Method and apparatus for improving mitral valve function

• US 20060136053A1
• Filed: 11/23/2005
• Published: 06/22/2006
• Est. Priority Date: 05/27/2003
• Status: Abandoned Application

• Current Assignee: Guided Delivery Systems, Inc.
• Original Assignee: Guided Delivery Systems, Inc.
• Inventors: Taylor, Daniel C., Barnes, Terrence G., Rourke, Jonathan M., Blacker, Steven J.
• Application Number:
  US11/286,906
• Publication Number:
  US 20060136053A1
• Time in Patent Office: Days
• US Class Current: 623/2.360
• CPC Class Codes: A61F 2/2451 Inserts in the coronary sinus for correcting the valve shape

Abstract

A method and apparatus for reducing mitral regurgitation. The apparatus is inserted into the coronary sinus of a patient in the vicinity of the posterior leaflet of the mitral valve, the apparatus being adapted to straighten the natural curvature of at least a portion of the coronary sinus in the vicinity of the posterior leaflet of the mitral valve, whereby to move the posterior annulus anteriorly and thereby improve leaflet coaptation and reduce mitral regurgitation. The apparatus is also configured to work in conjunction with an electrical lead for an implantable bi-ventricular pacing device, an electrical lead for an implantable cardio defibrillator, etc.

Claims

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

an elongated carrier of material sufficiently flexible to assume a first configuration generally conforming to a coronary sinus upon insertion of the carrier into the coronary sinus, and to assume a straighter second configuration when biased toward the straighter configuration, the carrier having a plurality of lumens extending lengthwise therethrough; and

a plurality of straightening rods adapted to be received by the lumens in the carrier, each of the straightening rods being formed so as to be;

(i) more rigid than the anatomical tissue surrounding the posterior leaflet of the mitral valve; and

(ii) have a shape straighter than the shape of the coronary sinus in the vicinity of the posterior leaflet of the mitral valve; and

(iii) have an adequate length relative to the radius of curvature of the coronary sinus;

such that when the straightening rods are positioned in the lumens while the carrier is positioned in the coronary sinus adjacent to the posterior leaflet of the mitral valve, the straightening rods will impart a straightening force to the wall of the coronary sinus, whereby to move the posterior annulus anteriorly so as to improve leaflet coaptation and, as a result, reduce mitral regurgitation;

wherein at least one of the lumens is sized so as to receive an electrical lead therein.

2. An assembly according to claim 1 wherein the carrier is of a circular cross-section in at least a portion thereof.

3. An assembly according to claim 1 wherein the carrier is of an ovoid cross-section in at least a portion thereof.

4. An assembly according to claim 1 wherein the straightening rods are provided with varying degrees of stiffness along the length thereof.

5. An assembly according to claim 1 wherein the straightening rods are selected from a kit comprising a plurality of rods having different degrees of stiffness.

6. An assembly according to claim 1 wherein the straightening rods are selected from a kit comprising a plurality of rods having different lengths.

7. An assembly according to claim 1 wherein the assembly further comprises a guidewire, and the carrier further comprises an opening through which the guidewire is movable.

8. An assembly according to claim 7 wherein the opening comprises one of the lumens.

9. An assembly according to claim 8 wherein the lumens are of different diameters.

10. An assembly according to claim 8 wherein a first straightening rod is of a stiffness different from the stiffness of a second straightening rod.

11. An assembly according to claim 10 wherein the stiffness of the first straightening rod along at least a portion thereof is inversely coordinated with the stiffness of the second straightening rod along at least a portion thereof.

12. An assembly according to claim 1 wherein the assembly further comprises a sheath for constraining said carrier, said sheath being removable from said carrier.

13. An assembly according to claim 12 wherein the sheath constrains the carrier in a first cross-sectional configuration and, upon removal of the sheath, frees the carrier to assume a second cross-sectional configuration.

14. An assembly according to claim 1 wherein the straightening rods are substantially straight in an unstressed condition.

15. An assembly according to claim 1 wherein the straightening rods are substantially curved after insertion into the coronary sinus.

16. An assembly according to claim 1 wherein the straightening rods comprise first and second end portions connected together by an intermediate portion, wherein the intermediate portion comprises first and second regions connected together by a central region, wherein the central region and the first and second end portions are substantially curved after the elongated body is inserted into the coronary sinus, and further wherein the first and second regions are substantially straight after the elongated body is inserted into the coronary sinus.

17. An assembly according to claim 16 wherein the first and second regions are stiffer than the central region, and further wherein the central region is stiffer than the first and second end portions.

