|Publication number||US20050267580 A1|
|Application number||US 11/181,782|
|Publication date||Dec 1, 2005|
|Filing date||Jul 15, 2005|
|Priority date||Apr 23, 2003|
|Also published as||CA2523131A1, CA2523131C, EP1615600A2, EP1615600A4, US6969405, US20040215342, US20090248160, WO2004093723A2, WO2004093723A3|
|Publication number||11181782, 181782, US 2005/0267580 A1, US 2005/267580 A1, US 20050267580 A1, US 20050267580A1, US 2005267580 A1, US 2005267580A1, US-A1-20050267580, US-A1-2005267580, US2005/0267580A1, US2005/267580A1, US20050267580 A1, US20050267580A1, US2005267580 A1, US2005267580A1|
|Original Assignee||Loubert Suddaby|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (30), Referenced by (53), Classifications (19)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This application is a division of application Ser. No. 10/420,803, filed Aug. 23, 2003.
This invention relates to orthopedic surgery, more particularly to a prosthetic intervertebral disc replacement system which can be implanted into a suitably prepared intervertebral disc space via minimally invasive surgical techniques to provide for and restore substantial functional normalcy.
The normal intervertebral disc is in essence a complex joint which allows for various articular motions between adjacent vertebral segments. These articular motions, in turn, account for the flexibility and functional mobility of the normal human spine. In the course of a day, the normal intervertebral disc encounters a variety of compressional, rotations and associated flexion or extension movements. In these day to day activities, movements in varying and repetitive combinations accumulate and contribute to the deterioration of natural discs that occurs over time. As with other joints in the human body that deteriorate over time, it would be desirable to have disc replacement prostheses which could be inserted in place of a failed or worn normal disc when it is determined the disc is irreparably damaged and that preservation of functional mobility is required. The time honored method of addressing debilitating symptoms and signs of a degenerative disc is to remove the disc and fuse the two adjacent vertebral bones together. Fusion eliminates motion at the abnormal segment, and while useful at improving debilitating symptoms, the consequence of eliminating natural motions at a single segment is that greater degrees of stress occur above or below that segment. This in turn accelerates degeneration of neighboring intervertebral discs, often necessitating additional fusion surgeries. It would be desirable, therefore, to preserve motion at every disc space and thus retain natural motion and eliminate the adjacent level degeneration that discectomy and fusion seems to produce. Toward this end, an intervertebral disc replacement prosthesis ought ideally to restore and preserve disc space height while permitting sufficient natural motion (flexion, extension, rotation and lateral bending) to prevent excessive stresses on spinal segments above and below the prosthesis.
Several intervertebral disc replacement prostheses are now in production, but none has the capacity to be implanted posteriorly through traditional exposures of the spine, or through smaller incisions, known collectively as minimally invasive surgical techniques.
An object of the invention is to provide for a complete and functional disc replacement that simultaneously restores sufficient disc space height and mobility to provide for functional normalcy, while allowing for a variety of surgical approaches and the use of minimally invasive surgical techniques.
To achieve this objective, the component parts of the replacement disc are bonded to the surface of sacks or chambers which are distensible or inflatable. In this manner, the replacement discs can be inserted through a small opening and then inflated within a disc space thereby assuming its final functional configuration. The sacks are nonporous and allow no escape of their contents. The sacks, or chambers, are initially inflated with a radio opaque liquid contrast material under fluoroscopic guidance to check for functional positioning and anatomic alignment, as well as functional integrity of the chambers themselves. Once ideal placement is confirmed, the radio opaque contrast material is removed and replaced with a hardenable material or resin which forms a solid construct once suitably mature. In this fashion, infinite anatomic variation of disc heights and configurations can be accommodated, and insertion of the replacement disc can be facilitated through a small annulotomy favoring minimally invasive surgical techniques.
The preferred embodiment contains at least two inflatable chambers, although one, or any number of chambers might be conceived and created, depending on specific needs.
For example, in the two component version, one chamber sits atop the other with the disc space between the vertebral end plates. On the cranial or superior surface of the cranial chamber, teeth, digits, or corrugations are found which impress themselves into the end plate when the sack or chamber is inflated. A similar set of components is found on the caudal or inferior surface of the caudal or inferior chamber. These teeth or digits transgress the end plate surface and fixate the replacement disc in situ when the chambers are inflated. The juxtaposing surface between the cranial and caudal chambers contain mating surfaces that allow for functional motion between the cranial and caudal chambers when they are inflated to their final size. The mating surfaces are formed of male and female components that interdigitate, largely in a ball and socket fashion, but other similar functional relationships may be considered, provided that the adjacent surface interaction provides for the cardinal movements of a functioning intervertebral disc. These cardinal movements will allow for approximately 15 degrees of flexion, 5 degrees of extension, 5 degrees of lateral bending, 2 degrees of axial rotation and 1-5 mm of translation. When fully expanded, the fulcrum of movement on flexion and extension is located near the junction of the posterior one third and anterior two thirds of the vertebral body. The relationship between the components is such that it allows for varying degrees of rotation, flexion, extension and translational movements while simultaneously retarding the extremes of these motions to prevent disengagement of the cranial and caudal components at the extremes of functional movement. The mating surfaces are lined with polyethylene or similar materials suited for long term frictional wear. These linings may include plastics, ceramics, metals, carbon composites or combinations thereof.
