The present invention relates to the field of spinal implants and, more particularly, to implants comprising intervertebral disc replacements that provide dynamic spinal stabilisation.
The spine is a complicated structure comprised of various anatomical components, which, while being extremely flexible, provides structure and stability for the body. The spine is made up of vertebrae, each having a ventral body of a generally cylindrical shape. Opposed surfaces of adjacent vertebral bodies are connected together and separated by intervertebral discs (or “discs”), comprised of a fibrocartilaginous material. The vertebral bodies are also connected to each other by a complex arrangement of ligaments acting together to limit excessive movement and to provide stability. A stable spine is important for preventing incapacitating pain, progressive deformity and neurological compromise.
The anatomy of the spine allows motion (translation and rotation in a positive and negative direction) to take place without much resistance but as the range of motion reaches the physiological limits, the resistance to motion gradually increases to bring the motion to a gradual and controlled stop.
Intervertebral discs are highly functional and complex structures. They contain a hydrophilic protein substance that is able to attract water thereby increasing its volume. The protein, also called the nucleus pulposis is surrounded and contained by a ligamentous structure called the annulus fibrosis. The main function of the discs is load bearing and motion. Through their weight bearing function, the discs transmit loads from one vertebral body to the next while providing a cushion between adjacent bodies. The discs allow movement to occur between adjacent vertebral bodies but within a limited range thereby giving the spine structure and stiffness.
Due to a number of factors such as age, injury, disease etc., it is often found that intervertebral discs lose their dimensional stability and collapse, shrink, become displaced, or otherwise damaged. It is common for diseased or damaged discs to be replaced with prostheses and various versions of such prostheses, or implants, as are known in the art. One of the known methods involves replacement of a damaged disc with a spacer into the space occupied by the disc. However, such spacers also fuse together the adjacent vertebrae thereby preventing any relational movement there-between.
More recently, disc replacement implants that allow movement between adjacent vertebrae have been proposed. Examples of some prior art implants are provided in the following U.S. patents: U.S. Pat. No. 5,562,738 (Boyd et al.); U.S. Pat. No. 6,179,874 (Cauthen); and U.S. Pat. No. 6,572,653 (Simonson).
Unfortunately, the disc replacement (i.e. implant) solutions taught in the prior art are generally deficient in that they do not take into consideration the unique and physiological function of the spine. For example, many of the known artificial disc implants are unconstrained with respect to the normal physiological range of motion of the spine in the majority of motion planes. Although some of the prior art devices provide a restricted range of motion, such restrictions are often outside of the normal physiological range of motion; thereby rendering such devices functionally unconstrained. Further, the known unconstrained implants rely on the normal, and in many cases diseased structures such as degenerated facets, to limit excessive motion. This often leads to early facet joint degeneration and other collateral damage to spinal components.
In addition, many of the artificial discs known in the art do not provide mechanisms for minimising stress upon adjacent structures caused by sudden motions.
Thus, there exists a need for an intervertebral disc implant that overcomes at least some of the deficiencies in the prior art solutions. More particularly, there exists a need for a spinal implant that allows for the reconstruction of spinal structures while preserving motion and protecting the facet joints of the affected segment of the spine from accelerated degeneration.
In one aspect, the present invention provides an implant for replacing intervertebral discs.
In another aspect, the invention provides an artificial intervertebral disc that allows adjacent vertebrae a range of motion about various axes. Such motion is limited to a predetermined range within which movement of adjacent vertebrae does not lead to deterioration of neighbouring spinal structural components.
In another aspect, the above-mentioned motion about various axes can be coupled to more closely simulate natural movement.
Thus, in one aspect, the invention provides an artificial intervertebral disc for implantation between first and second adjacent vertebrae of a spine, the disc comprising:
an outer casing comprising cooperating first and second shells and defining a first compartment, the first and second shells being relatively moveable with respect to each other;
an inner casing comprising a cup and a cooperating lid, the cup and lid being relatively moveable with respect to each other, the inner casing defining a second compartment; and,
a resilient nucleus;
wherein,
a) the lid and cup of the inner casing are sized to have one of the cup or lid received within the other of the cup or lid;
b) the inner casing is substantially contained within the first compartment of the outer casing; and,
c) the resilient nucleus is substantially contained within the second compartment of the inner casing, the nucleus being biased against the cup and lid for elastically separating the cup and lid.
