In situ formation of intervertebral disc implants

• US 20060089719A1
• Filed: 10/21/2004
• Published: 04/27/2006
• Est. Priority Date: 10/21/2004
• Status: Abandoned Application

• Current Assignee: SDGI Holdings Incorporated (Medtronic Plc)
• Original Assignee: SDGI Holdings Incorporated (Medtronic Plc)
• Inventors: Trieu, Hai H.
• Application Number:
  US10/970,762
• Publication Number:
  US 20060089719A1
• Time in Patent Office: Days
• US Class Current: 623/17.130
• CPC Class Codes: A61F 2/442 Intervertebral or spinal discs, e.g. resilient non-disc-shaped intervertebral inflatable pockets A61F2/441; non-disc-shaped intervertebral fusion implants A61F2/4455
• CPC Class Codes: A61F 2/4611 of spinal prostheses
• CPC Class Codes: A61F 2002/30062 (bio)absorbable, biodegradable, bioerodable, (bio)resorbable, resorptive
• CPC Class Codes: A61F 2002/30092 using shape memory or superelastic materials, e.g. nitinol
• CPC Class Codes: A61F 2002/302 toroidal, e.g. rings
• CPC Class Codes: A61F 2002/30291 spirally-coiled, i.e. having a 2D spiral cross-section
• CPC Class Codes: A61F 2002/30331 made by longitudinally pushing a protrusion into a complementarily-shaped recess, e.g. held by friction fit
• CPC Class Codes: A61F 2002/305 Snap connection
• CPC Class Codes: A61F 2002/30579 with mechanically expandable devices, e.g. fixation devices
• CPC Class Codes: A61F 2002/30594 slotted, e.g. radial or meridian slot ending in a polar aperture, non-polar slots, horizontal or arcuate slots
• CPC Class Codes: A61F 2002/3082 Grooves
• CPC Class Codes: A61F 2002/30841 Sharp anchoring protrusions for impaction into the bone, e.g. sharp pins, spikes
• CPC Class Codes: A61F 2002/30892 parallel
• CPC Class Codes: A61F 2002/444 for replacing the nucleus pulposus
• CPC Class Codes: A61F 2002/4495 having a fabric structure, e.g. made from wires or fibres
• CPC Class Codes: A61F 2002/4627 with linear motion along or rotating motion about the instrument axis or the implantation direction, e.g. telescopic, along a guiding rod, screwing inside the instrument
• CPC Class Codes: A61F 2002/4628 with linear motion along or rotating motion about an axis transverse to the instrument axis or to the implantation direction, e.g. clamping
• CPC Class Codes: A61F 2210/0004 bioabsorbable
• CPC Class Codes: A61F 2210/0014 using shape memory or superelastic materials, e.g. nitinol
• CPC Class Codes: A61F 2220/0025 Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
• CPC Class Codes: A61F 2220/0033 : made by longitudinally pushing a protrusion into a complementary-shaped recess, e.g. held by friction fit
• CPC Class Codes: A61F 2230/0065 : toroidal, e.g. ring-shaped, doughnut-shaped
• CPC Class Codes: A61F 2230/0091 : helically-coiled or spirally-coiled, i.e. having a 2-D spiral cross-section
• CPC Class Codes: A61P 19/08 : for bone diseases, e.g. rachitism, Paget's disease

Abstract

Nucleus pulposus implants that are resistant to migration in and/or expulsion from an intervertebral disc space are provided. In one form of the invention, an implant includes a load bearing elastic body surrounded in the disc space by an anchoring, preferably resorbable, biocompatible material which may be in the form of an outer shell. In certain forms of the invention, the elastic body is surrounded by a supporting member, such as a band or jacket, and the supporting member is surrounded by the outer shell. Kits for forming such implants are also provided. In another form of the invention, an implant is provided that has locking features and optional shape memory characteristics. In yet another aspect of the invention, nucleus pulposus implants are provided that have shape memory characteristics and are configured to allow short-term manual, or other deformation without permanent deformation, cracks, tears, breakage or other damage. Methods of forming and implanting the implants are also described, as are delivery devices and components thereof for delivering the implants.

Claims

1. A method of implanting an intervertebral disc nucleus pulposus implant so as to cause minimal trauma during implantation, yet maximum retention and performance after implantation, said method comprising:

(a) providing a load bearing elastic body having shape memory and sized for placement into an intervertebral disc space;

wherein said elastic body is configurable to a first, folded configuration effective to serve as a prosthetic disc nucleus;

wherein said elastic body is configurable into a second, straightened configuration for insertion through an opening in an intervertebral disc annulus fibrosis;

wherein said shape memory is effective to return said elastic body to its first, folded configuration after the elastic body is straightened to its second, straightened configuration and inserted in a disc space;

(b) implanting said load bearing elastic body in an intervertebral disc space while the elastic body is in its second, straightened configuration;

(c) allowing said load bearing elastic body to assume its first, folded configuration, and thereby to partially fill the disc space; and

(d) providing around said load bearing elastic body an amount of biocompatible material sufficient to fill or substantially fill the remaining disc space.

