MINIMALLY INVASIVE SYSTEMS, DEVICES, AND SURGICAL METHODS FOR PERFORMING ARTHRODESIS IN THE SPINE

• US 20110264098A1
• Filed: 02/24/2011
• Published: 10/27/2011
• Est. Priority Date: 02/26/2010
• Status: Abandoned Application

• Current Assignee: Charles S. Cobbs
• Original Assignee: Charles S. Cobbs
• Inventors: COBBS, CHARLES S.
• Application Number:
  US13/034,150
• Publication Number:
  US 20110264098A1
• Time in Patent Office: Days
• US Class Current: 606/93
• CPC Class Codes: A61B 17/1617 with mobile or detachable parts
• CPC Class Codes: A61B 17/1633 Sleeves, i.e. non-rotating parts surrounding the bit shaft, e.g. the sleeve forming a single unit with the bit shaft A61B17/1644 takes precedence
• CPC Class Codes: A61B 17/1642 for producing a curved bore
• CPC Class Codes: A61B 17/1671 for the spine
• CPC Class Codes: A61B 17/7097 Stabilisers comprising fluid filler in an implant, e.g. balloon; devices for inserting or filling such implants disc prostheses made of inflatable chambers or pockets filled with fluid A61F2/441; replacing the nucleus pulposus A61F2002/444
• CPC Class Codes: A61B 2017/0256 for the spine

Abstract

Systems, devices, and methods achieve percutaneous fusion of the spine. The systems, devices, and methods percutaneously manipulate instrumentation to achieve posterior percutaneous transpedicular access to an interior of a first targeted vertebral body through a pedicle of the vertebra. The systems, devices, and methods percutaneously manipulate instrumentation through the achieved percutaneous transpedicular access, to achieve percutaneous cephalad trans-disc access to an interior of a second targeted vertebral body at a next adjacent superior level to the first targeted vertebral body. The systems, devices, and methods percutaneously manipulate instrumentation through the achieved percutaneous transpedicular access and percutaneous cephalad trans-disc access, to achieve percutaneous disc cavity creation comprising forming an enlarged cavity in the intervertebral disc space between the first and second targeted vertebral bodies. The systems, devices, and methods percutaneously manipulate instrumentation through the achieved percutaneous transpedicular access and percutaneous cephalad trans-disc access, to place a support structure in the enlarged cavity that achieves disc cavity support, into which a volume of a filling material is conveyed that, over time, hardens to promote fusion of the targeted first and second vertebral bodies.

Claims

1. A system for percutaneous fusion of the spine comprising

a first instrumentation component that is sized and configured to achieve posterior percutaneous transpedicular access to an interior of a first targeted vertebral body through a pedicle of the vertebra,

a second instrumentation component that is sized and configured to achieve percutaneous cephalad trans-disc access to an interior of a second targeted vertebral body at a next adjacent superior level to the first targeted vertebral body,

a third instrumentation component that is sized and configured to achieve percutaneous disc cavity creation comprising a device for forming an enlarged cavity in the intervertebral disc space between the first and second targeted vertebral bodies, and

a fourth instrumentation component that is sized and configured to achieve percutaneous disc cavity support comprising a support matrix placed in the enlarged cavity formed by the third instrumentation component and that is sized and configured to separate and hold the first and second vertebral bodies apart, to thereby distract nerve roots and relieve pressure on the nerves, and a device for conveying in a percutaneous manner a volume of a filling material into the support matrix that, over time, hardens to promote fusion of the targeted first and second vertebral bodies.

2. A system according to claim 1

wherein the filling material comprises a flowable polymer material or a bone graft material that, upon setting, helps the vertebrae heal together or fuse.

3. A system according to claim 1

wherein the first instrumentation component comprises a guide tube including a proximal slotted side wall and distal slotted side wall oriented, in use, to face in a caphalad direction.

4. A system according to claim 1

wherein the second instrumentation component comprises a stylus or suture instrument having a curvature that is sized and configured to be passed through a guide tube in a curvilinear path to direct a distal end of the stylus or suture instrument through the superior end plate of the first targeted vertebral body into and through the intervertebral disc between the first and second targeted vertebral bodies and into and through the inferior (caudal) end plate of the second targeted vertebral body.

