Precursor stent gasket for receiving bilateral grafts having controlled contralateral guidewire access

• US 6,270,525 B1
• Filed: 09/23/1999
• Issued: 08/07/2001
• Est. Priority Date: 09/23/1999
• Status: Expired due to Term

• Current Assignee: Cardinal Health Switzerland 515 GmbH (Cardinal Health, Inc.)
• Original Assignee: Cordis Corporation (Cardinal Health, Inc.)
• Inventors: Toyos, Ivan A., Solovay, Kenneth S., Letendre, Robert P.
• Primary Examiner(s): Snow, Bruce
• Assistant Examiner(s): Pellegrino, Brian E
• Application Number:
  US09/404,660
• Time in Patent Office: 684 Days
• Field of Search: 623/1.11, 623/1.12, 623/1.13, 623/1.18, 623/1.23, 623/1.31, 623/1.35, 623/1.24
• US Class Current: 623/1.35
• CPC Class Codes: A61F 2/07 Stent-grafts
• CPC Class Codes: A61F 2/89 the wire-like elements comprising two or more adjacent rings flexibly connected by separate members
• CPC Class Codes: A61F 2/90 characterised by a net-like or mesh-like structure
• CPC Class Codes: A61F 2002/072 Encapsulated stents, e.g. wire or whole stent embedded in lining
• CPC Class Codes: A61F 2002/075 the stent being loosely attached to the graft material, e.g. by stitching
• CPC Class Codes: A61F 2230/0034 D-shaped
• CPC Class Codes: A61F 2230/0054 V-shaped

Abstract

A precursor stent for implantation within the body of a patient is utilized in combination with an aortic graft for repairing an abdominal aortic aneurysm. The stent is designed to receive a pair of grafts placed side by side within the interior of the stent. The stent includes a substantially cylindrical and expandable member having a proximal end, a distal end, a longitudinal axis extending therebetween and an interior. The stent further includes an occlusive member attached to the expandable member. The occlusive member at least partially occludes a passageway or stent lumen which extends through the interior of the expandable member extending between its distal end and proximal end. The occlusive member has an opening extending therethrough designed to receive a guidewire for one of the grafts. Therefore, when the guidewire for the other graft is introduced, after deployment of the stent within a body, it will go through the portion of the interior not covered by the occlusive member. This helps to ensure proper side by side placement of the two grafts.

Claims

1. A precursor stent for implantation within the body of a patient, said stent designed to receive a pair of grafts, said stent comprising;

a) a substantially cylindrical and expandable member having a proximal end, a distal end, a longitudinal axis extending therebetween and an interior; and

b) an occlusive member attached to said expandable member, said occlusive member occludes about one half of a passageway through said interior of said expandable member, from its distal end to its proximal end, as taken from a plane bisecting said expandable member perpendicular to said longitudinal axis, said occlusive member having an opening extending therethrough.

2. The precursor stent according to claim 1, wherein said expandable member further comprises at least two spaced apart longitudinal legs having distal and proximal ends, said distal ends of said legs attached to said proximal end of said member, said legs extending proximally away from said member, at least one of said legs further including a flange adjacent its proximal end.

3. The precursor stent according to claim 2, wherein said legs extend distally and axially from said expandable member when said precursor stent is deployed within a body.

4. The precursor stent according to claim 2 wherein said at least one flange on said longitudinal legs are substantially I-shaped.

5. The precursor stent according to claim 1 wherein said self-expanding member is made from a superelastic Nickel-Titanium alloy.

6. The precursor stent according to claim 1 wherein said occlusive member is made from a material selected from the group comprising:

polyurethane, polyethylene, polytetrafluoroethylene and Dacron.

7. A precursor stent for implantation within the body of a patient, said stent designed to receive and engage a pair of grafts, said stent comprising:

a) an expandable member having a substantially cylindrical wall, a proximal end, a distal end, a longitudinal axis extending therebetween and an interior, said expandable member further including a gasket member substantially surrounding said wall; and

b) an occlusive member attached to said expandable member, said occlusive member occludes about one half of a passageway through said interior of said expandable member, from its distal end to its proximal end, as taken from a plane bisecting said expandable member perpendicular to said longitudinal axis, said occlusive member having an opening extending therethrough.

8. The stent according to claim 7, wherein said expandable member further comprises at least two spaced apart longitudinal legs having distal and proximal ends, said distal ends of said legs attached to said proximal end of said member, said legs extending proximally away from said member, at least one of said legs further including a flange adjacent its proximal end.

9. The stent according to claim 8 wherein said legs extend distally and axially from said expandable member when said precursor stent is deployed within a body.

10. The precursor stent according to claim 8 wherein said at least one flange on said longitudinal legs are substantially I-shaped.

11. The stent according to claim 7, wherein said expandable member is made from a superelastic Nickel-Titanium alloy.

12. The precursor stent according to claim 7 wherein said occlusive member is made from a material selected from the group comprising:

polyurethane, polyethylene, polytetrafluoroethylene and Dacron.

13. An aortic graft for intravascular delivery to repair an abdominal aortic aneurysm in an aorta having two iliac arteries associated therewith, said graft comprising:

a) first and second graft members having distal and proximal ends, each graft member is designed to be inserted through a femoral artery in a collapsed condition, and inserted within the aneurysm and deployed therein, said distal ends of said graft members being distal to said aneurysm adjacent an arterial wall; and

b) a precursor stent, surrounding said distal ends of each of said graft members and coupled thereto, said precursor stent comprising an expandable member having a substantially cylindrical wall, a proximal end, a distal end, a longitudinal axis extending therebetween and an interior, said expandable member further including a gasket member substantially surrounding said wall and an occlusive member attached to said expandable member, said occlusive member occludes about one half of a passageway through said interior of said expandable member, from its distal end to its proximal end, as taken from a plane bisecting said expandable member perpendicular to said longitudinal axis, said occlusive member having an opening extending therethrough, said precursor stent further including at least two spaced apart longitudinal legs having distal and proximal ends, said distal ends of said legs attached to said proximal end of said member, said legs extending proximally away from said member, each said leg including a flange adjacent its proximal end.

14. The aortic graft of claim 13 wherein said gasket comprises an open cell foam.

15. The aortic graft of claim 13 wherein said precursor stent is made from a superelastic nickel-titanium alloy.

16. The aortic graft according to claim 13 wherein said occlusive member is made from a material selected from the group comprising:

polyurethane, polyethylene, polytetrafluoroethylene and Dacron.