US20060293754A1 - Intervertebral Prosthesis - Google Patents
Intervertebral Prosthesis Download PDFInfo
- Publication number
- US20060293754A1 US20060293754A1 US11/468,601 US46860106A US2006293754A1 US 20060293754 A1 US20060293754 A1 US 20060293754A1 US 46860106 A US46860106 A US 46860106A US 2006293754 A1 US2006293754 A1 US 2006293754A1
- Authority
- US
- United States
- Prior art keywords
- plate
- serrations
- prosthesis
- midline
- region
- Prior art date
- Legal status (The legal status 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 status listed.)
- Abandoned
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS 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
- A61F2/00—Filters 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
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/44—Joints for the spine, e.g. vertebrae, spinal discs
- A61F2/442—Intervertebral or spinal discs, e.g. resilient
- A61F2/4425—Intervertebral or spinal discs, e.g. resilient made of articulated components
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- A61F2/00—Filters 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
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/30767—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
- A61F2/30771—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
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- A61F2/00—Filters 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
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/46—Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor
- A61F2/4603—Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor for insertion or extraction of endoprosthetic joints or of accessories thereof
- A61F2/4611—Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor for insertion or extraction of endoprosthetic joints or of accessories thereof of spinal prostheses
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- A61F2/00—Filters 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
- A61F2/02—Prostheses implantable into the body
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- A61F2002/30001—Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
- A61F2002/30003—Material related properties of the prosthesis or of a coating on the prosthesis
- A61F2002/3006—Properties of materials and coating materials
- A61F2002/3008—Properties of materials and coating materials radio-opaque, e.g. radio-opaque markers
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- A61F2002/30001—Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
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- A61F2002/30329—Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
- A61F2002/30331—Connections 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
- A61F2002/30362—Connections 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 with possibility of relative movement between the protrusion and the recess
- A61F2002/30364—Rotation about the common longitudinal axis
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- A61F2002/30331—Connections 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
- A61F2002/30362—Connections 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 with possibility of relative movement between the protrusion and the recess
- A61F2002/30369—Limited lateral translation of the protrusion within a larger recess
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- A61F2002/30518—Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements with possibility of relative movement between the prosthetic parts
- A61F2002/30528—Means for limiting said movement
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS 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
- A61F2250/00—Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
- A61F2250/0058—Additional features; Implant or prostheses properties not otherwise provided for
- A61F2250/0096—Markers and sensors for detecting a position or changes of a position of an implant, e.g. RF sensors, ultrasound markers
- A61F2250/0098—Markers and sensors for detecting a position or changes of a position of an implant, e.g. RF sensors, ultrasound markers radio-opaque, e.g. radio-opaque markers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS 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
- A61F2310/00—Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
- A61F2310/00005—The prosthesis being constructed from a particular material
- A61F2310/00011—Metals or alloys
- A61F2310/00017—Iron- or Fe-based alloys, e.g. stainless steel
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS 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
- A61F2310/00—Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
- A61F2310/00005—The prosthesis being constructed from a particular material
- A61F2310/00011—Metals or alloys
- A61F2310/00029—Cobalt-based alloys, e.g. Co-Cr alloys or Vitallium
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS 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
- A61F2310/00—Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
- A61F2310/00005—The prosthesis being constructed from a particular material
- A61F2310/00179—Ceramics or ceramic-like structures
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS 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
- A61F2310/00—Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
- A61F2310/00389—The prosthesis being coated or covered with a particular material
- A61F2310/00592—Coating or prosthesis-covering structure made of ceramics or of ceramic-like compounds
- A61F2310/00856—Coating or prosthesis-covering structure made of compounds based on metal nitrides
- A61F2310/0088—Coating made of titanium nitride
Definitions
- This invention relates to an intervertebral prosthesis.
- intervertebral prosthesis is sold by Waldemar Link GmbH & Co under the trademark LINK® SB Charotti.
- This prosthesis includes upper and lower prosthesis plates which locate against and engage the adjacent vertebral bodies, and a low friction core between the plates.
