Kink resistant endovascular graft

• US 20040176836A1
• Filed: 03/06/2003
• Published: 09/09/2004
• Est. Priority Date: 03/06/2003
• Status: Active Grant

• Current Assignee: Endologix
• Original Assignee: Trivascular Incorporated
• Inventors: Chobotov, Michael V., Kari, Stuart E.
• Granted Patent: US 7,150,758 B2
• Time in Patent Office: Days
• US Class Current: 623/1.32
• CPC Class Codes: A61F 2/06 Blood vessels
• 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 2002/072 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 2002/8486 provided on at least one of the ends
• CPC Class Codes: A61F 2250/0003 having an inflatable pocket filled with fluid, e.g. liquid or gas

Abstract

An intracorporeal device, such as an endovascular graft, having a tubular section with circumferential or helical radial support members. The radial support members may be inflatable channels which support the tubular structure of the graft and which are appropriately sized and longitudinally spaced to prevent or reduce kinking of the tubular structure upon bending of the tubular structure.

Claims

1. A tubular intracorporeal device comprising a longitudinal section which comprises a plurality of circumferential radial support members with a substantially constant longitudinal spacing between the circumferential radial support members that is about 50 to about 200 percent of a longitudinal thickness of the circumferential radial support members.

2. The device of claim 1 wherein the circumferential radial support members comprise circumferential inflatable channels in an inflated state.

3. The device of claim 1 wherein a transverse cross section of the circumferential radial support members has a substantially annular configuration.

4. The device of claim 1 wherein the longitudinal section comprises a tubular section and a longitudinal thickness of the circumferential radial support members is about 10 to about 30 percent of an outer transverse dimension of the tubular section.

5. The device of claim 1 wherein the substantially constant longitudinal spacing between the circumferential radial support members that is about 70 to about 110 percent of a longitudinal thickness of the circumferential radial support members.

6. The device of claim 2 wherein the device comprises an endovascular graft.

7. The device of claim 2 wherein the longitudinal section comprises a tubular section and the circumferential inflatable channels are formed integrally with a flexible material of the tubular section.

8. The device of claim 2 wherein the longitudinal section comprises a tubular section and the circumferential inflatable channels are formed separately from the tubular section and secured thereto.

9. The device of claim 2 wherein a longitudinal section of the circumferential inflatable channels in an inflated state has a substantially round configuration.

10. The device of claim 1 wherein a longitudinal section of the circumferential radial support members has a substantially round configuration.

11. A tubular intracorporeal device comprising a longitudinal section which comprises a helical radial support member with a substantially constant longitudinal spacing between adjacent coils of the helical radial support member that is about 50 to about 200 percent of a longitudinal thickness of the helical radial support member.

12. The device of claim 11 wherein the helical radial support member comprises a helical inflatable channel in an inflated state.

13. The device of claim 11 wherein the longitudinal section comprises a tubular section and a longitudinal thickness of the helical radial support member is about 10 to about 30 percent of an outer transverse dimension of the tubular section.

14. The device of claim 11 wherein the substantially constant longitudinal spacing between adjacent coils of the helical radial support member that is about 70 to about 110 percent of a longitudinal thickness of the helical radial support member.

15. The device of claim 11 wherein the device comprises an endovascular graft.

16. The device of claim 12 wherein the longitudinal section comprises a tubular section and the helical inflatable channel is formed integrally with a flexible material of the tubular section.

17. The device of claim 12 wherein the longitudinal section comprises a tubular section and the helical inflatable channel is formed separately from the tubular section and secured thereto.

18. An endovascular graft comprising:

a) a first longitudinal section which comprises a plurality of circumferential inflatable channels with a substantially constant longitudinal spacing between the circumferential inflatable channels that is about 50 to about 75 percent of a longitudinal thickness of the circumferential inflatable channels with the circumferential inflatable channels in an inflated state; and

b) a second longitudinal section which comprises a plurality of circumferential inflatable channels with a substantially constant longitudinal spacing between the circumferential inflatable channels that is about 100 to about 200 percent of a longitudinal thickness of the circumferential inflatable channels of the second longitudinal section with the circumferential inflatable channels in an inflated state.

19. The endovascular graft of claim 18 wherein the longitudinal spacing of the circumferential inflatable channels of the first and second longitudinal sections is configured to substantially correspond to a bend radii of corresponding longitudinal sections of a patient'"'"'s vascular conduit upon deployment.

