Apparatus and method for fixing electrodes in a blood vessel

• US 6,161,029 A
• Filed: 03/08/1999
• Issued: 12/12/2000
• Est. Priority Date: 03/08/1999
• Status: Expired due to Term

• Current Assignee: Medtronic Incorporated (Medtronic Plc)
• Original Assignee: Medtronic Incorporated (Medtronic Plc)
• Inventors: Heynen, Henri G., Hess, Douglas N, von Venrooij, Paulus C., Struble, Chester I., Spreigl, William T.
• Primary Examiner(s): COHEN, LEE S
• Application Number:
  US09/265,445
• Time in Patent Office: 645 Days
• Field of Search: 600/374, 600/381, 600/375, 607/122, 607/126
• US Class Current: 600/381
• CPC Class Codes: A61B 5/283 Invasive
• CPC Class Codes: A61B 5/29 for permanent or long-term implantation
• CPC Class Codes: A61B 5/6853 with a balloon
• CPC Class Codes: A61N 1/056 Transvascular endocardial electrode systems
• CPC Class Codes: A61N 2001/0585 Coronary sinus electrodes

Abstract

Endocardial implantable cardiac leads are disclosed for applying electrical stimulation to and/or sensing electrical activity of the heart at one or more distal electrode positioned at a cardiac implantation site within a cardiac vessel adjacent to and at a desired orientation to the left ventricle or atrium of the heart. The distal electrode(s) is supported by a tubular electrode support having a diameter large enough to bear against the blood vessel wall and a support lumen that allows blood to flow through it. A retention stent extends proximally from a distal stent end fixed to the tubular electrode support to a proximal stent end. After advancement to the cardiac implantation site employing a lead delivery mechanism, the retention stent is expandable from a collapsed stent state in which the outer diameter of the retention stent is less than the inner diameter of the vessel to an expanded stent state. The expanded stent is lodged against the blood vessel wall and inhibits movement of the stent and distal electrode support. The expanded stent lumen is aligned with the electrode support lumen for allowing blood to flow through the aligned electrode support lumen and expanded stent lumen. The retention stent may take any of the known forms that can be introduced in the collapsed stent state within an introducer lumen or mounted to an introducer and can either self-expand upon release in the blood vessel or be mechanically expanded within the blood vessel.

Claims

1. An implantable electrical lead for locating at least one distal electrode at a desired implantation site in a body vessel having a predetermined vessel diameter of the type comprising an elongated insulated lead body extending between a proximal lead end and a distal lead end and enclosing at least one electrical conductor having a proximal end and a distal end, the distal lead end further comprising:

a tubular electrode support coupled to said distal lead end having a fixed tubular support outer tall diameter and having a tubular support lumen extending between a proximal support end and a distal support end;

a first electrode coupled with said electrical conductor and supported on said tubular electrode support outer wall; and

a tubular retention stent mounted to and extending axially from said tubular electrode support, said retention stent having a retention stent lumen axially aligned with said tubular support lumen, said retention stent adapted to assume a collapsed stent state having a collapsed stent diameter smaller than the vessel diameter to enable introduction of said distal lead end to said desired implantation site and to assume an expanded stent state having an expanded stent diameter sufficient to engage the retention stent against the body vessel to inhibit movement,

whereby the aligned retention stent lumen and tubular support lumen enable flow of body fluids therethrough.

2. The electrical lead of claim 1, wherein said fixed tubular support outer wall diameter is correlated to the body vessel diameter such that the support outer wall engages the body vessel and said first electrode is placed in contact with the body vessel.

3. The electrical lead of claim 2, wherein:

said tubular electrode support is non-conductive; and

said lead body encloses a second lead conductor extending from said proximal lead end to said distal lead end, and further comprising;

a second electrode supported by said tubular electrode support spaced from and electrically insulated from said first electrode and electrically connected to said second lead conductor at said distal lead end.

4. The electrical lead of claim 1, wherein:

said tubular electrode support is non-conductive; and

said lead body encloses a second lead conductor extending from said proximal lead end to said distal lead end, and further comprising;

a second electrode supported by said tubular electrode support spaced from and electrically insulated from said first electrode and electrically connected to said second lead conductor at said distal lead end.

5. The electrical lead of claim 1, wherein said retention stent is formed of a tubular stent body adapted to be expanded from said collapsed stent state to said expanded stent state through the application of expansion force applied within said retention stent lumen while said retention stent is in said collapsed stent state.

6. The electrical lead of claim 1, wherein said retention stent is formed of a tubular stent body adapted to be restrained in said collapsed state and to expand from said collapsed stent state to said expanded stent state upon release of a restraint applied thereto.

