Device and method for modifying the shape of a body organ

• US 8,172,898 B2
• Filed: 03/08/2010
• Issued: 05/08/2012
• Est. Priority Date: 12/05/2001
• Status: Expired due to Term

• Current Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Original Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Inventors: Adams, John M., Mathis, Mark L., Reuter, David G., Beeson, Cruz, Kowalsky, Leonard, Alferness, Clifton A.
• Primary Examiner(s): Isabella, David
• Assistant Examiner(s): Sharma, Yashita
• Application Number:
  US12/719,758
• Publication Number:
  US 20100168847A1
• Time in Patent Office: 792 Days
• Field of Search: 623/1.11, 623/1.15, 623/2.1, 623/2.36, 623/2.37
• US Class Current: 623/2.36
• CPC Class Codes: A61F 2/2451 Inserts in the coronary sinus for correcting the valve shape
• CPC Class Codes: A61F 2250/001 for adjusting a diameter
• CPC Class Codes: A61F 2250/0059 temporary

Abstract

An intravascular support device includes a support or reshaper wire, a proximal anchor and a distal anchor. The support wire engages a vessel wall to change the shape of tissue adjacent the vessel in which the intravascular support is placed. The anchors and support wire are designed such that the vessel in which the support is placed remains open and can be accessed by other devices if necessary. The device provides a minimal metal surface area to blood flowing within the vessel to limit the creation of thrombosis. The anchors can be locked in place to secure the support within the vessel.

Claims

1. A device for treating mitral valve regurgitation, comprising:

a distal anchor having a collapsed configuration within a delivery device and an expanded configuration with an expanded diameter;

a proximal anchor having a collapsed configuration within the delivery device and an expanded configuration with an expanded diameter; and

a connecting element connecting the distal and proximal anchors,

wherein the diameter of the proximal anchor in the expanded configuration is at least about 133% greater than the diameter of the distal anchor in the expanded configuration,

wherein each of the distal and proximal anchors are adapted to have the expanded configurations with the expanded diameters external to a patient'"'"'s body.

2. The device of claim 1 wherein the distal and proximal anchors each have collapsed diameters in their collapsed configurations, and wherein the collapsed diameter of the distal anchor within the delivery device is substantially the same as the collapsed diameter of the proximal anchor within the delivery device.

3. The device of claim 1 wherein the diameter of the proximal anchor in the expanded configuration is at least about 200% greater than the diameter of the distal anchor in the expanded configuration.

4. The device of claim 1 wherein the diameter of the proximal anchor in the expanded configuration is at least about 333% greater than the diameter of the distal anchor in the expanded configuration.

5. The device of claim 1 further comprising a distal lock adapted to lock the distal anchor in a locked configuration.

6. The device of claim 5 wherein the distal lock is adapted to lock the distal anchor in the expanded configuration.

7. The device of claim 1 further comprising a proximal lock adapted to lock the proximal anchor in a locked configuration.

8. The device of claim 7 wherein the proximal lock is adapted to lock the proximal anchor in the expanded configuration.