The present invention relates to a system and a method for a spinal stabilization implant assembly, and more particularly to a spinal stabilization implant assembly that includes a stabilization plate an intervertebral insert and bone fasteners.
Fibula strut grafts have a proven history of effectiveness for anterior cervical corpectomies but are inherently vulnerable to complications such as early or late fracture, dislodgement, displacement, telescoping into the vertebral body, or nonunion. The settling and resultant segmental kyphosis after multi-level anterior cervical reconstruction have also been documented. The risk of graft migration, displacement, or fracture appears more likely with more vertebral bodies removed and longer grafts, and with corpectomies involving a fusion ending at the C7 vertebral body. Newer interbody stabilization options have emerged such as polyetherketone (PEEK) which have the advantages of greater endplate coverage leading to a more stable construct and with similar modulus of elasticity as bone. However, PEEK cages require separate graft material for interbody fusion. Other options include metal expandable cages but these can be bulky, risk adjacent body fracture, and have limited room for bone graft, and therefore, do not provide the most ideal biologic environment. Stacking PEEK cages intuitively can also fill a corpectomy space by stacking the appropriate heights end-to-end. Improved cervical stabilization assemblies and methods are desirable.
The present invention relates to a spinal stabilization implant assembly that includes a stabilization plate, an intervertebral insert and bone fasteners.
In general, in one aspect, the invention features a spinal stabilization implant assembly configured for implantation at least partially between a superior vertebra and an inferior vertebra. The spinal stabilization implant assembly includes a cervical stabilization plate and one or more bone fasteners. The cervical stabilization plate includes an elongated body having left and right side surfaces, front and back surfaces and top and bottom surfaces. The elongated body has a central portion, a top portion and a bottom portion. The top portion is bent at a first angle relative to the central portion and is dimensioned for capturing and fastening to a corner ridge of a vertebral wall of a superior vertebra. The bottom portion is bent at a second angle relative to the central portion and the second angle is opposite to the first angle and is dimensioned for capturing and fastening to a corner ridge of a vertebral wall of an inferior vertebra. The back surface has a protruding indent-tab, and the indent-tab is shaped and dimensioned to be implanted in an intervertebral space between the superior and the inferior vertebras. The elongated body further includes one or more through-openings extending from the front surface to the back surface and the one or more bone fasteners are shaped and dimensioned to be inserted through the one or more through-openings, respectively, and to be attached to locations in the vertebral walls of the superior and inferior vertebras.
Implementations of this aspect of the invention may include one or more of the following features. Each of the one or more through-openings has a first diameter at the front surface of the elongated body, a second diameter at the back surface of the elongated body and a third diameter in the area between the front the back surfaces of the elongated body. The third diameter is larger than the first diameter and the second diameter, thereby forming a lip at the top of the through-openings and a groove within an inner wall of the through openings. Each of the one or more bone fasteners includes a threaded main body and a head. The head has one or more flexible structures configured to be flexed inwards when inserted into the groove and then configured to be unflexed and to be captured within the groove. The elongated body further includes a central through opening configured to be packed with graft material. The elongated body further includes one or more spikes extending from the back surface and being shaped and dimensioned to be inserted into the vertebral walls of the superior and inferior vertebras. The spinal stabilization implant assembly further includes an intervertebral cage configured to be implanted in the intervertebral space between the superior and inferior vertebras. The intervertebral cage comprises front, back, left, right, top, and bottom surfaces. The intervertebral cage is integral with the back surface of the elongated body. The intervertebral cage further comprises first and second fins extending from back surface of the intervertebral cage. The intervertebral cage has a U-shaped body and an integrated central support bar configured to prevent movement between the superior and the inferior vertebras. The intervertebral cage is attached to the back surface of the elongated body with a screw. The top and bottom portions of the elongated body are pivotally connected to the central portion of the elongated body. The spinal stabilization implant assembly further includes top and bottom locking tabs configured to lock the angular positions of the top and bottom portions relative to the central portion. The spinal stabilization implant assembly further includes a keystone and the keystone has top and bottom angled surfaces configured to lock the angular positions of the top and bottom portions relative to the central portion, when the keystone is attached to the central portion. The cervical stabilization plate has an adjustable length. The length of the cervical stabilization plate is adjusted via a ratchet mechanism, or by rotating a threaded rod, or via a cam mechanism, or via a side-sliding mechanism. The side-sliding mechanism includes inserting plates of different height in a space between the top and central portions or the space between the bottom and central portions. The cam mechanism includes an oval shaped cam configured to be rotated in a space between the top and bottom portions. The back surface of the elongated body has a recess and the intervertebral cage is shaped and dimensioned to be inserted into the recess and to slidably engage the elongated body. The elongated body may be made of metal and the intervertebral implant may be made of PEEK. The height of the indent-tab matches the height of the intervertebral cage.
