Cardiac valve annulus restraining device

• US 20070027533A1
• Filed: 07/28/2005
• Published: 02/01/2007
• Est. Priority Date: 07/28/2005
• Status: Abandoned Application

• Current Assignee: Medtronic Vascular, Inc. (Medtronic Plc)
• Original Assignee: Medtronic Vascular, Inc. (Medtronic Plc)
• Inventors: Douk, Nareak
• Application Number:
  US11/193,674
• Publication Number:
  US 20070027533A1
• Time in Patent Office: Days
• US Class Current: 623/2.110
• CPC Class Codes: A61F 2/2433 using balloon catheter
• CPC Class Codes: A61F 2/2445 Annuloplasty rings in direct contact with the valve annulus
• CPC Class Codes: A61F 2/2466 Delivery devices therefor
• CPC Class Codes: A61F 2250/001 for adjusting a diameter

Abstract

A catheter based system for treating mitral valve regurgitation includes a restraining device having a flexible member, a plurality of movable anchor members attached to the outer surface of the flexible member, and an adjustment filament attached to the ends of the flexible member. One embodiment of the invention includes a method for attaching a flexible restraining device to the annulus of a mitral valve, and adjusting the length of the adjustment filament attached to the flexible member of the restraining device, thereby reshaping the mitral valve annulus so that the anterior and posterior leaflets of the mitral valve close during ventricular contraction.

Claims

1. A system for treating mitral valve regurgitation, the system comprising:

a catheter;

a flexible restraining device having a plurality of anchor members extendable therefrom;

the anchor members being integrally formed with or fixedly attached to the flexible restraining device;

the anchor members shaped for penetration into the annulus of a mitral valve

the anchor members being movable from a delivery configuration to a deployment configuration; and

an adjustment member extending from end portions of the flexible restraining device.

2. The system of claim 1 wherein the flexible restraining device has an elongated, essentially linear configuration and an arcuate configuration;

the flexible restraining device has an inner surface and an outer surface and the anchor members are positionable in a catheter delivery configuration, in which the anchor members are parallel to the outer surface of the flexible restraining device; and

the anchor members are positionable in a deployment configuration, in which the anchor members extend radially from flexible restraining device and when the device is deployed from a catheter the anchor members extend to the deployment configuration.

3. The system of claim 1 wherein the flexible restraining device and anchor members comprise a shape memory alloy.

4. The system of claim 1 wherein the flexible restraining device and anchor members comprise nitinol.

5. The system of claim 1 further comprising means for seating the flexible restraining device against the annulus of a mitral valve and implanting the anchor members into the annulus.

6. The system of claim 1 wherein the catheter comprises:

an outer sheath;

a delivery chamber within the sheath at a distal end of the catheter; and

a deployment device positioned within the delivery chamber, wherein when the system is delivered to a location adjacent to a mitral valve, the flexible restraining device is deployed from the delivery chamber and positioned in a supra-annular position adjacent to the annulus of the mitral valve.

7. The system of claim 6 further wherein the catheter further comprises an inflatable balloon attached thereto and when the balloon is inflated, the flexible restraining device is seated against the annulus of the mitral valve.

8. The system of claim 1 wherein the adjustment member is selected from the group consisting of a string, a wire, a cord, a filament, and a cable.

9. The system of claim 8 wherein the flexible restraining device is a generally tubular member and the adjustment member is routed through the restraining device such that the ends of the adjustment member extend from the ends of the restraining device, and wherein when the restraining device is in an arcuate configuration, the adjustment member may be used to draw the ends of the flexible restraining device toward each other and maintain the ends of the restraining device in a fixed position.

10. A device for treating mitral valve regurgitation comprising:

a flexible restraining device having a plurality of anchor members extending therefrom;

the anchor members being integrally formed with or fixedly attached to the flexible restraining device;

the anchor members being movable from a delivery configuration to a deployment configuration; and

an adjustment member extending from end portions of the flexible restraining device.

11. The device of claim 10 wherein the flexible restraining device has an inner surface, an outer surface, an arcuate configuration and an elongated, essentially linear configuration;

the anchor members are positionable in a catheter delivery configuration, in which the anchor members lie on the outer surface of the flexible restraining device; and

the anchor members are positionable in a deployment configuration, in which the anchor members extend radially from flexible restraining device and when the device is deployed from a catheter the anchor members extend to the deployment configuration.

12. The device of claim 10 wherein the adjustment member is selected from the group consisting of a string, a wire, a cord, a filament, and a cable.

13. The device of claim 10 wherein the flexible restraining device is a generally tubular member and the adjustment member is routed through the restraining device such that the ends of the adjustment member extend from the ends of the restraining device, and wherein when the restraining device is in an arcuate configuration, the adjustment member may be used to draw the ends of the flexible restraining device toward each other and maintain the ends of the restraining device in a fixed position.

14. The device of claim 13 further comprising means for securing the ends of the adjustment members such the ends of the restraining device can be maintained in a fixed position.

15. The device of claim 10 wherein the flexible restraining device and anchor members comprise a shape memory alloy.

16. The system of claim 12 wherein the flexible restraining device and anchor members comprise nitinol.

17. A method of treating mitral valve regurgitation, the method comprising:

delivering a flexible restraining device, having shape-memory anchor members, to a location adjacent a mitral valve via a catheter;

deploying the flexible restraining device from the distal tip of the catheter thereby causing the flexible restraining device to assume an arcuate configuration;

moving the anchor members from a delivery to a deployment configuration responsive to the deployment of the flexible restraining device;

positioning the flexible restraining device against an annulus of the mitral valve;

inserting the anchor members into the annulus;

altering the shape of the flexible restraining device by altering the radius of the arcuate configuration; and

reshaping the annulus in response to the altering of the radius of the arcuate configuration the flexible restraining device.

18. The method of claim 17 wherein inserting the shape memory anchor members into the annulus further comprises inflating a balloon to exert force on the flexible ring, and causing the anchor members to penetrate the annulus.

19. The method of claim 17 wherein altering the radius of an arcuate configuration of the flexible restraining device further comprises drawing the ends of the device toward each other when the device is in the arcuate configuration.

20. The method of claim 17 wherein reshaping the annulus of the mitral valve reduces mitral valve regurgitation.