Cannula stent

• US 7,172,623 B2
• Filed: 10/09/2002
• Issued: 02/06/2007
• Est. Priority Date: 10/09/2001
• Status: Expired due to Term

• Current Assignee: Cook Medical Technologies, LLC (Cook Group Incorporated)
• Original Assignee: Cook Incorporated (Cook Group Incorporated), William Cook Europe ApS (Cook Group Incorporated)
• Inventors: Hansen, Palle M., Parker, Fred T., Ehrlinspiel, Michael
• Primary Examiner(s): TRUONG, KEVIN THAO
• Application Number:
  US10/267,385
• Publication Number:
  US 20030088310A1
• Time in Patent Office: 1,581 Days
• Field of Search: 623/1.15, 623/1.16, 623/1.11, 623/1.12, 623/1.2, 606191-198
• US Class Current: 623/1.15
• CPC Class Codes: A61F 2/91 made from perforated sheet material or tubes, e.g. perforated by laser cuts or etched holes
• CPC Class Codes: A61F 2/915 with bands having a meander structure, adjacent bands being connected to each other
• CPC Class Codes: A61F 2002/91516 the meander having a change in frequency along the band
• CPC Class Codes: A61F 2002/91525 within the whole structure different bands showing different meander characteristics, e.g. frequency or amplitude
• CPC Class Codes: A61F 2002/91533 characterised by the phase between adjacent bands
• CPC Class Codes: A61F 2002/91558 connected peak to peak
• CPC Class Codes: A61F 2002/91575 connected peak to trough
• CPC Class Codes: A61F 2230/0054 V-shaped

Abstract

A stent (30) formed from cannula and having flexible segments (31) and high hoop strength segments (32) alternating therealong. Longitudinal struts or tie bars (41) interconnect the segments. Minimal length reduction of the strut occurs upon expansion. In the high hoop strength segment (32), struts (37) in a zig-zag configuration (Gianturco Z-stent) are initially parallel in the unexpanded strut condition. In the flexible segment (31), struts (58) extend from a respective C-shaped bend (59) to converge at the opposite ends thereof when unexpanded. In one embodiment, certain adjacent struts (39–41) of the hoop segment are spaced apart by elongated openings or gaps (46, 48) interposed therebetween and interconnected at their respective ends (42, 44) to form a T-shaped strut interconnection (45). The selected width (50, 51) of the first and third struts (54, 57) increases toward the ends (47, 48) of the elongated openings (46, 48) adjacent the strut interconnection (45). This strut width increase about one end of the strut significantly reduces the tensile strain exhibited about the opening end when the stent is radially expanded during manufacture. The tip length (52, 55) of the struts about the interconnection (45) is also adjusted (increased) along with the other C-shaped strut interconnections (59, 71) to further distribute the tensile strain developed during radial expansion.

Claims

1. A cannula stent comprising:

a cannula having a passageway extending longitudinally therein and a wall of biocompatible material extending at least partially around said passageway, said wall having a plurality of struts extending longitudinally therein and a plurality of elongated openings therethrough, said openings extending at least partially between said plurality of struts, at least first, second, and third ones of said struts being adjacent and having respective ends laterally interconnected at a strut interconnection, a first opening of said openings extending between the first and the second struts and having a first opening end longitudinally adjacent the strut interconnection between the first and the second struts, a second opening of said openings extending between the second and the third struts and having a second opening end longitudinally adjacent the strut interconnection between the second and the third struts, wherein the first strut has a selected width that increases along the first strut toward the first opening end and wherein the second strut has a selected width that decreases along the second strut toward the strut interconnection.

2. The cannula stent of claim 1 wherein the third strut has a selected width that increases along the third strut toward the second opening end.

3. The cannula stent of claim 2 wherein the selected width of the third strut increases longitudinally along the third strut toward the second opening end.

4. The cannula stent of claim 2 wherein the third selected width of the third strut has a third outside diameter selected width and a third inside diameter selected width less than the third outside diameter selected width.

5. The cannula stent of claim 1 wherein the selected width of the first strut increases longitudinally along the first strut toward the first opening end.

6. The cannula stent of claim 1 wherein the strut interconnection has a first interconnection length that extends longitudinally from the first opening end to a first edge of the strut interconnection that is longitudinally opposite the first opening end, wherein the selected width of the first strut extends at least partially along a length of the first strut, and wherein the first interconnection length is greater than the selected width of the first strut.

7. The cannula stent of claim 6 wherein the first interconnection length is greater than the selected width of the first strut by 10 to 30 percent.

