JP2013063316A - Dental implant repair system - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a dental implant repair system that includes an aesthetic implant abutment for the installation of a repair dental prosthesis in an oral cavity of a patient.SOLUTION: The dental implant repair system includes: an implant; an abutment that is fixed to the implant; and a dental prosthesis that has been arranged on the abutment. The abutment is a single unit structure produced with a ceramic material, and is multicolor to agree with the color of the dental prosthesis, and a surrounding tooth row and the surrounding tissue of teethridge over the whole.

Description

  This application is a continuation-in-part of US patent application Ser. No. 10 / 799,513 filed Mar. 12, 2004, and is hereby incorporated by reference.

  The present invention relates generally to restorative dentistry. In particular, the present invention relates to a dental implant repair system.

  Restorative dentistry has made significant progress in the use of dental implants that support dental restorations intended to permanently replace natural teeth. Dental implants provide an alternative to removable dentures, fixed partial dentures and single tooth restorations.

  In a jaw-fixed dental restoration, a well-designed implant is surgically implanted into the patient's jawbone, leaving the gum surface exposed. A support post, commonly referred to as an abutment, is securely secured to the exposed surface of the implant at the same time. The dental prosthesis is secured to the abutment by going through screws and abutments (retained screws) or conventional cementing techniques (retained cement) extending through the holes in the prosthesis .

  As described above, for example, U.S. Pat. No. 4,988,298 to Lazzara et al., Contains all the content that is hereby incorporated by reference and as shown in FIG. The dental implant repair system 10 generally includes a dental implant 14, a support post or abutment 16, and a prosthesis 12. The implant is typically manufactured from a biocompatible material such as titanium or a titanium alloy, and the gum surface 22 is flush with or embedded in a jaw bone that is substantially flush with the gum surface AA of the jawbone. Entered. The gum end includes a female threaded recess 24 and a multi-faced male projection for abutment with the abutment 16. The abutment 16 is securely attached under the prosthesis 12 or at the end of the gums and functions to provide a rigid interconnection between the implant 14 and the prosthesis 12.

  The passage extends through the abutment 16 and provides a recess in the portion of the trans gum for engaging the protrusion of the implant. The screw 26 abuts against the shoulder 28 of the abutment and engages the screw recess 24 of the implant to press fit the precision-formed abutment surface 29 into the attached contact surface having the gum surface of the implant. The prosthesis 12 is fabricated around the top of the abutment and can be connected to the abutment via screws 26 or cement. The prosthesis is colored to match the surrounding dentition.

  In general, the abutment is made of a metal such as titanium, and the prosthesis is made of a ceramic material such as a ceramic material such as porcelain or a polymer resin material. However, a fully metallic abutment can be seen through the prosthesis, resulting in a dark color, which makes it more distinct from natural teeth when shadows like the central rod are exposed to bright light. So the prosthesis is a bit not beautiful. Various methods for preventing or masking the appearance of shadows are known in the art.

  One attempt to solve the attractive problem involves making the support posts entirely from a tooth-colored ceramic material. This approach can result in a secure, almost seamless connection between the prosthesis and the support post, with the direct surface bonded to the support post by the porcelain top and / or the interaction of the prosthesis. While presenting variations of the attractiveness of using titanium support posts, the proposed description presents many challenges.

  Ceramic materials generally have a much higher hardness than titanium. When an all-ceramic support post is used, for example, biting of the support post is unavoidable by biting, resulting in high stress interactions between the metal implant and the ceramic material of the post. Because ceramic support posts are harder than titanium implants, they can cause damage to the implant. If sufficient damage occurs, the final surgical intervention will require removing and replacing the titanium implant. In addition, ceramic materials are generally not radiopaque and the interface between the two elements is easy when using conventional x-ray imaging to examine the connection between the abutment and the titanium implant It is not visible, and sufficient inspection cannot be performed. Furthermore, the destruction of all ceramic posts is also a problem to consider.

