Stentless aortic valve replacement with high radial strength

• US 8,568,477 B2
• Filed: 06/07/2006
• Issued: 10/29/2013
• Est. Priority Date: 06/07/2005
• Status: Active Grant

• Current Assignee: Speyside Medical, LLC
• Original Assignee: Direct Flow Medical, Inc.
• Inventors: Lashinski, Randall T., Bishop, Gordon B.
• Primary Examiner(s): Isabella, David
• Assistant Examiner(s): LEVINE, JOSHUA H
• Application Number:
  US11/422,841
• Publication Number:
  US 20070005133A1
• Time in Patent Office: 2,701 Days
• Field of Search: 623/2.12, 623/2.14, 623/2.17, 623/2.18
• US Class Current: 623/2.38
• CPC Class Codes: A61F 2/2409 Support rings therefor, e.g. for connecting valves to tissue annuloplasty rings A61F2/2442
• CPC Class Codes: A61F 2/2415 Manufacturing methods
• CPC Class Codes: A61F 2/2418 Scaffolds therefor, e.g. support stents
• CPC Class Codes: A61F 2/2427 Devices for manipulating or deploying heart valves during implantation
• CPC Class Codes: A61F 2/2469 with resilient valve members, e.g. conical spiral
• CPC Class Codes: A61F 2/2476 Valves implantable in the body not otherwise provided for
• CPC Class Codes: A61F 2220/0066 stapled
• CPC Class Codes: A61F 2250/0003 having an inflatable pocket filled with fluid, e.g. liquid or gas

Abstract

Disclosed is a stentless transluminally implantable heart valve, having a formed in place support. The formed in place support exhibits superior crush resistance when compared to conventional balloon expandable or self expandable stent based valves.

Claims

1. A cardiovascular prosthetic valve comprising:

a stentless support structure, the stentless support structure comprising an inflatable cuff comprising at least one inflatable channel that forms, at least in part, a distal inflatable toroidal structure and a proximal inflatable toroidal structure, the inflatable cuff also comprising a waist that extends between the distal inflatable toroidal structure and the proximal inflatable toroidal structure, wherein the inflatable cuff is transformable from a reduced cross sectional configuration for transluminal deployment to a functional enlarged configuration to form a flow path through the support structure;

a valve coupled to the inflatable cuff and positioned in the flow path, the valve configured to permit flow in a first axial direction and to inhibit flow in a second axial direction opposite to the first axial direction;

a hardenable media positioned within the inflatable cuff holding the inflatable cuff in the functional enlarged configuration; and

wherein the inflatable cuff in the functional enlarged configuration exhibits sufficient crush resistance that it will deform radially no more than about 0.3 inches under a load of about 4 pounds when the hardenable media in the inflatable cuff is hardened.

2. The cardiovascular prosthetic valve of claim 1, wherein the at least one inflatable channel includes a first chamber associated with the distal inflatable toroidal structure and a second, independent, chamber associated with the proximal inflatable toroidal structure.

3. A prosthetic valve for replacing an aortic valve positioned between the left ventricle and the aorta of the heart, the prosthetic valve comprising:

a stentless support structure, the stentless support structure comprising an inflatable structure comprising a distal end and a proximal end, wherein the inflatable structure is transformable from a reduced cross sectional configuration for transluminal deployment to a functional enlarged configuration surrounding a flow path for blood; and

a valve member coupled to the inflatable structure, the valve member being positioned generally between the distal and proximal ends of the inflatable structure and in the flow path for blood;

a hardenable media positioned within the inflatable structure holding the inflatable structure in the functional enlarged configuration;

wherein the distal end of the inflatable structure is configured to be positioned within the left ventricle and the proximal end of the inflatable structure is configured to be positioned within the aorta; and

wherein the inflatable structure in the functional enlarged configuration exhibits sufficient crush resistance that it will deform radially no more than about 0.3 inches under a load of about 4 pounds when the hardenable media is hardened.

4. The prosthetic valve of claim 3, wherein the inflatable structure includes a first chamber associated with the distal end and a second separate chamber associated with the proximal end.