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Official Description

Antibody; Yersinia

© Copyright 2026 American Medical Association. All rights reserved.

Common Language Description

The CPT® Code 86793 refers to the laboratory test for the detection of antibodies against Yersinia, a genus of bacteria known for causing serious infections, including bubonic plague. This test is performed on a blood sample collected from the patient. The presence of antibodies indicates that the immune system has responded to an infection by Yersinia, suggesting either a current or past infection. The test is crucial for diagnosing infections caused by this bacterium, which can lead to severe health complications if not identified and treated promptly. Understanding the immune response through antibody testing is essential for healthcare providers in determining the appropriate course of treatment and management for affected individuals.

© Copyright 2026 Coding Ahead. All rights reserved.

1. Indications

The antibody test for Yersinia (CPT® Code 86793) is indicated for the following conditions:

  • Suspected Yersinia Infection The test is performed when a patient presents with symptoms suggestive of an infection caused by Yersinia, such as fever, abdominal pain, and swollen lymph nodes.
  • Exposure History Individuals who have been in contact with confirmed cases of Yersinia infection or have been in areas where the bacteria are prevalent may be tested to determine if they have developed antibodies.
  • Diagnostic Confirmation The test aids in confirming a diagnosis of bubonic plague or other Yersinia-related infections, particularly in patients exhibiting clinical signs consistent with these diseases.

2. Procedure

The procedure for testing antibodies to Yersinia involves several key steps:

  • Sample Collection A healthcare professional collects a blood sample from the patient, typically via venipuncture. This process involves inserting a needle into a vein, usually in the arm, to draw a sufficient volume of blood for testing.
  • Sample Preparation Once the blood sample is collected, it is processed in the laboratory. This may involve centrifugation to separate the serum from the blood cells, as the serum is required for the antibody testing.
  • Testing Methodology The laboratory performs the antibody test using specific immunological techniques, such as enzyme-linked immunosorbent assay (ELISA) or indirect immunofluorescence, to detect the presence of antibodies against Yersinia in the serum sample.
  • Result Interpretation After the testing is completed, the laboratory analyzes the results. A positive result indicates the presence of antibodies, suggesting a current or past infection with Yersinia, while a negative result suggests no detectable antibodies.

3. Post-Procedure

After the antibody test for Yersinia is performed, the patient may experience minimal discomfort at the site of blood collection, which typically resolves quickly. There are no specific post-procedure care instructions required for this test. However, patients should be informed about the potential for receiving results that may require further clinical evaluation or treatment based on the presence of antibodies. It is essential for healthcare providers to discuss the implications of the test results with the patient, including any necessary follow-up actions or additional testing that may be warranted based on the findings.

Short Descr YERSINIA ANTIBODY
Medium Descr ANTIBODY YERSINIA
Long Descr Antibody; Yersinia
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 2
CCS Clinical Classification 235 - Other Laboratory
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.
91 Repeat clinical diagnostic laboratory test: in the course of treatment of the patient, it may be necessary to repeat the same laboratory test on the same day to obtain subsequent (multiple) test results. under these circumstances, the laboratory test performed can be identified by its usual procedure number and the addition of modifier 91. note: this modifier may not be used when tests are rerun to confirm initial results; due to testing problems with specimens or equipment; or for any other reason when a normal, one-time, reportable result is all that is required. this modifier may not be used when other code(s) describe a series of test results (eg, glucose tolerance tests, evocative/suppression testing). this modifier may only be used for laboratory test(s) performed more than once on the same day on the same patient.
Date
Action
Notes
1993-01-01 Added First appearance in code book in 1993.
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Description
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