The present invention relates to the field of spinal implants and, more particularly, to intervertebral disc prostheses, or artificial intervertebral discs.
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 (including load distribution and shock absorption) 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, are known in the art. One of such implants comprises a spacer that is inserted into the space occupied by the disc. However, such spacers have been found to result in fusion of the adjacent vertebrae, thereby preventing relative movement there-between. This often leads to the compressive forces between the vertebrae in question to be translated to adjacent vertebrae, thereby resulting in further complications such as damage to neighboring discs and/or damage to facet joints and the like.
More recently, disc replacement implants that allow various degrees of movement between adjacent vertebrae have been proposed. Examples of some prior art implants are provided in the following: 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, or 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 or further facet joint degeneration and other collateral damage to spinal components.
In addition, many of the artificial discs known in the art, such as U.S. Pat. Nos. 5,562,738 (mentioned above) and 5,542,773, and United States Patent Application Nos. 2005/0149189 and 2005/0256581, generally comprise a ball and socket joint that is implanted between adjacent vertebral bodies. One of the issues associated with such devices is the difficulty in designing constraints to motion. Quite often, such constraints are provided by the soft tissue adjacent to the implant, thereby resulting in a limited degree of constraint and/or damage to such tissue structures. Where constraints are provided, typical ball and socket implants are not easily adapted to for providing various types and degrees of constraint as may be required depending on the need.
In one aspect, the present invention provides an artificial disc or implant comprising a ball and ring combination, which generally combines the features of known ball and socket designs but which includes at least some degree of versatility in terms of the type and degree of constraint that can be built into the device. The implant of the invention also provides for variations in the type of motion and center of rotation.
In one aspect, the invention comprises an artificial disc having two main sections or components, each being adapted to be positioned against opposed vertebral body surfaces of adjacent vertebrae. One of the two sections including a “ball” structure comprising a convex bearing surface. The other of the sections including a “ring” structure comprising a ring adapted to receive and constrain at least a portion of the convex surface.
In another aspect, one or both of the aforementioned sections may include one or more “stops” or restrictive structures for limiting the range of relative movement between the two sections.
Thus, in one aspect, the invention provides an artificial intervertebral disc for implantation between adjacent superior and inferior vertebrae of a spine, the disc comprising first and second cooperating shells, each of the shells having opposed inner surfaces and oppositely directed outer surfaces, the outer surfaces being adapted for placement against the vertebrae; the inner surface of the first shell including a convex protrusion; and, the inner surface of the second shell including an articulation surface and a motion constraining ring adapted to receive the convex protrusion when the first and second shells are combined, wherein, when in use, the articulation surface of the second shell contacts and bears against the convex protrusion, and the ring constrains relative movement between the convex protrusion and the second shell.
The nature and mode of operation of the present invention will now be more fully described in the following detailed description of the invention in view of the accompanying drawing figures, in which:
a is a sagittal cross sectional view of the artificial intervertebral disc of the invention according to one embodiment;
b is a transverse cross sectional view of the disc of
a, 12a and 13a are sagittal cross sectional views of the artificial intervertebral disc of the invention according to other embodiments;
b, 12b and 13b are transverse cross sectional views of the artificial intervertebral discs of
a, 17a and 18a are sagittal cross sectional views of the artificial intervertebral disc of the invention according to other embodiments; and,
b, 17b and 18b are side perspective views of the rings of the discs shown in
At the outset, it should be appreciated that like drawing numbers on different drawing views identify identical, or functionally similar, structural elements of the invention. It also should be appreciated that figure proportions and angles are not always to scale in order to clearly portray the attributes of the present invention.
While the present invention is described with respect to what is presently considered to be the preferred aspects, it is to be understood that the invention as claimed is not limited to the disclosed aspects. The present invention is intended to include various modifications and equivalent arrangements within the spirit and scope of the appended claims.
Furthermore, it is understood that this invention is not limited to the particular methodology, materials and modifications described and, as such, may, of course, vary. It is also understood that the terminology used herein is for the purpose of describing particular aspects only, and is not intended to limit the scope of the present invention, which is limited only by the appended claims.
Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood to one of ordinary skill in the art to which this invention belongs. 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 and are not intended to limit the scope of the invention in any way. 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 patient's body when the spine is in the upright position. Similarly, the term “inferior” will be used to refer to the bottom portions of the implant while “anterior” will be used to refer to those portions that face the front of the patient's body when the spine is in the upright position. With respect to views shown in the accompanying figures, the term “coronal” will be understood to indicate a plane extending between lateral ends thereby separating the body into anterior and posterior portions. Similarly, the term “laterally” will be understood to mean a position parallel to a coronal plane. The term “sagittal” will be understood to indicate a plane extending anteroposterior thereby separating the body into lateral portions. The term “axial” will be understood to indicate a plane separating the body into superior and inferior portions. It will be appreciated that these positional and orientation terms are not intended to limit the invention to any particular orientation but are used to facilitate the following description. Although any methods, devices or materials similar or equivalent to those described herein can be used in the practice or testing of the invention, the preferred methods, devices, and materials are now described.
In general terms, 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 various degrees of motion between adjacent vertebral bodies, but preferably within acceptable limits. In one embodiment, the invention is designed to permit relative movement between the vertebrae adjacent to the artificial disc of the invention, such movement including various degrees of freedom but preferably limited to a specified range. In one embodiment, the artificial disc, or prosthesis, of the invention is provided with one or more “soft” and/or “hard” stops to limit motion between the adjacent vertebrae. In particular, the artificial disc of the invention provides for rotation, 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, or 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.
a illustrates an artificial intervertebral disc 10 according to an embodiment of the invention. As shown, disc 10 includes superior shell 12 and inferior shell 14. Each of shells 12 and 14 comprise a bone contacting surface for placement against the bony structures of vertically adjacent vertebral bodies in a region where the natural intervertebral disc has been excised. As discussed above, such discecotomy may be necessary in cases where the natural disc is damaged or diseased. Superior shell 12 includes superior surface 16 for placement against the inferior surface of one vertebra while inferior shell 14 includes inferior surface 18 for placement against the superior surface of an adjacent and vertically lower vertebra. It will be understood that the terms “upper” and “lower” are used in conjunction with a spine in the upright position. Although the term “shell” is used herein, it will be understood that such term is not intended to limit the present invention to any shape or configuration. Other terms that may apply to the shells would be plate, etc. The term “shell” will be understood by persons skilled in the art to apply to the structures shown and/or described herein as well as any equivalent structures.
In the embodiment shown in
b illustrates ring 22 of
a also illustrates superior surface 24 of inferior shell 14, which is provided with a convex structure, or “ball” 26, generally extending in the superior (or upward) direction. Although the term “ball” is used herein, it will be apparent to persons skilled in the art that this term is not intended to refer to a full or partial spherical structure. In one embodiment, as shown in
When implanting artificial disc 10 into an intervertebral disc space, two shells 12 and 14 are first aligned with inferior surface of superior shell 12 facing the superior surface of inferior shell 14. In this alignment, ball 26 and ring 22 are engaged with ball 26 being positioned within the lumen of ring 22. In this orientation, disc 10 is then inserted within the intervertebral space, between the adjacent vertebral bodies. In this position, the outer surfaces of shells 12 and 14 are in contact with the respective vertebral bodies. Once so implanted, the normal compressive force exerted by one vertebra against the other will serve to maintain disc 10 in position. It will be understood that any other artificial means may be used to prevent dislodging of the disc. For example, the outer surfaces of the shells may be provided with an adhesive or bone cement, etc., to ensure proper positioning.
