BONE ANCHORS FOR ORTHOPEDIC APPLICATIONS

• US 20100082072A1
• Filed: 03/27/2009
• Published: 04/01/2010
• Est. Priority Date: 03/28/2008
• Status: Abandoned Application

• Current Assignee: Warsaw Orthopedic Incorporated (Medtronic Plc)
• Original Assignee: Warsaw Orthopedic Incorporated (Medtronic Plc)
• Inventors: O'Brien, Michael F., Berven, Sigurd, Boachie-Adjei, Oheneba, Shelokov, Alexis P., Winterbottom, John M., Boden, Scott, Sybert, Daryl R., Betz, Randal R.
• Application Number:
  US12/413,013
• Publication Number:
  US 20100082072A1
• Time in Patent Office: Days
• US Class Current: 606/326
• CPC Class Codes: A61B 17/68 Internal fixation devices , including fasteners and spinal fixators, even if a part thereof projects from the skin bone staples A61B17/0642
• CPC Class Codes: A61B 17/686 Plugs, i.e. elements forming interface between bone hole and implant or fastener, e.g. screw
• CPC Class Codes: A61B 2017/00004 (bio)absorbable, (bio)resorbable, resorptive for implantable prostheses A61F2210/0004
• CPC Class Codes: A61B 2017/00946 malleable
• CPC Class Codes: A61C 8/0012 characterised by the material or composition, e.g. ceramics, surface layer, metal alloy use of specific materials A61K6/00

Abstract

Bone anchors and related methods for their use are described. The inventive anchor is suitable for placement in bone and for use in orthopedic surgery and dentistry. The bone anchor can be made from a bone/polymer or bone substitute/polymer composite, and can provide a firm and secure base for attaching a fastening device. The bone anchor can be used in various orthopedic and dental procedures including spinal surgery, where normal, cancellous, cortical, diseased or osteoporotic bone is present. The bone anchor can be resorbed and/or replaced with native bone tissue over a period of time. In certain embodiments, the bone anchor is made malleable or flowable and formed in situ or in vivo.

Claims

1. A bone anchor comprising:

an elongate element having a near end, a distal end, an inner surface and an outer surface, wherein the element is adapted for placement within a void in a bone and is adapted to receive and secure a fastening device; and

wherein the element is formed from a composite comprising;

a plurality of particles selected from the group consisting of;

particles of bone-derived material, bone particles, particles of bone substitute material, inorganic particles, and any combination thereof; and

a polymer with which the plurality of particles have been combined.

2. The bone anchor as claimed in claim 1, wherein the composite can undergo a phase transition from a formable, moldable, pliable or flowable state to a substantially solid state, and

the phase transition occurs within biocompatible temperature ranges or biocompatible chemical conditions.

3. The bone anchor as claimed in claim 2, wherein the bone anchor was transitioned to a substantially solid state after placement in the void in a bone.

4. The bone anchor as claimed in claim 1, wherein the element is tubular in shape, having at least one inner diameter and at least one outer diameter, and a wall extending the length of the element between the at least one inner diameter and the at least one outer diameter.

5. The bone anchor as claimed in claim 4, further comprising:

at least one slot incorporated into at least a portion of the anchor'"'"'s wall, the at least one slot running in a direction along the length of the anchor; and

wherein

insertion of the fastening device into the central core of the anchor expands the portion of the wall incorporating the slots radially outward.

6. The bone anchor as claimed in claim 4, further comprising a shape feature selected from the following group:

an inner diameter substantially constant along the length of the anchor, an outer diameter substantially constant along the length of the anchor, an inner diameter gradually decreasing from the near end to the distal end, an outer diameter gradually decreasing from the near end to the distal end, and an outer diameter gradually increasing from the near end to the distal end.

7. The bone anchor as claimed in claim 4, wherein the maximum outer diameter is in a range between about 5 millimeters and about 10 millimeters, and the maximum inner diameter is in a range between about 2 millimeters and about 8 millimeters.

8. The bone anchor as claimed in claim 4, wherein the maximum outer diameter is in a range between about 10 millimeters and about 20 millimeters, and the maximum inner diameter is in a range between about 8 millimeters and about 17 millimeters.

9. The bone anchor as claimed in claim 4, wherein the length of the anchor is in a range between about 3 millimeters and about 5 millimeters.

10. The bone anchor as claimed in claim 4, wherein the length of the anchor is in a range between about 5 millimeters and about 10 millimeters.

11. The bone anchor as claimed in claim 4, wherein the length of the anchor is in a range between about 10 millimeters and about 20 millimeters.

12. The bone anchor as claimed in claim 4, wherein the anchor incorporates a feature selected from the group consisting of:

a smooth outer surface, a threaded outer surface, a ridged outer surface, a ribbed outer surface, an outer surface having protrusions, an outer surface having indentations, a grooved outer surface, and any combination thereof.

