Kit for implanting in a duct

• US 8,246,675 B2
• Filed: 12/23/2003
• Issued: 08/21/2012
• Est. Priority Date: 12/23/2003
• Status: Active Grant

• Current Assignee: W. L. Gore & Associates (W.L. Gore & Associates)
• Original Assignee: Laboratories Perouse
• Inventors: Zegdi, Rachid
• Primary Examiner(s): Pellegrino, Brian
• Assistant Examiner(s): MILLER, CHERYL L
• Application Number:
  US10/583,658
• Publication Number:
  US 20070198097A1
• Time in Patent Office: 3,164 Days
• Field of Search: 623 124- 126, 623 21- 219, 623/900, 606/106, 606/198, 606/200
• US Class Current: 623/1.24
• CPC Class Codes: A61F 2/2418 Scaffolds therefor, e.g. support stents
• CPC Class Codes: A61F 2002/9528 for retrieval of stents
• CPC Class Codes: A61F 2230/008 paraboloidal
• CPC Class Codes: A61F 2250/006 modular

Abstract

A kit for implanting in a duct, which includes a tubular endoprosthesis and a prosthetic valve is disclosed. The prosthetic valve includes a carrier frame that is radially deformable in elastic manner relative to a central axis of the tubular endoprosthesis between a deployed, implanted position, and a folded, implanting position. The carrier frame is urged elastically towards its deployed position. A flexible shutter is connected to the carrier frame. The shutter is deformable between an obstruction position in which it is extended transversely, and a release position in which it is contracted transversely under to allow a fluid to flow through the carrier frame. The carrier frame also includes an integrated centripetal compressing mechanism for centripetally compressing the carrier frame towards folded position.

Claims

1. A kit for implanting in a duct, the kit comprising:

a tubular endoprosthesis; and

a prosthetic valve configured to be implanted in, and withdrawn from said tubular endoprosthesis;

wherein said prosthetic valve comprises;

a resilient carrier frame that is radially deformable in an elastic manner relative to a central axis of said tubular endoprosthesis between a deployed position in which said resilient carrier frame rests against said tubular endoprosthesis, and a folded position, said resilient carrier frame being biased towards the deployed position by its resiliency;

a flexible shutter connected to said resilient carrier frame, said flexible shutter being deformable between an obstruction position in which said flexible shutter is extended transverse to the central axis of said tubular endoprosthesis and a release position in which said flexible shutter is contracted transverse to the central axis of said tubular endoprosthesis to allow a fluid to flow through said resilient carrier frame; and

integrated centripetal compression means for compressing said resilient carrier frame from the deployed position towards the folded position,

wherein said integrated centripetal compression means comprises a clamp having at least two branches connected together at a common region located along a central axis of said resilient carrier frame in the deployed position, each branch having a connection segment connected to said flexible shutter and a drive segment for centripetally compressing said resilient carrier frame towards the folded position, and

wherein the common region is located at a distance from said connection segments of said branches, said drive segments are located between said connection segments and the common region, axially apart from said connection segments, and said drive segments are spaced axially away from said flexible shutter.

2. The kit according to claim 1, wherein said flexible shutter comprises a pouch having an end wall.

3. The kit according to claim 2, wherein said pouch includes an evacuation orifice formed in said end wall.

4. The kit according to claim 2, wherein said end wall of said pouch is generally hemispherical.

5. The kit according to claim 1, wherein said resilient carrier frame is fork-shaped, each of said branches is elastically deformable, and said branches are welded together at the common region such that said drive segments and said connection segments are located on a first side of the common region.

6. The kit according to claim 1, wherein said at least two branches of said clamp is two branches.

7. The kit according to claim 1, wherein said at least two branches of said clamp is three branches.

8. The kit according to claim 1, wherein

said flexible shutter comprises a pouch having an end wall;

and

said prosthetic valve further comprises a plurality of threads respectively connecting each of said branches to said end wall of said pouch.

9. The kit according to claim 1, wherein said tubular endoprosthesis is adapted to be positioned against an inside surface of the duct.

10. A method for implanting a kit according to claim 1 in the duct, the method comprising:

implanting the tubular endoprosthesis in the duct by an endoluminal technique; and

removably implanting the prosthetic valve inside the tubular endoprosthesis by the endoluminal technique.

11. The method according to claim 10, further comprising:

compressing the prosthetic valve to the folded position by the integrated centripetal compression means;

removing the prosthetic valve from the tubular endoprosthesis in a transluminal manner; and

implanting a new prosthetic valve in the tubular endoprosthesis by the endoluminal technique.

12. The kit according to claim 1, wherein said resilient carrier frame, said flexible shutter, and said integrated centripetal compression means are shaped and arranged such that contacting said centripetal compression means causes said resilient carrier frame to be compressed toward the folded position for removal or adjustment.

13. The kit according to claim 1, wherein said drive segments are curved to be convex inwardly toward said flexible shutter.