7. An assembly to facilitate the advancement of an electrical lead within a patient'"'"'s body to position and fix a first distal electrode of the electrical lead at a desired implantation site in an elongated body vessel, the electrical lead including a lead body extending between a proximal lead end and a distal lead end and a first lead conductor extending within said lead body between said proximal and distal lead ends and electrically connected to said first distal electrode, said arrangement comprising:

a tubular electrode support coupled to said distal lead end having a fixed tubular support outer wall supporting said first electrode, said tubular electrode support having an outer wall diameter and having a tubular support lumen extending between a proximal support end and a distal support end; and

a tubular retention stent mounted to and extending axially from said tubular electrode support, said retention stent having a retention stent lumen axially aligned with said tubular support lumen and adapted to assume a collapsed stent state having a collapsed stent diameter smaller than the vessel diameter to enable introduction of said distal lead end to said desired implantation site and to assume an expanded stent state having an expanded stent diameter sufficient to engage the retention stent against the body vessel to inhibit movement; and

lead delivery means for engaging and advancing said distal lead end to the desired implantation site with said retention stent in said collapsed stent state, said lead delivery means further comprising means for effecting the expansion of said retention stent from said collapsed stent state to said expanded stent state and for releasing said distal lead end at the desired implantation site,

whereby the aligned retention stent lumen and tubular support lumen enable flow of body fluids therethrough.

8. The assembly of claim 7, wherein:

said retention stent is formed of a tubular stent body formed of a bent wire adapted to be expanded from said collapsed stent state to said expanded stent state through the application of expansion force applied within said retention stent lumen while said retention stent is in said collapsed stent state; and

said lead delivery means further comprises expansion force applying means for selectively applying expansion force within said retention stent lumen while said retention stent is in said collapsed stent state and at said desired implantation site to expand said tubular stent body from said collapsed stent state to said expanded stent state.

9. The assembly of claim 8, herein said expansion force applying means further comprises:

a balloon catheter having an expandable balloon fitted within said retention stent lumen adapted to be expanded to apply expansion force to said retention stent while said retention stent is in said collapsed stent state and at said desired implantation site to expand said tubular stent body from said collapsed stent state to said expanded stent state.

10. The assembly of claim 8, herein said expansion force applying means further comprises:

a balloon catheter having an expandable balloon fitted within said retention stent lumen adapted to be expanded to apply expansion force to said retention stent while said retention stent is in said collapsed stent state and at said desired implantation site to expand said tubular stent body from said collapsed stent state to said expanded stent state; and

an introducer having an introducer lumen for receiving said lead body and said balloon catheter coupled with said retention stent while said retention stent is in said collapsed stent state with said expandable balloon fitted within said retention stent lumen,

whereby, upon advancement of the introducer to the desired implantation site, the retention stent and the balloon of the balloon catheter are adapted to be advanced distally from the introducer lumen and the balloon inflated to apply expansion force to said retention stent when said retention stent is in said collapsed stent state and at said desired implantation site to expand said tubular stent body from said collapsed stent state to said expanded stent state.

11. The assembly of claim 7, wherein:

said retention stent is formed of a tubular stent body adapted to be expanded from said collapsed stent state to said expanded stent state through the application of expansion force applied within said retention stent lumen while said retention stent is in said collapsed stent state; and

said lead delivery means further comprises expansion force applying means for selectively applying expansion force within said retention stent lumen while said retention stent is in said collapsed stent state and at said desired implantation site to expand said tubular stent body from said collapsed stent state to said expanded stent state.

12. The assembly of claim 11, wherein said expansion force applying means further comprises:

a balloon catheter having an expandable balloon fitted within said retention stent lumen adapted to be expanded to apply expansion force to said retention stent while said retention stent is in said collapsed stent state and at said desired implantation site to expand said tubular stent body from said collapsed stent state to said expanded stent state.

13. The assembly of claim 11, wherein said expansion force applying means further comprises:

a balloon catheter having an expandable balloon fitted within said retention stent lumen adapted to be expanded to apply expansion force to said retention stent while said retention stent is in said collapsed stent state and at said desired implantation site to expand said tubular stent body from said collapsed stent state to said expanded stent state; and

an introducer having an introducer lumen for receiving said lead body and said balloon catheter coupled with said retention stent while said retention stent is in said collapsed stent state with said expandable balloon fitted within said retention stent lumen,

whereby, upon advancement of the introducer to the desired implantation site, the retention stent and the balloon of the balloon catheter are adapted to be advanced distally from the introducer lumen and the balloon inflated to apply expansion force to said retention stent when said retention stent is in said collapsed stent state and at said desired implantation site to expand said tubular stent body from said collapsed stent state to said expanded stent state.

14. The assembly of claim 13, wherein said retention stent extends proximally from the proximal support end of said tubular electrode support, said lead body extends proximally from said tubular electrode support and through said stent lumen, and said tubular electrode support extends distally from a distal end of said introducer when said retention stent and balloon catheter are received within said introducer lumen.

15. The assembly of claim 7, wherein said retention stent is formed of a tubular stent body adapted to be restrained in said collapsed state and to expand from said collapsed stent state to said expanded stent state upon release of a restraint applied thereto;

and

said lead delivery means further comprises restraining force applying means for selectively applying restraining force to said retention stent to maintain said retention stent is in said collapsed stent state and restraining force release means for releasing the restraining force at said desired implantation site to allow said tubular stent body to expand from said collapsed stent state to said expanded stent state.

