WO1999011203A1 - Prosthesis of the spinal column - Google Patents

Prosthesis of the spinal column Download PDF

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Publication number
WO1999011203A1
WO1999011203A1 PCT/AT1998/000201 AT9800201W WO9911203A1 WO 1999011203 A1 WO1999011203 A1 WO 1999011203A1 AT 9800201 W AT9800201 W AT 9800201W WO 9911203 A1 WO9911203 A1 WO 9911203A1
Authority
WO
WIPO (PCT)
Prior art keywords
prosthesis
vertebral body
spinal
anchoring
implant
Prior art date
Application number
PCT/AT1998/000201
Other languages
German (de)
French (fr)
Inventor
Ronald J. Sabitzer
Franz K. Fuss
Original Assignee
Sabitzer Ronald J
Fuss Franz K
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
Application filed by Sabitzer Ronald J, Fuss Franz K filed Critical Sabitzer Ronald J
Priority to AU89636/98A priority Critical patent/AU8963698A/en
Priority to EP98941133A priority patent/EP1009339A1/en
Publication of WO1999011203A1 publication Critical patent/WO1999011203A1/en

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Classifications

    • 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
    • A61F2/442Intervertebral or spinal discs, e.g. resilient
    • 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
    • A61F2/30767Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
    • A61F2/30771Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
    • 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
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30108Shapes
    • A61F2002/30199Three-dimensional shapes
    • A61F2002/30224Three-dimensional shapes cylindrical
    • 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
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30108Shapes
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    • A61F2002/30242Three-dimensional shapes spherical
    • A61F2002/30245Partial spheres
    • AHUMAN NECESSITIES
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    • 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
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    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
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    • A61F2002/30252Three-dimensional shapes quadric-shaped
    • A61F2002/30253Three-dimensional shapes quadric-shaped ellipsoidal or ovoid
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    • 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
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
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    • A61F2002/30301Three-dimensional shapes saddle-shaped
    • AHUMAN NECESSITIES
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    • 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
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30316The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
    • A61F2002/30329Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2002/30331Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by longitudinally pushing a protrusion into a complementarily-shaped recess, e.g. held by friction fit
    • A61F2002/30354Cylindrically-shaped protrusion and recess, e.g. cylinder of circular basis
    • 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
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30316The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
    • A61F2002/30329Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2002/30405Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by screwing complementary threads machined on the parts themselves
    • 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
    • A61F2/30767Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
    • A61F2/30771Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
    • A61F2002/30878Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves with non-sharp protrusions, for instance contacting the bone for anchoring, e.g. keels, pegs, pins, posts, shanks, stems, struts
    • 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
    • A61F2/30767Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
    • A61F2/30771Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
    • A61F2002/30904Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves serrated profile, i.e. saw-toothed
    • 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
    • A61F2/46Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor
    • A61F2002/4631Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor the prosthesis being specially adapted for being cemented
    • 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
    • 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
    • A61F2220/0033Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by longitudinally pushing a protrusion into a complementary-shaped recess, e.g. held by friction fit
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    • 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
    • A61F2230/0069Three-dimensional shapes cylindrical
    • 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
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    • 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
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    • A61F2230/0073Quadric-shaped
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    • 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
    • A61F2230/0095Saddle-shaped