The features of the invention will become more apparent in the following detailed description in which reference is made to the appended drawings wherein:
In the following description, the terms “superior”, “inferior”, “anterior”, “posterior” and “lateral” will be used. These terms are meant to describe the orientation of the implants of the invention when positioned in the spine. Thus, “superior” refers to a top portion and “posterior” refers to that portion of the implant (or other spinal components) facing the rear of the body when the spine is in the upright position. It will be appreciated that these positional terms are not intended to limit the invention to any particular orientation but are used to facilitate description of the implant.
The present invention provides artificial discs or implants for replacing intervertebral discs that are damaged or otherwise dysfunctional. The implants of the present invention are designed to allow motion between adjacent vertebral bodies but within normal limitations.
In general terms, the present invention provides a spinal implant for replacing intervertebral discs. The implant of the invention is generally comprised of various interlocking sections that are moveable relative to each other and which contain a resilient, force-absorbing nucleus. The relative movement between the components of the disc of the invention includes various degrees of freedom but is limited to a specified range. The present invention provides an artificial spinal disc for the replacement of intervertebral discs in the spinal column. The present invention, as will be described further below, allows for unconstrained and partially constrained vertebral motions at the site of spinal column insertion. In particular, the artificial disc of the invention provides for rotational, flexion, extension and lateral motions that are similar to normal movements in the neutral and elastic zones (i.e. the movements associated with a normal or intact disc). In addition, the device of the invention also allows various combinations of such motions, such as coupled motions. For example, the disc of the invention can be subjected to flexion and translation, or lateral flexion and lateral translation, or flexion and rotation. Various other motions will be apparent to persons skilled in the art given the present disclosure.
One embodiment of the spinal implant of the invention is illustrated in FIGS. 2 to 4. In the embodiment illustrated in these figures, the implant 10 is comprised of two overlapping casings, an internal casing 12 that is substantially enveloped by an external casing 14. As shown in the figures and as will be understood by persons skilled in the art, the term “substantially” as used in this context means that the inner casing 12 is for the most part surrounded by the outer casing 14 but that some portion of the inner casing may be exposed (i.e. not enveloped). Each of the casings 12 and 14 are comprised of two co-operating sections. The anterior and posterior ends of the implant are shown at 11 and 13, respectively. As shown, the inner casing 12 is comprised of a superior section or lid 16 (or “superior annulus”) and an inferior section or cup 18 (or “inferior annulus”). Similarly, the outer casing 14 is comprised of a superior section or superior shell 20 (or “superior endplate”) and an inferior section or inferior shell 22 (or “inferior endplate”). These sections are discussed further below. It is noted that although the term “annulus” is used throughout this description, it is done purely as a matter of convenience and this term is not meant to indicate that the lid 16 or cup 18 must have a fenestration, although this may be possibility in one embodiment of the invention.
As illustrated in FIGS. 2 to 4, the outer casing 14 has a generally ovoid or ellipsoid shape when viewed in the superior aspect (i.e.
In addition to the provision of increased surface area, the outer surfaces of the superior and inferior shells may be provided with one or more other promoters for bony in-growth. Such factors may be physical and/or chemical in nature. For example, the outer surface may be provided with a plurality of holes or pins and the like to which bone can attach. Alternatively or in combination, the outer surfaces of the shells may be provided with chemical bone growth components. These and other bone growth factors will be known to persons skilled in the art.
The inferior shell 22 (or inferior endplate) of the outer casing 14 includes a generally circular recess 28 (or “discoid recess”) for receiving the cup or inferior annulus 18. As illustrated in
The cup 18 (or inferior annulus) of the inner casing 12 includes a generally circular base 34 with a generally upwardly extending sidewall 36. As shown in
The base 34 of the cup 18 is adapted to receive and contain a resilient nucleus 37, which is discussed further below. The nucleus 37, according to the embodiment of the invention shown in
The lid 16 (or superior annulus) of the inner casing 12 is adapted to fit over the cup 18. The lid 16 comprises a generally circular cover 38 having, as shown in
b illustrates a variation in the sizing of the groove 42. As shown, in one aspect, the groove 42 of the lid 16 may be wider (or oversized) than the sidewall 36 of the cup 18. As will be understood, such difference in size will enable a degree of relative translational movement between the cup and lid. Thus, in this aspect, the disc would limit flexion but would allow some degree of ventral or dorsal translation. It will be understood that the degree of translational movement allowed will depend on the amount of clearance provided to the sidewall 36 within the groove 42. It will also be understood that a similar oversizing may be provided in the opposite groove 44 of the lid 16.
