Stent element

• US 9,510,936 B2
• Filed: 06/01/2012
• Issued: 12/06/2016
• Est. Priority Date: 06/03/2011
• Status: Active Grant

• Current Assignee: Vascutek Limited (Terumo Corporation)
• Original Assignee: Vascutek Limited (Terumo Corporation)
• Inventors: McDonald, Gary Peter, Stevenson, David Granville
• Primary Examiner(s): Lynch, Robert
• Application Number:
  US14/123,649
• Publication Number:
  US 20140114393A1
• Time in Patent Office: 1,649 Days
• US Class Current: 1/1
• CPC Class Codes: A61F 2/07 Stent-grafts
• CPC Class Codes: A61F 2/86 Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure
• CPC Class Codes: A61F 2/89 the wire-like elements comprising two or more adjacent rings flexibly connected by separate members
• CPC Class Codes: A61F 2002/075 the stent being loosely attached to the graft material, e.g. by stitching
• CPC Class Codes: A61F 2230/0054 V-shaped
• CPC Class Codes: A61F 2230/006 Y-shaped
• CPC Class Codes: Y10T 29/49826 Assembling or joining

Abstract

There is provided a stent element comprising a central portion with two arms extending therefrom, optionally in a V-shaped or Y-shaped configuration. The arms of the stent-element are resiliently deformable to facilitate packing and suitable material for forming the stent-element is nitinol or PEEK. The stent element can be used to stabilise two adjacent ring stents on a stent graft by attachment to the graft material between the ring stents, for example by sewing. The stent element stabilises the ring stent without risk of fracture. A stent graft having two ring stents and the stent element located between the ring stents is also described.

Claims

1. A stent graft comprising:

i) a sleeve having a first end and a second end with a lumen extending therethrough;

ii) at least two unconnected ring stents attached to the sleeve a pre-selected distance apart; and

iii) a stent element having a central portion with at least two arms extending outwardly therefrom, wherein the stent element is attached to the sleeve so that it bridges the pre-selected distance between the ring stents.

2. The stent graft of claim 1 wherein said stent element is in a V-shaped or Y-shaped configuration.

3. The stent graft of claim 1 wherein said stent element comprises from four arms in an X-shaped configuration.

4. The stent graft of claim 1 wherein the arms of the stent element are each resiliently deformable.

5. The stent graft of claim 1 wherein the stent element is formed from nitinol.

6. The stent graft of claim 1 wherein the ring stents are formed from multiple windings of nitinol wire.

7. The stent graft as claimed in claim 1, wherein the stent element is configured to flex and bend independently of the at least two ring stents.

8. The stent graft as claimed in claim 1, wherein at least one of the at least two arms of the stent element bridges the pre-selected distance between the ring stents.

9. An implantable prosthesis comprising:

i) a compliant and substantially fluid impervious tubular sleeve having a proximal end and a distal end with a conduit therethrough;

ii) a first ring stent formed from multiple windings of wire of a shape memory material, attached to said sleeve at a first location;

iii) a second ring stent formed from multiple windings of wire of a shape memory material, attached to said sleeve at a second location; and

iv) a stent element having a central portion and at least two resilient arms extending therefrom, wherein a first portion of said stent element is attached to said sleeve at said first location, and wherein a second portion of said stent element is attached to said sleeve at said second location,

wherein the first ring stent and the second ring stent are unconnected ring stents.

10. The prosthesis of claim 9 wherein said stent element is in a V-shaped or Y-shaped configuration.

11. The prosthesis of claim 9 wherein said stent element comprises from four arms in an X-shaped configuration.

12. The prosthesis of claim 9 wherein the arms of the stent element are each resiliently deformable.

13. The prosthesis of claim 9 wherein the stent element is formed from nitinol.

14. The prosthesis of claim 9 wherein the ring stents are formed from multiple windings of nitinol wire.

15. A method of treating a body lumen, said method comprising inserting a stent graft comprising:

i) a sleeve having a first end and a second end with a lumen extending therethrough;

ii) at least two unconnected ring stents attached to the sleeve a pre-selected distance apart; and

iii) a stent element having a central portion with at least two arms extending outwardly therefrom, wherein the stent element is attached to the sleeve so that it bridges the distance between the ring stents.

16. The method as claimed in claim 15 wherein said stent element has a V-shaped or Y-shaped configuration.

17. The method as claimed in claim 15 wherein said stent element has four arms in an X-shaped configuration.

18. The method as claimed in claim 15 the arms of the stent element are each resiliently deformable.

19. The method as claimed in claim 15 wherein the stent element is formed from nitinol.

20. A method of treating a patient in need thereof, said method comprising implanting a prosthesis comprising:

i) a compliant and substantially fluid impervious tubular sleeve having a proximal end and a distal end with a conduit therethrough;

ii) a first ring stent formed from multiple windings of wire of a shape memory material, attached to said sleeve at a first location;

iii) a second ring stent formed from multiple windings of wire of a shape memory material, attached to said sleeve at a second location; and

iv) a stent element having a central portion and at least two resilient arms extending therefrom, wherein a first portion of said stent element is attached to said sleeve at said first location, and wherein a second portion of said stent element is attached to said sleeve at said second location,

wherein the first ring stent and the second ring stent are unconnected ring stents.

21. The method as claimed in claim 20 wherein said stent element has a V-shaped or Y-shaped configuration.

22. The method as claimed in claim 20 wherein said stent element has four arms in an X-shaped configuration.

23. The method as claimed in claim 20 the arms of the stent element are each resiliently deformable.

24. The method as claimed in claim 20 wherein the stent element is formed from nitinol.

25. A method of manufacturing a prosthesis suitable for implantation into the body, said method comprising:

(i) providing a flexible tubular conduit;

(ii) attaching a stent element to said conduit such that said stent element is attached at two distinct locations on said conduit;

(iii) attaching a first stent element to the conduit at or adjacent said first attachment point; and

(iv) attaching a second ring stent to said conduit at or adjacent said second attachment point,

wherein the first ring stent and the second ring stent are unconnected ring stents.

26. The method as claimed in claim 25 wherein said stent is attached to the conduit by stitching.

27. The method as claimed in claim 25 wherein said stent element has a V-shaped or Y-shaped configuration.

28. The method as claimed in claim 25 wherein said stent element has four arms in an X-shaped configuration.

29. The method as claimed in claim 25 wherein the stent element is formed from nitinol.

30. A stent graft comprising:

a sleeve having a first end and a second end with a lumen extending therethrough;

at least two ring stents attached to the sleeve a pre-selected distance apart; and

a stent element having a central portion with at least two arms extending outwardly therefrom,

wherein the stent element is attached to the sleeve such that it bridges the pre-selected distance between the at least two ring stents, and

wherein the at least two ring stents are separate and distinct ring stents, and wherein the stent element is a separate and distinct component from the at least two ring stents.

31. A stent graft comprising:

a sleeve having a first end and a second end with a lumen extending therethrough;

at least two ring stents attached to the sleeve a pre-selected distance apart; and

a stent element having a central portion with at least two arms extending outwardly therefrom,

wherein the stent element is attached to the sleeve such that it bridges the pre-selected distance between the at least two ring stents, and

wherein the stent element is only attached to the sleeve.

32. A stent graft comprising:

a sleeve having a first end and a second end with a lumen extending therethrough;

at least two ring stents attached to the sleeve a pre-selected distance apart; and

a stent element having a central portion with at least two arms extending outwardly therefrom,

wherein the stent element is attached to the sleeve such that it bridges the pre-selected distance between the at least two ring stents, and,

wherein the stent element is not directly coupled to the at least two ring stents.