U.S. patent application number 11/526849 was filed with the patent office on 2007-03-29 for artificial functional spinal unit assemblies.
Invention is credited to Charles Gordon, Corey Harbold.
Application Number | 20070073406 11/526849 |
Document ID | / |
Family ID | 34116123 |
Filed Date | 2007-03-29 |
United States Patent
Application |
20070073406 |
Kind Code |
A1 |
Gordon; Charles ; et
al. |
March 29, 2007 |
Artificial functional spinal unit assemblies
Abstract
An artificial functional spinal unit is provided comprising,
generally, an expandable artificial intervertebral implant that can
be placed via a posterior surgical approach and used in conjunction
with one or more artificial facet joints to provide an anatomically
correct range of motion. Expandable artificial intervertebral
implants in both lordotic and non-lordotic designs are disclosed,
as well as lordotic and non-lordotic expandable cages for both PLIF
(posterior lumber interbody fusion) and TLIF (transforaminal lumbar
interbody fusion) procedures. The expandable implants may have
various shapes, such as round, square, rectangular, banana-shaped,
kidney-shaped, or other similar shapes. By virtue of their
posteriorly implanted approach, the disclosed artificial FSU's
allow for posterior decompression of the neural elements,
reconstruction of all or part of the natural functional spinal
unit, restoration and maintenance of lordosis, maintenance of
motion, and restoration and maintenance of disc space height.
Inventors: |
Gordon; Charles; (Tyler,
TX) ; Harbold; Corey; (Tyler, TX) |
Correspondence
Address: |
MEYERTONS, HOOD, KIVLIN, KOWERT & GOETZEL, P.C.
700 LAVACA, SUITE 800
AUSTIN
TX
78701
US
|
Family ID: |
34116123 |
Appl. No.: |
11/526849 |
Filed: |
September 25, 2006 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
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10634950 |
Aug 5, 2003 |
|
|
|
11526849 |
Sep 25, 2006 |
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Current U.S.
Class: |
623/17.15 |
Current CPC
Class: |
A61B 17/7005 20130101;
A61F 2002/3079 20130101; A61F 2220/0075 20130101; A61F 2002/30649
20130101; A61B 17/7052 20130101; A61F 2002/30492 20130101; A61F
2250/0007 20130101; A61F 2/30771 20130101; A61F 2002/30578
20130101; A61B 17/704 20130101; A61B 17/7008 20130101; A61F 2/30767
20130101; A61F 2002/3055 20130101; A61F 2002/3071 20130101; A61F
2002/443 20130101; A61F 2230/0015 20130101; A61B 17/7064 20130101;
A61F 2250/0085 20130101; A61F 2/4425 20130101; A61F 2002/30662
20130101; A61B 17/7041 20130101; A61F 2002/30462 20130101; A61F
2002/30365 20130101; A61F 2002/30507 20130101; A61F 2002/30785
20130101; A61F 2310/00796 20130101; A61B 17/7023 20130101; A61B
17/7037 20130101; A61F 2310/00976 20130101; A61F 2/4405 20130101;
A61B 17/7032 20130101; A61F 2002/30616 20130101; A61F 2220/0033
20130101; A61B 17/86 20130101; A61B 17/1671 20130101; A61F
2002/30133 20130101; A61F 2002/30579 20130101; A61F 2310/00407
20130101; A61B 17/746 20130101; A61F 2220/0025 20130101; A61B
2017/0256 20130101; A61F 2002/30515 20130101; A61F 2002/30538
20130101; A61F 2002/30624 20130101; A61F 2002/30556 20130101; A61F
2250/0006 20130101; A61F 2002/30364 20130101; A61F 2002/30841
20130101; A61B 17/8897 20130101; A61B 17/1757 20130101; A61F
2002/30369 20130101; A61F 2250/0009 20130101 |
Class at
Publication: |
623/017.15 |
International
Class: |
A61F 2/44 20060101
A61F002/44 |
Claims
1-106. (canceled)
107. A spinal implant assembly comprising: at least one
intervertebral implant comprising: a lower body having an inferior
surface and a superior surface, the superior surface having an
upwardly projecting wall forming a channel thereupon, the wall
having an opening defined therethrough; an upper body located above
the lower body, the upper body having a superior surface and a
substantially concave inferior surface; a joint insert having an
inferior surface and a substantially convex superior surface, the
joint insert residing within the channel on the lower body; and an
expansion device capable of being inserted through the opening in
the wall on the lower body such that, upon insertion of the
expansion device, the joint insert is lifted above the channel
causing the insert to articulate with the substantially concave
inferior surface of the upper body; and at least one artificial
facet joint.
108. The spinal implant assembly of claim 107, wherein at least one
artificial facet joint comprises: an upper multi-axial pedicle
screw having a non-locking head with a hole defined therethrough; a
lower multi-axial pedicle screw having a non-locking head with a
hole defined therethrough; and a rod having a central rod portion
and two washer-type heads on each end of the central rod portion,
the central rod portion slidingly positioned through the hole in
the non-locking head of the upper multi-axial pedicle screw and the
lower multi-axial pedicle screw such that the heads of the upper
and lower multi-axial pedicle screws slide freely along the central
rod portion.
109. The spinal implant assembly of claim 107, wherein at least one
artificial facet joint comprises: an upper pedicle screw having a
lockable head with a hole defined therethrough; a lower multi-axial
pedicle screw having a non-locking head with a hole defined
therethrough; and a rod having a central rod portion, an upper end
and a lower end, the lower end having a washer-type head, the
central rod portion slidingly positioned through the hole in the
non-locking head of the lower multi-axial pedicle screw such that
the washer-type lower head prohibits dislocation of the lower
multi-axial pedicle screw from the central rod portion, and the
upper end of the rod slidingly positioned through the hole in the
lockable head of the upper pedicle screw such that, upon locking of
the lockable head, rotational and translational motion of the upper
end of the rod is prohibited.
