This invention relates generally to a spinal implant assembly for implantation into the intervertebral space between adjacent vertebral bones to simultaneously provide stabilization and continued flexibility and proper anatomical motion, and more specifically to such a device that has the ability to provide sliding action between elements of the device.
The bones and connective tissue of an adult human spinal column consists of more than twenty discrete bones coupled sequentially to one another by a tri-joint complex that consists of a disc and the two posterior facet joints. The discs of adjacent bones are cushioned by spacers referred to as intervertebral discs. These more than twenty bones are anatomically categorized as being members of one of four classifications: cervical, thoracic, lumbar, or sacral. The cervical portion of the spine, which comprises the top of the spine, up to the base of the skull, includes the first seven vertebrae. The intermediate twelve bones are the thoracic vertebrae, and connect to the lower spine comprising the five lumbar vertebrae. The base of the spine is the sacral bones (including the coccyx). The component bones of the cervical spine are generally smaller than those of the thoracic spine, which are in turn smaller than those of the lumbar region. The sacral region connects laterally to the pelvis.
The spinal column is highly complex in that it includes these more than twenty bones coupled to one another, housing and protecting critical elements of the nervous system having innumerable peripheral nerves and circulatory bodies in close proximity. In spite of these complications, the spine is a highly flexible structure, capable of a high degree of curvature and twist in nearly every direction.
Genetic or developmental irregularities, trauma, chronic stress, tumors, and degenerative wear are a few of the causes that can result in spinal pathologies for which surgical intervention may be necessary. A variety of systems have been disclosed in the art that achieve immobilization and/or fusion of adjacent bones by implanting artificial assemblies in or on the spinal column. The region of the back that needs to be immobilized, as well as the individual variations in anatomy, determine the appropriate surgical protocol and implantation assembly. With respect to the failure of the intervertebral disc, the interbody fusion cage has generated substantial interest because it can be implanted laparoscopically into the anterior of the spine, thus reducing operating room time and patient recovery time scarification.
Many intervertebral body cages comprise 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 may be inserted side by side with the external threads threading into the upper and lower surfaces of the adjacent vertebral bones. The cages may 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.
These cages of the prior art have enjoyed medical success in promoting fusion and approximating proper disc height. It is, however, 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. Thus, 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 borne by the now-fused joint, are transferred onto the nearby facet joints and intervertebral discs. It would therefore, be a considerable advance in the art to provide an implant assembly which does not promote fusion, but rather, which mimics the biomechanical action of the natural disc cartilage, thereby permitting continued normal motion and stress distribution.
Some artificial intervertebral discs have been designed that permit greater flexibility of the spine, specifically of adjacent vertebral bodies. See, for example, that which is detailed in U.S. patent application Ser. No. 10/256,160 (filed Sep. 26, 2002) entitled “Artificial Intervertebral Disc,” which is a continuation-in-part application of U.S. patent application Ser. No. 10/175,417 (filed Jun. 19, 2002) entitled “Artificial Intervertebral Disc Utilizing a Ball Joint Coupling”, which is a continuation-in-part application of U.S. patent application Ser. No. 10/151,280 (filed May 20, 2002) entitled “Tension Bearing Artificial Disc Providing a Centroid of Motion Centrally Located Within an Intervertebral Space”, which is a continuation-in-part application of both U.S. patent application Ser. No. 09/970,479 (filed Oct. 4, 2001) entitled “Intervertebral Spacer Device Utilizing a Spirally Slotted Belleville Washer Having Radially Extending Grooves” as well as U.S. patent application Ser. No. 10/140,153, (filed May 7, 2002) entitled “Artificial Intervertebral Disc Having a Flexible Wire Mesh Vertebral Body Contact Element”, the former being a continuation-in-part application of U.S. patent application Ser. No. 09/968,046 (filed Oct. 1, 2001) entitled “Intervertebral Spacer Device Utilizing a Belleville Washer Having Radially Extending Grooves” and the latter being a continuation-in-part application of both U.S. patent application Ser. No. 09/970,479 (detailed above) as well as U.S. patent application Ser. No. 10/128,619 (filed Apr. 23, 2002) entitled “Intervertebral Spacer Having a Flexible Wire Mesh Vertebral Body Contact Element”, which is a continuation-in-part application of both U.S. patent application Ser. No. 09/906,119 (filed Jul. 16, 2001) and entitled “Trial Intervertebral Distraction Spacers” as well as U.S. patent application Ser. No. 09/982,148 (filed Oct. 18, 2001) and entitled “Intervertebral Spacer Device Having Arch Shaped Spring Elements,” the disclosures of which are incorporated herein by reference as if fully set forth herein. But still, what is needed is artificial discs that closely mimic the natural movement of the spine.
