Implantable Valve System

• US 20130310927A1
• Filed: 05/18/2012
• Published: 11/21/2013
• Est. Priority Date: 05/18/2012
• Status: Abandoned Application

• Current Assignee: Quintessenza, James
• Original Assignee: Quintessenza, James
• Inventors: Quintessenza, James
• Application Number:
  US13/475,938
• Publication Number:
  US 20130310927A1
• Time in Patent Office: Days
• US Class Current: 623/2.12
• CPC Class Codes: A61F 2/2412 with soft flexible valve members, e.g. tissue valves shaped like natural valves check valves with flexible valve members in general F16K15/14
• CPC Class Codes: A61F 2/2415 Manufacturing methods
• CPC Class Codes: A61F 2/2418 Scaffolds therefor, e.g. support stents
• CPC Class Codes: A61F 2220/0075 sutured, ligatured or stitched, retained or tied with a rope, string, thread, wire or cable

Abstract

An implantable valve system comprises a flexible tube and a flexible valve structure. The flexible tube and flexible valve structure can be made of a synthetic polymer material. The flexible valve structure is disposed within the flexible tube. The flexible valve structure can comprises a first leaflet, a second leaflet, and a valve orifice between the first leaflet and the second leaflet. Additional leaflets are possible. Each of the first leaflet and the second leaflet comprises an upper portion forming the valve orifice and a lower portion attached to the flexible tube. The valve orifice has a maximum circumference less than an internal circumference of the flexible tube.

Claims

1. An implantable valve system comprising:

a flexible tube; and

a flexible valve structure within the flexible tube, the flexible valve structure comprising a first leaflet, a second leaflet, and a valve orifice between the first leaflet and the second leaflet, each of the first leaflet and the second leaflet comprising an upper portion forming the valve orifice and a lower portion attached to the flexible tube, the valve orifice having a maximum circumference less than an internal circumference of the flexible tube.

2. The system of claim 1, wherein each of the lower portions comprises a curved attachment region attached to the flexible tube.

3. The system of claim 2, wherein curved attachment region corresponds to a substantially parabolic edge of the lower portion.

4. The system of claim 2, further comprising sutures connecting the flexible tube to the curved attachment region of each lower portion.

5. The system of claim 1, wherein each of the upper portions includes a top edge sized at about half of the internal circumference of the flexible tube.

6. The system of claim 1, wherein the upper portion of the first leaflet is joined to the upper portion of the second leaflet at a first commissural region and at a second commissural region, and the valve orifice is bounded by the first commissural region and the second commissural region.

7. The system of claim 6, further comprising a first attachment suture at the first commissural region and a second attachment suture at the second commissural region, the first attachment suture connecting the first commissural region to the flexible tube, the second attachment suture connecting the second commissural region to the flexible tube.

8. The system of claim 6, further comprising a first commissural suture at the first commissural region and a second commissural suture at the second commissural region, the first commissural suture located at or about an end of the valve orifice, and the second commissural suture located at or about another end of the valve orifice.

9. The system of claim 6, wherein each of the upper portions includes a top edge, each top edge comprises end segments and a medial segment connecting the end segments, the first and second commissural regions join the end segments of the first leaflet to the end segments of the second leaflet, and the medial segments define the valve orifice and are configured to move relative to each other from a separated state to a coaptated state.

10. The system of claim 9, wherein each of the end segments is sized from about 1 mm to about 2 mm.

11. The system of claim 10, wherein the top edge is sized at about half of the internal circumference of the flexible tube.

12. The system of claim 1, wherein the flexible tube is configured to maintain an internal circumference without substantial enlargement upon application of an expansion force to the flexible tube.

13. The system of claim 12, wherein the flexible tube is configured to stretch axially.

14. The system of claim 1, wherein the first leaflet and the second leaflet are formed of a single, continuous sheet material that is neither human tissue nor animal tissue.

15. The system of claim 1, wherein the flexible tube is formed of a material that is neither human tissue nor animal tissue.

16. The system of claim 1, wherein the flexible tube, the first leaflet, and the second leaflet are formed of PTFE.

17. The system of claim 1, wherein the flexible tube has an inner surface having a texture that allows for ingrowth or adhesion of biological tissue to the inner surface when implanted in a human or animal body.

18. The system of claim 17, wherein the flexible tube has an outer surface that that is substantially fluid-tight.

19. The system of claim 17, wherein the flexible tube has an outer surface that is substantially smooth and resistant to tissue ingrowth in comparison to the inner surface.

20. The system of claim 1, further comprising a tubular stent, wherein the flexible tube is disposed within the tubular stent, and the tubular stent comprises interconnected stent struts.

21. The system of claim 20, further comprising a catheter carrying the flexible tube and the flexible valve, the catheter extending through the flexible tube and the valve orifice.