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The CPT® Code 0588T refers to the procedure involving the revision or removal of a percutaneously placed integrated single device neurostimulation system specifically designed for bladder dysfunction. This system includes an electrode array and a receiver or pulse generator. The procedure encompasses not only the physical removal or revision of the device but also includes essential components such as analysis, programming, and imaging guidance when performed, particularly focusing on the posterior tibial nerve. The underlying purpose of this neurostimulation system is to address conditions like overactive bladder (OAB), which is characterized by an increased urgency to urinate, frequent urination, and potential involuntary loss of urine, known as incontinence. The implanted device works by sending electrical signals to the posterior tibial nerve, which plays a crucial role in the bladder's function. By altering the communication between the sympathetic and parasympathetic nervous systems involved in the voiding reflex, the device aims to improve bladder storage capacity and reduce the frequency and urgency of urination. The procedure is typically performed under local anesthesia, and the device is implanted through a small incision or via an injection method near the tibial neurovascular bundle. This comprehensive approach ensures that the device can be effectively revised or removed, allowing for adjustments to be made to optimize the patient's treatment outcomes.
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The procedure associated with CPT® Code 0588T is indicated for patients experiencing bladder dysfunction, particularly those suffering from overactive bladder (OAB). OAB is a chronic condition that leads to symptoms such as:
The procedure for the revision or removal of the neurostimulation device involves several key steps:
Post-procedure care involves monitoring the patient for any immediate complications related to the incision site and ensuring that the neurostimulation device is functioning correctly. Patients may be advised on activity restrictions to promote healing and prevent strain on the surgical site. Follow-up appointments are typically scheduled to assess the effectiveness of the device and make any necessary adjustments to the stimulation settings. It is essential for patients to report any unusual symptoms or discomfort during their recovery period to their healthcare provider.
| Short Descr | REVISION/REMOVAL ISDNS PTN | Medium Descr | REVJ/ OR RMVL PERQ ISDNS BLDR DYSF PTN | Long Descr | Revision or removal of percutaneously placed integrated single device neurostimulation system for bladder dysfunction including electrode array and receiver or pulse generator, including analysis, programming, and imaging guidance when performed, posterior tibial nerve | Status Code | Carriers Price the Code | Global Days | YYY - Carrier Determines Whether Global Concept Applies | PC/TC Indicator (26, TC) | 0 - Physician Service Code | 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 | Hospital Part B services paid through a comprehensive APC | ASC Payment Indicator | Office-based surgical procedure added to ASC list in CY 2008 or later without MPFS nonfacility PE RVUs; payment based on OPPS relative payment weight. | Berenson-Eggers TOS (BETOS) | none | MUE | 1 |
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| 2024-01-01 | Changed | Medium and Long Descriptions changed. Guideline information changed. |
| 2020-01-01 | Added | Code added. |
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