Endoluminal device having enhanced affixation characteristics

• US 8,663,316 B2
• Filed: 12/27/2005
• Issued: 03/04/2014
• Est. Priority Date: 02/26/2003
• Status: Expired due to Fees

• Current Assignee: Lifeshield Sciences LLC (Acacia Research Corporation)
• Original Assignee: Lifeshield Sciences LLC (Acacia Research Corporation)
• Inventors: Elliott, Christopher J.
• Primary Examiner(s): Isabella, David
• Assistant Examiner(s): SCHILLINGER, ANN M
• Application Number:
  US11/318,736
• Publication Number:
  US 20060100684A1
• Time in Patent Office: 2,989 Days
• Field of Search: 623 111- 154
• US Class Current: 623/1.35
• 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 2/90 characterised by a net-like or mesh-like structure
• CPC Class Codes: A61F 2002/065 Y-shaped blood vessels
• CPC Class Codes: A61F 2002/077 having means to fill the space between stent-graft and aneurysm wall, e.g. a sleeve
• CPC Class Codes: A61F 2220/0008 Fixation appliances for connecting prostheses to the body
• CPC Class Codes: A61F 2220/0016 with sharp anchoring protrusions, e.g. barbs, pins, spikes
• CPC Class Codes: A61F 2230/0054 V-shaped
• CPC Class Codes: A61F 2230/0071 spherical
• CPC Class Codes: A61F 2230/0076 ellipsoidal or ovoid
• CPC Class Codes: A61F 2230/008 paraboloidal
• CPC Class Codes: A61F 2250/0039 differing in diameter

Abstract

An endoluminal device for affixation to a wall of a body lumen having a neck region defined by a relatively narrow width and a shoulder region that diverges from the neck region to a relatively wider width. The device comprises a bulbous portion having a shoulder portion with a diameter profile that conforms to the shoulder region of the lumen, and a converging diameter portion sized not to conform to the body lumen diameter profile. In some embodiments, a plurality of affixation members in an area of the device that typically extends from a distal end of the device through the shoulder portion. In one embodiment, the device comprises an endograft for repair of an aneurysm, such as an abdominal aortic aneurysm (AAA).

Claims

1. A self-expanding endoluminal device having a compressed configuration and a self-expanded configuration, the device in the self-expanded configuration comprising a first neck, a bulbous portion defining a convex exterior surface, a second neck, a first shoulder portion located between the first neck and the bulbous portion and defining a concave exterior surface therebetween, and a second shoulder portion located between the second neck and the bulbous portion and defining a concave exterior surface therebetween, the first neck having a first diameter, the bulbous portion having a geometry characterized by a diverging and converging diameter greater than the first diameter, the diverging and converging diameter forming the first and second shoulder portions, respectively, wherein the first neck is configured in a polygonally wound stent architecture to exert a first radial self-expansion force applied to a lumen wall and the bulbous portion is configured in a braided stent architecture to exert a second radial self-expansion force applied to the lumen wall in a shoulder region that is less than the first radial expansion force.

2. The device of claim 1, wherein the bulbous portion of the device comprises a stent having at least one superelastic section and at least one plastically deformable section.

3. The device of claim 1 further comprising a plurality of affixation members at least on part of the device shoulder portion.

4. The endoluminal device of claim 3, wherein the affixation members comprise hooks, barbs, or other members that project radially outward from the device.

5. The endoluminal device of claim 3, wherein the device has a distal end adapted to be positioned in an upstream portion of a lumen and the plurality of affixation members are disposed in an area of the device extending proximally from the distal end of the device through the first shoulder portion.

6. The endoluminal device of claim 5, wherein an area in which the plurality of affixation members are disposed extends axially to a maximum diameter portion of the first shoulder portion.

7. The endoluminal device of claim 1, wherein the device comprises a stent.

8. The device of claim 7, wherein the stent comprises at least one superelastic section and at least one plastically deformable section.

9. The device of claim 1, wherein the first shoulder portion of the device comprises a stent having at least one superelastic section and at least one plastically deformable section.

