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Official Description

Antibody; rotavirus

© Copyright 2026 American Medical Association. All rights reserved.

Common Language Description

The CPT® Code 86759 refers to a laboratory test specifically designed to measure antibodies against rotavirus. Rotavirus is a significant pathogen that primarily affects infants and young children, leading to gastrointestinal illnesses characterized by symptoms such as diarrhea, vomiting, fever, and abdominal pain. These symptoms can be severe and may result in dehydration, which sometimes necessitates hospitalization for appropriate treatment. The test evaluates different types of antibodies: a positive IgM antibody titer indicates a recent infection, while a positive IgG titer suggests a past infection. However, in infants, the presence of IgG may also indicate the passive transfer of maternal antibodies, complicating the interpretation of results. Additionally, a positive IgA antibody titer is typically observed during the recovery phase following an infection. To conduct this test, a blood sample is collected through a procedure known as venipuncture, which is reported separately. The serum obtained from the blood sample is then analyzed for the presence of IgG, IgM, and IgA antibodies using an indirect enzyme immunoassay technique, providing valuable information regarding the patient's immune response to rotavirus.

© Copyright 2026 Coding Ahead. All rights reserved.

1. Indications

The antibody test for rotavirus (CPT® Code 86759) is indicated for the following conditions:

  • Gastrointestinal Illness The test is performed when a patient presents with symptoms of gastrointestinal illness, particularly in infants and young children, which may include diarrhea, vomiting, fever, and abdominal pain.
  • Dehydration Risk It is indicated in cases where the symptoms may lead to dehydration, necessitating further evaluation and potential hospitalization for treatment.
  • Recent Infection Assessment The test is used to determine if there has been a recent rotavirus infection, as indicated by a positive IgM antibody titer.
  • Past Infection Evaluation It is also indicated for assessing past infections through the measurement of IgG antibodies, although interpretation in infants may require consideration of maternal antibody transfer.
  • Convalescent Phase Monitoring The test may be utilized to monitor patients during the convalescent phase of rotavirus infection, where a positive IgA antibody titer is expected.

2. Procedure

The procedure for conducting the rotavirus antibody test (CPT® Code 86759) involves several key steps:

  • Step 1: Patient Preparation Prior to the test, the patient may be prepared by explaining the procedure and ensuring that they understand the purpose of the test. In pediatric cases, it is essential to reassure both the child and the guardians to minimize anxiety.
  • Step 2: Venipuncture A qualified healthcare professional performs venipuncture to obtain a blood sample. This involves using a sterile needle to access a vein, typically in the arm, and collecting the blood into a designated collection tube. Proper technique is crucial to minimize discomfort and ensure a successful draw.
  • Step 3: Serum Separation After blood collection, the sample is processed to separate the serum from the cellular components. This is typically done by centrifugation, which spins the blood at high speeds to allow the serum to rise to the top of the tube.
  • Step 4: Antibody Testing The separated serum is then subjected to testing for the presence of IgG, IgM, and IgA antibodies against rotavirus. This is accomplished using an indirect enzyme immunoassay, which detects the antibodies based on their binding to specific antigens in the test system.
  • Step 5: Result Interpretation Once the testing is complete, the results are interpreted by a qualified laboratory professional. The presence of specific antibodies is evaluated to determine the patient's immune response to rotavirus, and the findings are documented for clinical review.

3. Post-Procedure

After the rotavirus antibody test is completed, the patient may be monitored briefly to ensure there are no immediate adverse reactions to the venipuncture. The healthcare provider will typically provide instructions regarding any necessary follow-up based on the test results. If the test indicates a recent infection or significant antibody levels, further clinical evaluation and management may be warranted. Additionally, the patient may be advised on signs of dehydration or worsening symptoms that would require immediate medical attention. The results of the test will be communicated to the patient or their guardians, along with any recommendations for further testing or treatment as needed.

Short Descr ROTAVIRUS ANTIBODY
Medium Descr ANTIBODY ROTAVIRUS
Long Descr Antibody; rotavirus
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
Date
Action
Notes
1993-01-01 Added First appearance in code book in 1993.
Code
Description
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