Endoluminal prosthetic device

• US 8,348,988 B2
• Filed: 01/18/2005
• Issued: 01/08/2013
• Est. Priority Date: 01/20/2004
• Status: Active Grant

• Current Assignee: Cook Medical Incorporated (Cook Group Incorporated)
• Original Assignee: Cook Medical Incorporated (Cook Group Incorporated)
• Inventors: Lad, Ashvin, DeBruyne, Michael P., Osborne, Thomas A.
• Primary Examiner(s): Nguyen, Tuan V
• Assistant Examiner(s): MCEVOY, THOMAS M
• Application Number:
  US11/037,792
• Publication Number:
  US 20050159803A1
• Time in Patent Office: 2,912 Days
• Field of Search: 623/1.11, 623/1.13, 623/1.14, 623/1.16, 623/1.44, 623/1.23, 623/1.32, 623/1.33, 623/1.36
• US Class Current: 623/1.13
• CPC Class Codes: A61F 2/07 Stent-grafts
• CPC Class Codes: A61F 2/848 having means for fixation to the vessel wall, e.g. barbs
• 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 2002/067 modular
• CPC Class Codes: A61F 2002/075 the stent being loosely attached to the graft material, e.g. by stitching
• CPC Class Codes: A61F 2220/0016 with sharp anchoring protrusions, e.g. barbs, pins, spikes
• CPC Class Codes: A61F 2220/0075 sutured, ligatured or stitched, retained or tied with a rope, string, thread, wire or cable
• CPC Class Codes: A61F 2230/005 Rosette-shaped, e.g. star-shaped
• CPC Class Codes: A61F 2230/0054 V-shaped
• CPC Class Codes: A61F 2230/0067 conical

Abstract

An endoluminal prosthetic device for placement in a body lumen is formed by stitching stents to a graft. A first or anchoring stent is used for securing a graft made of biocompatible material that forms at least one lumen. There is also a second stent. The first and second stents each include a plurality of struts and apices between the struts. At least two of the apices in each of the first and second stents are secured to the graft by stitches. A running suture links at least one stitch of the first stent and one stitch of the second stent. The running suture linking the first stent and the second stent adds strength to the stitches and better secures the first stent to the device. The endoluminal prosthetic device may be used in an aortic vessel to treat stenoses or aneurysms.

Claims

1. An endoluminal prosthetic device, comprising:

a graft comprising a bio-compatible material and at least one lumen extending longitudinally therein;

a first stent comprising a plurality of struts and apices between the struts, wherein at least one apex in the first stent is secured to the graft by looping a thread around and at the apex and through the graft material forming a first knotted stitch, and wherein the first knotted stitch prevents the at least one apex in the first stent from moving relative to the graft; and

a second stent comprising a plurality of struts and apices between the struts, wherein at least one apex in the second stent is secured to the graft by looping the thread around and at the apex and through the graft material forming a second knotted stitch, wherein the second knotted stitch is formed by the same thread forming the first knotted stitch, and wherein the second knotted stitch prevents the at least one apex in the second stent from moving relative to the graft,

wherein the thread forms a running suture linking the first knotted stitch of the first stent and the second knotted stitch of the second stent, wherein the running suture extends at least partially in a longitudinal direction from the first knotted stitch to the second knotted stitch; and

wherein the running suture strengthens the endoluminal prosthetic device by adding strength to bonds between the first stent, the second stent, and the graft.

2. The endoluminal prosthetic device of claim 1, wherein the first stent is an anchoring stent and the second stent is an internal stent.

3. The endoluminal prosthetic device of claim 1, wherein the graft is made of material selected from the group consisting of polyester, polyurethane, polyethylene, polypropylene and polytetrafluoroethylene.

4. The endoluminal prosthetic device of claim 1, wherein the suture further comprises monofilament or braided multifilament material selected from the group consisting of polyester, nylon, polyaramid, polypropylene, and polyethylene.

5. The endoluminal prosthetic device of claim 1, wherein the stents comprise material selected from the group consisting of stainless steel, titanium, and shape memory material.

