Anchor for electrode delivery system

• US 8,019,438 B2
• Filed: 06/28/2005
• Issued: 09/13/2011
• Est. Priority Date: 06/28/2005
• Status: Active Grant

• Current Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Original Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Inventors: Johnson, Eric T., Tockman, Bruce A.
• Primary Examiner(s): Patel; Niketa I
• Assistant Examiner(s): Lavert; Nicole F
• Application Number:
  US11/168,282
• Publication Number:
  US 20060293741A1
• Time in Patent Office: 2,268 Days
• Field of Search: 607116-118, 607/122, 600370-374
• US Class Current: 607/116
• CPC Class Codes: A61F 2/86 Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure
• CPC Class Codes: A61F 2/95 Instruments specially adapted for placement or removal of stents or stent-grafts
• CPC Class Codes: A61N 1/057 Anchoring means; Means for fixing the head inside the heart
• CPC Class Codes: A61N 2001/0585 Coronary sinus electrodes

Abstract

The present invention is device for delivering an electrode into a lateral vein of the coronary sinus. The device includes a support structure, a stent, a tether coupled to the stent and a removable sheath disposed about the stent. The stent is carried on the support structure and is deployable from a first collapsed configuration to a second expanded configuration for engaging the inner walls of the selected vessel. The sheath is sized to retain the stent in the first collapsed configuration. The electrode is carried on the stent or on a lead threaded over the tether.

Claims

1. An electrode delivery system configured to deliver an electrode into a coronary vein, the electrode delivery system comprising:

a support structure having a proximal end and a distal end;

a stent deployable from a first collapsed configuration to a second expanded configuration, the stent disposed about the distal end of the support structure, the support structure being adapted to be removed from the stent to deploy the stent within the coronary vein, the stent sized to receive at least a portion of a lead carrying the electrode;

a tether attached to the stent, the tether having a first portion extending distal to the stent, the first portion having a proximal region coupled to the stent and a distal region, the tether having a second portion coupled to the distal region of the first portion and extending proximally from the distal region through the stent such that the lead can be advanced along the tether into the stent while the tether remains attached to the stent such that an electrode on the lead can be positioned at a desired location relative to the coronary vein; and

a removable sheath disposed around the stent and sized to retain the stent in the first collapsed configuration,

wherein, in the second configuration, the stent frictionally engages the coronary vein to anchor the tether.

2. The electrode delivery system of claim 1 wherein the stent is coated with a material adapted to reduce tissue ingrowth.

3. The electrode delivery system of claim 1 wherein the stent is coated with a drug-eluting material.

4. The electrode delivery system of claim 1 wherein either of the stent and the tether are formed from a material that is biodegradable or bioabsorbable.

5. The electrode delivery system of claim 1 wherein the tether is detachably coupled to the stent.

6. The electrode delivery system of claim 1 wherein the sheath is a dissolvable coating formed about the stent.

7. The electrode delivery system of claim 1 wherein the support structure is a catheter.

8. The electrode delivery system of claim 7 further comprising a cardiac lead having an electrode and an internal lumen extending therethrough for receiving the tether.

9. The electrode delivery system of claim 1 wherein the support structure is a cardiac lead, the cardiac lead having an electrode and an internal lumen extending therethrough for receiving the tether.

10. The electrode delivery system of claim 1 further comprising an electrode coupled to the stent, wherein the electrode is electrically coupled to the tether.

11. The electrode delivery system of claim 10 wherein the electrode is an electrically active region of the stent.

12. The electrode delivery system of claim 10 wherein the electrode has a concave shape to facilitate contacting a surface of the heart.

13. The electrode delivery system of claim 10 wherein the electrode is electrically isolated from the stent.

14. The electrode delivery system of claim 1, wherein the first portion extends from the stent at an angle such that the lead can be advanced along the tether through and distal of the stent.

15. A device configured to deliver an electrode into a branch vein of the coronary sinus, the device comprising:

a support structure;

an expandable stent means disposed about the support structure, the support structure being adapted to permit removable of the support structure from the expandable stent means to leave the expandable stent means within the branch vein, the expandable stent means for anchoring an electrode in the branch vein;

a tether having a distal end and a proximal end, wherein a first portion of the tether extends distal to the stent, the first portion having a proximal region coupled to the stent means and a distal region, the tether having a second portion coupled to the distal region of the first portion and extending proximally from the distal region through the stent means such that a lead can be advanced along the tether into the stent means in order to position an electrode on the lead at a desired location relative to the branch vein while the tether remains fixedly attached to the expandable stent means;

a sheath removably disposed about the stent means; and

an electrode coupled to the stent means.

16. The device of claim 15 wherein the electrode is an electrically active region of the stent means, and further wherein the electrode is electrically coupled to the tether.

17. The device of claim 16 wherein the stent means is coated with a non-conductive material except for the electrically active region.

18. The device of claim 15 wherein the electrode is electrically isolated from the stent means.

19. The electrode delivery system of claim 15, wherein the first portion extends from the expandable stent means at an angle such that the lead can be advanced along the tether through and distal of the expandable stent means.

20. An electrode delivery system configured to deliver an electrode into a coronary vein, the electrode delivery system comprising:

an implantable lead including an electrode disposed on the implantable lead;

a support structure having a proximal end and a distal end;

a stent deployable from a first collapsed configuration to a second expanded configuration, the stent disposed about the distal end of the support structure, the support structure configured to permit removal of the support structure to deploy the stent within the coronary vein, the stent sized to accommodate the implantable lead;

a tether attached to the stent, the tether including a portion that extends distally of the stent such that the lead can be advanced along the tether into the stent in order to position the electrode at a desired location relative to the coronary vein while the tether remains attached to the stent; and

a removable sheath disposed around the stent and sized to retain the stent in the first collapsed configuration,

wherein, in the second configuration, the stent frictionally engages the coronary vein to anchor the tether.