Biocompatible wires and methods of using same to fill bone void

• US 20050015148A1
• Filed: 07/18/2003
• Published: 01/20/2005
• Est. Priority Date: 07/18/2003
• Status: Abandoned Application

• Current Assignee: Boston Scientific Scimed (Boston Scientific Corporation)
• Original Assignee: Boston Scientific Scimed (Boston Scientific Corporation)
• Inventors: Jansen, Lex P., Patel, Mukund
• Application Number:
  US10/623,381
• Publication Number:
  US 20050015148A1
• Time in Patent Office: Days
• US Class Current: 623/17.110
• CPC Class Codes: A61B 17/1671 for the spine
• CPC Class Codes: A61B 17/1697 specially adapted for wire insertion
• 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 17/7094 Solid vertebral fillers; devices for inserting such fillers

Abstract

Devices, kits, and methods are provided for reducing a bone fracture, e.g., a vertebral compression fracture, is provided. The device comprises a plurality of resilient wires composed of a biocompatible material, such as a biocompatible polymer (e.g., polymethylmethacrylate (PMMA)). The wires can be introduced into the cavity of the bone structure to form a web-like arrangement therein. The web-like arrangement can be stabilized by applying uncured bone cement onto the arrangement to connect the wires at their contacts point. The bone cavity can then be filled with a bone growth enhancing medium.

Claims

1. A device for treating a bone structure having a cavity, comprising:

a single elongate laterally resilient wire composed of a biocompatible material, the wire configured to be introduced into the cavity of the bone structure.

2. The device of claim 1, wherein the bone structure is a vertebral body.

3. The device of claim 1, wherein the biocompatible material is polymethylmethacrylate (PMMA).

4. The device of claim 1, further comprising a plurality of individual elongate laterally resilient wires, each of which is composed of a biocompatible material and is configured to be introduced into the cavity of the bone structure.

5. The device of claim 4, wherein the bone structure comprises a compression fracture, and wherein the web-like arrangement is configured to at least partially reduce the compression fracture.

6. The device of claim 5, wherein the bone structure is a vertebral cavity and the compression fracture is a vertebral compression fracture.

7. A kit for treating a bone structure having a cavity, comprising:

a plurality of biocompatible laterally resilient wires; and

a cannula configured for introducing the wires within the cavity of the bone structure in a web-like arrangement.

8. The kit of claim 7, wherein the bone structure is a vertebral body.

9. The kit of claim 7, wherein the wires are composed of a polymer.

10. The kit of claim 9, wherein the polymer is polymethylmethacrylate (PMMA).

11. The kit of claim 7, further comprising a device configured for applying uncured bone cement onto the web-like arrangement of wires.

12. The kit of claim 11, wherein the device is configured to be introduced within the cannula.

13. The kit of claim 11, further comprising the uncured bone cement.

14. The kit of claim 13, wherein both the wires and uncured bone cement are composed of polymethylmethacrylate (PMMA).

15. The kit of claim 7, further comprising a plunger assembly configured to be introduced within the cannula to apply a bone growth inducing material between the resilient wires in the web-like arrangement.

16. The kit of claim 15, further comprising the bone growth inducing material.

17. The kit of claim 7, wherein the bone structure comprises a compression fracture, and wherein the web-like arrangement comprises a structure that at least partially reduces the compression fracture.

18. The kit of claim 17, wherein the bone structure is a vertebral cavity and the compression fracture is a vertebral compression fracture.

19. The kit of claim 17, further comprising a separate compression fracture reducing device configured to facilitate reduction of the compression fracture.

20. A method of treating a bone structure, comprising:

introducing a plurality of biocompatible wires within the bone structure to create a web-like arrangement within the cavity of the bone structure.

21. The method of claim 20, wherein the bone structure is a vertebral body.

22. The method of claim 20, wherein the wires are composed of a polymer.

23. The method of claim 20, wherein the wires are composed of polymethylmethacrylate (PMMA).

24. The method of claim 20, wherein the web-like arrangement comprises points of contact between the wires, the method further comprising applying uncured bone cement onto the web-like arrangement of wires to interconnect the wires at the points of contact.

25. The method of claim 24, wherein the uncured bone cement is sprayed onto the web-like arrangement.

26. The method of claim 25, wherein both the wires and uncured bone cement are composed of polymethylmethacrylate (PMMA).

27. The method of claim 20, further comprising applying a bone growth inducing material between the wires.

28. The method of claim 20, wherein the bone structure comprises a compression fracture, the method further comprising at least partially reducing the compression fracture by forming the web-like arrangement of wires within the cavity of the bone structure.

29. The method of claim 28, wherein the bone structure is a vertebral cavity and the compression fracture is a vertebral compression fracture.

30. The method of claim 28, further comprising inserting a separate compression fracture reducing device into the cavity of the bone structure, reducing the compression fracture with the fracture reducing device, and removing the fracture reducing device to relax the compression fracture, wherein the web-like arrangement of wires is formed within the cavity of the bone structure subsequent to the relaxation of the compression fracture.