Pressure sensitive trial instrument and method

1. A trial implant instrument comprising:

a handle including an elongate shaft;

a pressure sensitive trial coupled to the elongate shaft, the pressure sensitive trial including a superior end plate exterior surface configured to engage a first end plate of a first vertebral body, a separate inferior end plate exterior surface configured to engage a second end plate of a second vertebral body, and one or more lateral side surfaces between the superior end plate exterior surface and the inferior end plate exterior surface, the pressure sensitive trial having a non-adjustable thickness between the superior end plate exterior surface and the inferior end plate exterior surface; and

a pressure sensitive film disposed on at least one of the superior end plate exterior surface and the inferior end plate exterior surface, and further disposed on at least a portion of the one or more lateral side surfaces,

wherein the pressure sensitive film is operable to indicate whether a predetermined target pressure is achieved following contact of the first end plate of the first vertebral body to the superior end plate exterior surface, and further following contact of the second end plate of the second vertebral body to the inferior end plate exterior surface.

2. The trial implant instrument of claim 1 , wherein the pressure sensitive film is disposed on both the superior end plate exterior surface and the inferior end plate exterior surface.

3. The trial implant instrument of claim 1 , wherein the pressure sensitive film is adhered to at least one of the superior end plate exterior surface and the inferior end plate exterior surface with an adhesive material.

4. The trial implant instrument of claim 1 , wherein the one or more lateral side surfaces includes at least two lateral side surfaces, and wherein the pressure sensitive film is held in position on at least one of the superior end plate exterior surface and the inferior end plate exterior surface with an exterior film sleeve wrapping around the at least two lateral side surfaces of the pressure sensitive trial.

5. The trial implant instrument of claim 4 , wherein the pressure sensitive trial is reusable and the pressure sensitive film is disposable.

6. The trial implant instrument of claim 1 , wherein the pressure sensitive trial with the pressure sensitive film disposed on at least one of the superior end plate exterior surface and the inferior end plate exterior surface is single use.

7. The trial implant instrument of claim 1 , wherein the pressure sensitive trial includes a threaded bore, and the elongate shaft includes a threaded distal end configured to removably couple to the threaded bore.

8. The trial implant instrument of claim 7 , wherein the handle further includes a coupling knob connected to the elongate shaft and configured to receive rotational input and transmit the rotational input to rotate the elongate shaft.

9. A implant sizing system comprising:

an instrument handle including an elongate shaft extending from a distal end; and

a plurality of pressure sensitive trial implants couplable to a distal end of the elongate shaft, each pressure sensitive trial implant of the plurality of pressure sensitive trial implants corresponding to a predetermined size for an implant, each pressure sensitive trial implant of the plurality of pressure sensitive trial implants having a non-adjustable thickness between a superior end plate exterior surface and a separate inferior end plate exterior surface, each pressure sensitive trial implant of the plurality of pressure sensitive trial implants including one or more lateral side surfaces between the superior end plate exterior surface and the inferior end plate exterior surface,

wherein at least one of the superior end plate exterior surface and the inferior end plate exterior surface of each pressure sensitive trial implant is covered in a pressure sensitive film, wherein the pressure sensitive film is further disposed on at least a portion of the one or more lateral side surfaces,

wherein the pressure sensitive film is configured to change color in localized areas in response to a pressure or force applied to the pressure sensitive trial implant, wherein the pressure sensitive film is operable to indicate whether a predetermined target pressure is achieved following contact of a first end plate of a first vertebral body to the superior end plate exterior surface, and

further following contact of a second end plate of a second vertebral body to the inferior end plate exterior surface, wherein the predetermined target pressure corresponds to the predetermined size for the implant.

10. The implant sizing system of claim 9 , further comprising a vertebral body distraction instrument configured to engage a superior vertebral body and an inferior vertebral body to enable distraction of a disc space between the superior vertebral body and the inferior vertebral body to allow insertion of a pressure sensitive trial implant of the plurality of pressure sensitive trial implants.

11. The implant sizing system of claim 9 , wherein the pressure sensitive film is disposed on both the superior end plate exterior surface and the inferior end plate exterior surface of each pressure sensitive trial implant of the plurality of pressure sensitive trial implants.

12. The implant sizing system of claim 9 , wherein the pressure sensitive film is adhered to the at least one superior end plate exterior surface and inferior end plate exterior surface of each pressure sensitive trial implant with an adhesive material.

