Table 8.
Device | FDA approved device | Device specifics | MR Safety |
---|---|---|---|
Barorefelex activation therapy | Barostim Neo (CVRx, Inc., Minneapolish, MN) |
Carotid sinus lead and subcutaneous pulse generator in ipsilateral chest. | MR Conditional for head, neck and lower extremity imaging |
Phrenic nerve stimulation | remedē System (Zoll, Minnetonka, MN) |
Transvenous phrenic nerve stimulation and sensing leads and subcutaneous pulse generator in chest. | MR Unsafe |
Cardiac contractility modulation | Optimizer System, (Impulse Dynamics, Marlton, NJ) |
Right ventricular pacemaker leads (2) and subcutaneous pulse generator in ipsilateral chest. | MR conditional at 1.5T for head and extremity imaging |
Interatrial shunt devices | Corvia Atrial Shunt System (Corvia Medical, Inc., Tewksbury, MA) V-Wave (V-Wave Ltd., Caesarea, Israel) |
Interatrial septal device creating a small left to right atrial shunt. | MR Conditional |