5. A system according to claim 4

wherein the curvature of the stylus or suture instrument is pre-formed.

6. A system according to claim 4

wherein the curvature of the stylus or suture instrument is set at an instance of use.

7. A system according to claim 4

wherein the stylus or suture instrument includes a center lumen sized and configured to receive a curved guide wire, and

wherein the second instrumentation includes a cannulated drill that is sized and configured for passage over the guide wire to clear an access channel through cortical bone of the end plate of the first targeted vertebral body, into and through adjoining disc tissue, and into and through the end plate into cortical bone of the second targeted vertebral body.

8. A system according to claim 4

wherein the stylus or suture instrument includes a center lumen sized and configured to receive a curved guide wire to guide passage of the third instrumentation component.

9. A system according to claim 1

wherein the first instrumentation component comprises a guide tube including a proximal slotted side wall and distal slotted side wall oriented, in use, to face in a caphalad direction, and

wherein the second instrumentation component comprises a curved stylus or suture instrument that is sized and configured to be passed through the guide tube in a curvilinear path through the slotted proximal and distal side walls to direct the distal end of the stylus or suture instrument through the superior end plate of the first targeted vertebral body into and through the intervertebral disc between the first and second targeted vertebral bodies and into and through the inferior (caudal) end plate of the second targeted vertebral body.

10. A system according to claim 9

wherein the curvature of the stylus or suture instrument is pre-formed.

11. A system according to claim 9

wherein the curvature of the stylus or suture instrument is set at an instance of use.

12. A system according to claim 9

wherein the stylus or suture instrument includes a center lumen sized and configured to accommodate placement of a curved guide wire, and

wherein the second instrumentation includes a cannulated drill that is sized and configured for passage over the guide wire to clear an access channel through cortical bone of the end plate of the first targeted vertebral body, into and through adjoining disc tissue, and into and through the end plate into cortical bone of the second targeted vertebral body.

13. A system according to claim 9

wherein the stylus or suture instrument includes a center lumen sized and configured to receive a curved guide wire to guide passage of the third instrumentation component.

14. A system according to claim 1

wherein the third instrumentation component comprises a flexible tissue drilling unit including, at a distal end, a tissue cutter that is sized and configured to assume a collapsed, lay-flat low profile condition for passage through a guide tube and to be expanded toward a radially enlarged deployed condition for cutting tissue and forming an enlarged cavity in the intervertebral disc space between the first and second targeted vertebral bodies.

15. A system according to claim 14

wherein the first instrumentation component comprises a guide tube including a proximal slotted side wall and distal slotted side wall oriented, in use, to face in a caphalad direction, and

wherein the second instrumentation component comprises a curved stylus or suture instrument that is sized and configured to be passed through the guide tube in a curvilinear path through the slotted proximal and distal side walls to direct the distal end of the stylus or suture instrument through the superior end plate of the first targeted vertebral body into and through the intervertebral disc between the first and second targeted vertebral bodies and into and through the inferior (caudal) end plate of the second targeted vertebral body, the stylus or suture instrument including a center lumen sized and configured to accommodate placement of a curved guide wire to guide passage of the flexible tissue drilling unit during use.

16. A system according to claim 1

wherein the fourth instrumentation component includes a self-expanding support matrix or structure that is sized and configured so that, when expanded within the enlarged cavity, an interior chamber is formed that can accommodate the filling material.

17. A system according to claim 16

wherein the fourth instrumentation includes a flexible bone filling material delivery cannula that is sized and configured conveys the filling material into the interior chamber of the self-expanding support matrix or structure after its expansion within the enlarged cavity.

18. A system according to claim 16

wherein the first instrumentation component comprises a guide tube including a proximal slotted side wall and distal slotted side wall oriented, in use, to face in a caphalad direction, and

wherein the second instrumentation component comprises a curved stylus or suture instrument that is sized and configured to be passed through the guide tube in a curvilinear path through the slotted proximal and distal side walls to direct the distal end of the stylus or suture instrument through the superior end plate of the first targeted vertebral body into and through the intervertebral disc between the first and second targeted vertebral bodies and into and through the inferior (caudal) end plate of the second targeted vertebral body, the stylus or suture instrument including a center lumen sized and configured to accommodate placement of a curved guide wire to guide delivery of the self-expanding support matrix or structure.