20. The endovascular graft of claim 18 wherein the first and second longitudinal sections comprise tubular sections and a longitudinal thickness of the circumferential inflatable channels is about 10 to about 30 percent of an outer transverse dimension of the tubular sections with the circumferential inflatable channel in an expanded state.

21. The device of claim 18 wherein the first longitudinal section is axially adjacent the second longitudinal section.

22. An endovascular graft comprising:

a) a first longitudinal section which comprises a helical inflatable channel with a substantially constant longitudinal spacing between coils of the helical inflatable channel that is about 50 to about 75 percent of a longitudinal thickness of the helical inflatable channel with the helical inflatable channel in an inflated state; and

b) a second longitudinal section which comprises a helical inflatable channel with a substantially constant longitudinal spacing between coils of the helical inflatable channel that is about 100 to about 200 percent of a longitudinal thickness of the helical inflatable channel of the second longitudinal section with the circumferential inflatable channels in an inflated state.

23. The endovascular graft of claim 22 wherein the longitudinal spacing of each longitudinal section is configured to substantially correspond to a bend radii of corresponding longitudinal sections of a patient'"'"'s vascular conduit upon deployment of the endovascular graft.

24. The endovascular graft section of claim 22 wherein the first and second longitudinal sections comprise tubular sections and wherein a longitudinal thickness of the helical inflatable channel is about 10 to about 30 percent of an outer transverse dimension of the tubular sections with the helical inflatable channel in an expanded state.

25. The device of claim 22 wherein the first longitudinal section is axially adjacent the second longitudinal section.

26. An endovascular graft section comprising a plurality of circumferential inflatable channels having a longitudinal spacing between a first segment of a first circumferential inflatable channel and an adjacent segment of a second circumferential inflatable channel that is about 50 to about 200 percent of a longitudinal thickness of the first segment when the first segment is in an expanded state.

27. The endovascular graft section of claim 26 wherein the endovascular graft section comprises a tubular section and the circumferential inflatable channels are integrally formed with the tubular section.

28. The endovascular graft section of claim 26 wherein the endovascular graft section comprises a tubular section and the circumferential inflatable channels are formed separately from the tubular section and secured to the tubular section.

29. The endovascular graft section of claim 26 wherein the circumferential inflatable channels are in an inflated state with an internal inflation pressure of about 3 to about 25 psi.

30. The endovascular graft section of claim 26 wherein the endovascular graft section comprises a tubular section and the tubular section is comprised of a flexible material.

31. The endovascular graft section of claim 30 wherein the flexible material comprises ePTFE.

32. The endovascular graft section of claim 26 wherein the endovascular graft section comprises a tubular section and a longitudinal thickness of the circumferential inflatable channels is about 10 to about 30 percent of an outer transverse dimension of the tubular section with the circumferential inflatable channels in an expanded state.

33. The endovascular graft section of claim 26 wherein the longitudinal thickness of the circumferential inflatable channels in the graft section is substantially the same.

34. The endovascular graft section of claim 33 wherein the longitudinal spacing between adjacent segments of the circumferential inflatable channels in the graft section is substantially the same.

35. An endovascular graft section comprising a helical inflatable channel having a longitudinal spacing between a first segment of the helical inflatable channel and an adjacent second segment of the helical inflatable channel disposed longitudinally from the first segment that is about 50 to about 200 percent of a longitudinal thickness of the first segment when the helical inflatable channel is in an expanded state.

36. The endovascular graft section of claim 35 wherein the endovascular graft section comprises a tubular section and the helical inflatable channel is integrally formed with the tubular section.

37. The endovascular graft section of claim 35 wherein the endovascular graft section comprises a tubular section and the helical inflatable channel is formed separately from the tubular section and secured to the tubular section.

38. The endovascular graft section of claim 35 wherein the helical inflatable channel is in an inflated state with an internal inflation pressure of about 5 to about 20 psi.

39. The endovascular graft section of claim 35 wherein the endovascular graft section comprises a tubular section and the tubular section is comprised of a flexible material.

40. The endovascular graft section of claim 39 wherein the flexible material comprises ePTFE.

41. The endovascular graft section of claim 35 wherein the endovascular graft section comprises a tubular section and a longitudinal thickness of the helical inflatable channel is about 10 to about 30 percent of an outer transverse dimension of the tubular section with the helical inflatable channel in an expanded state.

42. The endovascular graft section of claim 35 wherein the longitudinal thickness of the helical inflatable channel in the graft section is substantially the same.

43. The endovascular graft section of claim 42 wherein the longitudinal spacing between adjacent segments of the helical inflatable channel in the graft section is substantially the same.