Method and apparatus for forming insulated implantable electrodes

• US 20070255320A1
• Filed: 04/28/2006
• Published: 11/01/2007
• Est. Priority Date: 04/28/2006
• Status: Abandoned Application

• Current Assignee: LivaNova USA, Inc. (LivaNova Plc)
• Original Assignee: Cyberonics, Inc
• Inventors: Guzman, Albert, Inman, D., Parnis, Steven
• Application Number:
  US11/414,013
• Publication Number:
  US 20070255320A1
• Time in Patent Office: Days
• US Class Current: 607/2
• CPC Class Codes: A61N 1/0551 Spinal or peripheral nerve electrodes
• CPC Class Codes: A61N 1/36071 Pain
• CPC Class Codes: A61N 1/36114 Cardiac control, e.g. by vagal stimulation stimulating the heart A61N1/362

Abstract

A method, system, and an apparatus are provided for insulating an electrode implanted in a body of a patient. The method comprises surgically exposing a nerve of the patient, implanting at least one electrode in the body of the patient, wherein the implanting comprises coupling theat least one electrode to the nerve of the patient, providing a mold form, disposing the mold form around at least a portion of the at least one electrode and the nerve, introducing into the mold form a curable liquid insulant, allowing the curable liquid insulant to cure, removing the mold form from around the at least one electrode and from the patient'"'"'s body, and surgically closing the exposure of the nerve.

Claims

1. A method for insulating an electrode implanted in a body of a patient, the method comprising:

surgically exposing a nerve of the patient;

implanting at least one electrode in the body of the patient, wherein said implanting comprises coupling said at least one electrode to said nerve of the patient;

providing a mold form;

disposing said mold form around at least a portion of said at least one electrode and said nerve;

introducing into said mold form a curable liquid insulant;

allowing said curable liquid insulant to cure;

removing said mold form from around said at least one electrode and from said patient'"'"'s body; and

surgically closing said exposure of said nerve.

2. The method of claim 1, wherein implanting at least one electrode comprises implanting a lead having a proximal and a distal end, and wherein said distal end of said lead comprises at least one electrode, said method further comprising:

providing an implantable medical device;

implanting said implantable medical device in the body of the patient; and

coupling said proximal end of said lead to said implantable medical device.

3. The method of claim 1 wherein exposing said nerve comprises exposing a cranial nerve selected from the group consisting of a vagus nerve, a trigeminal nerve, a glossopharyngeal nerve, and branches of the foregoing.

4. The method of claim 1, wherein introducing said curable liquid insulant comprises introducing at least one of a polymer mixture and a gel into the insulation form.

5. The method of claim 1, wherein allowing said curable liquid insulant to cure comprises at least one of cross-linking said curable liquid insulant, thickening said curable liquid insulating, and evaporating a solvent from said curable liquid insulant.

6. The method of claim 1 wherein said mold form comprises a material selected from a rigid sheath, a semi-rigid sheath, and a flexible sheath.

7. An implanted medical device system for treating a medical condition of a patient, the implanted medical device system comprising:

a medical device implanted in the body of the patient for at least one of generating a therapeutic electrical signal and sensing electrical activity on a nerve;

an implanted electrode coupled to a nerve and to the implanted medical device; and

an in situ formed sealed insulation capsule covering the implanted electrode and at least a portion of the nerve to prevent intercellular body fluids outside the nerve from contacting the implanted electrode.

8. The implanted medical device system of claim 7, wherein said implanted electrode is a circumneural electrode such that said insulator substantially surrounds said at least a portion of said nerve.

9. The implanted medical device system of claim 8, wherein said implanted electrode further comprises:

a first helical electrode that surrounds a first portion of said nerve to form a positive electrode; and

a second helical electrode that surrounds a second portion of said nerve to form a negative electrode.

10. The implanted medical device system of claim 7, wherein said medical device further comprises:

a controller to selectively perform an operation selected from the group consisting of providing a therapeutic electrical signal to said implanted electrode and sensing electrical activity on the nerve.

11. The implanted medical device system of claim 7, further comprising a lead coupled to said medical device and to said implanted electrode, wherein said implanted electrode further comprises a plurality of insulated electrodes, each insulated electrode corresponding to a stimulation or sensing channel.

12. The implanted medical device system of claim 7, wherein said sealed insulation capsule is capable of providing strain relief between said proximal end of said lead and said implanted electrode.

13. A method of insulating an implanted electrode coupled to a nerve, the method comprising:

providing a lead assembly comprising at least one lead body having proximal and distal ends, and at least one electrode coupled to said distal end;

surgically exposing a cranial nerve;

implanting said lead assembly in the body of the patient, wherein implanting comprises coupling the at least one electrode to the cranial nerve;

providing a mold form disposed around said at least one electrode and around at least a portion of said cranial nerve;

introducing into said mold form a liquid insulation comprising at least one of a polymer mixture and a gel;

curing said liquid insulation to form a sealed insulation capsule around said at least one electrode; and

surgically closing said exposure of said cranial nerve.

14. The method of claim 13, wherein curing said liquid insulation comprises at least one of cross-linking said liquid insulation, thickening said liquid insulation, and evaporating a solvent from said liquid insulation to provide a sealed insulation capsule preventing intercellular body fluids outside said cranial nerve from contacting the at least one electrode.

15. The method of claim 13 further comprising allowing the at least one electrode to remain in the patient'"'"'s body for a predetermined time period.

16. The method of claim 15, further comprising allowing the at least one electrode to remain in the patient'"'"'s body for at least one month.

17. The method of claim 13 further comprising removing said mold form from the patient'"'"'s body.

18. The method of claim 13, further comprising providing a medical device;

implanting said medical device in the body of the patient; and

coupling said medical device to said proximal end of said lead assembly.

19. The method of claim 18, further comprising performing an operation selected from the group consisting of generating a therapeutic electrical signal using said medical device and applying said signal to said at least one electrode, and sensing electrical activity on said cranial nerve.

20. The method of claim 13, wherein said cranial nerve is selected from the group consisting of a vagus nerve, a trigeminal nerve, a glossopharyngeal nerve, and branches of the foregoing.