Implantable medical device with optimized shape

• US 7,637,937 B2
• Filed: 04/06/2005
• Issued: 12/29/2009
• Est. Priority Date: 04/08/2004
• Status: Active Grant

• Current Assignee: Cook Medical Incorporated (Cook Group Incorporated)
• Original Assignee: Cook Incorporated (Cook Group Incorporated)
• Inventors: Case, Brian C., Flagle, Jacob A.
• Primary Examiner(s): Manahan; Todd E
• Assistant Examiner(s): BLATT, ERIC D
• Application Number:
  US11/099,713
• Publication Number:
  US 20050228472A1
• Time in Patent Office: 1,728 Days
• Field of Search: 623 115- 12, 623/1.24, 623/1.11
• US Class Current: 623/1.15
• CPC Class Codes: A61F 2/2418 Scaffolds therefor, e.g. support stents
• CPC Class Codes: A61F 2/2475 Venous valves
• CPC Class Codes: A61F 2/90 characterised by a net-like or mesh-like structure
• CPC Class Codes: A61F 2002/30014 differing in elasticity, stiffness or compressibility
• CPC Class Codes: A61F 2002/3011 Cross-sections or two-dimensional shapes
• CPC Class Codes: A61F 2220/0016 with sharp anchoring protrusions, e.g. barbs, pins, spikes
• CPC Class Codes: A61F 2220/005 using adhesives
• CPC Class Codes: A61F 2220/0058 soldered or brazed or welded
• CPC Class Codes: A61F 2230/0002 Two-dimensional shapes, e.g. cross-sections
• CPC Class Codes: A61F 2230/0017 Angular shapes
• CPC Class Codes: A61F 2230/0054 V-shaped
• CPC Class Codes: A61F 2250/0018 differing in elasticity, stiffness or compressibility
• CPC Class Codes: A61F 2250/0036 differing in thickness

Abstract

Medical devices for implantation in a body vessel, and methods of using and making the same, are provided. Embodiments of the invention relate to medical devices comprising a frame having cross-section that can substantially conform to body vessel shapes that have elliptical or circular cross-sections, and dynamically respond to changes in the cross-section of a body vessel. Frames with directionally-dependent radial compressibility or expandability characteristics are also provided. Medical devices comprising a frame and one or more valve members adapted to regulate fluid flow in a body vessel, such as a vein, are also provided.

Claims

1. A method of treating a subject with a medical device for implantation in a body vessel of the venous system, said body vessel comprising an elliptical cross-section having a major axis and a minor axis wherein the cross-section of the body vessel can undergo change as a result of blood flowing therethrough, comprising the steps of:

(a) radially compressing a medical device into a radially compressed delivery configuration, the medical device comprising

(i) an elliptical annular frame having a tubular configuration defining a lumen about a longitudinal axis, the frame being movable between an expanded configuration and a compressed configuration, the frame in the expanded configuration having an elliptical cross- section having a major axis and a minor axis, where the frame has a first maximum radial distance along the major axis greater than a second maximum radial distance along the minor axis, the frame having a circular cross-section in the radially compressed delivery configuration, the frame including at least one annular ring member having at least two circumferential regions forming a closed ring frame, each circumferential region having a different radial compressibility, wherein the radial compressibility of the circumferential region along the major axis is greater than the radial compressibility along the minor axis, and

(ii) one or two valve leaflets attached to the frame, the valve leaflet having a free edge unattached to the frame and positioned within the lumen of the frame along the major axis of the elliptical cross-section of the frame, the free edge of the one or more valve leaflets moveable in response to fluid flow through the lumen;

(b) delivering the medical device in the radially compressed delivery configuration to a point of treatment within said body vessel of the venous system; and

(c) deploying the medical device at the point of treatment by radially expanding the medical device from the radially compressed delivery configuration to a radially expanded configuration such that the major and minor axes of the frame are substantially aligned with the major and minor axes of said body vessel respectively, wherein the cross-section of the frame is configured to move between the elliptical cross-section and the circular cross-section to conform to the changing cross-section of said body vessel of the venous system.

2. The method of claim 1, wherein the frame includes a first annular ring member and a second annular ring member longitudinally adjacent to the first annular ring member, wherein the frame having an elliptical cross-section at the first annular ring member and a circular cross-section at the second annular ring member.

3. The method of claim 2, wherein the first and second annular ring members each have a first radial compressibility along a first radial direction perpendicular to the longitudinal axis that is greater than a second radial compressibility along a second radial direction perpendicular to the longitudinal axis and the first radial direction, the first and second radial compressibility of the second annular ring member being different than the first and second radial compressibility of the first annular ring member.

4. The method of claim 1, wherein the medical device further comprises a means for orienting the medical device within a body vessel.

5. The method of claim 1, wherein the at least one annular ring member of the frame comprises a plurality of interconnected linear struts and bends arranged in a zig-zag pattern extending circumferentially around the longitudinal axis to form the closed ring frame.

6. The method of claim 5, wherein each annular ring has a first circumferential region and a second circumferential region,

the first circumferential region having a first strut density per unit of circumferential distance;

and

the second circumferential region having a second strut density per unit of circumferential distance, that is less than the first strut density.

7. The method of claim 5, wherein each annular ring has a first circumferential region and a second circumferential region,

the first circumferential region having struts with a first strut cross-sectional area;

and

the second circumferential region having struts with a second strut cross-sectional area that is less than the first strut cross-sectional area.

8. The method of claim 1, where the frame comprises a material selected from the group consisting of:

a stainless steel, a NiTi alloy and a cobalt-chromium alloy.