110. The spinal implant assembly of claim 107, wherein at least one
artificial facet joint comprises: an upper pedicle screw having a
lockable head with a hole defined therethrough; a lower pedicle
screw having a lockable head with a hole defined therethrough; and
a rod having an upper end, a lower end and a central ball joint
connecting the upper and lower end that permits the rod to bend,
the upper end of the rod slidingly positioned within the hole of
the head of the upper pedicle screw, the lower end of the rod
slidingly positioned within the hole of the lower pedicle screw,
the lockable heads of the upper and lower pedicle screw being
locked such that rotational and translational motion of the rod is
prohibited.
111. The spinal implant assembly of claim 107, wherein at least one
intervertebral implant comprises osteoconductive scaffolding into
which bone may grow disposed on the superior surface of the upper
body.
112. The spinal implant assembly of claim 107, wherein at least one
expandable intervertebral implant comprises osteoconductive
scaffolding into which bone may grow disposed on the inferior
surface of the lower body.
113. The spinal implant assembly of claim 107, wherein the upper
body and lower body have substantially similar shapes.
114. The spinal implant assembly of claim 113, wherein the shape of
the upper body when viewed proximally is round.
115. The spinal implant assembly of claim 113, wherein the shape of
the upper body when viewed proximally is banana-shaped.
116. An artificial functional spinal unit, comprising: at least one
intervertebral implant, wherein at least one intervertebral implant
comprises a lower body configured to couple to a first human
vertebra and an upper body configured to couple to a second human
vertebra, and wherein the upper body is moveable relative to the
lower body to accommodate at least flexion of the first human
vertebra relative to the second human vertebra; and at least one
artificial facet joint configured to couple to the first human
vertebra and the second human vertebra.
117. The artificial functional spinal unit of claim 116, wherein at
least one artificial facet joint comprises: a first pedicle screw;
a second pedicle screw; and a rod configured to couple to the first
pedicle screw and the second pedicle screw such that a head of the
first pedicle screw and a head of the second screw are able to
slide relative to the rod after installation of the artificial
facet joint.
118. The artificial functional spinal unit of claim 116, wherein at
least one artificial facet joint comprises: a first pedicle screw;
a second pedicle screw; and a rod configured to couple to the first
pedicle screw and the second pedicle screw such that the rod is
secured to a head of the first pedicle screw, and the rod is able
to slide relative to a head of the second pedicle screw after
installation of the artificial facet joint.
119. The artificial functional spinal unit of claim 116, wherein at
least one artificial facet joint comprises: a first pedicle screw;
a second pedicle screw; a rod configured to couple to the first
pedicle screw and the second pedicle screw, wherein the rod
includes a ball joint that allows the rod to bend, and wherein the
rod is secured to a head of the first pedicle screw and to a head
of the second pedicle screw during installation of the artificial
facet joint.
120. The artificial functional spinal unit of claim 116, wherein at
least one intervertebral implant comprises osteoconductive
scaffolding into which bone may grow.
121. The artificial functional spinal unit of claim 116, wherein
the shape of the upper body when viewed proximally is round.
122. The artificial functional spinal unit of claim 116, wherein
the shape of the upper body when viewed proximally is
banana-shaped.
123. A method of forming an artificial functional spinal unit,
comprising: placing one or more intervertebral implants between a
first human vertebra and a second human vertebra, wherein at least
one intervertebral implant is configured to accommodate flexion of
the first human vertebra relative to the second human vertebra; and
securing at least one artificial facet joint to the first human
vertebra and the second human vertebra.
124. The method of claim 123, wherein placing at least one of the
intervertebral implants comprises inserting the intervertebral
implant between the first human vertebra and the second human
vertebra, and expanding the intervertebral implant.
125. The method of claim 123, wherein securing at least one
artificial facet joint to the first human vertebra and the second
human vertebra comprises: placing a first pedicle screw in the
first human vertebra; placing a second pedicle screw in the second
human vertebra; coupling a rod to the first pedicle screw and the
second pedicle screw, wherein the rod is able to move relative to
the first pedicle screw after the rod is coupled to the first
pedicle screw.
126. The method of claim 123, wherein at least one artificial facet
joint comprises a ball joint configured to accommodate flexion of
the first human vertebra relative to the second human vertebra.
Description
PRIORITY CLAIM
[0001] This application is a continuation of U.S. patent
application Ser. No. 10/634,950 entitled "ARTIFICIAL FUNCTIONAL
SPINAL UNIT ASSEMBLIES" filed on Aug. 5, 2003, the disclosure of
which is hereby incorporated by reference.
BACKGROUND
[0002] 1. Field of the Invention
[0003] The present invention generally relates to functional spinal
implant assemblies for insertion into the intervertebral space
between adjacent vertebral bones and reconstruction of the
posterior elements to provide stability, flexibility and proper
biomechanical motion. More specifically, the present invention
relates to artificial functional spinal units comprising an
expandable artificial intervertebral implant that can be inserted
via a posterior surgical approach and used in conjunction with one
or more artificial facet joints to provide a more anatomically
correct range of motion.
[0004] 2. Description of Related Art
[0005] The human spine is a complex mechanical structure composed
of alternating bony vertebrae and fibrocartilaginous discs that are
connected by strong ligaments and supported by musculature that
extends from the skull to the pelvis and provides axial support to
the body. The intervertebral discs primarily serve as a mechanical
cushion between adjacent vertebral segments of the spinal column
and generally comprise three basic components: the nucleus
pulposus, the anulus fibrosis, and two vertebral end plates. The
end plates are made of thin cartilage overlying a thin layer of
hard cortical bone that attaches to the spongy, cancellous bone of
the vertebral body. The anulus fibrosis forms the disc's perimeter
and is a tough outer ring that binds adjacent vertebrae together.
The vertebrae generally comprise a vertebral foramen bounded by the
anterior vertebral body and the neural arch, which consists of two
pedicles and two larninae that are united posteriorly. The spinous
and transverse processes protrude from the neural arch. The
superior and inferior articular facets lie at the root of the
transverse process. The term "functional spinal unit" ("FSU")
refers to the entire motion segment: the anterior disc and the
posterior facet joints, along with the supporting ligaments and
connective tissues.
