Stent improvements

• US 20050240278A1
• Filed: 04/26/2004
• Published: 10/27/2005
• Est. Priority Date: 04/26/2004
• Status: Abandoned Application

• Current Assignee: ACMI Corp. (Olympus Corporation)
• Original Assignee: ACMI Corp. (Olympus Corporation)
• Inventors: Nishtala, Vasu, Aliski, Peter, Tremaglio, Anthony, Shia, Benedict
• Application Number:
  US10/833,210
• Publication Number:
  US 20050240278A1
• Time in Patent Office: Days
• US Class Current: 623/23.700
• CPC Class Codes: A61F 2/04 Hollow or tubular parts of organs, e.g. bladders, tracheae, bronchi or bile ducts A61F2/18, A61F2/20 take precedence; devices, other than stent-grafts, providing patency to, or preventing collapsing of, tubular structures of the body other than stent-grafts, e.g. stents A61F2/82; instruments specially adapted for placement or removal of stents or stent-grafts A61F2/95
• CPC Class Codes: A61M 27/008 pre-shaped, for use in the urethral or ureteral tract

Abstract

In accordance with the invention, there are provided medical devices for providing a fluid passage between two areas in the body. An embodiment of the present invention relates to a stent comprising a tubular member at least a portion of which comprises a reinforcement structure. The tubular member includes a wall and an axial lumen therein having a lumen surface. The reinforcement structure extends at least a portion of a length of the body portion adjacent the distal end portion. One advantage of this embodiment of the invention is, for example, that the reinforcement structure increases patient comfort by providing enhanced flexibility. A second advantage of this embodiment of the invention is, for example, that the reinforcement structure improves axial stiffness and radial stiffness allowing for a thinner tubular member wall thickness and larger lumen diameter.

Claims

1. A stent comprising:

an elongated tubular member having a body portion, a proximate end portion and a distal end portion, the tubular member having a wall and an axial lumen therein having a lumen surface; and

a reinforcement structure extending at least a portion of a length of the body portion adjacent the distal end portion.

2. The stent of claim 1, where the reinforcement structure comprises:

a coiled filament embedded within the wall of the tubular structure, the coiled filament adapted to provide a predetermined axial stiffness and radial stiffness.

3. The sent of claim 1, where the reinforcement structure comprises:

a coiled filament adjacent to and in abutment with the lumen surface of the tubular structure, the coiled filament adapted to provide a predetermined axial stiffness and radial stiffness.

4. The stent of claim 1, where the reinforcement structure comprises:

a plurality of rings; and

a plurality of longitudinal members, the longitudinal members coupled to the plurality of rings spaced apart to define a tube-like structure, the reinforcement structure embedded within the wall of the tubular structure, the reinforcement structure adapted to provide a predetermined axial stiffness and radial stiffness to at least a portion of the body portion.

5. The stent of claim 1, where the reinforcement structure comprises:

a plurality of rings; and

a plurality of longitudinal members, the longitudinal members coupled to the plurality of rings spaced apart to define a tube-like structure, the reinforcement structure adjacent to and in abutment with the lumen surface of the tubular structure, the reinforcement structure adapted to provide a predetermined axial stiffness and radial stiffness to at least a portion of the body portion.

6. The stent of claim 1, where the reinforcement structure comprises:

a cross-web member comprising a plurality of interconnected webs that bisect the lumen, the webs intersect at an axis of the lumen and extend radially to abut the lumen surface, the webs defining a plurality of laterally running fluid passages suitable for providing a fluid path traversing the at least a portion of the body portion comprising the cross-web member.

7. The stent of claim 6, further comprising:

a plurality of apertures adapted to provide fluid communication between an exterior of the tubular member and the fluid passages defined by the webs, the apertures substantially aligned with the fluid passages; and

a portion of the tubular member disposed directly adjacent an edge of the webs defining a frame adapted to reduce any potential for trauma to any abutting body tissue.

8. The stent of claim 7, wherein the apertures define a plurality of annular rings adapted to retain a guide within one of the fluid passages.

9. The stent of claim 1, wherein the distal end portion comprises a retaining structure.

10. The stent of claim 1, wherein the stent comprises a ureteral drainage stent.

11. A ureteral stent for maintaining drainage between the kidney and bladder comprising:

an elongated flexible tubular member having proximal end portion and a distal end portion coupled by a body portion having an axis including a central lumen to provide fluid communication between the proximal end portion and distal end portion, the proximal end portion adapted for placement in the bladder, the distal end portion including retention means adapted for retaining the distal end portion in the kidney, at least a portion of the body portion comprising a reinforcement structure extending at least a portion of a length of the body portion adjacent the distal end portion.

12. The ureteral stent of claim 11, where the reinforcement structure comprises:

a coiled filament embedded within the wall of the tubular structure, the coiled filament adapted to provide a predetermined axial stiffness and radial stiffness.

13. The sent of claim 11, where the reinforcement structure comprises:

a coiled filament adjacent to and in abutment with the lumen surface of the tubular structure, the coiled filament adapted to provide a predetermined axial stiffness and radial stiffness.

