Endoluminal prosthesis

• US 20070088425A1
• Filed: 10/10/2006
• Published: 04/19/2007
• Est. Priority Date: 10/13/2005
• Status: Active Grant

• Current Assignee: Cook Medical Technologies, LLC (Cook Group Incorporated)
• Original Assignee: Cook Incorporated (Cook Group Incorporated)
• Inventors: Schaeffer, Darin
• Granted Patent: US 7,670,369 B2
• Time in Patent Office: Days
• US Class Current: 623/1.130
• 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 2002/061 provided with means for allowing access to secondary lumens
• CPC Class Codes: A61F 2002/065 Y-shaped blood vessels
• 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 2002/821 Ostial stents
• CPC Class Codes: A61F 2250/0018 differing in elasticity, stiffness or compressibility
• CPC Class Codes: A61F 2250/0039 differing in diameter
• CPC Class Codes: A61F 2250/0048 differing in mechanical expandability, e.g. in mechanical, self- or balloon expandability

Abstract

An endoluminal prosthesis is disclosed and comprises a first generally tubular stent, a second generally tubular stent, and a generally tubular graft member concentrically disposed between the first and second stents. One or more of the first and second stents may have a body portion and a flaring portion. The first and second stents each may have a recoil force such that the combined application of the first and second recoil forces secures the graft member between the first and second stents.

Claims

1. An endoluminal prosthesis having a compressed configuration and an expanded configuration, the prosthesis comprising:

a first generally tubular stent;

a second generally tubular stent disposed radially about the first tubular stent; and

a generally tubular graft member disposed between the first stent and the second stent,

where the first stent has a first recoil force and the second stent has a second recoil force such that the combined application of the first and second recoil forces secures the graft member between the first and second stents.

2. The prosthesis of claim 1 where the first stent comprises a flaring portion and a body portion, and where in the compressed configuration, the flaring portion and the body portion lie in the same plane.

3. The prosthesis of claim 2 where in the compressed configuration, the flaring portion of the first stent extends longitudinally beyond an end of the second stent.

4. The prosthesis of claim 1 where the second stent comprises a flaring portion and a body portion, and where in the compressed configuration, the flaring portion and the body portion lie in the same plane.

5. The prosthesis of claim 1 where the second recoil force is greater than the first recoil force.

8. The prosthesis of claim 1 where at least one of the first and second stents comprises a series of stent rings.

9. The prosthesis of claim 8 where the stent rings are interconnected.

10. The prosthesis of claim 1, where the first stent and the second stent are balloon-expandable.

11. The prosthesis of claim 1, where the first stent and the second stent are self-expanding.

12. The prosthesis of claim 1, where one of the first and second stent is balloon-expandable and the other of the second and first stent is self-expanding.

13. The prosthesis of claim 1 where the first and second stents are made of biocompatible material selected from the group of stainless steel, platinum, gold, titanium, Nitinol, nickel-titanium alloys, MP35N, nickel-cobalt alloys, Cobalt L-605, cobalt-chromium alloys, biocompatible metals, metal-alloys and polymeric materials.

14. The prosthesis of claim 1:

where one of the first stent and the second stent comprises a flaring portion and a body portion, and where in the compressed configuration, the flaring portion and the body portion lie in the same plane and where in the compressed configuration, the flaring portion of the one of the first and second stent extends longitudinally beyond an end of the other of the second and first stent;

where the second recoil force is greater than the first recoil force, the first recoil force decreasing the diameter of the first stent by about 0% to about 7% and the second recoil force decreasing the diameter of the second stent by about 4% to about 10%;

where at least one of the first and second stents comprises a series of interconnected stent rings; and

where one of the first stent and the second stent is balloon-expandable and the other of the second and the first stent is self-expanding; and

where the first and second stents are made of biocompatible material selected from the group of stainless steel, platinum, gold, titanium, Nitinol, nickel-titanium alloys, MP35N, nickel-cobalt alloys, Cobalt L-605, cobalt-chromium alloys, biocompatible metals, metal-alloys and polymeric materials.

6. The prosthesis of claim 6 where the first recoil force decreases the diameter of the first stent by about 0% to about 7%.

7. The prosthesis of claim 6 where the second recoil force decreases the diameter of the second stent by about 4% to about 10%.

15. A system for repairing a branched vessel having a main lumen and a branch lumen, the system comprising:

a main vessel stent graft having a fenestration and being deployable within the main lumen so that the fenestration is aligned with the branch lumen;

a branch vessel stent graft having a body portion and a flaring portion and being deployable within the branch lumen so that the flaring portion extends at least partially through the fenestration, the branch vessel stent graft comprising;

a first generally tubular stent having a first body portion and a first flaring portion;

a second generally tubular stent having a second body portion, where one of the first and second stent is disposed concentrically about the other of the second and first stent to define an outer stent and an inner stent; and

a generally tubular graft member disposed between the first and second body portion;

where the first stent has a first recoil force and the second stent has a second recoil force such that the combined application of the first and second recoil forces secures the graft member between the first and second stents.

16. The system of claim 15 where the second stent has a flaring portion, and where the flaring portion of the first stent is at least partially aligned with the flaring portion of the second stent and the tubular portion of the first stent is at least partially aligned with the tubular portion of the second stent.

17. The system of claim 15 where the recoil force of the outer stent is greater than the recoil force of the inner stent.

18. The prosthesis of claim 17 where the recoil force of the inner stent decreases the diameter of the inner stent by about 0% to about 7% and the recoil force of the outer stent decreases the diameter of the outer stent by about 4% to about 10%.

19. The system of claim 15 where at least one of the first and the second stent comprises a series of stent rings.

20. The system of claim 15:

where the second stent has a flaring portion, and where the flaring portion of the first stent is at least partially aligned with the flaring portion of the second stent and the tubular portion of the first stent is at least partially aligned with the tubular portion of the second stent; and

where the recoil force of the outer stent is greater than the recoil force of the inner stent, the recoil force of the inner stent decreasing the diameter of the inner stent by about 0% to about 7% and the recoil force of the outer stent decreasing the diameter of the outer stent by about 4% to about 10%; and

where at least one of the first and the second stents comprises a series of stent rings.