Once in position, superior surface of ball 26 would contact inferior surface 20 of superior plate 12. This contact provides the desired separation between the adjacent vertebral bodies. Relative movement between ball 26 and surface 20 provides the essential articulation between the vertebral bodies. Further, ring 22 serves to constrain the relative movement between ball 26 and inferior surface 20. That is, ring 22 limits the amount of movement of the ball over surface 20 to a defined articulation region. Surface 23 of ring 22 that contacts ball 26 is referred to herein as the articulation surface of the ring. It will be understood that ring 22 is dimensioned to be of sufficient height (as measured inferiorly from the inferior surface of the superior shell) to provide the required limit, or “stop”, for ball 26. In a typical application, ring 22 would have a height of 1 to 5 mm. However, it will be understood that various other sizes may be used or needed depending, for example, on the associated anatomy. The invention is not limited to any specific dimensions as may be mentioned herein, and may be modified to fit within any disc space of the human spine, i.e., the cervical, thoracic, or lumbar regions. Further, as mentioned above, and as discussed further below, ring 22 can be sized to limit or constrain various movements of ball 26 including translation, lateral bending, flexion, extension and any coupled movements involving one or more of such specific movements. This flexibility in design will therefore allow the artificial disc of the invention to function similarly to naturally occurring discs while also allowing correction or prevention of any malformations.
In one embodiment, as shown in
As indicated above, in one embodiment, the ball may be hemispheric in cross section but the shape may be varied in size in any direction. Thus, ball 26 may comprise a hemisphere or a convex shape that is elongated in the anteroposterior and/or lateral directions. In general, ball 26 may comprise any convex shape that provides the desired amount and type of intervertebral movements. This variability in structure of ball 26 would allow for a variety of different movements to occur within the physical constraints of ring 22. As discussed further below, further motion constraints may be provided on ball 26 itself.
Although
In other embodiments, inferior shell 14 may be adapted to provide resistance to the movement of ring 22. In one embodiment, inferior shell 14 may be provided with one or more hard stops or bumpers to limit the movement of ring 22 over ball 26. The term “hard stops” is understood to mean a physical motion limiter. In particular, a “hard stop” would serve to limit motion so as not to exceed the aforementioned elastic zone. A “soft stop”, on the other hand would serve to commence limitation of motion once the elastic zone is entered. According to an embodiment of the invention, such stops may be built into the shell around the ball, at any distance, or may be formed as part of the ball itself. In one aspect, the hard stops may be of a height that is only a few millimeters below the maximum height of ball 26.
An example of such hard stops is illustrated in
In another embodiment, hard stops 28 may be located anteriorly to limit flexion in the anteroposterior direction and in still another embodiment, they would be located posteriorly. Any combination could be used to provide hard stops to constrain motion. The stops could be any manner of shapes from rectangular with rounded edges to domes and of variable height. It will be understood that in one embodiment, hard stops 28 may be provided to restrict movement in all directions if such limited movement is required. “Bumpers” 28 may be of various shapes for example linear or curved. Similarly, it will be understood that in other embodiments, no such hard stops may be needed.
Another embodiment of the above mentioned hard stop function is shown in
In another embodiment, hard stops may be placed laterally on either side of ball 26 to a height only a few millimeters below the maximum height of the ball to limit lateral flexion.
Another embodiment of the invention is shown in
In a similar manner, a further embodiment of the invention would have hard stop 36 (or extension 30 of
Another embodiment of the invention is illustrated in
Another embodiment of the invention is shown in
A further embodiment of a resilient force absorbing means is illustrated in
Another position adjusting means is illustrated in
Much of the above discussion has focused on variations that may be implemented to inferior shell 14 and/or ball 26 of the invention. However, in a similar manner, superior shell 12 and/or ring 22 may also be varied to achieve a variety of positions and functions. For example, in one embodiment, the ring may be formed in various sizes and shapes. These would include variations in the height of the limiting edge of ring 22 and variations in its shape, including circular, ovoid and rectangular forms etc. For example, by varying the shape of ring 22, it will be understood that the shape and area for articulation with the ball would also be varied thereby allowing the ball's constraint of motion to be tailored as needed. Similarly, the location of ring 22 may also be varied on superior shell 12 so as to match the position of the ball 26. In addition, superior shell 12 may be provided with one or more “stops”, such as hard stops and/or soft stops, similar to those described above, for constraining or limiting the relative movements between the superior and inferior shells. Such stops may comprise separate elements attached to the superior shell or may form part of ring 22 itself. For example, in one embodiment, the stops may comprise raised edges of the ring. Further examples and aspects of the invention are discussed further below.
