The present invention relates generally to an abutment system for a dental implant system. More particularly, the present invention relates to a gingival healing abutment system having scanning features and provisionalization features.
The dental restoration of a partially or wholly edentulous patient with artificial dentition is typically done in two stages. In the first stage, an incision is made through the gingiva to expose the underlying bone. An artificial tooth root, in the form of a dental implant, is placed in the jawbone for osseointegration. The dental implant generally includes a threaded bore to receive a retaining screw for holding mating components thereon. During the first stage, the gum tissue overlying the implant is sutured and heals as the osseointegration process continues.
Once the osseointegration process is complete, the second stage is initiated. Here, the gingival tissue is re-opened to expose an end of the dental implant. A healing component or healing abutment is fastened to the exposed end of the dental implant to allow the gingival tissue to heal therearound. It should be noted that the healing abutment can be placed on the dental implant immediately after the implant has been installed and before osseointegration. In recent years, for some situations, the osseointegration step and gingival healing steps have been combined into a one-step process. Alternatively, instead of a healing abutment, a temporary abutment may be used to support a temporary prosthesis and also serves the purpose of shaping the gingiva above the dental implant, just like a healing abutment.
In more recent years, scanning technologies have been used to aid in the development of permanent prostheses. The scanning technologies are used to locate the underlying dental implant to which the final prosthesis is supported, as well as the adjacent soft tissue, the adjacent dentition, and the opposing dentition. The present disclosure is directed at gingival healing abutment systems (including temporary abutment systems), components, and methods that can be used in conjunction with scanning technologies.
In one aspect, the present invention includes a healing abutment assembly for attachment to a dental implant having a threaded bore. The healing abutment assembly includes a base, a polymeric abutment cap, and a screw. The base has a lower region and an upper region. The lower region includes an anti-rotational feature for non-rotationally mating with the dental implant. The upper region includes a first anti-rotational structure and at least one retention groove. The base has a though-bore extending through the lower and upper regions. The polymeric abutment cap is coupled to the upper region of the base. The polymeric abutment cap has at least one projection configured to mate with the at least one retention groove of the base. The polymeric abutment cap has a second anti-rotational structure to mate with the first anti-rotational structure of the base. A top surface of the polymeric abutment cap includes one or more information markers providing information concerning the polymeric abutment cap and the underlying dental implant. The screw extends through the through-bore of the base and engages the threaded bore of the dental implant. The screw holds the base on the dental implant.
In a further aspect, the present invention is a healing abutment kit for use with a dental implant having a threaded bore. The kit includes a base, a plurality of polymeric abutment caps, and a screw. The base includes a lower region and an upper region. The lower region includes an anti-rotational feature for non-rotationally mating with one of the dental implants. The upper region includes a first anti-rotational structure and a first axial-retention structure. Each of the plurality of polymeric abutment caps has a second anti-rotational structure being configured to mate with the first anti-rotational structure of the base. Each of the plurality of polymeric abutment caps has a second axial-retention structure for mating with the first axial-retention structure of the base. Each of the polymeric abutment caps has different geometric dimensions. Each of the polymeric abutment caps has an upper surface that includes a unique code that indicates (i) the geometric dimensions of the polymeric abutment cap and/or (ii) information concerning the underlying dental implant. The screw is for extending through the through-bore of the base and engaging the threaded bore of the dental implant so as to hold the base on the dental implant.
In yet another aspect, an abutment system is for attachment to a dental implant having a threaded bore and for engaging and/or shaping the surrounding gingival tissue. The abutment system includes a base and a polymeric abutment cap. The base includes a lower region and an upper region. The lower region includes an anti-rotational feature for non-rotationally mating with one of the dental implants. The upper region includes a first anti-rotational structure and a first axial retention structure. The polymeric abutment cap has a second anti-rotational structure for mating with the first anti-rotational structure and a second axial retention structure for mating with the first axial retention structure. The abutment cap has an upper surface that includes information markers. The information markers provide information concerning the abutment cap and the underlying dental implant.
In a further aspect, the present invention is a method of using a healing abutment kit with a dental implant having a threaded bore. The kit including a base and a plurality of polymeric abutment caps. Each of the polymeric abutment caps has different geometric dimensions. The method includes mating the base onto the dental implant, and selecting one of the plurality of polymeric abutment caps for mating with the base. The method further includes attaching the selected polymeric abutment cap with the base, and permitting gingival tissue to heal around the combination of the base and the selected polymeric cap. The method also includes scanning the upper surface polymeric abutment cap to identify a unique code that indicates the geometric dimensions of the polymeric abutment cap and information concerning the underlying dental implant.
The above summary is not intended to represent each embodiment or every aspect of the present disclosure. Rather, the summary merely provides an exemplification of some of the novel features presented herein. The above features and advantages, and other features and advantages of the present disclosure, will be readily apparent from the following detailed description of exemplary embodiments and best modes for carrying out the present invention when taken in connection with the accompanying drawings and the appended claims.
The foregoing and other advantages of the invention will become apparent upon reading the following detailed description and upon reference to the drawings.
While the present disclosure is susceptible to various modifications and alternative forms, specific embodiments have been shown by way of example in the drawings and will be described in detail herein. It should be understood, however, that the present disclosure is not intended to be limited to the particular forms disclosed. Rather, the present disclosure is to cover all modifications, equivalents, and alternatives falling within the spirit and scope of the present disclosure as defined by the appended claims.
