WO2001039678A1 - Dispositif de stabilisation intervertebral - Google Patents

Dispositif de stabilisation intervertebral Download PDF

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Publication number
WO2001039678A1
WO2001039678A1 PCT/FR2000/003368 FR0003368W WO0139678A1 WO 2001039678 A1 WO2001039678 A1 WO 2001039678A1 FR 0003368 W FR0003368 W FR 0003368W WO 0139678 A1 WO0139678 A1 WO 0139678A1
Authority
WO
WIPO (PCT)
Prior art keywords
implant
vertebrae
intervertebral
chambers
extra
Prior art date
Application number
PCT/FR2000/003368
Other languages
English (en)
Inventor
Henry Graf
Original Assignee
Henry Graf
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from FR9915160A external-priority patent/FR2801782B3/fr
Priority claimed from FR9916662A external-priority patent/FR2803188A1/fr
Priority claimed from FR0006640A external-priority patent/FR2809304A1/fr
Application filed by Henry Graf filed Critical Henry Graf
Priority to CA002392868A priority Critical patent/CA2392868C/fr
Priority to JP2001541414A priority patent/JP4294901B2/ja
Priority to US10/148,693 priority patent/US7291150B2/en
Priority to AU21824/01A priority patent/AU778410B2/en
Priority to EP00985390A priority patent/EP1233711B1/fr
Priority to DE60030313T priority patent/DE60030313T2/de
Publication of WO2001039678A1 publication Critical patent/WO2001039678A1/fr
Priority to US11/982,761 priority patent/US8172880B2/en

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Classifications

    • AHUMAN NECESSITIES
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    • A61B17/56Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor
    • A61B17/58Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor for osteosynthesis, e.g. bone plates, screws, setting implements or the like
    • A61B17/68Internal fixation devices, including fasteners and spinal fixators, even if a part thereof projects from the skin
    • A61B17/70Spinal positioners or stabilisers ; Bone stabilisers comprising fluid filler in an implant
    • A61B17/7001Screws or hooks combined with longitudinal elements which do not contact vertebrae
    • A61B17/7002Longitudinal elements, e.g. rods
    • A61B17/7019Longitudinal elements having flexible parts, or parts connected together, such that after implantation the elements can move relative to each other
    • A61B17/7025Longitudinal elements having flexible parts, or parts connected together, such that after implantation the elements can move relative to each other with a sliding joint
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/44Joints for the spine, e.g. vertebrae, spinal discs
    • A61F2/442Intervertebral or spinal discs, e.g. resilient
    • A61F2002/444Intervertebral or spinal discs, e.g. resilient for replacing the nucleus pulposus
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/44Joints for the spine, e.g. vertebrae, spinal discs
    • A61F2002/448Joints for the spine, e.g. vertebrae, spinal discs comprising multiple adjacent spinal implants within the same intervertebral space or within the same vertebra, e.g. comprising two adjacent spinal implants
    • A61F2002/4485Joints for the spine, e.g. vertebrae, spinal discs comprising multiple adjacent spinal implants within the same intervertebral space or within the same vertebra, e.g. comprising two adjacent spinal implants comprising three or more adjacent spinal implants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2220/00Fixations or connections for prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2220/0025Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2220/005Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements using adhesives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2230/00Geometry of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2230/0063Three-dimensional shapes
    • A61F2230/0065Three-dimensional shapes toroidal, e.g. ring-shaped, doughnut-shaped
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2230/00Geometry of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2230/0063Three-dimensional shapes
    • A61F2230/0071Three-dimensional shapes spherical
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2310/00Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
    • A61F2310/00005The prosthesis being constructed from a particular material
    • A61F2310/00011Metals or alloys
    • A61F2310/00023Titanium or titanium-based alloys, e.g. Ti-Ni alloys