[0006] The spine as a whole is a highly flexible structure capable
of a high degree of curvature and twist in nearly every direction.
However, genetic or developmental irregularities, trauma, chronic
stress, and degenerative wear can result in spinal pathologies for
which surgical intervention may be necessary.
[0007] It is common practice to remove a spinal disc in cases of
spinal disc deterioration, disease or spinal injury. The discs
sometimes become diseased or damaged such that the intervertebral
separation is reduced. Such events cause the height of the disc
nucleus to decrease, which in turn causes the anulus to buckle in
areas where the laminated plies are loosely bonded. As the
overlapping laminated plies of the anulus begin to buckle and
separate, either circumferential or radial anular tears may occur.
Such disruption to the natural intervertebral separation produces
pain, which can be alleviated by removal of the disc and
maintenance of the natural separation distance. In cases of chronic
back pain resulting from a degenerated or herniated disc, removal
of the disc becomes medically necessary.
[0008] In some cases, the damaged disc may be replaced with a disc
prosthesis intended to duplicate the function of the natural spinal
disc. U.S. Pat. No. 4,863,477 discloses a resilient spinal disc
prosthesis intended to replace the resiliency of a natural human
spinal disc. U.S. Pat. No. 5,192,326 teaches a prosthetic nucleus
for replacing just the nucleus portion of a human spinal disc.
[0009] In other cases it is desired to fuse the adjacent vertebrae
together after removal of the disc, sometimes referred to as
"intervertebral fusion" or "interbody fusion."
[0010] Many techniques and instruments have been devised to perform
intervertebral fusion. There is common agreement that the strongest
intervertebral fusion is the interbody (between the lumbar bodies)
fusion, which may be augmented by a posterior or facet fusion. In
cases of intervertebral fusion, either structural bone or an
interbody fusion cage filled with morselized bone is placed
centrally within the space where the spinal disc once resided.
Multiple cages or bony grafts may be used within that space.
[0011] Such practices are characterized by certain disadvantages,
most important of which is the actual morbidity of the procedure
itself. Placement of rigid cages or structural grafts in the
interbody space either requires an anterior surgical approach,
which carries certain unavoidable risks to the viscous structures
overlying the spine (intestines, major blood vessels, and the
ureter), or they may be accomplished from a posterior surgical
approach, thereby requiring significant traction on the overlying
nerve roots. The interval between the exiting and traversing nerve
roots is limited to a few millimeters and does not allow for safe
passage of large intervertebral devices, as may be accomplished
from the anterior approach. Alternatively, the anterior approach
does not allow for inspection of the nerve roots, is not suitable
alone for cases in which the posterior elements are not competent,
and most importantly, the anterior approach is associated with very
high morbidity and risk where there has been previous anterior
surgery.
[0012] Another significant drawback to fusion surgery in general is
that adjacent vertebral segments show accelerated deterioration
after a successful fusion has been performed at any level. The
spine is by definition stiffer after the fusion procedure, and the
natural body mechanics place increased stress on levels proximal to
the fused segment. Other drawbacks include the possibility of "flat
back syndrome" in which there is a disruption in the natural
curvature of the spine. The vertebrae in the lower lumbar region of
the spine reside in an arch referred as having a sagittal
alignment. The sagittal alignment is compromised when adjacent
vertebral bodies that were once angled toward each other on their
posterior side become fused in a different, less angled orientation
relative to one another. Finally, there is always the risk that the
fusion attempt may fail, leading to pseudoarthrosis, an often
painful condition that may lead to device failure and further
surgery.
[0013] Conventional interbody fusion cages generally comprise a
tubular metal body having an external surface threading. They are
inserted transverse to the axis of the spine, into preformed
cylindrical holes at the junction of adjacent vertebral bodies. Two
cages are generally inserted side by side with the external
threading tapping into the lower surface of the vertebral bone
above, and the upper surface of the vertebral bone below. The cages
include holes through which the adjacent bones are to grow.
Additional materials, for example autogenous bone graft materials,
may be inserted into the hollow interior of the cage to incite or
accelerate the growth of the bone into the cage. End caps are often
utilized to hold the bone graft material within the cage.
[0014] These cages of the prior art have enjoyed medical success in
promoting fusion and grossly approximating proper disc height. As
previously discussed, however, cages that would be placed from the
safer posterior route would be limited in size by the interval
between the nerve roots. It would therefore, be a considerable
advance in the art to provide a fusion implant assembly which could
be expanded from within the intervertebral space, thereby
minimizing potential trauma to the nerve roots and yet still
providing the ability to restore disc space height.
[0015] Ultimately though, it is important to note that the fusion
of the adjacent bones is an incomplete solution to the underlying
pathology as it does not cure the ailment, but rather simply masks
the pathology under a stabilizing bridge of bone. This bone fusion
limits the overall flexibility of the spinal column and
artificially constrains the normal motion of the patient. This
constraint can cause collateral injury to the patient's spine as
additional stresses of motion, normally bone by the now-fused
joint, are transferred onto the nearby facet joints and
intervertebral discs. Thus, it would be an even greater advance in
the art to provide an implant assembly that does not promote
fusion, but instead closely mimics the biomechanical action of the
natural disc cartilage, thereby permitting continued normal motion
and stress distribution.
SUMMARY
[0016] Accordingly, an artificial functional spinal unit (FSU) is
provided comprising, generally, an expandable artificial
intervertebral implant that can be placed via a posterior surgical
approach and used in conjunction with one or more artificial facet
joints to provide an anatomically correct range of motion.
Expandable artificial intervertebral implants in both lordotic and
non-lordotic designs are disclosed, as well as lordotic and
non-lordotic expandable cages for both PLIF (posterior lumber
interbody fusion) and TLIF (transforaminal lumbar interbody fusion)
procedures. The expandable implants may have various shapes, such
as round, square, rectangular, banana-shaped, kidney-shaped, or
other similar shapes. By virtue of their posteriorly implanted
approach, the disclosed artificial FSU's allow for posterior
decompression of the neural elements, reconstruction of all or part
of the natural functional spinal unit, restoration and maintenance
of lordosis, maintenance of motion, and restoration and maintenance
of disc space height.
