Methods and systems for heart valve therapy

• US 9,050,188 B2
• Filed: 05/02/2014
• Issued: 06/09/2015
• Est. Priority Date: 10/23/2013
• Status: Active Grant

• Current Assignee: Caisson Interventional, LLC (LivaNova Plc)
• Original Assignee: Caisson Interventional, LLC (LivaNova Plc)
• Inventors: Schweich, Cyril J. Jr., Mortier, Todd J.
• Primary Examiner(s): Iwamaye, Andrew
• Assistant Examiner(s): LOPEZ, LESLIE ANN
• Application Number:
  US14/268,076
• Publication Number:
  US 20150112427A1
• Time in Patent Office: 403 Days
• Field of Search: 623/1.24, 623/1.26, 623 217- 218, 623 236- 238
• US Class Current: 1/1
• 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 2/243 Deployment by mechanical expansion
• CPC Class Codes: A61F 2/2436 Deployment by retracting a sheath
• CPC Class Codes: A61F 2002/9534 for repositioning of stents
• CPC Class Codes: A61F 2220/0016 with sharp anchoring protrusions, e.g. barbs, pins, spikes
• CPC Class Codes: A61F 2230/0006 circular
• CPC Class Codes: A61F 2230/0034 D-shaped
• CPC Class Codes: A61F 2250/006 modular
• CPC Class Codes: A61F 2310/00023 Titanium or titanium-based alloys, e.g. Ti-Ni alloys

Abstract

Systems and methods for medical interventional procedures, including approaches to valve implantation. In one aspect, the methods and systems involve a modular approach to mitral valve therapy.

Claims

1. A method of replacing a mitral valve of a heart in a multiple step approach, the mitral valve including commissural clefts, an anterior leaflet, a posterior leaflet, an annulus and a sub-annular gutter, comprising:

inserting an anchor assembly within the heart, the anchor assembly including a first expandable frame movable between a compressed configuration and an expanded configuration, a retention structure, a plurality of projections, and a generally central hub of the first expandable frame positioned lower than the plurality of projections and positioned radially inward from the retention structure;

expanding the anchor assembly to the expanded configuration while positioned supra-annularly to the mitral valve;

arranging at least one of the plurality of projections so that the one projection is placed into engagement with the sub-annular gutter;

subsequent to inserting the anchor assembly and arranging the at least one of the plurality of projections of the anchor assembly, inserting an artificial valve within the heart, the artificial valve comprising a second expandable frame and valve leaflets attached to the second expandable frame, wherein the inserted anchor assembly leaves the leaflets of the mitral valve unaffected and the anchor assembly does not interrupt leaflet, chordae, or native valve function of the mitral valve until placement of the artificial valve; and

arranging the artificial valve into engagement with the retention structure of the anchor assembly.

2. The method of claim 1, wherein the anchoring assembly is sized and shaped to be implanted without reshaping the annulus.

3. The method of claim 1, wherein the artificial valve is configured to sealingly engage natural tissue.

4. The method of claim 1, wherein the artificial valve is inserted within the heart using a catheter, wherein the artificial valve is self-expanded within the anchor assembly.

5. The method of claim 1, further comprising employing an orientation frame to align the plurality of projections with native anatomy.

6. The method of claim 5, wherein the orientation frame defines a part of the anchoring assembly.

7. The method of claim 5, wherein the orientation frame defines structure separate and distinct from the anchor assembly.

8. The method of claim 1, wherein said arranging the artificial valve comprises engaging a generally D-shaped outer peripheral region of the second expandable frame of the artificial valve with the retention structure of the anchor assembly while a circular valve orifice of the artificial valve is positioned radially inward from the generally D-shaped outer peripheral region and carries the valve leaflets that define a circular perimeter at the circular valve orifice.

9. The method of claim 8, wherein the first expandable frame of the anchor assembly comprises a first nitinol wire construction that is at least partially covered in a mesh material and that is movable between the compressed configuration and the expanded configuration, and wherein the second expandable frame of artificial valve comprises a second nitinol wire construction that is at least partially covered in a tissue material and that is expandable independently from the first expandable frame of the anchoring assembly.

10. The method of claim 9, wherein the plurality of projections of the anchor assembly comprise sub-annular projections that are positioned lower than the retention structure of the anchor assembly, and wherein the generally central hub is positioned lower than the sub-annular projections.

11. The method of claim 10, wherein said inserting the anchor assembly within the heart comprises inserting the anchor assembly into the left atrium via an anchor delivery catheter, and said inserting the anchor assembly within the heart comprises inserting the valve assembly into the left atrium via a valve delivery catheter after the anchor assembly engages with the sub-annular gutter of the mitral valve.

12. A method of replacing a mitral valve of a heart in a multiple step approach, the mitral valve including commissural clefts, an anterior leaflet, a posterior leaflet, an annulus and a sub-annular gutter, comprising:

inserting an anchor assembly within the heart using an anchor delivery catheter covering the anchor assembly, the anchor assembly including a first expandable frame movable between a compressed configuration and an expanded configuration, a retention structure, a plurality of projections, and a generally central hub of the first expandable frame positioned lower than the plurality of projections and positioned radially inward from the retention structure;

at least partially uncovering the anchor assembly while positioned supra-annular to the mitral valve;

arranging at least one of the plurality of projections so that the one projection is placed into engagement with the sub-annular gutter;

subsequent to inserting the anchor assembly and arranging the at least one of the plurality of projections of the anchor assembly, inserting an artificial valve within the heart, the artificial valve comprising a second expandable frame and valve leaflets attached to the second expandable frame, wherein the inserted anchor assembly leaves the leaflets of the mitral valve unaffected and the anchor assembly does not interrupt leaflet, chordae, or native valve function of the mitral valve until placement of the artificial valve; and

arranging the artificial valve into engagement with the retention structure of the anchor assembly.

13. The method of claim 12, wherein the anchoring assembly is sized and shaped to be implanted without reshaping the annulus.

14. The method of claim 12, wherein the artificial valve is configured to sealingly engage natural tissue.

15. The method of claim 12, wherein the artificial valve has a sealing surface and the sealing surface is configured to engage natural leaflets.

16. The method of claim 12, wherein the artificial valve is self-expanded within the anchor assembly.

17. The method of claim 12, wherein said arranging the artificial valve comprises engaging a generally D-shaped outer peripheral region of the second expandable frame of the artificial valve with the retention structure of the anchor assembly while a circular valve orifice of the artificial valve is positioned radially inward from the generally D-shaped outer peripheral region and carries the valve leaflets that define a circular perimeter at the circular valve orifice.

18. The method of claim 17, wherein the first expandable frame of the anchor assembly comprises a first nitinol wire construction that is at least partially covered in a mesh material and that is movable between the compressed configuration and the expanded configuration, and wherein the second expandable frame of artificial valve comprises a second nitinol wire construction that is at least partially covered in a tissue material and that is expandable independently from the first expandable frame of the anchoring assembly.

19. The method of claim 18, wherein the plurality of projections of the anchor assembly comprise sub-annular projections that are positioned lower than the retention structure of the anchor assembly, and wherein the generally central hub is positioned lower than the sub-annular projections.

20. The method of claim 19, wherein said inserting the anchor assembly within the heart comprises inserting the anchor assembly into the left atrium via the anchor delivery catheter, and said inserting the anchor assembly within the heart comprises inserting the valve assembly into the left atrium via a valve delivery catheter after the anchor assembly engages with the sub-annular gutter of the mitral valve.