Medical electrical lead with proximal armoring

• US 8,099,175 B2
• Filed: 02/13/2009
• Issued: 01/17/2012
• Est. Priority Date: 02/15/2008
• Status: Active Grant

• Current Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Original Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Inventors: Reddy, G. Shantanu
• Primary Examiner(s): MANUEL, GEORGE C
• Application Number:
  US12/371,264
• Publication Number:
  US 20090210043A1
• Time in Patent Office: 1,068 Days
• Field of Search: 607/122
• US Class Current: 607/122
• CPC Class Codes: A61N 1/056 Transvascular endocardial electrode systems

Abstract

A medical electrical lead includes a flexible, insulative body defining a proximal region, an intermediate region, and a distal region. The proximal region is configured to be implanted at a subcutaneous implantation site, and is dimensioned to extend from an implantation location of the pulse generator to a location distal to a cardiovascular system entry site. The intermediate region is configured to extend distally from the proximal region to a location distal to a superior vena cava of a patient'"'"'s heart, and the distal region is configured to extend distally from the intermediate region within the patient'"'"'s heart. The lead further includes an armoring layer disposed on the lead body covering at least the proximal region.

Claims

1. A medical electrical lead configured to be coupled to a pulse generator in a cardiac rhythm management system, the lead comprising:

a proximal connector configured to mechanically and electrically couple the lead to the pulse generator;

a flexible body extending distally from the connector, the body defining a proximal region, an intermediate region, and a distal region terminating in a distal tip;

an armoring layer disposed over the proximal region of the lead body and not over the distal region of the lead body, the armoring layer including a polymeric material having a lubricious outer surface configured to resist abrasion, and a reinforcing material disposed within the armoring layer, wherein the proximal region is configured to be implanted substantially subcutaneously, and is dimensioned to extend from an implantation location of the pulse generator to a location distal to a cardiovascular entry site;

at least one electrode coupled to the lead body in the distal region; and

at least one electrical conductor extending from the at least one electrode to the connector for electrically coupling the at least one electrode thereto.

2. The lead of claim 1 wherein the polymeric material is ePTFE or PTFE.

3. The lead of claim 2 wherein the polymeric material is ePTFE tape wound circumferentially about the lead body.

4. The lead of claim 1 wherein the reinforcing material includes a flexible braid embedded within the polymeric material.

5. The lead of claim 1 wherein the reinforcing material includes a wire or ribbon configured as a helical coil embedded within the polymeric material of the armoring layer.

6. The lead of claim 1 wherein:

the reinforcing material is a flexible braid disposed over the lead body; and

the polymeric material is disposed over the braid.

7. The lead of claim 1 wherein:

the reinforcing material is a wire or ribbon configured as a helical coil wound about the lead body; and

the polymeric material is disposed over the coil.

8. The lead of claim 1 wherein:

the intermediate region is configured to extend distally from the proximal region to a location distal to a superior vena cava of a patient'"'"'s heart; and

the distal region is configured to extend distally from the intermediate region within the patient'"'"'s heart.

9. The lead of claim 8 wherein:

the at least one electrode includes;

a coil electrode coupled to the lead body in the distal region; and

a tip electrode in the form of a fixation helix configured to penetrate cardiac tissue extending distally from the distal tip of the body; and

the at least one electrical conductor includes;

a first conductor extending from the cod electrode to the connector; and

a second connector extending from the tip electrode to the connector.

10. The lead of claim 9 further comprising a layer of polymeric material disposed over at least a portion of the coil electrode for inhibiting tissue ingrowth thereto.

11. The lead of claim 10 wherein the layer of polymeric material disposed over at least a portion of the coil electrode is an ePTFE ribbon wrapped circumferentially about at least a portion of the coil electrode.

12. The lead of claim 11 wherein the armoring layer is further disposed over the intermediate region of the lead body.

13. The lead of claim 12 wherein the ePTFE ribbon extends proximally from the coil electrode to form the polymeric material of the armoring layer.

14. The lead of claim 13 wherein the reinforcing material is a flexible braid disposed between the lead body and the ePTFE ribbon in the intermediate and proximal regions of the lead.

15. The lead of claim 13 wherein the reinforcing material is a flexible wire or ribbon helically wrapped about the lead body between the lead body and the ePTFE ribbon in the intermediate and proximal regions of the lead.

16. A medical electrical lead configured to be coupled to a pulse generator in a cardiac rhythm management system, the lead comprising:

a proximal connector configured to mechanically and electrically couple the lead to the pulse generator;

a flexible body extending distally from the connector, the body defining a proximal region, an intermediate region, and a distal region terminating in a distal tip;

at least one electrode coupled to the lead body in the distal region; and

at least one electrical conductor extending from the at least one electrode to the connector for electrically coupling the at least one electrode thereto; and

armoring means for reinforcing and increasing abrasion resistance of at least the proximal region, the armoring means extending over the proximal region of the lead body but not the distal region of the lead body, wherein the proximal region is configured to be implanted substantially subcutaneously, and is dimensioned to extend from an implantation location of the pulse generator to a location distal to a cardiovascular entry site.

17. The lead of claim 16 further comprising armoring means for reinforcing and increasing abrasion resistance of the intermediate region.

18. A medical electrical lead configured to be coupled to a pulse generator in a cardiac rhythm management system, the lead comprising:

a proximal connector configured to mechanically and electrically couple the lead to the pulse generator;

a flexible body extending distally from the connector, the body defining;

a proximal region configured to be implanted substantially subcutaneously, and is dimensioned to extend from an implantation location of the pulse generator to a location distal to a cardiovascular entry site;

an intermediate region configured to extend distally from the proximal region to a location distal to a superior vena cava of a patient'"'"'s heart; and

a distal region terminating in a distal tip, the distal region being configured to extend distally front the intermediate region within the patient'"'"'s heart;

an armoring layer disposed over only the proximal and intermediate regions of the lead body, the armoring layer including a lubricious polymeric material and a reinforcing material embedded in the polymeric material, the armoring layer extending distally from the connector and terminating proximal to the intermediate region of the lead body;

at least one electrode coupled to the lead body in the distal region; and

at least one electrical conductor extending from the at least one electrode to the connector for electrically coupling the at least one electrode thereto.