[0017] The posterior implantation of an interbody device provides
critical benefits over other anterior implanted devices. Placement
of posterior devices that maintain mobility in the spine have been
limited due to the relatively small opening that can be afforded
posteriorly between the exiting and transversing nerve roots.
Additionally, placement of posterior interbody devices requires the
removal of one or both facet joints, further destabilizing the
spine. Thus conventional posteriorly placed interbody devices have
been generally limited to interbody fusion devices.
[0018] Since a properly functioning natural FSU relies on intact
posterior elements (facet joints) and since it is necessary to
remove these elements to place a posterior interbody device, a
two-step procedure is disclosed that allows for placement of an
expandable intervertebral implant and replacement of one or both
facets that are necessarily removed during the surgical procedure.
The expansile nature of the disclosed devices allow for restoration
of disc height once inside the vertebral interspace. The expandable
devices are collapsed prior to placement and then expanded once
properly inserted in the intervertebral space. During the process
of expansion, the endplates of the natural intervertebral disc,
which essentially remain intact after removal or partial removal of
the remaining natural disc elements, are compressed against the
device, which thereby facilitates bony end growth onto the surface
of the artificial implant. Once the interbody device is in place
and expanded, the posterior element is reconstructed with the
disclosed pedicle screw and rod system, which can also be used to
distract the disk space while inserting the artificial implant.
Once the interbody device is in place and expanded, the posterior
element is further compressed, again promoting bony end growth into
the artificial implant. This posterior compression allows for
anterior flexion but replaces the limiting element of the facet and
interspinous ligament and thereby limits flexion to some degree,
and in doing so maintains stability for the anteriorly located
interbody device.
[0019] The posterior approach avoids the potential risks and
morbidity of the anterior approach, which requires mobilization of
the vascular structures, the ureter, and exposes the bowels to
risk. Also, the anterior approach does not offer the surgeon an
opportunity to view the posterior neural elements and thereby does
not afford an opportunity for decompression of those elements. Once
an anterior exposure had been utilized a revision procedure is
quite risky and carries significant morbidity.
[0020] The artificial FSU generally comprises an expandable
intervertebral implant and one or more artificial facet joints. The
expandable intervertebral implant generally comprises a pair of
spaced apart plate members, each with a vertebral body contact
surface. The general shape of the plate members may be round,
square, rectangular, banana shaped, kidney shaped, or some other
similar shape, depending on the desired vertebral implantation
site. Because the artificial intervertebral implant is to be
positioned between the facing surfaces of adjacent vertebral
bodies, the plate members are arranged in a substantially parallel
planar alignment (or slightly offset relative to one another in
accordance with proper lordotic angulation) with the vertebral body
contact surfaces facing away from one another. The plate members
are to mate with the vertebral bodies so as to not rotate relative
thereto, but rather to permit the spinal segments to axially
compress and bend relative to one another in manners that mimic the
natural motion of the spinal segment. This natural motion is
permitted by the performance of an expandable joint insert, which
is disposed between the plate members. The securing of the plate
members to the vertebral bone is achieved through the use of a
osteoconductive scaffolding machined into the exterior surface of
each plate member. Alternatively, a mesh of osteoconductive surface
may be secured to the exterior surface of the plate members by
methods known in the art. The osteoconductive scaffolding provides
a surface through which bone may ultimately grow. If an
osteoconductive mesh is employed, it may be constructed of any
biocompatible material, both metal and non-metal. Each plate member
may also comprise a porous coating (which may be a sprayed
deposition layer, or an adhesive applied beaded metal layer, or
other suitable porous coatings known in the art, i.e. hydroxy
appetite). The porous coating permits the long-term ingrowth of
vertebral bone into the plate member, thus permanently securing the
prosthesis within the intervertebral space.
[0021] In more detail, the expandable artificial implant of the
present invention comprises four parts: an upper body, a lower
body, an expandable joint insert that fits into the lower body, and
an expansion device, which may be an expansion plate, screw, or
other similar device. The upper body generally comprises a
substantially concave inferior surface and a substantially planar
superior surface. The substantially planar superior surface of the
upper body may have some degree of convexity to promote the joining
of the upper body to the intact endplates of the natural
intervertebral disc upon compression. The lower body generally
comprises a recessed channel, having a rectangular cross section,
which extends along the superior surface of the lower body in the
medial-lateral direction and substantially conforms to the shape of
the upper and lower bodies. The lower body further comprises a
substantially planar inferior surface that may have some degree of
convexity to promote the joining of the lower body to the intact
endplates of the natural intervertebral disc upon compression. The
expandable joint insert resides within the channel on the superior
surface of the lower body. The expandable joint insert has a
generally flat inferior surface and a substantially convex superior
surface that articulates with the substantially concave inferior
surface of the upper body. Prior to expansion of the artificial
implant, the generally flat inferior surface of the expandable
joint insert rests on the bottom surface of the channel. The
expandable joint insert is raised above the bottom of the channel
by means of an expansion screw, an expansion plate, or other
similar device, that is inserted through an expansion hole or slot.
The expansion hole or slot is disposed through the wall of the
lower body formed by the channel. The expansion hole or slot gives
access to the lower surface of the channel and is positioned such
that the expansion device can be inserted into the expansion hole
or slot via a posterior surgical approach. As the expansion device
is inserted through the expansion slot, into the channel, and under
the expandable joint insert, the expandable joint insert is raised
above the floor of the channel and lifts the upper body above the
lower body to the desired disc height. The distance from the
inferior surface of the lower body and the superior surface of the
upper body should be equal to the ideal distraction height of the
disk space. As the artificial implant is flexed and extended, the
convex superior surface of the expandable joint insert articulates
with the concave inferior surface of the upper body.
