The present invention relates to intervertebral implants for stabilization of the vertebral column adapted to form a wedge to be inserted between the facing plates of two adjacent vertebrae to maintain a constant disc spacing.
The document EP 0 307 241 A describes one example of an intervertebral implant taking the form of a cage of parallelepiped shape. This form of cage is not well suited to use in the vertebral column, in particular because the longitudinal edges of this kind of cage may cause lesions to the spinal cord or the roots during insertion of the implant between the adjacent vertebrae. Relatively ineffective retention of the adjacent vertebrae is also encountered, and is likely to be caused by the parallelepiped shape of the cage.
There has also been proposed an intervertebral implant of parallelepiped shape in which the upper and lower larger faces are plane and at an angle to each other that is open toward the front, to maintain the adjacent vertebrae at an appropriate physiological lordosis angle. The shape of the implant necessitates the formation of large recesses in the vertebral plates, to allow insertion of the intervertebral implant by front to back movement in translation during fitting, which creates inappropriate trauma.
The document U.S. Pat. No. 5,888,227 A describes an intervertebral implant with a peripheral wall around a single large interior cavity open at the front and at the rear. The upper and lower faces are divergent toward the front and have a double front-to-back and transverse curvature. The structure has insufficient mechanical strength and the retention of the adjacent vertebrae is insufficient.
The document WO 02/15825 A describes an implant of cylindrical general shape with upper and lower walls each provided with two orifices, an anterior wall with a threaded hole for manipulation by a fitting tool, and lateral walls each having a longitudinal groove whose edges oppose axial rotation of the implant during fitting.
The problem addressed by the present invention is that of defining a new intervertebral implant structure that very significantly reduces the risks of nervous lesions during fitting, improves positioning and locking of the vertebrae to each other, and minimizes bone trauma during fitting. Particular requirements are improved mechanical strength and good bone attachment, facilitating fusion of two adjacent vertebrae.
To achieve the above and other objects, the intervertebral implant of the invention for stabilizing adjacent vertebrae, comprises a solid biocompatible material implant body having a tubular general structure delimited by an upper wall and a lower wall that are convex and slightly divergent toward the front, two opposite lateral walls that are plane and slightly divergent toward the front, and a posterior wall with a threaded axial hole, with a single interior cavity providing communication between orifices provided in the upper wall and the lower wall; according to the invention:
the upper wall and the lower wall each comprise a respective single large upper orifice or lower orifice,
an interchangeable compression plug is adapted to be fitted by screwing it into the threaded axial hole in the posterior wall,
the interior cavity is closed toward the front by an anterior wall,
the width of the implant defined by the lateral walls is less than its height defined by the upper wall and the lower wall.
A structure of the above kind with a large central cavity and large openings in the upper and lower walls encourages contact between a graft inserted inside the implant body and the two vertebral plates between which the intervertebral implant is inserted. Fitting the graft is facilitated. The interchangeable compression plug compresses the graft against the two adjacent vertebrae after fitting. Finally, the implant may be fitted between two vertebrae by being turned 90° so that its lateral faces that are closer together are at the top and at the bottom, facing the vertebral plates of the two adjacent vertebrae. It is then rotated 90° to bring the graft into contact with the vertebrae. This reduces the trauma to the vertebral region and minimizes the quantity of material that has to be removed to insert the intervertebral implant between the adjacent vertebrae.
In one advantageous embodiment, because of the upper orifice and the lower orifice, the interior cavity is open over the whole of its width between the lateral walls and over the whole of its length between the posterior wall and the anterior wall. This facilitates fitting the graft and maximizes its contact with the adjacent vertebrae.
The interchangeable compression plug preferably comprises a conical interior end portion. This facilitates penetration of the plug into the graft, to compress it.
To obtain effective compression the interchangeable compression plug and the threaded axial hole that receives it advantageously have a diameter substantially equal to the width of the interior cavity in the vicinity of the posterior wall.