Recognizing the advantages of metallic supports, US Pat. No. 5,685,714 to Beaty et al. Describes an abutment having two different cross sections. As shown in FIG. 2, the abutment 12 includes an inner or core 36 made of titanium or a titanium alloy and an outer periphery or cuff 34 made of ceramic, typically aluminum oxide. The metal core 36 provides the necessary strength to the abutment and provides a framework for connecting the prosthesis 38 to the implant 40. A ceramic cuff 34 preferably surrounds all outer surfaces of the core 36 and protects the shadow of the metal core 36 through the prosthesis 38. PureForm ^TM (TM) (Centerpulse Dental Inc., Carlsbad, CA) (Centerpulse Dental Inc., Carlsbad, Calif.) , For example, the tooth-shaped consisting of titanium core and ceramic cuff made of alumina / zirconia mixed It is an abutment. Screw-carrying alumina or zirconia or alumina-based abutments are trademarks of Bio-Cera ^™ (Bio-Rock International, Deerfield Beach, Florida) (Bio-Lok International, Inc., Deerfield Beach, Fla. .), CerAdapt ^TM (TM) (Nobel Biocare (TM) Corporation, Gothenburg, ^{Sweden) (Nobel Biocare TM AB, Goteborg} , SE), and, ZiReal ^TM (trademark) post (implant Innovations, Inc., Wilmington, Delaware) (Implant Innovations, Inc., Wilmington, Del.).

  US Pat. No. 6,497,573 to Wagner et al. Describes a three-part dental abutment that includes a shield between a metal core and a polymeric cuff. The shield is preferably formed in an opaque material such as a mixture of several mono- and dimethacrylates, providing various colors for the best shield or any grayish or metallic color of the core Various dyes that also mask can be included.

  US Pat. No. 7,179,089 is directed to a two-part abutment having a top made of metal, zirconia or alumina cylinder and a shoulder attached to the cylinder and made of hybrid ceramic material, thereby A pigment can be added to the hybrid ceramic material to match the color of the patient's gingival tissue.

  Each of the devices described above, however, has certain drawbacks. The three part system is inherently expensive in both time and material. The two part system of US Pat. No. 7,179,089 requires the mounting of a cylinder on the shoulder component. In addition, the two part system effectively masks the shadow of the metal core while requiring additional time and expertise in prosthesis fabrication. When using a fully metallic abutment, the engineer recognized that the result was simply a shading and was making a prosthesis that fits the surrounding dentition. For the addition of cuff components, however, the cuff color and the color of the prosthetic bond to the alloy create the final restoration color so that the technician can take into account the abutment color when making the prosthesis. There must be.

  This is particularly important when the prosthesis is made of ceramic. Since most ceramic restorations have an inherent translucency, it is imperative that the abutment be shaded to supplement the desired shade of the restoration. This process is similar to determining the natural tooth shade prior to the fabrication of an all-ceramic crown. In that case, it is recognized that the underlying natural tooth or “stamp” affects the shade of the final restoration.

  US Pat. No. 6,231,342 and US Pat. No. 5,989,029 are hereby incorporated by reference for purposes of customized abutment. The abutment is customized by making a series of measurements at the tooth site and making the abutment based on the measurements. Despite the abutment being a customized single unit structure, there are no color and shade considerations.

Conventional abutments include, for example, PureForm ^™ (trademark) Ceramic Coping (Center Pulse Dental Inc., Carlsbad, Calif.) (Centerpulse Dental Inc., Carlsbad, Calif.), Bio-Cera ^™ (trademark) (Bio-Rock International, Inc.) Deerfield Beach, Florida) (Bio-Lock International, Inc. , Deerfield Beach, Fla.), CerAdapt TM ( TM) (Nobel Biocare ^TM (trademark), Gothenburg, ^{Sweden), (Nobel Biocare TM AB,} Goteborg, SE), ZiReal ^TM (trademark) (implant Innovations, Inc., Will mint , Delaware) (Implant Innovations, Inc., Wilmington, Del.), Regardless of the material to be manufactured, one standard color selected by the manufacturer usually available. Thus, a “perfect match” between the abutment and the prosthesis is not achieved. CerAdapt ^TM (TM) abutment, for example, Vita-Shade ^TM (TM) A-3 (Vita Shade ^TM (TM) guide, Bidento, Brea, ^{California) (Vita-Shade TM Guide,} Vident, Brea, Calif.) And Available.