Definitions

  • the invention relates to a spinal prosthesis for insertion into the intervertebral space of the spine after surgical removal of the intervertebral disc.
  • intervertebral disc intervertebral disc, intervertebral disc
  • the intervertebral disc has two functions: ensuring the mobility of two vertebrae to one another and the effect of a shock absorber. It may be necessary to remove the disc (disc) for various medical reasons. First of all, there is no standard surgical therapy for or after disc removal. Three surgical methods are generally used as an operative option: A: fusion, B: neither disc replacement nor fusion, C: disc replacement (only available in the lumbar spine).
  • intervertebral space intervertebral gap
  • the implant consists of only one piece, which may have elastic properties and is not connected to the vertebral bodies. These implants ensure reduced mobility and possibly a certain shock absorber effect. The fulcrum of these implants lies in the implant itself and not in the lower vertebral body, as is physiologically the case. aa) no elastic properties: a steel ball is installed as an implant (Fernström ball-bearing prosthesis)
  • the implant consists of a single piece, which consists of hard cover plates and an elastic core.
  • the cover plates may have connecting or anchoring means in relation to the vertebral bodies.
  • These implants ensure reduced mobility and a certain shock absorber effect.
  • the fulcrum of these implants lies in the implant itself and not in the lower vertebral body, as is physiologically the case.
  • This relates to implants with the following patent numbers: CH 671 691 A5, WO 90/11740, US-A 4 911 718, US-A 5 071 437, US-A 5 171 281, EP 0 346 269 A2, EP 0 310 837 AI.
  • the implant is fixed to both vertebral bodies and consists of at least two parts that are movably connected to one another, as can be seen, for example, from FR-A 2 718 635. Each part is firmly connected to a vertebral body. Elastic elements can be installed between these parts. These two parts ensure reduced mobility and possibly a certain shock absorber effect.
  • the mobility is generated within the prosthesis; only with the Fernström ball-bearing prosthesis does the movement between the implant and both vertebrae take place. There is no implant that is movable with respect to one vertebral body and immovable with respect to the other.
  • shock absorber effect is eliminated: this does not put any strain on the neighboring segments, since there are other structures that take on this shock absorber effect (ligaments, muscles); in addition, there are no devices that act as shock absorbers for the large joints of the lower extremity (hip, knee, ankle).
  • the implant is firmly connected to both vertebrae: the fulcrum is right there! in the wrong place, in the middle of the implant or on its edge. Because parts of the implant are firmly connected to the vertebrae, the (non-physiological) kinematics of the implant prescribe the kinematics to the vertebrae. This in turn leads to an unnatural strain on the other spinal devices (ligaments, joints, muscles) and to shear forces between the implant and vertebra. Due to the fixed connection of the implant to both vertebrae, the implant cannot be forced out of the intervertebral space due to the unnatural kinematics.
  • the object of the invention relates to a prosthesis that maintains the physiological or natural mobility and maintains the center of rotation in its physiological position.
  • the spinal prosthesis according to the invention is essentially characterized in that the prosthesis, which is formed in one piece in the installed state, has a curved surface on the upper side of the prosthesis and is movable relative to the cranial vertebral body, in that the prosthesis by means of anchoring and connecting means on the underside of the prosthesis is immovably connected to the caudal vertebral body and that the axis of rotation between the neighboring vertebral bodies lies in the caudal vertebral body when bending forwards and backwards.
  • the prosthesis must be inserted into the intervertebral space during operations in which the disc (disc) is removed.
  • the implant or the prosthesis is constructed according to the invention in such a way that the cranial (upper [standing person]) vertebral body is movable relative to the one-piece prosthesis and the prosthesis is not movable relative to the caudal (lower) vertebral body.
  • the inventive design of the spinal prosthesis not only succeeds in reliably anchoring the prosthesis in the caudal vertebral body, but it can also provide the physiological or natural mobility of the adjacent vertebral bodies by providing the mobility of the prosthesis, which is designed in one piece when installed, in accordance with the invention the axis of rotation between the adjacent vertebral bodies in the caudal vertebral body, as corresponds to the natural axis of rotation between adjacent vertebral bodies, are maintained.
  • the prosthesis consists of two equally large, essentially symmetrical, parts that can be put together, but this embodiment also results in a one-piece prosthesis in the installed state, which is relative to the cranial vertebral body is movable along the curved surface, while the prosthesis according to the invention is immovably anchored in the caudal vertebral body.
  • the curved surface of the prosthesis facing the cranial vertebral body is at least one section of a spherical surface. , Ellipsoid, saddle or cylinder surface is formed, with the appropriate choice of the curved surface and a corresponding orientation when Installation of the prosthesis allows different degrees of freedom of movement to be achieved between the adjacent vertebral bodies.
  • a different selection of degrees of freedom can be achieved in that the curved surface has a different curvature or curvature along two essentially normal intersection lines, as corresponds to a preferred embodiment of the prosthesis according to the invention.
  • the anchoring and connecting means are formed by at least one web or extension, which in particular has a granular, porous, ribbed, toothed or roughened surface.
  • the connecting and anchoring means are releasably fixed to the prosthesis via a plug-in or threaded connection.
  • the implant can be used in all spine sections (cervical, thoracic and lumbar spine), since it takes into account the individual kinematics of each section and can be produced in any necessary size; b) it can be installed from the ventral (front) and dorsal (rear); c) it consists of one part (or from two parts, left and right part) which is only connected to the lower vertebral body; d) because of its shape it guarantees a maximum of three degrees of freedom of movement and maintains the physiological axes of movement in their natural position, the pivot point in the case of ante- and retroversion being in the middle of the caudal vertebral body; e) the cranial vertebral body is movable relative to the prosthesis, so that the bone tissue of the prosthesis can adapt through physiological remodeling processes; and f) due to points d) and e) the structures associated with the movement segment (ligaments, joints, muscles) are not overused.
  • Fig. 1 shows an intact spine segment in a side view
  • FIG. 2 shows a spinal movement segment from the side with a spinal prosthesis according to the invention (kinematic spinal prosthesis);
  • FIG. 3 shows a sagittal section (section viewed from the side) through an embodiment of a prosthesis according to the invention
  • FIG. 4 shows a frontal section (sectional area seen from the front) through further modified embodiments of the prosthesis according to the invention with different curvature of the surface in accordance with arrows IV of FIGS. 2 and 3, FIG. 3 showing a view in the direction of arrow III 4 is.
  • a natural, intact spinal movement segment (Fig. 1) from the side (front to left, back to the right, standing person) consists of the cranial (upper) vertebral body 1, the caudal (lower) vertebral body 3 and the discus in between ( 2, intervertebral disc).
  • the direction of movement 5 of the upper vertebra 1 during forward and backward bending (ante / retro version) takes place around a pivot point 4 which lies in the lower vertebra 3.
  • the prosthesis or the implant 6 (FIG. 2) is inserted between the vertebral bodies 1, 3.
  • the direction of movement 5) of the upper vertebra 1 during forward and backward bending (ante / retro version) is now carried out by one rotation.
  • the one-piece prosthesis 6 (FIG. 3) is divided into an upper side 8 and a lower side 10.
  • a sinking of the prosthesis 6 in the lower vertebral body 3 is drawn as anchoring means.
  • the frontal section (section viewed from the front) through the prosthesis (FIG. 4) shows modified embodiments of possible different curvatures of the surface of the prosthesis 6: spherical surface 9a, ellipsoid surface 9b, saddle surface 9c, cylinder surface 9d.
  • the top 8 has a curved surface 9.
  • the curvature defines the kinematics in the direction of movement 5 of the upper or cranial vertebral body. With forward and backward bending (ante- and retroversion) of the spine, the fulcrum 7 of the movement lies in the lower vertebral body 3.
  • the center of curvature of the prosthesis (in the case of a sagittally cut prosthesis, cutting surface viewed from the side; FIG. 3) must therefore lie at the same point. If the curvature corresponds to the circular geometry, then the center of curvature is equal to pivot point 7 (center of rotation). if the implant is viewed from the front (frontal cut, cut surface viewed from the front; Fig. 4), then the curvature can be different. If the curvature from the side view 9 is identical to that from the front view 9a, then the top of the prosthesis corresponds to the circular geometry. The prosthesis therefore guarantees three degrees of freedom of movement:
  • the top of the prosthesis corresponds either to the ellipsoid geometry or the saddle geometry.
  • the prosthesis 6 then ensures only two degrees of freedom of movement: -a) forward / backward bending about a horizontal axis -b) lateral bending about a sagittal axis
  • the top of the prosthesis corresponds to the cylinder geometry.
  • the prosthesis then only guarantees one degree of freedom of movement: -a) Forward / backward bending around a horizontal axis
  • the underside 10 of the one-piece prosthesis 6 must be designed in such a way that it cannot move relative to the lower or caudal vertebral body 3 (be it rotation or translation).
  • This immobility is given by the anchoring and connecting means 11.
  • These can be: webs or one or more extensions 11 which are sunk into the lower vertebral body 3; a granular, porous, ribbed, serrated or roughened surface surface 13 into which the bone tissue can grow; Bone cement for connecting the prosthesis and bone.
  • the connecting means do not necessarily have to be permanently connected to the prosthesis, but can also be fastened to the prosthesis for easier installation by means of a plug connection or thread, as is indicated in FIG. 4 by a detachable connection 14.
  • the prosthesis can also consist of two parts of the same size (right part and left part), as indicated in Fig. 4 when the prosthesis is formed with the curvature 9a by the parts 6 and 6 ', the Division takes place essentially along the section line 12.
  • the composition of the parts in the intervertebral gap however, the one-piece form of the prosthesis 6 described above results in the installed state.
  • the advantage in this case is that the prosthesis can also be installed from the back (dorsal), particularly on the lumbar spine.

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Abstract

In a spinal column prosthesis for insertion into the intervertebral space of the spinal column after surgical removal of the intervertebral disk, it is provided that the prosthesis (6), which in the inserted state is designed in a single piece, has a curved surface (9) at its top side, is movable relative to the cranial vertebra (1) and is fixed to the caudal vertebra (3) by anchoring and connecting means (11) arranged on the bottom side (10) of the prosthesis. The axis of rotation (7) between adjacent vertebrae (1, 3) when bending forwards and backwards (5) lies in the caudal vertebra (3). This makes it possible to preserve the natural mobility between adjacent vertebrae (1, 3) and to keep the natural centre of rotation in its physiological position.

