Tapered helical stent and method for manufacturing the stent

• US 20080221664A1
• Filed: 03/08/2007
• Published: 09/11/2008
• Est. Priority Date: 03/08/2007
• Status: Active Grant

• Current Assignee: PST, LLC
• Original Assignee: PST, LLC
• Inventors: Slater, Charles, Bales, Thomas O., Jahrmarkt, Scott
• Granted Patent: US 8,623,070 B2
• Time in Patent Office: Days
• US Class Current: 623/1.22
• CPC Class Codes: A61F 2/88 the wire-like elements formed as helical or spiral coils forming a net-like or mesh-like structure A61F2/90
• CPC Class Codes: A61F 2/885 comprising a coil including a plurality of spiral or helical sections with alternate directions around a central axis
• CPC Class Codes: A61F 2/90 characterised by a net-like or mesh-like structure
• 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 2002/91508 the meander having a difference in amplitude along the band
• 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 2002/91541 Adjacent bands are arranged out of phase
• CPC Class Codes: A61F 2002/91558 connected peak to peak
• CPC Class Codes: A61F 2230/0078 hyperboloidal
• CPC Class Codes: A61F 2250/0039 differing in diameter

Abstract

A tapered helical implantation device for peripheral arteries and other body lumina of locally varying diameter, including struts connected by loops and shaped in a helical winding. The helical winding defines turns and, when expanded, has a first end with a first expanded circumference and a second end with a second expanded circumference greater than the first expanded circumference to form a stent tapering outward from the first end towards the second end. Bridges connect adjacent ones of the turns. The struts, the loops, and the bridges define a series of pores aligned along the helix, the pores having a substantially uniform pore size. The pores has a substantially similar area. The pore size limits a size of a particle that can pass therethrough. In particular, the pore size limits a size of a spherical particle that can pass therethrough.

Claims

1. A tapered helical implantation device for peripheral arteries and other body lumina of locally varying diameter, comprising:

struts connected by loops and shaped in a helical winding, said helical winding defining turns and, when expanded, having a first end with a first expanded circumference, and a second end with a second expanded circumference greater than said first expanded circumference to form a stent tapering outward from said first end towards said second end;

bridges connecting adjacent ones of said turns; and

said struts, said loops, and said bridges defining a series of pores aligned along said helix, said pores having a substantially uniform pore size.

2. The device according to claim 1, wherein said pores have a substantially similar area.

3. The device according to claim 1, wherein said pore size limits a size of a particle that can pass therethrough.

4. The device according to claim 1, wherein said pore size limits a size of a spherical particle that can pass therethrough.

5. The device according to claim 1, wherein:

said winding defines a longitudinal axis of said stent and an axis of said helical winding; and

said struts extend one of;

longitudinally along said longitudinal axis; and

perpendicular to said axis of said helical winding.

6. The device according to claim 1, wherein said bridges connect adjacent loops on adjacent ones of said turns.

7. The device according to claim 1, wherein said bridges are placed at locations on said helix corresponding to at least one of every third strut pair, every fifth strut pair, and every seventh strut pair.

8. The device according to claim 1, wherein said bridges are disposed in a 5-up-and-5-down pattern.

9. The device according to claim 1, wherein said bridges are disposed in a 5-up-and-7-down pattern.

10. The device according to claim 1, wherein:

said stent has an overall length; and

a number of said struts per one of said turns remains the same throughout said overall length.

11. The device according to claim 1, wherein:

said stent has an overall length; and

said struts increase in one of width and length from said first end to said second end at least one of in steps, by linear proportion, and by geometric proportion.

12. The device according to claim 1, wherein:

said stent has an overall length;

said struts of each of said turns have the same size; and

said struts increase in size from one of said turns to another of said turns from said first end to said second end at least one of in steps, by linear proportion, and by geometric proportion.

13. The device according to claim 1, wherein:

said stent has an overall length; and

a density of said bridges is substantially even over said overall length to have an equal number of said struts disposed between adjacent bridges in all areas of said stent.

14. The device according to claim 13, wherein a number of said struts per one of said turns is constant and a pattern of said bridges remains constant along said overall length.

15. The device according to claim 1, wherein:

said stent has an overall length; and

a density of said bridges is varied over said overall length to have a different number of said struts disposed between adjacent ones of said bridges in different areas of said stent.

16. The device according to claim 1, wherein a circumferential distance between ends of said struts at said second end are substantially the same as a circumferential distance between ends of said struts at said first end to create said substantially uniform pore size.

17. The device according to claim 1, wherein a number of said struts at said second end is proportionally larger than a number of said struts at said first end.

18. The device according to claim 1, wherein said stent has a length and, when expanded and placed in a lumen, provides a constant hoop force over said length against the lumen.

19. The device according to claim 1, wherein said stent has a constant metal ratio from said first end to said second end.

20. The device according to claim 1, wherein said first end has a diameter between approximately 4 mm and approximately 6 mm and said second end has a diameter between approximately 6 mm and approximately 10 mm.

21. The device according to claim 1, wherein the lumen is one of a carotid artery, a common bile duct, and a location where an iliac artery joins a superficial femoral artery.

22. The device according to claim 1, wherein said stent is a balloon-expanded stent and has a resistance to expansion at each point along a length of said stent proportional to an intended vessel size in which said stent is to be implanted.

23. The device according to claim 1, wherein said struts and said loops define a kerf having a width, said width of said kerf between said struts defines said width of said struts, and said kerf is varied along said stent to create a taper of said stent when expanded.

