INTERVERTEBRAL IMPLANT AND TOOL ASSEMBLY
20240189114 ยท 2024-06-13
Inventors
- Ahmnon D. Moskowitz (Rockville, MD, US)
- Pablo A. Valdivia Y. Alvarado (Cambridge, MA, US)
- Mosheh T. Moskowitz (Rockville, MD, US)
- Nathan C. Moskowitz (Rockville, MD, US)
Cpc classification
A61B17/92
HUMAN NECESSITIES
A61B17/0644
HUMAN NECESSITIES
A61F2002/2835
HUMAN NECESSITIES
A61F2002/30772
HUMAN NECESSITIES
A61B17/809
HUMAN NECESSITIES
A61F2002/30878
HUMAN NECESSITIES
A61F2002/4687
HUMAN NECESSITIES
A61B17/86
HUMAN NECESSITIES
A61F2002/4627
HUMAN NECESSITIES
A61B2017/0641
HUMAN NECESSITIES
A61F2/447
HUMAN NECESSITIES
A61F2002/30579
HUMAN NECESSITIES
A61B17/8894
HUMAN NECESSITIES
A61F2002/448
HUMAN NECESSITIES
A61B17/0642
HUMAN NECESSITIES
A61F2002/30507
HUMAN NECESSITIES
A61F2220/0025
HUMAN NECESSITIES
A61F2/4465
HUMAN NECESSITIES
A61B17/7064
HUMAN NECESSITIES
A61F2002/4681
HUMAN NECESSITIES
International classification
A61B17/70
HUMAN NECESSITIES
A61B17/80
HUMAN NECESSITIES
A61B17/88
HUMAN NECESSITIES
A61B17/86
HUMAN NECESSITIES
Abstract
A self-drilling bone fusion screw apparatus is disclosed which includes at least first and second sliding boxes. A first screw member having a tapered end and a threaded body is disposed within the first sliding box, and a second screw member having a tapered end and a threaded body disposed within the second sliding box. An adjuster adjusts the height of the sliding boxes. The screw members are screwed into vertebral bodies in order to fuse the vertebral bodies together. A plurality of the self-drilling bone fusion screw apparatuses may be attached together and/or integrated via a plate or cage. Also disclosed is a cervical facet staple that includes a curved staple base and at least two prongs attached to the bottom surface of the curved staple base.
Claims
1-20. (canceled)
21. A tool assembly comprising: a spinal spacer implant configured for implantation in a patient's spine, the spinal spacer implant comprising: a first expandable portion, the first expandable portion comprising a first surface for contacting a first bone surface of the patient's spine; and a second expandable portion, the second expandable portion comprising a second surface for contacting a second bone surface of the patient's spine; wherein the spinal spacer implant is configured to be expanded from a closed configuration to an expanded configuration by movement of the first expandable portion and second expandable portion relative to one another, and wherein the first surface and the second surface are configured to contact the first bone surface and the second bone surface of the patient's spine, respectively, when the spinal spacer implant is in the expanded configuration; and an insertion tool configured for manipulating and inserting the spinal spacer implant into the patient's spine, the insertion tool comprising: a first tool body having a first end and a second end, the first tool body defining a lumen between the first end and the second end, the second end comprising prongs configured to engage the spinal spacer implant; and a second tool body having a third end and a fourth end, a diameter of the second tool body being smaller than an inner diameter of the lumen of the first tool body such that the second tool body is sized to be inserted through the first tool body so that the third end of the second tool body extends beyond the first end of the first tool body and the fourth end of the second tool body is configured to engage the spinal spacer implant, wherein the fourth end of the second tool body is configured to expand the spinal spacer implant in response to rotating the second end of the second tool body.
22. The tool assembly of claim 21, wherein the first bone surface comprises a first location in the patient's spine and the second bone surface comprises a second location in the patient's spine, the second location being different from the first location.
23. The tool assembly of claim 22, wherein the second tool body is configured to move the first expandable portion and the second expandable portion concurrently by rotating the fourth end of the second tool body, and the first expandable portion of the spinal spacer implant is configured to engage the first location of the patient's spine and the second expandable portion configured to engage the second location of the patient's spine concurrently when the spinal spacer implant is in the expanded configuration.
24. The tool assembly of claim 23, wherein the first expandable portion and the second expandable portion are positioned opposite one another, and the first location of the patient's spine is a first vertebral surface and the second location of the patient's spine is a second vertebral surface.
25. The tool assembly of claim 21, the spinal spacer implant further comprising an opening defined in the first surface of the first expandable portion, the opening configured to receive a material for encouraging bone fusion.
26. The tool assembly of claim 21, the first expandable portion comprising an angled rail and the second expandable portion comprising an angled ramp, the angled rail configured to slidably engage the angled ramp, and the second tool body is configured to expand the spinal spacer implant by sliding the angled rail along the angled ramp by a rotation of the fourth end of the second tool body.