Description

WIRBELSÄULEN-PROTHESE SPINE PROSTHESIS
Die Erfindung betrifft eine Wirbelsäulen-Prothese zum Einbringen in den Zwischenwirbelspalt der Wirbelsäule nach chirurgischer Entfernung der Bandscheibe.The invention relates to a spinal prosthesis for insertion into the intervertebral space of the spine after surgical removal of the intervertebral disc.
Der Discus intervertebralis (Zwischenwirbelscheibe, Bandscheibe) hat zwei Aufgaben: Gewährleistung der Beweglichkeit zweier Wirbel zueinander und Stoßdämpferwirkung. Aus ver- schiedenen medizinischen Gründen kann eine Entfernung des Discus (der Bandscheibe) nötig sein. Vorweg gesagt, es gibt keine chirurgische Standardtherapie für bzw. nach Discusent- fernung. Als operative Möglichkeit werden im allgemeinen drei Operationsmethoden verwendet: A: Fusion, B: weder Discus-Ersatz noch Fusion, C: Discusersatz (gibt es nur in der Lendenwirbelsäule).The intervertebral disc (intervertebral disc, intervertebral disc) has two functions: ensuring the mobility of two vertebrae to one another and the effect of a shock absorber. It may be necessary to remove the disc (disc) for various medical reasons. First of all, there is no standard surgical therapy for or after disc removal. Three surgical methods are generally used as an operative option: A: fusion, B: neither disc replacement nor fusion, C: disc replacement (only available in the lumbar spine).
Bei Fusion werden mittels diverser Verblockungsmöglichkeiten zwei benachbarte Wirbelkörper so miteinander verbunden, daß sowohl die Beweglichkeit als auch die Stoßdämpferwirkung verloren gehen.In Fusion, two adjacent vertebral bodies are connected to one another by means of various blocking options so that both the mobility and the shock absorber effect are lost.
Weder Discusersatz noch Fusion führen zu einer abnormen Beweglichkeit mit fehlender Stoßdämp erwirkung.Neither disc replacement nor fusion lead to abnormal mobility with no shock absorber effect.
Es gibt folgende Prothesen- bzw. Implantattypen (nur für die Lendenwirbelsäule), die zur Einbringung in den Zwischenwirbelraum (Intervertebralspalt) gedacht sind:The following types of prostheses or implants (only for the lumbar spine) are intended for insertion into the intervertebral space (intervertebral gap):
a) Das Implantat besteht nur aus einem einzigen Stück, welches eventuell elastische Eigenschaften aufweist und mit den Wirbelkörpem nicht verbunden ist. Diese Implantate gewährleisten eine reduzierte Beweglichkeit und eventuell eine gewisse Stoßdämpferwirkung. Der Drehpunkt dieser Implantate liegt im Implantat selbst und nicht im unteren Wirbelkörper, wie dies physiologischerweise der Fall ist. aa) keine elastischen Eigenschaften: Als Implantat wird eine Stahlkugel eingebaut (Fernström ball-bearing prothesis)a) The implant consists of only one piece, which may have elastic properties and is not connected to the vertebral bodies. These implants ensure reduced mobility and possibly a certain shock absorber effect. The fulcrum of these implants lies in the implant itself and not in the lower vertebral body, as is physiologically the case. aa) no elastic properties: a steel ball is installed as an implant (Fernström ball-bearing prosthesis)
ab) elastische Eigenschaften: Implantate mit folgenden Pa- tentnummern: WO 94/23671, WO 93/16664, DE 37 41 493 AI, US-Aab) elastic properties: implants with the following patent numbers: WO 94/23671, WO 93/16664, DE 37 41 493 AI, US-A
4 874 382, US-A 5 047 055, US-A 5 108 438, US-A 5 192 326, EP-A 0 304 305, US-A 5 320 644.4,874,382, US-A 5 047 055, US-A 5 108 438, US-A 5 192 326, EP-A 0 304 305, US-A 5 320 644.
b) Das Implantat besteht aus einem einzigen Stück, welches aus harten Deckplatten und aus einem elastischen Kern besteht. Die Deckplatten besitzen eventuell Verbindungs- oder Verankerungsmittel gegenüber den Wirbelkörpern. Diese Implantate gewährleisten eine reduzierte Beweglichkeit und eine gewisse Stoßdämpferwirkung. Der Drehpunkt dieser Im- plantate liegt im Implantat selbst und nicht im unteren Wirbelkörper, wie dies physiologischerweise der Fall ist. Das betrifft Implantate mit folgenden Patentnummern: CH 671 691 A5, WO 90/11740, US-A 4 911 718, US-A 5 071 437, US-A 5 171 281, EP 0 346 269 A2 , EP 0 310 837 AI.b) The implant consists of a single piece, which consists of hard cover plates and an elastic core. The cover plates may have connecting or anchoring means in relation to the vertebral bodies. These implants ensure reduced mobility and a certain shock absorber effect. The fulcrum of these implants lies in the implant itself and not in the lower vertebral body, as is physiologically the case. This relates to implants with the following patent numbers: CH 671 691 A5, WO 90/11740, US-A 4 911 718, US-A 5 071 437, US-A 5 171 281, EP 0 346 269 A2, EP 0 310 837 AI.
c) Das Implantat ist fix mit beiden Wirbelkörpem verbunden und besteht aus mindestens zwei Teilen, die beweglich miteinander verbunden sind, wie dies beispielsweise der FR-A 2 718 635 zu entnehmen ist. Jeder Teil ist mit einem Wirbel- körper fest verbunden. Zwischen diesen Teilen können elastische Elemente eingebaut sein. Diese zwei Teile gewährleisten eine reduzierte Beweglichkeit und eventuell eine gewisse Stoßdämpferwirkung. Der Drehpunkt dieser Implantate liegt im Implantat selbst oder am Rand des Implantats und nicht - wie normalerweise - im unteren Wirbelkörper. Unter "Rand" ist zu verstehen: Oberseite des Implantats (= Unterseite des oberen Wirbels; WO 93/10725), Unterseite des Implantats (= Oberseite des unteren Wirbels; US-A 5 314 477), Hinterseite des Implantats (US-A 4 759 769).c) The implant is fixed to both vertebral bodies and consists of at least two parts that are movably connected to one another, as can be seen, for example, from FR-A 2 718 635. Each part is firmly connected to a vertebral body. Elastic elements can be installed between these parts. These two parts ensure reduced mobility and possibly a certain shock absorber effect. The fulcrum of these implants lies in the implant itself or on the edge of the implant and not - as is usually the case - in the lower vertebral body. “Edge” is to be understood as: top of the implant (= bottom of the upper vertebra; WO 93/10725), bottom of the implant (= top of the lower vertebra; US Pat. No. 5,314,477), rear side of the implant (US Pat. No. 4 759 769).
ca) keine elastischen Eigenschaften: Implantate mit folgenden Patentnummern: US-A 5 314 477, EP 0 560 141 AI, US-A 5 258 031, US-A 5 246 458, EP-A 0 177 728, DE 35 29 761 AI, WO 93/10725.ca) no elastic properties: implants with the following patent numbers: US-A 5 314 477, EP 0 560 141 AI, US-A 5 258 031, US-A 5 246 458, EP-A 0 177 728, DE 35 29 761 AI, WO 93/10725.