8. The cannula stent of claim 6 wherein the first interconnection length is greater than the selected width of the first strut by 15 to 25 percent.

9. The cannula sent of claim 6 wherein the first interconnection length is greater than the selected width of the first strut by about 20 percent.

10. The cannula stent of claim 6 wherein the strut interconnection has a second interconnection length that extends longitudinally from the second opening end to a second edge of the strut interconnection that is longitudinally opposite the second opening end, wherein the selected width of the third strut extends at least partially along a length of the third strut, and wherein the second interconnection length is greater than the selected width of the third strut.

11. The cannula stent of claim 10 wherein the second interconnection length is greater than the selected width of the third strut by 10 to 30 percent.

12. The cannula stent of claim 10 wherein the first and the second interconnection lengths are equivalent.

13. The cannula stent of claim 10 wherein the second interconnection length is greater than the selected width of the third strut by 15 to 25 percent.

14. The cannula stent of claim 10 wherein the second interconnection length is greater that the selected width of the third strut by about 20 percent.

15. The cannula stent of claim 2 wherein the first and the second opening ends are laterally adjacent.

16. The cannula stent of claim 2 wherein the selected widths of the first and the third struts are equivalent and wherein the increases of the selected widths of the first and the third struts are equivalent.

17. The cannula stent of claim 2 wherein the first and the second opening ends have the same axial position along the cannula.

18. The cannula stent of claim 2 wherein the increases of the selected widths of the first and the third struts are over an equivalent length of the first and the third struts.

19. The cannula stent of claim 18 wherein the increases of the selected widths of the first and the third struts are over 10 to 30 percent of the lengths of the first and the third struts.

20. The cannula stent of claim 18 wherein the increases of the selected widths are over 12.5 to 25 percent of the lengths of the first end the third struts.

21. The cannula stent of claim 18 wherein the increases of the selected widths of the first and the third struts are over less than 20 percent of the lengths of the first and the third struts.

22. The cannula stent of claim 2 wherein the width of the first and the second elongated openings is greater about the first and the second opening ends than the remainder of the first and the second elongated openings between the first and the second struts and between the second and the third struts, respectively.

23. The cannula stent of claim 2 wherein the first and the second elongated openings are rounded about the first and the second opening ends.

24. The cannula stent of claim 23 wherein the first and the second elongated openings are at least partially elliptical about the first and the second opening ends.

25. The cannula stent of claim 2 wherein the respective ends of the first and the third struts at the strut interconnection are rounded.

26. The cannula stent of claim 25 wherein the respective ends of the first and the third struts at the strut interconnection are convex.

27. The cannula stent of claim 26 wherein the respective end of the second strut at the strut interconnection is concave.

29. The cannula stent of claim 1 wherein the first selected width of the first strut has a first outside diameter selected width and a first inside diameter selected width less than the first outside diameter selected width.

30. The cannula stent of claim 29 wherein the first inside diameter selected width to the first outside diameter selected width establishes a first selected strut width ratio.

31. The cannula stent of claim 30 wherein the first selected strut width ratio increases along the first strut toward the first opening end.

32. The cannula stent of claim 31 wherein the first elongated opening is at least partially elliptical about the first opening end and wherein the first selected strut width ratio increases more rapidly along the first elongated opening where at least partially elliptical than the remaining portion of the first elongated opening.

33. The cannule stent of claim 1 wherein the first elongated opening is at least partially elliptical about the first opening end;

wherein the first elongated opening has a first outside diameter opening width and a first inside diameter opening width;

wherein the first inside diameter opening width to the first outside diameter opening width establishes a first opening width ratio; and

wherein the first opening width ratio decreases along the first elongated opening where at least partially elliptical.

28. A cannula stent comprising:

a cannula having a passageway extending longitudinally therein end a wall of biocompatible material extending at least partially around said passageway, said wall having a plurality of struts extending longitudinally therein and a plurality of elongated openings therethrough, said openings extending at least partially between said plurality of struts, at least first, second, and third ones of said struts being adjacent and having respective ends laterally interconnected at a strut interconnection, a first opening of said openings extending between the first and the second struts and having a first opening end longitudinally adjacent the strut interconnection between the first and the second struts, a second opening of said openings extending between the second and the third struts and having a second opening end longitudinally adjacent the strut interconnection between the second and the third struts, wherein the first and the second openings are equivalent in shape and at least partially elliptical and the first and the second opening ends are positioned at the same axial position along the elongated member, wherein the first strut has a width that increases along the first strut toward the first opening end and wherein the second strut has a selected width that decreases along the second strut toward the strut interconnection.