Helically formed coil for a neural cuff electrode

• US 8,954,167 B2
• Filed: 03/05/2010
• Issued: 02/10/2015
• Est. Priority Date: 05/26/2009
• Status: Expired due to Fees

• Current Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Original Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Inventors: Zarembo, Paul E., Ruble, Stephen
• Primary Examiner(s): Koharski, Christopher D
• Assistant Examiner(s): OROPEZA, FRANCES P
• Application Number:
  US12/718,462
• Publication Number:
  US 20100305674A1
• Time in Patent Office: 1,803 Days
• Field of Search: 607/118
• US Class Current: 607/118
• CPC Class Codes: A61N 1/0556 Cuff electrodes

Abstract

A lead assembly for an implantable medical device includes a lead body having a proximal end and a distal end. One or more connectors at the proximal end of the lead body are each adapted for connection to a pulse generator. One or more conductive elements are coupled to the one or more connectors at the proximal end and extend through the lead body to the distal end. Each of the one or more conductive elements includes an electrode coil that extends from the distal end of the lead body that is formed into a helix having a diameter greater than a diameter of the electrode coil.

Claims

1. A lead assembly for an implantable medical device, the lead assembly comprising:

a lead body having a proximal end and a distal end;

one or more connectors at the proximal end of the lead body that are each adapted for connection to a pulse generator; and

one or more conductive elements coupled to the one or more connectors at the proximal end and extending through the lead body to the distal end, wherein each of the one or more conductive elements comprises an electrode coil that extends from the distal end of the lead body, and wherein the electrode coil is formed into a helix at the distal end having a diameter greater than a diameter of the electrode coil.

2. The lead assembly of claim 1, wherein each electrode coil includes a lumen extending through the electrode coil to the distal end of the conductive element.

3. The lead assembly of claim 2, wherein the lumen is accessible with a mandrel employable to unwind the helix during implantation.

4. The lead assembly of claim 3, wherein the mandrel is provided on a comb-like structure including a plurality of mandrels each employable to unwind the helix of one of the one or more electrode coils.

5. The lead assembly of claim 1, wherein each electrode coil is at least partially surrounded by a biocompatible insulator.

6. The lead assembly of claim 5, wherein the biocompatible insulator is selected from the group consisting of expanded polytetrafluoroethylene (ePTFE), PTFE, polyurethane, ethylene tetrafluoroethylene (ETFE), ultra-high molecular weight polyethylene (UHMWPE), and silicone rubber.

7. The lead assembly of claim 1, wherein each electrode coil is comprised of a biocompatible material selected from the group consisting of MPTa, Pt-clad Ta, Pt-clad MP35N, MP35N, MPAg, and Nitinol.

8. A lead assembly for nerve stimulation, the lead assembly comprising:

a lead body having a proximal end and a distal end;

one or more connectors at the proximal end of the lead body that are each adapted for connection to a pulse generator; and

one or more conductive elements coupled to the one or more connectors at the proximal end and extending through the lead body to the distal end, wherein each of the one or more conductive elements includes an electrode coil coupled to a distal end of the conductive element, and wherein the electrode coil is formed into a helix having an inner diameter that is sized to couple to a nerve.

9. The lead assembly of claim 8, wherein each electrode coil includes a lumen extending through the electrode coil.

10. The lead assembly of claim 9, wherein the lumen is accessible with a mandrel employable to straighten the helix during implantation.

11. The lead assembly of claim 8, wherein each electrode coil is at least partially surrounded by a biocompatible insulator.

12. The lead assembly of claim 11, wherein the biocompatible insulator is electrically porous, and wherein portions of each helix that do not confront the nerve are electrically sealed.

13. The lead assembly of claim 11, wherein the biocompatible insulator is not electrically porous, and wherein portions of each helix that confront the nerve are ablated.

14. The lead assembly of claim 11, wherein the biocompatible insulator is selected from the group consisting of expanded polytetrafluoroethylene (ePTFE), PTFE, polyurethane, ethylene tetrafluoroethylene (ETFE), ultra-high molecular weight polyethylene (UHMWPE), and silicone rubber.

15. The lead assembly of claim 8, wherein each electrode coil is comprised of a biocompatible material selected from the group consisting of MPTa, Pt-clad Ta, Pt-clad MP35N, MP35N, MPAg, and Nitinol.

16. A neurostimulation system comprising:

a stimulation device; and

one or more conductive elements each comprising a coil that is electrically coupled to the stimulation device, each coil including a distal end that is formed into a helix that is sized to couple to a nerve such that an inner surface of the helix confronts the nerve, wherein the inner surface of each helix is configured to deliver electrical energy to the nerve.

17. The neurostimulation system of claim 16, wherein the stimulation device comprises a pulse generator, and wherein the neurostimulation system further comprises:

a lead body having a proximal end and a distal end, wherein the one or more conductive elements extend through the lead body; and

one or more connectors at the proximal end of the lead body that are connectable to the pulse generator, wherein the one or more conductive elements are connected to the one or more connectors at the proximal end.

18. The neurostimulation system of claim 16, wherein the stimulation device comprises an implantable microstimulator.

19. The neurostimulation system of claim 16, wherein each coil includes a lumen extending through the helix.

20. The neurostimulation system of claim 19, wherein the lumen is accessible with a mandrel employable to straighten the helix during implantation.

21. The neurostimulation system of claim 16, wherein each helix is at least partially surrounded by a biocompatible insulator.

22. The neurostimulation system of claim 21, wherein the biocompatible insulator is electrically porous, and wherein portions of each helix that do not confront the nerve are electrically sealed.

23. The neurostimulation system of claim 21, wherein the biocompatible insulator is not electrically porous, and wherein portions of each helix that confront the nerve are ablated.

24. The neurostimulation system of claim 21, wherein the biocompatible insulator is selected from the group consisting of expanded polytetrafluoroethylene (ePTFE), PTFE, polyurethane, ethylene tetrafluoroethylene (ETFE), ultra-high molecular weight polyethylene (UHMWPE), and silicone rubber.