cb) elastische Eigenschaften: Implantate mit folgenden Pa- tentnummern: WO 94/26213, EP 0 566 810 AI, DE 41 09 941 AI,cb) elastic properties: implants with the following patent numbers: WO 94/26213, EP 0 566 810 AI, DE 41 09 941 AI,
DE 42 13 771 Cl, US-A 4 309 777, US-A 5 002 576, US-A 4 759 769, US-A 4 946 378, US-A 4 873 477.DE 42 13 771 Cl, US-A 4 309 777, US-A 5 002 576, US-A 4 759 769, US-A 4 946 378, US-A 4 873 477.
Bei all diesen Implantattypen entsprechend dem oben ange- führten Stand der Technik wird die Beweglichkeit innerhalb der Prothese erzeugt; nur bei der Fernström ball-bearing prothesis erfolgt die Bewegung zwischen Implantat und beiden Wirbelkörpern. Es gibt kein Implantat, das gegenüber einem Wirbelkörper beweglich und gegenüber dem anderen unbeweglich ist.With all these types of implants according to the state of the art mentioned above, the mobility is generated within the prosthesis; only with the Fernström ball-bearing prosthesis does the movement between the implant and both vertebrae take place. There is no implant that is movable with respect to one vertebral body and immovable with respect to the other.
Die Probleme, die sich nach operativer Versorgung ergeben, sind folgende:The problems that arise after operative care are as follows:
a) die Beweglichkeit ist aufgehoben: Dadurch werden die Nachbarsegmente (benachbarte Bandscheiben) insofern überbelastet, als sie die verlorengegangene Beweglichkeit mitübernehmen müssen.a) The mobility is eliminated: This causes the neighboring segments (adjacent intervertebral discs) to be overloaded insofar as they have to take over the lost mobility.
b) die Stoßdämpferwirkung ist aufgehoben: Dies führt zu keiner Belastung der Nachbarsegmente, da es weitere Strukturen gibt, die diese Stoßdämpferwirkung übernehmen (Bänder, Muskeln) ; außerdem gibt es bei den großen Gelenken der unteren Extremität (Hüft-, Knie-, Sprunggelenk) auch keine als Stoßdämpfer wirkenden Einrichtungen.b) the shock absorber effect is eliminated: this does not put any strain on the neighboring segments, since there are other structures that take on this shock absorber effect (ligaments, muscles); in addition, there are no devices that act as shock absorbers for the large joints of the lower extremity (hip, knee, ankle).
c) eine Beweglichkeit ist vorhanden und das Implantat ist mit den Wirbeln nicht verbunden: Der Drehpunkt liegt hierbei an falscher Stelle und zwar mitten im Implantat. Dies führt zu einer unnatürlichen Beanspruchung der weiteren Einrichtungen der Wirbelsäule (Bänder, Gelenke, Muskeln) und zu Schmerzen in diesen Strukturen, sodaß diese nicht mehr optimal funktionieren können. Weiters kommt es durch den fal- sehen Drehpunkt zu Scherkräften, die das Implantat aus dem Zwischenwirbelspalt herausdrängen können.c) There is mobility and the implant is not connected to the vertebrae: the pivot point is in the wrong place, namely in the middle of the implant. This leads to an unnatural strain on the other facilities of the spine (ligaments, joints, muscles) and pain in these structures, so that they can no longer function optimally. Furthermore, see pivot point to shear forces that can force the implant out of the intervertebral gap.
d) eine Beweglichkeit ist vorhanden und das Implantat ist mit beiden Wirbeln fest verbunden: Der Drehpunkt liegt hiebe! an falscher Stelle, mitten im Implantat oder an dessen Rand. Dadurch, daß Teile des Implantats mit den Wirbeln fest verbunden sind, schreibt die (unphysiologische) Kinematik des Implantats den Wirbeln die Kinematik vor. Dies führt wiederum zu einer unnatürlichen Beanspruchung der weiteren Einrichtungen der Wirbelsäule (Bänder, Gelenke, Muskeln) und zu Scherkräften zwischen Implantat und Wirbel. Durch die feste Verbindung des Implantats mit beiden Wirbeln kann nun das Implantat durch die unnatürliche Kinematik nicht aus dem Zwischenwirbelspalt herausgedrängt werden. Dadurch werden die Befestigungsmittel und der Knochen überbeansprucht, sodaß die Gefahr einer Implantatlockerung besteht. Dies ist die einzige Möglichkeit des Knochens, auf die unnatürliche Kinematik zu reagieren, da er durch die feste Verbindung keine weitere Möglichkeit der Anpassung besitzt.d) there is mobility and the implant is firmly connected to both vertebrae: the fulcrum is right there! in the wrong place, in the middle of the implant or on its edge. Because parts of the implant are firmly connected to the vertebrae, the (non-physiological) kinematics of the implant prescribe the kinematics to the vertebrae. This in turn leads to an unnatural strain on the other spinal devices (ligaments, joints, muscles) and to shear forces between the implant and vertebra. Due to the fixed connection of the implant to both vertebrae, the implant cannot be forced out of the intervertebral space due to the unnatural kinematics. As a result, the fasteners and the bone are overstressed, so that there is a risk of implant loosening. This is the only way for the bone to react to the unnatural kinematics, since it has no further possibility of adaptation due to the fixed connection.
Weitere Nachteile ergeben sich dadurch, daß Implantate, die aus zwei oder mehr Teilen bestehen, aufgrund der geringen Größe nicht an der Halswirbelsäule eingebaut werden können.Further disadvantages result from the fact that implants consisting of two or more parts cannot be installed on the cervical spine due to the small size.
Die Aufgabenstellung der Erfindung betrifft eine Prothese, die die physiologische bzw. natürliche Beweglichkeit aufrechterhält und das Bewegungs-Drehzentrum in seiner physiologischen Lage bewahrt. Zur Lösung dieser Aufgabe ist die erfindungsgemäße Wirbelsäulen-Prothese im wesentlichen dadurch gekennzeichnet, daß die in eingebautem Zustand einstückig ausgebildete Prothese eine gewölbte Oberfläche an der Prothesen-Oberseite aufweist und gegenüber dem cranialen Wirbelkörper beweglich ist, daß die Prothese durch Veranke- rungs- und Verbindungsmittel an der Prothesen-Unterseite mit dem caudalen Wirbelkörper unbeweglich verbunden ist und daß die Rotationsachse zwischen den benachbarten Wirbelkörpem bei Vor- und Zurückbeugen im caudalen Wirbelkörper liegt. Die Prothese ist bei Operationen, bei welchen der Discus (Bandscheibe) entfernt wird, in den Zwischenwirbelraum einzubringen. Das Implantat bzw. die Prothese ist erfindungs- gemäß so konstruiert, daß der craniale (obere [am stehenden Menschen]) Wirbelkörper gegenüber der einstückig ausgebildeten Prothese beweglich ist und die Prothese gegenüber dem caudalen (unteren) Wirbelkörper nicht beweglich ist. Durch die erfindungsgemäße Ausbildung der Wirbelsäulen-Prothese gelingt nicht nur eine zuverlässige Verankerung der Prothese in dem caudalen Wirbelkörper, sondern es kann durch die gleichzeitig erfindungsgemäß vorgesehene Beweglichkeit der in eingebautem Zustand einstückig ausgebildeten Prothese die physiologische bzw. natürliche Beweglichkeit der