Definitions

  • the present invention relates to an intervertebral stabilization device.
  • such a device is intended to replace all or part of an intervertebral disc, when the latter has been destroyed by surgery or disease.
  • the invention proposes to produce a stabilization device which, while ensuring satisfactory freedom of movement between the vertebrae which are adjacent to it, induces only slight mechanical stresses at the level of the entire spinal chain.
  • an intervertebral stabilization device intended to connect two neighboring vertebrae, characterized in that it comprises an implant intended to be inserted at least partially between the vertebral bodies of the two neighboring vertebrae, said implant being able to give said two neighboring vertebral bodies at least a degree of mutual freedom, said device also comprising at least one extra-discal organ, disposed at the rear of the intervertebral space, capable of absorbing a displacement between said vertebrae, at least in the direction of intervertebral flexion.
  • the two neighboring vertebrae have a single degree of freedom, it is a degree of freedom in rotation, around a transverse axis of the patient, corresponding to the flexion and extension movements of this patient.
  • the or each extra-discal organ is capable of absorbing a displacement between these neighboring vertebrae at least in the direction of the intervertebral flexion, in which the patient leans forward.
  • This intervertebral flexion corresponds to the extension of each extra-discal organ, that is to say to its elongation in its main direction, which is substantially the main direction of the vertebral chain, that is to say the vertical when the patient is standing.
  • FIG. 1 is a schematic side view, illustrating two neighboring vertebrae between which is placed a stabilization device according to the invention
  • - Figure 2 is a side view, on a larger scale, illustrating an implant belonging to the stabilization device of Figure 1;
  • FIGS. 3 to 6 are views similar to Figure 2, illustrating alternative embodiments of the implant belonging to the stabilization device of Figure 1;
  • FIG. 7 is a top view, illustrating an additional variant of the invention.
  • FIG. 8 is a rear view, illustrating the two damping members belonging to the stabilization device of Figure 7;
  • Figure 9 is a schematic side view, similar to Figure 1, illustrating an additional alternative embodiment of the invention.
  • FIG. 10 is a perspective view, illustrating the device of Figure 9;
  • FIG. 11 to 13 are top views, illustrating the device of Figure 9, then two alternative embodiments.
  • FIG. 14 is a side view illustrating a last alternative embodiment of the invention.
  • FIG 1 shows two vertebrae respectively upper 2 and lower 2 'which are connected by means of a stabilization device according to the invention.
  • Each vertebra comprises a vertebral body 4, 4 'extended by a pedicle 6, 6', an upper articular 8, 8 'and a lower articular 10, 10'.
  • the intervertebral space is designated by 12, by 14 and 14 ′ the facing articular facets and by 16 and 16 ′ the articular capsules.
  • the two vertebrae 2, 2 ' are connected to each other by means of a stabilization device, comprising an interbody implant 18, housed in the intervertebral space 12, as well as a damping member, generally designated by the reference 20, the two ends of which are fixed to the corresponding vertebrae by means of pedicle screws 22, 22 '.
  • a stabilization device comprising an interbody implant 18, housed in the intervertebral space 12, as well as a damping member, generally designated by the reference 20, the two ends of which are fixed to the corresponding vertebrae by means of pedicle screws 22, 22 '.
  • the damping member is for example in accordance with the teaching of FR-A-2 676 911, or even that of FR-A-2 751 864. It can also comprise a ligament, in accordance for example with the teaching of FR-A-2 694 182.
  • the implant 18 is shown more precisely in FIG. 2.
  • the right side corresponds to the posterior part of the intervertebral space 12
  • the left side corresponding to the anterior part.
  • the implant 18 comprises respectively upper 24 and lower 26 elements, coming into contact with the vertebral bodies 4, 4 ', by respective contact surfaces 24', 26 ', which are planar.
  • these contact surfaces can be of different shapes, in particular convex.
  • the elements 24, 26 comprise respective yokes 24 '', 26 '', which are articulated by means of an axis 28 extending transversely.
  • This axis 28, which is arranged on the posterior side of the intervertebral space 12, gives a degree of freedom between the surfaces 24 'and 26', and therefore between the vertebral bodies 4, 4 '.
  • This unique degree of freedom is a rotation around the transverse, or sagittal, axis 28 or an extension, which thus corresponds to a bending of the patient towards the front of the latter towards the rear.
  • FIG. 3 illustrates a second embodiment of the intervertebral implant, designated by the reference 68.
  • the latter comprises two elements respectively upper 74 and lower 76, coming into contact with the vertebral bodies 4, 4 'via surfaces flat contact 74 ', 76'.
  • One of these elements, in this case the upper element is provided with a 74 '' spherical housing, forming a cup, disposed towards the rear part of the space. intervertebral 12.
  • This housing 74 '' cooperates with a spherical projection 76 '' of the other element, namely the lower element 76.
  • this implant 68 with one or more springs, similar to that 30, or with a resilient block, extending between the upper and lower elements, for example on the anterior side of the intervertebral space.
  • FIG. 4 illustrates a third embodiment of the intervertebral implant, which is designated as a whole by the reference 118.
  • This implant comprises two upper 124 and lower 126 elements, forming plates. Each of these plates, which bears against a respective vertebral body via a flat surface 124 ', 126', is provided with a spherical recess 124 '', 126 ''.
  • a ball 128 which has a radius of curvature substantially less than that of the recesses 124 '', 126 '', is interposed between the plates 124, 126.
  • This ball 128 is free to move in the vicinity of the adjacent surface of the plates 124, 126, which gives three degrees of freedom in rotation to the two vertebral bodies 4, 4 ′ around a movable point, as well as two degrees of freedom in translation authorized by the sliding of the plates on this ball.
  • the latter can be replaced by a non-spherical member, for example oval or cylindrical, bearing against the plates 124, 126 by means of a contact surface whose radius of curvature is less than that of the recesses 124 '', 126 '' above, to allow mutual movement of this member relative to the plate.
  • FIG. 5 represents a fourth alternative embodiment of the intervertebral implant, designated as a whole by the reference 168.
  • the latter comprises a coating, formed by two rigid plates 74, 176, between which is interposed an elastic core 178.
  • the plates 174, 176 partially cover the core 178, in the sense that they are arranged on the edges of this core adjacent to the vertebral bodies.
  • the plates are for example made of titanium while the core, which is for example glued to the plate, is made for example of silicone or elastomer, in particular rubber.
  • the plates 174, 176 come into contact with the vertebral bodies 4, 4 'via flat surfaces 174', 176 '.
  • This implant is inserted into the intervertebral space by impaction, like implants 18, 68 and 118. It is also conceivable that the distance separating the contact surfaces 174 ′, 176 ′, which corresponds to the vertical dimension of the implant placed , increases towards its anterior part, in the vertical anatomical position of the patient's rest.
  • FIG. 6 illustrates a fifth embodiment of the intervertebral implant, designated as a whole by the reference 218.
  • the latter comprises a rigid ball 228 surrounded by a peripheral ring 226, of main axis parallel to the main axis of the spine, this ring being made of an elastic material such as rubber.
  • the lateral ends of the ring are integral with plates 224 which come into contact with the respective vertebral bodies 4, 4 '.
  • the implants 18, 68, 118, 168, 218 described above are total disc prostheses. It is also possible to use an implant 268, illustrated in FIG. 7, which is a partial disc prosthesis.
  • the latter 268, which is inserted into the disc 270, is arranged offset, relative to the main axis A of the spinal chain which, when the patient is in a standing position, is a vertical axis passing through the median plane P extending from back to front of the patient.
  • This prosthesis can be inserted by screwing or impacting into the intervertebral space.
  • This partial prosthesis 268 is associated with a damping member 20A, which is arranged, offset, on the same side of the axis A as the partial prosthesis 268.
  • partial prosthesis 268 a additional prosthesis 268 ', located on the other side of the axis A.