27. A method of using the tool assembly of claim 21, the method comprising: aligning the spinal spacer implant with the prongs of the first tool body; engaging the prongs with the spinal spacer implant using a handle positioned at the first end of the first tool body; engaging the spinal spacer implant with the second end of the second tool body; expanding the spinal spacer implant to fit a space in the patient's spine by turning the first end of the second tool body within the lumen of the first tool body; and removing the first and second tool bodies from the patient's spine while leaving the spinal spacer implant in place.
28. The method of claim 27, wherein the spinal spacer implant is inserted into the patient's spine in a first compressed state and expanding the spinal spacer implant to fit the space in the patient's spine comprises expanding the spinal spacer implant after insertion to engage two bone surfaces of the patient's spine.
29. The method of claim 28, wherein expanding the spinal spacer implant comprises rotating the fourth end of the second tool body to slide the first expandable portion relative to the second expandable portion until the first surface and the second surface are in contact with the first and second bone surfaces of the patient's spine, respectively.
30. The method of claim 28, wherein rotating the fourth end of the second tool body is configured to turn a drive screw of the spinal spacer implant to slide the first expandable portion relative to the second expandable portion.
31. The method of claim 28, wherein the spinal spacer implant comprises at least one engaging mechanism for attaching to the two bone surfaces of the patient's spine.
32. The method of claim 27, wherein engaging the prongs with the spinal spacer implant comprises positioning the prongs within indentations of the spinal spacer implant.
33. The method of claim 27, further comprising adding a bone graft material to the spinal spacer implant.
34. The method of claim 27, further comprising visualizing using fluoroscopy the patient's spine during the expanding the spinal spacer implant to fit a space in the patient's spine.
35. The method of claim 27, further comprising positioning a second spinal spacer implant within the patient's spine using the insertion tool.
36. The method of claim 30, further comprising fixing the spinal spacer implant in the patient's spine with one or more screws.
37. A spinal spacer implant comprising: a first expandable portion, the first expandable portion comprising a first surface for contacting a first vertebral surface of a patient's spine and a second surface comprising a first angled ramp; a second expandable portion, the second expandable portion comprising a third surface for contacting a second vertebral surface of the patient's spine and a fourth surface comprising a second angled ramp, the first surface positioned opposite the third surface, the second angled ramp of the fourth surface configured to engage the first angled ramp of the second surface; an opening defined in the first surface of the first expandable portion, the opening configured to receive a material for encouraging bone fusion; a space defined between the first expandable portion and the second expandable portion; and a drive screw positioned in the space defined between the first expandable portion and the second expandable portion, the drive screw configured to move the first expandable portion relative to the second expandable portion; wherein the first surface and the second surface comprise surface features configured to engage the first and second vertebral surfaces of the patient's spine; and wherein the spinal spacer implant is configured to be expanded from a closed configuration to an expanded configuration by movement of the first expandable portion and second expandable portion relative to one another, and wherein the first surface and the second surface are configured to contact the first vertebral surface and the second vertebral surface of the patient's spine, respectively, when the spinal spacer implant is in the expanded configuration.
38. The spinal spacer implant of claim 37, wherein the spinal spacer implant is configured to be positioned between adjacent vertebrae such that the first vertebral surface and the second vertebral surface comprise surfaces of two adjacent vertebrae.
39. The spinal spacer implant of claim 37, wherein the first angled ramp is configured to slidably engage the second angled ramp, and the first expandable portion is configured to move relative to the second expandable portion by sliding the first angled ramp along the second angled ramp by a rotation of the drive screw.
40. The spinal spacer implant of claim 37, wherein the drive screw is configured to move the first expandable portion and the second expandable portion concurrently.
Description
BRIEF DESCRIPTION OF DRAWINGS
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[0046] Figures E-G illustrate the sequential steps (I-III) of the positioning tooll/screw guide/box expander assembly. Step I (
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DETAILED DESCRIPTION OF THE INVENTION
1. The Medical Device
[0060] Referring to
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[0062] The expandable box 100 consists of top and bottom triangular sliding bases 103, 104 (
[0063] Transvertebral screw 101 penetrates the top base 103, and transvertebral screw 102 traverses the bottom base 104 of the screw box 100. The two screws 101, 102 traverse the screw box 100 in opposing directions, bi-directionally (whether they are lateral or medially oriented). The external edges of the triangular bases 103, 104 in contact with vertebral body surfaces include ridges 107. This facilitates the screw box's 100 incorporation into and fusion with the superior and inferior vertebral bodies (
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[0069] The key components of this device include an Allen key 501, a spring 502, a handle 503, a griper 504 and a screw guide 505. The Allen key 501 when inserted in the insertion 514 and turned, turns the screw adjuster (
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2. The Surgical Method
[0083] Exemplary surgical steps for practicing one or more of the foregoing embodiments will now be described.
[0084] The posterior lumbar spine implantation of all the screw box 100, 200, 300 embodiments, with BDFT screws, and horizontal mini-plate 400 can be implanted via previously described posterior lumbar interbody fusion (PLIF) or posterior transforaminal lumbar interbody fusion (TLIF) procedures. The procedures can be performed open, microscopic, closed tubular or endoscopic. Fluoroscopic guidance can be used with any of these procedures.
