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The CPT® Code 87513 refers to the detection of the infectious agent Helicobacter pylori (H. pylori) by nucleic acid testing, specifically focusing on clarithromycin resistance. This procedure utilizes advanced molecular techniques, such as the amplification refractory mutation system combined with quantitative real-time polymerase chain reaction (ARMS‐PCR), the H. pylori with Clarithromycin Resistance Prediction (HPFRP) real-time polymerase chain reaction, or fluorescence in situ hybridization. These methods are designed to identify specific mutations in the 23S ribosomal RNA of H. pylori that confer resistance to the macrolide antibiotic clarithromycin. The presence of these mutations is critical, as they can significantly impact treatment decisions for infections caused by H. pylori. The testing is performed on gastric secretions or gastric mucosa, allowing for the detection of the 23S rRNA gene and associated mutations that lead to antibiotic resistance, all without the need for traditional culture methods. This molecular approach enhances the accuracy and speed of diagnosing clarithromycin resistance in H. pylori, facilitating timely and appropriate therapeutic interventions.
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The procedure associated with CPT® Code 87513 is indicated for the detection of clarithromycin resistance in Helicobacter pylori (H. pylori) infections. This testing is particularly relevant in the following scenarios:
The procedure for CPT® Code 87513 involves several key steps to accurately detect clarithromycin resistance in H. pylori:
After the completion of the testing procedure associated with CPT® Code 87513, the following post-procedure considerations are important:
Results from the molecular testing are typically available within a short timeframe, allowing for prompt clinical decision-making. Physicians should review the findings to determine the presence of clarithromycin resistance, which will inform the choice of antibiotic therapy for the patient. It is essential to communicate the results to the patient and discuss potential treatment options based on the resistance profile. Additionally, any necessary follow-up care or further diagnostic evaluations should be planned based on the outcomes of the test.
| Short Descr | H PYLRI CLRTHMCN RST AMP PRB | Medium Descr | IADNA H PYLORI CLARITHROMYCIN RESIST AMP PRB TQ | Long Descr | Infectious agent detection by nucleic acid (DNA or RNA); Helicobacter pylori (H. pylori), clarithromycin resistance, amplified probe technique | 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) | none | MUE | Not applicable/unspecified. |
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| 2025-01-01 | Added | Code Added. |
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