Mitral valve prosthesis

• US 20050075727A1
• Filed: 10/29/2002
• Published: 04/07/2005
• Est. Priority Date: 10/29/2001
• Status: Abandoned Application

• Current Assignee: The University Court Of The University Of Glasgow
• Original Assignee: The University Court Of The University Of Glasgow
• Inventors: Wheatley, David John
• Application Number:
  US10/493,950
• Publication Number:
  US 20050075727A1
• Time in Patent Office: Days
• US Class Current: 623/2.170
• CPC Class Codes: A61F 2/2412 with soft flexible valve members, e.g. tissue valves shaped like natural valves check valves with flexible valve members in general F16K15/14
• CPC Class Codes: A61F 2/2457 Chordae tendineae prostheses

Abstract

The present invention relates to a mitral valve prosthesis comprising flexible leaflet-like elements with curved coapting surfaces and means for maintaining continuity of the valve when inserted into the mitral annulus, which mimics the continuity between the papillary muscles, the chordae tendineae, the mitral valve leaflets and the mitral annulus of a natural valve. The present invention also relates to a method of fitting such a prosthesis to heart of a patient.

Claims

1. A heart valve prosthesis comprising:

a support adapted to be coupled to the mitral annulus;

a valve element coupled to the support and moveable between an open position and a closed position;

at least one continuity member having one end coupled to said support and the other end for coupling to papillary muscle; and

restraining means for securing the continuity member to an area of heart muscle and for permiitting adjustment of the continuity member externally of the heart.

3. The prosthesis of claim 1, wherein the support has a ring-like structure.

4. The prosthesis of claim 1 wherein the support comprises a semi-rigid structure.

5. The prosthesis of claim 1 wherein the support is incorporated into a fabric sewing ring.

6. The prosthesis of claim 5, wherein said fabric sewing ring is formed of polytetrafluoroethylene.

7. The prosthesis of claim 1, wherein the valve element is flexible.

8. The prosthesis of claim 1, wherein a plurality of valve elements are provided.

9. The prosthesis of claim 1 wherein two flexible valve elements are provided.

10. The prosthesis of claim 9, wherein the valve elements are formed and arranged to mimic the function of the anterior and posterior leaflets of a working biological valve in vivo.

11. The prosthesis of claim 1, wherein the valve element comprises elongate reinforcing elements.

12. The prosthesis of claim 11, wherein the reinforcing elements are in the form of elongate strands.

13. The prosthesis of claim 12, wherein the strands are multifilament.

14. The prosthesis of claim 11, wherein the reinforcing elements are of at least one of polytetrafluoroethylene (PTFE), polypropylene and carbon fibre.

15. The prosthesis of claim 11, wherein the reinforcing elements are attached around the support and radiate therefrom.

16. The prosthesis of claim 11 wherein the reinforcing strands are embedded in a single plane within the valve element.

17. The prosthesis of any of claim 11 wherein the reinforcing strands lie in at least two separate planes with polymer material therebetween.

18. The prosthesis of claim 15, wherein the reinforcing elements comprise primary elements extending in one direction and secondary elements extending in another direction.

19. The prosthesis of claim 11, wherein the reinforcing elements comprise short strand discontinuous fibres of high aspect ratio.

20. The prosthesis of claim 19, wherein the short strand discontinuous fibres of high aspect ratio are nanotubes.

21. The prosthesis of claim 18, wherein primary elements are mutually coupled by secondary elements to create a netlike structure.

22. The prosthesis of claim 21, wherein the net-like structure is coupled to a flexible material forming at least one surface of the valve element.

23. The prosthesis of claim 21, wherein the net-like structure is embedded within a biostable polymer.

24. The prosthesis of claim 23, wherein the polymer comprises polyurethane.

25. The prosthesis of claim 21, wherein the net-like structure is of a size and shape corresponding to the valve element.

26. The prosthesis of claim 11, wherein the reinforcing elements continue beyond the valve element and ends of the elements form continuity members.

