The present invention generally relates to spinal implants inserted in the spine of a patient during surgical procedures and to method for surgically inserting the implants.
A spinal implant may be used to stabilize a portion of a spine. The implant may promote bone growth between adjacent vertebra that fuses the vertebra together. The implant may include a spherical protrusion, a threaded pin and an angled surface to facilitate remote adjustment of the implant position using an insertion instrument.
An intervertebral disc may degenerate. Degeneration may be caused by trauma, disease, and/or aging. An intervertebral disc that becomes degenerated may have to be partially or fully removed from a spinal column. Partial or full removal of an intervertebral disc may destabilize the spinal column. Destabilization of a spinal column may result in alteration of a natural separation distance between adjacent vertebra. Maintaining the natural separation between vertebra may prevent pressure from being applied to nerves that pass between vertebral bodies. Excessive pressure applied to the nerves may cause pain and nerve damage. Artificial discs maintain spacing and articulation between vertebral bodies normally allowed by the elastic properties of the natural disc, which directly connects two opposing vertebral bodies. Various artificial discs are described by Stefee et al. in U.S. Pat. No. 5,071,437, and Gill et al. in U.S. Pat. No. 6,113,637.
During a spinal fixation procedure, a spinal implant may be inserted in a space created by the removal or partial removal of an intervertebral disc between adjacent vertebra. The spinal implant may maintain the height of the spine and restore stability to the spine. Bone growth may fuse the implant to adjacent vertebra. Spine fusion helps eliminate pain, but limits the range of spinal motion for patients. It is thought that spine fusion creates increased degeneration in adjacent non-fused segments, commonly known as “adjacent segment disease.”
Traditional artificial disc surgery treatment requires removal of the natural human disc and the insertion of two plates through the abdomen, i.e. the anterior side of the patient. Anterior insertion of the disc necessitates surgical dissection of the two major blood vessels, the vena cava and the aorta. Rupture of these blood vessels are a life threatening complication of an anterior approach to the lumbar spine, as well as nerve damage resulting in retrograde ejaculation in males. Because of the risks, such surgery requires the attendance of both a general surgeon as well as an orthopedic surgeon.
As a result, there is a need for an artificial disk which may be inserted unilaterally (or bilaterally) from the posterior side of the patient.
An artificial disk and surgical insert method have been developed in which the disk components are inserted posteriorly and assembled in situ, e.g., within the vertebral interbody space. The components of the disk are small enough that combined with a lateral surgical approach, resection of the facet joints and manipulation of the spinal cord may be completely avoided. Other surgical techniques may be employed for the insertion of the disc components and assembling the components in situ. Assembling in situ allows for a fully functioning artificial disk to be inserted posteriorly.
In another embodiment, a spinal implant may be inserted during a spinal fixation procedure using an anterior, lateral, posterior, or transverse spinal approach. A discectomy may be performed to remove or partially remove a defective or damaged intervertebral disc. The discectomy may create a space for a spinal implant. The amount of removed disc material may correspond to the size and type of spinal implant to be inserted.
A method to insert an artificial disc in the spine of a patient has been developed that comprises: sequentially inserting at least two components of an artificial disk in an vertebral interbody space; assembling the components within the vertebral interbody space to form an artificial disc, and using the assembled artificial disc as a disc in the vertebral interbody space. The interbody space is between two adjacent vertebra. The components of the artificial disc are sequentially surgically inserted posteriorly into the patient or sequentially inserted with a lateral surgical approach, and are surgically inserted without resection of facet joints in the spine.
A method has been developed for forming an artificial spine disc assembly including: an upper spine support plate and lower spine support plate, wherein each plate has a generally planer surface adapted to face and engage a vertebra and a first coupling; an upper disc beam and a lower disc beam, each beam comprising one of a pair of opposing joint surfaces and second coupling adapted to connecting to one of the first coupling to a respective one of the support plates, the method comprising: surgically and individually inserting the disc beams into vertebral interbody space in a spine of a patient; assembling the upper disc beam and the lower disc beam by mating the opposing joint surfaces in the vertebral interbody space, and surgically and individually inserting the support plates into vertebral interbody space in a spine of a patient; attaching the coupling of each support plate to a corresponding one of the disc beams in the vertebral interbody space. Wherein the upper support plate is a pair of upper support plates and the lower support plate is a pair of lower support plates, such that attaching of the support plates includes attaching each of pair of upper support plates to opposite beams on the upper disc beam and attaching each of a pair of lower support plates to opposite beams on the lower disc beam. The method further comprises positioning the upper support plate opposite to a lower surface of an upper vertebra and positioning the lower support plate opposite to an upper surface of a lower vertebra.
An artificial spine disc assembly has been developed comprising: a first disc beam having a center block with a rounded joint surface and a pair of opposite beams extending outward from the center block; a second disc beam having a center block with a second joint surface and a pair of opposite beams extending outward from the center block, wherein the second joint surface seats into the first joint surface when the second disc beam is mounted on the first disc beam; a first pair of spine support plates, wherein each plate has a generally planer surface adapted to face and engage a vertebra and a coupling to engage one of the opposite beams of the first disc beam, and a second pair of spine support plates, wherein each plate has a generally planer surface adapted to face and engage a vertebra and a coupling to engage one of the opposite beams of the first disc beam. In the artificial spine disc assembly, the first joint surface is a concave surface in an upper face of the center block of the second disc beam, and the second joint surface is a convex surface on a lower face of the center block of the first disc beam. The concave surface is a rounded well in the upper face and the convex surface is a semi-hemispherical surface in the lower face. The artificial spine disc assembly is packaged with the disc beams and spine support plates disassembled in a sterile package to be shipped to a medical service provider.
