Embodiments are generally related to spinal implants and medical surgery devices and techniques. Embodiments also relate to the field of vertebral body spacers. Embodiments additionally relate to implanting techniques and surgical devices and component devices for spinal fusion. Embodiments further relate to expandable cage devices utilized in spinal surgery and interbody cage devices with multi-access capabilities.
In some instances, an intervertebral disc that becomes degenerated may need to be partially or fully removed from a spinal column. Intervertebral discs can degenerate due to various causes such as, for example, trauma, disease, or aging. Removal or partial removal of an intervertebral disc destabilizes the spinal column. A spinal implant may thus be inserted into a disc space created by the removal or partial removal of an intervertebral disc. The spinal implant may maintain the height of the spine and restore stability to the spine. Bone then grows from the adjacent vertebrae into the spinal implant. The bone growth fuses the adjacent vertebrae.
A spinal implant can be inserted utilizing an anterior, transforaminal, oblique, posterior or lateral spinal approach. For an anterior approach, extensive vessel retraction is often required and many vertebral levels are not readily accessible from this approach. Another approach is a posterior approach. This approach typically requires that both sides of the disc space on either side of the spinal cord be surgically exposed, which may require a substantial incision or multiple access locations as well as extensive retraction of the spinal cord.
Yet another approach is a postero-lateral approach to the disc space. The posterior-lateral approach is employed in a posterior lumbar interbody fusion (PLIF) or transforaminal lumber interbody fusion (TLIF) procedure, which may be performed as an open technique, which requires making a larger incision along the middle of the back. Through this incision, the surgeon then cuts away, or retracts, spinal muscles and tissue to access the vertebrae and disc space. The TLIF procedure may also be performed as a minimally invasive or as an extreme lateral interbody fusion procedure that involves a retroperitoneal transpoas approach to the lumbar spine as an alternative to “open” fusion surgery. In the minimally invasive procedure, the surgeon employs much smaller incisions, avoids disrupting major muscles and tissues in the back, and reduces the amount of muscle and tissue that is cut or retracted.
Anterior Lumbar Interbody Fusion (ALIF) using threaded devices such as cages and bone dowels have been in use for over ten years. Initially, threaded cages or dowels were expected to act as a stand-alone device that would promote fusion and maintain disc height without the need for posterior surgery and instrumentation of the spine. In spite of fusion rates better than 90 percent for single level fusion and 65 percent for two-level fusion, significant subsidence has been observed on follow-up X-rays at varying times following the procedure. This subsidence, or slow insinuation of the threaded devices into the vertebral bodies, has resulted in lost disc height, which in some patients has resulted in the failure to fuse and the recurrence of often very painful symptoms.
The implants may be constructed of any biocompatible materials sufficiently strong to maintain spinal distraction including, but not limited to, bone, metals, ceramics and/or polymers. Implants may be packed with bone graft or a synthetic bone graft substitute to facilitate spinal fusion. Implants may have a variety of shapes, which include, but are not limited to, threaded cylinders, unthreaded cylinders, and parallelepipeds.
A protective sleeve can be used during preparation and insertion of a spinal implant. The protective sleeve serves to protect abdominal organs, blood vessels, and other tissue during a spinal implant procedure using an anterior approach. The sleeve typically extends above the surgical opening during use. The sleeve maintains distraction of the vertebrae. Also, the sleeve serves as an alignment guide for tool and implant insertion during the surgical procedure. Protective sleeves can also be used during a spinal fusion procedure using a posterior or lateral approach.
Typically, most surgical corrections of a disc space include at least a partial discectomy, which is followed by restoration of normal disc space height and, in some instances, fusion of the adjacent vertebral bodies. Restoration of normal disc space height generally involves the implantation of a spacer and fusion typically involves inclusion of bone graft or bone graft substitute material into the intervertebral disc space to create bony fusion. Fusion rods may also be employed. Some implants further provide artificial dynamics to the spine. Such techniques for achieving interbody fusion or for providing artificial disc functions are well known.
