Osteointegration apparatus
View Patent ↗A method for effecting reduction, stabilization and enhancement of fusion of the human cranio-cervical junction, which may be performed in order to relieve mechanical stresses imparted to the spinal cord and brainstem as a result of an abnormal clivo-axial angle, includes steps of achieving the correct craniocervical relationship, of effecting a fusion of a first portion of a bone forming material based structural member to a human cranium, and effecting fusion of a second portion of the bone forming material based structural member to a least one portion of a human cervical spine. Fusion of the bone forming material based structural member to the human cranium may be promoted through the use an osteointegration apparatus that includes a porous ossomeric mesh and a frame member.
1. A method for stabilizing the occipitocervical junction comprising steps of:
positioning an osteointegration apparatus that normalizes the clivoaxial angle over a subocciput and a cervical vertebra of a patient, wherein the osteointegration apparatus comprises:
a porous mesh for facilitating osteointegration; and
a frame member that is connected to and reinforces the porous mesh, wherein the frame member comprises apertures for receiving fasteners anchoring the osteointegration apparatus to a cranium and the cervical vertebra; and stabilizing the occipitocervical junction.
2. The method of claim 1 , wherein the frame member is attached to a perimeter of the porous mesh.
3. The method of claim 1 , wherein the frame member is positioned at an internal region of the porous mesh.
4. The method of claim 1 , wherein the osteointegration apparatus comprises more than one frame member.
5. The method of claim 1 , wherein at least one of the frame member or the porous mesh is coated with an osteogenic bone graft material.
6. The method of claim 1 , wherein at least one of the frame member or the porous mesh is coated with an osteogenic bone graft material.
7. The method of claim 1 , wherein the porous mesh is rigid.
8. The method of claim 7 , wherein frame member is constructed from a material comprising titanium or carbon fiber.
9. The method of claim 1 , wherein the frame member is a continuous unitary structure that is attached to and positioned along an entire perimeter of the porous mesh.
10. The method of claim 1 , wherein the porous mesh comprises a plurality of apertures having a diameter of about 200 μm to about 1000 μm.
11. The method of claim 1 , wherein the porous mesh has a tensile strength of about 100 psi to about 5000 psi.
12. The method of claim 1 , wherein the porous mesh has a tensile strength of about 10,000 psi to about 25,000 psi.
13. The method of claim 1 , further comprising the steps of fastening the osteointegration apparatus to the cervical vertebra and a cranium.
14. The method of 1 , wherein the osteointegration apparatus has a structure that achieves or maintains a normalized clivoaxial angle such that the geometry of the osteointegration apparatus requires normalization of the clivoaxial angle when implanted in a patient.
15. The method of claim 14 , wherein the osteointegration apparatus has a structure and geometry that achieves or maintains a clivoaxial angle to about 145° to about 165°.
16. The method of claim 1 , further comprising the step of positioning the osteointegration apparatus over and fastening the osteointegration apparatus to one or more medical devices anchored to the cervical vertebra or the cranium.
17. The method of claim 1 , further comprising the step of positioning the osteointegration apparatus over and fastening the osteointegration apparatus to a portion of a plate attached to the cranium and a screw fastened to the cervical vertebra.
18. A system for stabilizing an occipitocervical junction comprising:
a cranial plate attachable to a cranium;
a vertebral clamp attachable to a vertebra; and
an osteointegration apparatus for facilitating fusion, wherein the osteointegration apparatus is positioned over and fastened to the cranial plate and the vertebral clamp, and wherein the osteointegration apparatus comprises:
a porous mesh for facilitating osteointegration;
a frame member that is connected to and reinforces the porous mesh, wherein the frame member comprises a plurality of apertures;
a first fastener that is positioned within a first aperture of the frame member and is attached to the cranial plate, wherein the first fastener anchors the osteointegration apparatus and the cranial plate to the cranium; and
a second fastener that is positioned within a second aperture of the frame member and is attached to the vertebra, wherein the second fastener anchors the osteointegration apparatus and the vertebral clamp to the vertebra,
wherein the osteointegration apparatus has a structure that achieves or maintains a normalized clivoaxial angle such that the geometry of the osteointegration apparatus requires normalization of the clivoaxial angle when implanted in a patient.
19. The system of claim 18 , wherein the frame member is attached to a perimeter of the porous mesh.
20. The system of claim 18 , wherein the frame member is positioned at an internal region of the porous mesh.
21. The system of claim 18 , wherein the osteointegration apparatus has a structure and geometry that achieves or maintains a clivoaxial angle of about 145° to about 165°.
22. The system of claim 21 , wherein the frame member is constructed from a material comprising titanium or carbon fiber and wherein the porous mesh has a trabecular configuration.
23. The system of claim 18 , wherein at least one of the frame member or the porous mesh is coated with an osteogenic bone graft material.
24. The system of claim 18 , wherein the porous mesh is rigid.
25. The system of claim 18 , wherein the frame member is a continuous unitary structure that is attached to and positioned along an entire perimeter of the porous mesh.
26. The system of claim 18 , wherein the porous mesh comprises a plurality of apertures having a diameter of about 200 μm to about 1000 μm.
27. The system of claim 18 , wherein the porous mesh has a tensile strength of about 100 psi to about 5000 psi.
28. The system of claim 18 , wherein the porous mesh has a tensile strength of about 10,000 psi to about 25,000 psi.
29. The system of claim 18 , wherein the osteointegration apparatus comprises more than one frame member.