Not medical advice.
The information on this website is provided for general educational purposes and does not constitute medical advice, diagnosis, or treatment. Always seek the advice of a qualified healthcare provider regarding any medical condition.
No patient-physician relationship.
Visiting this website, submitting an inquiry form, or corresponding with our team does not create a patient-physician relationship. That relationship is established only after formal evaluation and written consent.
Evidence status of cardioneuroablation.
Cardioneuroablation is an emerging therapy supported by a growing body of observational data, small randomized trials, and systematic reviews. It does not currently hold a Class I recommendation in major international guidelines. Larger multicenter randomized controlled trials are in progress. Individual results vary. Freedom-from-syncope rates reported in the literature range from approximately 73% to 92% depending on patient selection, follow-up duration, and technique.
Regulatory status in the United States.
Cardioneuroablation does not currently have a dedicated FDA indication or a specific CPT billing code in the United States. The catheters and 3D mapping systems used during the procedure are FDA-cleared devices manufactured in the United States. U.S. patients considering this procedure should consult with their local cardiologist and their insurance carrier regarding coverage and continuity of care.
Risks of the procedure.
As with any invasive cardiac procedure, cardioneuroablation carries potential risks including but not limited to: vascular complications at access sites, pericardial effusion or tamponade, thromboembolic events, transient or sustained arrhythmias, reinnervation over time, and risks associated with general anesthesia. A complete discussion of risks and alternatives occurs before the procedure as part of informed consent.
Testimonials and case descriptions.
Any patient case descriptions or testimonials featured on this website are shared with the patient's explicit written permission. They reflect one individual experience and are not a guarantee, warranty, or prediction of your own outcome. Individual recovery timelines, clinical response, and long-term results vary.
Cost comparisons.
The U.S. cost ranges cited on this website are based on publicly available price transparency data for catheter ablation for atrial fibrillation at U.S. academic medical centers (2024 to 2025). Cardioneuroablation does not have a dedicated billing code in the U.S. and is typically billed under the closest comparable procedure. Actual charges vary by hospital, region, insurance status, and individual case complexity. A detailed, itemized written quote for your specific case is provided only after teleconsultation.
Continuity of care.
We strongly recommend that all international patients identify a local cardiologist or electrophysiologist in their home country before traveling for any cardiac procedure. We actively communicate procedural documentation to your local providers upon request.
No guarantees.
We make no warranty, express or implied, that any procedure will cure, eliminate, or prevent recurrence of syncope, bradyarrhythmia, or any other condition. Treatment is individualized and based on the best evidence available at the time.