2. The method of claim 1 wherein said biocompatible material is provided by injecting said biocompatible material around said elastic body.

3. The method of claim 1 wherein said biocompatible material is an adhesive material.

4. The method of claim 1 wherein said biocompatible material is a tissue sealant material.

5. The method of claim 1 wherein said biocompatible material is a resorbable material.

6. The method of claim 1 wherein said biocompatible material is a non-resorbable material.

7. The method of claim 1 wherein said biocompatible material is a curable material.

8. The method of claim 7 wherein said biocompatible material is cured in situ.

10. The method of claim 1 wherein said biocompatible material is a natural material.

12. The method of claim 1 wherein said load bearing elastic body comprises a member selected from the group consisting of elastomeric materials, hydrogels, and hydrophilic polymers, or composites thereof.

13. The method of claim 12 wherein said load bearing elastic body comprises an elastomeric material selected from the group consisting of silicones, polyurethanes, copolymers of silicone and polyurethane, polyolefins, and vulcanized rubber.

14. The method of claim 13 wherein said polyurethane comprises one or more materials selected from the group consisting of thermoplastic polyurethanes, aliphatic polyurethanes, segmented polyurethanes, hydrophilic polyurethanes, polyether-urethanes, polycarbonate-urethanes and silicone polyether-urethanes.

15. The method of claim 12 wherein said load bearing elastic body comprises a hydrogel comprising one or more materials selected from the group consisting of natural hydrogels, and hydrogels formed from polyvinyl alcohol, acrylamides, polyurethanes, polyethylene glycol, poly(N-vinyl-2-pyrrolidone), acrylates, copolymers of acrylates with N-vinyl pyrrolidone, N-vinyl lactams, acrylamide, polyurethanes and polyacrylonitrile.

16. The method of claim 12 wherein said load bearing elastic body comprises a hydrophilic polymer comprising one or more materials selected from the group consisting of glucomannan gel, hyaluronic acid, and polysaccharides.

17. The method of claim 1 wherein said biocompatible material comprises a material selected from the group consisting of fibrin, albumin, collagen, elastin, silk, polyethylene oxide, cyanoacrylate, polylactic acid, polyglycolic acid, polypropylene fumarate, tyrosine-based polycarbonate, and demineralized bone matrix.

18. The method of claim 1 wherein said biocompatible material further includes a pharmacological agent.

19. The method of claim 18 wherein said pharmacological agent comprises a growth factor or an agent effective for treating degenerative disc disease, spinal arthritis, spinal infection, spinal tumor or osteoporosis.

20. The method of claim 19 wherein said growth factor comprises one or more members selected from the group consisting of bone morphogenetic protein, transforming growth factor-β

(TGF-β

), insulin-like growth factor, platelet-derived growth factor, and fibroblast growth factor.

21. The method of claim 18 wherein said pharmacological agent comprises one or more members selected from the group consisting of antibiotics, analgesics, and anti-inflammatory drugs, including steroids.

22. The method of claim 1 wherein said biocompatible material is introduced into said intervertebral disc space prior to introducing said elastic body into said intervertebral disc space.

23. The method of claim 1 wherein said biocompatible material is introduced into said intervertebral disc space after introducing said elastic body into said intervertebral disc space.

24. The method of claim 1 wherein said biocompatible material is introduced into said intervertebral disc space at the same time as said elastic body is introduced into said intervertebral disc space.

25. A method according to claim 1 wherein said load bearing elastic body has a substantially solid center when the implant is in its first, folded configuration.

26. A method according to claim 1 wherein said elastic body has an aperture in the center when the implant is in its first, folded configuration.

27. A method according to claim 26 wherein said elastic body is annular-shaped when the implant is in its first, folded configuration.

28. A method according to claim 26 wherein said elastic body is spiral-shaped when the implant is in its first, folded configuration.

29. A method according to claim 1 wherein said elastic body has a first end and a second end when the implant is in its second, straightened configuration, wherein said first end and said second end configured for mating engagement with each other when the implant is in its first, folded configuration.

30. A method according to claim 1 wherein said elastic body has a surface that includes at least one surface feature to enhance fixation of the implant to the outer shell.