[0022] After the insertion and expansion of the expandable
intervertebral implant, the posterior facet joints may be
reconstructed by employing the disclosed artificial facet joints.
One embodiment of the artificial facet joint generally comprises a
lower and upper multi-axial pedicle screw joined by a rod bridging
the vertebral bodies above and below the artificial implant. The
rod comprises a washer-type head at its lower (caudad) end. The rod
fits into the heads of the pedicle screws and a top loaded set
screw is placed in the pedicle screw heads. The disclosed pedicle
screw system may employ different types of pedicle screws so that
the top loaded set screw may or may not lock down on the rod
depending on surgeon preference. If a non-locking pedicle screw is
used the caudad end remains fully multi-axial. The upper (cephalad)
end of the rod is held within the head of the upper pedicle screw
with a set screw which locks down on the rod and eliminates any rod
movement at the cephalad end, which by nature has limited
multi-axial function. In an alternative embodiment of an artificial
facet joint, the rod may comprise washer-type heads on both ends
(caudad and cephalad) so that both pedicle screws can be of the
non-locking variety. In the event of a two level surgical
procedure, three pedicle screws would be employed with a single
rod, which would have washer-type heads at both ends. The middle
pedicle screw would be a locking-type and the upper most and lower
most pedicle screws would be of the non-locking variety.
[0023] In addition, another embodiment of the artificial facet
joint is disclosed that generally comprises two locked pedicle
screws joined by a rod having a ball and socket joint centrally
located on the rod between the two pedicle screws. The locking of
the pedicle screws prevents the screw head from swiveling, but
allows rotation and translation of the rod.
[0024] In instances where a fusion procedure is unavoidable, a PLIF
and TLIF cage are disclosed that utilize the expansion principal of
the functional artificial intervertebral implant. The cage
generally comprises three parts: An external body, an internal
body, and an expansion device. The external and internal bodies
will have substantially the same shape and will be shaped
accordingly to the procedures for which they will be used, more
specifically, a rectangular cage is employed for a PLIF procedure
and round or banana shaped cage is employed for the TLIF procedure.
Both the external and internal bodies comprise a mesh structure in
which an osteoconductive substance can be placed (i.e., morsilized
autograph or an osteobiologic substitute). The external body of the
cage contains an internal void space that houses the internal body.
The external body further comprises an expansion window on its
superior surface through which the internal body is raised upon
expansion of the cage. The internal body comprises a planar plate
member that is slightly larger than the expansion window in the
superior surface of the external body such that when the cage is
expanded the planar plate member secures itself against the
interior side of the expansion window, thereby interlocking the
external and internal bodies and eliminating mobility between the
two bodies. Similar to the functional expandable implant, an
expansion device is placed through an expansion slot. The expansion
device lifts the internal body relative to the external body,
interlocking the planar plate member of the internal body against
the interior of the expansion window, and pushing the mesh
structure of the internal body through the expansion window and
above the superior surface of the external body. Varying the height
of the expansion device and the dimensions of the external and
internal bodies allows for various distraction heights to regain
disc space. As with the functional intervertebral implant, the PLIF
and TLIF cages may take the form of either an expandable lordotic
cage or a non-lordotic cage.
BRIEF DESCRIPTION OF THE DRAWINGS
[0025] Advantages of the present invention will become apparent to
those skilled in the art with the benefit of the following detailed
description and upon reference to the accompanying drawings in
which:
[0026] FIG. 1 is a top view of a round, expandable intervertebral
implant of the present invention.
[0027] FIG. 2 is a side cross-sectional view of the round,
expandable intervertebral implant shown in FIG. 1.
[0028] FIG. 3a is a top view of a banana-shaped, expandable
intervertebral implant of the present invention.
[0029] FIG. 3b is a side cross-sectional view of the banana-shaped,
expandable intervertebral implant shown in FIG. 3a.
[0030] FIG. 4a is a cross-sectional illustration of an expandable
intervertebral implant in compression.
[0031] FIG. 4b is a cross-sectional illustration of an expandable
intervertebral implant in flexion.
[0032] FIG. 5a is a top view of a banana-shaped, expandable
intervertebral implant, illustrating the insertion of expansion
screws to expand the joint.
[0033] FIG. 5b is a top view of a banana-shaped, expandable
intervertebral implant, illustrating the insertion of a
non-threaded expansion device to expand the joint.
[0034] FIG. 6a is a top view of a banana-shaped, expandable
intervertebral implant, illustrating the insertion of an expansion
plate to expand the joint.
[0035] FIG. 6b is a side cross-sectional view of a banana-shaped,
expandable intervertebral implant, illustrating the insertion of an
expansion plate to expand the joint.
[0036] FIG. 6c is a side cross-sectional view of an expandable
intervertebral implant, featuring retaining pegs.
[0037] FIG. 6d is a side cross-sectional view of an expandable
intervertebral implant in flexion, featuring retaining pegs.
[0038] FIG. 7a is a cross-sectional view of an expandable
intervertebral implant, prior to expansion.
[0039] FIG. 7b is a cross-sectional view of an expandable
intervertebral implant, following expansion.
[0040] FIG. 8 is a side perspective view illustrating placement of
an expandable intervertebral implant within an intervertebral
space.
[0041] FIG. 9a is a side view of an artificial facet joint of the
present invention, featuring a rod with two washer-type heads.
[0042] FIG. 9b is a side view of an artificial facet joint of the
present invention, featuring a rod with a single washer-type
head.
[0043] FIG. 9c is a cross-sectional view of a pedicle screw
featuring a locking screw head.
[0044] FIG. 10 is a side view of an artificial facet joint of the
present invention, featuring a rod having a ball joint.
[0045] FIG. 11 is a posterior view of the spine after
reconstruction and implantation of an artificial functional spinal
unit including an expandable intervertebral implant and an
artificial facet joint.
[0046] FIG. 12a is a top view of an expandable PLIF cage in
accordance with the present invention.
[0047] FIG. 12b is a side cross-sectional view of an expandable
PLIF cage in accordance with the present invention prior to
expansion.