10. The endoluminal device of claim 1, wherein the first neck portion includes a renal neck portion adapted to be positioned at a distal end of an aneurysm and the first device shoulder portion is adapted to be positioned proximal a renal neck at the lumen shoulder region.

11. The endoluminal device of claim 1, wherein the first neck portion includes an iliac neck portion adapted to be positioned at a proximal end of an aneurysm and the first device shoulder portion is adapted to be positioned distally of the iliac neck.

12. The endograft of claim 1, wherein the plurality of affixation members are disposed in an area that extends axially from a distal end of the endograft to at least an intermediate location in the first bulbous portion.

13. The device of claim 1, wherein the device converging diameter length comprises a tapered or step-change diameter.

14. The endoluminal device of claim 1, wherein the device comprises an endograft comprising a stent that is at least partially covered or lined with a graft material.

15. The endoluminal device of claim 14, wherein the endograft is adapted to repair an aneurysm.

16. The endoluminal device of claim 15, wherein the endograft is adapted to repair an abdominal aortic aneurysm (AAA).

17. A self-expanding endoluminal device having a compressed configuration and a self-expanded configuration and having a distal end, the device in the self-expanded configuration comprising a distal first neck, a first bulbous portion defining a convex exterior surface, a distal second neck, a first shoulder portion located between the distal first neck and the first bulbous portion and defining a concave exterior surface therebetween, and a second shoulder portion located between the distal second neck and the first bulbous portion and defining a concave exterior surface therebetween, the distal first neck having a first diameter, the first bulbous portion having geometry characterized by a diverging and converging diameter greater than the first diameter, the diverging and converging diameter forming the first and second shoulder portions, respectively, at least the distal first neck and part of the first bulbous portion comprising a plurality of affixation members that project radially outward for affixation to a lumen wall of an abdominal aortic aneurysm, wherein the distal first neck is configured in a polygonally wound stent architecture to exert a first radial self-expansion force applied to the lumen wall and the bulbous portion is configured in a braided stent architecture to exert a second radial self-expansion force applied to the lumen wall in a shoulder region that is less than the first radial expansion force.

18. The device of claim 17, wherein the area in which the plurality of affixation members are disposed extends axially to a maximum diameter portion of the first bulbous portion.

19. The device of claim 17 further comprising a proximal end comprising at least one proximal neck having a second diameter and an additional corresponding bulbous portion located distally of the proximal neck and having a distally diverging then converging diameter greater than the second diameter, at least the proximal neck and part of the additional corresponding bulbous portion comprising a plurality of affixation members that project radially outward from the device for affixation to the lumen wall of the abdominal aortic aneurysm.

20. The device of claim 19 further comprising a plurality of affixation members at least on part of the device first distal shoulder portion and on part of the device proximal shoulder portion.

21. The endoluminal device of claim 19, wherein the device first distal shoulder portion and the device proximal shoulder portion comprises a non-modular device.

22. The endoluminal device of claim 19, wherein the device distal shoulder portion and the device proximal shoulder portion comprises a modular device.

23. The endoluminal device of claim 22, wherein a first modular component comprises the device first distal shoulder portion and a first device proximal shoulder portion, and a second modular component comprises a second device proximal shoulder portion.

24. The device of claim 19 comprising two proximal necks and two additional corresponding bulbous portions, each proximal neck and additional corresponding bulbous portion for deployment adjacent an iliac neck region of the abdominal aortic aneurysm.

25. The device of claim 24, wherein the distal first and second necks, first bulbous portion and first and second shoulder portions comprise a first modular component, and each proximal neck and additional corresponding bulbous portion comprise additional modular components.

26. The device of claim 24, wherein the distal first and second necks, first bulbous portion, first and second shoulder portions, one proximal neck, and one additional corresponding bulbous portion comprise a first modular component, and another proximal neck and additional corresponding bulbous portion comprise a second modular component.

27. The device of claim 17 wherein the device comprises a stent at least partially lined or covered by a graft material.

28. The endoluminal device of claim 27, wherein the endograft is adapted to repair the abdominal aortic aneurysm.

29. The endoluminal device of claim 17, wherein the endograft is adapted to repair an aneurysm.