IMPLANTABLE DEVICE FOR TREATMENT OF VENTRICULAR DILATION

• US 20090054724A1
• Filed: 08/22/2007
• Published: 02/26/2009
• Est. Priority Date: 08/22/2007
• Status: Active Grant

• Current Assignee: Edwards Lifesciences Corporation
• Original Assignee: Edwards Lifesciences Corporation
• Inventors: Hauser, David L., Solem, Jan Otto
• Granted Patent: US 8,100,820 B2
• Time in Patent Office: Days
• US Class Current: 600/37
• CPC Class Codes: A61F 2/2451 Inserts in the coronary sinus for correcting the valve shape
• CPC Class Codes: A61F 2/2481 Devices outside the heart wall, e.g. bags, strips or bands
• CPC Class Codes: A61F 2250/0007 for adjusting length
• CPC Class Codes: A61F 2250/0031 made from both resorbable and non-resorbable prosthetic parts, e.g. adjacent parts

Abstract

A device and method for reducing ventricular dilation by placing one or more cardiac bridges into vessels extending along a length of the ventricle. Each cardiac bridge preferably includes a pair of anchors and a bridge member secured therebetween. The tension in the bridge member is increased to compress the ventricle and thereby reduce the dilation. In another embodiment, the bridge member is tensioned to reshape the left ventricle for reducing tension on the chordae tendinae in the heart to improve valve function.

Claims

1. A method of reducing left ventricular dilation, comprising:

advancing at least a portion of a cardiac bridge into a posterior vein of a left ventricle, the cardiac bridge including a proximal anchor, a distal anchor and a bridge member connecting the proximal and distal anchors;

expanding the proximal and distal anchors; and

altering a curvature of the bridge member between the proximal and distal anchors such that the bridge member applies a compressive force to a wall of the left ventricle.

2. The method of claim 1, wherein the curvature of the bridge member is altered by increasing tension in the bridge member, thereby causing the bridge member to adjust toward a straighter configuration.

3. The method of claim 2, wherein a resorbable material is provided along the bridge member for maintaining the bridge member in an elongated configuration and wherein the resorbable material is resorbed over time for gradually reducing a length of the bridge member.

4. The method of claim 1, wherein the cardiac bridge is formed at least in part of a shape memory material.

5. The method of claim 1, wherein the proximal and distal anchors comprise expandable stents.

6. A method of reducing ventricular dilation, comprising:

advancing at least a portion of a first cardiac bridge into a first vein that branches from a coronary sinus and extends along a length of a left ventricle, the first cardiac bridge including a first proximal anchor, a first distal anchor and a first bridge member;

advancing at least a portion of a second cardiac bridge into a second vein that branches from the coronary sinus and extends along the length of the left ventricle, the second cardiac bridge including a second proximal anchor, a second distal anchor and a second bridge member;

joining the first and second bridge members; and

increasing tension in the first and second bridge members such that the bridge members applies a compressive force to the ventricular wall.

7. The method of claim 6, wherein joining the first and second bridge members comprises securing ends of the first and second bridge members with a coupling member at a location proximal to the first and second proximal anchors.

8. The method of claim 6, wherein joining the first and second bridge members comprises securing ends of the first and second bridge members with a coupling member at a location distal to the first and second distal anchors.

9. The method of claim 8, wherein the first and second bridge members are secured to the coupling member in a region along an apex of the heart.

10. The method of claim 7, wherein the coupling member is an advanceable clip which is configured to slide over the first and second bridge members and has an open configuration for advancement and a closed configuration for securing the bridge members.

11. The method of claim 7, further comprising removing a portion of the first and second bridge members proximal to the coupling member.

12. The method of claim 6, wherein joining the first and second bridge members comprises securing ends of the first and second bridge members to an anchoring member deployed in the coronary sinus.

13. A method for improving coaption of leaflets of a mitral valve, comprising:

advancing at least a portion of a cardiac bridge into a posterior vein of the left ventricle, the cardiac bridge including a proximal anchor, a distal anchor and a bridge member connecting the proximal and distal anchors;

expanding the proximal and distal anchors; and

applying tension to the bridge member for reducing a height of a left ventricle and thereby reducing tension on the chordae tendinae.

14. A device for treating left ventricular dilation, comprising:

a first cardiac bridge including a first proximal anchor, a first distal anchor and a first elongate bridge member;

a second cardiac bridge including a second proximal anchor, a second distal anchor and a second bridge member; and

a coupling member for securing ends of the first and second elongate bridge members;

wherein the first cardiac bridge member is configured to be deployed within a first vessel extending along a left ventricle and the second cardiac bridge member is configured to be deployed in a second vessel adjacent to the first vessel and wherein the bridge members are configured to be secured to the coupling member to form a compressive body for altering a shape of the left ventricle.