16. The assembly of claim 15, wherein:

said restraining force applying means further comprises an introducer having an introducer lumen for receiving said lead body extending therethrough and said retention stent in a distal portion of said introducer lumen while said retention stent is in said collapsed stent state; and

said release means further comprises a pusher catheter adapted to be advanced distally through said introducer lumen and to push against and move said retention stent distally out of said distal portion of said introducer lumen while said retention stent is in said collapsed stent state, thereby releasing the restraining force applied to said retention stent to allow said tubular stent body to expand from said collapsed stent state to said expanded stent state.

17. The assembly of claim 16, wherein said retention stent extends proximally from the proximal support end of said tubular electrode support, said lead body extends proximally from said tubular electrode support and through said stent lumen, and said tubular electrode support extends distally from a distal end of said introducer when said retention stent is received within said distal portion of said introducer lumen.

18. A method of advancing and fixing a first distal electrode of an electrical lead within a patient'"'"'s body at a desired implantation site in an elongated body vessel, the electrical lead including a lead body extending between a proximal lead end and a distal lead end and a first lead conductor extending within said lead body between said proximal and distal lead ends and electrically connected to said first distal electrode, said arrangement comprising:

providing a tubular electrode support coupled to said distal lead end having a fixed tubular support outer wall supporting said first electrode, said tubular electrode support having an outer wall diameter and having a tubular support lumen extending between a proximal support end and a distal support end;

providing a tubular retention stent mounted to and extending axially from said tubular electrode support, said retention stent having a retention stent lumen axially aligned with said tubular support lumen and adapted to assume a collapsed stent state having a collapsed stent diameter smaller than the vessel diameter to enable introduction of said distal lead end to said desired implantation site and to assume an expanded stent state having an expanded stent diameter sufficient to engage the retention stent against the body vessel to inhibit movement;

engaging and advancing said distal lead end to the desired implantation site with said retention stent in said collapsed stent state;

effecting the expansion of said retention stent from said collapsed stent state to said expanded stent state, whereby the aligned retention stent lumen and tubular support lumen enable flow of body fluids therethrough.

19. The method of claim 18, further comprising the step of:

forming said retention stent of a tubular stent body adapted to be expanded from said collapsed stent state to said expanded stent state through the application of expansion force applied within said retention stent lumen while said retention stent is in said collapsed stent state; and

said effecting step further comprises;

selectively applying expansion force within said retention stent lumen said retention stent is in said collapsed stent state and at said desired implantation site to expand said tubular stent body from said collapsed stent state to said expanded stent state.

20. The method of claim 19, wherein said engaging and advancing step further comprises the step of:

inserting a balloon catheter having an expandable balloon within said retention stent lumen while said retention stent is in said collapsed stent state; and

advancing said balloon catheter and said distal lead end to the desired implantation site; and

said expansion force applying step further comprises the steps of;

expanding the expandable balloon at said desired implantation site to apply expansion force to said retention stent to expand said tubular stent body from said collapsed stent state to said expanded stent state.

21. The method of claim 19, wherein said engaging and advancing step further comprises the step of:

inserting a balloon catheter having an expandable balloon within said retention stent lumen while said retention stent is in said collapsed stent state;

inserting the balloon catheter and said lead into an introducer lumen with said expandable balloon and said retention stent while said retention stent is in said collapsed stent state;

advancing said introducer, said balloon catheter, and said distal lead end to the desired implantation site; and

ejecting said expandable balloon and said retention stent distally from said introducer lumen; and

said expansion force applying further comprises the steps of;

expanding the expandable balloon at said desired implantation site to apply expansion force to said retention stent to expand said tubular stent body from said collapsed stent state to said expanded stent state.

22. The method of claim 18, further comprising the step of:

forming said retention stent of a tubular stent body adapted to be restrained in said collapsed state and to expand from said collapsed stent state to said expanded stent state upon release of a restraint applied thereto; and

said effecting step further comprises;

selectively applying restraining force to said retention stent to maintain said retention stent is in said collapsed stent state; and

releasing the restraining force at said desired implantation site to allow said tubular stent body to expand from said collapsed stent state to said expanded stent state.

23. The method of claim 22, wherein:

said restraining force applying step further comprises locating said lead body extending through an introducer lumen of an elongated introducer with said retention stent restrained in said collapsed stent state in a distal portion of said introducer lumen; and

said releasing step further comprises advancing a pusher catheter distally through said introducer lumen to push against and move said retention stent distally out of said distal portion of said introducer lumen while said retention stent is in said collapsed stent state, thereby releasing the restraining force applied to said retention stent to allow said tubular stent body to expand from said collapsed stent state to said expanded stent state.

24. The method of claim 18, wherein said body vessel constitutes the coronary sinus of the heart and body fluids constitute venous blood.

25. The method of claim 18, wherein said body vessel constitutes the great vein descending from the coronary sinus of the heart and body fluids constitute venous blood.