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Official Description

Implantation or replacement of carotid sinus baroreflex activation device; total system (includes generator placement, unilateral or bilateral lead placement, intra-operative interrogation, programming, and repositioning, when performed)

© Copyright 2025 American Medical Association. All rights reserved.

Common Language Description

The CPT® Code 0266T refers to the procedure of implantation or replacement of a carotid sinus baroreflex activation device, which is a specialized medical device used to treat patients suffering from refractory hypertension. This condition is characterized by high blood pressure that does not respond adequately to standard medical treatments. The carotid sinus baroreflex plays a crucial role in regulating arterial blood pressure and heart rate by sending electrical signals to the brainstem, which in turn modulates the autonomic nervous system's output to maintain blood pressure within a normal range. In patients with refractory hypertension, the functionality of this reflex is compromised, leading to persistent high blood pressure. The implantation of the baroreflex activation device aims to enhance the electrical activity of the carotid baroreceptor afferent nerves. By doing so, the device mimics the natural response of the carotid sinus to elevated blood pressure, prompting the central nervous system to adjust sympathetic and vagal nerve activity. This adjustment results in a decrease in both blood pressure and heart rate. The procedure involves the careful placement of electrodes on the carotid sinus wall, which requires precise surgical techniques to ensure the safety and effectiveness of the device. The entire process includes generator placement, lead placement (which can be unilateral or bilateral), intra-operative interrogation, programming of the device, and any necessary repositioning to achieve optimal results.

© Copyright 2025 Coding Ahead. All rights reserved.

1. Indications

The implantation or replacement of a carotid sinus baroreflex activation device is indicated for patients with refractory hypertension, which is defined as high blood pressure that remains uncontrolled despite the use of multiple antihypertensive medications. This procedure is specifically designed for individuals who have not achieved adequate blood pressure control through conventional treatment methods and may benefit from the modulation of their autonomic nervous system to lower blood pressure and heart rate.

  • Refractory Hypertension Patients who experience persistent high blood pressure that does not respond to standard medical therapies.

2. Procedure

The procedure for the implantation or replacement of a carotid sinus baroreflex activation device involves several critical steps to ensure proper placement and functionality of the device.

  • Step 1: Incision and Exposure An incision is made over the carotid bifurcation on one side of the neck to expose the common carotid artery. This step is crucial for accessing the carotid sinus where the electrodes will be placed.
  • Step 2: Identification and Protection of the Vagus Nerve The vagus nerve is carefully identified and protected during the procedure to prevent any damage that could affect the patient's autonomic functions.
  • Step 3: Mobilization of the Carotid Artery Bifurcation The carotid artery bifurcation is mobilized circumferentially, ensuring that the neurovascular bundle within the bifurcation remains undisturbed, which is essential for maintaining normal vascular function.
  • Step 4: Electrode Placement The first electrode is positioned on the bifurcation in the area of the carotid sinus. This electrode is then attached to the impulse generator, and its placement is tested to evaluate the hemodynamic response.
  • Step 5: Repositioning of the Electrode If necessary, the electrode is repositioned until an optimal hemodynamic response is achieved, ensuring that the device will effectively modulate blood pressure.
  • Step 6: Suturing the Electrode Once the optimal position is confirmed, the electrode is sutured in place to secure it for long-term functionality.
  • Step 7: Contralateral Procedure The procedure is then repeated on the contralateral side, ensuring that both sides are equipped with the necessary electrodes for effective treatment.
  • Step 8: Tunneling of Leads The leads from the electrodes are tunneled to the infraclavicular region, where a subcutaneous pocket for the impulse generator (IPG) is developed.
  • Step 9: Creation of Subcutaneous Pocket An incision is made in the skin to fashion a subcutaneous pocket for the IPG, which will house the device that generates the electrical impulses.
  • Step 10: Connection and Testing of the IPG The leads are connected to the impulse generator, and the device is tested to ensure it is functioning correctly.
  • Step 11: Programming the Device The optimal frequency and intensity of the electrical impulses are determined, and the generator is programmed accordingly to achieve the desired therapeutic effect.
  • Step 12: Final Placement and Closure After confirming that the leads and IPG are working properly and that the desired reduction in blood pressure and heart rate has been achieved, the IPG is placed into the pocket, sutured to the underlying tissue, and the pocket is closed.

3. Post-Procedure

Post-procedure care involves monitoring the patient for any immediate complications and ensuring that the device is functioning as intended. Patients may require follow-up visits to assess the effectiveness of the device in managing their blood pressure and to make any necessary adjustments to the programming of the impulse generator. It is essential to provide the patient with instructions regarding activity restrictions, wound care, and signs of potential complications that should prompt immediate medical attention. Regular follow-up appointments will help in evaluating the long-term efficacy of the device and the overall management of the patient's hypertension.

Short Descr IMPLT/RPL CRTD SNS DEV TOTAL
Medium Descr IM/REPL CARTD SINUS BAROREFLX ACTIV DEV TOT SYST
Long Descr Implantation or replacement of carotid sinus baroreflex activation device; total system (includes generator placement, unilateral or bilateral lead placement, intra-operative interrogation, programming, and repositioning, when performed)
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 Procedure or Service, Not Discounted when Multiple
ASC Payment Indicator Device-intensive procedure added to ASC list in CY 2008 or later; paid at adjusted rate.
Type of Service (TOS) 2 - Surgery
Berenson-Eggers TOS (BETOS) T2D - Other tests - other
MUE 1
CCS Clinical Classification 59 - Other OR procedures on vessels of head and neck
82 Assistant surgeon (when qualified resident surgeon not available): the unavailability of a qualified resident surgeon is a prerequisite for use of modifier 82 appended to the usual procedure code number(s).
AS Physician assistant, nurse practitioner, or clinical nurse specialist services for assistant at surgery
22 Increased procedural services: when the work required to provide a service is substantially greater than typically required, it may be identified by adding modifier 22 to the usual procedure code. documentation must support the substantial additional work and the reason for the additional work (ie, increased intensity, time, technical difficulty of procedure, severity of patient's condition, physical and mental effort required). note: this modifier should not be appended to an e/m service.
79 Unrelated procedure or service by the same physician or other qualified health care professional during the postoperative period: the individual may need to indicate that the performance of a procedure or service during the postoperative period was unrelated to the original procedure. this circumstance may be reported by using modifier 79. (for repeat procedures on the same day, see modifier 76.)
80 Assistant surgeon: surgical assistant services may be identified by adding modifier 80 to the usual procedure number(s).
GC This service has been performed in part by a resident under the direction of a teaching physician
GW Service not related to the hospice patient's terminal condition
LT Left side (used to identify procedures performed on the left side of the body)
Q0 Investigational clinical service provided in a clinical research study that is in an approved clinical research study
RT Right side (used to identify procedures performed on the right side of the body)
X5 Diagnostic services requested by another clinician: for reporting services by a clinician who furnishes care to the patient only as requested by another clinician or subsequent and related services requested by another clinician; this modifier is reported for patient relationships that may not be adequately captured by the above alternative categories; reporting clinician service examples include but are not limited to, the radiologist's interpretation of an imaging study requested by another clinician
Date
Action
Notes
2012-01-01 Added First appearance in code book
2011-07-01 Added Code implemented
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