US Pat. No. 4,988,298 US Pat. No. 5,685,714 US Pat. No. 6,497,573 US Pat. No. 7,179,089 US Pat. No. 6,231,342 US Pat. No. 5,989,029

  In an embodiment, the present invention provides an aesthetic implant abutment for attaching a restoration dental prosthesis in a patient's oral cavity. In accordance with the present invention, the implant abutment includes a core and a cuff surrounding the core, the cuff being colored to match the color of the prosthesis.

  In various embodiments, the core is made from a metal, such as titanium or a titanium alloy, and the cuff and prosthesis are made from a ceramic or polymeric material. In the preferred embodiment, the cuff and prosthesis are formed of ceramic.

  The present invention further provides a dental implant repair system including an implant, a dental abutment having a core and a cuff surrounding the core to be fixed to the implant, and a dental prosthesis to be fixed to the abutment. -The cuff is colored to match the color of the prosthesis.

  The present invention is also a method of manufacturing a dental implant restoration, wherein the implant is secured in the oral cavity of a patient, the dental abutment comprising a core and a cuff surrounding the core is secured to the implant, A dental prosthesis is attached to the abutment, and the abutment cuff provides a method that is colored to match the color of the prosthesis.

  In yet another embodiment, the single unit abutment is made of a ceramic material, shaded to match the color of the dental prosthesis, and / or surrounds the dentition and surrounds the gum tissue . The abutment is anatomically shaped and shaded to conform to the near net shape and shade of the prosthesis attached to it. As the abutment gets closer to the net shape and more shades appear more naturally, the restoration on the top is no longer needed and becomes the restoration itself. In addition, the abutment is shaded to match the color of the surrounding dentition and gum tissue.

1 is a partial cross-sectional view of a prior art dental abutment that is secured within a dental implant repair system. FIG. 1 is a partial cross-sectional view of a prior art dental abutment that is secured within a dental implant repair system. FIG. 1 is a partial cross-sectional view of a dental restoration system according to an embodiment of the present invention. It is a perspective view of the face side of the abutment according to one embodiment of the present invention. It is a perspective view of the side surface of the horizontal direction of the abutment of FIG. It is a perspective view of the upper part side of the abutment of FIG. FIG. 6 is a partial cross-sectional view of a dental implant system according to another embodiment of the present invention. FIG. 6 is a perspective view of a dental implant system according to another embodiment of the present invention. FIG. 9 is a facial perspective view of the abutment of the implant system of FIG. 8. FIG. 9 is a facial perspective view of the abutment of the implant system of FIG. 8. 11 is a perspective view of a hole in the abutment of FIGS. 9 and 10. FIG. FIG. 11 is a perspective view of another hole located in the abutment of FIGS. 9 and 10. FIG. 9 is a close-up cutaway view of the upper portion of the implant shown in FIG. 8. FIG. 14 is a top view of the implant of FIG. 13.

  FIG. 3 shows a dental repair system 100 that includes a prosthesis 102, an abutment 104, and an implant 106. The abutment and prosthesis are closely attached and connected to the implant as shown.

  The implant 106 has a coronal or gum end with a screw hole 110 and has a male engaging feature 112 extending upward. The coronal end extends downward along the cylinder to the end. The male engagement feature 112 connects to the abutment and may be a plurality of upwardly extending tines, polygons, or other types of functions known to those skilled in the art. Alternatively, the implant can have a female coupling function that matches the male projection on the abutment core. The implant may be any one of a variety of well-known implants, such as those manufactured by Sulzer Calcitek Inc. (Carlsbad, Calif.).

  The abutment 104 has two different and distinct parts, preferably formed from two different materials. The core part 120 has a cylindrical shape and extends from the upper part to the lower part. A passage 126 extends centrally through the core. The lower part abuts against the coronal end of the implant 106. The abutment 104 can include a female engagement feature 128 that is engaged by a male engagement feature 112 to provide a counter-rotating connection between the abutment and the implant. The engagement feature has a configuration that is adapted to provide a significant anti-rotation connection. Numerous configurations of the engagement feature are known to those skilled in the art and can be used (eg, Spline® tine, octagon and other polygons).

  The core 120 includes a shoulder 130 located generally along the interior of the passage 126 at the top. A corresponding ledge 132 is formed along the outer surface adjacent to the shoulder 130. Preferably, the core is fabricated from a biocompatible metal such as titanium or an alloy thereof. The metal core provides strength to the abutment and framework for connecting the prosthesis to the implant.