benachbar- ten Wirbelkörper durch Vorsehen der Rotationsachse zwischen den benachbarten Wirbelkörpem im caudalen Wirbelkörper, wie dies der natürlichen Drehachse zwischen benachbarten Wirbelkörpern entspricht, aufrechterhalten werden.The object of the invention relates to a prosthesis that maintains the physiological or natural mobility and maintains the center of rotation in its physiological position. To achieve this object, the spinal prosthesis according to the invention is essentially characterized in that the prosthesis, which is formed in one piece in the installed state, has a curved surface on the upper side of the prosthesis and is movable relative to the cranial vertebral body, in that the prosthesis by means of anchoring and connecting means on the underside of the prosthesis is immovably connected to the caudal vertebral body and that the axis of rotation between the neighboring vertebral bodies lies in the caudal vertebral body when bending forwards and backwards. The prosthesis must be inserted into the intervertebral space during operations in which the disc (disc) is removed. The implant or the prosthesis is constructed according to the invention in such a way that the cranial (upper [standing person]) vertebral body is movable relative to the one-piece prosthesis and the prosthesis is not movable relative to the caudal (lower) vertebral body. The inventive design of the spinal prosthesis not only succeeds in reliably anchoring the prosthesis in the caudal vertebral body, but it can also provide the physiological or natural mobility of the adjacent vertebral bodies by providing the mobility of the prosthesis, which is designed in one piece when installed, in accordance with the invention the axis of rotation between the adjacent vertebral bodies in the caudal vertebral body, as corresponds to the natural axis of rotation between adjacent vertebral bodies, are maintained.
Für den Fall von beengten Platzverhältnissen ist gemäß einer bevorzugten Ausführungsform vorgesehen, daß die Prothese aus zwei gleich großen, im wesentlichen symmetrischen, miteinander zusammensetzbaren Teilen besteht, wobei sich jedoch auch bei dieser Ausführungsform in eingebautem Zustand eine ein- stückige Prothese ergibt, welche relativ zum cranialen Wirbelkörper entlang der gewölbten Oberfläche beweglich ist, während die erfindungsgemäße Prothese im caudalen Wirbel- körper unbeweglich verankert ist.In the event of limited space, it is provided according to a preferred embodiment that the prosthesis consists of two equally large, essentially symmetrical, parts that can be put together, but this embodiment also results in a one-piece prosthesis in the installed state, which is relative to the cranial vertebral body is movable along the curved surface, while the prosthesis according to the invention is immovably anchored in the caudal vertebral body.
Zur Erzielung einer entsprechenden Anzahl von Freiheits- graden der Bewegung zwischen den benachbarten Wirbelkörpe bei Einbau der erfindungsgemäßen Prothese ist darüberhinaus gemäß einer weiters bevorzugten Ausführungsform vorgesehen, daß die zum cranialen Wirbelkörper gewandte, gewölbte Ober- fläche der Prothese in wenigstens einer Schnittanischt von einer Kugel-, Ellipsoid-, Sattel- oder Zylinder-Oberfläche gebildet ist, wobei sich durch entsprechende Wahl der gewölbten Oberfläche und eine entsprechende Orientierung beim Einbau der Prothese unterschiedliche Freiheitsgrade der Bewegung zwischen den benachbarten Wirbelkörpem erzielen lassen. Eine unterschiedliche Auswahl von Freiheitsgraden läßt sich hiebei dadurch erzielen, daß die gewölbte Ober- fläche entlang von zwei im wesentlichen normal aufeinander stehenden Schnittlinien eine unterschiedliche Wölbung bzw. Krümmung aufweisen, wie dies einer bevorzugten Ausführungs- form der erfindungsgemäßen Prothese entspricht.In order to achieve a corresponding number of degrees of freedom of movement between the adjacent vertebral bodies when the prosthesis according to the invention is installed, it is furthermore provided according to a further preferred embodiment that the curved surface of the prosthesis facing the cranial vertebral body is at least one section of a spherical surface. , Ellipsoid, saddle or cylinder surface is formed, with the appropriate choice of the curved surface and a corresponding orientation when Installation of the prosthesis allows different degrees of freedom of movement to be achieved between the adjacent vertebral bodies. A different selection of degrees of freedom can be achieved in that the curved surface has a different curvature or curvature along two essentially normal intersection lines, as corresponds to a preferred embodiment of the prosthesis according to the invention.
Für eine ordnungsgemäße Verankerung der Prothese im unteren bzw. caudalen Wirbelkörper ist erfindungsgemäß bevorzugt vorgesehen, daß die Verankerungs- und Verbindungsmittel von wenigstens einem Steg oder Fortsatz gebildet sind, welcher insbesondere eine körnige, poröse, gerippte, gezahnte oder aufgerauhte Oberfläche aufweist. Für eine Anpassung an unterschiedliche Einsatzzwecke bzw. für eine Verwendung unterschiedlicher Verankerungs- bzw. Verbindungsmittel mit einem Grundkörper der Prothese ist darübherinaus bevorzugt vorgesehen, daß die Verbindungs- und Verankerungsmittel an der Prothese über eine Steck- oder Gewindeverbindung lösbar festgelegt sind.For proper anchoring of the prosthesis in the lower or caudal vertebral body, it is preferably provided according to the invention that the anchoring and connecting means are formed by at least one web or extension, which in particular has a granular, porous, ribbed, toothed or roughened surface. In addition, for adaptation to different purposes or for using different anchoring or connecting means with a base body of the prosthesis, it is preferably provided that the connecting and anchoring means are releasably fixed to the prosthesis via a plug-in or threaded connection.
