Conical stent

• US 5,922,019 A
• Filed: 12/29/1995
• Issued: 07/13/1999
• Est. Priority Date: 11/27/1995
• Status: Expired due to Term

• Current Assignee: Boston Scientific Corporation
• Original Assignee: Schneider (Europe) GmbH (Boston Scientific Corporation)
• Inventors: Gianotti, Marc, Hofmann, Eugen, Hankh, Susanne
• Primary Examiner(s): Isabella, David J.
• Assistant Examiner(s): Black, John M.
• Application Number:
  US08/581,714
• Time in Patent Office: 1,292 Days
• Field of Search: 623/1, 623/11, 623/12, 606/190-200
• US Class Current: 623/1.13
• CPC Class Codes: A61F 2/90 characterised by a net-like or mesh-like structure
• CPC Class Codes: A61F 2210/0076 multilayered, e.g. laminated structures
• CPC Class Codes: A61F 2230/0067 conical
• CPC Class Codes: A61F 2250/0037 differing in height or in length
• CPC Class Codes: A61F 2250/0039 differing in diameter
• CPC Class Codes: D04C 1/06 Braid or lace serving particular purposes
• CPC Class Codes: D10B 2509/06 Vascular grafts; stents

Abstract

The stent comprises a flexible self-expandable braided tubular wall having a proximal segment having an outer diameter, and a distal segment having an outer diameter smaller than the outer diameter of the proximal segment. An intermediate segment is formed between proximal and distal segments, which forms a truncated cone of which the base is forming the proximal end of the intermediate segment and of which the top is forming the distal end of the intermediate segment. A covering layer is arranged within the tubular wall.

Claims

1. A stent for use in a body passageway, comprising:

a flexible self-expandable braided tubular wall having a longitudinal axis, characterized in that the tubular wall comprises a first proximal anchor segment adapted to provide a sufficiently high radial force to prevent migration of the stent in a body passageway and having proximal and distal ends and a first outer diameter, the proximal end of the first proximal anchor segment terminating at a first free end of the stent;

a second distal way-making segment having proximal and distal ends and a second outer diameter smaller than said first outer diameter of said first proximal anchor segment, a distal end of the second distal segment terminating at a second free end of the stent; and

a third intermediate segment having a proximal end connected to the distal end of the first segment and a distal end connected to the proximal end of the second distal way-making segment; and

the braided tubular wall having braiding with varying steep angle with respect to the longitudinal axis of the tubular wall where the radial force and flexibility over at least a portion of the flexible self-expandable braided tubular wall is not constant.

2. A stent according to claim 1, wherein said first proximal anchor segment and said second distal segment are cylindrical.

3. A stent according to claim 1, wherein said third intermediate segment is a truncated cone having a base forming the proximal end of the third intermediate segment and a top forming the distal end of the third intermediate segment.

4. A stent according to claim 1, further comprising a covering layer of elastic material surrounding said tubular wall.

5. A stent according to claim 4, wherein at least a proximal portion of the first proximal anchor segment is not covered by the covering layer.

6. A stent according to claim 4, wherein a distal portion of the second distal way-making segment is not covered by the covering layer.

7. A stent according to claim 1, further comprising a covering layer of elastic material arranged within said tubular wall.

8. The stent according to claim 1 further comprising the first proximal anchor segment having a shorter axial length than the third intermediate segment.

9. A stent for use in a body passageway, comprising:

a flexible self-expandable braided tubular wall having a longitudinal axis, characterized in that the tubular wall comprises a first proximal anchor segment adapted to provide a sufficiently high radial force to prevent migration of the stent in a body passageway and having proximal and distal ends and a first outer diameter, the proximal end of the first proximal anchor segment terminating at a first free end of the stent;

a second distal way-making segment having proximal and distal ends and a second outer diameter smaller than said first outer diameter of said first proximal anchor segment, the distal end of the second distal segment terminating at a second free end of the stent; and

a third intermediate segment having a proximal end connected to the distal end of the first segment and a distal end connected to the proximal end of the second distal way-making segment; and

the braided tubular wall having braiding with varying steep angle with respect to the longitudinal axis of the tubular wall

wherein the braided tubular wall is made of metal.

10. The stent of claim 9 wherein the metal is a spring steel.

11. The stent of claim 9 wherein the metal is a stainless steel.

12. The stent according to claim 9 further comprising a covering layer of elastic material surrounding the tubular wall.

13. The stent of claim 12 wherein the elastic material is adapted to prevent ingrowth through the stent.

14. The stent of claim 9 wherein the first proximal anchor segment and the second distal way-making segment are cylindrical.

15. The stent of claim 9 wherein the third intermediate segment is a truncated cone having a base forming the proximal end of the third intermediate segment and a top forming the distal end of the third intermediate segment.

16. The stent of claim 9 further comprising a covering layer of elastic material surrounding said tubular wall.

17. The stent of claim 16 wherein at least a proximal portion of the first proximal anchor segment is not covered by the covering layer.

18. The stent of claim 16 wherein a distal portion of the second distal way-making segment is not covered by the covering layer.

19. The stent according to claim 9 further comprising the first proximal anchor segment having a shorter axial length than the third intermediate segment.

20. A prosthesis comprising:

a proximal mesh segment, an intermediate mesh segment, and a distal mesh segment, the prosthesis having an inside and outside surface,

the proximal mesh segment including a plurality of filaments and having a first proximal end and a first distal end, a substantially constant braid angle and a substantially constant diameter in an unloaded state;

the intermediate mesh segment including a plurality of filaments and having a second proximal end and a second distal end, a varying braid angle over the intermediate mesh segment, and a tapering diameter from the second proximal end to the second distal end in an unloaded state, the intermediate mesh segment being distal of the proximal mesh segment, and the first distal end of the proximal mesh segment being connected to the second proximal end of the intermediate segment; and

a distal mesh segment including a plurality of filaments and having a third proximal end and a third distal end, a substantially constant braid angle and a substantially constant diameter smaller than the first diameter of the proximal mesh segment in an unloaded state, the distal mesh segment being distal of the intermediate mesh segment, and the third proximal end of the distal mesh segment being connected to the second distal end of the intermediate segment;

wherein the filaments are metal, the prosthesis is self-expanding, and the first proximal end of the proximal mesh segment and the third distal end of the distal mesh segment terminate at a first free end and a second free end, respectively.

21. The prosthesis of claim 20 wherein the varying braid angle decreases from the second proximal end to the second distal end.

22. The prosthesis of claim 20 further comprising one or more additional mesh segments between the proximal mesh segment and the distal mesh segment.

23. The prosthesis of claim 20 wherein the proximal mesh segment is adapted to provide an anchor portion for securing the prosthesis in a body passageway, and the intermediate mesh segment is adapted to provide transitional flexibility between the proximal mesh segment and distal mesh segment,

wherein over a length of the prosthesis, the prosthesis is adapted to provide a plurality of forces to the body passageway.

24. The stent according to claim 20 further comprising the proximal mesh segment having a shorter axial length than the intermediate mesh segment.