SUBPERIOSTEAL JAW IMPLANT
20180161129 ยท 2018-06-14
Inventors
Cpc classification
A61C8/0012
HUMAN NECESSITIES
B33Y80/00
PERFORMING OPERATIONS; TRANSPORTING
A61C8/0031
HUMAN NECESSITIES
International classification
Abstract
In a jaw implant for oral, subperiosteal placement over the alveolar ridge of the maxilla or of the mandible, the implant forms a body which in cross-section, in the condition in which it has been placed on the alveolar ridge transverse to the alveolar ridge, has been formed concave towards the alveolar ridge, wherein in or near a first portion forming the base of the body, in particular forming the base of the J, L or U, the body has been provided with one or more supporting areas for support members, such as pillars, for extending through the gingiva, the support members forming a support for an exo-prosthesis, wherein the supporting areas have been connected to the rest of the body via relatively weakened areas of the body, in particular have been connected to the rest of the body via those relatively weakened areas of the body only.
Claims
1-54. (canceled)
55. Jaw implant for oral, subperiosteal placement over the alveolar ridge of the maxilla or of the mandible, wherein the implant forms a body which in cross-section, in the condition in which it has been placed on the alveolar ridge transverse to the alveolar ridge, has been formed concave towards the alveolar ridge, such as J-shaped, L-shaped or U-shaped, wherein in or near a first portion forming the base of the body, in particular forming the base of the J, L or U, the body has been provided with one or more supporting areas for support members, such as pillars, for extending through the gingiva, in particular passing through it, said supporting areas being integrally formed with the body, said support members forming a support for an exo-prosthesis, such as a dental prosthesis or dentures, characterized in that the supporting areas have been connected to the rest of the body via relatively weakened areas of the body, in particular have been connected to the rest of the body via those relatively weakened areas of the body only.
56. Implant according to claim 55, wherein each supporting area has been connected to the rest of the body via its own weakened areas.
57. Implant according to claim 56, wherein, at least at the location of the supporting areas, the body has an open structure such as a framework or grid.
58. Implant according to claim 57, wherein the weakened areas have been restricted to within the bars or strips of the grid or framework.
59. Implant according to claim 55, wherein the relatively weakened areas have been formed by porous areas, wherein the pores may have a cross-section that is smaller than 1 mm, for instance in the order of a few tenths of one mm, such as 0.5 mm.
60. Implant according to claim 55, wherein the weakened areas are formed by hollow bar sections or hollow strip sections.
61. Implant according to claim 55, wherein the relatively weakened areas are formed by areas having a relatively reduced wall thickness.
62. Implant according to claim 55, wherein the relatively weakened areas are formed by areas having perforations in the material of the body, wherein the perforations have a cross-section that is smaller than the thickness of the body at that location.
63. Implant according to claim 55, manufactured by means of 3D printing, preferably made of titanium, tantalum or an alloy thereof.
64. Implant according to claim 55, wherein the body has been provided with attachment holes for screws for attaching the implant to the jawbone, wherein the holes have been provided on a second portion of the body in question abutting a side of the alveolar ridge, wherein, preferably, the second portion has been formed for attachment to the buccal side of the jawbone in question.
65. Implant according to claim 55, wherein the body has been provided with attachment holes for screws for attaching the implant to the jawbone, wherein the body has been provided with extensions, provided with one or more of the attachment holes, wherein the body has been configured for placement on the mandible wherein the body has been provided with such an extension for attachment to the corpus mandibulae and/or with such an extension for attachment to the ramus ascendens mandibulae, in particular for attachment to the frontal edge (trigonum retromolare) of the ramus ascendens mandibulae, over the trigonum retromolare in the direction of the processus coronoideus, or lateral from the ascending branch of the mandible, dorsally extending.
66. Implant according to claim 55, wherein the body has been configured for placement on the maxilla, wherein the body has been provided with extensions, provided with one or more of the attachment holes for screws for attaching the implant, wherein the body has been provided with such an extension for attachment adjacent to the apertura piriformis and/or has been provided with such an extension for attachment to the zygomatic pillar and/or the zygoma.
67. Implant according to claim 55, wherein the supporting areas at the convex side of the body in question have been provided with elevations which, at their end facing away from the body, have been provided with a means for attaching an exo-prosthesis thereto, either with or without the interposition of an intermediate pillar, wherein the elevations have been integrally formed with the body in question.
68. Implant according to claim 67, wherein the elevations protrude from the body in question up to a distance that is sufficient for their circumferential surface to extend above the gingiva after having been placed.