Die Vorteile der Erfindung ergeben sich dadurch, daß a) das Implantat in allen Wirbelsäulen-Abschnitten (Hals-, Brust- und Lendenwirbelsäule) eingesetzt werden kann, da es die individuelle Kinematik jedes Abschnittes berücksichtigt und in jeder nötigen Größe hergestellt werden kann; b) es von ventral (vorne) und von dorsal (hinten) eingebaut werden kann; c) es aus einem Teil (oder aus Einbaugründen aus zwei Teilen, linker und rechter Teil) besteht, der nur mit dem unteren Wirbelkörper verbunden ist; d) es aufgrund seiner Form maximal drei Freiheitsgrade der Bewegung gewährleistet und die physiologischen Bewegungs- achsen in ihrer natürlichen Lage bewahrt, wobei vor allem der Drehpunkt bei Ante- und Retroversion im mittleren Bereich des caudalen Wirbelkörpers liegt; e) der craniale Wirbelkörper gegenüber der Prothese beweglich ist, sodaß sich das Knochengewebe der Prothese durch physiologische Umbauvorgänge anpassen kann; und f) aufgrund der Punkte d) und e) die dem Bewegungssegment zugehörigen Strukturen (Bänder, Gelenke, Muskeln) nicht überbeansprucht werden.The advantages of the invention result from the fact that a) the implant can be used in all spine sections (cervical, thoracic and lumbar spine), since it takes into account the individual kinematics of each section and can be produced in any necessary size; b) it can be installed from the ventral (front) and dorsal (rear); c) it consists of one part (or from two parts, left and right part) which is only connected to the lower vertebral body; d) because of its shape it guarantees a maximum of three degrees of freedom of movement and maintains the physiological axes of movement in their natural position, the pivot point in the case of ante- and retroversion being in the middle of the caudal vertebral body; e) the cranial vertebral body is movable relative to the prosthesis, so that the bone tissue of the prosthesis can adapt through physiological remodeling processes; and f) due to points d) and e) the structures associated with the movement segment (ligaments, joints, muscles) are not overused.
Die Erfindung wird nachfolgend im Detail unter Bezugnahme auf die beiliegende Zeichnung anhand von schematisch darge- stellten Ausführungsbeispielen beschrieben, wobei:The invention is described in detail below with reference to the accompanying drawing using schematically illustrated exemplary embodiments, in which:
Fig. 1 ein intaktes Wirbelsäulensegment in einer Seitenansicht zeigt;Fig. 1 shows an intact spine segment in a side view;
Fig. 2 ein Wirbelsäulen-Bewegungssegment von der Seite mit einer erfindungsgemäßen Wirbelsäulen-Prothese (kinematische Wirbelsäulen-Prothese) zeigt;2 shows a spinal movement segment from the side with a spinal prosthesis according to the invention (kinematic spinal prosthesis);
Fig. 3 einen sagittalen Schnitt (Schnittfläche von der Seite gesehen) durch eine Ausführungsform einer erfindungsgemäßen Prothese zeigt; und Fig. 4 einen frontalen Schnitt (Schnittfläche von vorne ge- sehen) durch weitere abgewandelte Ausführungsformen der erfindungsgemäßen Prothese mit unterschiedlicher Krümmung der Oberfläche entsprechend den Pfeilen IV der Fig. 2 und 3 zeigt, wobei Fig. 3 eine Ansicht in Richtung des Pfeils III der Fig. 4 ist.Fig. 3 shows a sagittal section (section viewed from the side) through an embodiment of a prosthesis according to the invention; and FIG. 4 shows a frontal section (sectional area seen from the front) through further modified embodiments of the prosthesis according to the invention with different curvature of the surface in accordance with arrows IV of FIGS. 2 and 3, FIG. 3 showing a view in the direction of arrow III 4 is.
Ein natürliches, intaktes Wirbelsäulen-Bewegungssegment (Fig. 1) von der Seite (Vorderseite nach links, Hinterseite nach rechts, stehender Mensch) besteht aus dem cranialen (oberen) Wirbelkörper 1, dem caudalen (unteren) Wirbelkörper 3 und dem dazwischen befindlichen Discus (2, Bandscheibe). Die Bewegungsrichtung 5 des oberen Wirbels 1 bei Vor- und Rückbeugen (Ante/Retro-Version) erfolgt um einen Drehpunkt 4, der im unteren Wirbel 3 liegt.A natural, intact spinal movement segment (Fig. 1) from the side (front to left, back to the right, standing person) consists of the cranial (upper) vertebral body 1, the caudal (lower) vertebral body 3 and the discus in between ( 2, intervertebral disc). The direction of movement 5 of the upper vertebra 1 during forward and backward bending (ante / retro version) takes place around a pivot point 4 which lies in the lower vertebra 3.
Während der Operation wird die Prothese bzw. das Implantat 6 (Fig. 2) zwischen die Wirbelkörper 1, 3 eingebracht. Die Bewegungsrichtung 5) des oberen Wirbels 1 bei Vor- und Rückbeugen (Ante/Retro-Version) erfolgt nunmehr um einen Dreh- punkt 7, der im unteren Wirbel 3 liegt und durch die Prothesenform vorgegeben ist und im wesentlichen dem natürlichen Drehpunkt 4 gemäß Fig. 1 entspricht.During the operation, the prosthesis or the implant 6 (FIG. 2) is inserted between the vertebral bodies 1, 3. The direction of movement 5) of the upper vertebra 1 during forward and backward bending (ante / retro version) is now carried out by one rotation. Point 7, which lies in the lower vertebra 3 and is predetermined by the shape of the prosthesis and corresponds essentially to the natural pivot point 4 according to FIG. 1.
Die einstückig ausgebildete Prothese 6 (Fig. 3) gliedert sich in eine Oberseite 8 und eine Unterseite 10. An der Oberseite 8 befindet sich die für die Beweglichkeit relevante Oberfläche 9. Die Krümmung der Oberfläche bestimmt den Drehpunkt 7 für Vor- und Rückbeugen (Krümmungsmittelpunkt = RotationsZentrum bei Kreisgeometrie) . An der Unterseite 10 befinden sich Verankerungs- und Verbindungsmittel 11 für die Verankerung der Prothese 6 in dem unteren Wirbelkörper 3, sodaß die Unbeweglichkeit der Prothese 6 gegenüber dem unteren Wirbelkörper 3 gewährleistet ist. In Fig. 3 und auch in Fig. 2 ist eine Versenkung der Prothese 6 im unteren Wirbelkörper 3 als Verankerungsmittel gezeichnet.The one-piece prosthesis 6 (FIG. 3) is divided into an upper side 8 and a lower side 10. On the upper side 8 there is the surface 9 relevant for mobility. The curvature of the surface determines the pivot point 7 for forward and backward bending (center of curvature = Center of rotation for circular geometry). On the underside 10 there are anchoring and connecting means 11 for anchoring the prosthesis 6 in the lower vertebral body 3, so that the immobility of the prosthesis 6 with respect to the lower vertebral body 3 is ensured. In Fig. 3 and also in Fig. 2, a sinking of the prosthesis 6 in the lower vertebral body 3 is drawn as anchoring means.
Im frontalen Schnitt (Schnittfläche von vorne gesehen) durch die Prothese (Fig. 4) zeigen sich abgewandelte Ausführungs- formen möglicher unterschiedlicher Krümmungen der Oberfläche der Prothese 6: Kugel-Oberfläche 9a, Ellipsoid-Oberfläche 9b, Sattel-Oberfläche 9c, Zylinder-Oberfläche 9d.The frontal section (section viewed from the front) through the prosthesis (FIG. 4) shows modified embodiments of possible different curvatures of the surface of the prosthesis 6: spherical surface 9a, ellipsoid surface 9b, saddle surface 9c, cylinder surface 9d.
Bei Verwendung einer Prothese 6 ergeben sich für die Beweg- lichkeit folgende Verhältnisse:When using a prosthesis 6, the following conditions result for mobility:
-A) Die Oberseite 8 besitzt eine gewölbte Oberfläche 9. Die Wölbung gibt die Kinematik in der Bewegungsrichtung 5 des oberen bzw. cranialen Wirbelkörpers vor. Bei Vor- und Rückbeugung (Ante- und Retroversion) der Wirbelsäule liegt der Drehpunkt 7 der Bewegung im unteren Wirbelkörper 3.-A) The top 8 has a curved surface 9. The curvature defines the kinematics in the direction of movement 5 of the upper or cranial vertebral body. With forward and backward bending (ante- and retroversion) of the spine, the fulcrum 7 of the movement lies in the lower vertebral body 3.
Der Krümmungsmittelpunkt der Prothese (bei sagittal geschnittener Prothese, Schnittfläche von der Seite gesehen; Fig. 3) muß daher an derselben Stelle liegen. Entspricht die Krümmung der Kreisgeometrie, dann ist der Krümmungsmittelpunkt gleich dem Drehpunkt 7 (RotationsZentrum) . wird das Implantat von vorne betrachtet (frontaler Schnitt, Schnittfläche von vorne betrachtet; Fig. 4), dann kann die Wölbung unterschiedlich sein. Ist die Krümmung aus seitlicher Ansicht 9 identisch mit der aus vorderer Ansicht 9a, dann entspricht die Oberseite der Prothese der Kreisgeometrie. Die Prothese gewährleistet daher drei Freiheitsgrade der Bewegung:The center of curvature of the prosthesis (in the case of a sagittally cut prosthesis, cutting surface viewed from the side; FIG. 3) must therefore lie at the same point. If the curvature corresponds to the circular geometry, then the center of curvature is equal to pivot point 7 (center of rotation). if the implant is viewed from the front (frontal cut, cut surface viewed from the front; Fig. 4), then the curvature can be different. If the curvature from the side view 9 is identical to that from the front view 9a, then the top of the prosthesis corresponds to the circular geometry. The prosthesis therefore guarantees three degrees of freedom of movement:
-a) Vor/Rückbeugen um eine horizontale Achse -b) Seitenbeugen um eine sagittale Achse, und -c) Rotation um eine vertikale Achse.-a) forward / backward bending around a horizontal axis -b) side bending around a sagittal axis, and -c) rotation around a vertical axis.
Ist die Krümmung aus seitlicher Ansicht 9 nicht identisch mit der Krümmung aus vorderer Ansicht aber entweder gleichsinnig gekrümmt 9b oder gegensinnig gekrümmt 9c, dann entspricht die Oberseite der Prothese entweder der Ellipsoid- Geometrie oder der Sattel-Geometrie. Die Prothese 6 gewähr- leistet dann nur zwei Freiheitsgrade der Bewegung: -a) Vor/Rückbeugen um eine horizontale Achse -b) Seitbeugen um eine sagittale AchseIf the curvature from the side view 9 is not identical to the curvature from the front view but is either curved in the same direction 9b or curved in the opposite direction 9c, then the top of the prosthesis corresponds either to the ellipsoid geometry or the saddle geometry. The prosthesis 6 then ensures only two degrees of freedom of movement: -a) forward / backward bending about a horizontal axis -b) lateral bending about a sagittal axis
Ist die Krümmung aus seitlicher Ansicht 9 nicht identisch mit der aus vorderer Ansicht und letztere ist nicht gekrümmt 9b, dann entspricht die Oberseite der Prothese der Zylinder- Geometrie. Die Prothese gewährleistet dann nur einen Freiheitsgrad der Bewegung: -a) Vor/Rückbeugen um eine horizontale AchseIf the curvature from the side view 9 is not identical to that from the front view and the latter is not curved 9b, then the top of the prosthesis corresponds to the cylinder geometry. The prosthesis then only guarantees one degree of freedom of movement: -a) Forward / backward bending around a horizontal axis
Die unterschiedlichen Krümmungen der Oberflächen aus vorderer Ansicht (Fig. 4) sind nötig, um dem unterschiedlichen Bewegungsverhalten der einzelnen funktioneilen Wirbelsäulenabschnitte Rechnung zu tragen.The different curvatures of the surfaces from the front view (FIG. 4) are necessary in order to take into account the different movement behavior of the individual functional spinal column sections.
-B) Die Unterseite 10 der einstückigen Prothese 6 muß so beschaffen sein, daß eine Bewegung derselben gegenüber dem unteren bzw. caudalen Wirbelkörper 3 (sei es Rotation oder Translation) ausgeschlossen ist. Diese Unbeweglichkeit ist durch die Verankerungs- und Verbindungsmittel 11 gegeben. Diese können sein: Stege oder ein oder mehrere Fortsätze 11, die in den unteren Wirbelkörper 3 eingesenkt werden; eine körnige, poröse, gerippte, gezähnte oder aufgerauhte Unter- fläche 13, in die das Knochengewebe einwachsen kann; Knochenzement zur Verbindung von Prothese und Knochen. Die Verbindungsmittel müssen nicht unbedingt fix mit der Prothese verbunden sein, sondern können auch zwecks leichterem Einbau mittels Steckverbindung oder Gewinde an der Prothese befestigt werden, wie dies in Fig. 4 durch eine lösbare Verbindung 14 angedeutet ist.-B) The underside 10 of the one-piece prosthesis 6 must be designed in such a way that it cannot move relative to the lower or caudal vertebral body 3 (be it rotation or translation). This immobility is given by the anchoring and connecting means 11. These can be: webs or one or more extensions 11 which are sunk into the lower vertebral body 3; a granular, porous, ribbed, serrated or roughened surface surface 13 into which the bone tissue can grow; Bone cement for connecting the prosthesis and bone. The connecting means do not necessarily have to be permanently connected to the prosthesis, but can also be fastened to the prosthesis for easier installation by means of a plug connection or thread, as is indicated in FIG. 4 by a detachable connection 14.
-C) Als Variante kann die Prothese auch aus zwei gleich großen Teilen (rechter Teil und linker Teil) bestehen, wie dies in Fig. 4 bei der Ausbildung der Prothese mit der Krümmung 9a durch die Teile 6 und 6' angedeutet ist, wobei die Teilung im wesentlichen entlang der Schnittlinie 12 erfolgt. Dies ist dann der Fall, wenn knapp bemessene chirur- gische Zugangswege eine leichtere Einbringung der Prothese (hier: kleinere Teile der Prothese) erfordern. Nach Zusammensetzung der Teile im Zwischenwirbelspalt ergibt sich aber die oben beschriebene einstückige Form der Prothese 6 in eingebautem Zustand. Der Vorteil liegt in diesem Fall darin, daß die Prothese insbesondere an der Lendenwirbelsäule auch von hinten (dorsal) eingebaut werden kann. -C) As a variant, the prosthesis can also consist of two parts of the same size (right part and left part), as indicated in Fig. 4 when the prosthesis is formed with the curvature 9a by the parts 6 and 6 ', the Division takes place essentially along the section line 12. This is the case when tightly dimensioned surgical access routes require easier insertion of the prosthesis (here: smaller parts of the prosthesis). According to the composition of the parts in the intervertebral gap, however, the one-piece form of the prosthesis 6 described above results in the installed state. The advantage in this case is that the prosthesis can also be installed from the back (dorsal), particularly on the lumbar spine.