27. The prosthesis of claim 1, further including restraining means comprising a tubular member for receiving the other end portion of the continuity member.

28. The prosthesis of claim 27, wherein the tubular member is a tube which is at least semi-rigid.

29. The prosthesis of claim 27 wherein the tubular member is of a metal alloy.

30. The prosthesis of claim 29 wherein the alloy is Titanium.

31. The prosthesis of claim 29 wherein the alloy is Nitinol.

32. The prosthesis of claim 27, wherein the tubular member has an open mesh structure.

33. The prosthesis of claim 32, wherein the open mesh structure is adapted to permit tissue ingrowth.

34. The prosthesis of any of claims 27 wherein the tubular member comprises at least one integral flange.

35. The prosthesis of claim 34 wherein the integral flange comprises a mesh structure.

36. The prosthesis of claim 1 wherein the prosthesis is coated with a material selected to improve blood compatibility.

37. The prosthesis of claim 36 wherein the material to improve blood compatibility is one of a hydrogel and a fluoropolymer plasma.

38. The prosthesis of claim 28, wherein the leading end of the tube is in the form of a trocar, adapted to be pushed through the papillary muscle.

39. The prosthesis of claim 1, further comprising restraining means for securing the continuity member to an area of heart muscle and for permitting adjustment of the continuity member externally of the heart.

40. The prosthesis of claim 39, wherein the restraining means comprises a compressible crimping clip.

41. The prosthesis of claim 39 or 40, wherein the restraining means comprises a flange.

42. The prosthesis of claim 1 comprising at least first and second valve elements having free ends defining at least one fold.

43. The prosthesis of claim 42 wherein the valve elements comprise cut-out regions at free edges of at least one valve element.

44. The prosthesis of claim 43 wherein cut-out regions are provided in alternate folds in both valve elements.

45. The prosthesis of claim 1 wherein a free edge of the valve element is constructed using a 3D spline curve.

46. The prosthesis of claim 45 wherein the free edge curve with at least one fold is defined as:

f(t)=at⁶+bt⁵+ct⁴+dt³+et²+ft+g

where t is the x-, y-, or z-coordinate of a point along the free edge curve, f (t) is a function of this point, and a-g are coefficients.

2. A heart valve prosthesis comprising:

a support adapted to be coupled to the mitral annulus;

first and second valve elements coupled to the support

and moveable between an open position and a closed position, the elements defining curved coapting surfaces, each surface having at least two points of inflection; and

at least one continuity member having one end coupled to said support and the other end adapted for coupling to papillary muscle.

47. A method of inserting a heart valve prosthesis, the prosthesis comprising a support, a valve element coupled to the support and moveable between an open position and a closed position, and at least one continuity member having one end coupled to said support, said method comprising the steps of:

(i) securing the support to the mitral orifice of the heart;

(ii) passing the other end of the continuity member through the papillary muscle of the heart; and

(iii) adjusting the continuity member externally of the heart.

49. The method of claim 47, further comprising the steps of:

closing the patient'"'"'s chest; and

then further adjusting the continuity member.

50. The method of claim 47, further comprising the step of:

individually adjusting strands of the continuity member.

48. A method of inserting a heart valve prosthesis, the prosthesis comprising a support, a valve element coupled to the support and moveable between an open position and a closed position, and at least one continuity member having one end coupled to said support, said method comprising the steps of:

(a) excising a diseased valve from a patient, wherein papillary muscle tips and a rim of leaflet tissue at the mitral orifice are left intact;

(b) measuring the size of the patient'"'"'s valve cavity;

(c) determining appropriate sites within the patient'"'"'s papillary muscle to receive the continuity member;

(d) perforating the patient'"'"'s heart at the determined papillary muscle site;

(e) securing the support to the mitral orifice of the heart;

(f) passing the continuity member through the papillary muscle of the heart;

(g) adjusting the continuity member externally of the heart; and

(h) securing the continuity member to said papillary muscle.