13. The bone anchor as claimed in claim 4, wherein the anchor incorporates a feature selected from the group consisting of:

a smooth inner surface, a threaded inner surface, a ridged inner surface, a ribbed inner surface, an inner surface having protrusions, an inner surface having indentations, a grooved inner surface, and any combinations thereof.

14. The bone anchor as claimed in claim 4, wherein the anchor incorporates a plurality of inner diameters along the length of the anchor, each inner diameter corresponding to a portion of the length of the anchor, and at least one portion located at the distal end having a threaded inner surface;

wherein

a fastening device engages the threaded inner surface at the distal end and compresses the bone anchor along its length upon tightening the fastening device, the compressing action causing the walls along a portion of the bone anchor to expand radially outward.

15. The bone anchor as claimed in claim 4, wherein the anchor incorporates a feature at its near end selected from the group consisting of:

a flanged head, a pan head, a slotted head, a socket head, a hexagonal head, and a square head.

16. The bone anchor as claimed in claim 4 adapted to receive a bayonet fastening device, wherein the bayonet fastening device can be rotated to a locking position upon insertion.

17. The bone anchor as claimed in claim 4 adapted to receive a latching rivet-like fastening device, wherein the rivet-like fastening device can be tapped, pressed or driven into a locked position.

18. The bone anchor as claimed in claim 4, wherein the fastening device is a device selected from the group consisting of:

pedicle screw, screw, bolt, pin, post, rod, and spring pin.

19. The bone anchor as claimed in claim 4, wherein the fastening device is a device selected from the group consisting of:

cancellous, cortical, and malleolar screws.

20. The bone anchor as claimed in claim 1, wherein the polymer comprises a material selected from the group consisting of:

polylactides, polyglycolides, starch poly(caprolactone), poly(caprolactones), poly(L-lactide), poly(lactide-co-glycolide), poly(D,L-lactide-co-glycolide), poly(L-lactide-co-glycolide), poly(L-lactide-co-D,L-lactide), polyurethanes, polycarbonates, polyarylates, poly(propylene fumarates), polyphosphazenes, polymethylmethacrylates, polyacrylates, polyesters, polyethers, stereoisomers of the above, co-polymers of the above, lactide-glycolide copolymers, polyglyconate, poly(anhydrides), poly(hydroxy acids), poly(alkylene oxides), poly(propylene glycol-co fumaric acid), polyamides, polyureas, polyamines, polyamino acids, polyacetals, poly(orthoesters), poly(pyrolic acid), poly(glaxanone), poly(phosphazenes), poly(organophosphazene), poly(dioxanones), polyhydroxybutyrate, polyhydroxyvalyrate, polyhydroxybutyrate/valerate copolymers, poly(vinyl pyrrolidone), polycyanoacrylates, glucose-based polyurethanes, lysine-based polyurethanes, polysaccharides, chitin, starches, celluloses, PEGylated-poly(lactide-co-glycolide, PEGylated-poly(lactide), PEGylated-poly(glycolide), collagen, polysaccharides, agarose, glycosaminoglycans, alginate, chitosan, tyrosine-based polymers, polypyrrole, polyanilines, polythiophene, polystyrene, non-biodegradable polyesters, non-biodegradable polyureas, poly(vinyl alcohol), non-biodegradable polyamides, poly(tetrafluoroethylene), expanded polytetrafluoroethylene (ePTFE), poly(ethylene vinyl acetate), polypropylene, non-biodegradable polyacrylate, non-biodegradable polycyanoacrylates, non-biodegradable polyurethanes, copolymers of poly(ethyl methacrylate) with tetrahydrofurfuryl methacrylate, polymethacrylate, non-biodegradable poly(methyl methacrylate), polyethylene (including ultra high molecular weight polyethylene (UHMWPE)), polypyrrole, polyanilines, polythiophene, poly(ethylene oxide), poly(ethylene oxide co-butylene terephthalate), poly ether-ether ketones (PEEK), polyetherketoneketones (PEKK), and combinations thereof.

21. The bone anchor as claimed in claim 1, wherein the particles comprise from about 50% to about 70% by weight of the composite from which the bone anchor is formed.

22. The bone anchor as claimed in claim 1, wherein the particles comprise about 63% by weight of the composite from which the bone anchor is formed.

23. The bone anchor as claimed in claim 1, wherein the composite forming the bone anchor is osteoinductive or osteoconductive.

24. The bone anchor as claimed in claim 1, wherein the bone anchor is placed in a void in a vertebra or in the sacrum.

25. The bone anchor as claimed in claim 1, wherein the bone anchor is placed in a void in the pedicle of a vertebra or the body of a vertebra.

26. The bone anchor as claimed in claim 1, wherein the bone anchor is adapted to be resorbed over a period from about 1 month to about 6 months.

27. The bone anchor as claimed in claim 1, wherein the bone anchor is adapted to be resorbed over a period from about 6 months to about 1 year.

28. The bone anchor as claimed in claim 1, wherein the bone anchor is adapted to be resorbed over a period from about 1 year to about 2 years.