The inter-vertebral spacing (i.e., between neighboring vertebrae) in a healthy spine can be maintained via a compressible and somewhat elastic disc. The disc serves to allow the spine to move about the various axes of rotation and through the various arcs and movements required for normal mobility. The elasticity of the disc maintains spacing between the vertebrae allowing room or clearance for compression of neighboring vertebrae during flexion and lateral bending of the spine. In addition, the disc allows relative rotation about the vertical axis of neighboring vertebrae allowing twisting of the shoulders relative to the hips and pelvis. Clearance between neighboring vertebrae maintained by a healthy disc is also important to allow nerves from the spinal chord to extend out of the spine between neighboring vertebrae without being squeezed or impinged by the vertebrae.
In situations (based upon injury or otherwise) where a disc is not functioning properly, the inter-vertebral disc tends to compress and in doing so pressure is exerted on nerves extending from the spinal cord by this reduced inter-vertebral spacing. Various other types of nerve problems may be experienced in the spine, such as exiting nerve root compression in neural foramen, passing nerve root compression. A few medical procedures have been devised to alleviate such nerve compression and the pain that results from nerve pressure. Many of these procedures revolve around attempts to prevent the vertebrae from moving too close to each other by surgically removing an improperly functioning disc and replacing it with a lumber interbody fusion (LIF) device. Although prior interbody devices, including LIF cage devices, may be effective at improving patient condition, the vertebrae of the spine, body organs, the spinal cord, other nerves, and other adjacent bodily structures make obtaining surgical access to the location between the vertebrae where the LIF cage is to be installed difficult.
In case of lateral approach, it would be desirable to reduce the size of the LIF/VBR cage to minimize the size for the required surgical opening for installation of the LIF/VBR cage, while maintaining high strength, durability, and reliability of the LIF/VBR cage device. Instruments and lateral implants are not necessarily suited to efficiently distract the disc space without damaging the adjacent endplates. In an effort to address the foregoing difficulties, it is believed that the implant device for spinal fusion from lateral approach, as discussed herein, can address many of the problems with traditional lateral implants.
The following summary is provided to facilitate an understanding of some of the innovative features unique to the disclosed embodiment and is not intended to be a full description. A full appreciation of the various aspects of the embodiments disclosed herein can be gained by taking the entire specification, claims, drawings, and abstract as a whole.
It is, therefore, one aspect of the disclosed embodiments to provide for spinal implants.
It is another aspect of the disclosed embodiments to provide an interbody cage apparatus that can be utilized in a multi-access approach in the context of spinal implants and spinal surgery.
It is yet another aspect of the disclosed embodiments to provide for an interbody cage apparatus that can be inserted in a MIS exposure and then expanded insitu.
The aforementioned aspects and other objectives and advantages can now be achieved as described herein. An implant apparatus and a method for spinal fusion from oblique, lateral, ALIF, PLIF, and TLIF approach are disclosed. Such an apparatus can be configured in some embodiments to include an expandable implant cage and an inserter. The cage can be inserted between endplates of upper and lower vertebra using an oblique, lateral, ALIF, PLIF, and/or TLIF approach. The cage generally includes a male and female screw configuration and a cage expansion mechanism. The inserter inserts the cage in a spinal disc space and tightens the male and female screw arrangement. Once the cage is inserted to the desired position, viewed by X-ray you will begin to tighten the male portion of the screw in the device and continue to tighten until final deployment of cage has been achieved. This provides a much greater footprint that allows the device to reach the cortical ring or apophyseal ring of the vertebral body. Tightening of male and female screw arrangement operates the cage expansion mechanism to expand the cage size. The cage can be inserted through a smaller surgical opening and then expanded to a full size assembly between the vertebrae.
