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Code deleted, to report see 88346, 88350

Official Description

Immunofluorescent study, each antibody; indirect method

© Copyright 2026 American Medical Association. All rights reserved.

Common Language Description

The CPT® Code 88347 refers to an immunofluorescent study that employs an indirect method for testing antibodies. In this procedure, antibodies are treated with a fluorescent dye, which allows for the visualization of specific antigens in suspected diseased red blood cells. This technique is particularly useful in diagnosing various conditions related to blood disorders and autoimmune diseases. The test is performed by applying the fluorescently labeled antibodies to a sample, which can be blood serum rather than a tissue sample, to identify the presence of specific antigens. It is important to note that this code is billed once for each antibody utilized in the testing process, ensuring that the complexity and scope of the diagnostic work are accurately represented in the coding. The use of the indirect method indicates that the antibodies are not directly bound to the target antigens but rather require a secondary antibody for detection, enhancing the sensitivity and specificity of the test results.

© Copyright 2026 Coding Ahead. All rights reserved.

1. Indications

The immunofluorescent study represented by CPT® Code 88347 is indicated for various clinical scenarios where there is a suspicion of disease affecting red blood cells. The following conditions may warrant the use of this procedure:

  • Autoimmune Hemolytic Anemia This condition occurs when the immune system mistakenly attacks and destroys red blood cells, leading to anemia.
  • Hemolytic Disease of the Newborn This condition arises when there is an incompatibility between the blood types of the mother and the fetus, potentially leading to the destruction of the fetus's red blood cells.
  • Transfusion Reactions These reactions can occur when a patient receives incompatible blood, prompting an immune response against the transfused red blood cells.
  • Other Blood Disorders Various other hematological conditions may also necessitate the use of immunofluorescent studies to identify specific antibodies or antigens.

2. Procedure

The procedure for conducting an immunofluorescent study using CPT® Code 88347 involves several key steps that ensure accurate testing and diagnosis. Each step is crucial for the successful identification of antibodies in the blood serum.

  • Step 1: Sample Collection The first step involves the collection of a blood sample from the patient. This sample is typically processed to obtain serum, which is the liquid portion of the blood that remains after clotting. The serum is essential for the subsequent testing of antibodies.
  • Step 2: Preparation of Antibodies In this step, specific antibodies that are suspected to react with the target antigens in the red blood cells are selected. These antibodies are then labeled with a fluorescent dye, which will allow for visualization under a fluorescence microscope.
  • Step 3: Incubation The fluorescently labeled antibodies are added to the serum sample and incubated for a specified period. This incubation allows the antibodies to bind to any corresponding antigens present in the serum, forming antigen-antibody complexes.
  • Step 4: Washing After incubation, the sample is washed to remove any unbound antibodies. This step is critical to reduce background fluorescence and enhance the specificity of the test results.
  • Step 5: Visualization The final step involves examining the sample under a fluorescence microscope. The presence of fluorescence indicates a positive reaction, confirming the presence of specific antibodies against the target antigens in the serum.

3. Post-Procedure

Post-procedure care following an immunofluorescent study coded with CPT® 88347 typically involves monitoring the patient for any immediate reactions, especially if the test was part of a broader diagnostic workup for blood disorders. The results of the immunofluorescent study will be analyzed and interpreted by a qualified healthcare professional, who will then discuss the findings with the patient. Depending on the results, further testing or treatment may be necessary. It is also important for healthcare providers to document the findings accurately and ensure that any follow-up actions are clearly communicated to the patient and relevant medical staff.

Short Descr IMMUNOFLUORESCENT STUDY
Medium Descr IMMUNOFLUORESCENT STUDY EA ANTIBODY INDIR METHOD
Long Descr Immunofluorescent study, each antibody; indirect method
Status Code Active Code
Global Days XXX - Global Concept Does Not Apply
PC/TC Indicator (26, TC) 1 - Diagnostic Tests for Radiology Services
Multiple Procedures (51) 0 - No payment adjustment rules for multiple procedures apply.
Bilateral Surgery (50) 0 - 150% payment adjustment for bilateral procedures does NOT apply.
Physician Supervisions 09 - Concept does not apply.
Assistant Surgeon (80, 82) 0 - Payment restriction for assistants at surgery applies to this procedure...
Co-Surgeons (62) 0 - Co-surgeons not permitted for this procedure.
Team Surgery (66) 0 - Team surgeons not permitted for this procedure.
Diagnostic Imaging Family 99 - Concept Does Not Apply
APC Status Indicator STV-Packaged Codes
Type of Service (TOS) 5 - Diagnostic Laboratory
Berenson-Eggers TOS (BETOS) T1G - Lab tests - other (Medicare fee schedule)
MUE Not applicable/unspecified.
CCS Clinical Classification 234 - Pathology
Date
Action
Notes
2016-01-01 Deleted Code deleted, to report see 88346, 88350
1990-01-01 Added First appearance in code book in 1990.
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Description
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