  • This partial prosthesis 268' which is shown in phantom, may be similar to the partial prosthesis 268, it being understood that it is possible to confer these two partial prostheses 268, 268 'of different heights, so as to compensate for a possible collapse of the disc occurring asymmetrically, when viewed from behind.
  • the partial prosthesis 268 ' is associated with an additional damping member 20B, shown in phantom, which is provided on the same side of the axis A as the partial prosthesis 268'.
  • damping members have a metal part and are for example in accordance with the teaching of FR-A-2 751 864. They are advantageously connected to each other by means of a transverse rod 272, extending substantially horizontally.
  • the connection between each member 20, 20A and the rod 272 is rigid, and for example involves welding. It is advantageously carried out at the middle part of these damping members.
  • FIGS 9 to 11 illustrate a further variant of the invention, in which there are provided two upper pedicle screws 322, 324, arranged on either side of the main axis of the spine, as well as two screws lower pedicle 322 ', 324'.
  • the stabilization device comprises an implant 318, for example analogous to that 168, as well as an extra-discal member 320, which is analogous to that 20.
  • This stabilization device also comprises an upper stop element 326, comprising a horizontal branch 328 as well as two vertical branches 330.
  • This branch 328 is hollowed out by two circular openings intended for the passage of the rod of the upper pedicle screws 322, 324.
  • the walls of each opening are extended by an axial sheath 329, covering part of the screw.
  • This sheath which may have come integrally with the branch 328, receives a stop screw 331 capable of selectively immobilizing the abutment element relative to the pedicle screw, along a translation parallel to the main axis of the latter.
  • This device also comprises a lower stop element 334, comprising a horizontal branch 336 extended, at its two ends, by rods 337 provided with spheres 338.
  • This lower element is hollowed out by two openings, intended for the passage of the rod of the two screws lower pedicle 322 ', 324'.
  • each opening is provided with an axial sheath 329 ', provided with a screw 331'.
  • At least one of the openings can be an oblong opening. This thus makes it possible to adapt the dimensions of the abutment elements to different spacings of the pedicle screws.
  • the horizontal branches 328 and 336 can have variable lengths, for example being telescopic.
  • Each vertical branch 330 is folded back, so that its end has a flat surface 326 ′ extending obliquely. This means that this end is neither parallel to the median transverse axis A ', extending from the right to the left of the patient, nor parallel to the median sagittal axis A' ', extending from back to front of the patient
  • Each surface 326 ' cooperates with a corresponding sphere 338, according to a substantially punctual contact.
  • two rotations around the axes A 'and A' ' are authorized between the upper and lower stop elements and, in doing so, between the two vertebrae 2 and 2'.
  • rotation around the vertical axis A is prohibited between these two vertebrae.
  • any mutual translation of the two vertebrae 2, 2 ' is prohibited, in both directions, along the transverse axis A'.
  • a mutual translation between these two vertebrae is authorized, in both directions, along the vertical axis A.
  • the upper stop element can be provided with at least one sphere 338 ′, cooperating with a vertical branch, terminated by an oblique planar surface 336 ′, extending from the horizontal branch 336 of the lower element (figure 12). It is possible to call on the cooperation of two adjacent spherical bearing surfaces 342, 342 ′, each of which belongs to a respective stop element (FIG. 13).
  • at least one of the vertical branches 330 can, at least partially, be made of an elastic material, the elasticity of which allows permanent contact between each branch 330 and a corresponding sphere 338.
  • FIG. 14 illustrates an additional variant embodiment of the invention.
  • the device described therein comprises an implant 368, intended to be inserted at least partially into the intervertebral space.
  • This implant includes two chambers respectively front 368 'and rear 368 '', surrounded by two shells 369.
  • Each of these, which has a cross section substantially in an arc, is made of a rigid material, such as titanium.
  • These shells 369, which are intended to come into contact with the vertebral bodies 4, 4 ′, are subject to the chambers, for example by gluing.
  • a damping fluid comprises at least one liquid, such as water or oil. It may also contain air, or else a hydrophilic body, such as hydrogel.
  • the stabilization device illustrated in this FIG. 11 also comprises a damping member 370, arranged at the rear of the intervertebral space.
  • This member comprises a rigid tank 372 inside which is disposed a piston 374, which comprises a head 376, forming an upper end, the transverse dimensions of which are close to those of the tank.
  • An O-ring seal 378 is mounted between the walls facing the head and the tank.
  • the head 376 of the piston extends from a vertical rod 380 which sealingly passes through the lower wall
  • the lower end of the rod 380, opposite the head 376, is ball-mounted on the head of the lower screw 371.
  • the head of the piston delimits respectively upper 386 and lower 388 chambers, belonging to the tank 372.
  • the upper chamber receives a spring 390, working in compression, which extends vertically between the upper wall of the tank and the wall opposite the head. This spring allows the piston to be returned to its low position, which corresponds to a lordotic posture of the patient, physiologically advantageous.
  • the front chamber of the implant 368 is placed in fluid communication with the upper chamber of the member 370, by means of a conduit 392, while the rear chamber of the implant is put in fluid communication with the lower chamber 388 via a conduit additional 394.
  • arrow F when the patient leans forward, according to arrow F, fluid is expelled from the front chamber in the direction of the upper chamber, which contributes to lowering the piston 374 into the tank, opposite the upper screw 373. This rise induces a displacement of fluid, via the conduit 394, from the lower chamber towards the rear chamber. This bending movement is therefore damped by these different fluid flows.
  • the implant belonging to the stabilization device of the invention can be partial or total.
  • several implants of this type can be placed between two same vertebrae. This implant can be placed either by the anterior route or by the posterior route.
  • intervertebral implant in the form of an envelope containing a hydrophilic gel or water, this implant constituting a nucleus prosthesis.
  • the intervertebral implant may contain a damping fluid, and be in accordance with one of the embodiments described in the French patent application, filed on December 29, 1999, under number 99 16662.
  • This fluidic intervertebral implant is capable of cooperate with an extra-disc mechanical type organ, for example analogous to that 20.
  • the extra-discal member may also contain such a damping fluid, and be in accordance with one of the embodiments described in the application for French patent above mentioned.
  • This fluid extra-discal organ is capable of cooperating with a mechanical intervertebral implant, such as for example that 18.
  • the invention makes it possible to achieve the objectives mentioned above.
  • the device of the invention makes it possible to restore the posterior stability, which had been significantly reduced due to the surgery.
  • the intervertebral implant makes it possible to restore the height of the disc and to recall the natural intervertebral movement, since it gives at least one degree of freedom to the vertebral bodies facing. Furthermore, the extra-discal damping member guarantees an additional component to this posterior stabilization.
  • the stabilization device of the invention thus guarantees that the relative movement of the two vertebrae which it connects is sufficiently close to the movement authorized by a natural vertebral disc, so that no major dysfunction appears on the whole. of the spinal chain.
  • connection means between these two damping members is advantageous, insofar as it ensures a significant reduction in horizontal intervertebral shear, as in the event of rupture or absence of one or two posterior articular massifs.
  • Achieving the intervertebral implant in the form of at least a partial prosthesis is advantageous. Indeed, such prostheses, because of their dimensions, can be introduced from the rear of the patient, so that a single operation can be used, during which these prostheses are implanted at the same time as the 'damping device.
  • Providing a single prosthesis, associated with a single extra-discal damping member, both offset on the same side of the main axis of the vertebral chain makes it possible to remedy asymmetrical collapses of the intervertebral space, seen from behind. Such asymmetrical collapses can also be remedied by using two prostheses of different heights, arranged on either side of the main axis of the spinal chain.