Additionally, in a preferred embodiment, an interbody cage apparatus can be utilized in a multi-access approach. Such a device can be inserted in a MIS exposure and then can be expanded insitu. Such a multi access device can expand in width to cover a larger area for fusion to occur. Such device includes a unique feature that allows for the graft material to stay in place upon deployment. Such a cage device can be configured with four graft boxes that can be filled with allograft or autograft material to allow for fusion to occur. Along with the graft boxes, such a cage can also be configured with a unique feature in the posterior piece of the device that has small cut outs or ports to allow for moldable allograft material to be injected through the inserter device. Such ports allow the device to be completely filled in the vacant spaces for material to be placed for an even larger area for fusion to occur.
Such a cage can be also configured with a unique feature that allows it to be deployed in a controlled matter, allowing the surgeon to open and close the device for specific placement. Such a cage can also include in some embodiments, a central post system made up of a female and male post that is threaded and a barrel t-post that allows the device to be a deployed in a controlled matter.
Such an embodiment allows a surgeon to implant the device through a small exposure to get the largest footprint for stability and structural support. The cage once deployed will be resting on the cortical ring of the vertebral body, which is the strongest part of the body structure.
Along with the implant, a unique implant inserter can include an inserter instrument that attaches to the cage. The driver can be cannulated to allow for a separate driver that slides down the cannulation and inserts the screw on the device that can then be rotated to allow the cage to deploy. Once deployed the driver can then be removed and the surgeon can then insert an luer tip syringe filled with, for example, bmp or allograft material, which can be injected down the inserter through the cannulation and fill the voids inside the cage.
The accompanying figures, in which like reference numerals refer to identical or functionally similar elements throughout the separate views and which are incorporated in and form a part of the specification, further illustrate the disclosed embodiments and, together with the detailed description of the invention, serve to explain the principles of the disclosed embodiments.
The particular values and configurations discussed in these non-limiting examples can be varied and are cited merely to illustrate at least one embodiment and are not intended to limit the scope thereof.
Based on the foregoing, it can be appreciated that an implant apparatus 1800 and a method for spinal fusion from oblique, lateral, ALIF, PLIF, and/or TLIF approaches are disclosed. The apparatus/device 1800 can be configured to include an expandable implant cage 1828/1834 and an inserter such as, for example, inserters 2102, 2104, and 2106. The cage can be inserted between endplates of upper and lower vertebra using oblique, lateral, ALIF, PLIF, and TLIF approach. The cage generally includes a male and female screw configuration and a cage expansion mechanism. The inserter inserts the cage in a spinal disc space and tightens the male and female screw arrangement.
Once the cage is inserted to the desired position, viewed by X-ray, a user can begin to tighten the male portion of the screw in the device and continue to tighten until final deployment of the cage has been achieved. This provides a much greater footprint that allows the device to reach the cortical ring or apophyseal ring of the vertebral body. Tightening of male and female screw arrangement operates the cage expansion mechanism to expand the cage size. The cage can be inserted through a smaller surgical opening and then expanded to a full size assembly between the vertebrae.
Based on the foregoing, it can be appreciated that various embodiments are disclosed, including preferred and alternative embodiments. For example, in an embodiment, an implant apparatus for spinal fusion can include an expandable implant cage positioned between endplates of upper and lower vertebra comprising a male and female screw arrangement and a cage expansion mechanism, wherein the cage expansion mechanism expands the cage size on tightening the male and female screw arrangement; and an inserter for inserting the cage in a spinal disc space that maintains a handle, a shaft, and a coupling arrangement, wherein the inserter is operated to engage the coupling arrangement with the male and female screw arrangement and to tighten the male and female screw arrangement.
In some embodiments, the cage expansion mechanism can comprise a pin and hinge configuration. In other embodiments, the cage expansion mechanism can comprise a cage compartment configuration. In yet other embodiments, the cage expansion mechanism can comprise a combination of a cage compartment configuration and a pin and hinge configuration. In still other embodiments, the disclosed cage expansion mechanism can be positioned on at least one sidewall of the cage. In some embodiments, the disclosed spinal fusion can be an oblique approach. In other embodiments, the spinal fusion can be a lateral approach. In yet other embodiments, the spinal fusion can be an ALIF approach, a PLIF approach, or a TLIF approach.