Claims

P a t e n t a n s p r ü c h e Patent claims
1. Wirbelsäulen-Prothese zum Einbringen in den Zwischenwirbelspalt der Wirbelsäule nach chirurgischer Entfernung der Bandscheibe, dadurch gekennzeichnet, daß die in eingebautem Zustand einstückig ausgebildete Prothese (6) eine gewölbte Oberfläche (9, 9a, 9b, 9c, 9d) an der Prothesen-Oberseite (8) aufweist und gegenüber dem cranialen Wirbelkörper (1) beweglich ist, daß die Prothese (6) durch Verankerungs- und Verbindungsmittel (11) an der Prothesen-Unterseite (10) mit dem caudalen Wirbelkörper (3) unbeweglich verbunden ist und daß die Rotationsachse (7) zwischen den benachbarten Wirbelkörpem (1, 3) bei Vor- und Zurückbeugen (5) im caudalen Wirbelkörper (3) liegt.1. Spinal prosthesis for insertion into the intervertebral space of the spine after surgical removal of the intervertebral disc, characterized in that the prosthesis (6), which is formed in one piece in the installed state, has a curved surface (9, 9a, 9b, 9c, 9d) on the prosthesis. Top (8) and is movable relative to the cranial vertebral body (1), that the prosthesis (6) is immovably connected to the caudal vertebral body (3) by anchoring and connecting means (11) on the underside of the prosthesis (10) and that the axis of rotation (7) between the adjacent vertebral bodies (1, 3) when bending forward and backward (5) lies in the caudal vertebral body (3).
2. Wirbelsäulen-Prothese nach Anspruch 1, dadurch gekennzeichnet, daß die Prothese (6) aus zwei gleich großen, im wesentlichen symmetrischen, miteinander zusammensetzbaren Teilen besteht.2. Spinal prosthesis according to claim 1, characterized in that the prosthesis (6) consists of two equal, substantially symmetrical, parts that can be assembled together.
3. Wirbelsäulen-Prothese nach Anspruch 1 oder 2, dadurch gekennzeichnet, daß die zum cranialen Wirbelkörper (1) gewandte, gewölbte Oberfläche der Prothese (6) in wenigstens einer Schnittansicht von einer Kugel- (9a), Ellipsoid- (9b), Sattel- (9c) oder Zylinder-Oberfläche (9d) gebildet ist.3. Spinal prosthesis according to claim 1 or 2, characterized in that the curved surface of the prosthesis (6) facing the cranial vertebral body (1) in at least one sectional view of a ball (9a), ellipsoid (9b), saddle - (9c) or cylinder surface (9d) is formed.
4. Wirbelsäulen-Prothese nach Anspruch 1, 2 oder 3, dadurch gekennzeichnet, daß die Verankerungs- und Verbindungsmittel von wenigstens einem Steg oder Fortsatz (11) gebildet sind, welcher insbesondere eine körnige, poröse, gerippte, gezahnte oder aufgerauhte Oberfläche (13) aufweist.4. spinal prosthesis according to claim 1, 2 or 3, characterized in that the anchoring and connecting means are formed by at least one web or extension (11), which in particular a granular, porous, ribbed, toothed or roughened surface (13) having.
5. Wirbelsäulen-Prothese nach einem der Ansprüche 1 bis 4, dadurch gekennzeichnet, daß die Verbindungs- und Veranke- rungsmittel (11) an der Prothese (6) über eine Steck- oder Gewindeverbindung (14) lösbar festgelegt sind. 5. spinal prosthesis according to one of claims 1 to 4, characterized in that the connecting and anchoring means (11) on the prosthesis (6) via a plug or thread connection (14) are releasably fixed.
6. Wirbelsäulen-Prothese nach einem der Ansprüche 1 bis 5, dadurch gekennzeichnet, daß die gewölbte Oberfläche (9, 9a, 9b, 9c, 9d) entlang von zwei im wesentlichen normal aufeinander stehenden Schnittlinien eine unterschiedliche Wöl- bung bzw. Krümmung aufweisen. 6. Spinal prosthesis according to one of claims 1 to 5, characterized in that the curved surface (9, 9a, 9b, 9c, 9d) have a different curvature or curvature along two substantially normal cutting lines.
PCT/AT1998/000201 1997-08-28 1998-08-26 Prosthesis of the spinal column WO1999011203A1 (en)

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EP2907481A1 (en) * 2014-02-12 2015-08-19 HO-MED Handelsgesellschaft m.b.H. Implant for insertion between vertebrae of the spine and construction kit for making such an implant
US11147682B2 (en) 2017-09-08 2021-10-19 Pioneer Surgical Technology, Inc. Intervertebral implants, instruments, and methods
USD907771S1 (en) 2017-10-09 2021-01-12 Pioneer Surgical Technology, Inc. Intervertebral implant
USD968613S1 (en) 2017-10-09 2022-11-01 Pioneer Surgical Technology, Inc. Intervertebral implant

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AT405237B (en) 1999-06-25
ATA144897A (en) 1998-11-15
EP1009339A1 (en) 2000-06-21
AU8963698A (en) 1999-03-22

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