In general, in one aspect, the invention features a spinal stabilization implant assembly including a first cervical stabilization plate comprising an elongated body having a top portion and a bottom portion, and a second cervical stabilization plate comprising an elongated body having a top portion and a bottom portion. The bottom portion of the first cervical stabilization plate is configured to be attached to a first vertebra and the top portion of the second stabilization plate is configured to be stacked end-to-end below the bottom portion of the first cervical stabilization plate and to be attached to the same first vertebra. The top portion of the first cervical stabilization plate is configured to be attached to a second vertebra, and the bottom portion of the second stabilization plate is configured to be attached to a third vertebra. The second vertebra is superior to the first vertebra, and the third vertebra is inferior to the first vertebra.
In general, in one aspect, the invention features a spinal stabilization method including providing a spinal stabilization implant assembly and implanting the spinal stabilization implant assembly at least partially between a superior vertebra and an inferior vertebra. The spinal stabilization implant assembly includes a cervical stabilization plate and one or more bone fasteners. The cervical stabilization plate has an elongated body having left and right side surfaces, front and back surfaces and top and bottom surfaces. The elongated body includes a central portion, a top portion and a bottom portion. The top portion is bent at a first angle relative to the central portion and is dimensioned for capturing and fastening to a corner ridge of a vertebral wall of the superior vertebra. The bottom portion is bent at a second angle relative to the central portion and the second angle is opposite to the first angle and is dimensioned for capturing and fastening to a corner ridge of a vertebral wall of the inferior vertebra. The back surface has a protruding indent-tab. The indent-tab is shaped and dimensioned to be implanted in an intervertebral space between the superior and the inferior vertebras. The elongated body further includes one or more through-openings extending from the front surface to the back surface and the one or more bone fasteners are shaped and dimensioned to be inserted through the one or more through-openings, respectively, and to be attached to locations in the vertebral walls of the superior and inferior vertebras. The method further includes inserting an intervertebral cage in the intervertebral space between the superior and inferior vertebras, and the height of the indent-tab matches the height of the intervertebral cage.
In general, in one aspect, the invention features a spinal stabilization method including providing a first cervical stabilization plate comprising an elongated body having a top portion and a bottom portion, providing a second cervical stabilization plate comprising an elongated body having a top portion and a bottom portion, attaching the bottom portion of the first cervical stabilization plate to a first vertebra, stacking the top portion of the second stabilization plate end-to-end below the bottom portion of the first cervical stabilization plate, and attaching the top portion of the second stabilization plate to the same first vertebra. The method further includes attaching the top portion of the first cervical stabilization plate to a second vertebra, and attaching the bottom portion of the second stabilization plate to a third vertebra. The second vertebra is superior to the first vertebra, and the third vertebra is inferior to the first vertebra.
The details of one or more embodiments of the invention are set forth in the accompanying drawings and description below. Other features, objects, and advantages of the invention will be apparent from the following description of the preferred embodiments, the drawings, and the claims
Referring to the figures, wherein like numerals represent like parts throughout the several views:
The present invention relates to a spinal stabilization implant assembly 100 that includes a cervical stabilization plate 110, an intervertebral cage insert 150 and one or more bone fasteners 120, as shown in
Referring to
The one or more bone fasteners 120 are configured to be inserted through the one or more through-openings 114a, 114b, respectively, and to be attached to locations in the spinal vertebras, thereby attaching the cervical plate to the spinal vertebras. The through-openings comprise a first diameter 131a at the front surface 111c of the elongated body 111, a second diameter 131b at the back surface 111d of the elongated body 111 and a third diameter 131c in the area between the front 111c and back 111d surfaces of the elongated body 111. The first diameter 131a is smaller than the third diameter 131c, thereby forming a lip 132 at the top of the through-openings. The third diameter 131c is larger than the second diameter 131b and the first diameter 131a is larger than the second diameter 131b, thereby forming a groove 133 within the inner wall of the through-openings. The bone fasteners 120 comprise a threaded main body 124 and a head 122. The threaded main body 124 comprises threads 124a for engaging the spinal vertebras and the head 122 comprises one or more flexible structures 121a, 121b, 121c configured to be flexed and inserted into the groove 133 and then unflex and remain captured within the groove 133.