- the core has upper and lower convexly curved surfaces and the plates have corresponding, concavely curved recesses which cooperate with the curved surfaces of the core. This allows the plates to slide over the core to allow required spinal movements to take place.
- the curved recesses in the plates are surrounded by annular ridges which locate, at the limit of sliding movement of the plates over the core, in opposing peripheral channels surrounding the curved surfaces of the core.
- EP 0 560 141 also describes one alternative arrangement in which the curved surfaces of the core carry opposing, elongate keys that locate in elongate grooves in the plates and another alternative arrangement in which the plates have opposing elongate keys that locate in elongate grooves in the opposite curved surfaces of the core.
- These key and groove arrangements allow the plates to slide freely over the core, within the limits of the length of the grooves, in one plane only. Although allowance is made for some lateral play of the keys in the grooves, very little sliding movement of the plates over the core can take place in the orthogonal vertical plane, and this is considered to be a serious drawback of this design.
- EP 0 560 140 and EP 0 560 141 have been discussed above.
- U.S. Patent Publication Nos. US2002/0035400 and US2002/0128715 describe intervertebral prostheses with center-posts received in passages in a core.
- the core possesses an annular flange structure engaged by extensions on the plates.
- an intervertebral prosthesis for insertion between adjacent vertebrae, the prosthesis comprising upper and lower prosthesis plates locatable against the respective vertebrae and having opposing, concavely curved recesses therein and a core located between the plates, the core having opposed, convexly curved surfaces received in the recesses of the plates to allow the plates to slide in articulated manner over the core, characterized in that:
- only one of the plates typically the operatively lower plate, includes a peg.
- both plates include pegs, the pegs opposing one another and locating loosely in respective openings located centrally in the opposed curved surfaces of the core.
- each peg and the opening in which it locates are conical in shape.
- a prosthesis plate for use in a prosthesis as summarized above, the prosthesis plate having a coarse surface locatable against a vertebra, an oppositely facing concavely curved surface which is complemental in shape to a convexly curved surface of a core of the prosthesis, characterized in the concavely curved surface of the plate has a spherical curvature and in that the plate includes a conical locating peg extending centrally from the concavely curved surface, the peg being locatable loosely in a central opening in the convexly curved surface of the core.
- a core for use in the prosthesis comprising a one piece plastics body having operatively upper and lower curved surfaces, characterized in that the curved surfaces of the body are spherically curved and at least one of the surfaces has a central, conical opening therein dimensioned to receive a conical locating peg of a prosthesis plate loosely.
- FIG. 1 shows a cross-sectional view of a prosthesis plate used in a prosthesis according to the invention
- FIG. 2 shows a plan view of the prosthesis plate seen in FIG. 1 ;
- FIG. 3 shows a cross-sectional view of a core used in a prosthesis according to the invention
- FIG. 4 shows a plan view of the core seen in FIG. 3 ;
- FIG. 5 shows a cross-sectional view of an intervertebral prosthesis according to a first embodiment of the invention in a neutral condition before articulation has taken place;
- FIG. 6 shows the prosthesis of FIG. 5 articulated to a limit position
- FIG. 7 shows a cross-sectional view of an intervertebral prosthesis according to a second embodiment of the invention.
- the prosthesis plate 10 seen in FIGS. 1 and 2 may be formed from titanium, typically being formed in one piece of grade 5 titanium. Other suitable materials include titanium nitrides, cobalt chrome alloys, and ceramics.
- the prosthesis plate includes a major surface 12 which is machined to a coarse, serrated finish 14 . Projecting from the surface 12 is an elongate fin 16 pierced by transverse holes 18 .
- the opposite surface of the plate 10 is formed with a recess 20 surrounding a projecting conical peg 22 of round cross-section at the centre of the recess.
- the recess is bounded by an annular rim 24 .
- the surface 26 of the recess is concavely, spherically curved and has a titanium nitride finish.
- a first embodiment of prosthesis of the invention includes a pair of identical prosthesis plates 10 arranged in opposition to one another.
- the prosthesis 28 also includes a core 30 illustrated in FIGS. 3 and 4 .
