Use of an expandable stent as an implant conduit in the lateral approach to the spine

Patent metadata

Field	Value
Publication number	US-9314231-B2
Application number	US-201313887838-A
Country	US
Kind code	B2
Filing date	May 6, 2013
Priority date	May 6, 2013
Publication date	Apr 19, 2016
Grant date	Apr 19, 2016

Abstract

The use of a memory metal mesh stent as a retractor in a lateral approach to the spine. The expanded stent is used as a conduit through which an implant can pass. This advance is predicated upon the appreciation that modern stent implants have diameters that are large enough to accommodate passage of an intervertebral spinal implant therethrough.

First claim

We claim:

1. A spinal surgery device, comprising:
an electrified probe having an outer surface b) a mesh stent having an inner surface and an outer surface, an unexpanded condition and an expanded condition, wherein the inner surface of the stent in its unexpanded condition contacts the outer surface of the electrified probe,
c) an elongated sheath having a distal end, an inner surface, an outer surface and a throughhole extending from the inner surface to the outer surface of the sheath, wherein the inner surface of the sheath contacts the outer surface of the stent in its unexpanded condition.

2. The device of claim 1 wherein the electrified probe is electrically connected to an electrical impulse generator.

3. The device of claim 1 wherein the electrified probe is electrically connected to a neuromonitoring system.

4. The device of claim 1 wherein the stent has a fabric thereon for preventing tissue ingress.

5. The device of claim 4 wherein the coating is electrically conductive.

6. The device of claim 1 wherein the elongated sheath is sized to be rotatable about the mesh.

7. The device of claim 1 wherein the stent is electrically conductive.

8. The device of claim 1 wherein the sheath is electrically-resistive or has an electro-resistive coating thereon.

9. The device of claim 1 wherein the throughhole does not open onto the distal end of the sheath.

10. The device of claim 9 wherein the probe does not extend past the distal end of the sheath.

11. A method of performing surgery, comprising the steps of:
a) advancing an electrified elongated probe having an outer surface through a target tissue while performing neuromonitoring with the probe,
b) providing an assembly comprising:
i) an expandable mesh stent in an unexpanded condition, the stent having an outer surface and an inner surface, and
ii) an elongated sheath having a distal end, an inner surface and an outer surface and a throughhole extending from the inner surface to the outer surface of the elongated sheath, wherein the inner surface of the sheath contacts the outer surface of the stent,
c) sliding the assembly over the probe so that the inner surface of the stent contacts the outer surface of the probe,
d) rotating the sheath while performing neuromonitoring with the probe.

12. The method of claim 11 further comprising the step of:
e) withdrawing the sheath from the stent to produce an expanded stent having a bore.

13. The method of claim 12 further comprising the step of:
f) anchoring the stent to a bone with the probe.

14. The method of claim 12 further comprising the step of:
f) passing an implant through the bore of the expanded stent.

15. The method of claim 12 further comprising the step of:
f) passing an instrument through the bore of the expanded stent.

16. The method of claim 11 wherein the target tissue is a psoas muscle having a lumbar plexus.

17. The method of claim 16 further comprising a step before step a), comprising:
positioning a retractor proximal to the psoas muscle.

18. The method of claim 17 further comprising expanding the retractor to provide an access portal for the probe.

19. The method of claim 11 further comprising the step of:
e) re-positioning the probe within the target tissue after performing step d).

20. The method of claim 11 wherein the throughhole does not open onto the distal end of the sheath.

21. A spinal surgery device, comprising:
a) an electrified probe having an outer surface;
b) an electrically-conductive cannula having an inner surface and an outer surface, wherein the inner surface of the cannula contacts the outer surface of the electrified probe,
c) an electrically-resistive elongated sheath having a distal end, an inner surface, an outer surface and a throughhole extending from the inner surface to the outer surface of the sheath, wherein the inner surface of the sheath contacts the outer surface of the cannula.

22. The device of claim 21 wherein the electrified probe is electrically connected to an electrical impulse generator.

23. The device of claim 21 wherein the electrified probe is electrically connected to a neuromonitoring system.

24. The device of claim 21 wherein the elongated sheath is sized to be rotatable about the cannula.

25. The device of claim 21 wherein the elongated sheath is sized to be slidable over the cannula.

26. The device of claim 21 wherein the throughhole does not open onto the distal end of the sheath.

27. A spinal surgery device, comprising:
a) an electrified probe having an outer surface;
b) an electrically-resistive cannula having a distal end, an inner surface, an outer surface and a throughhole extending from the inner surface to the outer surface of the cannula, wherein the inner surface of the cannula contacts the outer surface of the probe.

28. The device of claim 27 wherein the throughhole does not open onto the distal end of the cannula.

29. The device of claim 27 wherein the electrified probe is electrically connected to an electrical impulse generator.

30. The device of claim 27 wherein the electrified probe is electrically connected to a neuromonitoring system.

31. The device of claim 27 wherein the cannula is sized to be rotatable about the probe.

32. The device of claim 27 wherein the cannula is sized to be slidable over the probe.

33. The device of claim 27 wherein the probe does not extend past the distal end of the cannula.

34. The device of claim 27 wherein the probe comprises a bare proximal end portion.

35. The device of claim 27 wherein the probe comprises a bare distal end portion.

36. The device of claim 27 wherein the distal end portion is an island.

Assignees

• O'Neil Michael J
• Dimauro Thomas M
• Depuy Synthes Products Inc

Inventors

• O'Neil Michael J
• Dimauro Thomas M

Classifications

• A61B5/4893

  Nerves · CPC title

• A61B5/4041

  Evaluating nerves condition · CPC title

• A61B2017/3488

  Fixation to inner organ or inner body tissue · CPC title

• A61B2017/00261

  Discectomy · CPC title

• A61B2017/00867

  shape memory effect · CPC title