Granted Patent B2

US 9,226,835 · App. 14/191,969 · Granted Jan 5, 2016

Abstract

Claims (35)

1. A percutaneous fusion method to correct disc compression in a patient, comprising:

making a posterolateral incision to access a desired spinal motion segment;

determining a target level of a disc space between adjacent vertebral bodies for implantation of a spinal implant;

locating a path to the disc space at the target level;

inserting a guide wire to maintain the path to the target level, the guide wire extending to the disc space between the adjacent vertebral bodies to the target level at the location for placing the spinal implant;

selecting an appropriately sized spinal implant to correct disc compression, the spinal implant having a substantially square or substantially rectangular cross section midway from a proximal or distal end with height to width ratio in a range of 1:1 to 2:1 sized for full insertion between two adjacent vertebrae, the implant having a body, the body having a distal end, a proximal end, the body having a length extending from the distal end to the proximal end and opposing sides or walls extending between the distal and proximal ends to support the adjacent vertebrae on opposing upper and lower surfaces, the length being greater than the width or the height of the body of the implant, and a longitudinal axis and defining at least one implant aperture therethrough, the body being aligned with the longitudinal axis, the at least one implant aperture being in communication with a proximal and distal opening, the openings in alignment with one another to allow the passage of a guide wire therethrough the body, the distal end being an atraumatic tapered distal end, the tapered distal end having a profile having a cross section along the length of the body of a frustoconical shape or an elliptic parabolic shape; an elongate cannulated insertion tool defining an interior insertion tool pathway, wherein a distal end of the elongate cannulated insertion tool has a shape or configuration that correspondingly matingly engages at least a portion of at least one corresponding external surface of the implant so rotational alignment of the insertion tool and the implant is maintained after insertion to tense the soft tissue without damaging the nerve to reestablish the normal disc height of the two adjacent vertebral bodies; and an elongate lockshaft positioned therein the insertion tool pathway and defining a longitudinal interior lockshaft pathway, wherein a distal end of the elongate lockshaft selectively engages and attaches to a portion of the implant, and wherein rotation of the elongate lockshaft can draw and tighten the matingly engaged surfaces of the insertion tool to the implant wherein when the distal end of the elongate lockshaft is engaged with a proximal end portion of the implant, the interior lockshaft pathway and the implant aperture are aligned to receive the guide wire, the implant having a height and a length sized to accommodate being evenly spaced on each side of the spinous process;

placing the spinal implant over the guide wire by passing the guide wire through the aperture;

sliding the spinal implant along the guide wire to position the spinal implant into the disc space at the target level;

removing the guide wire; and

fixating at least a portion of the desired spinal motion segment, thereby enabling fusion of the adjacent vertebral bodies.

2. The method of claim 1 , wherein the step of fixating at least a portion of the desired spinal motion segment comprises fixating at least one facet screw into a desired facet joint.

3. The method of claim 1 , wherein the posterolateral incision is made through a Kambin's Triangle of the desired spinal motion segment.

4. The method of claim 1 , wherein the body comprises two opposing longitudinal gripping facets each defining a ridged surface.

5. The method of claim 4 , wherein the body further defines an implant cavity in communication with the implant aperture and open to at least one of the gripping facets.

6. The method of claim 5 , further comprising the step of loading a graft into the implant cavity prior to sliding the spinal implant over the guide wire, wherein the graft is composed of a material selected from the group consisting of autologous bone, allograft bone, bone substitute, and osteoinductive agent.

7. The method of claim 6 , further comprising the step of turning the insertion tool to position the two opposing longitudinal gripping facets in contact with portions of the adjacent vertebral bodies.

8. The method of claim 1 , further comprises the step of turning the insertion tool to position the two opposing implant upper and lower surfaces in contact with portions of the adjacent vertebral bodies.

9. The method of claim 1 , wherein the spinal implant comprises bio-compatible material.

10. The method of claim 9 , wherein the bio-compatible material is selected from the group consisting of PolyEtherEtherKetone, ceramic, allograft bone, and PolyEtherEtherKetone with BaSO4.

11. The method of claim 1 , wherein locating the path to the disc space at the target level comprising using a nerve monitoring probe with a transfer sleeve to measure the proximity of an existing nerve root.

12. The method of claim 11 , further comprising the step of removing the nerve monitoring probe, leaving the transfer sleeve in place, wherein the step of inserting the guide wire to maintain a path to the disc space is achieved through the transfer sleeve.

13. The method of claim 12 , further comprising the step of removing the transfer sleeve, and placing a dilator over the guide wire to distract the adjacent vertebral bodies.

14. The method of claim 13 , further comprising the step of positioning an access portal over the dilator and into the disc space, and removing the dilator and guide wire.

15. The method of claim 14 , further comprising the step of performing a discectomy and decorticating selected vertebral endplates via the access portal.

16. The method of claim 15 , further comprising introducing a bone graft into the disc space via the access portal, wherein the bone graft is composed of a material selected from the group consisting of autologous bone, allograft bone, bone substitute, and osteoinductive agent.

17. The method of claim 16 , further comprising the steps of reintroducing a guide wire via the access portal and removing the access portal.

18. The method of claim 1 , wherein the step of fixating at least a portion of the desired spinal motion segment comprises:

locating a path to the desired facet joint;

inserting a guide wire to a depth equal to or deeper than a desired facet screw depth;

performing facet arthrodesis, using the guide wire as a guide;

inserting a graft into the facet joint;

introducing the at least one facet screw to the desired facet screw depth, compressing the facet joint onto the graft.

19. The method of claim 18 , further comprising the step of decorticating one or more surfaces of the facet joint.

20. The method of claim 1 , further comprising the step of performing a foramen nerve root decompression.

21. The method of claim 1 , further comprising the step of performing a central nerve root decompression.

Assignments (8)