Esophageal stent

• US 9,687,367 B2
• Filed: 06/04/2013
• Issued: 06/27/2017
• Est. Priority Date: 06/05/2012
• Status: Active Grant

• Current Assignee: Merit Medical Systems, Inc.
• Original Assignee: Merit Medical Systems, Inc.
• Inventors: Gill, Darla, Eller, Zeke, Snider, Rich, Clegg, Trent
• Primary Examiner(s): Prone, Christopher D
• Assistant Examiner(s): Diop, Rokhaya
• Application Number:
  US13/909,427
• Publication Number:
  US 20130325141A1
• Time in Patent Office: 1,484 Days
• Field of Search: 623 11, 623 112, 623 113, 623 114, 623 115, 623 116, 623 12, 623 121, 623 122, 623 124, 623 126, 623 13, 623 131, 623 134, 623 2364, 623 237
• CPC Class Codes: A61F 2/2418 Scaffolds therefor, e.g. support stents
• CPC Class Codes: A61F 2/90 characterised by a net-like or mesh-like structure
• CPC Class Codes: A61F 2/915 with bands having a meander structure, adjacent bands being connected to each other
• CPC Class Codes: A61F 2002/044 Oesophagi or esophagi or gullets
• CPC Class Codes: A61F 2220/005 using adhesives
• CPC Class Codes: A61F 2220/0058 soldered or brazed or welded
• CPC Class Codes: A61F 2220/0075 sutured, ligatured or stitched, retained or tied with a rope, string, thread, wire or cable
• CPC Class Codes: A61F 2230/0054 V-shaped
• CPC Class Codes: A61F 2250/0018 differing in elasticity, stiffness or compressibility

Abstract

Stent embodiments formed of a scaffolding structure are disclosed. Some embodiments may include a valve. A portion of the scaffolding structure may include a lattice structure formed by a plurality of interconnected arms arranged to form quadrilateral-shaped cells, such as diamond-shaped cells. The scaffolding structure may be formed by rows of strut arms arranged as annular segments and adjacent annular segments interconnected by connectors that extend in the longitudinal direction. The scaffolding structure may also be formed by rows of strut arms arranged in a helical pattern. The scaffolding structure has components configured to allow at least a portion of the stent to decrease in diameter in response to an axial force applied to the stent. Further, the components and elements of the stent may be configured to balance transverse forces applied to the stent, thus reducing the incidence of infolding.

Claims

1. An implantable device to be disposed within a body lumen, the implantable device comprising:

a scaffolding structure defining a cylindrical shape and a lumen through the scaffolding structure, wherein at least a first portion of the scaffolding structure comprises a lattice structure formed by a plurality of interconnected arms the first portion having a first stiffness, and a second portion of the scaffolding structure comprises a second plurality of interconnected arms with adjacent arms arranged at acute angles relative to each other in rows around a longitudinal axis of the cylindrical shape, wherein each row is defined as a pattern of alternating peaks and valleys formed by adjacent interconnected arms, wherein at least a first row, a second row, and a third row are arranged in a longitudinal direction along the longitudinal axis of the cylindrical shape, the first row being proximal to the second row and distal to the third row, wherein the first row is connected to each of the second row and the third row by a plurality of connectors extending in the longitudinal direction of the cylindrical shape to form cells that are non-quadrilateral in shape, wherein the first portion extends longitudinally from a distal end of the scaffolding structure to an intermediate location on the scaffolding structure and the second portion extends longitudinally from the intermediate location on the scaffolding structure to a proximal end of the scaffolding structure, and wherein the second portion of the scaffolding structure has a second stiffness that is less than the first stiffness; and

a valve coupled to an inside diameter of the first portion of the scaffolding structure;

wherein a length of the implantable device is between about 70 mm and about 150 mm; and

wherein the scaffolding structure lacks a plane of symmetry that is transverse to the longitudinal axis of the cylindrical shape.

2. The implantable device of claim 1, further comprising a plurality of eyelets configured to receive a suture, the eyelets disposed adjacent the proximal end of the scaffolding structure.

3. The implantable device of claim 2, further comprising a plurality of rounded knobs wherein the knobs are disposed adjacent the distal end of the scaffolding structure.

4. The implantable device of claim 1, further comprising a polymeric cover applied to and between the scaffolding structure.

5. The implantable device of claim 4, wherein the polymeric cover comprises a first layer and a second layer, and wherein at least one of the first and second layers comprises silicone.

6. The implantable device of claim 1, wherein the scaffolding structure comprises a memory alloy with a thickness of about 0.30 mm to about 0.60 mm.

7. The implantable device of claim 6, wherein the scaffolding structure is laser cut from a tube of nitinol.

8. The implantable device of claim 1, wherein the scaffolding structure is configured to reduce in diameter in response to an axial force applied to a longitudinal end of the implantable device in a longitudinal direction away from the implantable device.

9. The implantable device of claim 1, further comprising one or more radiopaque indicia indicating a position of the valve.

10. The implantable device of claim 1, wherein the first portion of the scaffolding structure is less compressible in a transverse direction than the second portion of the scaffolding structure.

11. The implantable device of claim 1, wherein the plurality of interconnected arms of the lattice structure of the first portion of the scaffolding structure are arranged to form quadrilateral-shaped cells.