  The abutment cuff 140 is connected to the outer surface of the core 120 and preferably surrounds all outer surfaces. The cuff has a somewhat cylindrical configuration and extends from the top to the bottom. The cuff can be shaped around the core to have a variety of configurations, such as a cylindrical or elliptical configuration or anatomical shape that resembles the cross section of a natural tooth, for example.

  As shown in FIG. 3, the cuff 140 tapers outward and upward from the coronal end of the implant 106 to form a frustoconical shape. This taper extends to the ledge 146 and transitions inward at the top of the cuff 140. The shoulder 148 is located along the inner surface. This shoulder 148 is fitted by a fitting ledge 132 on the outside of the core.

  The prosthesis 102 is shaped like a natural tooth and includes a passage 150 that aligns with the abutment passage 126. The screw 152 passes through these passages until the screw head 154 abuts against the top of the core. As shown, the lower portion of the head includes a taper 156 that abuts against the shoulder 130 along the interior of the core. The screw includes a shank 158 extending from the head. The shank has a female thread 160 that mates with the coronal end of the implant to engage the corresponding thread of the screw hole 110. The screw holds the prosthesis attached to the abutment and implant. The head 154 also includes a recess 162. The recess is provided to engage a tool (not shown) for tightening and loosening the screw, or to engage another screw (not shown) in a passable manner to secure the prosthesis. Can be provided.

In accordance with one embodiment of the present invention, the color of the abutment cuff 140 is matched to the color of the prosthesis 102. The cuff 140 and prosthesis 102 are preferably manufactured from a ceramic material, while the zirconia / prosthesis 102 described in, for example, US Pat. No. 6,380,113 to Kim et al. Alumina composites and various polymers and polymer combinations such as acrylic polymers, fibers, glass, silica and alumina, reinforced polymers, thermoset and photosensitive polymers, vinyl esters, and epoxy type materials may also be used. it can. Suitable polymers, Sculpture ^TM (TM) or FibreKor ^TM (TM), Generic / Pentoron Inc. (Wallingford (Connecticut)) (Jeneric / Pentron, Inc. (Wallingford, Conn.)) And Targis ^TM (TM) or Vectris ^TM (TM), Ibokuraru Bibadento Inc. (Schaan, Liechtenstein) (Ivoclar Vivadent, Inc. (Schaan (LI))) are included.

  In the context of the present invention, “adapting” the color of the abutment cuff to the color of the prosthesis means selecting the color for the abutment cuff that is most similar to the color of the prosthesis. . Generally, restorations are made in multiple shades, typically darker on the gum surface and lighter on the top. However, the color of the abutment is selected to match the overall color at the prosthesis, especially the abutment 140 and restoration 104 interface.

  Several methods for determining the color of dental restorations are known in the art. The most commonly used are dental shade guides, which typically have basic support for multiple tabs or other indicia, each corresponding to a different color. The tab / indicator color represents the standard tooth color range. U.S. Pat. No. 6,139,318 to Foser, for example, is hereby incorporated by reference in its entirety to select an appropriate color for a dental restoration. The following are particularly useful color keys. The color key includes a removable number, tooth sample elements formed in the same material, the same color, and the same method as a dental restoration. In addition, the tooth sample element includes a first surface having a texture and curvature that matches a natural tooth and a second surface that is smooth and flat. The first surface also offers the possibility of testing the impression that the generated restoration has at the same location, while the second surface is easier in the patient's oral cavity for comparison by surrounding the dentition Provides an improved assessment of color alone so that it can be placed on.

Other commercially available dental shade guides include, for example, Chromoscop ^™ (Ivoclar Vivadent, Schaan, Liechtenstein) (Ivoclar Vivadent, Inc., Schaan, LI), Vitapan Classical ^™ (Vita-Lumimin). ^TM (TM) vacuum shade guide) (Vita-Lumin ^TM (TM) vacuum shade Guide) and Vitapan 3-D Master ^TM (TM) (Bidento, Brea, California) (Vident, Brea, Calif. ), and, Bioform ^TM (Trademark) and TruMatch ^™ (trademark) (Dentspray International, Milford, Delaware) (Dentspl y International, Inc., Milford, Del.).