- the core is made in one piece of a low friction plastics material, in this case a polyethylene known as Orthosol, but a variety of other high molecular weight polyethylenes might also find use.
- the core could be composed of a metal, such as cobalt chrome, or of a ceramic.
- the core is generally in the form of a circular, doughnut-shaped toroid and has identical upper and lower surfaces 32 which are convexly, spherically curved.
- the upper and lower surfaces 32 are formed centrally with conical openings 34 , in this case forming the opposite ends of a circular cross-section passage 36 passing axially and centrally through the body of the core.
- the core surfaces 32 and recess surface 26 have the same radius of curvature which is, in this case, 18 mm.
- the plates 10 are arranged in opposition to one another with the core 30 located between them.
- the pegs 22 of the plates locate in the openings 34 , i.e. in the ends of the passage 36 .
- the combined length of the pegs is less than the length of the passage 36 , so the inner ends of the pegs are spaced apart from one another by a short distance 38 , as shown in FIG. 5 .
- the transverse dimension of each peg is, at all points along the length of the peg, considerably less than the diameter of the passage 36 at the corresponding point along the length of the passage.
- the cooperating spherical surfaces 26 and 32 and the relative dimensions of the pegs 22 and the passage 36 allow the plates 10 to slide or articulate over the core through a fairly large range of angles and in all directions or degrees of freedom, including rotation about the central axis.
- the rims 24 of the plates contact with one another as indicated by the numeral 40 in FIG. 6 . Further articulation of the prosthesis 28 beyond this point is not possible. At the limit of articulation, the pegs 22 also come into abutment with the side of the passage 36 , as also illustrated in FIG. 6 .
- openings 34 at the ends of the passage 36 are defined by similar cone angles to the pegs 22 , so that contact between the pegs and the sides of the openings takes place complementally over virtually the entire length of each peg.
- the pegs 22 remain in the passage 36 and prevent the core from separating laterally from the plates 10 .
- the core is held captive by the pegs during all possible articulations which can take place.
- the plates 10 are limited to 12° of articulation before the rims 24 abut one another, i.e. 12° is the maximum articulation which can take place.
- the pegs 22 locate in a passage 32 which passes right through the core 30 . It will however be understood that in other embodiments, the pegs could merely locate in blind recesses or openings in the opposite surfaces of the core without such openings actually being joined to one another to form a continuous passage.
- FIG. 7 illustrates a prosthesis according to a second embodiment of the invention in a view similar to that of FIG. 5 .
- components corresponding to components illustrated in the earlier Figures are indicated by the same reference numerals.
- the lower prosthesis plate 10 in FIG. 7 is identical to the prosthesis plates of the first embodiment.
- the upper prosthesis plate, designated 10 . 1 has no central peg. Instead, the surface 26 is continuously, spherically curved. In all other respects the plate 10 . 1 is identical to the plate 10 .
- the core is held captive by the action of the single peg 22 carried by the lower prosthesis plate 10 .
- the core 30 is identical to the core described previously but once again it will be appreciated that core could have a blind recess in its downwardly facing, curved surface 32 only to receive the single peg 22 .
- the prosthesis 28 , 50 is surgically implanted between adjacent spinal vertebrae in place of a damaged disc.
- adjacent vertebrae are forcibly separated from one another to provide the necessary space for insertion.
- the plates 10 , 10 . 1 are slipped laterally into place between the vertebrae with their fins 16 entering slots cut in the opposing vertebral surfaces to receive them.
- the vertebra After insertion of the core between the opposing plates, the vertebra are allowed to move together to hold the assembled prosthesis in place.
- the surfaces 12 of the plates 10 , 10 . 1 locate against the opposing vertebrae and, with passage of time, firm connection between the plates and the vertebrae will be achieved as bone tissue grows over the serrated finish. Bone tissue growth will also take place about the fins 16 and through the holes 18 therein, further enhancing the connection which is achieved.
- the core 30 used in the embodiments described above is formed with narrow, angularly spaced, blind passages which accommodate titanium pins 42 .
- the core itself is transparent to X-radiation and so would normally be invisible in a post-operative X-ray examination.