The superior external surface 46 of the lid 16 is provided with a convexly curved anterior portion 48 and a generally flat posterior portion 50 or “turtledeck”. The inferior surface of the lid 16 includes an anterior section 47 that is adapted to contain the thicker anterior portion 39 of the nucleus. The inferior surface of the lid also includes a posterior section 49 that is angled so as to contain the ramped surface 45 of the nucleus. Thus, the combination of the superior surface of the cup 18 and the inferior surface of the lid 16 forms a nucleus cavity, for containing the nucleus 37 there-within. As will be understood, during the application of a compressive force on the implant, the volume of the nucleus cavity will be reduced. For this reason, as shown in
It should be noted that the position and radius of curvature of the curved portion 48 may be changed in other embodiments. For example, depending upon the range of motion desired, the curved portion may be placed further posteriorly. In addition, it will be understood that the radius of curvature of the curved portion 48 will also affect the range of motion offered by the disc of the invention. This is discussed further herein.
The superior shell 20 (or superior endplate) includes an inner surface having an anterior end provided with a concave surface 52 that is adapted to slide over the convex surface 48 of the lid 16 (as discussed further below). Similarly, the posterior end of the superior shell 20 inner surface is includes a generally horizontal surface 53 that is adapted to slide over the turtledeck 50 of the lid 16. As shown in
The posterior end of the superior shell 20 includes a generally downwardly extending flange 54 terminating with a hook 56. As illustrated in
As shown in
As also illustrated in
The nucleus 37 of the invention, as indicated above, comprises a resilient material. In one embodiment, such material comprises a hydrogel, which is a material known in the art. However, alternative materials may also be used for the nucleus. For example, the nucleus may comprise a combination of mechanical springs, or an alternative compressible material as would be known to an individual of skill in the art. Generally, the nucleus is made from resiliently compressible materials. As can be seen in
FIGS. 6 to 8 illustrate another embodiment of the invention wherein elements common with the embodiment described above are identified with common reference numerals but with the letter “a” added for clarity. As with the embodiment described above, the artificial disc 10a illustrated in
As can be seen, in the embodiment illustrated in
A further embodiment of the invention is illustrated in
A further embodiment of the invention is illustrated in
A further embodiment of the invention is illustrated in
Summary of Features of the Invention
As discussed above, the artificial disc of the present invention includes various features, which will now be summarised. Firstly, in one aspect, the disc isolates axial rotation, lateral bending, and flexion/extension into component vectors and includes various structural components to accommodate such movements. In the result, the disc generally reproduces neutral zone and elastic zone movements associated with an intact disc along such individual component vectors. Further, the invention allows for unconstrained and partially constrained coupled movements making use of engineered end-points that prevent excessive or non-physiological movement. The fully constrained stop mechanisms (i.e. the “hard stops”) ensure that movement is not extended past the elastic zone.
In another embodiment, the disc of the invention may be generally wedge shaped in the sagittal plane so as to integrate with and promote a lordotic spine configuration. Such an implant may be used in cases where spinal re-alignment is sought. For example, the disc may have a larger height at the anterior end as compared to the height of the posterior end to provide the aforementioned wedge shape. Similarly, such a difference in height may also be provided between the lateral sides of the disc, that is in the coronal plane. This type of configuration may be used, for example, to correct a malalignment such as scoliosis.
The generally spherically curved external surfaces of the shells provide the disc of the invention with an ovoid curvature in the coronal plane. This structure maximises disc to bone surface area and thereby promotes bony ingrowth. Such structure also maximises prosthetic occupation of the disc space while stabilizing disc against bone after implantation. It will also be understood that the ovoid lateral curvature also maximises stability on floating annulus/nucleus complex in the coronal plane.
As will be appreciated by persons skilled in the art, the wedge shaped configuration of the nucleus and of the inner casing 12, in combination with the generally loose integration of the superior and inferior shells (20 and 22), facilitates the removal and replacement of the annulus/nucleus complex from an anterior approach. This is an important feature when the nucleus and/or annulus needs to be extracted after implantation for later revision or replacement.
As discussed above, the superior shell 20 associates loosely with the inferior shell 22 thereby allowing the superior shell 20 to float on the annulus and nucleus structures. Therefore, the annulus and nucleus serve to provide a “rotating platform” which supports the shells 20 and 22.
Vertically extending shell, or endplate stabilisers serve to provide a “hard stop” against excessive coronal or sagittal translation of the shells, while allowing moderate degrees of translation in these same planes between the endplate, annulus, and nucleus components. The shell stabilisers also provide a hard stop for axial rotation after a predefined amount of angular motion is achieved.