13. The implant sizing system of claim 9 , wherein the one or more lateral side surfaces includes at least two lateral side surfaces, and wherein the pressure sensitive film is held in position on the at least one superior end plate exterior surface and inferior end plate exterior surface with an exterior film sleeve wrapping around the at least two lateral side surfaces of each pressure sensitive trial implant.

14. The implant sizing system of claim 13 , wherein each pressure sensitive trial implant is reusable and the pressure sensitive film is disposable.

15. The implant sizing system of claim 9 , wherein each pressure sensitive trial implant with the pressure sensitive film disposed on the at least one superior end plate exterior surface and inferior end plate exterior surface is single use.

16. The implant sizing system of claim 9 , wherein each pressure sensitive trial implant includes a threaded bore, and the distal end of the elongate shaft is threaded to removably couple to the threaded bore.

17. The implant sizing system of claim 16 , wherein the handle further includes a coupling knob connected to the elongate shaft and configured to receive rotational input and transmit the rotational input to rotate the elongate shaft.

18. A method for implant sizing, the method comprising:

selecting an implant size including obtaining a pressure sensitive trial implant corresponding to the selected implant size;

preparing a trialing instrument including coupling the pressure sensitive trial implant to a distal end of an elongate shaft portion of the trialing instrument, the pressure sensitive trial implant having a non-adjustable thickness between a superior end plate exterior surface and a separate inferior end plate exterior surface, the pressure sensitive trial implant including one or more lateral side surfaces between the superior end plate exterior surface and the inferior end plate exterior surface, wherein at least one of the superior end plate exterior surface and the inferior end plate exterior surface of the pressure sensitive trial implant is covered in a pressure sensitive film, and wherein the pressure sensitive film is further disposed on at least a portion of the one or more lateral side surfaces;

trialing the pressure sensitive trial implant in an intervertebral disc space between a first vertebral body and a second vertebral body, the intervertebral disc space prepared to receive an intervertebral implant; and

determining whether the selected implant size is correct based at least in part on comparing a state of the pressure sensitive film disposed on at least one of the superior end plate exterior surface and the inferior end plate exterior surface of the pressure sensitive trial implant to a known standard, wherein the pressure sensitive film is operable to indicate whether a predetermined target pressure is achieved following contact of a first end plate of the first vertebral body to the superior end plate exterior surface, and further following contact of a second end plate of the second vertebral body to the inferior end plate exterior surface, wherein the predetermined target pressure corresponds to the selected implant size.

19. The method for implant sizing of claim 18 , further comprising distracting the intervertebral disc space prior to trialing the pressure sensitive trial implant.

20. The method for implant sizing of claim 18 , further comprising disposing of the pressure sensitive trial implant after use.

21. The method for implant sizing of claim 18 , wherein comparing the state of the pressure sensitive film to the known standard indicates that the selected implant size is incorrect.

22. The method for implant sizing of claim 21 , further comprising:

selecting a second implant size based on the indication that the selected implant size is incorrect;

preparing the trialing instrument including coupling a second pressure sensitive trial implant to the distal end of the elongate shaft portion, wherein the second pressure sensitive trial implant corresponds to the second implant size, the second pressure sensitive trial implant having a second, different non-adjustable thickness between a second superior end plate exterior surface and a second separate inferior end plate exterior surface, the second pressure sensitive trial implant including one or more second lateral side surfaces between the second superior end plate exterior surface and the second inferior end plate exterior surface, wherein at least one of the second superior end plate exterior surface and the second inferior end plate exterior surface of the second pressure sensitive trial implant is covered in a second pressure sensitive film, and wherein the second pressure sensitive film is further disposed on at least a portion of the one or more second lateral side surfaces;

trialing the second pressure sensitive trial implant; and

determining whether the second implant size is correct based at least in part on comparing a state of the second pressure sensitive film disposed on at least one of the second superior end plate exterior surface and the second inferior end plate exterior surface of the second pressure sensitive trial implant to the known standard.

23. The method for implant sizing of claim 18 , wherein comparing the state of the second pressure sensitive film includes examining color changes across a surface of the at least one of the second superior end plate exterior surface and the second inferior end plate exterior surface with the second pressure sensitive film.

24. The method for implant sizing of claim 18 , wherein comparing the state of the pressure sensitive film includes comparing color, color density, or color intensity to the known standard.