- the pins 42 serve as radiographic markers and enable the position of the core 30 to be ascertained during such examination.
- Annular grooves 44 are provided in the plates 10 , 10 . 1 to facilitate holding and manipulation of the prosthesis by appropriate instruments during placement into the intervertebral disc space.
- the prostheses 28 , 50 described above have a number of advantages, as follows:
- the principles of the invention are applicable to prosthetic disc implants for lumbar vertebrae as well as cervical vertebrae. In the latter case, the fins 16 will typically be omitted.
Abstract
An intervertebral prosthesis for insertion between adjacent vertebrae includes a first prosthesis plate and a second prosthesis plate. The first and second prosthesis plates each comprise a midline, an engagement surface to engage a first vertebra and a bearing surface disposed opposite the engagement surface. The bearing surfaces of the first and second plates are arranged to cooperate to form an articulate joint. A first region of serrations is disposed on the engagement surface of the first plate on one side of the midline of the first plate, and a second region of serrations is disposed on the engagement surface of the first plate on an opposite side of the first plate midline. Each region comprises at least several serrations, and each serration comprises a base attached to one of the plates and tapers from the base to a tip.
Description
- The present application is a continuation of U.S. patent application Ser. No. 11/084,224 (Atty. Docket No. 022031-001710US), filed on Mar. 18, 2005, which is a continuation-in-part of PCT/IB2003/001529 (Atty. Docket No. 022031-001700PC), filed on Apr. 24, 2003, designating the United States, which claimed priority from South African Application No. 2002/7517, filed on Sep. 19, 2002; the full disclosures of which are incorporated herein by reference.
- 1. Field of the Invention
- This invention relates to an intervertebral prosthesis.
- In the event of damage to a spinal disc it is known practice to implant an intervertebral prosthesis surgically to replace the damaged organ. Several types of prosthesis for this purpose are known and in common use.
- One type of known intervertebral prosthesis is sold by Waldemar Link GmbH & Co under the trademark LINK® SB Charité. This prosthesis includes upper and lower prosthesis plates which locate against and engage the adjacent vertebral bodies, and a low friction core between the plates. The core has upper and lower convexly curved surfaces and the plates have corresponding, concavely curved recesses which cooperate with the curved surfaces of the core. This allows the plates to slide over the core to allow required spinal movements to take place. The curved recesses in the plates are surrounded by annular ridges which locate, at the limit of sliding movement of the plates over the core, in opposing peripheral channels surrounding the curved surfaces of the core.
- This type of configuration is also described in European Patent Publication Nos. EP 0 560 140 and EP 0 560 141 (both Waldemar Link GmbH & Co). However a drawback of such configurations is that the provision of the peripheral ribs and channels limits the areas available for bearing and sliding contact between the plates and core, and accordingly the loads which can be transmitted by the prosthesis. As a result of the relatively small bearing areas, it is believed that at least the core will be subject to rapid wear and have a relatively short life-span.
- EP 0 560 141 also describes one alternative arrangement in which the curved surfaces of the core carry opposing, elongate keys that locate in elongate grooves in the plates and another alternative arrangement in which the plates have opposing elongate keys that locate in elongate grooves in the opposite curved surfaces of the core. These key and groove arrangements allow the plates to slide freely over the core, within the limits of the length of the grooves, in one plane only. Although allowance is made for some lateral play of the keys in the grooves, very little sliding movement of the plates over the core can take place in the orthogonal vertical plane, and this is considered to be a serious drawback of this design.
- 2. Description of the Background Art
- European Patent Publication Nos. EP 0 560 140 and EP 0 560 141 have been discussed above. U.S. Patent Publication Nos. US2002/0035400 and US2002/0128715 describe intervertebral prostheses with center-posts received in passages in a core. The core possesses an annular flange structure engaged by extensions on the plates.
