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The procedure described by CPT® Code 0424T involves the insertion or replacement of a neurostimulator system specifically designed for the treatment of central sleep apnea (CSA). Central sleep apnea is a condition characterized by the brain's failure to signal the muscles responsible for breathing, leading to temporary cessation of breath during sleep. This condition can be exacerbated by various factors, including cardiovascular diseases, strokes, anatomical issues affecting the neck or brainstem, morbid obesity, and the use of narcotic medications. The neurostimulator system comprises several key components: an implantable pulse generator (IPG), which is surgically placed in a subcutaneous pocket typically located in the pectoral region, usually on the right side; a stimulation lead that is inserted into either the right brachiocephalic vein or the left pericardiophrenic vein (the latter being the preferred site) to facilitate unilateral phrenic nerve stimulation; and a pressure sensing lead that is positioned in the azygos vein to monitor respiratory activity. The primary function of the IPG is to deliver electrical impulses to the phrenic nerve, which in turn stimulates the diaphragm to contract, thereby restoring normal breathing patterns. This procedure is performed under conscious sedation, allowing the patient to remain communicative throughout the process, which is crucial for ensuring proper placement and function of the leads during the procedure.
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The procedure is indicated for patients diagnosed with central sleep apnea (CSA), which may arise from various underlying conditions. The following factors may contribute to the occurrence of CSA:
The procedure for the insertion or replacement of the neurostimulator system involves several detailed steps to ensure proper placement and functionality of the device:
After the procedure, patients are typically monitored for any immediate complications related to the insertion of the neurostimulator system. Recovery may involve observation for signs of infection, bleeding, or other adverse effects at the incision site. Patients may be advised on activity restrictions and follow-up appointments to assess the functionality of the neurostimulator system and to monitor for any potential complications. It is essential for patients to report any unusual symptoms or concerns to their healthcare provider during the recovery period.
| Short Descr | INSJ/RPLC NSTIM APNEA COMPL | Medium Descr | INSJ/RPLC NSTIM SYSTEM SLEEP APNEA COMPLETE | Long Descr | Insertion or replacement of neurostimulator system for treatment of central sleep apnea; complete system (transvenous placement of right or left stimulation lead, sensing lead, implantable pulse generator) | Status Code | Carriers Price the Code | Global Days | XXX - Global Concept Does Not Apply | 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 | Procedure or Service, Not Discounted when Multiple | Berenson-Eggers TOS (BETOS) | P5E - Ambulatory procedures - other | MUE | Not applicable/unspecified. |
| 53 | Discontinued procedure: under certain circumstances, the physician or other qualified health care professional may elect to terminate a surgical or diagnostic procedure. due to extenuating circumstances or those that threaten the well being of the patient, it may be necessary to indicate that a surgical or diagnostic procedure was started but discontinued. this circumstance may be reported by adding modifier 53 to the code reported by the individual for the discontinued procedure. note: this modifier is not used to report the elective cancellation of a procedure prior to the patient's anesthesia induction and/or surgical preparation in the operating suite. for outpatient hospital/ambulatory surgery center (asc) reporting of a previously scheduled procedure/service that is partially reduced or cancelled as a result of extenuating circumstances or those that threaten the well being of the patient prior to or after administration of anesthesia, see modifiers 73 and 74 (see modifiers approved for asc hospital outpatient use). | GC | This service has been performed in part by a resident under the direction of a teaching physician | GY | Item or service statutorily excluded, does not meet the definition of any medicare benefit or, for non-medicare insurers, is not a contract benefit | Q0 | Investigational clinical service provided in a clinical research study that is in an approved clinical research study | Q1 | Routine clinical service provided in a clinical research study that is in an approved clinical research study |
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