24. The device according to claim 1, wherein:

said struts and said loops define a kerf;

said stent has an overall length;

a width of said struts remains constant throughout said overall length;

a width of said kerf between said struts remains constant throughout said overall length;

a number of struts per one of said turns stays the same along an entirety of said overall length; and

said length of said struts varies from said smaller end to said larger end.

25. The device according to claim 1, wherein:

said struts and said loops define a kerf;

said stent has an overall length;

both said width and said length of said struts transition in a constantly increasing manner from said smaller end of said stent to said larger end;

said kerf transitions in a constantly decreasing manner from said smaller end to said larger end; and

a number of said struts per one of said turns remains the same along an entirety of said overall length.

26. The device according to claim 1, wherein:

said struts and said loops define a kerf;

said stent has an overall length;

both said width and said length of said struts transition in a constantly increasing manner from said smaller end to said larger end;

said kerf remains constant throughout said overall length; and

a number of said struts per one of said turns decreases along said overall length from said smaller end to said larger end.

27. The device according to claim 1, wherein:

said stent has an overall length; and

said length and said width of said struts and a count of said struts varies along said overall length to have a number of said struts at said smaller end be larger than a number of said struts at said larger end.

28. The device according to claim 1, wherein:

said stent has an overall length; and

said stent is a tapered balloon-expanded stent and has a resistance to expansion at each point along said overall length proportional to an intended implantation vessel size.

29. The device according to claim 1, wherein said struts and said loops are shaped to expand asymmetrically when said stent is expanded by a uniform expansion force.

30. The device according to claim 29, wherein said stent has a uniform resistance to expansion and has uniform expansion properties over said overall length when expanded to an asymmetric shape.

31. The device according to claim 1, wherein:

said stent has an overall length; and

said stent is a self-expanding tapered helical stent and generates expansion forces and resistance to external forces proportional to an adjacent lumen diameter at each point along said overall length to apply a substantially equal pressure to an implantation lumen wall at every point along said overall length.

32. The device according to claim 1, wherein:

said stent has an overall length; and

an opening angle between struts of a pair of said struts is uniform over said overall length.

33. A tapered helical implantation device for peripheral arteries and other body lumina of locally varying diameter, comprising:

a helical winding of struts connected by loops, said helical winding defining a first end, a second end, and helical turns;

said struts each having a length and a width, at least one of;

said length of said struts;

said width of said struts; and

a frequency of said struts per one of said turns,

being varied from said first end to said second end to form a diameter-varying implantable stent outwardly tapered from said first end to said second end when expanded;

bridges connecting adjacent ones of said turns; and

said struts, said loops, and said bridges defining a series of pores aligned along said helix, said pores having a substantially uniform pore size.

34. An implantation device for lumina of locally varying diameter, comprising:

a helical winding defining turns and, when expanded, having a first end with a first expanded circumference and a second end with a second expanded circumference greater than said first expanded circumference to form a stent tapering outward from said first end towards said second end;

bridges connecting adjacent ones of said turns; and

said winding and said bridges defining a series of pores aligned along said helix, said pores having a substantially uniform pore size.

35. A tapered helical implantation device for peripheral arteries and other body lumina of locally varying diameter, comprising:

struts connected by loops and shaped in a helical winding, said helical winding defining turns and, when expanded, having a first end with a first expanded circumference, and a second end with a second expanded circumference greater than said first expanded circumference to form a stent tapering outward from said first end towards said second end;

bridges connecting adjacent ones of said turns; and

said struts, said loops, and said bridges defining a series of pores aligned along said helix, said pores being shaped to permit particles no greater than a given size to pass therethrough, said given size being substantially constant from said first end to said second end.

36. A tapered helical implantation device for peripheral arteries and other body lumina of locally varying diameter, comprising:

a helical winding of struts connected by loops, said helical winding defining a first end, a second end, and helical turns;

said struts each having a length and a width, at least one of;

said length of said struts;

said width of said struts; and

a frequency of said struts per one of said turns,

being varied from said first end to said second end to form a diameter-varying implantable stent outwardly tapered from said first end to said second end when expanded;

bridges connecting adjacent ones of said turns; and

said struts, said loops, and said bridges defining a series of pores aligned along said helix, said pores being shaped to permit particles no greater than a given size to pass therethrough, said given size being substantially constant from said first end to said second end.

37. A tapered helical implantation device for peripheral arteries and other body lumina of locally varying diameter, comprising:

metal struts connected by metal loops and shaped in a helical winding, said helical winding defining turns and, when expanded, having a first end with a first expanded circumference, and a second end with a second expanded circumference greater than said first expanded circumference to form a stent tapering outward from said first end towards said second end;

said first end having a first end turn and said second end having a second end turn;

metal bridges connecting adjacent ones of said turns; and

said struts, said loops, and said bridges between said first and second end turns having a substantially constant metal-to-total area proportion.

38. A tapered helical implantation device for peripheral arteries and other body lumina of locally varying diameter, comprising:

a helical winding of struts connected by loops, said helical winding defining a first end, a second end, and helical turns;

said first end having a first end turn and said second end having a second end turn;

said struts each having a length and a width, at least one of;

said length of said struts;

said width of said struts; and

a frequency of said struts per one of said turns,

being varied from said first end to said second end to form a diameter-varying implantable stent outwardly tapered from said first end to said second end when expanded;

bridges connecting adjacent ones of said turns; and

said struts, said loops, and said bridges between said first and second end turns having a substantially constant metal-to-total area proportion.