  Once the color of the prosthesis is determined, the abutment with the cuff fits most closely to the color used in the implant restoration. With the dental shade guide system, a series of colored abutments can be selected that are specific to that system.

  The principles of the present invention thus provide several advantages over conventional dental implant repair systems. The present invention simplifies the repair process in that the fabrication of the prosthesis no longer needs to take into account the color of the abutment. The abutment includes a cuff that matches the color selected for the prosthesis. Thus, the interface between the abutment and the restoration is aesthetically emphasized and less visually observable. In contrast, the color of the restoration according to the prior art was determined by the combination of the color of the abutment and the prosthesis. In general, the technician creating the restoration obtains a standard abutment, then determines the color of the prosthesis and, when combined with the color of the abutment, the desired color of the final restoration It becomes.

  By utilizing an abutment having the same color as the prosthesis, the final restoration has a greater depth and provides a more natural appearance. Just as a damaged tooth “stump” provides a natural color framework for tooth reconstruction, the abutment of the present invention provides a natural color framework for the fabrication of prostheses.

  In some cases, the restoration can include a layer of dental cement between the abutment and the prosthesis. Prior to the present invention, the specialist selects a cement with a color that properly combines with the color of the abutment and prosthesis to obtain the desired color for the final restoration. However, since the abutment matches the color of the prosthesis, no additional determination is required for the present invention and a transparent cement can be used.

  In a typical jawbone-fixed dental restoration, the gingiva is repaired around the system so that the implant system extends above the lower surface of the prosthesis after being fixed in the patient's mouth. However, due to normal aging, it is not uncommon for the gingival line to recede, exposing the lower surface of the prosthesis in the same way as part of the abutment. Prior art abutments can result in an unsightly, unnatural appearance. According to the present invention, however, as the prosthesis color and abutment cuff are adapted, the appearance of the abutment is inconspicuous, even when exposed, and the implant restoration naturally follows the surrounding dentition. To be mixed.

  4-6 show another embodiment of the abutment 200 of the present invention. The abutment 200 is a unitary or single unit structure and can be secured to the implant 202 shown in FIG. A dental prosthesis, such as the crown 204 shown in FIG. 7, is placed on the abutment 200 that is connected to the implant 202 having the screw 206 to hole 207 attachment of the abutment 200. In this type of design, the abutment has a female connection component and the implant body has a male connection component. It should be mentioned that the means of attachment of the abutment 200 to the implant is not limited to the outer anti-rotation connection as illustrated in FIG. Other modes and methods of attachment include, but are not limited to, interconnecting components and can be used. As used herein, an abutment may be adapted to connect to any type of implant.

  The abutment 200 is a single unit structure made of a ceramic material. As shown in FIGS. 4-7, the abutment 200 is manufactured from a single piece of ceramic material, combining the core and cuff of the previous embodiment into a single unit. The abutment foundation includes a collar 208, has a planar lower side 210, and fits snugly into an implant such as implant 202. The upper side of the collar 208 has a lip 212 that extends around the periphery of the collar 208. The coronal portion or upper portion 214 extends upward and is shaped similar to the tooth structure. A dental prosthesis such as the crown 204 of FIG. 7 fits over the lip 212 and the top 214 of the abutment 200.

  The collar 208 is preferably gum or pink to match the gum tissue surrounding the implant 202 in the patient's mouth. By covering the collar 208 with a pink or gum shade, the abutment surrounds and camouflages the dentition and gum tissue in the patient's oral cavity when the gum tissue in the patient's oral cavity is retracted.

  The abutments described herein may be used, or may require changing and preparing a customized abutment to fit the patient more accurately. As shown in FIGS. 4 and 5, the lip 212 forms the original cervical line of the abutment 200. In preparing the abutment to better fit the patient's mouth, it may be necessary to move the cervical line to match the cervical line in the patient's mouth when the gingival tissue is retracted. To adjust the cervical line, the collar 208 can be made of different colored layers of material. The inner core of the collar 208 may be a dentin color (to fit the tooth neck region of the tooth) and the outer layer may be a gum color. The colored layer of the gums can vary from about 0.25 to about 1.00 mm thick. The technician lowers the cervical line as shown in FIGS. 4 and 5 by removing the colored layer of the gums covering the area 213 from the point of the original cervical line 212 to the new cervical line 215. Can do. By removing the gum layer in region 215, a dentin colored layer appears and the cervical line moves from line 212 to line 213. The abutment can be effectively camouflaged by the patient's existing dentition and gum tissue.

