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The CPT® Code 87285 refers to a specific laboratory test that detects the presence of the infectious agent Treponema pallidum, which is the bacterium responsible for causing syphilis. This test employs an immunofluorescent technique, a method that utilizes fluorescently labeled antibodies to identify the antigen associated with T. pallidum in a specimen. Syphilis is classified as a sexually transmitted disease (STD) and can have serious health implications if left untreated. The test is particularly significant in diagnosing primary syphilis, where a characteristic sore known as a chancre forms at the site of infection. In certain cases, such as when congenital syphilis is suspected, tissue samples from the umbilical cord may also be analyzed. The importance of this test is underscored by the potential consequences of undiagnosed syphilis during pregnancy, which can lead to severe outcomes for the infant, including stillbirth or immediate postnatal death. Additionally, untreated infants may face long-term developmental challenges. The immunofluorescent antigen detection process involves scraping the suspicious lesion to collect a specimen, followed by the application of a specific reagent that binds to the T. pallidum antigen. After incubation, the specimen is examined under a fluorescence microscope, where positive results are indicated by the appearance of bright green or orange-yellow fluorescence, signifying successful antigen-antibody binding.
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The test coded as CPT® 87285 is indicated for the detection of Treponema pallidum in various clinical scenarios, particularly when there is a suspicion of syphilis. The following conditions warrant the performance of this test:
The procedure for performing the test under CPT® 87285 involves several critical steps to ensure accurate detection of the T. pallidum antigen. The following outlines the procedural steps:
Post-procedure care for patients undergoing the test coded as CPT® 87285 typically involves no specific requirements, as the test is minimally invasive and does not necessitate recovery time. However, it is essential for healthcare providers to communicate the results to the patient promptly. If the test result is positive, further evaluation and treatment for syphilis should be initiated, including counseling on the implications of the diagnosis and potential treatment options. Additionally, if congenital syphilis is suspected, appropriate follow-up care for the infant should be arranged to address any potential health issues arising from the infection.
| Short Descr | TREPONEMA PALLIDUM AG IF | Medium Descr | IAADI TREPONEMA PALLIDUM | Long Descr | Infectious agent antigen detection by immunofluorescent technique; Treponema pallidum | 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) |
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| 2011-01-01 | Changed | Short description changed. |
| 2001-01-01 | Changed | Code description changed. |
| 1998-01-01 | Added | First appearance in code book in 1998. |
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