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Official Description

Antibody; Haemophilus influenza

© Copyright 2026 American Medical Association. All rights reserved.

Common Language Description

The CPT® Code 86684 refers to a laboratory test that measures the presence of antibodies against Haemophilus influenzae type B (HIB) in a patient's blood. This test specifically evaluates the IgG antibodies, which are crucial for determining the immune response to the HIB vaccine. The assessment of these antibodies is particularly important in understanding a patient's immune status, especially after vaccination, and can be instrumental in diagnosing immunodeficiency response syndromes. Haemophilus influenzae is a significant encapsulated bacterium known for its potential to cause severe infections, particularly in vulnerable populations such as children under five years of age. Among the six identified types of this bacterium (A-F), type B is the most prevalent and is associated with serious health conditions, including meningitis, bacteremia, cellulitis, epiglottitis, pneumonia, and septic arthritis. The test is performed by obtaining a blood sample through venipuncture, which is a separately reportable procedure. The serum obtained from the blood sample is then analyzed using an enzyme-linked immunosorbent assay (ELISA), a common laboratory technique used to detect and quantify proteins, such as antibodies, in the serum.

© Copyright 2026 Coding Ahead. All rights reserved.

1. Indications

The antibody test for Haemophilus influenzae type B (HIB) is indicated for several specific clinical scenarios, particularly in assessing the immune response to vaccination and evaluating potential immunodeficiency. The following conditions may warrant the use of this test:

  • Post-Vaccination Assessment This test is performed to determine the immune status of a patient following vaccination against HIB, ensuring that the individual has developed adequate antibody levels to provide protection against infections caused by this bacterium.
  • Evaluation of Immunodeficiency The test aids in the diagnosis of immunodeficiency response syndromes, where the patient's immune system may not respond effectively to vaccinations or infections, thereby increasing the risk of severe diseases associated with H. influenzae.
  • Monitoring High-Risk Populations It is particularly relevant for children under the age of 5 years, who are at a higher risk for severe infections caused by H. influenzae type B, allowing for timely intervention if antibody levels are found to be insufficient.

2. Procedure

The procedure for conducting the antibody test for Haemophilus influenzae type B involves several key steps that ensure accurate measurement of IgG antibodies in the serum. The following outlines the procedural steps:

  • Step 1: Patient Preparation Prior to the test, the patient may be instructed to avoid certain medications or supplements that could interfere with the test results. It is essential to ensure that the patient is adequately informed about the procedure and any necessary preparations.
  • Step 2: Venipuncture A qualified healthcare professional performs a 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. The venipuncture procedure is crucial as it must be performed with precision to minimize discomfort and ensure an adequate sample for testing.
  • Step 3: Serum Separation After the blood sample is collected, it is processed to separate the serum from the cellular components. This is typically done by centrifugation, which spins the blood at high speeds to separate the serum, which contains the antibodies, from the red and white blood cells.
  • Step 4: Testing Using ELISA The serum is then subjected to an enzyme-linked immunosorbent assay (ELISA). This laboratory technique involves adding specific antigens related to H. influenzae type B to the serum sample. If antibodies are present, they will bind to the antigens, and a series of reactions will produce a measurable signal, indicating the level of antibodies in the sample.
  • Step 5: Result Interpretation Once the ELISA is complete, the results are analyzed and interpreted by laboratory personnel. The presence and concentration of IgG antibodies against HIB are reported, providing critical information regarding the patient's immune status.

3. Post-Procedure

After the procedure, the patient may experience minor discomfort or bruising at the venipuncture site, which typically resolves quickly. There are no specific post-procedure care instructions required for this test, but patients should be advised to monitor the site for any unusual symptoms, such as excessive swelling or pain. The results of the antibody test will be communicated to the healthcare provider, who will discuss the findings with the patient and determine any necessary follow-up actions based on the immune status indicated by the test results.

Short Descr HEMOPHILUS INFLUENZA ANTIBDY
Medium Descr ANTIBODY HAEMOPHILUS INFLUENZA
Long Descr Antibody; Haemophilus influenza
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.
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.
Date
Action
Notes
2013-01-01 Changed Short Descriptor changed.
2004-01-01 Changed Code description changed.
1993-01-01 Added First appearance in code book in 1993.
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Description
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