19. A system according to claim 1

wherein the fourth instrumentation component includes an in-situ molding component that is sized and configured to cast in place within the enlarged cavity formed by the third instrumentation component a polymeric support matrix or structure that is sized and configured so that, after being cast, presents a structure having the physical geometry and mechanical strength that restores the functionality of the intervertebral disc.

20. A system according to claim 19

further including a flexible tissue drilling unit to form an enlarged central lumen through the cast-in-place polymer support matrix that is sized and configured to receive the filling material.

21. A system according to claim 19

wherein the first instrumentation component comprises a guide tube including a proximal slotted side wall and distal slotted side wall oriented, in use, to face in a caphalad direction, and

wherein the second instrumentation component comprises a curved stylus or suture instrument that is sized and configured to be passed through the guide tube in a curvilinear path through the slotted proximal and distal side walls to direct the distal end of the stylus or suture instrument through the superior end plate of the first targeted vertebral body into and through the intervertebral disc between the first and second targeted vertebral bodies and into and through the inferior (caudal) end plate of the second targeted vertebral body, the stylus or suture instrument including a center lumen sized and configured to accommodate placement of a curved guide wire to guide delivery of the fourth instrumentation component.

22. A system according to claim 1

wherein the first instrumentation component comprises a guide tube including a proximal slotted side wall and distal slotted side wall oriented, in use, to face in a caphalad direction, and

wherein the second instrumentation component comprises a curved stylus or suture instrument that is sized and configured to be passed through the guide tube in a curvilinear path through the slotted proximal and distal side walls to direct the distal end of the stylus or suture instrument through the superior end plate of the first targeted vertebral body into and through the intervertebral disc between the first and second targeted vertebral bodies and into and through the inferior (caudal) end plate of the second targeted vertebral body, the stylus or suture instrument including a center lumen sized and configured to accommodate placement of a curved guide wire to guide subsequent delivery of the third and fourth instrumentation components.

23. A method for percutaneous fusion of the spine comprising

(i) percutaneously manipulating instrumentation to achieve posterior percutaneous transpedicular access to an interior of a first targeted vertebral body through a pedicle of the vertebra,

(ii) percutaneously manipulating instrumentation through the percutaneous transpedicular access achieved during (i), to achieve percutaneous cephalad trans-disc access to an interior of a second targeted vertebral body at a next adjacent superior level to the first targeted vertebral body,

(iii) percutaneously manipulating instrumentation through the percutaneous transpedicular access achieved during (i) and the percutaneous cephalad trans-disc access achieved during (ii), to achieve percutaneous disc cavity creation comprising forming an enlarged cavity in the intervertebral disc space between the first and second targeted vertebral bodies, and

(iv) percutaneously manipulating instrumentation through the percutaneous transpedicular access achieved during (i) and the percutaneous cephalad trans-disc access achieved during (ii), to achieve percutaneous disc cavity support comprising placing a support matrix in the enlarged cavity formed during (iii) that is sized and configured to separate and hold the first and second vertebral bodies apart, to thereby distract nerve roots and relieve pressure on the nerves, and conveying a volume of a filling material into the support matrix that, over time, hardens to promote fusion of the targeted first and second vertebral bodies.

24. A method according to claim 23

wherein (i) includes placing a guide tube including a proximal slotted side wall and distal slotted side wall oriented, in when placed, to face in a caphalad direction, and

wherein (ii) includes placing a curved stylus or suture instrument through the guide tube in a curvilinear path through the slotted proximal and distal side walls to direct the distal end of the stylus or suture instrument through the superior end plate of the first targeted vertebral body into and through the intervertebral disc between the first and second targeted vertebral bodies and into and through the inferior (caudal) end plate of the second targeted vertebral body, and placing a curved guide wire through the guide tube to guide subsequent percutaneous manipulation of instrumentation during (iii) and (iv).

