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The CPT® Code 86717 refers to a laboratory test specifically designed to measure antibodies against Leishmania, a parasitic organism. Leishmania is primarily found in tropical and subtropical regions, as well as Southern Europe, and is transmitted to humans through the bite of infected sand flies. The infection can manifest in two primary forms: cutaneous and visceral. The cutaneous form is marked by the development of skin sores or ulcers, which may become scabbed or crusted, and is often associated with swollen lymph nodes. In contrast, the visceral form of the disease occurs when the parasite invades internal organs such as the liver, spleen, and bone marrow. Symptoms of visceral leishmaniasis can vary widely; some individuals may remain asymptomatic, while others may experience significant clinical manifestations including fever, weight loss, enlargement of the spleen and liver, anemia, leukopenia, or thrombocytopenia. The presence of a positive IgG antibody titer in the test results indicates either a current or past infection with Leishmania. To perform this test, a blood sample is collected from the patient through a procedure known as venipuncture, which is reported separately. The serum obtained from the blood sample is then analyzed using a semi-quantitative immunoassay to determine the level of antibodies present.
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The antibody test for Leishmania (CPT® Code 86717) is indicated for the following conditions:
The procedure for conducting the Leishmania antibody test involves several key steps:
After the procedure, patients 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 report any unusual symptoms or prolonged discomfort. The results of the test will be communicated to the healthcare provider, who will discuss the findings with the patient and determine any necessary follow-up actions or treatments based on the results.
| Short Descr | LEISHMANIA ANTIBODY | Medium Descr | ANTIBODY LEISHMANIA | Long Descr | Antibody; Leishmania | 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 | 8 | 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. |
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| 1993-01-01 | Added | First appearance in code book in 1993. |
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