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The CPT® Code 87260 refers to a laboratory test specifically designed for the detection of adenovirus antigens using an immunofluorescent technique. Adenoviruses are a group of more than 50 viruses that can cause a variety of illnesses in humans, categorized into six distinct species (A-F). These viruses are known to lead to conditions such as gastroenteritis, respiratory illnesses (including colds, croup, bronchitis, and pneumonia), conjunctivitis, hemorrhagic cystitis, and skin rashes. The test is performed on respiratory or fecal samples, which can be collected through various methods. For respiratory samples, collection techniques include nasopharyngeal swabs, aspirates, or washings, as well as bronchoalveolar lavage (BAL) or tracheal aspirates. Fecal samples can be obtained via rectal swabs or stool sampling. During the test, the collected sample is inoculated with antibodies that are specifically conjugated to fluorescein isothiocyanate, a fluorescent dye. The sample is then examined under an epifluorescence microscope. If adenovirus antigens are present, the antibodies will bind to these antigens, resulting in a bright green fluorescence in the cytoplasm and/or nuclei of the infected cells. In contrast, non-infected surrounding cells will exhibit a dull red fluorescence. This immunofluorescent test is valuable for diagnosing acute adenoviral infections and can also help identify asymptomatic carriers, as active adenovirus can be shed in respiratory secretions and feces for extended periods, sometimes lasting weeks or months.
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The CPT® Code 87260 is indicated for the detection of adenovirus antigens in patients presenting with symptoms associated with adenoviral infections. The following conditions may warrant the use of this test:
The procedure for the CPT® Code 87260 involves several critical steps to ensure accurate detection of adenovirus antigens. The following procedural steps are outlined:
After the procedure, the laboratory will analyze the results and report the findings. If adenovirus antigens are detected, this may confirm an active infection, which can assist in guiding treatment decisions. It is important to note that adenovirus can be shed in respiratory secretions and feces for weeks or even months, which may have implications for infection control and public health measures. Clinicians should consider follow-up testing or monitoring in cases where asymptomatic carriers are identified.
| Short Descr | ADENOVIRUS AG IF | Medium Descr | IAADI ADENOVIRUS | Long Descr | Infectious agent antigen detection by immunofluorescent technique; adenovirus | 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. | GV | Attending physician not employed or paid under arrangement by the patient's hospice provider | 59 | Distinct procedural service: under certain circumstances, it may be necessary to indicate that a procedure or service was distinct or independent from other non-e/m services performed on the same day. modifier 59 is used to identify procedures/services, other than e/m services, that are not normally reported together, but are appropriate under the circumstances. documentation must support a different session, different procedure or surgery, different site or organ system, separate incision/excision, separate lesion, or separate injury (or area of injury in extensive injuries) not ordinarily encountered or performed on the same day by the same individual. however, when another already established modifier is appropriate it should be used rather than modifier 59. only if no more descriptive modifier is available, and the use of modifier 59 best explains the circumstances, should modifier 59 be used. note: modifier 59 should not be appended to an e/m service. to report a separate and distinct e/m service with a non-e/m service performed on the same date, see modifier 25. |
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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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