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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; Entamoeba histolytica dispar group

© Copyright 2026 American Medical Association. All rights reserved.

Common Language Description

The CPT® Code 87336 refers to a laboratory test designed to detect the presence of antigens associated with the Entamoeba histolytica dispar group. This test employs various immunoassay techniques, including enzyme immunoassay (EIA), enzyme-linked immunosorbent assay (ELISA), fluorescence immunoassay (FIA), and immunochemiluminometric assay (IMCA). The primary purpose of this test is to identify the antigen in a fecal sample, which is crucial for diagnosing infections caused by this parasite. Entamoeba histolytica is known to be a pathogenic organism that can lead to serious health issues such as liver abscesses, intestinal inflammation, acute colitis, and in severe cases, toxic megacolon and peritonitis. Symptoms of infection typically manifest as abdominal pain and diarrhea. The transmission of this parasite can occur through sexual contact or ingestion of contaminated food and water. The Entamoeba histolytica species has two distinct morphological forms: a resilient, tetra-nucleated cyst that is infective, and a fragile trophozoite that can cause disease. While the E. histolytica dispar group is generally considered non-invasive and non-pathogenic, it can occasionally lead to diarrheal illnesses. In contrast, the E. histolytica group is more invasive and pathogenic, often linked to acute clinical presentations. For the test, a fecal sample is collected and either preserved in a fixative or sent fresh to the laboratory for analysis. The immunoassay techniques utilized in this test are sensitive and capable of detecting minute quantities of the antigen when it binds to its specific antibody. The detection process involves adding a secondary enzyme-labeled antibody, which facilitates a chromogenic reaction that results in a visible color change or fluorescence, allowing for qualitative or semi-quantitative assessment of the antigen's presence.

© Copyright 2026 Coding Ahead. All rights reserved.

1. Indications

The CPT® Code 87336 is indicated for the detection of antigens related to the Entamoeba histolytica dispar group in fecal samples. This test is performed under the following circumstances:

  • Abdominal Pain Patients presenting with abdominal pain that may suggest an underlying parasitic infection.
  • Diarrhea Individuals experiencing diarrhea, particularly when associated with potential exposure to contaminated food or water.
  • Potential Exposure Cases where there is a history of sexual transmission or ingestion of contaminated substances that could lead to infection.
  • Diagnostic Confirmation To confirm a diagnosis of Entamoeba histolytica infection, especially in symptomatic patients.

2. Procedure

The procedure for conducting the test under CPT® Code 87336 involves several key steps, which are outlined as follows:

  • Sample Collection A fecal sample is collected from the patient. This sample can either be placed in a fixative to preserve the integrity of the specimen or sent fresh to the laboratory for immediate processing.
  • Preparation of the Sample In the laboratory, the fecal sample is prepared for analysis. This may involve homogenizing the sample to ensure that any antigens present are evenly distributed for accurate testing.
  • Immunoassay Technique The prepared sample undergoes testing using one of the immunoassay techniques, such as EIA, ELISA, FIA, or IMCA. Each of these methods utilizes specific antibodies that bind to the Entamoeba histolytica dispar antigens if they are present in the sample.
  • Detection of Antigen In the case of EIA and ELISA, a secondary enzyme-labeled antibody is added to the sample. This antibody binds to the antigen-antibody complex, and a chromogenic reaction occurs, resulting in a color change that can be measured. For FIA, a fluorescent compound is used to detect the binding of the antibody to the antigen, while IMCA employs a chemiluminescent substance to quantify the antigen-antibody complex through light emission.
  • Result Interpretation The results of the test are assessed qualitatively or semi-quantitatively based on the colorimetric readings or fluorescence emitted, indicating the presence or absence of the antigen 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. The interpretation of the results will guide further clinical management and treatment decisions. If the test is positive, it may indicate an active infection with the Entamoeba histolytica dispar group, necessitating appropriate therapeutic interventions. In cases of negative results, further investigation may be warranted if clinical symptoms persist. It is essential for healthcare providers to consider the patient's clinical history and symptoms in conjunction with the test results for accurate diagnosis and treatment planning.

Short Descr ENTAMOEB HIST DISPR AG IA
Medium Descr IAAD IA ENTAMOEBA HISTOLYTICA DISPAR GRP
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; Entamoeba histolytica dispar group
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)
GA Waiver of liability statement issued as required by payer policy, individual case
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.
2001-01-01 Added First appearance in code book in 2001.
Code
Description
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