Self-molding annuloplasty ring

• US 6,726,716 B2
• Filed: 08/24/2001
• Issued: 04/27/2004
• Est. Priority Date: 08/24/2001
• Status: Expired due to Term

• Current Assignee: Edwards Lifesciences Corporation
• Original Assignee: Edwards Lifesciences Corporation
• Inventors: Marquez, Salvador
• Primary Examiner(s): Prebilic, Paul B.
• Application Number:
  US09/938,902
• Publication Number:
  US 20030040793A1
• Time in Patent Office: 977 Days
• Field of Search: 623/2.36, 623/2.37, 623/2.14, 623/2.18, 623/2.42, 623/900, 623/2.38, 623/1.13, 63/39, 63/38, 63/52, 63/6, 24/17.B, 24/20.S, 244/82
• US Class Current: 623/2.36
• CPC Class Codes: A61F 2/2445 Annuloplasty rings in direct contact with the valve annulus
• CPC Class Codes: A61F 2/2448 D-shaped rings
• CPC Class Codes: Y10S 623/902 Method of implanting

Abstract

The resilient self molding annuloplasty ring which may be enlarged prior to implantation to facilitate implantation within a dilated or otherwise incompetent valve annulus having sufficient contractive force to render a valve competent. The self molding annuloplasty ring of the invention may further comprise integral attachment devices to aid in the implantation process. The invention further discloses an illustrative method of implantation.

Claims

1. A sizable self-molding annuloplasty ring for implantation in a heart valve annulus, comprising:

a resilient inner sizing member;

a plurality of support members positioned on said inner sizing member; and

,

an outer attachment sheath enclosing said sizing member and said support members;

wherein the inner sizing member is biased toward a fully relaxed diameter but can be stretched to a fully expanded diameter; and

wherein the plurality of support members constrain contraction of the inner sizing member to a contracted diameter that is larger than the fully relaxed diameter but smaller than the fully expanded diameter.

2. The annuloplasty ring of claim 1 wherein each support member comprises a body member having a lumen formed therein, said lumen being capable of receiving said sizing member therein.

3. The annuloplasty ring of claim 1 wherein said resilient inner sizing member comprises a biologically compatible elastomer.

4. The annuloplasty ring of claim 1 wherein said outer attachment sheath is selected from the group consisting of:

biologically compatible fabric mesh;

polyethylene terepthalate;

polyester knit;

PTFE knit; and

ePTFE knit.

5. The annuloplasty ring of claim 1 wherein said outer attachment sheath comprises a medicament to induce tissue growth.

6. The annuloplasty ring of claim 1 wherein said annuloplasty ring further comprises a plurality of attachment devices positioned thereon.

7. The annuloplasty ring of claim 6 wherein said attachment devices are selected from the group consisting of:

needles;

barbs; and

hooks.

8. The annuloplasty ring of claim 6 wherein said attachment devices are manufactured from stainless steel.

9. The annuloplasty ring of claim 6 wherein said attachment devices are manufactured from a Nickel-Titanium alloy.

10. A sizable self-molding annuloplasty ring for implantation in a heart valve annulus, comprising:

a resilient inner sizing member in the shape of a continuous ring that has a relaxed diameter and can be stretched to a expanded diameter; and

a plurality of support members each having a receiving lumen formed therein which is capable of receiving the inner sizing member, the inner sizing member being positioned within the lumens of the support members;

wherein the plurality of support members are biased by the inner sizing member to engage one another and limit contraction of the inner sizing member to a contracted diameter;

wherein the contracted diameter is larger than the relaxed diameter but smaller than the expanded diameter.

11. The annuloplasty ring of claim 10 wherein said outer attachment sheath is selected from the group consisting of:

biologically compatible fabric mesh;

polyethylene terepthalate;

polyester knit;

PTFE knit; and

ePTFE knit.

12. The annuloplasty ring of claim 10 wherein said outer attachment sheath comprises a medicament to induce tissue growth.

13. The annuloplasty ring of claim 10 wherein said resilient inner sizing member comprises a biologically compatible elastomer.

14. The annuloplasty ring of claim 10 wherein said annuloplasty ring further comprises a plurality of attachment devices positioned thereon.

15. The annuloplasty ring of claim 14 wherein said attachment devices are selected from the group consisting of:

needles;

barbs; and

hooks.

16. The annuloplasty ring of claim 14 wherein said attachment devices are manufactured from stainless steel.

17. The annuloplasty ring of claim 14 wherein said attachment devices are manufactured from a Nickel-Titanium alloy.