[0048] FIG. 12c is a side cross-sectional view of an expandable
PLIF cage in accordance with the present invention following
expansion.
[0049] FIG. 12d is a side cross-sectional view of an expandable
TLIF cage in accordance with the present invention prior to
expansion.
[0050] FIG. 12e is a side cross-sectional view of an expandable
TLIF cage in accordance with the present invention following
expansion.
[0051] FIG. 13a is a posterior view of a banana-shaped lordotic
expandable intervertebral implant.
[0052] FIG. 13b is a top view of a banana-shaped lordotic
expandable intervertebral implant.
[0053] FIG. 14a is a lateral view of a banana-shaped lordotic
expandable intervertebral implant prior to expansion.
[0054] FIG. 14b is a lateral view of a banana-shaped lordotic
expandable intervertebral implant following expansion.
[0055] FIG. 15a is a side cross-sectional view of an expandable
lordotic cage prior to expansion.
[0056] FIG. 15b is a side cross-sectional view of an expandable
lordotic cage following expansion.
[0057] FIG. 16a is a lateral view of a banana-shaped lordotic
expandable intervertebral implant featuring an inclined expansion
plate.
[0058] FIG. 16b is a side cross-sectional view of an expandable
lordotic cage featuring an inclined expansion plate.
[0059] While the invention may be susceptible to various
modifications and alternative forms, specific embodiments thereof
are shown by way of example in the drawings and will herein be
described in detail. The drawings may not be to scale. It should be
understood, however, that the drawings and detailed description
thereto are not intended to limit the invention to the particular
form disclosed, but to the contrary, the intention is to cover all
modifications, equivalents, and alternatives falling within the
spirit and scope of the present invention as defined by the
appended claims.
DETAILED DESCRIPTION
[0060] In the following detailed description of the preferred
embodiments, reference is made to the accompanying drawings, which
form a part hereof, and in which are shown by way of illustration
specific embodiments in which the invention may be practiced. It is
to be understood that other embodiments may be utilized and
structural changes may be made without departing from the scope of
the present invention.
[0061] FIGS. 1 and 2 show a round, expandable artificial
intervertebral implant designated generally at 10. The device is
implemented through a posterior surgical approach by making an
incision in the annulus connecting adjacent vertebral bodies after
removing one or more facet joints. The natural spinal disc is
removed from the incision after which the expandable artificial
intervertebral implant is placed through the incision into position
between the vertebral bodies. The implant is preferably made of a
biocompatible metal having a non-porous quality and a smooth
finish; however, it may also be constructed of ceramic or any other
suitable inert material.
[0062] The expandable artificial intervertebral implant 10
generally comprises an upper body 12 and a lower body 14 in a
substantially parallel planar configuration. The superior surface 2
of the upper body 12 and the inferior surface 4 of the lower body
14 comprise a machined osteoconductive scaffolding 13 through which
the bone may ultimately grow. Osteoconductive scaffolding 13 may
also include spines or barbs that project into and secure against
the bony endplates of the adjacent bony vertebral bodies upon
expansion of the joint and minimize the possibility of sublaxation
and/or dislocation. The upper body 12 has a substantially concave
inferior surface 16. The lower body 14 has a channel 15 in superior
surface 17. Channel 15 has a rectangular cross-section that extends
along the lower body 14 in the medial-lateral direction and
substantially conforms to the shape of the upper 12 and lower 14
bodies. An expandable joint insert 19 resides within the channel 15
on the lower body. The expandable joint insert 19 has a generally
flat inferior surface 20 and a substantially convex superior
surface 21 that articulates with the substantially concave inferior
surface 16 of the upper body 12. The expandable joint insert 19 is
lifted from the bottom of channel 15 by means of an expansion screw
21, or other device, that is inserted between the generally flat
inferior surface 20 of the expandable joint insert 19 and the
bottom of the channel 15 extending along the lower body 14 through
an expansion slot 18. A void space is created between the
expandable joint insert 19 and the floor of the channel 15 in cross
sections not including the expansion device. A securing means, such
as the cables 25, may be employed to ensure the upper body 12 and
the lower body 14 remain intact during flexion and extension of the
FSU. Alternative means for securing the upper body 12 and lower
body 14 may also be employed, such as retaining pegs, torsion
springs, or similar devices.
[0063] FIGS. 3a and 3b show a banana-shaped expandable artificial
intervertebral implant 50. As with the round implant 10 shown in
FIG. 1, the banana-shaped implant also comprises an upper body 52
and a lower body 54 in a substantially planar configuration, each
having an external osteoconductive scaffolding 53. Note that the
channel 55 and the expandable joint insert 59, which is disposed
within the channel 55, substantially conforms to the shape of the
upper 52 and lower 54 bodies. Whereas the round expandable implant
may comprise a single expansion device, the banana-shaped implant
may contain one or more expansion devices 61 that are inserted into
expansion slots 60. Otherwise, the cross-section of the
banana-shaped implant is substantially similar to FIG. 2.
[0064] Turning to FIGS. 4a and 4b, an expandable artificial
intervertebral implant is shown in flexion and extension,
respectively. The concave inferior surface of 16 of upper body 12
articulates with the convex superior surface 21 of expandable joint
insert 19. As stated above, securing means 25 may be employed to
prevent dislocation of the implant.
[0065] FIGS. 5a and 5b illustrate the insertion of expansion
devices into a banana-shaped implant. The artificial intervertebral
implant 50 in FIG. 5a employs expansion screws 70 to expand joint
insert 19. One or more expansion screws 70 may be inserted through
one or more threaded expansion slots 71. Alternatively, as shown in
FIG. 5b, artificial implant 55 may employ a non-threaded expansion
device 72 inserted through a non-threaded expansion slot 73 to
accomplish the expansion of joint insert 19. The non-threaded
expansion slot 73 preferably has an arcuate shape to facilitate
insertion after the artificial disc prosthesis has been properly
placed within the intervertebral space. The non-threaded expansion
device 72 has substantially the same shape as expansion slot 73. A
threaded end cap 74 may be employed to retain the expansion device
72 inside the expansion slot 73.