- According to the invention there is provided an intervertebral prosthesis for insertion between adjacent vertebrae, the prosthesis comprising upper and lower prosthesis plates locatable against the respective vertebrae and having opposing, concavely curved recesses therein and a core located between the plates, the core having opposed, convexly curved surfaces received in the recesses of the plates to allow the plates to slide in articulated manner over the core, characterized in that:
-
- the opposed surfaces of the core and the recesses of the plates have cooperating spherical curvatures,
- the recess of a plate surrounds a locating peg projecting centrally from the base of the recess, and
- the peg locates loosely in an opening located centrally in a curved surface of the core, whereby the plates can slide over the core in all directions while the peg holds the core captive.
- In some embodiments, only one of the plates, typically the operatively lower plate, includes a peg. In other embodiments, both plates include pegs, the pegs opposing one another and locating loosely in respective openings located centrally in the opposed curved surfaces of the core. In each embodiment it is preferred that each peg and the opening in which it locates are conical in shape.
- According to another aspect of the invention there is provided a prosthesis plate for use in a prosthesis as summarized above, the prosthesis plate having a coarse surface locatable against a vertebra, an oppositely facing concavely curved surface which is complemental in shape to a convexly curved surface of a core of the prosthesis, characterized in the concavely curved surface of the plate has a spherical curvature and in that the plate includes a conical locating peg extending centrally from the concavely curved surface, the peg being locatable loosely in a central opening in the convexly curved surface of the core.
- According to yet another aspect of the invention there is provided a core for use in the prosthesis, the core comprising a one piece plastics body having operatively upper and lower curved surfaces, characterized in that the curved surfaces of the body are spherically curved and at least one of the surfaces has a central, conical opening therein dimensioned to receive a conical locating peg of a prosthesis plate loosely.
- Other features of the invention are set forth in the appended claims.
- The invention will now be described in more detail, by way of example only, with reference to the accompanying drawings in which:
-
FIG. 1 shows a cross-sectional view of a prosthesis plate used in a prosthesis according to the invention; -
FIG. 2 shows a plan view of the prosthesis plate seen inFIG. 1 ; -
FIG. 3 shows a cross-sectional view of a core used in a prosthesis according to the invention; -
FIG. 4 shows a plan view of the core seen inFIG. 3 ; -
FIG. 5 shows a cross-sectional view of an intervertebral prosthesis according to a first embodiment of the invention in a neutral condition before articulation has taken place; -
FIG. 6 shows the prosthesis ofFIG. 5 articulated to a limit position; and -
FIG. 7 shows a cross-sectional view of an intervertebral prosthesis according to a second embodiment of the invention. - The
prosthesis plate 10 seen inFIGS. 1 and 2 may be formed from titanium, typically being formed in one piece of grade 5 titanium. Other suitable materials include titanium nitrides, cobalt chrome alloys, and ceramics. The prosthesis plate includes amajor surface 12 which is machined to a coarse,serrated finish 14. Projecting from thesurface 12 is anelongate fin 16 pierced bytransverse holes 18. The opposite surface of theplate 10 is formed with arecess 20 surrounding a projectingconical peg 22 of round cross-section at the centre of the recess. The recess is bounded by anannular rim 24. Thesurface 26 of the recess is concavely, spherically curved and has a titanium nitride finish. - A first embodiment of prosthesis of the invention, indicated generally by the
numeral 28 inFIGS. 5 and 6 , includes a pair ofidentical prosthesis plates 10 arranged in opposition to one another. Theprosthesis 28 also includes acore 30 illustrated inFIGS. 3 and 4 . The core is made in one piece of a low friction plastics material, in this case a polyethylene known as Orthosol, but a variety of other high molecular weight polyethylenes might also find use. Alternatively, the core could be composed of a metal, such as cobalt chrome, or of a ceramic. The core is generally in the form of a circular, doughnut-shaped toroid and has identical upper andlower surfaces 32 which are convexly, spherically curved. The upper andlower surfaces 32 are formed centrally withconical openings 34, in this case forming the opposite ends of acircular cross-section passage 36 passing axially and centrally through the body of the core. - The
core surfaces 32 andrecess surface 26 have the same radius of curvature which is, in this case, 18 mm. - In the assembled
