Prosthetic valve with sealing members and methods of use thereof

Patent metadata

Field	Value
Publication number	US-9545306-B2
Application number	US-201113091765-A
Country	US
Kind code	B2
Filing date	Apr 21, 2011
Priority date	Apr 21, 2010
Publication date	Jan 17, 2017
Grant date	Jan 17, 2017

Abstract

Embodiments of the present invention provide prosthetic valves having sealing members on the external surface thereof. The prosthetic heart valves of the present invention are preferably delivered by catheter directly through the apex of the heart or by other close range transcatheter delivery methods. Because these methods of implantation require a shorter length of catheter, a prosthetic valve can be more accurately oriented in the desired implantation location. Fluoroscopy can be used to further assist in orientation of the valve. The sealing members of the present invention can be positioned on the prosthetic valve such that, when the prosthetic valve is implanted in a native annulus, each provided sealing member is located adjacent to a commissural point of the native valve leaflets. Because the sealing members are precisely oriented on the prosthetic valve, a physician can ensure that the sealing members are aligned with the commissural points of the native valve leaflets. In embodiments of the present invention, the prosthetic valve can have a waisted middle section, and the sealing members can be located in the waisted middle section such that the crimped diameter of the prosthetic valve is not negatively impacted by the sealing members.

First claim

What is claimed is:

1. A prosthetic heart valve assembly comprising:
a prosthetic valve including a circumferential wall having an inner surface and an outer surface, wherein the prosthetic valve is radially contractible and expandable for transcatheter delivery to a native annulus; and
two or more sealing members mounted on the prosthetic valve and substantially evenly placed around the prosthetic valve, wherein the sealing members have a size and shape corresponding to gaps existing between the implanted prosthetic valve and the native valve and are configured to engage the gaps to prevent paravalvular leakage;
wherein the two or more sealing members protrude from the outer surface of the prosthetic valve in both a crimped configuration before the prosthetic valve is implanted and a deployed configuration after the prosthetic valve is implanted; and
wherein the two or more sealing members do not extend beyond a maximum diameter of the outer surface of the prosthetic valve when the prosthetic valve is in the crimped configuration before the prosthetic valve is implanted.

2. The prosthetic heart valve assembly of claim 1 , wherein the prosthetic valve comprises an inflow section, an outflow section, and a waisted middle section having an expanded diameter less than the expanded diameters of the inflow section and the outflow section, and wherein the sealing members are positioned in the waisted middle section of the prosthetic valve.

3. The prosthetic heart valve assembly of claim 1 , wherein the sealing members include at least three sealing members configured to engage three commissure points of leaflets of a native tricuspid valve to prevent paravalvular leakage.

4. The prosthetic heart valve assembly of claim 3 , wherein the sealing members include three additional sealing members positioned approximately midway between the commissural points of a native tricuspid valve.

5. The prosthetic heart valve assembly of claim 1 , wherein the sealing members comprise at least one pad.

6. The prosthetic heart valve assembly of claim 5 , wherein at least one of the sealing members includes two pads.

7. The prosthetic heart valve assembly of claim 5 , wherein the prosthetic valve comprises support arms extending from the outer surface of the circumferential wall, and the support arms are configured to contact tissue adjacent to an outflow end of a native annulus to brace the prosthetic valve in position.

8. The prosthetic heart valve assembly of claim 1 , wherein the sealing members comprise polyethylene terephthalate.

9. The prosthetic heart valve assembly of claim 1 , wherein the sealing members comprise biological tissue.

10. The prosthetic valve of claim 1 further comprising:
two or more commissural posts, wherein each of the at least two sealing members is longitudinally aligned with a corresponding one of the two or more commissural posts.

11. The prosthetic valve of claim 10 , wherein each of the at least two sealing members have a size capable of occluding gaps created between the native annulus and the commissural posts.

Assignees

• Tabor Charles
• Medtronic Inc

Inventors

• Tabor Charles

Classifications

• A61F2220/0075

  sutured, ligatured or stitched, retained or tied with a rope, string, thread, wire or cable · CPC title

• A61F2250/0069

  Sealing means · CPC title

• A61F2/86

  Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure · CPC title

• A61F2/2433

  using balloon catheter · CPC title

• A61F2/2436

  Deployment by retracting a sheath · CPC title