CERVICAL DISTRACTION METHOD

• US 20130123922A1
• Filed: 12/20/2012
• Published: 05/16/2013
• Est. Priority Date: 12/29/2006
• Status: Active Grant

• Current Assignee: Providence Medical Technology, Inc.
• Original Assignee: Providence Medical Technology, Inc.
• Inventors: McCormack, Bruce M.
• Granted Patent: US 8,834,530 B2
• Time in Patent Office: Days
• US Class Current: 623/17.12
• CPC Class Codes: A61B 17/562 Implants for placement in joint gaps without restricting joint motion, e.g. to reduce arthritic pain
• CPC Class Codes: A61B 17/7064 Devices acting on, attached to, or simulating the effect of, vertebral facets; Tools therefor
• CPC Class Codes: A61B 2017/681 Alignment, compression, or distraction mechanisms
• CPC Class Codes: A61F 2/4405 for apophyseal or facet joints, i.e. between adjacent spinous or transverse processes devices implanted between spinous or transverse processes A61B17/7062
• CPC Class Codes: A61F 2/441 made of inflatable pockets or chambers filled with fluid, e.g. with hydrogel
• CPC Class Codes: A61F 2/4611 of spinal prostheses

Abstract

A device and method for a minimally invasive surgical implantation to reduce radicular symptoms by inserting an expandable cervical distraction implant in the facet joint and distracting the adjacent cervical vertebrae to increase the foraminal dimension. The implant, when positioned in the cervical facet joint, expands to via delivery of an inflation medium to increase the space between the vertebrae, thereby increasing the foraminal area or dimension, and reducing pressure on the nerves and blood vessels of the cervical spine.

Claims

1. A method of implanting an implant in a facet joint comprising an inferior articulating surface of an upper vertebra and a superior articulating surface of a lower vertebra, the method comprising:

a) minimally invasively accessing the facet joint with a guide tool;

b) minimally invasively routing the implant into the facet joint by routing along the guide tool the implant in a non-expanded configuration and operably coupled to a distal end of a delivery tool, the implant comprising an upper wall, a lower wall, a proximal end and a distal end, wherein the upper wall and lower wall comprise an inelastic material and the implant is configured to transition to an expanded configuration from the non-expanded configuration; and

c) acting at the implant with the delivery tool to cause the implant to transition from the non-expanded configuration to the expanded configuration, the transition of the implant causing the upper wall to act against the inferior articulating surface and the lower wall to act against the superior articulating surface.

2. The method of claim 1, further comprising selecting the implant from a number of predetermined sizes.

3. The method of claim 1, wherein the guide tool comprises a guidewire.

4. The method of claim 1, wherein the delivery tool comprises a catheter.

5. The method of claim 1, wherein step a) further comprises puncturing an access hole in a facet capsule of the facet joint.

6. The method of claim 5, wherein an introducer needle punctures the access hole in the facet capsule.

7. The method of claim 1, wherein the implant further comprises a transverse cross section when in the expanded configuration that is generally round, elliptical or square.

8. The method of claim 1, wherein the upper wall and lower wall are generally parallel to each other when viewed via a longitudinal cross section when the implant is in the expanded configuration.

9. The method of claim 1, wherein the upper wall and lower wall form a generally wedge shaped relationship to each other when viewed via a longitudinal cross section when the implant is in the expanded configuration.

10. The method of claim 9, wherein the distal end forms a narrow end of the wedge shaped relationship, and the proximal end forms a wide end of the wedge shaped relationship.

11. The method of claim 1, wherein acting at the implant with the delivery tool to cause the implant to transition from the non-expanded configuration to the expanded configuration comprises acting at the proximal end of the implant with the delivery tool.

12. The method of claim 11, wherein acting at the proximal end of the implant with the delivery tool to cause the implant to transition further comprises employing the delivery tool to deliver something between the upper wall and the lower wall.

13. The method of claim 12, wherein the something comprises a fluid, the implant further comprising a reservoir between the upper wall and the lower wall.

14. The method of claim 11, wherein acting at the proximal end of the implant with the delivery tool to cause the implant to transition further comprises employing the delivery tool to make a delivery between the upper wall and the lower wall.

15. The method of claim 14, wherein making the delivery between the upper wall and lower wall comprises delivering a fluid between the upper wall and lower wall, the implant comprising a reservoir between the upper wall and the lower wall.

16. The method of as in any of claim 13 or 15, in which the fluid comprises a hydrogel.

17. The method of claim 16, wherein the implant comprises a maximum inflation capacity.

18. The method of as in any of claim 12 or 14, further comprising selecting the implant from a number of predetermined sizes.

19. The method of as in any of claim 13 or 15, in which the proximal end of the implant comprises a port through which the fluid is delivered.

20. The method of claim 1, wherein an exterior surface of at least one of the upper wall or lower wall is configured to inhibit motion of the at least one of the upper wall or lower wall relative to the respective inferior articulating surface or the superior articulating surface.

21. The method of claim 20, wherein the exterior surface, in being configured to inhibit motion, comprises at least one of a surface roughness or texture.

22. The method of claim 1, further comprising performing step c) with a patient under conscious sedation and obtaining intra-operative symptom feedback from the patient.

23. The method of claim 1, wherein the implant is sized to accommodate a geometry of anatomy of a patient.

24. The method of claim 1, wherein the facet joint is adjacent a nerve root canal between the upper vertebra and the lower vertebra, the nerve root canal comprising a stenosed intervertebral foraminal height,

25. The method of claim 24, wherein prior to step c) a distance between the superior articulating surface and the inferior articulating surface is narrowed at least in part because of the stenosed intervertebral foraminal height.

26. The method of claim 25, wherein causing the upper wall to act against the inferior articulating surface and the lower wall to act against the superior articulating surface increases the distance between the superior articulating surface and the inferior articulating surface, thereby increasing the stenosed intervertebral foraminal height.