prosthesis 28, theplates 10 are arranged in opposition to one another with the core 30 located between them. Thepegs 22 of the plates locate in theopenings 34, i.e. in the ends of thepassage 36. The combined length of the pegs is less than the length of thepassage 36, so the inner ends of the pegs are spaced apart from one another by ashort distance 38, as shown inFIG. 5 . The transverse dimension of each peg is, at all points along the length of the peg, considerably less than the diameter of thepassage 36 at the corresponding point along the length of the passage. - The cooperating
spherical surfaces pegs 22 and thepassage 36 allow theplates 10 to slide or articulate over the core through a fairly large range of angles and in all directions or degrees of freedom, including rotation about the central axis. - At a predetermined limit of articulated movement of the plates relative to the core, the
rims 24 of the plates contact with one another as indicated by the numeral 40 inFIG. 6 . Further articulation of theprosthesis 28 beyond this point is not possible. At the limit of articulation, thepegs 22 also come into abutment with the side of thepassage 36, as also illustrated inFIG. 6 . - It will also be noted in
FIG. 6 that theopenings 34 at the ends of thepassage 36 are defined by similar cone angles to thepegs 22, so that contact between the pegs and the sides of the openings takes place complementally over virtually the entire length of each peg. - Throughout the range of possible articulation, the
pegs 22 remain in thepassage 36 and prevent the core from separating laterally from theplates 10. In other words, the core is held captive by the pegs during all possible articulations which can take place. In the illustrated embodiment, theplates 10 are limited to 12° of articulation before therims 24 abut one another, i.e. 12° is the maximum articulation which can take place. - In the
prosthesis 28 described above, thepegs 22 locate in apassage 32 which passes right through thecore 30. It will however be understood that in other embodiments, the pegs could merely locate in blind recesses or openings in the opposite surfaces of the core without such openings actually being joined to one another to form a continuous passage. -
FIG. 7 illustrates a prosthesis according to a second embodiment of the invention in a view similar to that ofFIG. 5 . InFIG. 7 , components corresponding to components illustrated in the earlier Figures are indicated by the same reference numerals. - The
lower prosthesis plate 10 inFIG. 7 is identical to the prosthesis plates of the first embodiment. However, the upper prosthesis plate, designated 10.1, has no central peg. Instead, thesurface 26 is continuously, spherically curved. In all other respects the plate 10.1 is identical to theplate 10. - In the assembled prosthesis 50, the core is held captive by the action of the
single peg 22 carried by thelower prosthesis plate 10. Thecore 30 is identical to the core described previously but once again it will be appreciated that core could have a blind recess in its downwardly facing,curved surface 32 only to receive thesingle peg 22. - The
prosthesis 28, 50 is surgically implanted between adjacent spinal vertebrae in place of a damaged disc. Those skilled in the art will understand that the adjacent vertebrae are forcibly separated from one another to provide the necessary space for insertion. Theplates 10, 10.1 are slipped laterally into place between the vertebrae with theirfins 16 entering slots cut in the opposing vertebral surfaces to receive them. - After insertion of the core between the opposing plates, the vertebra are allowed to move together to hold the assembled prosthesis in place.
- The
surfaces 12 of theplates 10, 10.1 locate against the opposing vertebrae and, with passage of time, firm connection between the plates and the vertebrae will be achieved as bone tissue grows over the serrated finish. Bone tissue growth will also take place about thefins 16 and through theholes 18 therein, further enhancing the connection which is achieved. - Referring to
FIGS. 3 and 4 , the core 30 used in the embodiments described above is formed with narrow, angularly spaced, blind passages which accommodate titanium pins 42. The core itself is transparent to X-radiation and so would normally be invisible in a post-operative X-ray examination. Thepins 42 serve as radiographic markers and enable the position of the core 30 to be ascertained during such examination. -
Annular grooves 44 are provided in theplates 10, 10.1 to facilitate holding and manipulation of the prosthesis by appropriate instruments during placement into the intervertebral disc space. - Compared to known prostheses, the
prostheses 28, 50 described above have a number of advantages, as follows: - 1. The peg or pegs 22 hold the core captive and prevent it from slipping out sideways.
