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Official Description

Removal and replacement of pulse generator for wireless cardiac stimulator for left ventricular pacing, including device interrogation and programming; battery component only

© Copyright 2025 American Medical Association. All rights reserved.

Common Language Description

The procedure described by CPT® Code 0520T involves the removal and replacement of a pulse generator specifically designed for a wireless cardiac stimulator that facilitates left ventricular pacing. This procedure is particularly relevant for patients who require enhanced cardiac resynchronization therapy (CRT) due to limitations associated with conventional pacemakers. In traditional setups, the use of a wire lead to stimulate the left ventricle can lead to complications such as difficult placement, dislodgment of the lead, unintended nerve stimulation, and inadequate response from the ventricle. The wireless LV pacing device addresses these challenges by eliminating the need for a physical lead, thereby improving the effectiveness of CRT. The removal and replacement of the pulse generator battery is performed when the existing battery has reached its end of life, ensuring that the pacing system continues to function optimally. The procedure involves accessing the subcutaneous pocket where the battery is housed, carefully removing the old battery, and installing a new one while ensuring all connections are secure and the system is functioning correctly before closing the incision.

© Copyright 2025 Coding Ahead. All rights reserved.

1. Indications

The procedure for the removal and replacement of the pulse generator for a wireless cardiac stimulator is indicated for patients who require ongoing left ventricular pacing and whose existing battery has reached its end of life. This procedure is particularly relevant for individuals experiencing:

  • Inadequate Cardiac Resynchronization Therapy (CRT) - Patients who do not achieve effective CRT due to limitations of conventional pacing methods.
  • Anatomic Challenges - Individuals who have experienced difficulties with the placement of LV pacing wires due to anatomical issues.
  • Lead Dislodgment - Patients who have had leads dislodged, leading to unintended nerve stimulation and poor ventricular response.
  • Battery End of Life - Patients whose pulse generator battery has reached its end of life and requires replacement to maintain device functionality.

2. Procedure

The procedure for the removal and replacement of the pulse generator battery involves several critical steps to ensure the safe and effective transition to a new battery. The following steps outline the process:

  • Step 1: Incision An incision is made over the previous battery implant scar site, which is typically located to the left of the existing transmitter pocket. This approach minimizes additional trauma to the surrounding tissue.
  • Step 2: Accessing the Pocket The subcutaneous pocket that houses the battery is accessed through the incision. Care is taken to avoid damaging surrounding structures during this process.
  • Step 3: Battery Removal The old battery is carefully removed from the pocket. This step is crucial to ensure that no residual components are left behind that could interfere with the new device.
  • Step 4: Disconnecting the Transmitter Cable A torque wrench is utilized to disconnect the transmitter cable from the old battery. This ensures a secure and proper disconnection without damaging the cable.
  • Step 5: Inspection The cable connection is inspected for any signs of fluid leaks or foreign substances that may have accumulated. This step is vital for ensuring the integrity of the system.
  • Step 6: Connecting the New Battery The transmitter’s cable is then inserted into the new battery, and the screws are tightened to secure the connection. This ensures that the new battery is properly integrated into the existing system.
  • Step 7: Positioning the New Battery The new battery is positioned into the existing pocket and sutured into place. Proper positioning is essential for the stability and functionality of the device.
  • Step 8: System Evaluation The entire system is evaluated for proper functioning using the previous settings. The programmer checks for appropriate biventricular pacing capture and makes any necessary adjustments to optimize performance.
  • Step 9: Closing the Pocket Once the system is confirmed to be functioning correctly, the subcutaneous pocket is closed, completing the procedure.

3. Post-Procedure

After the procedure, patients are typically monitored for any immediate complications related to the surgery. Expected recovery includes managing any discomfort at the incision site and ensuring that the new battery is functioning as intended. Follow-up appointments may be scheduled to assess the performance of the wireless cardiac stimulator and to make any further adjustments to the programming as needed. Patients should be advised on signs of infection or other complications that may arise post-operatively, and they should be instructed to follow up with their healthcare provider for routine evaluations of their cardiac pacing system.

Short Descr RMV&RPLCMT PG WCS LV BATTERY
Medium Descr RMVL&RPLCMT PG WCS LV PACG BATTERY COMPNT ONLY
Long Descr Removal and replacement of pulse generator for wireless cardiac stimulator for left ventricular pacing, including device interrogation and programming; battery component only
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) 2 - Standard 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) 1 - Statutory 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
Berenson-Eggers TOS (BETOS) none
MUE 1
Q0 Investigational clinical service provided in a clinical research study that is in an approved clinical research study
Date
Action
Notes
2024-01-01 Changed Short, Medium and Long Descriptions changed.
2019-01-01 Added Added
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