In another embodiment, an implant apparatus for spinal fusion can include, for example, an expandable implant cage positioned between endplates of upper and lower vertebra comprising a male and female screw arrangement and a cage expansion mechanism, wherein the cage expansion mechanism expands the cage size on tightening the male and female screw arrangement. Such an apparatus can also include an inserter for inserting the cage in a spinal disc space that maintains a handle, a shaft, and a coupling arrangement, wherein the inserter is operated to engage the coupling arrangement with the male and female screw arrangement and to tighten the male and female screw arrangement. Additionally, in such an apparatus, the cage expansion mechanism can comprise at least one of: a pin and hinge configuration, a cage compartment configuration, or a combination of the cage compartment configuration and the pin and hinge configuration. In an alternative embodiment of such an apparatus, the cage expansion mechanism can be positioned on at least one sidewall of the cage. In yet another embodiment of such an apparatus, the spinal fusion can be, for example, a lateral approach, an ALIF approach, a PLIF approach, a TLIF approach, and/or an oblique approach.
In still another embodiment, a method for spinal fusion may be implemented, which includes, for example, the steps of locating an expandable implant cage between endplates of upper and lower vertebra comprising a male and female screw arrangement and a cage expansion mechanism, wherein the cage expansion mechanism expands the cage size on tightening the male and female screw arrangement; providing an inserter for inserting the cage in a spinal disc space that maintains a handle, a shaft, and a coupling arrangement; and operating the inserter to engage the coupling arrangement with the male and female screw arrangement and to tighten the male and female screw arrangement.
In another embodiment of such a method, a step may be implemented for positioning the cage expansion mechanism on at least one sidewall of the cage. In other embodiments of such a method, a step may be implemented for configuring the cage expansion mechanism to comprise at least one of: a pin and hinge configuration; a cage compartment configuration; or a combination of the cage compartment configuration and the pin and hinge configuration.
Note that in a preferred embodiment, an interbody cage can be utilized in a multi-access approach. Such a device can be inserted in a MIS exposure and then can be expanded insitu. Such a multi access device can expand in width to cover a larger area for fusion to occur. Such device includes a unique feature that allows for the graft material to stay in place upon deployment. Such a cage device can be configured with four graft boxes that can be filled with allograft or autograft material to allow for fusion to occur. Along with the graft boxes, such a cage can also be configured with a unique feature in the posterior piece of the device that has small cut outs or ports to allow for moldable allograft material to be injected through the inserter device. Such ports allow the device to be completely filled in the vacant spaces for material to be placed for an even larger area for fusion to occur.
Such a cage can be also configured with a unique feature that allows it to be deployed in a controlled matter, allowing the surgeon to open and close the device for specific placement. Such a cage can also include in some embodiments, a central post system made up of a female and male post that is threaded, and a barrel t-post that allows the device to be a deployed in a controlled matter.
Such an embodiment allows a surgeon to implant the device through a small exposure to get the largest footprint for stability and structural support. The cage once deployed will be resting on the cortical ring of the vertebral body, which is the strongest part of the body structure.
Along with the implant, a unique implant inserter can include an inserter instrument that attaches to the cage. The driver can be cannulated to allow for a separate driver that slides down the cannulation and inserts the screw on the device that can then be rotated to allow the cage to deploy. Once deployed, the driver can then be removed and the surgeon can then insert a luer tip syringe filled with, for example, bmp or allograft material, which can be injected down the inserter through the cannulation and fill the voids inside the cage.
It will be appreciated that variations of the above disclosed and other features and functions, or alternatives thereof, may be desirably combined into many other different systems or applications. Also, that various presently unforeseen or unanticipated alternatives, modifications, variations or improvements therein may be subsequently made by those skilled in the art which are also intended to be encompassed by the following claims.
This patent application claims the benefit under 35 U.S.C. §119(e) of U.S. Provisional Application Ser. No. 61/584,894 entitled, “Expandable Interbody (Lateral, Posterior, Anterior) Multi-Access Cage for Spinal Surgery,” which was filed on Jan. 10, 2012 and is incorporated herein by reference in its entirety.