Low profile thermally set wrapped cover for a percutaneously deployed stent

• US 5,741,326 A
• Filed: 07/15/1996
• Issued: 04/21/1998
• Est. Priority Date: 07/15/1996
• Status: Expired due to Term

• Current Assignee: Cordis Corporation (Cardinal Health, Inc.)
• Original Assignee: Cordis Corporation (Cardinal Health, Inc.)
• Inventors: Solovay, Kenneth S.
• Primary Examiner(s): Weiss, John G.
• Assistant Examiner(s): Black, John M.
• Application Number:
  US08/680,435
• Time in Patent Office: 645 Days
• Field of Search: 623/1, 623/11, 623/12
• US Class Current: 623/2.25
• CPC Class Codes: A61F 2/07 Stent-grafts
• CPC Class Codes: A61F 2/90 characterised by a net-like or mesh-like structure
• CPC Class Codes: A61F 2/958 Inflatable balloons for placing stents or stent-grafts
• CPC Class Codes: A61F 2002/072 Encapsulated stents, e.g. wire or whole stent embedded in lining
• CPC Class Codes: A61F 2002/075 the stent being loosely attached to the graft material, e.g. by stitching
• CPC Class Codes: A61F 2002/9583 Means for holding the stent on the balloon, e.g. using protrusions, adhesives or an outer sleeve

Abstract

An endoprosthesis assembly for percutaneous deployment on a balloon catheter is disclosed. The assembly includes a radially expandable stent overlied by a tubular, low profile stent cover wrapped over the stent. The wrapped cover is thermally set to maintain its low profile wrapped configuration during deployment of the assembly. At the treatment site, the balloon portion of the catheter is inflated causing the stent to expand radially and the stent cover to unwrap and open to conform to the expanded configuration of the stent.

Claims

1. An endoprosthesis assembly for implantation at a treatment site within a patient'"'"'s body, the assembly comprising:

a) an expandable stent releasably affixed to a delivery catheter, the stent being in a first configuration during deployment of the assembly to the treatment site and adapted to be expanded to a second expanded configuration and to detach from the catheter during implantation of the assembly at the treatment site; and

b) a stent cover affixed to the stent and wrapped around an outer surface of the stent when the stent is in the first configuration, the cover being releasably set to maintain a wrapped configuration during deployment of the assembly to the treatment site within the body and adapted to at least partially unwrap during implantation to conform to the outer surface of the stent when the stent is expanded to the second expanded configuration, the stent cover being wrapped around the outer surface of the stent such that the stent cover has a substantially uniform cross sectional area over an entire length of the stent cover along a longitudinal axis of the stent cover when the stent cover is in the wrapped configuration.

2. The endoprosthesis assembly of claim 1 wherein the stent is cylindrical and expands radially outwardly when expanded from the first configuration to the second expanded configuration.

3. The endoprosthesis assembly of claim 2 wherein the stent cover is cylindrical and has an unwrapped inner diameter at least as great as an outer diameter of the stent when the stent is expanded to the second expanded configuration.

4. The endoprosthesis assembly of claim 3 wherein the entire length of the stent cover is less than a length of the stent along a longitudinal axis of the stent.

5. The endoprosthesis assembly of claim 3 wherein a radial force necessary to unwrap the stent cover is less than the radial force necessary to expand the stent from the first configuration to the second expanded configuration.

6. The endoprosthesis assembly of claim 3 wherein the unwrapped inner diameter of the stent cover is substantially equal to the outer diameter of the stent when the stent is expanded to the second expanded configuration.

7. The endoprosthesis assembly of claim 1 wherein the cover is thermally set in the wrapped configuration.

8. The endoprosthesis assembly of claim 7 wherein the stent and the stent cover in the wrapped configuration are heated at a temperature of substantially 220 degrees Celsius for substantially five minutes to thermally set the stent cover in the wrapped configuration.

9. The endoprosthesis assembly of claim 2 wherein the stent is adapted to be expanded to an outer diameter of substantially 5 millimeters and the assembly, when affixed to the delivery catheter, will pass through an introducer providing a passageway into the patient'"'"'s body wherein the passageway has a size of substantially 2.33 millimeters.

10. The endoprosthesis assembly of claim 2 wherein the stent is adapted to be expanded to an outer diameter of substantially 12 millimeters and the assembly, when affixed to the delivery catheter, will pass through an introducer providing a passageway into the patient'"'"'s body wherein the passageway has a size of substantially 2.67 millimeters.

11. The endoprosthesis assembly of claim 1 wherein the stent cover is comprised of a woven polyester material.

12. The endoprosthesis assembly of claim 11 wherein the stent cover is comprised of woven polyethylene terephthalate polyester.

13. The endoprosthesis assembly of claim 11 wherein the stent cover is comprised of a single layer of woven polyester material having a thickness of substantially 0.1 millimeters.

14. An endoprosthesis assembly for implantation at a treatment site within a patient'"'"'s body, the assembly comprising:

a) a stent having a first unexpanded configuration for deployment of the assembly to the treatment site and adapted to be expanded to a second expanded configuration for implantation of the assembly at the treatment site; and

b) a stent cover affixed to the stent and wrapped around an outer surface of the stent when the stent is in the first unexpanded configuration, the cover being thermally set to maintain a wrapped configuration during deployment of the assembly to the treatment site within the body and adapted to at least partially unwrap during implantation to conform to the outer surface of the stent when the stent is expanded to the second expanded configuration.

15. A stent delivery assembly comprising:

a) a delivery catheter;

b) an expandable stent releasably affixed to a delivery catheter, the stent being in a first configuration during deployment of the assembly to the treatment site and adapted to be expanded to a second expanded configuration and to detach from the catheter during implantation of the assembly at the treatment site; and

c) a stent cover affixed to the stent and wrapped around an outer surface of the stent when the stent is in the first configuration, the cover being releasably set to maintain a wrapped configuration during deployment of the assembly to the treatment site within the body and adapted to at least partially unwrap during implantation to conform to the outer surface of the stent when the stent is expanded to the second expanded configuration, the stent cover having a uniform cross sectional area over an entire length of the stent cover along a longitudinal axis of the stent cover when the stent cover is in the wrapped configuration.

16. The stent delivery assembly of claim 15 wherein the stent is releasably crimped to a radially expandable balloon portion of the delivery catheter and the assembly detaches from the catheter when the balloon portion is inflated.