Abstract

Ce dispositif comprend un implant (18) destiné à être inséré au moins partiellement entre les corps vertébraux (4, 4') des deux vertèbres voisines, ledit implant (18) étant apte à conférer auxdits deux corps vertébraux voisins (4, 4') au moins un degré de liberté mutuel, ledit dispositif comprenant également au moins un organe extra-discal (20), disposé à l'arrière de l'espace intervertébral (12), propre à amortir un déplacement entre lesdites vertèbres (2, 2'), au moins dans le sens de la flexion intervertébrale.

Description

DISPOSITIF DE STABILISATION INTERVERTEBRAL
La présente invention concerne un dispositif de stabili- sation intervertébral .
De manière habituelle, un tel dispositif est destiné à remplacer tout ou partie d'un disque intervertébral, lorsque ce dernier a été détruit par la chirurgie ou la maladie.
L'invention se propose de réaliser un dispositif de stabilisation qui, tout en assurant une liberté de mouvement satisfaisante entre les vertèbres qui lui sont adjacentes, induise seulement de faibles sollicitations mécaniques au niveau de l'ensemble de la chaîne vertébrale.
A cet effet, elle a pour objet un dispositif de stabili- sation intervertébral destiné à relier deux vertèbres voisines, caractérisé en ce qu'il comprend un implant destiné à être inséré au moins partiellement entre les corps vertébraux des deux vertèbres voisines, ledit implant étant apte à conférer auxdits deux corps vertébraux voisins au moins un degré de liberté mutuel, ledit dispositif comprenant également au moins un organe extra-discal, disposé à l'arrière de l'espace intervertébral, propre à amortir un déplacement entre lesdites vertèbres, au moins dans le sens de la flexion intervertébrale . Dans le cas où les deux vertèbres voisines possèdent un unique degré de liberté, il s'agit d'un degré de liberté en rotation, autour d'un axe transversal du patient, correspondant aux mouvements de flexion et d'extension de ce patient. Le ou chaque organe extra-discal est propre à amortir un déplacement entre ces vertèbres voisines au moins dans le sens de la flexion intervertébrale, dans laquelle le patient se penche vers l'avant. Cette flexion intervertébrale correspond à l'extension de chaque organe extra-discal, c'est-à-dire à son allongement selon sa direction principale, qui est sensiblement la direction principale de la chaîne vertébrale, soit la verticale lorsque le patient est debout.
L'invention va être décrite ci-dessous, en référence aux dessins annexés, donnés uniquement à titre d'exemples non limitatifs et dans lesquels :
- la figure 1 est une vue schématique de côté, illustrant deux vertèbres voisines entre lesquelles est placé un dispositif de stabilisation conforme à l'invention ; - la figure 2 est une vue de côté, à plus grande échelle, illustrant un implant appartenant au dispositif de stabilisation de la figure 1 ;
- les figures 3 à 6 sont des vues analogues à la figure 2, illustrant des variantes de réalisation de l'implant appartenant au dispositif de stabilisation de la figure 1 ;
- la figure 7 est une vue de dessus, illustrant une variante supplémentaire de l'invention ; et
- la figure 8 est une vue de derrière, illustrant les deux organes d'amortissement appartenant au dispositif de stabilisation de la figure 7 ;
- la figure 9 est une vue schématique de côté, analogue à la figure 1, illustrant une variante supplémentaire de réalisation de l'invention ;
- la figure 10 est une vue en perspective, illus- trant le dispositif de la figure 9 ;
- les figures 11 à 13 sont des vues de dessus, illustrant le dispositif de la figure 9, puis deux variantes de réalisations ; et
- la figure 14 est une vue de côté illustrant une dernière variante de réalisation de l'invention.
La figure 1 représente deux vertèbres respectivement supérieure 2 et inférieure 2' qui sont reliées par l'intermédiaire d'un dispositif de stabilisation conforme à l'invention. Chaque vertèbre comprend un corps vertébral 4, 4' prolongé par un pédicule 6, 6', une articulaire supérieure 8, 8' et une articulaire inférieure 10, 10' . On désigne par 12 l'espace intervertébral, par 14 et 14' les facettes articulaires en regard et par 16 et 16' les capsules articulaires.
Les deux vertèbres 2, 2' sont reliées mutuellement par l'intermédiaire d'un dispositif de stabilisation, comprenant un implant intersomatique 18, logé dans l'espace intervertébral 12, ainsi qu'un organe d'amortissement, désigné dans son ensemble par la référence 20, dont les deux extrémités sont fixées sur les vertèbres correspondantes par l'intermédiaire de vis pédiculaires 22, 22'.
L'organe d'amortissement est par exemple conforme à l'enseignement de FR-A-2 676 911, ou bien encore à celui de FR-A-2 751 864. Il peut également comprendre un ligament, conformément par exemple à l'enseignement de FR-A-2 694 182.
L'implant 18 est représenté de façon plus précise sur la figure 2. Sur cette dernière, comme sur les figures suivantes, le côté droit correspond à la partie postérieure de l'espace intervertébral 12, le côté gauche correspondant à la partie antérieure .
L'implant 18 comprend des éléments respectivement supérieur 24 et inférieur 26, entrant en contact avec les corps vertébraux 4, 4', par des surfaces de contact 24', 26' respectives, qui sont planes. A titre de variante, ces surfaces de contact peuvent être de formes différentes, notamment convexes .
Les éléments 24, 26 comportent des chapes respectives 24'', 26'', qui sont articulées au moyen d'un axe 28 s'éten- dant transversalement. Cet axe 28, qui est disposé du côté postérieur de l'espace intervertébral 12, confère un degré de liberté entre les surfaces 24' et 26', et donc entre les corps vertébraux 4, 4' . Ce degré de liberté unique est une rotation autour de l'axe 28 transversal, ou sagittal, ou à une extension ce qui correspond ainsi à une flexion du patient vers l'avant de celui-ci vers l'arrière.
