Methods and apparatus for treatment of aneurysms adjacent to branch arteries

• US 8,715,336 B2
• Filed: 04/19/2007
• Issued: 05/06/2014
• Est. Priority Date: 04/19/2007
• Status: Active Grant

• Current Assignee: Medtronic Vascular, Inc. (Medtronic Plc)
• Original Assignee: Medtronic Vascular, Inc. (Medtronic Plc)
• Inventors: Chu, Jack, Erickson, David R., Ganesan, Prema, Hanson, Curtis, Rust, Matthew, Thomas, Charles, Machek, James, Morris, Jonathon
• Primary Examiner(s): Sweet, Thomas J
• Assistant Examiner(s): PRESTON, REBECCA STRASZHEIM
• Application Number:
  US11/737,432
• Publication Number:
  US 20080262595A1
• Time in Patent Office: 2,574 Days
• Field of Search: None
• US Class Current: 623/1.16
• CPC Class Codes: A61F 2/064 with special features to facilitate anastomotic coupling anastomosis of natural blood vessels A61B17/11
• 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 2/954 for placing stents or stent-grafts in a bifurcation
• CPC Class Codes: A61F 2002/061 provided with means for allowing access to secondary lumens
• CPC Class Codes: A61F 2002/067 modular
• CPC Class Codes: A61F 2002/075 the stent being loosely attached to the graft material, e.g. by stitching
• CPC Class Codes: A61F 2002/821 Ostial stents
• CPC Class Codes: A61F 2002/9511 the retaining means being filaments or wires
• CPC Class Codes: A61F 2220/005 using adhesives
• CPC Class Codes: A61F 2220/0075 sutured, ligatured or stitched, retained or tied with a rope, string, thread, wire or cable

Abstract

A stent graft includes at least one aperture extending through the main body thereof, into which an extension portion may be deployed for positioning within an adjacent branch flow lumen. The extension portions include self biasing features, wherein the extension is biased into engagement with the main body to seal the interface thereof. Additionally, the extension portion may be configured for tortuous or deviated anatomy, to enable sealing of the extension portion with the body while extending the extension portion in a substantially non-radial direction from the main body.

Claims

1. An exclusion device for excluding fluid contact to an abnormality in a body flow lumen, comprising:

a body portion having a wall portion and at least opposed first and second open ends;

an aperture extending through said wall portion, said aperture alignable with an opening of a branch feature into the body flow lumen; and

an extension receivable within said aperture and extendible there from into the branch feature extending from the body flow lumen, said extension including;

a generally tubular body having a first end and a second end, the generally tubular body including an excluding material and at least one stent; and

a flange having a generally frustoconical internal support feature separate from the at least one stent of the generally tubular body, the generally frustoconical internal support feature encapsulated within a biocompatible polymer or held by one of the following overmolded materials;

silicone polyurethane, polyurethane blends, polyurethane alloys, ePTFE, PET, polypropylene, polyethylene or other biocompatible materials, the biocompatible polymer or overmolded material defining a generally tapered outer circumferential surface of the flange, the flange located adjacent to and coupled to said first end of said generally tubular body and adapted to sealingly engage with said body portion adjacent said aperture, the generally tapered outer circumferential surface tapering from a first end having a first diameter to a second end having a second diameter, wherein the first diameter is larger than the second diameter;

wherein said extension is configured to urge said flange of said extension and said body portion in contact adjacent to said aperture such that the generally tapered outer circumferential surface of said flange is adapted to engage against said aperture, the first end of the generally tapered outer circumferential surface is configure to be disposed within said body portion, and the second end of the generally tapered outer circumferential surface is configured to be disposed outside of the body portion.

2. An exclusion device for excluding fluid contact to an abnormality in a body flow lumen, comprising:

a body portion having a wall portion and at least opposed first and second open ends;

an aperture extending through said wall portion, said aperture alignable with an opening of a branch feature into the body flow lumen; and

an extension receivable within said aperture and extendible there from into the branch feature extending from the body flow lumen;

said extension including;

a generally tubular body having a first end and a second end, the generally tubular body including an excluding material and at least one stent; and

a flange having a generally frustoconical internal support feature separate from the at least one stent of the generally tubular body, the generally frustoconical internal support feature encapsulated within a biocompatible polymer or held by one of the following overmolded materials;

silicone polyurethane, polyurethane blends, polyurethane alloys, ePTFE, PET, polypropylene, polyethylene or other biocompatible materials, the biocompatible polymer or overmolded material defining a generally tapered outer circumferential surface of the flange, the flange adapted to be located adjacent to and coupled to said first end of said generally tubular body to sealingly engage with said body portion adjacent said aperture, the generally tapered outer circumferential surface tapering from a first end having a first diameter to a second end having a second diameter, wherein the first diameter is larger than the second diameter;

wherein said extension is configured to urge said flange of said extension and said body portion in contact adjacent to said aperture such that the generally tapered outer circumferential surface of said flange is adapted to engage against said aperture, the first end of the generally tapered outer circumferential surface is configured to be disposed within said body portion, and the second end of the generally tapered outer circumferential surface is configured to be disposed outside of the body portion.

3. The exclusion device of claim 2, wherein said generally frustoconical internal support feature is formed of a retained biased structure.

4. The exclusion device of claim 3, wherein said retained biased structure is a wire mesh.

5. The exclusion device of claim 3, wherein said retained biased structure includes at least one wire basket.

6. An exclusion device for excluding fluid contact to an abnormality in a body flow lumen, comprising:

a body portion having a wall portion and at least opposed first and second open ends;

an aperture extending through said wall portion, said aperture alignable with an opening of a branch feature into the body flow lumen; and

an extension receivable within said aperture and extendible there from into the branch feature extending from the body flow lumen, said extension including;

a generally tubular body having a first end and a second end, the generally tubular body including an excluding material and at least one stent; and

a flange including a first flange portion and a second flange portion, a generally frustoconical internal support feature encapsulated within a biocompatible material and disposed within one of the first and second flange portions, the generally frustoconical internal support structure being separate from the at least one stent of the generally tubular body, wherein the first end of the generally tubular body is received within the flange, wherein said first flange portion is configured to be retained within said body portion, and said second flange portion is configured to be positioned exterior to said body portion.

7. The exclusion device of claim 6, wherein said frustoconical support feature includes a first frustoconical support feature disposed within said first flange portion and a second frustoconical support feature disposed within said second flange portion.

8. An exclusion device for excluding fluid contact to an abnormality in a body flow lumen, comprising:

a body portion having a wall portion and at least opposed first and second open ends;

an aperture extending through said wall portion, said aperture alignable with an opening of a branch feature into the body flow lumen; and

an extension receivable within said aperture and extendible there from into the branch feature extending from the body flow lumen, said extension including;

a generally tubular body having a first end and a second end, the generally tubular body including an excluding material and at least one stent;

a flange having a first flange portion retained within said body portion and a second flange portion positioned exterior to said body portion; and

a polymer sheet portion disposed between the second flange portion and the first end of the generally tubular body, wherein said first flange portion is positioned about a first flange axis and the generally tubular body includes a longitudinal axis centerline which is angularly offset from the first flange axis when said extension is in a deployed configuration with said first flange portion within said body portion, said second flange portion exterior to said body portion, and said generally tubular body disposed within the branch feature and in a radially expanded configuration.