IP Library Granted Patent US 7,769,472
Granted Patent B2
US 7,769,472 · App. 11/194,041 · Granted Aug 3, 2010

Electrical stimulation lead with conformable array of electrodes

Assignee: Medtronic, Inc.
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Quick Facts
Patent No.
US 7,769,472
App. No.
11/194,041
Granted
Aug 3, 2010
Kind
B2
Abstract

An implantable electrical lead may include a conformable array of electrodes. The array of electrodes may be distributed across a rounded surface to position the electrodes in various positions and orientations relative to a target stimulation site. The lead may be useful in a variety of applications such as spinal cord stimulation to alleviate chronic pain, gastrointestinal stimulation to alleviate gastroparesis or obesity, pelvic floor stimulation to alleviate incontinence or sexual dysfunction, or deep brain stimulation to alleviate neurological disorders.

Claims (49)

1. An implantable electrical stimulation lead comprising:

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

a plurality of electrical conductors within the lead body; and

a plurality of stimulation electrodes, each of the electrodes being coupled to at least one of the conductors,

wherein a cross-section of the distal end taken in a direction substantially perpendicular to a longitudinal axis of the lead body defines a substantially continuous concave surface and a substantially convex surface, the convex surface being on an opposite side of the cross-section as the substantially concave surface, the electrodes are positioned at various positions on the concave surface and the convex surface, the electrodes comprise conductive pads, the substantially continuous concave surface defines a channel-like region at the distal end, the substantially concave surface comprises a first portion comprising at least one of the electrodes and a second portion that faces toward the first portion and comprises at least one of the electrodes, wherein at least one of the electrodes is positioned on the concave surface but not the convex surface, and wherein an outer width of the cross-section of the distal end is greater than an outer diameter of the lead body.

2. The lead of claim 1 , wherein the distal end is flexible and at least partially conformable to a target stimulation site.

3. The lead of claim 1 , wherein the distal end defines an inflation chamber that is at least partially inflatable to expand the distal end.

4. The lead of claim 1 , wherein the stimulation electrodes include at least sixteen stimulation electrodes.

5. The lead of claim 1 , wherein the distal end is formed at least partially from an elastomeric material.

6. The lead of claim 1 , further comprising one or more sensing electrodes positioned on at least one of the concave surface or the convex surface of the distal end.

7. The lead of claim 1 , wherein the distal end is configured to compress inward toward a longitudinal axis of the lead body.

8. An implantable electrical stimulator comprising:

an implantable pulse generator that generates electrical stimulation pulses; and

an implantable lead coupled to the implantable pulse generator, the lead including a lead body extending between a proximal end and a distal end, a plurality of electrical conductors within the lead body, and a plurality of stimulation electrodes, each of the electrodes being coupled to at least one of the conductors,

wherein a cross-section of the distal end taken in a direction substantially perpendicular to a longitudinal axis of the lead body defines a substantially continuous concave surface and a substantially convex surface, the convex surface being on an opposite side of the cross-section as the substantially concave surface, the electrodes are positioned at various positions on the concave surface and the convex surface, the electrodes comprise conductive pads, the substantially continuous concave surface defines a channel-like region, the concave surface comprises a first portion comprising at least one of the electrodes and a second portion that faces toward the first portion and comprises at least one of the electrodes, wherein at least one of the electrodes is positioned on the concave surface but not the convex surface, and wherein an outer width of the cross-section of the distal end is greater than an outer diameter of the lead body.

9. The stimulator of claim 8 , wherein the distal end is flexible and at least partially conformable to a target stimulation site.

10. The stimulator of claim 8 , wherein the distal end defines an inflation chamber that is inflatable to expand the distal end.

11. The stimulator of claim 8 , wherein the stimulation electrodes include at least sixteen stimulation electrodes.

12. The stimulator of claim 8 , wherein the distal end is formed at least partially from an elastomeric material.

13. The stimulator of claim 8 , further comprising one or more sensing electrodes positioned on at least one of the concave surface or the convex surface of the distal end.

14. The stimulator of claim 8 , wherein parameters of the electrical stimulation pulses are selected to alleviate symptoms of one or more of chronic pain, a gastrointestinal disorder, a urinary tract disorder, or sexual dysfunction.