18. An assembly according to claim 16 wherein the central region, the first and second end portions and the first and second regions have a length such that the elongated body applies an anteriorly-directed force to the walls of the coronary sinus substantially adjacent to the posterior leaflet of the valve, and applies a posteriorly-directed force to the walls of the coronary sinus substantially adjacent to the commissures of the valve.

19. An assembly according to claim 1 wherein the straightening rods are formed at least in part out of a resilient material.

20. An assembly according to claim 1 wherein the straightening rods effect valve remodeling on a continuous basis over a prolonged period of time.

21. An assembly according to claim 1 wherein the straightening rods are formed at least in part out of a superelastic material.

22. An assembly according to claim 1 wherein the assembly further comprises a stabilizing scaffold engaging to said elongated carrier.

23. An assembly according to claim 1 wherein at least a portion of the elongated carrier is configured to facilitate tissue in-growth.

24. An assembly according to claim 1 wherein the assembly further comprises an electrical lead extending through a lumen.

25. An assembly according to claim 24 wherein the electrical lead is positioned in the lumen prior to positioning the elongated carrier in a patient.

26. An assembly according to claim 24 wherein the electrical lead is positioned in the lumen after positioning the elongated carrier in a patient.

27. A method for reducing mitral regurgitation, the method comprising the steps of:

providing a flexible carrier having a plurality of lumens extending lengthwise therethrough;

advancing an electrical lead through the vascular system of a patient until a distal end of the electrical lead is disposed in the coronary sinus of the patient, and advancing a guidewire through the vascular system of a patient until a distal end of the guidewire is disposed in the coronary sinus of the patient;

advancing the carrier over the electrical lead and the guidewire until a distal end of the carrier is disposed in the coronary sinus; and

advancing a plurality of straightening rods into the plurality of lumens so as to exert a straightening force on the carrier and thereby on the coronary sinus to move the annulus of the mitral valve anteriorly, whereby to reduce mitral regurgitation.

28. A method according to claim 27 wherein the electrical lead is advanced into the coronary sinus of the patient prior to advancing the guidewire into the coronary sinus of the patient.

29. A method according to claim 27 wherein the guidewire is advanced into the coronary sinus of the patient prior to advancing the electrical lead into the coronary sinus of the patient.

30. A method according to claim 27 wherein the electrical lead and the guidewire extend through the lumens.

31. A method for reducing mitral regurgitation, the method comprising the steps of:

providing a flexible carrier having a plurality of lumens extending lengthwise therethrough;

advancing an electrical lead through the vascular system of a patient until a distal end of the electrical lead is disposed in the coronary sinus of the patient;

advancing the carrier over the electrical lead until a distal end of the carrier is disposed in the coronary sinus; and

advancing a plurality of straightening rods into the plurality of lumens so as to exert a straightening force on the carrier and thereby on the coronary sinus to move the annulus of the mitral valve anteriorly, whereby to reduce mitral regurgitation.

32. A method according to claim 31 wherein the electrical lead extends through the lumens.

33. A method for reducing mitral regurgitation, the method comprising the steps of:

providing a flexible carrier having a plurality of lumens extending lengthwise therethrough;

advancing the carrier through the vascular system of a patient until a distal end of the carrier is disposed in the coronary sinus;

advancing an electrical lead through the carrier until the distal end of the electrical lead is disposed in the coronary sinus of the patient; and

advancing a plurality of straightening rods into the plurality of lumens so as to exert a straightening force on the carrier and thereby on the coronary sinus to move the annulus of the mitral valve anteriorly, whereby to reduce mitral regurgitation.

34. A method according to claim 33 wherein the flexible carrier is advanced into the coronary sinus of the patient over a guidewire.

35. A method according to claim 33 wherein the flexible carrier is advanced into the coronary sinus of the patient using a stylet delivery.

36. A method according to claim 33 wherein the electrical lead extends through a lumen.

37. A method for reducing mitral regurgitation, the method comprising the steps of:

providing a flexible carrier having a plurality of lumens extending lengthwise therethrough, and an electrical lead extending through a lumen;

advancing the carrier through the vascular system of a patient until a distal end of the carrier is disposed in the coronary sinus, and positioning the electrical lead in heart tissue; and

advancing a plurality of straightening rods into the plurality of lumens so as to exert a straightening force on the carrier and thereby on the coronary sinus to move the annulus of the mitral valve anteriorly, whereby to reduce mitral regurgitation.

38. A method according to claim 37 wherein the flexible carrier is advanced into the coronary sinus of the patient over a guidewire.

39. A method according to claim 37 wherein the flexible carrier is advanced into the coronary sinus of the patient using a stylet delivery.

40. A method according to claim 38 wherein the guidewire extends through the lumens.