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Official Description

Infectious agent antigen detection by immunofluorescent technique; Bordetella pertussis/parapertussis

© Copyright 2026 American Medical Association. All rights reserved.

Common Language Description

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.

© Copyright 2026 Coding Ahead. All rights reserved.

1. Indications

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:

  • Whooping Cough Diagnosis The test is performed to confirm the presence of B. pertussis or B. parapertussis in patients exhibiting symptoms of whooping cough, which include severe coughing fits, inspiratory whoop, and post-tussive vomiting.
  • Respiratory Infection Evaluation It is utilized in the assessment of respiratory infections, especially in cases where the clinical presentation suggests a Bordetella infection.
  • Outbreak Investigation The test may be employed during outbreaks of whooping cough to identify the causative agents and implement appropriate public health measures.

2. Procedure

The procedure for performing the antigen detection test using CPT® Code 87265 involves several key steps:

  • Sample Collection A respiratory sample is obtained from the patient using one of three methods: a nasopharyngeal swab, aspirate, or washing. This step is critical as it ensures that the sample contains potential antigens from the pathogens being tested.
  • Sample Preparation Once the sample is collected, it is treated with a detecting reagent that contains specific antibodies targeting Bordetella pertussis and Bordetella parapertussis. A counterstain is also added to enhance visualization under the microscope.
  • Microscopic Examination The prepared sample is then examined under an epifluorescence microscope. During this examination, if B. pertussis or B. parapertussis antigens are present, the antibodies in the detecting reagent will bind to these antigens, resulting in a distinct color change that can be observed through the microscope.

3. Post-Procedure

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)
Date
Action
Notes
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.
Code
Description
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