- 2. At a predetermined maximum limit of articulation, the
rims 24 contact one another to prevent further articulation. At the same time, the peg or pegs 22 contact the sides of theopenings 34, also preventing further articulation. - 3. An acceptable bearing area of the plates on the core is obtained with the central peg/central opening configurations described above. This is particularly advantageous compared to prior art prostheses where the core has peripheral channels on its upper and lower surfaces to receive peripheral rims on the plates at the limit of articulation.
- In practice, it may happen that there is imperfect alignment of the prosthesis plates. In the case of very poor alignment, the dual peg configuration of
FIGS. 5 and 6 gives rise to the possibility that thepegs 22 are laterally offset from one another by a substantial distance. This can in turn lead to the undesirable consequence that the range of articulation which can be accommodated is unduly limited, and attempts to articulate past the limit could result in damage to the core by the misaligned pegs. In the embodiment ofFIG. 7 the single peg can be received centrally by the core, thereby avoiding this potential problem. - The principles of the invention are applicable to prosthetic disc implants for lumbar vertebrae as well as cervical vertebrae. In the latter case, the
fins 16 will typically be omitted. - While the present invention has been described with respect to particular embodiments and specific examples thereof, it should be understood that other embodiments may fall within the spirit and scope of the invention. Therefore, the scope of the invention is limited solely by the claims and their full range of equivalents.
Claims (21)
1. An intervertebral prosthesis for insertion between adjacent vertebrae, the prosthesis comprising:
a first prosthesis plate comprising a midline, an engagement surface to engage a first vertebra and a bearing surface disposed opposite the engagement surface;
a second prosthesis plate comprising a midline, an engagement surface to engage a second vertebra and a bearing surface disposed opposite the engagement surface, wherein the bearing surfaces of the first and second plates are arranged to cooperate to form an articulate joint;
a first region of serrations disposed on the engagement surface of the first plate on one side of the midline of the first plate; and
a second region of serrations disposed on the engagement surface of the first plate on an opposite side of the first plate midline; and
wherein each region comprises at least several serrations and each serration comprises a base attached to one of the plates and tapers from the base to a tip.
2. The prosthesis according to claim 1 wherein the serrations of the first region are parallel to the serrations of the second region.
3. The prosthesis according to claim 1 wherein the serrations of the first and second regions are parallel to the midline.
4. The prosthesis according to claim 1 wherein the serrations of the first and second regions are symmetrically disposed about the midline.
5. The prosthesis according to claim 1 further comprising a core located between the plates, the core comprising a first surface adapted to engage the bearing surface of the first plate and a second surface adapted to engage the bearing surface of the second plate, wherein the first surface of the core and the bearing surface of the first plate comprise cooperating spherical surfaces.
6. The prosthesis according to claim, 5 wherein second surface of the core and the bearing surface of the second plate comprise cooperating spherical surfaces.
7. A prosthesis according to claim 1 further comprising a fin to anchor the first plate in the first vertebra, the fin disposed along the midline between the rows of serrations disposed on the first plate, the fin adapted to enter a cut in the first vertebra.
8. The prosthesis according to claim 7 , wherein holes are formed transversely through the fin.
9. The prosthesis according to claim 1 , wherein the bearing surface of each plate is bounded by an annular rim, wherein the annular rims are arranged to contact one another at a predetermined limit of articulate movement of the plates.
10. The prosthesis according to claim 1 , wherein the bearing surface of each plate is bounded by an annular rim having a groove formed thereon, wherein the grooves are adapted to connect to a placement instrument while the prosthesis is inserted into the intervertebral space.
11. An intervertebral prosthesis for insertion between adjacent vertebrae, the prosthesis comprising:
a first prosthesis plate comprising a midline, an engagement surface to engage a first vertebra and a bearing surface disposed opposite the engagement surface;
a second prosthesis plate comprising a midline, an engagement surface to engage a second vertebra and a bearing surface disposed opposite the engagement surface, wherein the bearing surfaces of the first and second plates are arranged to cooperate to form an articulate joint;
a first region of serrations disposed on the engagement surface of the first plate on one side of the midline of the first plate;
a second region of serrations disposed on the engagement surface of the first plate on an opposite side of the first plate midline;
a third region of serrations disposed on the engagement surface of the second plate on one side of the midline of the second plate;
a fourth region of serrations disposed on the engagement surface of the second plate on an opposite side of the second plate midline; and
wherein each region comprises at least several serrations and each serration comprises a base attached one of the plates and tapers from the base to a tip.