Un ressort 30, travaillant en compression, est fixé aux éléments 24, 26, du côté antérieur de l'espace intervertébral 12. Ce ressort peut être remplacé par un bloc résilient, réalisé par exemple en élastomère, notamment en caoutchouc. La figure 3 illustre un second mode de réalisation de l'implant intervertébral, désigné par la référence 68. Ce dernier comprend deux éléments respectivement supérieur 74 et inférieur 76, entrant en contact avec les corps vertébraux 4, 4' par l'intermédiaire de surfaces de contact planes 74' , 76' . L'un de ces éléments, en l'occurrence l'élément supérieur, est pourvu d'un logement sphérique 74'', formant cupule, disposé vers la partie postérieure de l'espace intervertébral 12. Ce logement 74'' coopère avec une saillie sphéπque 76'' de l'autre élément, à savoir l'élément inférieur 76.
Etant donné que les rayons du logement 74'' et de la saillie 76'' sont sensiblement identiques, leur coopération assure trois degrés de liberté en rotation, autour du centre fixe 78 de la saillie sphéπque 76'', des surfaces de contact
74', 76' et donc des corps vertébraux 4, 4'.
Il est possible de munir cet implant 68 d'un ou plusieurs ressorts, analogues à celui 30, ou d'un bloc résilient, s 'étendant entre les éléments supérieur et inférieur, par exemple du côté antérieur de l'espace intervertébral.
La figure 4 illustre un troisième mode de réalisation de l'implant intervertébral, qui est désigné dans son ensemble par la référence 118. Cet implant comprend deux éléments supérieur 124 et inférieur 126, formant plateaux. Chacun de ces plateaux, qui prend appui contre un corps vertébral respectif par l'intermédiaire d'une surface plane 124', 126', est pourvu d'un renfoncement sphéπque 124' ' , 126' ' . Une bille 128 qui possède un rayon de courbure sensiblement inférieur à celui des renfoncements 124'', 126'', est intercalée entre les plateaux 124, 126.
Cette bille 128 est libre de se déplacer au voisinage de la surface adjacente des plateaux 124, 126, ce qui confère trois degrés de liberté en rotation, aux deux corps vertébraux 4, 4' autour d'un point mobile, ainsi que deux degrés de liberté en translation autorisés par les glissements des plateaux sur cette bille. Cette dernière peut être remplacée par un organe non sphéπque, par exemple ovale ou cylindrique, prenant appui contre les plateaux 124, 126 par l'intermédiaire d'une surface de contact dont le rayon de courbure est inférieur à celui des renfoncements 124'', 126'' précités, afin de permettre un déplacement mutuel de cet organe par rapport au plateau. La figure 5 représente une quatrième variante de réalisation de l'implant intervertébral, désigné dans son ensemble par la référence 168. Ce dernier comprend un enrobage, formé par deux plateaux rigides 74, 176, entre lesquels est intercalée une âme élastique 178. Les plateaux 174, 176 recouvrent partiellement l'âme 178, en ce sens qu'ils sont disposés sur les bords de cette âme adjacents aux corps vertébraux. Les plateaux sont par exemple réalisés en titane alors que l'âme, qui est par exemple collée au plateau, est réalisée par exemple en silicone ou en élastomère, notamment en caoutchouc.
Les plateaux 174, 176 entrent en contact avec les corps vertébraux 4, 4' par l'intermédiaire de surfaces planes 174', 176'. Cet implant est inséré dans l'espace intervertébral par impaction, comme les implants 18, 68 et 118. Il est également envisageable que la distance séparant les surfaces de contact 174', 176', qui correspond à la dimension verticale de l'implant posé, augmente vers sa partie antérieure, dans la position anatomique verticale du repos du patient.
La figure 6 illustre un cinquième mode de réalisation de l'implant intervertébral, désigné dans son ensemble par la référence 218. Ce dernier comprend une bille rigide 228 entourée par un anneau périphérique 226, d'axe principal parallèle à l'axe principal de la colonne vertébrale, cet anneau étant réalisé en un matériau élastique tel que du caoutchouc. Les extrémités latérales de l'anneau sont solidaires de plaques 224 qui entrent en contact avec les corps vertébraux respectifs 4, 4' . Les implants 18, 68, 118, 168, 218 décrits ci-dessus sont des prothèses totales de disque. Il est également possible de faire appel à un implant 268, illustré sur la figure 7, qui est une prothèse partielle de disque. Cette dernière 268, qui est insérée dans le disque 270, est disposée de façon décalée, par rapport à l'axe principal A de la chaîne vertébrale qui, lorsque le patient se trouve en position debout, est un axe vertical passant par le plan médian P s 'étendant d'arrière en avant du patient. Cette prothèse peut être insérée par vissage ou impactage dans l'espace intervertébral. Cette prothèse partielle 268 est associée à un organe d'amortissement 20A, qui est disposée, de façon décalée, du même côté de l'axe A que la prothèse partielle 268.
On peut associer à la prothèse partielle 268, une prothèse supplémentaire 268', située de l'autre côté de l'axe A. Cette prothèse partielle 268', qui est représentée en traits mixtes, peut être analogue à la prothèse partielle 268 étant entendu qu' il est possible de conférer à ces deux prothèses partielles 268, 268' des hauteurs différentes, de manière à compenser un éventuel effondrement du disque se produisant de façon asymétrique, en vue de derrière. La prothèse partielle 268' est associée à un organe d'amortissement supplémentaire 20B, représenté en traits mixtes, qui est prévu du même côté de l'axe A que la prothèse partielle 268' .
La figure 8 représente les deux organes d'amortissement
20A, 20B disposés de part et d'autre des articulaires 8, 10.
Ces organes d'amortissement présentent une partie métallique et sont par exemple conformes à l'enseignement de FR-A- 2 751 864. Ils sont avantageusement reliés l'un à l'autre au moyen d'une tige transversale 272, s 'étendant sensiblement horizontalement. La liaison entre chaque organe 20, 20A et la tige 272 est rigide, et fait par exemple intervenir une soudure. Elle est avantageusement réalisée au niveau de la partie médiane de ces organes d'amortissement.
Les figures 9 à 11 illustrent une variante supplémentaire de l'invention, dans laquelle il est prévu deux vis pédiculai- res supérieures 322, 324, disposées de part et d'autre de l'axe principal de la colonne vertébrale, ainsi que deux vis pédiculaires inférieures 322', 324'. Le dispositif de stabilisation comprend un implant 318, par exemple analogue à celui 168, ainsi qu'un organe extra-discal 320, qui est analogue à celui 20.