The upper or coronal portion 214 is preferably divided into three regions: a neck 216, a central region 218, and a cut end 220, and have different shades or collars to simulate the natural appearance of the teeth. Depending on the size, shape, and dentition that the abutment must correlate or match, these regions are just approximations and vary from abutment to abutment. Each region has different requirements for visual appearance. Thus, the appearance of the lower or neck region 216 of the abutment, which can vary from part to part, preferably conforms to the neck of the prosthesis and the neck of the surrounding dentition. The central area 218 of the abutment preferably matches the central area of the prosthesis and the central area of the surrounding dentition. The cut edge 220 preferably matches the cut edge of the prosthesis and the cut edge of the surrounding dentition. Shade determination for the three coronal areas is determined using commercially available dental shade guides such as Chromoscop ^™ (Ivoclar Vivadent, Schaan, Liechtenstein) (Ivoclar Vivadent, Inc., Schaan, LI), Vitapan Classic. ^TM (TM) (Vita-Lumin ^TM (TM) vacuum shade ^{guide) (Vita-Lumin TM vacuum shade} Guide), and, Vitapan 3-D Master ^TM (TM) (Bidento, Brea, California) (Vident, Brea, Calif .); And Bioform ^™ (trademark) and TruMatch ^™ (trademark) (Dent Spray International, Milford) (Dentsply International, Inc., Milford, Del.) Or can be customized for individual patients, or commercially available intraoral spectrophotometers such as Easyshade ( Vident, Brea, California) (Vident, Brea, Calif.) And Shade Vision (X-Rite, Grand Rapids, Michigan) (Shade Vision (X-Rite, Inc., Grand Rapids, Mich.)) It can be determined by using one. Thus, the natural tooth color of the abutment emphasizes the natural appearance of the prosthesis.

  Reference is further made to FIGS. 8-10 illustrating an abutment 300 showing alternate shapes of attachment to the implant 302 and crown 303. The abutment 300 includes a hole 304 that fits snugly over the conical top 306 of the implant 302. The implant 302 and the upper portion 306 of the hole 304 can vary in size, shape and / or design. The holes 304 are preferably tapered. FIG. 9 is a face view of the abutment 300, and FIG. 10 is a side view of the abutment 300. 11 and 12 show variations in the shape of the hole 304. FIG. 11 shows a cone-shaped hole with a bevel edge 306. FIG. 12 shows a hole 308 in the shape of a hemisphere. Similar to the abutment 200, the abutment 300 is a single unit structure made of ceramic material.

  FIGS. 13 and 14 show a close-up of another example of the upper portion 310 of the implant 302. The upper portion 310 includes one or more chamfered portions 312 that prevent rotation of the abutment 300 on the implant 302 when stress is applied by the patient, for example, while chewing.

  All of the above variations with respect to the abutment 200 apply to the abutment 300. Herein, the abutment can be customized in shape and color to enhance the natural feel provided by the dental prosthesis. By measuring the desired tooth replacement site and determining the type of tooth to be replaced, the type of abutment can be selected from the list and / or naturally into the patient's existing dentition It can be customized to the appropriate shape and color to fit.

  Similar to the abutment 104 having the core portion 120 and the cuff 140, all the above-described shape and structural variations can be applied to the single unit abutments 200 and 300, which includes the core and cuff in one monolithic unit. To join.

  The abutment is coated with an oxide powder with one or more colored substances to produce a colored powder, pressed against the colored powder to produce a molded body, It may be shaded during manufacture by sintering. The reference is commonly owned, co-pending U.S. Patent Application Publication No. 20070292597, which discloses a method of making a zirconia multicolor blank and its product, U.S. Pat. , 379,593 and U.S. Pat. No. 4,970,032, which discloses layered blanks for machining dental materials, all of which are incorporated herein by reference. To do. Partially or completely sintered blanks can also be made and can be further machined to the desired abutment shape.