Good results are obtained if the interchangeable compression plug has a length such that, at the end of screwing it into the threaded axial hole that receives it, its interior end portion penetrates the interior cavity to a distance of at least one quarter of the length of said interior cavity.
The implant is preferably provided with at least two interchangeable compression plugs having different lengths, so that the practitioner can choose the most suitable plug for compressing the graft.
In one advantageous embodiment, the posterior wall of the implant body includes an external diametral groove for actuating axial rotation of the implant, to move it from an insertion position, with its lateral walls at the top and at the bottom, to a vertebrae supporting orientation with the upper and lower walls bearing on the adjacent vertebral plates.
The implant may be made from a solid biocompatible material such as titanium or advantageously from a PEEK type polymer, which has the advantage of being radio transparent.
Other objects, features and advantages of the present invention will emerge from the following description of particular embodiments given with reference to the appended drawings, in which:
FIGS. 3 to 6 show the structure of the implant body from
In the embodiment shown in the figures, the intervertebral implant of the invention comprises a solid biocompatible material implant body 1 that has a tubular general structure delimited by an upper larger wall 2 and a lower larger wall 3 that are convex and slightly divergent toward the front, two opposite lateral walls 4 and 5 that are plane and slightly divergent toward the front, a posterior wall 6 with a threaded axial hole 7, and an anterior wall 8.
The interior of the implant body 1 is a single interior cavity 9, open at the top via an upper orifice 10 and open at the bottom via a lower orifice 11. The interior cavity 9 therefore provides communication between the upper orifice 10 and the lower orifice 11 provided in the upper larger face 2 and the lower larger face 3 of the implant body 1.
In the embodiment shown in the figures, as seen best in
The posterior wall 6 has an external diametral groove 12 for engaging a tool such as a screwdriver blade for imparting axial rotation to the implant body.
The anterior wall 8 includes an eccentric threaded hole 13, as shown in
The upper larger wall 2 and the lower larger wall 3 include annular toothed anti-expulsion ribs, such as an anterior rib 14, a median rib 15 and a posterior rib 16.
The lateral walls such as the wall 4 may include small lateral openings such as the holes 17 and 18.
As seen in
Like the threaded axial hole 7, the interchangeable compression plug 19 has a diameter substantially equal to the smallest width of the interior cavity 9 i.e. the distance between the lateral walls 4 and 5 in the vicinity of the posterior wall 6.
In the embodiment shown in
The interchangeable compression plug 19 may be made of titanium, so that it can be detected in an x-ray. On the other hand, the implant body 1 may advantageously be made of a radiotransparent material, advantageously from a PEEK (polyetheretherketone) type polymer.
In this case, a titanium marker may advantageously be provided in the implant body 1 away from the interchangeable compression plug 19.
In the embodiment shown in the figures, the upper wall 2 and the lower wall 3 each have a conical general shape and the upper orifice 10 and the lower orifice 11 are each bordered at its anterior and posterior ends by a respective flat 21 or 22 perpendicular to the lateral walls 4 and 5.
The implant of the invention may be fitted between two adjacent vertebrae to be treated by means of the following steps:
the plate regions between which the implant has to be lodged are squared off,
a bone graft is placed in the interior cavity 9 of the implant body 1,
the implant body 1 is oriented so that its plane lateral faces 4 and 5 are parallel to the plates of the vertebrae to be treated, so that the implant has a minimum height,
the implant body 1 oriented in this manner is inserted between the two adjacent vertebrae to be treated, which are held apart,
the implant body 1 is turned axially 90° to place its upper wall 2 and its lower wall 3 against the plates of the vertebrae to be treated, after which the vertebrae are released,
the interchangeable compression plug 19 is screwed in to compress the graft and thereby to press it against the vertebral plates to be treated.
The present invention is not limited to the embodiments that have been described explicitly, but includes variants and generalizations thereof contained within the scope of the following claims.
Number | Date | Country | Kind |
---|---|---|---|
02/16234 | Dec 2002 | FR | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
---|---|---|---|---|
PCT/FR03/03734 | 12/16/2003 | WO | 6/14/2005 |