Ce dispositif de stabilisation comprend également un élément de butée supérieur 326, comportant une branche horizontale 328 ainsi que deux branches verticales 330. Cette branche 328 est creusée de deux ouvertures circulaires destinées au passage de la tige des vis pédiculaires supérieures 322, 324. Les parois de chaque ouverture sont prolongées par un fourreau axial 329, recouvrant une partie de la vis. Ce fourreau, qui peut être venu de matière avec la branche 328, reçoit une vis d'arrêt 331 apte à immobiliser de façon sélective l'élément de butée par rapport à la vis pédiculaire, selon une translation parallèle à l'axe principal de cette dernière .
Ce dispositif comprend également un élément de butée inférieur 334, comportant une branche horizontale 336 prolongée, à ses deux extrémités, par des tiges 337 pourvues de sphères 338. Cet élément inférieur est creusé de deux ouvertures, destinées au passage de la tige des deux vis pédiculaires inférieures 322', 324'. De façon analogue à ce qui a été décrit ci -dessus pour l'élément supérieur, chaque ouverture est pourvue d'un fourreau axial 329' , muni d'une vis 331' .
Par ailleurs, en variante, au moins une des ouvertures peut être une lumière oblongue. Ceci permet ainsi d'adapter les dimensions des éléments de butée à différents espacements des vis pédiculaires. Les branches horizontales 328 et 336 peuvent présenter des longueurs variables, en étant par exemple télescopiques .
Chaque branche verticale 330 est repliée, de sorte que son extrémité possède une surface plane 326' s 'étendant de façon oblique. Ceci signifie que cette extrémité n'est ni parallèle à l'axe transversal médian A', s'étendant de la droite vers la gauche du patient, ni parallèle à l'axe sagittal médian A'', s'étendant d'arrière en avant du patient
(figure 11) . L'axe principal D de cette surface plane 326' est parallèle à une droite D' passant par l'intersection de ces deux axes A' et A'', notamment une bissectrice.
Chaque surface 326' coopère avec une sphère 338 correspondante, selon un contact sensiblement ponctuel. De la sorte, deux rotations autour des axes A' et A' ' sont autorisées entre les éléments de butée supérieur et inférieur et, ce faisant, entre les deux vertèbres 2 et 2' . En revanche, la rotation autour de l'axe vertical A est interdite entre ces deux vertèbres .
Par ailleurs, une mise en translation mutuelle des deux vertèbres 2, 2', selon l'axe sagittal A'', est autorisée dans un unique sens. Ainsi, la vertèbre supérieure ne peut se déplacer vers l'avant, par rapport à la vertèbre inférieure, mais en revanche est libre de se déplacer vers l'arrière par rapport à cette vertèbre inférieure.
En outre, toute translation mutuelle des deux vertèbres 2, 2' est interdite, dans les deux sens, selon l'axe transversal A' . Enfin, une translation mutuelle entre ces deux vertèbres est autorisée, dans les deux sens, selon l'axe vertical A.
D'autres agencements peuvent être envisagés. Ainsi, l'élément de butée supérieur peut être muni d'au moins une sphère 338', coopérant avec une branche verticale, terminée par une surface plane oblique 336', s'étendant à partir de la branche horizontale 336 de l'élément inférieur (figure 12) . Il peut être fait appel à la coopération de deux surfaces d'appui sphériques adjacentes 342, 342', dont chacune appartient à un élément de butée respectif (figure 13) . A titre de variante supplémentaire, au moins une des branches verticales 330 peut, au moins partiellement, être réalisée en un matériau élastique, dont l'élasticité autorise un contact permanent entre chaque branche 330 et une sphère correspondante 338. Il est également envisageable de réaliser au moins une branche verticale en deux parties, possédant un certain débattement mutuel en rotation, autour de l'axe principal de la branche. Cette possibilité de débattement peut être provisoire, pour la mise en place des deux éléments de butée, ou permanente afin d'assurer à chaque instant une adaptation angulaire entre la branche et la sphère.
Il est possible de prévoir une unique branche verticale 330, coopérant avec une unique sphère 338, notamment dans le cas où une partie de l'articulation postérieure naturelle n'a pas été détruite. Etant donné que chaque élément supérieur ou inférieur est monté sur deux vis pédiculaires à la fois, ceci permet d'éviter toute desolidarisation de ces vis par rapport aux corps vertébraux, une fois celles-ci mises en place.
La figure 14 illustre une variante supplémentaire de réalisation de l'invention. Le dispositif qui y est décrit comprend un implant 368, destiné à être inséré au moins partiellement dans l'espace intervertébral. Cet implant comprend deux chambres respectivement avant 368' et arrière 368'', entourées par deux coquilles 369. Chacune de ces dernières, qui présente une section transversale sensiblement en arc de cercle, est réalisée en un matériau rigide, tel que du titane. Ces coquilles 369, qui sont destinées à entrer en contact avec les corps vertébraux 4, 4', sont assujetties aux chambres, par exemple par collage.
Ces deux chambres 368, 368', qui sont séparées par une membrane 396, éventuellement poreuse, sont remplies d'un fluide d'amortissement. Ce dernier comprend au moins un liquide, tel que de l'eau ou de l'huile. Il peut également contenir de l'air, ou encore un corps hydrophile, tel de 1 ' hydrogel .
Le dispositif de stabilisation illustré sur cette figure 11 comprend également un organe d'amortissement 370, disposé à l'arrière de l'espace intervertébral. Cet organe comprend une cuve rigide 372 à l'intérieur de laquelle est disposé un piston 374, qui comprend une tête 376, formant extrémité supérieure, dont les dimensions transversales sont voisines de celles de la cuve. Un joint torique d'étanchéité 378 est monté entre les parois en regard de la tête et de la cuve.
La tête 376 du piston s'étend à partir d'une tige 380 verticale qui traverse, de façon étanche, la paroi inférieure