29. The bone anchor as claimed in claim 1, wherein the bone anchor is adapted to be resorbed over a period from about 2 years to about 3 years.

30. The bone anchor as claimed in claim 1, wherein the bone anchor is adapted to be resorbed over a period from about 3 years to about 5 years.

31. The bone anchor as claimed in claim 1, wherein the composite can undergo a reversible phase transition from a formable, moldable, pliable or flowable state to a substantially solid state;

and

the phase transition occurs within a temperature range selected from the group consisting of;

between about 40°

C. and about 45°

C., between about 45°

C. and about 50°

C., between about 50°

C. and about 55°

C., between about 55°

C. and about 60°

C., between about 60°

C. and about 70°

C., between about 70°

C. and about 80°

C., between about 80°

C. and about 90°

C., between about 90°

C. and about 100°

C., between about 100°

C. and about 110°

C., between about 110°

C. and about 120°

C., and between about 120°

C. and about 130°

C.

36. A method of placing the bone anchor of claim 1, the method comprising:

implanting the bone anchor into a void in the pedicle or the body of a vertebra or the sacrum of a subject; and

securing a fastening device into the bone anchor.

37. The method of claim 36, wherein the implanting is repeated for multiple vertebrae of a subject.

38. The method of claim 36, wherein the implanting comprises molding or adapting the shape of the anchor for conformity with a void in a vertebra or sacrum.

39. The method of claim 36, wherein the implanting comprises sequentially placing pieces of the anchor into a void in a vertebra or sacrum.

32. A bone anchor for spinal surgery comprising:

a substantially cylindrical, conical or tulip shaped elongate element adapted for placement in a void in the pedicle of a vertebra of a subject, the elongate element further adapted to receive and secure a fastening device;

wherein the elongate element is formed from a composite comprising;

bone particles; and

a polymer; and

wherein

at least a portion of the bone anchor expands radially outward upon insertion of a fastening device into the elongate element.

33. (canceled)

34. A method of forming a bone anchor in vivo, the method comprising:

placing a fastening-device form into a void in a bone;

injecting a flowable composite into the vacancy between the fastening-device form and the surrounding bone, the composite comprising a plurality of particles of a bone substitute material, bone-derived material, bone particles, inorganic material, or any combination thereof combined with a polymer;

transforming the composite to a substantially solid state; and

removing the fastening-device form.

35. The method of claim 34, wherein the injecting comprises injecting the anchor into a void of a vertebra or sacrum.

40. A method of placing a bone anchor, the method comprising:

rendering a composite into a flowable state, the composite comprising (1) a plurality of particles of an inorganic material, a bone-substitute material, a bone-derived material, bone particles, or any combination thereof; and

(2) a polymer;

injecting the composite into a void within a bone; and

forming a hole in the composite bone anchor to receive a fastening device

41. (canceled)

42. (canceled)

43. (canceled)

44. (canceled)

45. (canceled)

46. (canceled)

47. A method of placing a bone anchor in a vertebra, the method comprising:

evaluating a characteristic of at least a portion of the vertebra;

selecting a type of bone anchor based upon the evaluated characteristics;

preparing a site in the vertebra to receive the bone anchor; and

providing the bone anchor to the prepaired site.

48. The method of claim 47, wherein the evaluated characteristic comprises bone density, bone disease, bone structure, or bone defect.

49. The method of claim 47, wherein the portion of the vertebra comprises a pedicle.

50. The method of claim 47, wherein the portion of the vertebra comprises the vertebral body.

51. The method of claim 47, wherein the selected type of bone anchor comprises an anchor structure preformed from bone/polymer or bone substitute/polymer composite.

52. The method of claim 47, wherein the selected bype of bone anchor comprises a moldable anchor formed from bone/polymer or bone substitute/polymer composite.

53. The method of claim 47, wherein the step of preparing the site comprises forming a void in the site.

54. The method of claim 47, wherein the step of preparing the site comprises reaming, drilling, grinding, cutting, or threading bone at the site.

55. The method of claim 47, wherein the step of preparing the site comprises revising prior surgical intervention at the site.

56. The method of claim 47, wherein the step of providing the bone anchor comprises inserting or affixing the bone anchor at the site.

57. The method of claim 47, wherein the step of providing the bone anchor comprises pressing or tamping the bone anchor into the site.

58. The method of claim 47, further comprising reaming, drilling, cutting, grinding, or threading the bone anchor placed at the site.

59. A bone anchor formed from a composite comprising:

a plurality of particles selected from the group consisting of;

particles of bone-derived material, bone particles, particles of bone substitute material, inorganic particles, and any combination thereof; and

a polymer with which the plurality of particles have been combined.

60. (canceled)

61. (canceled)

62. (canceled)

63. (canceled)

64. (canceled)

65. (canceled)

66. (canceled)

67. (canceled)

68. (canceled)

69. (canceled)

70. (canceled)

71. (canceled)

72. (canceled)

73. (canceled)

74. (canceled)

75. (canceled)

76. (canceled)

77. (canceled)