Stent

• US 9,421,084 B2
• Filed: 02/04/2011
• Issued: 08/23/2016
• Est. Priority Date: 07/22/2005
• Status: Active Grant

• Current Assignee: Newtec Vascular Products Ltd.
• Original Assignee: Newtec Vascular Products Ltd.
• Inventors: Barker, Stephen Edward George
• Primary Examiner(s): Sevilla, Christian
• Assistant Examiner(s): Mathew, Seema
• Application Number:
  US13/021,162
• Publication Number:
  US 20110172761A1
• Time in Patent Office: 2,027 Days
• Field of Search: 623/1.35, 623/1.36, 604/8
• US Class Current: 1/1
• CPC Class Codes: A61B 17/11 for performing anastomosis; Buttons for anastomosis
• CPC Class Codes: A61B 2017/1107 for blood vessels
• CPC Class Codes: A61B 2017/1132 End-to-end connections
• CPC Class Codes: A61B 2017/1135 End-to-side connections, e.g. T- or Y-connections Y-shaped blood vessel prostheses A61F2002/065
• CPC Class Codes: A61F 2/064 with special features to facilitate anastomotic coupling anastomosis of natural blood vessels A61B17/11
• CPC Class Codes: A61F 2002/30062 (bio)absorbable, biodegradable, bioerodable, (bio)resorbable, resorptive
• CPC Class Codes: A61F 2210/0004 bioabsorbable

Abstract

An elongate device, actuate in cross-section, for placement around a vessel, comprises an essentially non-porous outer layer and a biodegradable inner layer.

An alternative device comprises a tubular portion for placement around a graft and a portion, arcuate in cross-section, that can straddle a native vessel, at the site of an end-to-side anastomosis.

Claims

1. An arteriovenous bypass grafting procedure, which comprises fitting an elongate device around an external surface of a vessel to be grafted, wherein the device is arcuate in cross-section and self-supporting, and wherein the device comprises inner and outer layers that are maintained in contact by their natural elasticity or by bonding, wherein the outer layer is more rigid than the inner layer such that it provides a structural framework for the device, wherein the inner layer stimulates neovascularisation and degrades faster than the outer layer, and wherein the device is fitted around the external surface of the vessel such that there is a space between the device and the vessel.

2. The procedure according to claim 1, which comprises fitting the device at the site of an end-to-side anastomosis.

3. The procedure according to claim 1, wherein the device is substantially Y- or T-shaped.

4. The procedure according to claim 1, wherein the outer layer is non-porous.

5. The procedure according to claim 1, wherein the arcuate cross-section includes an angle of up to 270°

.

6. The procedure according to claim 1, wherein the device is essentially tubular.

7. The procedure according to claim 6, wherein the tubular portion has an internal diameter of up to 8 mm.

8. The procedure according to claim 1, wherein the device includes an elongate slit.

9. The procedure according to claim 1, wherein the device includes an active agent.

10. The procedure according to claim 1, wherein the inner and outer layers are discrete.

11. The procedure according to claim 1, wherein the device is spaced apart from the vessel by at least 1 mm.

12. The procedure according to claim 11, wherein the inner layer is spaced apart from the vessel along the device'"'"'s entire length, including at the ends of the device such that the ends of the device are open.

13. The procedure according to claim 1, wherein the inner layer is spaced apart from the vessel along the device'"'"'s entire length, including at the ends of the device such that the ends of the device are open.