Intraluminal stent graft

• US 20070162109A1
• Filed: 01/11/2006
• Published: 07/12/2007
• Est. Priority Date: 01/11/2006
• Status: Abandoned Application

• Current Assignee: Cordis Corporation (Cardinal Health, Inc.)
• Original Assignee: Cordis Corporation (Cardinal Health, Inc.)
• Inventors: Feller, Frederick, Davila, Luis
• Application Number:
  US11/329,567
• Publication Number:
  US 20070162109A1
• Time in Patent Office: Days
• US Class Current: 623/1.350
• 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 2002/067 modular
• CPC Class Codes: A61F 2230/0067 conical

Abstract

A modular intraluminal stent graft. The intraluminal stent graft is bifurcated having a primary section and a secondary section extending therefrom. The primary section tapers from a larger diameter at an upstream end to a smaller diameter at a downstream end. The downstream end of the primary section has a pair of independent openings each having an expanded diameter. The secondary section provides a first endoleg having an upstream end that is received through the expanded diameter of one opening of the primary section, and a second endoleg having an upstream end that is received through the second opening of the primary section. The upstream ends of each endoleg, in its expanded state, is larger than the downstream portion of the respective endolegs and expands within the primary section to help assemble the graft in situ. The first and second endolegs also expand within the respective openings each is received within to assemble the stent graft in situ as well. The primary section is positioned within a blood vessel trunk, whereas the endolegs of the secondary section are positioned within a blood vessel branched from the blood vessel trunk. A typical application would be to place the primary section within the abdominal aorta infrarenally, with the endolegs positioned in the ipsilateral and contralaterial iliacs, respectively. By minimizing the number of stent segments in the primary section of the stent graft a lower delivery profile is achieved.

Claims

1. A expandable modular intraluminal stent graft comprising:

a primary section that tapers in its expanded state from a larger upstream end diameter to a smaller downstream end diameter;

a series of radially expandable stent segments at the upstream end of the primary section;

a first opening and a second opening, each opening having a diameter in its expanded state that combines to comprise the smaller downstream end diameter of the primary section;

a band of radially expandable stent segment within each opening;

a secondary section comprised of a first endoleg and a second endoleg, each endoleg having an upstream end and a downstream end, the upstream end of each endoleg received within the primary section through a respective one of the openings of the primary section and expanded therein the primary section and the downstream end of the endolegs extending therefrom thre respective one of the openings to assemble the stent graft in situ;

a radially expandable stent segment in the upstream end of each endoleg;

a series of radially expandable stent segments in the downstream end of each endoleg; and

graft material surrounding the primary and secondary sections.

2. The modular intraluminal stent graft of claim 1, further comprising:

longitudinal ribs extending between the upstream end and the downstream end of the primary section.

3. The modular intraluminal stent graft of claim 1, wherein the radially expandable stent segment in the respective openings of the primary section are offset relative to one another.

4. The modular intraluminal stent graft of claim 1, wherein the primary section further comprises one or more barbs at the upstream end thereof.

5. The modular intraluminal stent graft of claim 1, wherein one or both of the primary section and the secondary section further comprises one of foams, textiles or films to effect a seal between the primary and secondary sections.

6. The modular intraluminal stent graft of claim 1, wherein the radially expandable stent segments are comprised of self-expanding materials.

7. The modular intraluminal stent graft of claim 6, wherein the radially expandable stent segments are comprised of Nitinol.

8. The modular intraluminal stent graft of claim 1, wherein the radially expandable stent segments are comprised of balloon expandable materials.

9. The modular intraluminal stent graft of claim 1, further comprising a suprarenal fixation stent extending upstream from the upstream end of the primary section.

10. The modular intraluminal stent graft of claim 9, wherein the suprarenal fixation stent is comprised of self-expanding material.

11. The modular intraluminal stent graft of claim 10, wherein the suprarenal fixation stent is comprised of Nitinol.

12. The modular intraluminal stent graft of claim 9, wherein the suprarenal fixation stent is comprised of balloon expandable materials.

13. The modular intraluminal stent graft of claim 1, wherein one or both endolegs further comprises an expandable section at the downstream end thereof that helps anchor the respective endoleg in a vessel.

14. The modular intraluminal stent graft of claim 1, wherein the primary section is configured for deployment within a blood vessel trunk, and each endoleg of the secondary section is configured for deployment within a blood vessel branched from the blood vessel trunk.

15. A method for delivering an intraluminal stent graft to an intended treatment site, the method comprising:

delivering a primary section of the intraluminal stent graft within a vessel trunk via a catheter;

expanding upstream and downstream ends of the primary section within the vessel trunk by withdrawal of the catheter, wherein the downstream end of the primary section comprises first and second openings;

delivering a first endoleg through one of the first and second openings of the primary section via a catheter;

assembling the first endoleg in situ by expanding the upstream end of the first endoleg within the primary section, a portion of a downstream end of the first endoleg in the first opening of the primary section, and a remaining portion of the downstream end of the first endoleg in a first blood vessel branch;

delivering a second endoleg into the primary section through the second opening of the primary section via a separate catheter, the second endoleg having an upstream end and a downstream end; and

assembling the second endoleg in situ by expanding the upstream end of the second endoleg within the primary section, a portion of the downstream end of the second endoleg within the second opening of the primary section, and a remaining portion of the second endoleg in another blood vessel branch, the expanded upstream ends of the first and second endolegs each having at least one stent segment that interfacing with a region of the primary section that otherwise omits stent segments.

16. The method of claim 15, wherein the primary section and the first endoleg are delivered using the same catheter.

17. The method of claim 15, wherein the catheter delivering the primary section and the catheter delivering the first endoleg are different.

18. The method of claim 15, wherein at least one stent segment in each of the upstream ends of each endoleg expands to fill a region of the primary section that otherwise omits stent segments.

19. The method of claim 15, further comprising providing barbs at the upstream end of the primary section and anchoring the barbs within the blood vessel trunk.

20. The method of claim 15, wherein the blood vessel trunk is an abdominal aorta, the first blood vessel branch is an ipsilateral iliac, and the second blood vessel branch is a contralateral iliac.

21. The method of claim 20, further comprising deploying an expandable suprarenal fixation stent in the abdominal aorta with the primary section.

22. The method of claim 15, further comprising expanding downstream ends of at least one of the first and second endolegs to anchor within the respective blood vessel branch the endoleg is deployed within.

23. The method of claim 20, wherein graft material surrounds the primary and secondary sections, and not the suprarenal fixation stent.