Method and apparatus for reducing mitral regurgitation

• US 7,241,310 B2
• Filed: 01/14/2003
• Issued: 07/10/2007
• Est. Priority Date: 01/14/2002
• Status: Expired due to Term

• Current Assignee: Guided Delivery Systems, Inc.
• Original Assignee: Viacor, Inc.
• Inventors: Cohn, William E., Liddicoat, John R., Davenport, Todd F., Streeter, Richard B., Taylor, Daniel C., Woolfson, Steven B., Rourke, Jonathan, Kordis, Thomas F.
• Primary Examiner(s): McDermott; Corrine
• Assistant Examiner(s): Sweet; Thomas J.
• Application Number:
  US10/342,034
• Publication Number:
  US 20040019377A1
• Time in Patent Office: 1,638 Days
• Field of Search: 623/2.11, 623/2.36
• US Class Current: 623/2.36
• CPC Class Codes: A61B 17/3468 for implanting or removing devices, e.g. prostheses, implants, seeds, wires devices for implanting seeds A61M37/0069
• CPC Class Codes: A61B 17/3478 Endoscopic needles, e.g. for infusion biopsy needles A61B10/0233; catheters with injection needles A61M25/0067
• CPC Class Codes: A61B 2017/00247 Making holes in the wall of the heart, e.g. laser Myocardial revascularization
• CPC Class Codes: A61B 2018/00392 Transmyocardial revascularisation
• CPC Class Codes: A61F 2/2451 Inserts in the coronary sinus for correcting the valve shape
• CPC Class Codes: A61F 2250/0007 for adjusting length
• CPC Class Codes: A61F 2250/0063 Nested prosthetic parts
• CPC Class Codes: Y10S 623/904 Heart

Abstract

A method and device for reducing mitral regurgitation. An elongated body is positioned in a coronary sinus of a patient in a vicinity of a heart mitral valve posterior leaflet. The body is adapted to straighten a natural curvature of at least a portion of the coronary sinus in the vicinity of the posterior leaflet to move a posterior annulus anteriorly, which in turn moves the posterior leaflet anteriorly, thereby to improve leaflet coaptation.

Claims

1. An assembly for reducing mitral regurgitation, the assembly comprising:

a flexible delivery catheter for insertion into a coronary sinus of a patient in a vicinity of a posterior leaflet portion of a mitral valve;

structure for anchoring a distal end of said catheter in the coronary sinus;

a generally flexible push rod adapted for passage through said delivery catheter; and

an elongated substantially straight rod portion comprising a portion of said push rod and defining a more rigid portion of the length of said generally flexible push rod and disposed proximal to a distal end of said push rod and configured for moving through said catheter and into a position within said catheter and in the vicinity of the posterior leaflet portion of the mitral valve, said elongated substantially straight rod portion being of a metallic material more rigid than tissue proximate the posterior leaflet portion of the mitral valve, and being sized whereby to straighten a natural curvature of at least a portion of the coronary sinus in the vicinity of the posterior leaflet portion of the mitral valve, to move a posterior annulus portion of the mitral valve anteriorly and thereby improve coaptation between the posterior leaflet and an anterior leaflet portion of the mitral valve.

2. The assembly in accordance with claim 1 wherein said anchoring structure comprises barbs on said catheter for engaging with internal wall portions of the coronary sinus.

3. The assembly in accordance with claim 1 wherein said anchoring structure comprises a balloon attached to said catheter, the balloon engaging internal wall portions of the coronary sinus.

4. The assembly in accordance with claim 1 wherein said anchoring structure comprises a stent adjacent said catheter, said stent being adapted upon expansion thereof for engaging internal wall portions of the coronary sinus.

5. The assembly in accordance with claim 1 wherein said anchoring structure comprises hooks attached to said catheter and adapted to engage internal wall portions of the coronary sinus.

6. The assembly in accordance with claim 5 wherein said hooks are fixed on a stent and are adapted to engage the wall portions of the coronary sinus by expansion of the stent.

7. The assembly in accordance with claim 5 wherein said hooks are adapted for engaging with the internal wall and perforating the wall.

8. The assembly in accordance with claim 1 wherein said anchoring structure comprises an expandable foam body attached to said catheter, said foam body being adapted upon expansion for engaging internal wall portions of the coronary sinus.

9. The assembly in accordance with claim 1 wherein said anchoring structure comprises a plurality of selected ones of balloons and foam bodies disposed around the catheter and having gaps therebetween to facilitate blood flow therethrough.