382 de la cuve 372, avec interposition d'un joint torique 384.
L'extrémité inférieure de la tige 380, opposée à la tête 376, est montée à rotule sur la tête de la vis inférieure 371.
La tête du piston délimite des chambres respectivement supérieure 386 et inférieure 388, appartenant à la cuve 372. La chambre supérieure reçoit un ressort 390, travaillant en compression, qui s'étend verticalement entre la paroi supérieure de la cuve et la paroi en regard de la tête. Ce ressort permet le rappel du piston dans sa position basse, qui correspond à une posture lordosée du patient, physiologique- ment avantageuse.
La chambre avant de l'implant 368 est mise en communica- tion fluidique avec la chambre supérieure de l'organe 370, par l'intermédiaire d'un conduit 392, alors que la chambre arrière de l'implant est mise en communication fluidique avec la chambre inférieure 388 par l'intermédiaire d'un conduit supplémentaire 394. De la sorte, lorsque le patient se penche vers l'avant, selon la flèche F, du fluide est chassé de la chambre avant en direction de la chambre supérieure, ce qui contribue à faire descendre le piston 374 dans la cuve, à l'opposé de la vis supérieure 373. Cette remontée induit un déplacement de fluide, par le conduit 394, de la chambre inférieure vers la chambre arrière. Ce mouvement de flexion est donc amorti par ces différents écoulements de fluide.
L'invention n'est pas limitée aux exemples décrits et représentés.
L'implant appartenant au dispositif de stabilisation de l'invention peut être partiel ou total. Dans le cas où il s'agit d'un implant partiel, plusieurs implants de ce type peuvent être disposés entre deux mêmes vertèbres. Cet implant peut être mis en place, soit par voie antérieure, soit par voie postérieure.
Par ailleurs, on peut prévoir d'utiliser une bille unique, analogue à celle 228, qui confère trois degrés de liberté en rotation, ainsi que deux degrés de liberté en translation aux corps vertébraux 4, 4' . Il est également possible de réaliser l'implant intervertébral sous forme d'une enveloppe renfermant un gel hydrophile ou de l'eau, cet implant constituant une prothèse de nucleus.
Il est également possible de fixer l'implant sur la paroi verticale des corps vertébraux, par exemple par vissage, conformément à l'enseignement de EP-A-0 346 269, cet implant étant alors inséré seulement partiellement entre les deux corps vertébraux.
L'implant intervertébral peut renfermer un fluide d'amortissement, et être conforme à l'un des modes de réalisation décrits dans la demande de brevet français, déposée le 29 décembre 1999, sous le numéro 99 16662. Cet implant intervertébral fluidique est susceptible de coopérer avec un organe extra-discal de type mécanique, par exemple analogue à celui 20.
Par ailleurs, l'organe extra-discal peut également renfermer un tel fluide d'amortissement, et être conforme à l'un des modes de réalisation décrits dans la demande de brevet français ci -dessus mentionnée. Cet organe extra-discal fluidique est susceptible de coopérer avec un implant intervertébral mécanique, tel que par exemple celui 18.
L'invention permet de réaliser les objectifs précédemment mentionnés.
En cas de pathologie dégénérative du disque intervertébral, s'étendant aux nerfs qui lui sont adjacents, il est nécessaire pour le chirurgien de libérer la racine nerveuse ainsi comprimée. A cet effet, l'opération correspondante induit une destruction au moins partielle de l'articulation intervertébrale postérieure.
Le dispositif de l'invention permet de restaurer la stabilité postérieure, qui avait été sensiblement diminuée du fait de la chirurgie. L'implant intervertébral permet de restaurer la hauteur du disque et de rappeler le mouvement intervertébral naturel, étant donné qu'il confère au moins un degré de liberté aux corps vertébraux en regard. Par ailleurs, l'organe d'amortissement extra-discal garantit une composante supplémentaire à cette stabilisation postérieure.
Le fait de combiner cet implant intervertébral et cet organe extra-discal permet de réaliser ces deux éléments de manière simple et fiable. Il est ainsi possible de répartir, entre ces deux éléments, les différentes fonctions mécaniques qui sont nécessaires, en vue d'assurer une stabilité intervertébrale satisfaisante. Ceci permet donc de réduire les contraintes mécaniques exercées sur chacun de ces deux éléments, de sorte que ces derniers sont soumis à une usure restreinte. Ceci en allonge donc la durée de vie de façon correspondante.
Le dispositif de stabilisation de l'invention garantit ainsi que le mouvement relatif des deux vertèbres qu'il relie est suffisamment proche du mouvement autorisé par un disque vertébral naturel, pour que n'apparaisse pas de dysfonctionne- ment majeur au niveau de l'ensemble de la chaîne vertébrale.
L'emploi de deux organes d'amortissement extra-discaux, disposés de part et d'autres d'un axe principal de la colonne vertébrale est avantageux. En effet, il assure une composante supplémentaire d'amortissement, lorsque le patient se penche sur les côtés .
Prévoir des moyens de liaison entre ces deux organes d'amortissement est avantageux, dans la mesure où cela assure une réduction sensible du cisaillement horizontal intervertébral, comme en cas de rupture ou d'absence d'un ou de deux massifs articulaires postérieurs.
Réaliser l'implant intervertébral sous la forme d'au moins une prothèse partielle est avantageux. En effet, de telles prothèses, du fait de leur dimensions, peuvent être introduites depuis l'arrière du patient, de sorte qu'il peut être fait appel à une unique opération, au cours de laquelle ces prothèses sont implantées en même temps que l'organe d' amortissement . Prévoir une unique prothèse, associée à un unique organe d'amortissement extra-discal, tous deux décalés d'un même côté de l'axe principal de la chaîne vertébrale, permet de remédier à des effondrements asymétriques de l'espace intervertébral, vu de derrière. De tels effondrements asymétriques peuvent également être palliés en faisant appel à deux prothèses de hauteurs différentes, disposées de part et d'autre de l'axe principal de la chaîne vertébrale.

