Intravascular stent with enhanced rigidity strut members

• US 5,913,895 A
• Filed: 06/02/1997
• Issued: 06/22/1999
• Est. Priority Date: 06/02/1997
• Status: Expired due to Term

• Current Assignee: Cardinal Health Switzerland 515 GmbH (Cardinal Health, Inc.)
• Original Assignee: Isostent, Inc. (Cardinal Health, Inc.)
• Inventors: Burpee, Janet W., Fischell, David R.
• Primary Examiner(s): Prebilic, Paul B.
• Application Number:
  US08/867,488
• Time in Patent Office: 750 Days
• Field of Search: 623/1, 623/12, 606/191, 606/198
• US Class Current: 623/1.2
• 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 2002/91558 connected peak to peak
• CPC Class Codes: A61F 2230/0054 V-shaped

Abstract

Disclosed herein is a thin-walled cylindrical stent in which one or more of the sets of strut members are more radially rigid after stent expansion as compared to other sets of strut members. Each set of strut members consists of a multiplicity of structural struts that are connected together with the struts extending circumferentially when the stent is outwardly radially deployed within a vessel of a human body. The sets of strut members are those parts of the stent which unfold during radial expansion and provide the radially rigid structure which maintains vessel patency. This invention is a stent structure specifically designed to have enhanced radial rigidity either at the ends or the center of the stent. More radially rigid end struts reduce injury to the vessel from over expansion at the ends of the stent. The embodiment of the present invention with enhanced rigidity in the center would be particularly useful for the treatment of calcified obstructions. Enhanced rigidity can be achieved by either having a set of strut members that becomes more ring-like when radially deployed, or the strut members have a greater width as compared to other strut members of the stent.

Claims

1. A thin-walled, cylindrical stent formed from a single piece of metal, the stent having a nominal diameter when fully radially deployed into a vessel of the human body and having a longitudinal direction parallel to the axial axis of the cylindrical stent, the stent further comprising a multiplicity of sets of strut members with each set of strut members forming a circumferentially extending closed ring structure with adjacent sets of strut members being coupled each to the other by structures extending generally in the longitudinal direction, said stent having a proximal end, a distal end and a center section located approximately half-way between said proximal and distal ends, said stent having two types of circumferentially extending sets of strut members, a first type of set of strut members and a second type of set of strut members, the first type of set of strut members having a shorter total circumferential length as compared to the total circumferential length of the second type of set of strut members, the stent when radially deployed to its nominal diameter having the first type of set of strut members having greater radial rigidity as compared to the second type of set of strut members.

2. The stent as recited in claim 1 where said first type of set of strut members has a length in the longitudinal direction that is less than the length in the longitudinal direction of said second type of set of strut members.

3. The stent as recited in claim 1 where said sets of strut members are coupled each to the other by at least two substantially longitudinally extending undulating members.

4. The stent as recited by claim 3 where the substantially longitudinally extending undulating members are formed in an S-shaped contour.

5. The stent as recited by claim 3 where the substantially longitudinally extending undulating members are formed in a U-shaped contour.

6. The stent as recited by claim 1 where there is at least one of the first type of set of strut members situated at said proximal end of the stent.

7. The stent as recited by claim 6 where there is at least one of the first type of set of strut members situated at said distal end of the stent.

8. The stent as recited by claim 1 where there is at least one of the first type of set of strut members situated at said distal end of the stent.

9. The stent as recited by claim 1 where there is at least one of the first type of set of strut members at said center section of the stent.

10. The stent as recited by claim 7 where there is at least one of the first type of set of strut members situated at said center section of the stent.

11. The stent as recited in claim 1 where said first type of set of strut members has an average dimensional strut width of its strut members that is greater than the average dimensional strut width of the strut members of said second type of set of strut members.

12. The stent as recited in claim 1 where at least two adjacent sets of strut members are coupled each to the other by at least two substantially longitudinally extending linearly directed "H" cross bars.

13. The stent as recited in claim 1 where said stent is radially expanded responsive to inflation of a balloon onto which balloon the stent is mounted.

14. The stent as recited in claim 1 where said stent is a radially self-expanding stent.