Treatment of cardiac arrhythmia by modification of neuronal signaling through fat pads of the heart
View Patent ↗To control cardiac arrhythmias such as atrial fibrillation post-operatively, various non-ablative agents include polymers, fibroblasts, neurotoxins, and growth factors are introduced into one or more cardiac fat pads into the atrioventricular nodal fat pad in proximity to the autonomic ganglia therein. Any desired technique may be used for introducing the agent, including injection. The sinoatrial nodal fat pad target site and the atrioventricular nodal fat pad target site are identified using a stimulator, which may have electrodes coupled thereto or which may coupled to electrodes built into a delivery system.
1. A method of treating cardiac arrhythmia in a heart of a patient comprising:
preparing a source of non-ablative agent that is effective for modifying neuronal signaling by nerve tissue of the autonomic nervous system;
electrically stimulating a cardiac fat pad to locate a target site on the cardiac fat pad in proximity to autonomic ganglia therein, the autonomic ganglia being a part of the autonomic nervous system; and
delivering a therapeutically effective amount of the non-ablative agent from the source to the target site, wherein the non-ablative agent comprises a polymer, wherein the polymer is polyethylene glycol.
2. The method of claim 1 wherein the stimulation step comprises:
stimulating autonomic ganglia contained in an atrioventricular nodal (“AVN”) fat pad of the heart to identify an AVN fat pad target site; and
stimulating autonomic ganglia contained in a sinoatrial nodal (“SAN”) fat pad of the heart to identify an SAN fat pad target site; and
wherein the delivering step comprises delivering a therapeutically effective amount of the non-ablative agent from the source to the AVN fat pad target site and to the SAN fat pad target site.
3. The method of claim 1 further comprising performing coronary artery bypass graft surgery in open chest surgery, wherein the delivering step comprises delivering the therapeutically effective amount of the non-ablative agent from the source to the target site during the open chest surgery.
4. The method of claim 1 further comprising performing mitral valve surgery in open chest surgery, wherein the delivering step comprises delivering the therapeutically effective amount of the non-ablative agent from the source to the target site during the open chest surgery.
5. The method of claim 1 wherein the delivering step comprises delivering the therapeutically effective amount of the non-ablative agent from the source to the target site during a percutaneous translumenal procedure.
6. The method of claim 1 wherein the delivering step comprises delivering the therapeutically effective amount of the non-ablative agent from the source to the target site during a transthoracic minimally invasive procedure.
7. A method of treating cardiac arrhythmia in a heart of a patient comprising:
preparing a source of non-ablative agent that is effective for modifying neuronal signaling by nerve tissue of the autonomic nervous system; and
delivering a therapeutically effective amount of the non-ablative agent from the source into a cardiac fat pad in proximity to autonomic ganglia therein, the autonomic ganglia being a part of the autonomic nervous system, wherein the non-ablative agent comprises a polymer, wherein the polymer is polyethylene glycol.
8. The method of claim 7 further comprising performing coronary artery bypass graft surgery in open chest surgery, wherein the delivering step comprises delivering the therapeutically effective amount of the non-ablative agent during the open chest surgery.
9. The method of claim 7 further comprising performing mitral valve surgery in open chest surgery, wherein the delivering step comprises delivering the therapeutically effective amount of the non-ablative agent during the open chest surgery.
10. The method of claim 7 wherein the delivering step comprises delivering the therapeutically effective amount of the non-ablative agent through a catheter.
11. The method of claim 7 wherein the delivering step comprises delivering the therapeutically effective amount of the non-ablative agent during a percutaneous translumenal procedure.
12. The method of claim 7 wherein the delivering step comprises delivering the therapeutically effective amount of the non-ablative agent during a transthoracic minimally invasive procedure.
13. A method for treating cardiac arrhythmia in a heart of a patient, comprising:
establishing a dosing level of an injectable agent that is therapeutically effective for treating atrial fibrillation by interference with neuronal function in nerve ganglia of a cardiac fat pad; and
injecting the injectable agent at the dosing level into a cardiac fat pad in proximity to ganglia therein, wherein the injectable agent comprises a polymer, wherein the polymer is polyethylene glycol.
14. The method of claim 13 wherein the delivering step is performed in conjunction with cardiac surgery for treating prospective post-operative atrial fibrillation.
15. The method of claim 14 wherein the delivering step is performed epicardially during an open chest procedure.
16. The method of claim 13 wherein the delivering step is performed epicardially through a catheter.
17. The method of claim 13 wherein the delivering step is performed endocardially through a catheter.
18. The method of claim 13 wherein the delivering step comprises delivering the dosing level of the injectable agent in one injection.
19. The method of claim 13 wherein the delivering step comprises delivering the dosing level of the injectable agent in a plurality of injections.
20. The method of claim 13 wherein the injectable agent comprises a plurality of component materials.
21. The method of claim 13 wherein the injectable agent comprises a polymer at the dosing level in a range of from about 0.1 ml to about 5 ml.
22. The method of claim 13 wherein the injectable agent comprises a polymer at the dosing level in a range of from about 0.5 to about 2 ml.