The male and female component of the mating surface is bonded to the surface of its adjacent inflatable chamber such that proper union is assured when both chambers are inflated to their final proportions. Because the chambers are inflatable, they can be inserted into the disc in a collapsed state through a small opening and then inflated once they are appropriately positioned within the disc space.
As the chambers are inflated, teeth or digits on the superior or cranial and inferior or caudal surface of the chambers dig into the adjacent end plate and lock the prosthesis in position. The mating surface between the two inflated chambers in turn contains a ball and socket or male and female interacting component that permits functional movement between the cranial and caudal chambers when they are suitably inflated. By inflating them with a hardenable material, a solid, functional disc prosthesis can be formed with a final size that is much larger than its component parts. This allows not only for varying disc sizes and shapes, but also provides for use of the prosthesis in minimally invasive surgical techniques.
Suitable materials for the teeth or digits which bond to the end plate are any of a variety of metal or plastics or ceramics having sufficient strength to indent or puncture or bond with a vertebral end plate. Fabrics permitting tissue ingrowth might also be used.
Suitable materials for the walls of the inflatable chamber include Kevlar, polypropylene or any of a variety of plastics or fabrics having either elastic or non-elastic properties, but sufficiently pliable and having sufficient tensile strength to allow for deflated and inflated attitudes. The material should be sufficiently non-porous so as to prevent leakage of injected contents.
Suitable materials for the mating surfaces between the cranial and caudal chambers include any materials presently used in joint replacement having the capacity for long term frictional wear. These include various synthetics, such as polyethylene, plastics, ceramics and metal surfaces capable of long term cyclical frictional interactions.
Suitable materials to inflate the chamber to allow them to assume their final functional configuration include any hardenable material capable of maintaining function integrity under a variety of loads during various combinations of flexion, extension, rotation or translational movements. These materials include polymethyl methacrylate, polycarbonate, various polymerizing resins or indeed any material capable of being inject in a liquid or semisolid state and then capable of assuming a solid structural shape as determined by the recipient chamber into which it is injected.
In the simplest embodiment, a single chamber sitting between two metallic dishes conforming roughly to the shape of the vertebral end plates could be inflated to allow a friction fit of the metallic dishes to the end plates cranially and caudally. Once the injected material hardened within the chamber, functional mobility would be restored and retained.
In U.S. Pat. No. 3,875,595, Froning describes a bladder-like prosthesis which is inflated with liquid or plastic, but requires a valve as the material is non-hardenable and could potentially leak from the retaining bladder, causing the prosthesis to collapse.
Kuslich, in U.S. Pat. No. 5,571,189, describes an expandable porous fabric implant designed to stabilize a spinal segment. The fabric is porous and packed with biologic material which favors fusion of the interspace rather than functional mobility. It is packed with material which stabilizes a spinal segment by allowing ingrowth of bone and fibrous issues through pores on its surface.
In U.S. Pat. No. 5,674,295, Ray describes a pillow-shaped prosthetic spinal disc nucleus body made of a hydrogel core and a flexible constraining jacket which permits the hydrogel core to expand and contract. The constraining jacket is also porous, allowing entry and egress of fluids. The jacket is not filled with a hardenable material, since significant expansion and contraction is a pivotal feature to the biologic function of the prosthesis he describes.
These and other objects are attained by a inflatable intervertebral disc replacement prosthesis as described below.
In the accompanying drawings,
The drawings show several embodiments of the invention, having the characteristic feature that each prosthesis has at least one chamber 12 which can be inflated to conform to various intervertebral spaces.
Preferably, each chamber 12 is provided with studs 14, fingers, corrugations or other projecting structures designed to dig into the cranial and caudal surfaces of the vertebrae “V” against which they bear, to keep the prosthesis in place. The chamber 12 is at least partially made of a flexible material, not only so that it can expand, but also so that is can be collapsed to a small size, so that it can be inserted by minimally invasive techniques. The chamber wall 20 may be a strong fabric material, for example Kevlar, or it may be made of a strong polymeric film such as polypropylene. In the case of Kevlar, which is not substantially stretchable, the chambers may advantageously be formed in a particular shape, which will be attained on inflation, corresponding to the particular space being filled.
The chambers 12 may have rigid end plates 22 made, for example, of metal.
In the embodiments where two chambers 12, 12′ are used (
In any case, the prosthesis is placed by first preparing the intervertebral space, then inserting the prosthesis in the space, and then inflating its chamber(s) via valve(s) 42. The inflating fluid may be a liquid such as a gel or a hardenable material. Inflation is done to a degree determined by the surgeon to restore the space to its original height.
Since the invention is subject to modifications and variations, it is intended that the foregoing description and the accompanying drawings shall be interpreted as only illustrative of the invention defined by the following claims.
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|U.S. Classification||623/17.12, 623/17.14|
|International Classification||A61F2/00, A61F2/44, A61F2/30|
|Cooperative Classification||A61F2210/0085, A61F2002/30841, A61F2002/30583, A61F2/4425, A61F2002/30471, A61F2220/0091, A61F2002/30586, A61F2002/30579, A61F2/441, A61F2002/30649, A61F2002/30624, A61F2002/443|
|European Classification||A61F2/44B, A61F2/44D2|