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The CPT® Code 89325 refers to the test for sperm antibodies, commonly known as the antisperm antibody test. This diagnostic procedure is essential in evaluating cases of infertility that may be attributed to an immune response against sperm. In this context, the immune system of either the male or female partner may produce antibodies that target and damage sperm, leading to a condition known as immunologic infertility. Sperm antibodies are specific proteins that can be found in various bodily fluids, including blood, vaginal secretions, and semen. These antibodies recognize sperm as foreign entities and mount an immune response against them. In men, the development of sperm antibodies can occur due to several factors, including infections, traumatic injuries, or surgical procedures involving the testicles, such as biopsies or vasectomies. Notably, a significant number of men who experience fertility issues after undergoing a vasectomy reversal may be diagnosed with immunologic infertility. On the other hand, women can also produce antibodies against their partner's sperm or semen, which can further complicate fertility. To detect the presence of these sperm-bound antibodies, an immunobead test (IBT) is utilized. This test typically assesses both IgA and IgG antibody classes, and it is important to note that CPT® Code 89325 is reported separately for each immunoglobulin class tested. This detailed approach allows for a comprehensive evaluation of potential immunologic factors contributing to infertility.
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The sperm antibody test (CPT® Code 89325) is indicated in various clinical scenarios where infertility is suspected to be linked to an immune response against sperm. The following conditions may warrant the performance of this test:
The procedure for testing sperm antibodies involves several key steps to ensure accurate results. The following outlines the procedural steps associated with CPT® Code 89325:
After the sperm antibody test is completed, the patient may receive guidance based on the results. If sperm antibodies are detected, further evaluation and treatment options may be discussed with the healthcare provider. This could include potential interventions to address immunologic infertility or referrals to fertility specialists. It is important for patients to follow up with their healthcare provider to understand the implications of the test results and to explore appropriate next steps in their fertility journey.
| Short Descr | SPERM ANTIBODY TEST | Medium Descr | SPERM ANTIBODIES | Long Descr | Sperm antibodies | 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) |
| 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. |
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| Pre-1990 | Added | Code added. |
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