A “tongue and groove” relationship is provided between the superior and inferior annulus, which is achieved by the tongues extending from the inferior annulus being received within the anterior and posterior grooves 42 and 44, respectively, provided on the superior annulus. The preferred slanted or angled nature of the tongue and groove arrangement, in combination with the preferred wedge shaped design (as described above), serves to minimise translation (shear) across the nucleus while facilitating compression of the nucleus in flexion, neutral, or extension attitudes.
As illustrated in the figures, the surface areas of the base 43 of inferior annulus (or cup) 18 and the recess 28 of the inferior shell are relatively large in comparison with artificial disc. By maximising the surface areas of these components, it will be appreciated that any axial load on the disc is distributed over a greater area during all movements. In particular, such load distribution is achieved during flexion and extension movements, thereby minimising wear between the inferior annulus 18 and the inferior shell 22.
The posterior shell catch mechanism allows for angulation of its latch components to maintain locking competence during flexion and translation of the superior shell on the annulus/nucleus/inferior shell.
The floating configuration of the annulus/nucleus and superior/inferior shells transmits unconstrained axial loads through the nucleus even when the spine is not in a neutral position.
In other embodiments, the curved portion 48 of the superior annulus 16 may be moved more anterior or posterior to create different flexion/extension axes of rotation for different areas of the spine. In other embodiments, the radius of curvature of the curved portion 48 may be increased or decreased to create different flexion/extension axes of rotation.
The external surfaces of the superior and inferior shells may be curved or spherical (i.e. ovoid, elliptical) or straight (i.e. squared) for insertion into bi-concave or rectangular discectomy site at any area of the spine. The external surfaces may optionally be provided with anchoring ribs or keels for securing the disc to adjacent bone structures. The keels are preferably provided on the outer surfaces of the “squared” shells for increasing the stability of the prosthesis upon implantation. The keels, preferably provided in pairs on each surface, also serve to provide screw conduits for attachment of the artificial disc shells to an artificial vertebral body. Keels can also be used to run side to side (i.e. parallel to the coronal plane) particularly for implantation of discs from a lateral exposure.
In one embodiment, the superior shell may be larger in diameter, as taken in the sagittal plane (i.e. the anterior-posterior direction), than inferior shell so as to better approximate the “normal” condition.
In one embodiment, dimples or bumps may be provided on the anterior and posterior midline of the shell outer surfaces so that their alignment and positioning can be verified on x-rays.
In another embodiment, wedge shaped lordotic shells can be substituted for curved or squared shells to help realign the spine
The footprint of the disc is preferably maximised in both the coronal and sagittal planes to help eliminate subsidence. As will be understood, the size of the discs of the invention will vary to accommodate various sizes of discs in the normal spine.
The anterior end of the inferior shell and the discoid recess are provided with ledges to prevent anterior extrusion of the nucleus and/or the annulus once the prosthesis is implanted.
Other features of the invention will now be discussed with specific reference to directional movements.
1) Flexion and Extension
As indicated above, and as illustrated in
In other embodiments of the invention, the axis of rotation of the curve of the superior annulus may be positioned in other locations and/or the radius of curvature may be varied. For example in an alternate embodiment, the curved region of the superior annulus may be located further toward the posterior portion of the disc body in order to change the characteristics of spinal flexion and axial loading on the artificial disc. This can be seen in comparing
As will be apparent from the above discussion, neutral zone movement of the artificial disc of the invention, when in initial flexion, is provided by rotation of the superior shell over the superior annulus convex region. Elastic zone movement occurs with compression of the nucleus, which is necessitated by progressive distraction of posterior spinal elements during advanced flexion. Elastic zone movement in flexion unloads facets by rotating a superior facet away from an inferior facet of an adjacent vertebra without causing impaction of the facets or shear through them.
A “hard stop” in a flexion motion is provided by the posterior shell catch mechanism, or hooks after a predetermined amount of movement. Such a hard stop prevents excess motion beyond the elastic zone. The locking components of the posterior shell catch mechanism are preferably angled to maintain locking competence during flexion and translation. As will be appreciated, the compression of the nucleus prior to engagement of the hard stop (wherein the nucleus compression serves as a soft stop) serves to reduce the amount of wear on the catch mechanism.