The assembly 10 includes four spine support plates, 12, 14, 16 and 18. Each plate has a generally planer surface 20 that faces and engages an end of vertebra. The upper plates 14, 18 engage the lower end surface of an upper vertebra. The upper plates are positioned towards opposite sides of the upper vertebra end surface. The lower plates 12, 16 engage the upper end surface of a lower vertebra. The lower plates are positioned towards opposite sides of the lower vertebra end surface. The surface 20 of the plates 12, 14, 16 and 18 may include bumps 22, rough textured surface features or other surface treatments to promote adhesion between the surface and the end surface of the vertebra. The surface 20 of the plates may have a geometry that generally conforms to the end surface of the vertebra and provides a good amount of surface area to spread out loads applied between the vertebra.
The plates have a center slot 24 to receive a cantilever arms 26 from a disc beam 28, 30. The center slot may be in a relatively thick portion of the plates to ensure adequate structural support in the plates. The plates may have wings 32 extending from the center slot and become gradually thinner as they extend to an outer plate edge 34. The center slot may include an end lip 36 that may be a rectangular cutout in the end of the slot. The end lip receives a cantilever latch 40 on the arms 26 of the disc beam. The end lip and latch 40 snap together as the arm slides in through the slot 24. The secure engagement between the latch 40 and the lip 36 ensures that the plates do not slide off the arms after assembly of the artificial disc.
The beams may be integrally formed of a rigid biocompatible plastic material, e.g., Polyetheretherketone. The plates 12, 14, 16 and 18 may be formed of the same or other biocompatible plastic material.
When fully assembled, the artificial disc 10 replaces a spinal disc and fits between adjacent vertebra. The plate surfaces 20 of the upper and lower plates hold apart the vertebra. The disc beams hold the plates together and allow the plates limited movement, including pivoting and deformation. The deformation is provided by bending of the cantilevered arms 26 about the joint between the opposing disc beams 28, 30. Pivot movement is provided by the joint 38 formed by the insertion of a hemispherical ball joint 42 slidably fitting into a convex socket 44 cupped to receive the ball joint. The joint allows the ball to slide within the socket and thereby allows the upper plates to pivot with respect to the lower plates. The deformation and pivot movements of the artificial disc 10 replicate the natural movements between vertebra allowed by a healthy natural disc.
The arms 26 of each disc beam provide cantilever supports for the plates. The arms deform, e.g., bend, due to the pressure between the vertebra. The deformation provides a cushioning effect for the vertebra.
The base 46 for the disc beam 28 with the ball joint is relatively hollow with a peripheral walls extending around the four sides of the base. A ball joint 42 is seated within the hollowed out portion of the base 46. The base 46 for the disc beam 30 with the socket 44 is relatively solid but for a removed portion forming the socket. The base for the socket includes an annular ridge 50 having an inner curved surface that forms a portion of the socket. The materials for the ball and socket could be any combination of biocompatible ceramic, plastic (i.e. PEEK), stainless steel or wear resistant Cobalt-Chrome alloy.
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The latch 40 on each arm includes a beam 56 extending through a channel 58 in the arm. The cantilever beam 56 causes the latch 40 to snap into place against the lip 36 (
The artificial intervertebral disc assembly 10 may be assembled between the vertebra. The individual components of the disc assembly, e.g., disc beams and platforms, may be surgically inserted serially in between the vertebra. The components are assembled in place between adjacent vertebra. The components of the disc assembly are packaged in a sterile package (See
The components of the disc assembly 10 may be inserted during a spinal fixation procedure using an anterior, lateral, posterior or transverse spinal approach. A posterior spinal approach through the back of a patient has an advantage of being relatively minimally invasive, especially as compared to an anterior spinal approach. The components of the disc assembly may be inserted and assembled using an endoscope.
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With the disc beams in place and aligned, the first plate 12 is inserted through the incision by the endoscope 62 (or other insertion tool) such that its slot slides onto its respective arm 26 of one of the disc beams. A latch on the arm snaps into a groove in the plate to secure the plate to the arm. The positioning tool 66 may position the pair of disc beams such that the center slot in the plate is lined up with the arm of the disc beam. The second plate is inserted on its respective arm of the opposite disc beam.
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While the invention has been described in connection with what is presently considered to be the most practical and preferred embodiment, it is to be understood that the invention is not to be limited to the disclosed embodiment, but on the contrary, is intended to cover various modifications and equivalent arrangements included within the spirit and scope of the appended claims.
This application claims the benefit of U.S. Provisional Application Ser. Nos. 60/743,013 filed Dec. 5, 2005, and 60/743,065 filed Dec. 21, 2005, the entirety of both which applications are incorporated herein by reference.