[0066] FIGS. 6a and 6b illustrate an alternative embodiment of a
non-threaded expansion device. As shown in FIG. 6a, a banana-shaped
artificial intervertebral implant 80 having a wide expansion slot
81 on either the medial or lateral side of the implant 80.
Expansion plate 82 is impacted into place through expansion slot 81
after artificial implant 80 has been properly placed within the
intervertebral space. Similar to the previously described
embodiments, the artificial implant comprises an upper body 83 and
a lower body 84 in a substantially planar configuration, each
having an osteoconductive scaffolding 85 machined on their superior
and inferior surfaces, respectively. Note that the channel 86, as
well as expansion plate 82, substantially conforms to the shape of
the upper 83 and lower 84 bodies. Joint insert 87 also generally
conforms to the shape of the upper 83 and lower 84 bodies, however,
an advantageous shape for the banana-shaped implant 80 is more oval
to provide improved biomechanical motion of the implant. The bottom
floor of channel 86 may also employ a locking lip 88 to ensure that
the expansion plate 82 is properly installed and to minimize the
potential for dislocating expansion plate 82.
[0067] FIGS. 6c and 6d illustrate another embodiment of an
expandable intervertebral implant featuring retaining pegs 91 to
ensure against dislocation of upper body 83 from lower body 84
during flexion, extension and torsional motion. A plurality of
retaining pegs 91 project substantially upward from the superior
surface of lower body 84. On the inferior surface, upper body 83
comprises a plurality of holes, or containment wells 90,
dimensionally larger than captive pegs 91 and arranged such that
when upper body 83 is properly positioned upon lower body 84,
captive pegs 91 are housed within containment wells 90. As shown in
FIG. 6d, when the intervertebral implant is flexed or extended,
captive pegs 91 prohibit dislocation of upper body 83 from lower
body 84. While the pegs and containment wells may be any shape,
captive pegs 91 are preferably round and containment wells 90 are
preferably oval in shape, which gives limited torsional mobility as
well.
[0068] FIGS. 7a and 7b illustrate the expansion of joint insert 19
in more detail. As shown in FIG. 7a and prior to expansion of joint
insert 19, upper body 12 rests upon lower body 14 and the generally
flat inferior surface 20 of joint insert 19 rests upon the bottom
of channel 15, which extends along the lower body 14. Disposed
along the generally flat inferior surface 20 of expandable joint
insert 19 and adjacent to expansion slot 18, is a lifting notch 17
that engages with the expansion screw 70. Lifting notch 17
facilitates the lifting of expandable joint insert 19 and allows
expansion screw 70 to come into contact with the generally flat
inferior surface 20 of joint insert 19. Once inserted, as shown in
FIG. 7b, the generally flat inferior surface 20 of expandable joint
insert 19 rests upon expansion screw 70 and the upper body 12 is
lifted above lower body 14 to the desired intervertebral disc
height 71.
[0069] FIG. 8 shows an expandable artificial intervertebral implant
10 inserted into the spinal column. Note that the expandable
artificial implant 10 is posteriorly inserted and expanded through
void space 90, which is created by removal of a facet joint.
[0070] The disclosed techniques of expanding an artificial implant
by inserting an expansion plate or similar device may also be
employed to expand a PLIF or TLIF cage. As shown in FIGS. 12a, 12b
and 12c, a PLIF cage 300 is disclosed comprising a substantially
rectangular external cage element 301 housing an internal
expandable element 302. The PLIF cage element 301 has an
osteoconductive mesh structure 303, in which an osteoconductive
substance can be placed, on its inferior surface 304 and an
expansion window 305 located on its superior surface 306. The
internal expandable element 302 comprises a generally planar plate
member 307 having an inferior 308 and superior surface 309. A
second osteoconductive mesh structure 310 is secured upon the
superior surface 309 of the planar plate member 307 of the internal
expandable element 302. The inferior surface 308 of the planar
plate member 307 has a lifting notch 311 to facilitate the
expansion of the device upon installation of the expansion
plate312. The expansion plate 312 is inserted into the posteriorly
located expansion slot 313 of the PLIF external cage element 301
and engages the lifting notch 311 of the planar plate member 307 of
the internal expandable element 302. Locking lip 314 located within
expansion slot 313 minimizes the potential of expansion plate 312
dislocation.
[0071] FIGS. 12d and 12e show a TLIF cage similar to the PLIF cage
described above. The primary difference between the TLIF cage and
the PLIF cage is that the TLIF cage comprises a t-shaped
cross-sectional osteoconductive mesh structure 310 secured upon the
superior surface 309 of the planar plate member 307 of the internal
expandable element 302 such that the osteoconductive mesh structure
310 overhangs the superior surface 306 of the external cage element
301. Thus providing more surface area between the osteoconductive
mesh structure 310 and the bony endplates within the intervertebral
space.
[0072] One embodiment of an artificial facet joint 100 is shown in
FIG. 9a. Artificial facet joint 100 comprises an upper pedicle
screw 101 and a lower pedicle screw 102. Rod 103 is retained within
the head 104 of upper pedicle screw 101 and the head 105 of lower
pedicle screw 102. Rod 103 has washer-type ends 106 that allows for
posterior compression, but not extension.
[0073] Another embodiment of an artificial facet joint 110 is shown
in FIG. 9b. Rod 113 comprises a single washer-type end 116 on its
lower end 117. The head 115 of upper pedicle screw 112 has a
threaded locking screw 118, as shown in FIG. 9c, that holds rod 113
in place and prohibits the head 115 of pedicle screw 112 from
swiveling, but allows rod 113 to rotate and translate through the
head 115 of pedicle screw 102.
