Valve prosthesis fixation techniques using sandwiching

• US 8,771,345 B2
• Filed: 10/31/2011
• Issued: 07/08/2014
• Est. Priority Date: 09/19/2006
• Status: Active Grant

• Current Assignee: Medtronic Ventor Technologies LTD. (Medtronic Plc)
• Original Assignee: Medtronic Ventor Technologies LTD. (Medtronic Plc)
• Inventors: Tuval, Yosi, Kilemnik, Ido, Benary, Raphael
• Primary Examiner(s): Willse, David H
• Assistant Examiner(s): SHIPMON, TIFFANY P
• Application Number:
  US13/285,226
• Publication Number:
  US 20120046742A1
• Time in Patent Office: 981 Days
• Field of Search: 623 21- 219, 623 222- 226, 623 238- 241, 623 124- 126, 623/23.68
• US Class Current: 623/2.12
• CPC Class Codes: A61F 2/2409 Support rings therefor, e.g. for connecting valves to tissue annuloplasty rings A61F2/2442
• CPC Class Codes: A61F 2/2418 Scaffolds therefor, e.g. support stents
• CPC Class Codes: A61F 2/2427 Devices for manipulating or deploying heart valves during implantation
• CPC Class Codes: A61F 2/2436 Deployment by retracting a sheath
• CPC Class Codes: A61F 2/2469 with resilient valve members, e.g. conical spiral
• CPC Class Codes: A61F 2/9522 Means for mounting a stent or stent-graft onto or into a placement instrument
• CPC Class Codes: A61F 2220/0008 Fixation appliances for connecting prostheses to the body
• CPC Class Codes: A61F 2220/0016 with sharp anchoring protrusions, e.g. barbs, pins, spikes
• CPC Class Codes: A61F 2220/005 using adhesives
• CPC Class Codes: A61F 2220/0058 soldered or brazed or welded
• CPC Class Codes: A61F 2220/0075 sutured, ligatured or stitched, retained or tied with a rope, string, thread, wire or cable
• CPC Class Codes: A61F 2230/0006 circular
• CPC Class Codes: A61F 2230/005 Rosette-shaped, e.g. star-shaped
• CPC Class Codes: A61F 2230/0054 V-shaped
• CPC Class Codes: A61F 2230/0071 spherical
• CPC Class Codes: A61F 2230/008 paraboloidal
• CPC Class Codes: A61F 2250/0039 differing in diameter

Abstract

A prosthesis including a distal fixation member that defines two or more engagement arms that are configured to apply a first axial force to tissue of the subject on a downstream side of the native valve complex. The prosthesis also includes a proximal fixation member configured to apply a second axial force to tissue of the subject on an upstream side of the native valve complex such that application of the first and second axial forces couples the prosthesis to the native valve complex. The proximal fixation member and the distal fixation member are fabricated as one integrated structure. The engagement arms and the proximal fixation member are configured to capture leaflets of the native valve complex therebetween without folding over of leaflets of the native valve complex, upon implantation of the prosthesis.

Claims

1. A prosthesis for implantation at a native valve of a subject, the prosthesis comprising:

a frame comprising;

a distal fixation member configured to be positioned at least partially on a downstream side of the native valve, and shaped so as to define two or more leaflet engagement arms that are configured to apply a first force to tissue of the subject on a downstream side of the native valve, wherein the leaflet engagement arms are configured to contact a downstream side of a leaflet of the native valve without contacting commissures of the native valve upon implantation of the prosthesis;

a proximal fixation member configured to be positioned at least partially on an upstream side of the native valve, at least a portion of the proximal fixation member being configured to contact an upstream side of the native valve upon implantation of the prosthesis, the proximal fixation member being configured to apply a second force to tissue of the subject on an upstream side of the native valve,

wherein application of the first and second forces anchors the prosthesis to the native valve,

wherein the leaflet engagement arms and the proximal fixation member are configured to capture leaflets of the native valve therebetween, upon implantation of the prosthesis; and

a prosthetic valve positioned inside and coupled to the frame.

2. The prosthesis according to claim 1, wherein each of the leaflet engagement arms comprises a portion that is bent proximally.

3. The prosthesis according to claim 1, wherein the leaflet engagement arms and the proximal fixation member are configured to anchor the prosthesis to the native valve by sandwiching the native valve from a downstream side and the upstream side thereof, upon implantation of the prosthesis.

4. The prosthesis according to claim 1, wherein the prosthesis is configured, upon implantation thereof, to embrace, without squeezing, leaflets of the native valve.