14. The stent of claim 11, where the reinforcement structure comprises:

a plurality of rings; and

a plurality of longitudinal members, the longitudinal members coupled to the plurality of rings spaced apart to define a tube-like structure, the reinforcement structure embedded within the wall of the tubular structure, the reinforcement structure adapted to provide a predetermined axial stiffness and radial stiffness to at least a portion of the body portion.

15. The stent of claim 11, where the reinforcement structure comprises:

a plurality of rings; and

a plurality of longitudinal members, the longitudinal members coupled to the plurality of rings spaced apart to define a tube-like structure, the reinforcement structure adjacent to and in abutment with the lumen surface of the tubular structure, the reinforcement structure adapted to provide a predetermined axial stiffness and radial stiffness to at least a portion of the body portion.

16. The stent of claim 11, where the reinforcement structure comprises:

a cross-web member comprising a plurality of interconnected webs that bisect the lumen, the webs intersect at an axis of the lumen and extend radially to abut the lumen surface, the webs defining a plurality of laterally running fluid passages suitable for providing a fluid path traversing the at least a portion of the body portion comprising the cross-web member.

17. The stent of claim 16, further comprising:

a plurality of apertures adapted to provide fluid communication between an exterior of the tubular member and the fluid passages defined by the webs, the apertures substantially aligned with the fluid passages; and

a portion of the tubular member disposed directly adjacent an edge of the webs defining a frame adapted to reduce any potential for trauma to any abutting body tissue.

18. The stent of claim 17, wherein the apertures define a plurality of annular rings adapted to retain a guide within one of the fluid passages.

19. The stent of claim 11 wherein the distal end portion comprises a retaining structure.

20. The stent of claim 11 wherein the stent comprises a ureteral drainage stent.

21. A method for placing a stent comprising:

inserting a body portion into a ureter, a distal end portion into a kidney and a proximal end portion into a bladder, the stent comprising;

an elongated flexible tubular member having proximal end portion and a distal end portion coupled by a body portion having an axis including a central lumen to provide fluid communication between the proximal end portion and distal end portion, the proximal end portion adapted for placement in the bladder, the distal end portion including retention means adapted for retaining the distal end portion in the kidney, at least a portion of the body portion comprising a reinforcement structure extending at least a portion of a length of the body portion adjacent the distal end portion.

22. The method of claim 21, further comprising:

inserting a guidewire into the lumen of the stent, wherein the reinforcement structure comprises;

a coiled filament embedded within the wall of the tubular structure, the coiled filament adapted to provide a predetermined axial stiffness and radial stiffness.

23. The method of claim 21, further comprising:

inserting a guidewire into the lumen of the stent, wherein the reinforcement structure comprises;

a coiled filament adjacent to and in abutment with the lumen surface of the tubular structure, the coiled filament adapted to provide a predetermined axial stiffness and radial stiffness.

24. The method of claim 21, further comprising:

inserting a guidewire into the lumen of the stent, wherein the reinforcement structure comprises;

a plurality of rings; and

a plurality of longitudinal members, the longitudinal members coupled to the plurality of rings spaced apart to define a tube-like structure, the reinforcement structure embedded within the wall of the tubular structure, the reinforcement structure adapted to provide a predetermined axial stiffness and radial stiffness to at least a portion of the body portion.

25. The method of claim 21, further comprising:

inserting a guidewire into the lumen of the stent, wherein the reinforcement structure comprises;

a plurality of rings; and

a plurality of longitudinal members, the longitudinal members coupled to the plurality of rings spaced apart to define a tube-like structure, the reinforcement structure adjacent to and in abutment with the lumen surface of the tubular structure, the reinforcement structure adapted to provide a predetermined axial stiffness and radial stiffness to at least a portion of the body portion.

26. The method of claim 21, further comprising:

inserting a guidewire into the lumen of the stent, wherein the reinforcement structure comprises;

a cross-web member comprising a plurality of interconnected webs that bisect the lumen, the webs intersect at an axis of the lumen and extend radially to abut the lumen surface, the webs defining a plurality of laterally running fluid passages suitable for providing a fluid path traversing the at least a portion of the body portion comprising the cross-web member.

27. The method of claim 25, further comprising:

inserting a guidewire into the lumen of the stent, wherein the reinforcement structure comprises;

a plurality of apertures adapted to provide fluid communication between an exterior of the tubular member and the fluid passages defined by the webs, the apertures substantially aligned with the fluid passages; and

a portion of the tubular member disposed directly adjacent an edge of the webs defining a frame adapted to reduce any potential for trauma to any abutting body tissue.

28. The method of claim 26, wherein the apertures define a plurality of annular rings adapted to retain the guide within one of the fluid passages, the method further comprising:

inserting the guidewire into one of the fluid passages.

29. The method of claim 21 wherein the distal end portion comprises a retaining structure, the method further comprising:

inserting the guidewire into the distal end portion.