METHODS AND APPARATUS FOR A STENT HAVING AN EXPANDABLE WEB STRUCTURE

• US 20110004289A1
• Filed: 09/03/2010
• Published: 01/06/2011
• Est. Priority Date: 09/05/1998
• Status: Active Grant

• Current Assignee: Abbott Laboratories Limited (Abbott Laboratories Incorporated)
• Original Assignee: Abbott Laboratories Limited (Abbott Laboratories Incorporated)
• Inventors: Oepen, Randolf Von, Seibold, Gerd
• Granted Patent: US 8,303,645 B2
• Time in Patent Office: Days
• 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 2002/91508 the meander having a difference in amplitude along the band
• CPC Class Codes: A61F 2002/91533 characterised by the phase between adjacent bands
• CPC Class Codes: A61F 2002/91558 connected peak to peak

Abstract

The present invention provides a stent comprising a tubular flexible body having a wall with a web structure that is expandable from a contracted delivery configuration to deployed configuration. The web structure comprises a plurality of neighboring web patterns, where each web patterns is composed of adjoining webs, and the web patterns are interconnected. Each adjoining web comprises a central section interposed between two lateral sections to form concave or convex configurations.

Claims

1-35. -35. (canceled)

36. A stent comprising:

a tubular body having a longitudinal axis, and having proximal and distal ends and a lumen extending longitudinally therebetween, and a wall having areas thereof removed to define a web structure configured for circumferential expansion from a contracted delivery configuration to an expanded deployed configuration;

the web structure comprising a plurality of web patterns interconnected with one another at a plurality of interconnection locations, and that are arranged so that the web patterns are situated side-by-side along the longitudinal length of the tubular body, with each web pattern also extending circumferentially around the wall;

at least one of said interconnected web patterns comprising,

at least three webs joined end-to-end so as to extend between a first pair of interconnection locations with no intervening interconnection locations between the first pair of interconnection locations;

said three webs that are joined end-to-end being joined by two bends so that the bends permit the three webs to be generally foldable between the first pair of interconnection locations when said tubular body is in the contracted delivery configuration, and then unfolded when said tubular body is expanded to the deployed configuration;

a single web connected between a second pair of interconnection locations with no intervening interconnection locations between the second pair of interconnection locations; and

said at least three webs each comprising a plurality of web sections, with one of the web sections being angled relative to one other web section when the stent is in the expanded deployed configuration.

37. The stent of claim 36, further comprising a coating on the web structure that comprises a therapeutic agent, and wherein the therapeutic agent is chosen from the group consisting of therapeutic agents that retard thrombus formation, therapeutic agents that retard restenosis, and therapeutic agents for systemic or local delivery via the blood stream.

38. The stent of claim 36, wherein the interconnection locations are comprised of either or both connection elements and transition sections, and wherein each circumferential pair of connection elements or transition sections are separated by at least three webs.

39. The stent of claim 36, wherein at least some interconnection locations comprise transition sections that each define an H-shaped structure.

40. The stent of claim 39, wherein at least some of the arcuate webs span two H-shaped structures.

41. The stent of claim 39, wherein at least one of the H-shaped structures is disposed at an angle relative to the longitudinal axis of the stent.

42. The stent of claim 36, wherein each web comprises three web sections, with one of the sections being a central section joined at opposite ends thereof to two lateral sections, with at least one of the three web sections comprising a substantially straight section.

43. The stent of claim 42, wherein each web comprises three substantially straight sections, and wherein each of the lateral sections is angled relative to the central section when the stent is expanded, with each angle being expandable when the webs are unfolded to place the stent in the expanded deployed configuration.

44. The stent of claim 36, wherein the at least three webs are joined end-to-end in a manner that defines an S-shaped structure between the two and only two interconnection locations.

45. The stent of claim 36, wherein the stent is formed using a material so that the stent is balloon expandable when deployed.

46. The stent of claim 36, wherein the stent comprises a deformable material.

47. The stent of claim 46, wherein the deformable material is chosen from the group consisting of stainless steel and titanium.

48. The stent of claim 36, wherein the stent is formed using a shape memory alloy so that the stent is self-expanding when deployed.

49. The stent of claim 36, wherein at least a portion of the stent comprises a radiopaque material.

50. A stent comprising:

a tubular body having a longitudinal axis, and having proximal and distal ends and a lumen extending longitudinally therebetween, and a wall having areas thereof removed to define a web structure configured for circumferential expansion from a contracted delivery configuration to an expanded deployed configuration;

the web structure comprising a plurality of web patterns interconnected with one another at a plurality of interconnection locations, and that are arranged so that the web patterns are situated side-by-side along the longitudinal length of the tubular body, with each web pattern also extending circumferentially around the wall;

at least one of said interconnected web patterns comprising,

at least three webs joined end-to-end so as to extend between a first pair of interconnection locations defined as transition sections, with no intervening interconnection locations between the pair of transition sections;

said three webs that are joined end-to-end being joined by two bends so that the bends permit the three webs to be generally foldable between the first pair of transition sections when said tubular body is in the contracted delivery configuration, and then unfolded when said tubular body is expanded to the deployed configuration;

a single web connected between a second pair of interconnection locations defined as transition sections, with no intervening interconnection locations between the second pair of transition sections; and

each web comprising three web sections, with one of the web sections being a central section joined at opposite ends thereof to two lateral sections, each of the lateral sections being angled relative to the central section when the stent is in the expanded deployed configuration.

51. The stent of claim 50, further comprising a coating on the web structure that comprises a therapeutic agent, and wherein the therapeutic agent is chosen from the group consisting of therapeutic agents that retard thrombus formation, therapeutic agents that retard restenosis, and therapeutic agents for systemic or local delivery via the blood stream.

52. The stent of claim 50, wherein each transition section is separated, around the circumference of the wall, by at least five webs joined-end-to-end by four bends.

53. The stent of claim 50, wherein each transition section defines an H-shaped structure.

54. The stent of claim 50, wherein at least some of the arcuate webs span two H-shaped structures.

55. The stent of claim 53, wherein at least one of the H-shaped structures is disposed at an angle relative to a longitudinal axis of the stent.

56. The stent of claim 50, wherein at least one of the three web sections comprises a substantially straight section.

57. The stent of claim 56, wherein each web comprises three substantially straight sections, and wherein each of the lateral sections is angled relative to the central section when the stent is expanded, with each angle being expandable when the webs are unfolded to place the stent in the expanded deployed configuration.

58. The stent of claim 52, wherein the five webs are joined end-to-end in a manner that defines an S-shaped structure using at least three of the five webs.

59. The stent of claim 50, wherein the stent is formed using a material so that the stent is balloon expandable when deployed.

60. The stent of claim 50, wherein the stent comprises a deformable material.

61. The stent of claim 60, wherein the deformable material is chosen from the group consisting of stainless steel and titanium.

62. The stent of claim 50, wherein the stent is formed using a shape memory alloy so that the stent is self-expanding when deployed.

63. The stent of claim 50, wherein at least a portion of the stent comprises a radiopaque material.