Short body endoprosthesis

• US 6,306,164 B1
• Filed: 09/05/1997
• Issued: 10/23/2001
• Est. Priority Date: 09/05/1997
• Status: Expired due to Term

• Current Assignee: C.R. Bard, Inc. (Becton, Dickinson & Co)
• Original Assignee: C.R. Bard, Inc. (Becton, Dickinson & Co)
• Inventors: Kujawski, Dennis
• Primary Examiner(s): Milano, Michael J.
• Application Number:
  US08/925,809
• Time in Patent Office: 1,509 Days
• Field of Search: 623/1, 623/11, 623/12, 623/1.13, 623/1.16, 623/1.23, 623/1.27, 623/1.35, 623/1.36
• US Class Current: 623/1.35
• CPC Class Codes: A61F 2/07 Stent-grafts
• CPC Class Codes: A61F 2/89 the wire-like elements comprising two or more adjacent rings flexibly connected by separate members
• CPC Class Codes: A61F 2002/065 Y-shaped blood vessels
• CPC Class Codes: A61F 2002/075 the stent being loosely attached to the graft material, e.g. by stitching
• CPC Class Codes: A61F 2220/005 using adhesives
• CPC Class Codes: A61F 2220/0066 stapled
• CPC Class Codes: A61F 2220/0075 sutured, ligatured or stitched, retained or tied with a rope, string, thread, wire or cable

Abstract

The invention comprises, inter-alia, endoprosthetic implants for treating vascular defects, including abdominal aortic aneurysms. Implants according to the invention have a short main body that can be positioned within a patient'"'"'s aorta at a position above the renal end of an aortic aneurysm. The short main body includes a proximal, or renal, face that redirects the flow of blood into the openings of channels that can carry blood past the aneurysm. In this way, the flow of blood through the aorta is diverted into the two passageways and through the main body of the implant. Fluid exiting the implant can be carried by leg extensions and delivered to a healthy part of the patient'"'"'s aorta or the iliac arteries. Accordingly, the implant provides a system for allowing blood traveling through the aorta to be carried by a vascular graft that spans an aortic aneurysm, thereby relieving fluid pressure on the thin wall of aortic aneurysm, and reducing the risk of death caused by a ruptured aneurysm.

Claims

1. An endoprosthetic implant, comprising

a trunk having,

a proximal face including an aperture disposed therein,

a channel in fluid communication with said aperture and extending from said proximal face and hang a portion adapted for coupling to a leg extension,

an anchor coupled to a peripheral portion of said proximal face and adapted for engaging said proximal face to an interior tissue wall of a body lumen wherein said anchor comprises a tubular wire frame having a proximal opening and a distal opening, and

a vascular graft having a bifurcated portion disposed within said tubular wire frame and having a first and second channel and a peripheral portion mounted to said proximal opening of said tubular wire frame for forming said proximal face.

2. An endoprosthetic implant according to claim 1, wherein

said proximal face comprises a substantially flat surface formed of a fluid resistant, bio-compatible material suitable for disposition within a flow of fluid that occurs within the body lumen, said proximal face being adapted to redirect fluid flow through said channel.

3. An endoprosthetic implant according to claim 1, wherein

said anchor is radially compressible for allowing said trunk to be carried within a lumen of a catheter delivery system.

4. An endoprosthetic implant according to claim 1, wherein

said anchor includes a resilient wire frame capable of being placed under compression for providing a radially expansive force for sealing said trunk against the tissue wall of the body lumen.

5. An endoprosthetic implant according to claim 1, wherein

said trunk is dimensionally adapted for disposition within a short section of the body lumen, for disposition above a site of an aneurysm.

6. An endoprosthetic implant according to claim 1, wherein said trunk has a longitudinal length between approximately 1.0 cm.-3.0 cm.

7. An endoprosthetic implant according to claim 1, further comprising

a tubular leg extension having an interior channel and having an upper end being contractible radially for insertion into said channel and being dimensionally adapted for spanning an aneurysm.

8. An endoprosthetic implant according to claim 1, farther comprising

hook elements coupled to said trunk for joining said trunk to the tissue of the body lumen.

9. An endoprosthetic implant according to claim 1, wherein

said anchor is disposed proximate said proximal face.

10. An endoprosthetic implant according to claim 9, further including

an extension loop frame having a distal loop portion for coupling to a spoke element of a catheter delivery system, whereby said catheter delivery system may deliver, recapture and reposition said implant within the body lumen.

11. An endoprosthetic implant, comprising

a trunk having,

a proximal face including an aperture disposed therein,

a channel in fluid communication with said aperture and extending from said proximal face and having a portion adapted for coupling to a leg extension, and

an anchor coupled to a peripheral portion of said proximal face and adapted for engaging said proximal face to an interior tissue wall of a body lumen,

wherein said trunk comprises a solid plug of biocompatible material having two interior passageways extending therethrough for defining a first and second channel.

12. An endoprosthetic implant according to claim 11, wherein said biocompatible material is elastomeric.

13. A method of forming a bifurcated implant, comprising the steps of

providing an anchor formed of a resilient wire frame capable of big radially compressed and having a generally tubular shape including a proximal opening and a distal opening,

providing a vascular graft having a bifurcated portion and a proximal portion coupled thereto, wherein said step of providing a vascular graft includes the step of providing a bifurcated graft having a proximal portion formed as a unitary channel and having a bifurcated portion formed as two legs extending from said unitary channel,

disposing said bifurcated portion within said anchor, and

mounting said proximal portion of said graft to said proximal opening of said anchor to form a face for said implant having at least one opening for receiving fluid.

14. A method of forming a bifurcated implant, comprising the steps of

providing an anchor formed of a resilient wire frame capable of being radially compressed and having a generally tubular shape including a proximal opening and a distal opening,

providing a vascular graft having a bifurcated portion and a proximal portion coupled thereto, wherein said stop of providing a vascular graft includes the step of providing a bifurcated graft woven from a biocompatible material and having a bifurcated section formed therein,

disposing said bifurcated portion within said anchor, and

mounting said proximal portion of said graft to said proximal opening of said anchor to form a face for said implant baying atleast one opening for receiving fluid.

15. A method of forming a bifurcated implant, comprising the steps of

providing an anchor formed of a resilient wire frame capable of being radially compressed and having a generally tabular shape including a proximal opening and a distal opening,

providing a vascular graft having a bifurcated portion and a proximal portion coupled thereto, wherein said step of providing a vascular graft includes the step of

providing a graft formed as a unitary tubular body,

placing a stitch within said unitary tubular body along a centrally located longitudinal axis to form said bifurcated portion,

disposing said bifurcated portion within said anchor, and

mounting said proximal portion of said graft to said proximal opening of said anchor to form a face for said implant having at least one opening for receiving fluid.