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Code deleted, see 33277, 33287, 33288.

Official Description

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)

© Copyright 2026 American Medical Association. All rights reserved.

Common Language Description

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.

© Copyright 2026 Coding Ahead. All rights reserved.

1. Indications

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:

  • Cardiovascular Disease - Conditions affecting the heart and blood vessels that may impact respiratory function.
  • Stroke - Neurological events that can disrupt the brain's ability to regulate breathing.
  • Conditions Affecting the Neck or Brainstem - Anatomical or pathological issues that interfere with the neural pathways responsible for breathing control.
  • Morbid Obesity - Excess body weight that can lead to respiratory complications, including CSA.
  • Narcotic Use - The use of narcotic medications that may depress the central nervous system and impair respiratory drive.

2. Procedure

The procedure for the insertion or replacement of the neurostimulator system involves several detailed steps to ensure proper placement and functionality of the device:

  • Step 1: The procedure begins with the patient being placed under conscious sedation, allowing for communication with the physician throughout the process. Access to the venous system is achieved through a small incision made in the right axillary, cephalic, or subclavian vein.
  • Step 2: A sheath is inserted into the vein, and two long access wires are advanced into the vena cava to facilitate further catheterization.
  • Step 3: A guide catheter is then delivered over one of the access wires into the superior vena cava and advanced into the left brachiocephalic vein (LBC), positioning the tip at the junction with the left subclavian vein.
  • Step 4: Using contrast material, venous branches are identified, and an inner catheter is threaded into the guide catheter, extending beyond it to access the pericardiophrenic vein (PPV).
  • Step 5: The opening of the PPV is visualized and accessed with a coronary wire while the patient is instructed to take deep breaths to aid in the advancement of the catheter.
  • Step 6: The guide catheter is advanced further, and the inner catheter is removed. The stimulation lead is then loaded into the guide catheter and deployed to the target location within the PPV.
  • Step 7: The sensing lead is deployed next by threading a coronary sinus right guide catheter over the second venous access wire to a location between the tracheal carina and the junction of the brachiocephalic veins.
  • Step 8: The opening of the azygos vein is visualized using contrast, and a wire is advanced to the diaphragm level, again utilizing deep breaths or coughing to facilitate this process.
  • Step 9: The inner catheter is advanced over the wire, followed by the guide catheter, which is then advanced to the right lateral branch of the azygos vein for the deployment of the sensing lead.
  • Step 10: Once the lead placement is assessed, stimulation is measured to ensure complete contraction of the hemidiaphragm.
  • Step 11: The pulse generator is connected to the implanted leads and is placed in a subcutaneous pocket created below the clavicle. The unit is secured in place with a single ligature.
  • Step 12: Finally, the functionality of the neurostimulator system is checked to ensure proper operation before concluding the procedure.

3. Post-Procedure

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
Date
Action
Notes
2023-12-31 Deleted Code deleted, see 33277, 33287, 33288.
2017-01-01 Added First appearance in codebook.
2016-01-01 Added Added
Code
Description
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