fluorescence indicates the presence of the antigen, while FIA uses fluorescent compounds for detection. IMCA quantifies the antigen-antibody complex through light emission. The results are then interpreted as either qualitative (positive or negative) or semi-quantitative based on the intensity of the reaction.

3. Post-Procedure

Post-procedure care for patients undergoing testing with CPT® Code 87320 typically involves providing the patient with their test results and any necessary follow-up actions. If the test result is positive, the patient may require further evaluation and treatment for Chlamydia trachomatis infection. Counseling on safe sexual practices and the importance of notifying sexual partners may also be recommended to prevent reinfection and further transmission. In cases of negative results, patients may still be advised to undergo regular screenings, especially if they remain at risk for STIs. Additionally, healthcare providers should document the results and any follow-up plans in the patient's medical record to ensure continuity of care.

Short Descr CHLMYD TRACH AG IA
Medium Descr IAAD IA CHLAMYDIA TRACHOMATIS
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; Chlamydia trachomatis
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)
Date
Action
Notes
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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