12. The prosthesis according to claim 11 wherein the serrations of the third and fourth regions are identical the serrations of the first and second regions, respectively.
13. The prosthesis according to claim 11 wherein the serrations of the first region are parallel to the serrations of the second region and the serrations of the third region are parallel to the serrations of the fourth region.
14. The prosthesis according to claim 11 wherein the serrations of the first region and the serrations of the second region are parallel to the first plate midline and the serrations third region and the serrations of the fourth region are parallel to the second plate midline.
15. The prosthesis according to claim 11 wherein the serrations of the first and second regions are symmetrically disposed about the first plate midline and the serrations of the third and fourth regions are symmetrically disposed about the second plate midline.
16. The prosthesis according to claim 11 further comprising a core located between the plates, the core comprising a first surface adapted to engage the bearing surface of the first plate and a second surface adapted to engage the bearing surface of the second plate, wherein the first surface of the core and the bearing surface of the first plate comprise cooperating spherical surfaces.
17. The prosthesis according to claim, 11 wherein second surface of the core and the bearing surface of the second plate comprise cooperating spherical surfaces.
18. A prosthesis according to claim 11 further comprising:
a first fin to anchor the first plate in the first vertebra, the fin disposed along the midline between the regions of serrations disposed on the first plate, the fin adapted to enter a cut in the first vertebra; and
a second fin to anchor the second plate in the second vertebra, the fin disposed along the midline between the regions of serrations disposed on the second plate, the fin adapted to enter a cut in the second vertebra.
19. The prosthesis according to claim 18 , wherein holes are formed transversely through the fins.
20. The prosthesis according to claim 11 , wherein the bearing surface of each plate is bounded by an annular rim, wherein the annular rims are arranged to contact one another at a predetermined limit of articulate movement of the plates.
21. The prosthesis according to claim 11 , wherein the bearing surface of each plate is bounded by an annular rim having a groove formed thereon, wherein the grooves are adapted to connect to a placement instrument while the prosthesis is inserted into the intervertebral space.
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US11/468,618 Expired - Lifetime US7731754B2 (en) | 2002-09-19 | 2006-08-30 | Intervertebral prosthesis |
US11/982,420 Abandoned US20080294259A1 (en) | 2002-09-16 | 2007-10-31 | Intervertebral prosthesis |
US11/982,431 Abandoned US20080228277A1 (en) | 2002-09-19 | 2007-10-31 | Intervertebral prosthesis |
US12/129,868 Expired - Lifetime US8262732B2 (en) | 2002-09-19 | 2008-05-30 | Intervertebral prosthesis |
US12/731,993 Abandoned US20100179419A1 (en) | 2002-09-19 | 2010-03-25 | Intervertebral Prosthesis |
US15/284,344 Expired - Lifetime US9839525B2 (en) | 2002-09-19 | 2016-10-03 | Intervertebral prosthesis |
US15/458,913 Expired - Lifetime US10166113B2 (en) | 2002-09-19 | 2017-03-14 | Intervertebral prosthesis |
US15/812,209 Expired - Lifetime US10517738B2 (en) | 2002-09-19 | 2017-11-14 | Intervertebral prothesis |
US16/108,773 Expired - Lifetime US11285013B2 (en) | 2002-09-19 | 2018-08-22 | Intervertebral prosthesis |
US16/189,802 Expired - Lifetime US10413420B2 (en) | 2002-09-19 | 2018-11-13 | Intervertebral prosthesis |
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US15/458,913 Expired - Lifetime US10166113B2 (en) | 2002-09-19 | 2017-03-14 | Intervertebral prosthesis |
US15/812,209 Expired - Lifetime US10517738B2 (en) | 2002-09-19 | 2017-11-14 | Intervertebral prothesis |
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