31. A method according to claim 30 wherein said at least one surface feature includes a chemical modification.

32. A method according to claim 30 wherein said at least one surface feature includes a physical modification.

34. The method of claim 1 wherein said elastic body comprises a load bearing elastic body having shape memory and sized for placement into an intervertebral disc space, said body having a first end, a second end, and a central portion;

wherein said shape memory biases said body to a first configuration wherein said first end and said second end are positioned adjacent to said central portion to form at least one inner fold when the implant is in its first configuration;

said elastic body configurable into a second, straightened configuration for insertion through an opening in an intervertebral disc annulus fibrosis;

wherein said shape memory returns said body to said first configuration after said insertion;

wherein said elastic body has a surface that includes wrinkles, indents or projections that relieve stress and prevent cracking or tearing of the implant when the implant is straightened for implantation.

35. The method of claim 34 wherein said inner fold defines an aperture.

36. The method of claim 34 wherein said inner fold has a surface with projections;

and wherein said projections extend into said aperture.

37. The method of claim 34 wherein said elastic body further comprises a reinforcing material at said inner fold surface.

39. The method of claim 1 wherein said elastic body further includes at least one groove extending along an external side surface to relieve the compressive force on the external side of the implant when the implant is in its second, straightened configuration.

40. A method according to claim 1 wherein said elastic body is restrained by a flexible peripheral supporting band disposed circumferentially about said elastic body for reducing deformation of said body.

41. A method according to claim 40 wherein said elastic body comprises upper and lower surfaces, and wherein at least a portion of said upper and lower surfaces is free of said supporting band.

42. A method according to claim 41 wherein at least about 50% of each of said upper and lower surfaces is free of said peripheral supporting band.

43. A method according to claim 40 wherein said band is made of a solid material.

44. A method according to claim 40 wherein said band is made of a porous material.

45. A method according to claim 40 wherein said band is made of a made of a woven material.

46. A method according to claim 40 wherein said band is made of a braided material.

47. A method according to claim 40 wherein said band comprises a biocompatible material selected from one or more members of the group consisting of silicone, polyurethane, polyolefins, vulcanized rubber, shape memory materials, stainless steel, titanium, titanium alloy, cobalt chrome alloy, polyethylene, polyester, polyvinyl alcohol, polyacrylonitrile, polyamide, polytetrafluoroethylene, poly-paraphenylene terephthalamide, and cellulose, and combinations thereof.

48. A method according to claim 40 wherein said band is elastic.

49. A method according to claim 40 wherein said flexible peripheral supporting band is disposed in a groove circumferentially about said elastic body.

50. A method according to claim 40 wherein said implant further includes at least one strap extending along said upper surface and at least one strap extending across said bottom surface.

51. A method according to claim 50 wherein at least one of said at least one straps is attached to said supporting band.

52. A method according to claim 50 wherein at least one of said at least one straps is positioned in a groove on the surface of said elastic body.

53. A method according to claim 50 wherein said at least one straps comprises at least two straps.

54. A method according to claim 53 wherein said at least two straps are positioned generally parallel to each other.

55. A method according to claim 53 wherein said at least two straps are positioned generally perpendicular to each other.

9. (canceled)

11. (canceled)

33. (canceled)

38. (canceled)

56. A composite intervertebral disc nucleus pulposus implant secured in an intervertebral disc space, comprising:

(a) a load bearing elastic body surgically implanted in an intervertebral disc space;

wherein said elastic body has shape memory;

wherein said elastic body is in a first, folded configuration effective to serve as a prosthetic disc nucleus;

wherein said elastic body is configurable into a second, straightened configuration for insertion through an opening in an intervertebral disc annulus fibrosis;

wherein said shape memory is effective to return said elastic body to its first, folded configuration after the elastic body is straightened to its second, straightened configuration and inserted in a disc space; and

(b) a biocompatible material surgically implanted to fill or substantially fill the portion of the disc space that is not occupied by the load bearing elastic body.

57-107. -107. (canceled)

108. A kit for repairing an intervertebral disc nucleus, comprising:

a load bearing elastic body having shape memory and sized for placement into an intervertebral disc space;

wherein said elastic body is configurable to a first, folded configuration effective to serve as a prosthetic disc nucleus;

wherein said elastic body is configurable into a second, straightened configuration for insertion through an opening in an intervertebral disc annulus fibrosis;

wherein said shape memory is effective to return said elastic body to its first, folded configuration after the elastic body is straightened to its second, straightened configuration and inserted in a disc space; and

a container of biocompatible material sufficient to form an outer shell around said load bearing elastic body;

wherein said outer shell completely or substantially covers said elastic body.

109-151. -151. (canceled)