5. The prosthesis according to claim 1, wherein the native valve comprises three leaflets and three commissures, wherein the distal fixation member is shaped to define three leaflet engagement arms, wherein the leaflet engagement arms meet one another at junctures, wherein the leaflet engagement arms are shaped so as define three peak complexes at the junctures, and trough complexes, each of which is between the peak complexes, and wherein, upon implantation of the prosthesis, at least a portion of each of the peak complexes is disposed distal to and in rotational alignment with a respective one of commissures of the native valve and at least a portion of each of the trough complexes is disposed in rotational alignment with a respective one of the leaflets of the native valve.

6. The prosthesis according to claim 1, wherein the prosthetic valve comprises one or more prosthetic leaflets, and wherein the prosthetic valve is coupled to the frame such that at least 50% of an axial length of the prosthetic leaflets is distal to valve leaflets of the native valve upon implantation of the prosthesis.

7. The prosthesis according to claim 1, wherein the proximal fixation member comprises an inner support structure, and wherein the distal fixation member comprises an outer support structure that is disposed partially over the inner support structure.

8. The prosthesis according to claim 1, wherein the proximal fixation member is shaped to define a bulging proximal skirt, a proximal portion of which is configured to apply the second force.

9. The prosthesis according to claim 1, wherein a proximal portion of the frame is wider than a distal portion of the frame.

10. The prosthesis according to claim 1, wherein:

the first force is directed upstream; and

the second force is directed downstream.

11. The prosthesis according to claim 1, wherein the prosthesis is configured to apply the first force such that a ratio of (a) the first force to (b) a radial force applied outwardly by the prosthesis against the native valve is greater than 1.5:

1.

12. The prosthesis according to claim 1, wherein the prosthesis is configured to apply the first force with a force of at least 40 g.

13. The prosthesis according to claim 1, wherein the prosthesis is configured such that any radial force applied by the prosthesis outwardly against the native valve is insufficient by itself to chronically maintain the prosthesis in position with respect to the native valve under conditions of normal cardiac motion.

14. The prosthesis according to claim 1, wherein the prosthesis is configured to apply a radial force of less than 0.5 pounds outwardly against the native valve.

15. The prosthesis according to claim 14, wherein the prosthesis is configured to apply a radial force of less than 0.3 pounds outwardly against the native valve.

16. The prosthesis according to claim 15, wherein the prosthesis is configured to apply a radial force of less than 0.1 pounds outwardly against the native valve.

17. The prosthesis according to claim 1, wherein the native valve is a mitral valve.

18. The prosthesis according to claim 1, wherein the native valve is a mitral valve, an aortic valve, a pulmonary valve, or a tricuspid valve.

19. The prosthesis according to claim 1, wherein the native valve comprises two leaflets and two commissures, and wherein the prosthesis comprises two leaflet engagement arms.

20. The prosthesis according to claim 1, wherein the native valve comprises three leaflets and three commissures, and wherein the prosthesis comprises three leaflet engagement arms.

21. The prosthesis according to claim 1, wherein the native valve comprises two leaflets and two commissures, wherein the distal fixation member is shaped to define two leaflet engagement arms, wherein the leaflet engagement arms meet one another at junctures, wherein the leaflet engagement arms are shaped to define two peak complexes at the junctures, and trough complexes, each of which is between the peak complexes, and wherein, upon implantation of the prosthesis, at least a portion of each of the peak complexes is disposed distal to and in rotational alignment with a respective one of commissures of the native valve and at least a portion of each of the trough complexes is disposed in rotational alignment with a respective one of leaflets of the native valve.

22. The prosthesis according to claim 1, wherein the distal fixation member is shaped to define gaps between leaflet engagement arms, and wherein, upon implantation of the prosthesis, the gaps are rotationally aligned with commissures of the native valve and the leaflet engagement arms are rotationally aligned with leaflets of the native valve.

23. The prosthesis according to claim 1, wherein the frame is self-expandable, and wherein the prosthetic valve comprises pericardial tissue.

24. The prosthesis according to claim 1, wherein the valve prosthesis is configured to be implanted using a procedure selected from the group consisting of a transapical procedure, a transaortic procedure, a transseptal procedure, a transarterial procedure, a transcardiac procedure, a percutaneous procedure, and an endovascular procedure.

25. The prosthesis according to claim 1, wherein the number of leaflet engagement arms is equal to the number of leaflets of the native valve.