25. A method according to claim 24

wherein (iii) includes manipulating a flexible tissue drilling unit including, at a distal end, a tissue cutter that is sized and configured to assume a collapsed, lay-flat low profile condition for passage over the guide wire and to be expanded toward a radially enlarged deployed condition for cutting tissue and forming an enlarged cavity in the intervertebral disc space between the first and second targeted vertebral bodies.

26. A method according to claim 24

wherein (iv) includes manipulating a self-expanding support matrix or structure that is sized and configured so that, when expanded within the enlarged cavity formed during (iii), an interior chamber is formed that can accommodate the filling material.

27. A method according to claim 26

wherein (iv) includes manipulating a flexible bone filling material delivery cannula to convey the filling material into the interior chamber of the self-expanding support matrix or structure after its expansion within the enlarged cavity.

28. A method according to claim 24

wherein (iv) includes manipulating an in-situ molding component to cast in place within the enlarged cavity formed during (iii) a polymeric support matrix or structure that, after being cast, presents a structure having the physical geometry and mechanical strength that restores the functionality of the intervertebral disc, and forming an enlarged central lumen through the cast-in-place polymer support matrix that is sized and configured to receive the filling material.

29. A system for percutaneous lumbar fusion comprising

a first instrumentation component that is sized and configured to achieve posterior percutaneous transpedicular access to an interior of a first targeted vertebral body through a pedicle of the vertebra,

a second instrumentation component that is sized and configured to achieve percutaneous cephalad trans-disc access to an interior of a second targeted vertebral body at a next adjacent superior level to the first targeted vertebral body,

a third instrumentation component that is sized and configured to achieve percutaneous disc cavity creation comprising a device for forming an enlarged cavity in the intervertebral disc space between the first and second targeted vertebral bodies,

a fourth instrumentation component that is sized and configured to achieve percutaneous disc cavity support comprising a support matrix placed in the enlarged cavity formed by the third instrumentation component and that is sized and configured to separate and hold the first and second vertebral bodies apart, to thereby distract nerve roots and relieve pressure on the nerves, and a device for conveying in a percutaneous manner a volume of a filling material into the support matrix that, over time, hardens to promote fusion of the targeted first and second vertebral bodies, and

instructions for manipulating the first, second, third, and fourth instrumentation components comprising

(i) percutaneously manipulating the first instrumentation component to achieve posterior percutaneous transpedicular access to an interior of a first targeted vertebral body through a pedicle of the vertebra,

(ii) percutaneously manipulating the second instrumentation component through the percutaneous transpedicular access achieved during (i), to achieve percutaneous cephalad trans-disc access to an interior of a second targeted vertebral body at a next adjacent superior level to the first targeted vertebral body,

(iii) percutaneously manipulating the third instrumentation component through the percutaneous transpedicular access achieved during (i) and the percutaneous cephalad trans-disc access achieved during (ii), to achieve percutaneous disc cavity creation comprising forming an enlarged cavity in the intervertebral disc space between the first and second targeted vertebral bodies, and

(iv) percutaneously manipulating the fourth instrumentation component through the percutaneous transpedicular access achieved during (i) and the percutaneous cephalad trans-disc access achieved during (ii), to achieve percutaneous disc cavity support comprising placing a support matrix in the enlarged cavity formed during (iii) that is sized and configured to separate and hold the first and second vertebral bodies apart, to thereby distract nerve roots and relieve pressure on the nerves, and conveying a volume of a filling material into the support matrix that, over time, hardens to promote fusion of the targeted first and second vertebral bodies.

30. A system according to claim 29

wherein the instructions for use (i) includes placing a guide tube including a proximal slotted side wall and distal slotted side wall oriented, in when placed, to face in a caphalad direction, and

wherein the instructions for use (ii) includes placing a curved stylus or suture instrument through the guide tube in a curvilinear path through the slotted proximal and distal side walls to direct the distal end of the stylus or suture instrument through the superior end plate of the first targeted vertebral body into and through the intervertebral disc between the first and second targeted vertebral bodies and into and through the inferior (caudal) end plate of the second targeted vertebral body, and placing a curved guide wire through the guide tube to guide subsequent percutaneous manipulation of the third and instrumentation components during (iii) and (iv).