Among the advantages of the invention may be one or more of the following. The spinal stabilization implant assembly has ultra-low profile design, dual integrated screw lock mechanisms that prevent screw backout, pre-angled zero-step lock with variable screws, large graft window for visibility and anterior graft packing, tactile, audible and visual feedback of screw engagement, 20° variable screw angulation, and safe and simple screw recovery feature, among others. PEEK cages may be stacked around a fibula strut graft to fill a corpectomy defect. This practice may limit the chance of endplate fracture or graft dislodgment. There is space around the fibula graft for additional osteobiologics such as demineralized bone matrix (DBM). There may be benefit to designing PEEK cages that are stackable.
The method of implanting the spinal stabilization implant assembly of this invention includes the following. After determining cage size and inserting the cage in place, a void in the annulus remains. Next, place drill guide over annulus void. Indent of drill guide will fit through, thereby showing ideal location for plate placement and hole location on the vertebrae. Next, drilling through holes of drill guide and then removing the drill guide. Next, grabbing the plate with the plate holder and placing it over annulus void and screw holes. The plate size is adjusted to correspond to the cage size used in disc space. The indent of plate is selected to fit in the annulus void. Next, inserting screws to secure plate to the vertebral body. If performing multiple level fixation/fusion, repeat steps at next level. Each assembly includes a cervical plate, a cervical cage, a drill guide and a plate holder
Referring to
The present invention also provides a new approach to filling a corpectomy defect by stacking multiple PEEK cages around a fibula strut graft. The method has been used to treat a 45 year old male who underwent C5 corpectomy with a fibula strut allograft inside three PEEK cages stacked vertically around the graft. Follow-up at nine months showed improved strength, the patient returning to regular daily activities, and cervical spine x-rays demonstrating radiographic evidence of graft consolidation consistent with fusion. There was no evidence of subsidience or focal kyphosis.
In another case, the method was use to treat a 47 year old man with a massive C5-6 herniated disc. This patient's cervical radiculomyelopathy was attributed to the C5-6 herniated disc. The patient underwent anterior cervical decompression and fusion (ACDF). A 7 mm PEEK interbody cage (Invibio PEEK-OPTIMA) and a 19 mm cervical plate and screws (SpineFrontier Inc, Indus Invue Plate, Beverly, Mass.) were used to stabilize the spine. At six weeks postoperatively the patient still had residual pain and bilateral arm numbness. A repeat MRI illustrated improvement but computed tomography (CT) showed large posterior osteophytes causing residual stenosis at the level of the C5 and C6 endplates along with the functional compression at C3-C4. The patient underwent revision C5 corpectomy and a C3-4 ACDF. An 8 mm cage (Eminent Spine, Texas) with autograft corpectomized bone and DBM were placed at C3-4. Distraction pins were placed in the body of C4 and C6 and we measured for a 30 mm long fibula strut graft. A fibula strut allograft was fashioned and cut in half length wise and placed through three PEEK cages for a total length of 30 mm (12 mm, 10 mm, 8 mm in this order). The combined cages and fibula strut graft were placed in the trough and the distraction pins removed to allow the C4 and C6 vertebrae to collapse around the construct. Demineralized bone matrix (DBM) and autograft corpectomized bone were placed within the cages alongside the fibula strut graft. A 60 mm cervical plate with lordosis was placed with screws (SpineFrontier Inc, Indus Invue Plate, Beverly, Mass.). This plate felt solidly fixed and DBM was placed behind the plate and in front of the cages at all levels. At one year he had mild residual complaints of neck pain, numbness and tingling but was much improved overall. CT showed evidence of graft consolidation consistent with fusion. The plate and screws were stably fixed.
Although fibula strut grafts are historically an effective option for anterior cervical corpectomy, they are vulnerable to complications as the number of levels decompressed increases. Associated donor site morbidity is an additional consideration. Patients experiencing compliance difficulties with cervical bracing when fibula strut grafts are used without plating or with buttress plating may be at increased risk of graft failure. Patients with a history of heavy narcotic use or smoking may be at further risk for unfavorable outcomes without a stable fibula strut graft after corpectomy. In contrast, PEEK cages have good biomechanical characteristics and a comparable elastic coefficient to that of human bone. ACDF with a PEEK cage has shown good clinical results for single level cervical disorders, but this is not the case with multi-level ACDF.
Several embodiments of the present invention have been described. Nevertheless, it will be understood that various modifications may be made without departing from the spirit and scope of the invention. Accordingly, other embodiments are within the scope of the following claims.