The floating configuration of the superior shell on the superior annulus also allows for neutral zone movement during extension. Such movement narrows the gap or space above the turtledeck of the superior annulus. Compression of the superior shell horizontal region on the turtledeck during extension is transmitted to the nucleus providing elastic zone movement. The turtledeck also provides a hard stop after a predetermined amount of motion to prevent excessive movement.
The tongue and groove relationship of the superior annulus and the inferior annulus, in addition to the posterior shell catch mechanism, provide a hard stop in extension preventing excessive movement through the prosthesis after a predetermined amount of motion.
2) Rotation
The sidewalls of the superior shell constrain the superior annulus therewithin. Further, due to the fact that the inferior annulus is constrained by the superior annulus, it will be understood that any rotational movement of the superior shell forces the entire annulus (i.e. superior and inferior parts), and the resilient nucleus contained therein, to rotate with the superior shell against the inferior shell.
In a preferred embodiment, the discoid shape of the bottom of the inferior annulus integrates with the larger discoid recess in the inferior shell. This allows sagittal and lateral translation during twisting movements and, thereby eccentric rotation. As will be understood by persons skilled in the art, such movements serve to effectively mimic the physiological axis of rotation of normal discs. Further, the walls of the recess provided in the inferior shell also serve as hard stops for any excessive sagittal or lateral translation movement of the inferior annulus.
As explained above, the lateral shell stabilisers provide a hard stop for relative rotation of the superior shell and the inferior shell.
3) Lateral Bending
As indicated above, the superior annulus is adapted to fit over the inferior annulus whereby the inferior annulus is able to telescope inside the superior annulus. The space between the lateral walls of the superior annulus and the inferior annulus allows for lateral bending (bending in the coronal plane) with the eccentric compression of the nucleus. The neutral zone remains confined to neutral spinal alignment encouraging the spine to remain straight, avoiding a scoliotic attitude. The stabilisers provided laterally on the shells serve as a hard stop after a predetermined amount of lateral bending. It will be appreciated that such limitation prevents excessive lateral motion.
4) Coupling Motions
As described above, during flexion, the nucleus of the artificial disc compresses as the superior shell slides over the curvature of the superior annulus. Such movement causes the axis of rotation to descend with respect to the adjacent inferior vertebral body thereby mimicking the physiological relationships in the intact normal disc. Thus, the coupling of the movement of the superior shell over the curvature of the superior annulus and the flexion induced compression of the nucleus results in a gradual loading of the normal posterior elements in flexion until the hard stop is reached. As mentioned above, this combined movement reduces the wear on the posterior shell elements providing the hard stop.
The floating annulus/nucleus complex of the present invention, as described above, allows the aforementioned flexion/extension and axial rotation motions to be coupled with lateral bending thereby mimicking normal physiological movement.
Coupling of lateral angulation and lateral (coronal) translation with lateral bending occurs until the hard stop of the lateral shell stabilisers is encountered.
5) Compression
The tongue and groove arrangement provided on the anterior and posterior ends of the superior and inferior annuli provides stability and protects the resilient nucleus against translational shear. Further, such arrangement provides a defined limitation (i.e. a hard stop) on the degree of nucleus compression.
The generally trapezoidal shape of the resilient nucleus (when taken in sagittal cross section) allows maximum durability under loads of eccentric compression from directions other than true axial loading. As mentioned above, the nucleus cavity is designed to be larger than the nucleus itself. It will be understood that such extra space between the sides of the resilient nucleus and the superior annulus and the inferior annulus allows for lateral expansion during compression of the nucleus such as during axial loading of the disc.
The disc of the invention can be made with a variety of materials as will be known to persons skilled in the art. For example, the shells and annulus sections may be manufactured from steel, stainless steel, titanium, titanium alloy, porcelain, and plastic polymers. The nucleus may comprise mechanical springs (for example made of metal), hydraulic pistons, a hydrogel or silicone sac, rubber, or a polymer or elastomer material.
Although the invention has been described with reference to certain specific embodiments, various modifications thereof will be apparent to those skilled in the art without departing from the purpose and scope of the invention as outlined herein. The entire disclosures of all references recited above are incorporated herein by reference.
The present application is a Continuation of PCT application no. PCT/CA2006/000677, filed May 2, 2006, which claims priority from U.S. application No. 60/594,732, filed May 2, 2005. The entire disclosures of these applications are incorporated herein by reference.
Number | Date | Country | |
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60594732 | May 2005 | US |
Number | Date | Country | |
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Parent | PCT/CA2006/000677 | May 2006 | US |
Child | 11978872 | Oct 2007 | US |