An embodiment of the invention showing variations in the superior shell are illustrated in
A variant of ring 22h described above is illustrated in
b illustrates a further feature of ring 22j, namely a larger anteroposterior dimension as compared to a lateral dimension. As will be understood, such an arrangement serves to allow ball 26j a greater degree of freedom in movement in the sagittal plane and a restricted amount of movement in the coronal plane. In another embodiment, ring 22j may be elongated in the coronal plane thereby achieving the opposite effect. Thus, it will be understood that any combination of movements can be tailored by adjusting the dimensions of ring 22.
Further embodiments of the invention are illustrated in
a, 17a and 18a illustrate other embodiments of the invention. Where elements similar to those described above are identified, the same reference numerals are used but with the letters “r”, “t” and “u” added, respectively, for clarity.
a illustrates superior shell 12r that is similar to that shown in
As shown in
In the case of
b, 17b and 18b illustrate rings 22r, 22t and 22u depicted, respectively, in
Although
The structural components of the disc of the invention, in particular the ball and ring, may be formed of from any medically suitable material such as titanium, titanium alloys, nickel, nickel alloys, stainless steel, nickel-titanium alloys (such as Nitinol™ brand), cobalt-chrome alloys, polyurethane, porcelain, plastic and/or thermoplastic polymers (such as PEEK™ brand), silicone, rubber, carbothane or any combination thereof. In addition, it will be understood that the ball and ring may be made from materials that are the same or different from the remainder of the respective shells. For example, the ball may be made of titanium while the ring and both shells may be made of PEEK™ brand. Various other materials and combinations of materials will be known to persons skilled in the art.
As will be understood, and as explained above, the present invention may be adapted in various ways to meet any number of desired motion characteristics. That is, the shape, position, and size of the ball and/or ring may be chosen for various intervertebral joints of the spine and may be tailored for providing or restricting the degree and direction of motion. Various features and embodiments of the invention have been described and/or shown herein. It will be understood by persons skilled in the art that various combinations of such features and embodiments can be used depending on the need and requirements of the artificial disc. Further, although the figures illustrate various embodiments for the purposes of describing embodiments of the present, the relative or absolute dimensions shown are not intended to limit the scope of the invention in any way.
It will be apparent to persons skilled in the art that although the above discussion has focused on the superior shell being provided with the ring and the inferior shell being provided with the ball, the reverse may also be used. That is, in other embodiments, the superior shell may include the ball and the inferior shell may include the ring.
It will be apparent to persons skilled in the art that any bone contacting surfaces of the discs discussed above (such as the external surfaces of the shells) may be provided with a texture, treatment or coating to encourage or enhance bone ingrowth and/or adhesion to the adjacent bony structure. For example, such surfaces may be provided with a roughened or grooved texture and/or may be coated with a bone growth enhancing agent.
In addition, although the present invention has been described with reference to intervertebral joints, the present invention may equally be used in other joints such as, for example, knee joints.
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 in the claims appended hereto. Any examples provided herein are included solely for the purpose of illustrating the invention and are not intended to limit the invention in any way. Any drawings provided herein are solely for the purpose of illustrating various aspects of the invention and are not intended to be drawn to scale or to limit the invention in any way. The disclosures of all prior art recited herein are incorporated herein by reference in their entirety.
This application is filed under 35 U.S.C. §120 and §365(c) as a continuation of International Patent Application PCT/CA/2009/000233, filed Feb. 27, 2009, which application claims priority from U.S. Patent Application No. 61/067,545, filed Feb. 28, 2008, which applications are incorporated herein by reference in their entireties.
Number | Date | Country | |
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61067545 | Feb 2008 | US |
Number | Date | Country | |
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Parent | PCT/CA2009/000233 | Feb 2009 | US |
Child | 12870107 | US |