Bulbous valve and stent for treating vascular reflux

• US 20030208261A1
• Filed: 12/30/2002
• Published: 11/06/2003
• Est. Priority Date: 03/03/2000
• Status: Abandoned Application

• Current Assignee: Cook Incorporated (Cook Group Incorporated)
• Original Assignee: Cook Incorporated (Cook Group Incorporated)
• Inventors: Osse, Franciso J., Thorpe, Patricia E.
• Application Number:
  US10/220,650
• Publication Number:
  US 20030208261A1
• Time in Patent Office: Days
• US Class Current: 623/1.16
• CPC Class Codes: A61F 2/2415 Manufacturing methods
• CPC Class Codes: A61F 2/2418 Scaffolds therefor, e.g. support stents
• CPC Class Codes: A61F 2/2475 Venous valves
• CPC Class Codes: A61F 2230/0054 V-shaped
• CPC Class Codes: A61F 2240/002 Designing or making customized prostheses
• CPC Class Codes: A61F 2250/0039 differing in diameter
• CPC Class Codes: A61P 9/00 Drugs for disorders of the cardiovascular system

Abstract

A stent and valve device (43) assembly for manufacture using suitable biocompatible materials and for placement, preferably percutaneously, into a vascular lumen.

Claims

1. A self-expanding replacement valve assembly having a bulbous-shaped portion and which is configured for implantation within avascular lumen, the valve assembly comprising a plurality of flexible members, each flexible member conformed to cooperate with at least one other flexible member to unidirectionally admit vascular fluid through the valve assembly and to prevent retrograde flow of the vascular fluid through the valve assembly.

2. The assembly of claim 1, wherein at least a portion of one of said flexible members includes either sclera or small intestine sub-mucosa material.

3. The assembly of claim 1, in which the flexible members are supported by flexible and resilient struts configured for use in a vascular lumen.

4. The assembly of claim 3, in which the struts are manufactured with a resilient metallic material.

5. The assembly of claim 4, in which the struts material is selected from either nitinol or stainless steel.

6. The assembly of claim 3, in which the struts are manufactured from a biodegradable-like material designed to dissolve in a patient after a certain period of time.

7. The assembly of claim 3, in which the flexible members are cusps of a valve having edge portions configured for attachment to the struts, and edge portions configured to form free ends capable of reshaping to selectively form an opening through the valve assembly or an obstruction in the valve assembly.

8. The assembly of claim 1, in which the flexible members are bicusps.

9. The assembly of claim 1, in which the flexible members generally semi-elliptical in shape.

10. The assembly of claim 1, shaped as a generally tubular flexible member conformed to be implanted in a venous lumen in a fixed location.

11. The assembly of claim 3, in which the struts are connected to form a tubular shape and are flexible in a direction generally transverse to a longitudinal axis of the tubular shape, the flexible members being operably disposed in the tubular member.

12. The assembly of claim 11, in which each flexible member defines a first edge portion conformable to said tubular member and a second edge portion, the second edge portion of each flexible member cooperating to enable said unidirectional flow by forming a plurality of free ends which selectively engage and disengage each other.

13. A stent and valve assembly for use in a vascular lumen, comprising:

a. a flexible and resilient structure of a plurality of struts designed as a variably diametered tubular shape; and

b. a plurality of valve leaflets formed from either SIS or sclera material and attached along designated edge portions to a plurality of said struts to enable opening and closing of free edge portions to emulate the operation of a naturally occurring vascular valve.

14. The assembly of claim 13, having a two stage design of at least six struts in each stage.

15. The assembly of claim 13, in which the total length of the assembly is between about 1 and 2 cm, and the diameter of any stage is between about 8-20 mm.

16. A method of making a replacement valve assembly for implantation into a vascular lumen and to function as a check valve, the valve assembly comprising a plurality of flexible members, each flexible member conformed to cooperate with the other at least one flexible member to unidirectionally admit vascular fluid through the valve assembly, the method comprising the steps of:

providing a flexible biocompatible material;

constructing a plurality of flexible members from the flexible material; and

disposing the flexible members in a bulbous-shaped portion of a tubular member having at least one stage so as to function as a unidirectional flow valve.

17. The method of claim 16, in which sclera or SIS material is provided as the flexible material.

18. The method of claim 17, in which the tubular member is constructed as a two stage member to enhance stability during employment in a vascular lumen.

19. A method of treating chronic vascular insufficiency, the method comprising the steps of providing a replacement valve assembly shaped with a bulbous portion for implantation within a venous lumen, the valve assembly comprising a plurality of flexible members, each flexible member shaped to cooperate with the other at least one flexible member to unidirectionally admit vascular fluid through the valve assembly;

introducing at least one of said replacement valve assemblies into a venous lumen generally proximate an insufficient vascular valve; and

fixing said replacement valve assembly in said venous lumen by actuating a self expanding portion of the valve assembly to engage the inner lumenal wall of the venous lumen.

20. The method of claim 19, in which the replacement valve assembly is introduced into the venous lumen percutaneously.

21. The method of claim 20, in which the replacement valve assembly is introduced into the vascular lumen by a catheter with the replacement valve assembly within the catheter.

22. The method of claim 19, in which the venous replacement valve is made, at least partially, from mammalian tissue.

23. A method of making a vascular valve member assembly from mammalian sclera or small intestine sub-mucosa (SIS), the method comprising the steps of providing a mammalian tissue source;

removing said tissue from the tissue source; and

fashioning the valve member from the sclera or SIS.

24. The method of claim 23, in which a plurality of the valve members are attached at least in part to an inner portion of a self-expanding and generally tubular shaped strut assembly.