10. The assembly in accordance with claim 1 wherein said anchoring structure comprises a compressed wire ball fixed to said catheter, said wire ball being expandable to engage internal wall portions of the catheter.

11. The assembly in accordance with claim 1 wherein said anchoring structure comprises a cam member mounted in said catheter and moveable into a position for engaging internal wall portions of said catheter and expanding a diameter of said catheter to engage the coronary sinus.

12. The assembly in accordance with claim 1 wherein said anchoring structure comprises lumens in said catheter and extending lengthwise thereof, and side ports in communication with the lumens, the lumens and ports being adapted to flow adhesive therethrough, to bond the catheter distal end to wall portions of the coronary sinus.

13. The assembly in accordance with claim 1 wherein said anchoring structure comprises a mesh fixed to the exterior wall of said catheter for encouraging in-growth of patient body materials.

14. The assembly in accordance with claim 1 wherein said anchoring structure comprises lumens in said catheter and extending lengthwise thereof, and side ports in communication with the lumens, the lumens and the ports being adapted to convey a vacuum therethrough to draw wall portions of the coronary sinus into engagement with catheter wall portions.

15. The assembly in accordance with claim 1 and comprising second anchor structure for anchoring a proximal end of said catheter, said second anchor structure comprising a sewing cuff fixed to the proximal end of said catheter, for suturing to a patient'"'"'s outer skin.

16. The assembly in accordance with claim 1 and further comprising a cap for sealing closed a proximal end of said catheter, said cap being adapted to plug into the catheter proximal end.

17. The assembly in accordance with claim 1 and further comprising a cap for sealing closed a proximal end of said catheter, the cap comprising a wire mesh crimpable upon the catheter proximal end to seal the proximal end.

18. The assembly in accordance with claim 1 wherein said catheter is provided with at least one prolapse resistant portion comprising a reinforced portion which is less flexible than a remainder of said catheter.

19. The assembly in accordance with claim 1, wherein said elongated body is provided at one end thereof with a rounded non-traumatic tip, and strain relief taper, and in width-wise cross-section, a selected one of round and generally rectangular cross-section.

20. The assembly in accordance with claim 1 wherein said elongated body comprises an elastomeric outer portion disposed upon a core member.

21. The assembly in accordance with claim 20 wherein the core member comprises a selected one of a substantially rigid rod and a substantially rigid tube.

22. The assembly in accordance with claim 21 wherein the core member is a tube comprising a selected one of (i) empty and (ii) filled with a substantially rigid material.

23. The assembly in accordance with claim 20 wherein said outer portion is formed with barbs thereon.

24. The assembly in accordance with claim 1 wherein said elongated body is provided with strain relief steps at either end thereof.

25. The assembly in accordance with claim 1 wherein said elongated body is provided with strain relief segments mounted on a central rod.

26. The assembly in accordance with claim 1 wherein said elongated rod portion is comprised of a selected one of (i) nickel titanium and (ii) an alloy thereof.

27. The assembly is accordance with claim 1 wherein said body is anchored in said catheter by a selected one of barbs on said body, stents adjacent said body, and hooks attached to said body.

28. The assembly in accordance with claim 1 wherein said body is anchored in said catheter by an expansion member.

29. The assembly in accordance with claim 28 wherein the expansion member comprises a selected one of a balloon and an expandable foam.

30. The assembly in accordance with claim 1 wherein said body is anchored in said catheter by a selected one of an adhesive, a vacuum, an annular lock, a wedge lock, and a cam.

31. The assembly in accordance with claim 1 wherein said elongated body comprises:

an inner tubular member having a plurality of slots extending widthwise of said inner tubular member; and

an outer tubular member rotatably disposed on said inner tubular member, said outer tubular member having a plurality of slots extending widthwise of said outer tubular member;

the slots of said inner and outer tubular members being alignable with each other to permit bending of said elongated body; and

the slots of said inner and outer tubular members being movable to unaligned positions such that said elongated body resists bending.

32. The assembly in accordance with claim 1, the assembly further comprising:

a guidewire for insertion into the coronary sinus;

said delivery catheter being adapted for insertion into the coronary sinus overriding said guidewire; and

a push rod for moving the elongated body within said catheter to the position in the vicinity of the posterior leaflet.

33. The assembly in accordance with claim 1 wherein said elongated rod portion is of a shape memory alloy material.