  Alternatively, the abutment can be partially or fully sintered, and then stained with a stain to partially or fully sinter the abutment to fit the prosthesis surrounding the tooth surface and surrounding the gum tissue By doing so, it can be made of a shaded ceramic material.

The ceramic material is a high strength ceramic material, preferably zirconia, alumina and mixtures thereof, whereby the flexural strength is greater than about 1000 MPa, more preferably greater than about 1500 MPa, and most preferably greater than about 2000 MPa. Some applicable materials are yttria or ceria stable square zirconia (Y-TZP and Ce-TZP) zirconia reinforced alumina (ZTA), alumina reinforced zirconia (ATZ), mixtures thereof, composites and functional They are well known in the prior art as their stepwise composites. The flexural strength of these materials is customarily above 1000 MPa, better ones are further above 1500 MPa and most preferably even above 2000 MPa. Materials useful herein, ZirCAD ^TM (TM) block ^(ZirCAD TM blocks from Ivoclar Vivadent) of Ibokuraru Bibadento Tips - Ell nanoZir ^TM (TM) zirconia ^{(nanoZir TM zirconia from Hint-ELs} ) and Metokishito Inc. Ziraldent ^TM (TM) material ^(Ziraldent TM ^material from Metoxit AG) include but are not limited thereto.

  In addition to an abutment that is anatomically shaded as described above to simulate a natural dentition and further adapt to the surrounding dentition and gum tissue in the patient's oral cavity, Can also be anatomically shaped to match the shape of the surrounding dentition, gum tissue and prosthesis located in Most preferably, the abutment 200 has a shape that approximates the net tooth shape of the prosthesis, and the shade is a natural dentition so that it is attached and the color and translucent distribution features simulate the natural dentition. It is shaded anatomically to fit. Anatomically shaded multicolor abutment mimics the natural tooth color and translucent distribution, so that the crown placed on the abutment has a little or little appearance It is necessary to imitate porcelain into a replaced tooth. The abutment near net shape and shade eliminates the need to use a thick crown over the abutment and improves the overall strength and structural integrity of the implant system without aesthetic compromises. Since higher strength is provided by the abutment, less strength is needed in the crown or veneering layer (porcer or composite) located on the abutment. The aesthetic contribution of the veneering layer is at least more consistent and predictable when it is more important. As the abutment gets closer to the net shape and becomes more naturally shaded, it eliminates the need for an upper restoration and becomes the restoration itself. In addition to the aforementioned materials, as disclosed in commonly owned U.S. Patent Application Publication No. 20070042889, the net-shaped abutment has a flexural strength exceeding 600 MPa. It can be made of lithium disilicate and is hereby fully incorporated by reference.

  In selecting the correct shade for the abutment, the color components, colors, saturation and values are evaluated. Hue is the color dimension that allows us to distinguish one family of colors from the other, and saturation defines the relative intensity of a particular color, ie, a stronger color is its color. The degree will be at a higher level, and the value will describe the relative whiteness, or the blackness of a particular color, ie the lighter color will describe the higher value. In addition to these components, features such as opacity, fluorescence and translucency can also be considered during the determination of the correct shade for the abutment.

A complete dental restoration must be adapted to the color of the patient's teeth, i.e. it must be a "colored tooth". The color of human teeth is light, almost white-tan to light brown, and appears to occupy a very specific color space. This color space can be described by the L ^* , a ^* , b ^* rules commonly used in the commonly used CIE (Commission Internationale de l'Eclairage) Represents the color of the Cartesian coordinate system. L ^* or “value” is some degree of brightness or brightness and is represented on the vertical axis (black is 0 and white is 100). The a ^* and b ^* coordinates are one index of chromaticity, plus a ^* is red, minus a ^* is green, plus b ^* is yellow and minus b ^* is blue. Expressed as horizontal coordinates. U.S. Pat. No. 6,030,209, which is hereby incorporated by reference, shows that the tooth color CIE L ^* , a ^* , b ^* color coordinates indicate Vita Zahnfabrik (i.e. the color space of the tooth color). Vita Lumen (R) shade guide system manufactured by In the present specification, “tooth color” has the meaning that CIE, L ^* , a ^* , b ^* color coordinates are within the range of this color space or are in close proximity.