6. The endoluminal prosthetic device of claim 1 further comprising a cuff on the graft.

7. The endoluminal prosthetic device of claim 1, wherein the graft incorporates biomaterial selected from the group consisting of collagen, extracellular matrix material, and small intestine submucosa (SIS).

8. The endoluminal prosthetic device of claim 1, wherein at least one of the first stent and the second stent are secured by an additional stitch on at least two of the struts.

9. The endoluminal prosthetic device of claim 1, wherein the first stent is an anchoring stent and wherein at least one of the struts further comprises a barb for retaining the endoluminal prosthetic device in place.

10. The endoluminal prosthetic device of claim 1, further comprising additional stitches linked to the running suture.

11. The endoluminal prosthetic device of claim 1, wherein the amount of travel of the running suture between the first stitch and the second stitch in the longitudinal direction is less than the amount of travel in the circumferential direction.

12. A method of forming an endoluminal prosthetic device, the method comprising:

providing a graft comprising a bio-compatible material and at least one lumen extending longitudinally therein;

providing the device with a plurality of stitches;

joining a first stent to the graft, the first stent comprising a plurality of struts and apices between the struts, by at least one first stitch of the plurality of stitches,

wherein the at least one first stitch is formed by a thread looping around and at an apex of the plurality of apices and through the graft material thereby forming a first knotted stitch, and wherein each first stitch prevents one of the plurality of apices in the first stent from moving relative to the graft;

running the thread to a second stent at least partially in a longitudinal direction;

joining the second stent to the graft, the second stent comprising a plurality of struts and apices between the struts, by at least one second stitch of the plurality of stitches, wherein the at least one second stitch is formed by the thread a looping around and at an apex of the plurality of apices and through the graft material thereby forming a second knotted stitch, and wherein each second stitch prevents one of the plurality of apices in the second stent from moving relative to the graft; and

forming a running suture between the at least one first stitch and the at least one second stitch, wherein the running suture strengthens the endoluminal prosthetic device by adding strength to bonds between the first stent, the second stent, and the graft.

13. The method of claim 12, wherein the first stent is an anchoring stent and further comprising forming a barb on at least one strut of the anchoring stent.

14. The method of claim 12, further comprising folding the graft to form a cuff before the step of joining the first stent.

15. The method of claim 12, further comprising forming at least one penetration in the graft before the steps of joining.

16. The method of claim 12, further comprising linking at least one additional stitch to the running suture.

17. The method of claim 12, further comprising linking at least one additional stitch to the running suture, wherein at least two stitches share an opening in the graft.

18. The method of claim 12, further comprising linking at least one additional stitch to the running suture, wherein at least two stitches are within one suture diameter of each other.

19. An endoluminal prosthetic device, comprising:

a graft comprising a bio-compatible material and at least one lumen extending longitudinally therein;

a plurality of stitches;

a first stent comprising a plurality of struts and apices between the struts, wherein a first apex in the first stent is secured to the graft by looping a thread around the first apex and through the graft material forming a first knotted stitch, and wherein the first knotted stitch prevents the first apex in the first stent from moving relative to the graft;

a second stent comprising a plurality of struts and apices between the struts, wherein a first apex in the second stent is secured to the graft by looping the thread around the first apex of the second stent and through the graft material forming a second knotted stitch, and wherein the second knotted stitch prevents the first apex in the second stent from moving relative to the graft;

a second apex in the first stent is secured to the graft by looping the thread around the second apex of the first stent and through the graft material forming a third knotted stitch, wherein the third knotted stitch prevents the second apex in the first stent from moving relative to the graft;

wherein the device further comprises a running suture linking together the first knotted stitch to the second knotted and the second knotted stitch to the third knotted stitch, wherein the running suture is formed of the thread that also forms the first, second, and third knotted stitches; and

wherein the running suture strengthens the endoluminal prosthetic device by adding strength to bonds between the first stent, the second stent, and the graft.

20. The endoluminal prosthetic device of claim 19, wherein the amount of travel of the running suture between the first knotted stitch and the second knotted stitch in the longitudinal direction is less than the amount of travel between in the circumferential direction.