[0085] After adequate induction of anesthesia, the patient is placed in the prone position. A midline incision is made for a PLIF procedure, and one or two parallel paramedian incisions or a midline incision is made for the TLIF procedure. For the PLIF, a unilateral or bilateral facet sparing hemi-laminotomy is created to introduce screw box 100, 200, 300 embodiments I-III into the disc space, after it is adequately prepared.
[0086] For the TLIF procedure, after unilateral or bilateral dissection and drilling of the inferior articulating surface and the medial superior articulating facet the far lateral disc space is entered and a circumferential discectomy is performed. The disc space is prepared and the endplates exposed.
[0087] Then one screw box 100, 200, 300 of either embodiments I-III is placed on either right, left or both sides. Then another screw box of embodiments 100, 200, 300 I-III is placed on the contralateral side. For embodiment I the external screw guide 505/box expander is attached to the screw box (
[0088] For embodiments II-III the same method is used for placing screws, except the Allen key 501 is not utilized in the absence of plate expansion.
[0089] If bilateral constructs have been inserted, bone is packed into the intervertebral space, as well as within the device. Then the horizontal intervertebral zero profile mini-plate 400 is slid beneath the thecal sac and is secured to both left and right screw boxes with small mini-plate screws 210 (
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[0091] The anterior thoracic and lumbar spine implantation of one, two or three screw box constructs 100, 200, 300 and BDFT screws can be performed in a similar manner to the posterior application. Likewise, a horizontal mini-plate 400 can be used to cap two or three screw box constructs 100, 200, 300 (one placed midline deeply, one placed left and one placed right, forming a triangulation). Alternatively two screw box constructs may be placed into a circumferential ring for anterior placement. Anterior placement of these devices can be performed into the L4/5 and L5/S1 spaces on the supine anesthetized patient via previously described open microscopic or endoscopic techniques. Once the disc space is exposed and discectomy and space preparation are performed, placement of one, two or three screw box embodiments 100, 200, 300 (I-III) or a 2 in I construct can be placed. The screw placement is facilitated by the internal screw guides, and different positioning tools ((
[0092] The posterior placement of screw box constructs 100, 200, 300 alone or combined with horizontal mini-plates 400 into the thoracic spine can be performed via previously described transpedicular approaches; open or endoscopic. The anterior placement into the thoracic spine can be accomplished via a trans-thoracic approach. Once the disc space is exposed via either approach, any combination of the above mention Embodiments (I-III) can be inserted. Engagement of the devices is identical to what was mentioned above.
[0093] For posterior placement of cervical facet staple 700, 800 embodiments, after adequate induction of anesthesia the patient is flipped prone and his head and neck secured. A single midline or two para-median incisions are made for unilateral or bilateral or multilevel placement of staples. Ultimately the facet joint is exposed. Alternatively and preferably this can be performed percutaneously under fluoroscopic guidance with intravenous sedation. The staple 700, 800 (Embodiments I or II) is loaded into the impactor 900, 1000. The staple 700, 800 is placed on the two articulating cervical facets, and then impacted into the joint. To achieve modular calibrated fusion different combinations and permutations of cervical facet stales can be inserted ranging from a single unilateral two pronged staple providing a high degree of flexibility to a total of four bilaterally placed four pronged staples 800 (16 prongs) leading to the highest degree of rigidity. Additional bone may or may not be placed in its vicinity to facilitate permanent and solid fusion. This procedure can be performed open, closed, percutaneously, tubulary, endoscopically or microscopically.
[0094] We have previously described surgical placement of the lumbar facet joint staple in our two co-pending patents. The surgical procedure for this device is identical to that which has been previously mentioned.
[0095] The present inventions may provide effective and safe techniques that overcome the problems associated with current transpedicular based cervical, thoracic and lumbar fusion technology, and for many degenerative stable and unstable spine disease. These inventions could replace much pedicle screw-based instrumentation in many but not all degenerative spine conditions.
[0096] The speed and simplicity of placement of cervical and lumbar facet staples, and placement of Lumbar screw box-BDFT constructs far exceeds that of current pedicle screw technology. Furthermore, these devices have markedly significantly decreased risk of misguided screw placement, and hence decreased risk of neural and vascular injury, and blood loss. In the lumbar spine BDFT screw constructs and facet staples could be applied modularly in different combinations to achieve different degrees of rigidity (flexibility). Patients having these devices would have decreased recovery and back to work time. These devices most likely lead to similar if not equal fusion with significantly less morbidity, and hence overall make them a major advance in the evolution of spinal instrumented technology leading to advances in the care of the spinal patient.
[0097] Another major novelty and advance is the introduction of simple and safe modular calibrated cervical flexible fusion. To our knowledge neither a similar device nor a similar mathematical concept of modular joint flexibility/fusion calibration has been postulated for the cervical spine or for any other articulating joint.
[0098] To our knowledge there have not been any previously described similar posterior lumbar and thoracic combined spacer and screw constructs. These devices can similarly be modified to stabilize bone fractures throughout the entire body. To our knowledge the description of zero to subzero profile anterior or posterior horizontal spinal plates which traverse the diameter of the disc space has not been previously described.