In the fabrication of the abutment herein, the range of L ^* a ^* b ^* values is listed in Table 1 below, along with the amount of opacity selected.

  The value changes in the abutment depending on the shaded area. Table 2 lists the range of gums, cervix, center (adapted to dentin) and incisal area.

  Single unit abutments are an easy and effective way to provide a prosthesis that looks natural. The abutment gum color base can camouflage the coronal part, highlighting the surrounding gum tissue and the natural appearance of the prosthesis.

  Sufficient alveolar bone must first be present in the absence of teeth in order to properly treat patients with dental implants. After secure placement of the dental implant in the patient's jawbone, an appropriate abutment type is selected that provides support for the final restoration. Where the final restoration being considered is a full ceramic restoration, the choice of an implant abutment according to the invention, which is shaded like a natural tooth, is shaded through the ceramic prosthesis, and the ceramic restoration Suggested in contrast to metallic abutments that will affect the color of the skin. The impression and shade are sent to the lab for final restoration production using one of the well known shade guide systems. The abutment color will match the color chosen for the restoration. The final restoration is then fitted and permanently attached in the patient's mouth.

  It is relevant that the preferred embodiment is represented and that various modifications, additions, substitutions, etc. may be made without departing from the spirit of the invention despite the detailed description herein. It will be clear to the person skilled in the art and therefore they are considered to be within the scope of the invention as set forth in the claims that follow.

Claims (17)

Implants,
An abutment secured to the implant;
And a dental prosthesis disposed on the abutment,
A single unit structure comprises the abutment having a base end for mounting on an implant and a coronal end for supporting a dental prosthesis,
The single unit structure is made of ceramic material;
The dental implant repair system, wherein the single unit structure is multicolored to match the color of the dental prosthesis, the surrounding dentition and the surrounding gum tissue throughout.   The dental abutment repair system according to claim 1, wherein the abutment is attached to the implant either externally by screws or internally by a hole included in the abutment.   The dental implant repair system of claim 1, wherein the implant comprises the abutment comprising a male connection component and a female connection component connected to each other.   The dental implant repair system of claim 1, wherein the implant comprises the abutment comprising a female connection component and a male connection component connected to each other.   The dental implant repair system of claim 1, wherein the base end is a gum color, the coronal end is a cut edge color, and a region between the base and the coronal end is a dentin color.   The dental implant repair system according to claim 1, wherein the ceramic material comprises zirconia, alumina, and a mixture thereof, and the ceramic material has a bending strength exceeding 1000 MPa.   The dental implant repair system of claim 6, wherein the ceramic material includes a flexural strength of greater than 1500 MPa.   The dental implant repair system according to claim 6, wherein the ceramic material includes a bending strength exceeding 2000 MPa.   The abutment is a ready abutment, the unitary structure comprises a base and a crown, the base comprising a core and an outer layer of material covering the core; The dental implant repair system of claim 1, wherein the core is a dentin color and the outer layer is a gum color.   The dental implant repair system of claim 9, wherein the outer layer of material has a thickness in the range of about 0.25 to about 1.00 mm.   The dental implant repair system according to claim 9, wherein the abutment includes a cervical line, and the upper portion of the base portion and the lower portion of the coronal portion meet at the cervical line of the abutment.   The dental implant repair system of claim 11, comprising changing a position of the neckline after the abutment is prepared for placement on an implant.   13. Implant repair according to claim 12, wherein the abutment comprises being prepared using hand-held instruments and procedures, partially automated instruments and procedures, or fully automated instruments and procedures. system.   The dental implant repair system according to claim 1, wherein the dental prosthesis comprises a dental ceramic, porcelain, composite, or hybrid material.   Said dental ceramic, porcelain, composite or hybrid material is manufactured using hand-held instruments and procedures, partially automated instruments and procedures, or fully automated instruments and procedures 15. The dental implant repair system according to claim 14, comprising:   16. Dental implant repair according to claim 15, wherein the partially or fully automated instrument and procedure comprises CAD / CAM, rapid prototyping, plasma or flame deposition, electroforming, spraying or dipping. system.   The dental implant of claim 1, wherein the dental prosthesis is disposed on the abutment by pressing or layering a material that directly appears on the abutment. Repair system.