Implantable medical device with constrained expansion

• US 7,955,376 B2
• Filed: 10/10/2006
• Issued: 06/07/2011
• Est. Priority Date: 05/19/2003
• Status: Active Grant

• Current Assignee: Cook Medical Incorporated (Cook Group Incorporated)
• Original Assignee: Cook Medical Incorporated (Cook Group Incorporated)
• Inventors: Case, Brian C., Flagle, Jacob A., Hoffa, Andrew K., Garrison, Michael L., Osborne, Thomas A.
• Primary Examiner(s): Matthews; William (Howie) H
• Application Number:
  US11/539,925
• Publication Number:
  US 20070106372A1
• Time in Patent Office: 1,701 Days
• Field of Search: 623 11- 113, 623 124- 126, 623 13- 131, 623/2.18, 623/2.19
• US Class Current: 623/1.24
• CPC Class Codes: A61F 2/2418 Scaffolds therefor, e.g. support stents
• CPC Class Codes: A61F 2/2475 Venous valves
• CPC Class Codes: A61F 2220/0008 Fixation appliances for connecting prostheses to the body
• CPC Class Codes: A61F 2220/0016 with sharp anchoring protrusions, e.g. barbs, pins, spikes
• CPC Class Codes: A61F 2220/0075 sutured, ligatured or stitched, retained or tied with a rope, string, thread, wire or cable
• CPC Class Codes: A61F 2230/0026 trapezoidal
• CPC Class Codes: A61F 2230/0095 Saddle-shaped

Abstract

A medical device comprises a support structure and one or more graft members comprising a valve portion and a constraining portion. The support structure has a first, unexpanded configuration and a second, expanded configuration. The constraining portion is adapted to substantially prevent the support structure from achieving the second, expanded configuration. The valve portion is adapted to permit fluid flow through a body vessel in a first direction and substantially prevent fluid flow through the vessel in a second, opposite direction.

Claims

1. A medical device for implantation in a body vessel, comprising:

a support structure having a first, unexpanded configuration and a second, expanded configuration; and

a graft member connected to the support structure, the graft member having a proximal edge, a distal edge, a first lateral edge, a second lateral edge, and a lengthwise axis extending from the proximal edge to the distal edge, each of the first and second lateral edges extending from the proximal edge to the distal edge, the graft member comprising a valve portion, a constraining portion, and a transitional portion disposed between the valve portion and the constraining portion, the constraining portion sized to be drawn taught as the support structure expands from the first configuration to the second configuration and the valve portion adapted to permit fluid flow through said body vessel in a first direction and substantially prevent fluid flow through said body vessel in a second, opposite direction;

wherein prior to being connected to the support structure each of the first and second lateral edges comprises first and second outwardly directed curves relative to the lengthwise axis and an inwardly directed curve relative to the lengthwise axis disposed between the first and second outwardly directed curves;

wherein the valve portion has a first maximum width and the constraining portion has a second maximum width, each of the first and second maximum widths is measured from the first lateral edge to the second lateral edge along a lateral axis perpendicular to the lengthwise axis;

wherein the first maximum width is greater than the second maximum width; and

wherein the transitional portion has a width that tapers from the first maximum width to the second maximum width.

2. The medical device according to claim 1, further comprising a second graft member connected to the support structure and comprising a second valve portion and a second constraining portion.

3. The medical device according to claim 2, wherein the second graft member includes a second transitional portion disposed between the second valve portion and the second constraining portion.

4. The medical device according to claim 3, wherein the first and second valve portions cooperatively define a coaptation region.

5. The medical device according to claim 1, wherein the graft member comprises an extracellular matrix material.

6. The medical device according to claim 1, wherein the graft member comprises small intestine submucosa.

8. The medical device according to claim 6, wherein the support frame comprises a stent.

9. The medical device according to claim 1, wherein the valve portion comprises pleats.

10. The medical device according to claim 6, wherein the non-taught portion comprises pleats.

7. A medical device for implantation in a body vessel, comprising a graft member connected to an expandable support frame, the graft member having a proximal edge, a distal edge, a first lateral edge, a second lateral edge, and a lengthwise axis extending from the proximal edge to the distal edge, each of the first and second lateral edges extending from the proximal edge to the distal edge, the graft member including a taught portion adapted to constrain expansion of the support frame, a non-taught portion adapted to selectively permit and substantially prevent fluid flow through said body vessel, and a transitional portion located between the taught portion and the non-taught portion;

wherein prior to being connected to the expandable support frame each of the first and second lateral edges comprises first and second outwardly directed curves relative to the lengthwise axis and an inwardly directed curve relative to the lengthwise axis disposed between the first and second outwardly directed curves;

wherein the non-taught portion has a first maximum width and the taught portion has a second maximum width, each of the first and second maximum widths is measured from the first lateral edge to the second lateral edge along a lateral axis perpendicular to the lengthwise axis;

wherein the first maximum width is greater than the second maximum width; and

wherein the transitional portion has a width that tapers from the first maximum width to the second maximum width.