The present invention relates generally to artificial disc replacements.
As shown in
The bottom end plate member 12 may have a substantially flat top surface 14 with a plurality of protrusions 16 extending outwardly above top surface 14. Although reference words such as “upward” and “downward” may be used to describe the relationship between two features, the use of the terms is in no way meant to describe a gravitational reference point.
A core 20 may be disposed on top surface 14 of end plate 12. In a preferred embodiment, core 20 is comprised of a compressionable material. For example, the core 20 is preferably made from an ultra-high molecular weight polyethylene. The core may also be comprised of other materials such as ceramic and other plastics and even metal.
The core preferably includes a concave arch 22 remote from end plate 12. The concave arch 22 forms a cup. Core 20 also preferably includes an array of indents 24. Indents 24 are disposed on bottom surface 23 of core 20. The array of indents 24 is designed to receive protrusions 16 emanating upward from end plate 12. The array of indents 24 have a larger opening as compared to the length and width of the protrusions 16. This design enables core 20 to slide along end plate 12, as will later be described. The concave arch besides being spherical may also be in the shape of an elongated cylinder.
Top end plate 10 preferably includes a spherical convex lower surface 30 and an upper surface 32. Convex lower surface 30 has a concavity substantially equal to the concavity of concave surface 22 of core 20 such that a radius of the convex lower surface 30 can reside in the cup of the core. In the preferred embodiment, convex lower surface 30 extends past concave top surface 22. In the illustrated embodiment, convex lower surface 30 and concave upper surface 22 substantially form a ball-and-socket joint. The lower surface 30 may also be in the shape of various other curves and lines including but not limited to saddle shape curves, straight lines and cylindrical curves as well as combinations of the same.
The radius of both the convex lower surface 30 and concave arch 22 are preferably relatively large. The result is a relatively large surface contact area between the two elements that protects against migration and subsidence. A shoulder 34 may extend circumferentially around convex lower surface 30 and include a lip portion 36. The shoulder 34 and lip portion 36 may limit the articulation of end plate 10 along core 20 as a result of contact between shoulder 34 and a portion of core 20 as illustrated in
The resultant ball-and-socket design enables the present invention to articulate in the anterior/posterior direction, medial/lateral direction, as well as associated axial and sagittal angulations.
In a method of use, disc 1 of the present invention is disposed between two adjacent vertebrae, not shown in the drawings, with the upper surface 32 of end plate 10 abutting an upper vertebrae and a bottom surface 13 of end plate 12 abutting the lower vertebrae. Disc 1 is placed between the two vertebrae and anchored within. As shown in
As shown in
As illustrated in
As shown in
Additionally the design offers a strong primary anchorage system and reduces the risk of expulsion of the disc from the adjacent vertebrae.
The present design not only enables articulation in all four directions, i.e., anterior/posterior and medial/lateral as well as axial and sagittal angulation, but also increases maneuverability of the disc by providing sliding translation in the various directions as well. Additionally, by placing a compressionable material between the two end plates, some of the upward and downward forces placed on the adjacent vertebrae may be absorbed by the compressionable disc.