Claims

REVENDICATIONS
1. Dispositif de stabilisation intervertébral destiné à relier deux vertèbres voisines (2, 2'), caractérisé en ce qu'il comprend un implant (18 ; 68 ; 118 ; 168 ; 218 ; 268 ; 318 ; 368) destiné à être inséré au moins partiellement entre les corps vertébraux (4, 4') des deux vertèbres voisines, ledit implant (18 ; 68 ; 118 ; 168 ; 218 ; 268 ; 318 ; 368) étant apte à conférer auxdits deux corps vertébraux voisins (4, 4') au moins un degré de liberté mutuel, ledit dispositif comprenant également au moins un organe extra-discal (20 ; 320 ; 370), disposé à l'arrière de l'espace intervertébral (12) , propre à amortir un déplacement entre lesdites vertèbres (2, 2') , au moins dans le sens de la flexion intervertébrale.
2. Dispositif selon la revendication 1, caractérisé en ce que ledit implant (18 ; 68) est apte à conférer aux deux corps vertébraux (4, 4') au moins un degré de liberté en rotation, autour d'un pivot fixe (28 ; 78) dudit implant.
3. Dispositif selon la revendication 2, caractérisé en ce qu'il est prévu des moyens supplémentaires d'amortissement (30) au moins dans le sens de la flexion intervertébrale, disposés vers la partie antérieure dudit implant (18 ; 68) .
4. Dispositif selon la revendication 1, caractérisé en ce que ledit implant (118) est apte à conférer aux deux corps vertébraux (4, 4') au moins un degré de liberté en rotation, autour d'un pivot mobile (128 ; 228) dudit implant.
5. Dispositif selon la revendication 1, caractérisé en ce que ledit implant (168) comprend une âme élastique (178), notamment réalisée en un polymère de silicone ou un élastomè- re, partiellement recouverte par un enrobage (174, 176) réalisé en un matériau rigide.
6. Dispositif selon l'une quelconque des revendications précédentes, caractérisé en ce qu'il est prévu deux organes d'amortissement extra-discaux (20A, 20B) disposés de part et d'autre d'un axe principal (A) de la chaîne vertébrale.
7. Dispositif selon la revendication 6, caractérisé en ce qu'il est prévu en outre des moyens de solidarisation (272) des organes d'amortissement (20A, 20B) entre eux.
8. Dispositif selon l'une des revendications précédentes, caractérisé en ce que ledit implant comprend au moins une prothèse partielle (268, 268') de disque.
9. Dispositif selon la revendication 8, caractérisé en ce que ledit implant intervertébral comprend une unique prothèse partielle (268) , associée à un unique organe (20A) d'amortissement extra-discal, tous deux étant décalés d'un même côté par rapport à l'axe principal (A) de la chaîne vertébrale.
10. Dispositif selon la revendication 9, caractérisé en ce que ledit implant intervertébral comprend deux prothèses partielles (268, 268') disposées de part et d'autre dudit axe principal (A) , ainsi que deux organes (20A, 20B) d'amortisse- ment extra-discaux, disposés de part et d'autre dudit axe (A) .
11. Dispositif selon l'une des revendications précédentes, caractérisé en ce qu'il comprend en outre un élément de butée supérieur (326), solidaire d'une vertèbre supérieure, ainsi qu'un élément de butée inférieur (334), solidaire d'une vertèbre inférieure, ces éléments de butée extra-discaux possédant des surfaces d'appui mutuelles (326', 338 ; 336', 338' ; 342, 342') aptes à autoriser une rotation mutuelle desdites vertèbres supérieure (2) et inférieure (2') autour d'axes transversal (A') et sagittal (A'') du patient, ainsi qu'à empêcher une rotation mutuelle de ces deux vertèbres autour d'un axe vertical (A), ces surfaces d'appui étant en outre aptes à autoriser une translation mutuelle de ces vertèbres dans un unique sens selon l'axe sagittal (A''), à autoriser une translation entre ces deux vertèbres dans les deux sens selon l'axe vertical (A) , et à interdire une translation entre ces deux vertèbres dans les deux sens selon l'axe transversal (A') .
12. Dispositif selon la revendication 11, caractérisé en ce que l'un desdits éléments de butée comprend deux surfaces d'appui planes (326'), disposées de part et d'autre de l'axe vertical (A), ces deux surfaces s'étendant de façon oblique et coopérant avec deux sphères (338) dont est pourvu l'autre desdits éléments.
13. Dispositif selon les revendications 11 ou 12, caractérisé en ce que chaque élément de butée (326, 334) est solidaire de deux vis pédiculaires, respectivement supérieures (322, 324) et inférieures (322', 324').
14. Dispositif selon la revendication 13, caractérisé en ce qu'il est prévu des moyens (331, 331') permettant de solidariser en translation, de façon sélective, chaque élément de butée avec au moins une vis pédiculaire.
15. Dispositif selon l'une quelconque des revendications précédentes, caractérisé en ce que ledit implant (368) comprend au moins une chambre (368' , 368' ' ) et en ce que ledit organe extra-discal (370) comprend au moins une chambre (386, 388), lesdites au moins deux chambres renfermant un fluide, et en ce que sont prévus des moyens (392, 394) de mise en communication fluidique de ces chambres.
16. Dispositif selon la revendication 15, caractérisé en ce que les moyens de mise en communication comprennent au moins un conduit (392, 394) s'étendant entre ces chambres.
17. Dispositif selon la revendication 15, caractérisé en ce qu'un premier conduit assure la communication entre les chambres dans un premier sens, alors qu'un second conduit assure cette communication dans un second sens, opposé au premier, les sections de passage des premier et second conduits étant différentes.
18. Dispositif selon l'une des revendications 15 à 17, caractérisé en ce que l'implant (368) et/ou l'organe extradiscal comprend au moins deux chambres (368', 368'') et en ce qu'un élément poreux (396) sépare lesdites chambres.
19. Dispositif selon la revendication 18, caractérisé en ce que ledit organe poreux est mobile par rapport à ces chambres .
20. Dispositif selon l'une des revendications 15 à 19, caractérisé en ce qu'il est prévu au moins un piston (374), séparant deux chambres adjacentes.
21. Dispositif selon l'une des revendications 15 à 20, caractérisé en ce qu'au moins une chambre est pourvue d'une paroi déformable.
PCT/FR2000/003368 1999-12-01 2000-12-01 Dispositif de stabilisation intervertebral WO2001039678A1 (fr)

Priority Applications (7)

Application Number Priority Date Filing Date Title
CA002392868A CA2392868C (fr) 1999-12-01 2000-12-01 Dispositif de stabilisation intervertebral
JP2001541414A JP4294901B2 (ja) 1999-12-01 2000-12-01 椎間安定装置
US10/148,693 US7291150B2 (en) 1999-12-01 2000-12-01 Intervertebral stabilising device
AU21824/01A AU778410B2 (en) 1999-12-01 2000-12-01 Intervertebral stabilising device
EP00985390A EP1233711B1 (fr) 1999-12-01 2000-12-01 Dispositif de stabilisation intervertebral
DE60030313T DE60030313T2 (de) 1999-12-01 2000-12-01 Vorrichtung zur zwischenwirbelstabilisierung
US11/982,761 US8172880B2 (en) 1999-12-01 2007-11-05 Intervertebral stabilising device

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
FR99/15160 1999-12-01
FR9915160A FR2801782B3 (fr) 1999-12-01 1999-12-01 Dispositif de stabilisation intervertebral
FR9916662A FR2803188A1 (fr) 1999-12-29 1999-12-29 Dispositif et ensemble intervertebraux de stabilisation
FR99/16662 1999-12-29
FR0006640A FR2809304A1 (fr) 2000-05-24 2000-05-24 Dispositif de stabilisation intervertebral
FR00/06640 2000-05-24

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EP (1) EP1233711B1 (fr)
JP (1) JP4294901B2 (fr)
AT (1) ATE336952T1 (fr)
AU (1) AU778410B2 (fr)
CA (1) CA2392868C (fr)
DE (1) DE60030313T2 (fr)
ES (1) ES2270888T3 (fr)
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Cited By (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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AU778410B2 (en) 2004-12-02
US8172880B2 (en) 2012-05-08
DE60030313T2 (de) 2007-08-23
US20030055427A1 (en) 2003-03-20
EP1233711B1 (fr) 2006-08-23
JP4294901B2 (ja) 2009-07-15
US7291150B2 (en) 2007-11-06
DE60030313D1 (de) 2006-10-05
CA2392868A1 (fr) 2001-06-07
EP1233711A1 (fr) 2002-08-28
CA2392868C (fr) 2008-08-05
JP2003515381A (ja) 2003-05-07
AU2182401A (en) 2001-06-12
ES2270888T3 (es) 2007-04-16
US20080065078A1 (en) 2008-03-13
ATE336952T1 (de) 2006-09-15

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