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The CPT® Code 87265 refers to a laboratory test specifically designed for the detection of antigens associated with the infectious agents Bordetella pertussis and Bordetella parapertussis using an immunofluorescent technique. This test is crucial in diagnosing whooping cough, a highly contagious upper respiratory infection that manifests through severe coughing fits, an inspiratory whoop sound, and post-tussive vomiting. Bordetella pertussis is known for causing the more severe form of the disease, while Bordetella parapertussis typically results in milder symptoms and a shorter duration of illness, as it does not produce a toxin. Both pathogens can infect individuals simultaneously, complicating the clinical picture. The test is applicable across all age groups for B. pertussis infections, whereas B. parapertussis infections are predominantly observed in children under the age of 10. To perform the test, a respiratory sample is collected via nasopharyngeal swab, aspirate, or washing. This sample is then treated with a detecting reagent that contains specific antibodies targeting B. pertussis and B. parapertussis, along with a counterstain. The sample is examined under an epifluorescence microscope, where the presence of the antigens will result in a distinct color change due to the binding of antibodies to the antigens. While this immunofluorescent test offers a quicker turnaround time compared to traditional culture methods and reverse transcription-polymerase chain reaction (RT-PCR), it is important to note that it may be less sensitive in detecting the pathogens.
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The CPT® Code 87265 is indicated for the detection of Bordetella pertussis and Bordetella parapertussis antigens in respiratory samples. This test is particularly relevant in the following clinical scenarios:
The procedure for performing the antigen detection test using CPT® Code 87265 involves several key steps:
After the procedure, the laboratory will analyze the results of the immunofluorescent test. If the test indicates the presence of Bordetella pertussis or Bordetella parapertussis antigens, the healthcare provider will be informed, allowing for timely diagnosis and treatment of the patient. It is important to note that while this test provides rapid results, it may be less sensitive than culture methods or reverse transcription-polymerase chain reaction (RT-PCR). Therefore, clinicians may consider follow-up testing or additional diagnostic methods based on the clinical context and the patient's condition. Proper documentation of the test results and any subsequent actions taken is essential for patient care and compliance with healthcare regulations.
| Short Descr | PERTUSSIS AG IF | Medium Descr | IAADI BORDETELLA PRTUSSIS/PARAPRTUSSIS | Long Descr | Infectious agent antigen detection by immunofluorescent technique; Bordetella pertussis/parapertussis | 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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