Artificial valve prosthesis having a ring frame

• US 20070038295A1
• Filed: 08/11/2006
• Published: 02/15/2007
• Est. Priority Date: 08/12/2005
• Status: Abandoned Application

• Current Assignee: Cook Incorporated (Cook Group Incorporated)
• Original Assignee: Cook Incorporated (Cook Group Incorporated)
• Inventors: Bates, Brian, Flagle, Jacob, Case, Brian
• Application Number:
  US11/502,730
• Publication Number:
  US 20070038295A1
• Time in Patent Office: Days
• US Class Current: 623/2.180
• CPC Class Codes: A61F 2/2418 Scaffolds therefor, e.g. support stents
• CPC Class Codes: A61F 2/2475 Venous valves
• CPC Class Codes: A61F 2220/005 using adhesives
• CPC Class Codes: A61F 2220/0058 soldered or brazed or welded
• CPC Class Codes: A61F 2230/0026 trapezoidal
• CPC Class Codes: A61F 2230/0054 V-shaped
• CPC Class Codes: A61F 2230/0095 Saddle-shaped

Abstract

A radially expandable artificial valve prosthesis for regulating fluid flow through a body vessel is provided. The prosthesis includes a radially expandable ring frame, at least one valve leaflet attached to the ring frame forming a valve pocket and a support structure attached to the ring frame and adapted to position the ring frame within the bodily passage. The height of the valve pocket is less than the maximum cross sectional dimension of the lumen defined by the expanded ring frame. The valve leaflet is allows fluid flow in a first, antegrade, direction and restricts flow in a second, retrograde direction.

Claims

1. A radially expandable artificial valve prosthesis for regulating fluid flow through a body vessel, comprising:

a ring frame, wherein the ring frame is radially expandable to form an expanded ring frame having an expanded ring frame width;

a first valve leaflet, wherein a first portion of a perimeter of the valve leaflet is attached to the ring frame to form a valve pocket having a valve pocket height of less than the expanded ring frame width, and

a support structure attached to the ring frame, wherein the support structure positions the ring frame within the bodily vessel,

wherein the first valve leaflet allows fluid flow in a first, antegrade, direction and restricts flow in a second, retrograde direction.

2. The radially expandable artificial valve prosthesis of claim 1, wherein the first valve leaflet is deformable from a first position allowing fluid flow in a first, antegrade, direction to a second position restricting fluid flow in a second, retrograde, direction.

3. The radially expandable artificial valve prosthesis of claim 2, wherein the valve leaflet is positioned so as to create retrograde flow vortices sufficient to reduce stagnation of fluid in the valve pocket when the valve prosthesis is configured to restrict fluid flow in the retrograde direction.

4. The radially expandable artificial valve prosthesis of claim 1, wherein the first portion of a perimeter of the valve leaflet is attached to the ring frame by a method selected from the group consisting of suturing, tissue welding and adhesive bonding.

5. The radially expandable artificial valve prosthesis of claim 1, wherein the ring frame comprises a polymeric material.

6. The radially expandable artificial valve prosthesis of claim 1, wherein the ring frame comprises material selected from a group consisting of stainless steel, nickel, silver, platinum, gold, titanium, tantalum, iridium, tungsten, a self-expanding nickel titanium alloy, and inconel.

7. The radially expandable artificial valve prosthesis of claim 6, wherein the ring frame comprises a self-expanding nickel titanium alloy.

8. The radially expandable artificial valve prosthesis of claim 1, wherein the valve pocket height is less than 40 percent of the ring frame width.

9. The radially expandable artificial valve prosthesis of claim 8, wherein the height of the valve pocket height is less than 30 percent of the ring frame width.

10. The radially expandable artificial valve prosthesis of claim 9, wherein the valve pocket height is less than 15 percent of the ring frame width.

11. The radially expandable artificial valve prosthesis of claim 10, wherein the valve pocket height is less than 10 percent of the ring frame width.

12. The radially expandable artificial valve prosthesis of claim 1, wherein the expanded ring frame forms a substantially planar structure.

13. The radially expandable artificial valve prosthesis of claim 1, wherein a second portion of the perimeter of the valve leaflet is not attached to the ring frame.

14. The radially expandable artificial valve prosthesis of claim 13, wherein the second portion of the perimeter of the valve leaflet is extendable beyond the perimeter of the expanded ring frame.

15. The radially expandable artificial valve prosthesis of claim 14, the perimeter of the valve leaflet further comprising a third portion, wherein the third portion is not attached to the ring frame and wherein the third portion is adapted to allow limited retrograde fluid flow.

16. The radially expandable artificial valve prosthesis of claim 1, wherein at least a portion of the support structure is adapted to expand upon deployment to create an artificial sinus in the bodily passage adjacent to the artificial valve prosthesis and wherein the ring frame is positioned within the artificial sinus.

17. The radially expandable artificial valve prosthesis of claim 1, wherein the ring frame comprises a first ring frame portion and a second ring frame portion forming a continuous ring frame, wherein a first portion of the perimeter of the first valve leaflet is attached to the first ring frame portion and a first portion of a perimeter of a second valve leaflet is attached to the second ring frame portion, and wherein a second portion of the perimeter of the first valve leaflet and a second portion of the perimeter of the second valve leaflet define a lumen allowing antegrade fluid flow in the body vessel.

18. The radially expandable artificial valve prosthesis of claim 1, where the valve leaflet comprises a material selected from the group consisting of a synthetic biocompatible polymer, cellulose acetate, cellulose nitrate, silicone, polyethylene, teraphthalate, polyurethane, polyamide, polyester, polyorthoester, poly anhydride, polyether sulfone, polycarbonate, polypropylene, high molecular weight polyethylene, a fluoroplastic material, polytetrafluoroethylene, or mixtures or copolymers thereof;

polylactic acid, polyglycolic acid or copolymers thereof, a polyanhydride, polycaprolactone, polyhydroxy-butyrate valerate, polyhydroxyalkanoate, a polyetherurethane urea, naturally derived or synthetic collagenous material, an extracellular matrix material, submucosa, small intestinal submucosa, stomach submucosa, urinary bladder submucosa, uterine submucosa, renal capsule membrane, dura mater, pericardium, serosa, peritoneum or basement membrane materials, and liver basement membrane.

19. The radially expandable artificial valve prosthesis of claim 1, where the valve leaflet comprises a bioremodelable material.

20. The radially expandable artificial valve prosthesis of claim 1, wherein the valve leaflet comprises small intestinal submucosa.