15. A method comprising applying electrical stimulation pulses to a patient via an implanted lead, wherein the lead comprises a lead body extending between a proximal end and a distal end, a plurality of electrical conductors within the lead body, and a plurality of stimulation electrodes, each of the electrodes being coupled to at least one of the conductors, wherein a cross-section of the distal end taken in a direction substantially perpendicular to a longitudinal axis of the lead body defines a substantially continuous concave surface and a substantially convex surface, the convex surface being on an opposite side of the cross-section as the substantially concave surface, the electrodes are positioned at various positions on the concave surface and the convex surface, the electrodes comprise conductive pads, the substantially continuous concave surface defines a channel-like region, the concave surface comprises a first portion comprising at least one of the electrodes and a second portion that faces toward the first portion and comprises at least one of the electrodes, wherein at least one of the electrodes is positioned on the concave surface but not the convex surface, and wherein an outer width of the cross-section of the distal end is greater than an outer diameter of the lead body.

16. The method of claim 15 , further comprising positioning the distal end of the lead body proximate a target nerve site within the patient.

17. The method of claim 15 , wherein the target nerve site and parameters of the electrical stimulation pulses are selected to alleviate symptoms of one or more of chronic pain, a gastrointestinal disorder, a urinary tract disorder, or sexual dysfunction.

18. The method of claim 15 , wherein the distal end is flexible and at least partially conformable to a target stimulation site.

19. The method of claim 15 , wherein the stimulation electrodes include at least sixteen stimulation electrodes.

20. The method of claim 15 , wherein the distal end is formed at least partially from an elastomeric material.

21. The method of claim 15 , wherein the lead further comprises one or more sensing electrodes positioned on at least one of the concave surface or the convex surface of the distal end, the method further comprising sensing at least one electrical signal via the sensing electrodes.

22. The method of claim 15 , wherein the distal end defines an inflation chamber that is at least partially inflatable, the method further comprising inflating the inflation chamber upon deployment of the distal end of the lead within the patient to expand the distal end.

23. An implantable electrical stimulation lead comprising:

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

a plurality of electrical conductors within the lead body; and

a plurality of stimulation electrodes, each of the electrodes being coupled to at least one of the conductors,

wherein the distal end is substantially pliant and conformable to a target stimulation site, the distal end comprising a substantially continuous concave surface, wherein the substantially continuous concave surface comprises a first portion and a second portion that define a channel-like region, and wherein the plurality of stimulation electrodes comprises a first electrode comprising a first conductive pad positioned on a first surface of the first portion of the distal end but not a second surface of the first portion of the distal end, a second electrode comprising a second conductive pad positioned on the second surface of the first portion of the distal end but not the first surface of the first portion of the distal end, the second surface being on an opposite side of the first portion as the first surface, a third electrode comprising a third conductive pad positioned on the second portion of the distal end, and wherein an outer cross-sectional width of the distal end that defines the substantially concave surface is greater than an outer diameter of the lead body.

24. The lead of claim 23 , wherein the distal end defines an inflation chamber that is at least partially inflatable to expand the distal end.

25. The lead of claim 23 , wherein the stimulation electrodes include at least sixteen stimulation electrodes.

26. The lead of claim 23 , wherein the distal end is formed at least partially from an elastomeric material.

27. The lead of claim 23 , further comprising one or more sensing electrodes positioned on the concave surface of the distal end.

28. The lead of claim 23 , wherein the distal end has a pillow-like shape.

29. An implantable electrical stimulation lead comprising:

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

a plurality of electrical conductors within the lead body; and

a plurality of stimulation electrodes, each of the electrodes being coupled to at least one of the conductors,

wherein the distal end defines a substantially continuous concave surface that comprises a first distal portion and a second distal portion extending from the lead body, the first and second distal portions defining a channel-like region, and wherein the electrodes are positioned at various positions on each of the first and second distal portions, the plurality of stimulation electrodes comprising a first electrode comprising a first conductive pad positioned on a first surface of the first distal portion but not a second surface of the first portion of the distal end, and a second electrode comprising a second conductive pad positioned on the second surface of the first distal portion but not the first surface of the first portion of the distal end, the second surface being on an opposite side of the first distal portion as the first surface, and wherein an outer cross-sectional width of the distal end that defines the substantially concave surface is greater than an outer diameter of the lead body.

30. The lead of claim 29 , wherein the distal end is flexible and at least partially conformable to a target stimulation site.

31. The lead of claim 29 , wherein the stimulation electrodes include at least sixteen stimulation electrodes.

32. The lead of claim 29 , wherein the stimulation electrodes comprise conductive pads.

33. The lead of claim 29 , wherein the distal end is formed at least partially from an elastomeric material.

34. The lead of claim 29 , further comprising one or more sensing electrodes positioned on the concave surface of the distal end.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 19, 2005
From: GERBER, MARTIN T.
To: MEDTRONIC, INC.
Reel/Frame 017098/0410 →
Continuity (1)
Related Publication 20070027514A1 · Feb 1, 2007