The disc may also be sprayed with a coating such as a titanium plasma spray to increase bone ingrowth.
Although disc 1 has been described with reference to a core comprised of a single piece, the core may include 2 or more pieces. And the core may include two articulating surfaces, which may or may not confront each other. If the two articulating surfaces confront one another, the end plates of the present invention may both be designed with non-articulating surfaces, i.e., translation surfaces.
In an alternate embodiment, the core 20 may include more than 2 elements. For instance the core 20 may include a spherical or circular object sandwiched by two members. The two members may have arcuate surfaces confronting the spherical object and flat surfaces remote therefrom.
In an alternate embodiment, as shown in
As seen in
Disc 100 also preferably includes a core 120 disposed between end plate 110 and 112. Core 120 may be a single element or preferably consist of a bi-component having a spherical portion 122 and a base portion 124. Although the core 120 has been described including one or two elements, additional elements may also be included or comprise core 120.
In a preferred embodiment, base portion 124 is disposed on top surface 114 of end plate 112. Specifically, lower surface 130 of base portion 124 abuts top surface 114. Base portion 124 preferably includes ridge 134 extending circumferentially around the base portion at the base portion's latter edges as shown in
Spherical portion 122 is designed to cooperate with base portion 124. Spherical portion 122 preferably includes a upper convex surface 160 as shown in
In the preferred embodiment, convex surface 160 of spherical portion 122 is juxtaposed against concave surface 119 of end plate 110. The concavity of the two elements should be substantially equal much in the same way as a ball joint configuration. Additionally, as with the first embodiment, the radius of both surfaces is preferably large to create a large surface contact area.
As seen in
In a method of use, the present embodiment of the disc is disposed between two adjacent vertebrae with the upper vertebrae contacting the top surface 115 of end plate 110 and the lower vertebrae abutting the bottom surface 117 of end plate 112. Thus, similar to the first embodiment, when a person bends from side to side, a force may be placed against the upper end plate 110 by a vertebral body as designated by F″. As the force F″ is increased, end plate 110 articulates about spherical portion 122, specifically convex surface 160. The maximum articulation angle preferably is about 20°. As end plate 110 articulates, core 120 may translate or slide on top surface 114. The core 120 may slide until protrusion 118 abuts shoulder 138 of core 120. In the preferred embodiment, this maximum translation distance is approximately 2 mm along the direction X′ or 1 mm from a center position.
Although the present embodiment has been described with reference to a medial or lateral force, the disc may also articulate and translate with regard to an anterior or posterior force as well as any force having components in a combination of directions.
The embodiment as illustrated in
In the preferred embodiment, core 120 of disc 100 is comprised of a compressionable material such as, but not limited to, an ultra-high molecular weight polyethylene. The resultant design enables the disc to absorb some of the upward and downward force received by the vertebrae positioned adjacent disc 100.
In additional embodiments, the core, the base portion and spherical portion may consist of different materials. Preferably, at least one element is comprised of a compressionable material.
In a method of implanting disc 10, two vertebrae may be distracted using various tools known to those in the art. The distracting method may include placing trial spacers between the adjacent vertebrae until a desired distraction space is reached. The trial spacers may have the same outer contour as the disc 1 so that the correct positioning and alignment can be tested by the surgeon. The disc 1 may be inserted into the disc space by pushing the disc through two opposing rails at least partially positioned within the disc space or adjacent thereto.
Although the invention herein has been described with reference to particular embodiments, it is to be understood that these embodiments are merely illustrative of the principles and applications of the present invention. It is, therefore, to be understood that numerous modifications may be made to the illustrative embodiments and that other arrangements may be devised without departing from the spirit and scope of the present invention as defined by the appended claims.
This application claims the benefit of the filing date of U.S. Provisional Patent Application No. 60/603,060 filed Aug. 20, 2004, the disclosure of which is hereby incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| 60603060 | Aug 2004 | US |