69. Implant according to claim 67, wherein the elevations are pillar-shaped and at their outer ends have been provided with a means for direct attachment of an exo-prosthesis thereon.
70. Implant according to claim 69, wherein at their outer ends the elevations have been provided with a means for attaching an intermediate pillar thereto, which intermediate pillar at its opposite end has been provided with a means for attaching an exo-prosthesis thereon.
71. Method for manufacturing a subperiosteal jaw implant according to claim 55, wherein a scan is made of a jaw for which the implant is intended, on the basis of which scan a design of the implant is made, the design is entered as a CAD file into the operating system of a 3D printer which is fed with a bio-compatible printing material suitable for subperiosteal implants, after which the designed implant is printed by the 3D printer using the printing material, in accordance with the design in the CAD file.
72. Method according to claim 71, wherein the supporting areas at the convex side of the body in question have been provided with elevations which, at their end facing away from the body, have been provided with a means for attaching an exo-prosthesis thereto, either with or without the interposition of an intermediate pillar, wherein the elevations have been integrally formed with the body in question, and wherein the elevations are provided in a number that is an excess of the required number for the attachment of the exo-prothesis.
73. Method for intervening in cases of imminent onset of or full-blown peri-implantitis in the area of a support column forming the connection between a subperiosteal jaw implant and an exo-prosthesis, wherein a relatively weakened area forming the connection between the support column in question and a concave body of the implant placed against the jawbone is broken and the support column is removed.
74. Method according to claim 73, wherein the exo-prosthesis is placed back again after removal of the elevation.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0070] The invention will be elucidated on the basis of a number of exemplary embodiments shown in the attached drawings, in which:
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DETAILED DESCRIPTION OF THE DRAWINGS
[0085] The subperiosteal jaw implant 1 of
[0086] As can be seen in the cross-section of
[0087] The body 2 has furthermore been provided with integrally formed attachment lips 11 and 12, which have been provided with attachment holes 13 for osteosynthesis screws 14. The lips 11 are intended/configured for attachment to zygomatic pillars, the lips 12 are intended/configured for attachment to the bone adjacent to the apertura piriformis.
[0088] In
[0089] As can be seen in the cross-section of
[0090] The body 102 has furthermore been provided with integrally formed attachment lip 115, which has been provided with attachment holes 113 for osteosynthesis screws 114. The lips 115 are intended/configured for attachment to the frontal edge (trigonum retromolare) of the ramus ascendens mandibulae. Portion 105a has been provided with attachment holes 116, also for osteosynthesis screws 114.
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[0094] In
[0095] The embodiment of
[0096] The implant is placed in the patient by exposing the alveolar ridge by making a few incisions in the gingiva. The implant is placed on the alveolar ridge and attached to permanent jaw material using osteosynthesis screws. The gingiva is placed back again over the implant and sutured. The columns extend to above the gingiva.
[0097] Finally, the exo-prosthesis is placed on the columns.
[0098] After a while the implant will get osseointegrated with the bone membrane and with the gingiva. If the weakened areas 7, 107, 207, 307 have been formed by an incision at the bone side or have a porous surface at that location, this will be conducive to osseointegration. The forces resulting from chewing motions can be absorbed by the jaw via the various screw attachments. The motions of the implant relative to the gingiva and bone membrane will then remain within limits.
[0099] If a column extending through the gingiva has a mechanical problem or when there is question of peri-mucositis at said column, it is possible, after having detached the exo-prosthesis and cutting the gingiva around the column in question open in flaps, to detach the column 9 including its supporting area 8 from the body 2 of the subperiosteal implant 1, 101, 201, 301 through a machining action at the location of the weakened areas 7, 107, 207, 307. In case the body has been made of titanium or tantalum, or an alloy thereof, the machining action can be executed more easily than would be the case with the chromium-cobalt-molybdenum type alloys.
[0100] It is noted that the columns 9 can alternatively be executed as separate elements, and are then securely attached to the supporting areas 8, et cetera, inseparable therefrom.
[0101] Manufacturing using 3D printing enables shaping the weakenings in any wanted way, such as by porous areas, for instance with pores having a maximum cross-section of 0.5 mm, hollow areas, incisions, or perforations having a diameter that is smaller than the thickness of the body at that location.
[0102]
[0103] As can be seen in the cross-section of
[0104] Like in the preceding examples, weakenings 7 have been formed in the material of the body approximately halfway the bars 6, in accordance with what has been discussed above. Each column 9 therefore has its own supporting area 8, which has been provided with a weakening 7 in each connection 6 to the rest of the body 2.
