Implantable medical electrical stimulation lead fixation method and apparatus

• US 8,036,756 B2
• Filed: 02/13/2006
• Issued: 10/11/2011
• Est. Priority Date: 08/31/2001
• Status: Expired due to Fees

• Current Assignee: Medtronic Incorporated (Medtronic Plc)
• Original Assignee: Medtronic Incorporated (Medtronic Plc)
• Inventors: Carlton, Keith, Spinelli, Michele, Swoyer, John M., Hartle, Steven David, Gerber, Martin T., Mamo, George J.
• Primary Examiner(s): Patel; Niketa I
• Assistant Examiner(s): STOKLOSA, JOSEPH A
• Application Number:
  US11/352,552
• Publication Number:
  US 20060129218A1
• Time in Patent Office: 2,066 Days
• Field of Search: 607116-118
• US Class Current: 607/117
• CPC Class Codes: A61N 1/0551 Spinal or peripheral nerve electrodes
• CPC Class Codes: A61N 1/0558 Anchoring or fixation means therefor

Abstract

An implantable medical electrical lead particularly for stimulation of the sacral nerves comprises a lead body extending between a distal end and a proximal end, and the distal end having at least one electrode of an electrode array extending longitudinally from the distal end toward the proximal end. The lead body at its proximal end may be coupled to a pulse generator, additional intermediate wiring, or other stimulation device. A fixation mechanism is formed on or integrally with the lead body proximal to the electrode array that is adapted to be implanted in and engage subcutaneous tissue, particularly muscle tissue, to inhibit axial movement of the lead body and dislodgement of the stimulation electrodes.

Claims

1. A method of providing electrical stimulation of body tissue at a stimulation site employing an implantable pulse generator, the method comprising:

percutaneously introducing an introducer having an introducer lumen extending between an introducer lumen proximal end opening and an introducer lumen distal end opening through body tissue to locate the introducer lumen distal end opening adjacent to the stimulation site;

disposing an implantable medical lead within the introducer lumen, wherein the implantable medical lead comprises;

a lead body extending between a lead proximal end and a lead distal end;

P connector elements formed in a connector array along a first segment of the lead body proximate to the lead proximal end;

P stimulation electrodes arranged in an electrode array extending along a second segment of the lead body proximate to the lead distal end;

P lead conductors extending between the P connector elements and the P stimulation electrodes; and

a plurality of M tine elements formed in a tine element array extending along a third segment of the lead body between the second segment of the lead body and the lead proximal end, each tine element comprising N flexible tines, each tine having a tine width and a tine thickness and extending through a tine length from an attached tine end to a free tine end, the attached tine end attached to the lead body at a tine attachment site and supporting the tine extending outwardly of the lead body and toward the lead proximal end, whereby the M×

N tines are adapted to be folded inward against the lead body when fitted into and constrained by the introducer lumen, wherein the plurality of M tine elements are separate from and axially displaced from each other and from each of the P stimulation electrodes, and wherein all of the P stimulation electrodes are between the plurality of M tine elements and the lead distal end, and

wherein disposing the implantable medical lead within the introducer lumen comprises disposing the implantable medical lead within the introducer lumen with the M×

N tines folded inward against the lead body by constraint imposed by the introducer lumen without overlapping one another;

withdrawing the introducer proximally from the tine element array to successively release the N tines of each of the M tine elements to deploy outward and toward the lead proximal end to engage body tissue and inhibit axial dislodgement of the P stimulation electrodes; and

coupling the P connector elements to the implantable pulse generator.

2. The method of claim 1, further comprising advancing the implantable medical lead from the introducer lumen distal end opening to dispose the P electrodes in operative relation to body tissue to be stimulated prior to withdrawing the introducer proximally.

3. The method of claim 2, wherein disposing the implantable medical lead within the introducer lumen precedes percutaneously introducing the introducer.

4. The method of claim 1, wherein disposing the implantable medical lead within the introducer lumen precedes percutaneously introducing the introducer.

5. The method of claim 1, wherein percutaneously introducing the introducer precedes disposing the implantable medical lead within the introducer lumen.

6. The method of claim 1, wherein the tines of the tine elements are formed of a flexible implantable grade superelastic alloy.

7. The method of claim 1, wherein the tine attachment sites are separated longitudinally along the lead body in the tine element array by a distance that is substantially equal to or exceeds the tine length when folded toward the lead proximal end against the lead body.

8. The method of claim 1, wherein the tine attachment sites of adjacent tine elements along the lead body are radially offset from one another such that the tine free ends of the tines of adjacent tine elements engage against body tissue at radially and axially separated points along the tine array.

9. The method of claim 8, wherein tine lengths and tine widths of tines of a first tine element of the plurality of M tine elements are configured to enable the tines of the first tine element to fold toward the lead proximal end alongside and interleaved with a second tine element of the plurality of M tine elements, the second tine element being located closer to the lead proximal end than the first tine element.

10. The method of claim 9, wherein the N tines of the M tine elements are equal in number.

11. The method of claim 1, wherein the N tines of the M tine elements are equal in number.

12. The method of claim 1, wherein P is greater than 1, and wherein at least one of the P stimulation electrodes comprises an elongated, flexible electrode adapted to assume a curve when implanted in relation to body tissue.

13. The method of claim 1, wherein at least one of the plurality of M tine elements comprises a biocompatible plastic.

19. The method of claim 1, wherein P equals 1.

14. A method comprising:

percutaneously introducing an introducer comprising an introducer lumen extending between an introducer lumen proximal end opening and an introducer lumen distal end opening through body tissue to locate the introducer lumen distal end opening adjacent to a stimulation site;

disposing an implantable medical lead within the introducer lumen, wherein the implantable medical lead comprises;

a lead body extending between a lead proximal end and a lead distal end;

a plurality of connector elements formed in a connector array adjacent the lead proximal end;

a plurality of stimulation electrodes arranged in an electrode array extending along a first segment of the lead body proximate to the lead distal end;

a plurality of lead conductors extending between the connector elements and the stimulation electrodes; and

a plurality of tine elements attached to the lead body along a second segment of the lead body between the first segment of the lead body and the lead proximal end, each tine element comprising a plurality of flexible tines that are adapted to be folded inward against the lead body when fitted into and constrained by the introducer lumen and adapted to deploy outward to engage body tissue when the introducer is withdrawn, wherein the plurality of tine elements are separate from and axially displaced from each of the stimulation electrodes, and wherein the plurality of stimulation electrodes is between the plurality of tine elements and the lead distal end; and

withdrawing the introducer toward the lead proximal end from the plurality of tine elements to release the plurality of tines.

15. The method of claim 14, wherein each tine of each tine element has a tine length, and the tine elements are attached to the lead body at tine attachment sites, wherein the tine attachment sites are separated longitudinally along the lead body by a distance that is substantially equal to or exceeds the tine length when folded against the lead body.

16. The method of claim 14, wherein the tine elements are attached to the lead body at tine attachment sites, and the tine attachment sites of adjoining tine elements along the lead body are radially offset from one another around a circumference of the lead body.

17. The method of claim 14, wherein at least one of the stimulation electrodes comprises an elongated, flexible electrode adapted to assume a curve when implanted in relation to body tissue.

18. The method of claim 14, wherein at least one of the plurality of tines comprises a biocompatible plastic.