[0074] Another embodiment of an artificial facet joint 200 is shown
in FIG. 10. Artificial facet joint 200 generally comprises an upper
pedicle screw 201 and a lower pedicle screw 202 and rod 203
retained within the heads of pedicle screws 201, 202. Both pedicle
screws 201, 202 are secured with locking screws 218 that prevent
the heads 204, 205 of pedicle screws 201, 202 from swiveling, but
allow rotation and translation of rod 203. Rod 203 comprises two
rod members 206, 207 connected via a ball joint 208. Ball joint 208
allows for a generally upward rotation, away from the bony surfaces
of the vertebrae to which they are secured, but prohibit a
generally downward rotation, which would bring the ball joint in
contact with the vertebrae to which they are secured.
[0075] FIG. 11 shows the artificial facet joint 200 of FIG. 10 in
place on the spinal column. Note that artificial intervertebral
implant 10 has been posteriorly placed within the intervertebral
space through the void created by the surgical removal of the
natural facet joint. In addition, ball joint 208 generally rotates
in the posterior (upward) direction during posterior compression to
prevent impact upon the bony surfaces of the spine.
[0076] FIGS. 13a, 13b, 14a and 14b illustrate a lordotic,
banana-shaped expandable artificial intervertebral implant 400. The
lumbar spine is lordotic, thus the anterior disc height is
naturally larger than the posterior disc height. Therefore, an
expandable artificial intervertebral implant for the lumbar spine
must be capable of expanding into a lordotic position. FIG. 13a
shows the lordotic expandable artificial intervertebral implant 400
from a posterior view. Lordotic expandable artificial
intervertebral implant 400 generally comprises an upper body 412
and a lower hinged body 414 in a substantially planar configuration
prior to expansion. The superior surface 402 of the upper body 412
and the inferior surface 404 of the lower hinged body 414 comprise
an osteoconductive scaffolding 413 through which the bone may
ultimately grow. The upper body 412 has a substantially concave
inferior surface 416.
[0077] The lower hinged body 414 comprises a lower portion 420 and
an upper portion 430. Lower portion 420 and upper portion 430 are
posteriorly hinged via hinge 440. Hinge 440 effectively fixes the
posterior disk height 460 (shown in FIG. 14b). Upper portion 430 of
hinged body 414 has a generally flat inferior surface 431 and a
substantially convex superior surface 432. The lower portion 420
has a substantially planar configuration prior to expansion.
Located at the anterior end 421 of lower portion 420 is a
rotational lifting mechanism 422. Once placed in the intervertebral
space, the rotational lifting leg is rotationally engaged, thus
lifting the anterior end 421 of the expandable artificial
intervertebral implant 400 to achieve the desired anterior disc
height 470 and proper lordosis. Securing notch 425 is located on
the anterior end 421 of the upper portion 430 of hinged body 414.
Securing notch 425 engages with rotational lifting mechanism 422
once the expandable artificial intervertebral implant 400 has been
expanded. The height of rotational lifting mechanism 422 is
determined by the desired proper lordosis when the intervertebral
implant 400 is under neutral load.
[0078] Upper body 412 has a substantially concave inferior surface
416 that articulates with the substantially convex superior surface
432 of upper portion 430 of lower hinged body 414. When viewed in
the medial or lateral direction, as shown in FIGS. 14a and 14b,
upper body 412 has a downwardly projecting lobe 450 for the
attachment of safety bar 452. Safety bar 452 secures upper body 412
to upper portion 430 of lower hinged body 414 and minimizes the
possibility of dislocation.
[0079] FIG. 13b is a top view of lordotic expandable artificial
intervertebral implant 400 illustrating the placement of posterior
hinge 440, rotational lifting mechanism 422, and safety bar 452
affixed through upper body 412 and upper portion 430 of lower
hinged body 414.
[0080] The rotational lifting mechanism described above may also be
employed to achieve proper lordosis with an expandable PLIF and
TLIF cage, as shown in FIGS. 15a and 15b. Cage 500 is shown prior
to expansion in FIG. 15a and expanded in FIG. 15b. Cage 500
comprises an upper body 502 and a lower body 504. Hinge 506
posteriorly connects upper body 502 to lower body 504 and
effectively fixes posterior disc height 510 upon expansion of cage
500. The superior surface 512 of upper body 502 and the inferior
surface 514 of lower body 504 may include an osteoconductive
scaffolding or mesh 520 as previously described. Expansion of cage
500 is accomplished via rotational lifting mechanism 530, which
engages with securing notch 525, located on the anterior end 528 of
the inferior surface 513 of upper body 502, and minimizes the
potential for dislocation. The height of rotational lifting
mechanism 530, which effectively fixes anterior disc height 540, is
determined by the desired proper lordosis.
[0081] Another embodiment of an expandable lordotic artificial
intervertebral implant is illustrated in FIGS. 16aand 16b. Lordotic
expandable intervertebral implant 600 and lordotic cage 700 both
utilize an inclined expansion plate 650 to achieve proper lordosis.
Both devices are similar to those described above with the
exception of the expansion device and reference is made to FIGS.
14a and 14b for lordotic expandable intervertebral implant 600 and
FIGS. 15a and 15b for lordotic cage 700 for elements of the
intervertebral implants already identified. Expansion plate 650 is
generally wedged-shaped and comprises a lifting notch 620 on its
posterior end 622 to facilitate expansion. As shown in FIG. 16a,
expansion plate 650 is installed between the upper portion 430 and
lower portion 420 of lower hinged body 414. Located on the superior
surface 630 at the anterior end 624 is securing ridge 635. Securing
ridge 635 engages with securing notch 625 similar to the rotational
lifting mechanism described above. Located on the anterior superior
surface of lower portion 420 of lower hinged body 414 is a locking
lip 637, which minimizes the potential of dislocating inclined
expansion plate 650. FIG. 16b illustrate the use of expansion plate
650 in conjunction with lordotic cage 700.
[0082] Although the present invention has been described in terms
of specific embodiments, it is anticipated that alterations and
modifications thereof will no doubt become apparent to those
skilled in the art. It is therefore intended that the following
claims be interpreted as covering all alterations and modifications
that fall within the true spirit and scope of the invention.
* * * * *