[0105] The bodies 2a,b have furthermore been provided with integrally formed attachment lips 11 and 12, which have been provided with holes 13 for osteosynthesis screws 14. The lips 11 are intended for attachment to the zygomatic pillars and the zygoma, the lips 12 for attachment adjacent to the apertura piriformis. In
[0106] Prior to placing the segments 2a,b the alveolar ridge has been exposed by making a few incisions in the gingiva. Despite the presence of the rather long extensions 11 and 12, the segments 2a,b have in a controlled manner been successively introduced into the patient's mouth, and placed at the correct location on the maxillary alveolar ridge. See
[0107] Then the dentures 20 can be placed. In
[0108] The bridge part 20a then connects both segments 2a,b rigidly, wherein the stability of the segments is enhanced, which is advantageous for fixating the segments after that.
[0109] Subsequently the segments 2a,b are permanently fixated at intermediate distance from one another, to the labial/buccal side of the maxillary alveolar ridge using osteosynthesis screws 14, and are also attached to the zygomatic pillar and adjacent to the apertura piriformis using the osteosynthesis screws 14. The gingiva is placed back again, around the columns 9 and over the implant, and sutured. The columns 9 extend to above the gingiva.
[0110] In
[0111] As can be seen in the cross-section of
[0112] The segments or bodies 102a,b have furthermore been provided with integrally formed attachment lips or extensions 115a,b that have been provided with holes 113 for osteosynthesis screws 114. The lips 115a,b are intended for attachment to the lateral side of the ramus ascendens mandibulae, dorsally extending.
[0113] Despite the rather long extensions 115a,b, the segments or bodies 102a,b have in a controlled manner been successively introduced into the patient's mouth and placed at the correct location on the alveolar ridge. If so desired, the segments 102a,b could be kept in their place for the time being using a few temporary screws. After this has successively been done for both, the segment 102c is placed, optionally also by means of a temporary screw, in order to realize the situation of
[0114] In this example the dentures 120 to be placed are one-part like in
[0115] The screws 126 now also realize an angularly rigid connection of bridge part 120a to the segments 102a, 102b and 102c. The holes 125 are filled later on by a suitable filler.
[0116] The bridge part 120a then rigidly connects the three segments or bodies 102a,b,c, thus enhancing the stability of the segments placed on the alveolar ridge, at least until they have been fixated to the lateral side of the ramus ascendens mandibulae and to the alveolar ridge using osteosynthesis screws 114 in all holes 113. The gingiva can subsequently be placed back again and sutured.
[0117] In
[0118] The way of placement largely corresponds with placing the assembly of
[0119] After a while the implant segments will get osseointegrated with the bone membrane and with the gingiva. Until that time the bridge part ensures stabilization of the segments.
[0120] In one embodiment each segment has been provided to be ideally positioned by means of the precision attachment between the subperiosteal segments and the supra structure, which spatially define the segments in their ideal configuration relative to each other and relative to the jawbone.
[0121] Manufacturing the implants according to the invention, either in the segmented embodiment or not, can take place as follows. The patient is in need of an exo-prosthesis, yet due to an atrophied jawbone they have insufficient material to attach and anchor endosseous implants. Bone reconstruction using the patient's own bone or donor bone or using synthetic bone is not an option and neither is bone grafting. In such cases a subperiosteal implant may be the solution.
[0122] A three-dimensional image is made of the jaw or the jaw part in question of the patient's, which reveals the specific contours and condition of the jawbone. This is done using a 3D scanner, in particular a CT scanner, more in particular a CBCT scanner.
[0123] The 3D image is stored and made available to a designer of subperiosteal implants. The designer designs an optimal design of the subperiosteal implant for the patient using a CAD program. The designer then also decides on the locations of attachment by means of screws and the design of the weakenings and/or the division into segments. The scan also provides information about the locations where the bone is sufficiently thick to serve as location of attachment. Based on the scan, the designer is able to decide on the use of, the location and the shape of extensions/lips.
[0124] The design can be stored in a design file suitable for operating a 3D printer. The 3D printer in configured for printing medical implants made of biocompatible materials such as titanium or tantalum or alloys thereof.
[0125] The operating system of the 3D printer reads the design file and has the 3D printer print the body or the bodies in accordance with the design. The body obtained then forms the subperiosteal implant or the bodies obtained together form the subperiosteal implant constituting of segments. If required the body or the bodies/segments can be further finalized (such as finishing the threading), for instance in a CNC process.
[0126] The above description is included to illustrate the operation of preferred embodiments of the invention and not to limit the scope of the invention. Starting from the above explanation many variations that fall within the spirit and scope of the present invention will be evident to an expert.