Referring to
The base 22 also includes an anti-rotational feature 31 for non-rotationally holding the abutment cap 24 on the base 22. As shown, the anti-rotational feature 31 is a flat surface that mates of the corresponding flat surface (not shown) on the interior region of the abutment cap 24. One or more flat surfaces may be used for the anti-rotational feature 31 on the base 22 (e.g., the upper portion of the base 22 may include a polygonal shape, such as those shown in
The base 22 is typically made of metal, although it could be made of a polymeric material. The abutment cap 24 is preferably made of a polymeric material, such as polyether ether ketone (PEEK). The screw 26 is also preferably made of a metal.
In
In addition to providing information (e.g., dimensions, tapering angles, and shapes) about the healing abutment assemblies 21a, 21b, 21c, and 21d, the information markers 41-44 can also provide information regarding the underlying implant 120. For example, because the height dimension of the base 22 is known, and the height of the healing abutment cap 24 is known, the location of the table (the uppermost surface) of the implant 120 is also known in the z-direction (the direction of the central axis of the implant 120) and in the x-y direction. Additionally, the orientation of the anti-rotation feature 12 of the implant 120 can be aligned with one or more of the information markers 41, 42, 43, 44, or the orientation markers 32, 34. As an example, if the anti-rotation feature 12 is a hexagonal socket, the orientation marker 32 can be aligned with one of the six surfaces of the hexagonal socket. Or, an information marker location can be aligned with one of the six surfaces of the hexagonal socket. Alternatively, an arrow marker or diamond marker can be added to the upper surface to identify one of the flat surfaces of the anti-rotation feature 12. In summary, because the location of the anti-rotational feature 31 of the base 22 is at a known angular position relative to the anti-rotational feature 12 of the implant 120, a marker on the upper surface of the healing abutment cap 24 can also be used to locate one or more features of the implant 120. Additional information that can be identified by the information markers 41-44 is discussed below with respect to
Other types of coded systems could be used instead of the binary-coded type of system that is discussed with reference to
Alternatively, a first specified region on the healing cap 24 could include a code (e.g., a size of certain symbol, or a number of certain symbols) for identifying the healing cap's height. A second specified region on the healing cap 24 could include a different code (e.g., a size of certain symbol, or a number of certain second symbols) for identifying the healing cap's diameter. A third specified region on the healing cap 24 could include another code (e.g., a size of certain symbol, or a number of certain third symbols) for identifying the healing cap's taper. In addition to the unique codes being defined by symbols, the codes for defining the dimensions of the healing cap 24 can be presented in the form of alpha-numeric characters or different colors (or combinations thereof) that define one or more dimensions of the healing cap. Because the resolution and the photo-realistic data capture of the current intra-oral scanning systems and method has improved, these colors and alpha-numeric characters can be readily identified, such that the identification of healing cap 24 can be achieved. Accordingly, intra-oral scanning of the healing cap 24 may capture scan data corresponding to a unique combination of alpha-numeric character(s) and color(s) from the healing cap that serves as a code (or part of a code) for identifying the particular healing cap 24.
Further, because the data acquisition capabilities of current intra-oral scanning systems and methods has improved, the upper surface of the healing cap 24 can be scanned and shape-matched to help identify the healing cap due to its diametric dimension. In other words, the actual diametric size of the healing cap 24 serves as part of the information that is used to identify the healing cap 24. The location of any information marker on the upper surface relative to the scanned circumference of the upper surface provides an informational combination that can be matched against library of healing caps to identify the specific healing cap 24 that has been scanned. In that situation, the circumference of the healing cap 24 can be thought of as providing a diameter, whereas the marker(s) may provide the information for the height of the healing cap 24 and the location of the underlying implant's anti-rotation feature. The markers (e.g., a “Δ” symbol or a “o” symbol) can have the same size on all diametric sizes of the healing caps 24, such that the relative dimensions of the information marker to each healing cap's diameter is different, which assists with the shape-matching algorithm. Alternatively, the shape matching can rely on less than the entire upper surface, such as when the gingiva begins to grow slightly over the healing cap 24. The shape-matching algorithm may rely on a partial geometric match of the upper surface captured by the scan, wherein the partial geometry includes one or more markers and symbols on the upper surface, part of the upper surface itself, and perhaps other features, such as an exposed screw head (See
Because the gingival tissue will contact and surround the healing abutment assemblies 21a, 21b, 21c, and 21d, identifying which type of healing abutment cap 24 (and, thus, the healing abutment assembly 21) is mated to the implant 120 by inspection of the upper surface is important, especially when intraoral scanning is used. In this methodology, after the dental implant 120 has been installed, a clinician may select a healing abutment cap 24 that is best suited for the conditions in the patient's mouth. The base 22 can be attached to the implant 120 through the use of the screw 26. The selected healing abutment cap 24 can then be snapped onto the base 22 by the retaining action of the projection 28 on the base 22 and the groove 29 on the healing abutment cap 24. The clinician will likely choose the selected healing abutment cap 24 from a variety of possible healing abutment caps 24 that could have been placed on the base 22. But, the identification of the selected healing abutment cap 24 is readily known by simply reviewing the code defined by the information markers 41, 42, 43, 44 on the upper surface of the selected healing abutment cap 24. Using an intraoral scanner to identify the conditions in the patient's mouth after the gingival tissue has healed becomes very easy by use of the information markers 41, 42, 43, 44 and the orientation markers 32, 34 because the output of the intraoral scanner can be displayed on a common display used in conjunction with a computer terminal. Additionally, some of the vertical cylindrical surface of the healing abutment cap 24 below the upper surface can also be received as scan data to help locate the healing abutment assembly 21 and the underlying dental implant. Accordingly, a patient-specific custom abutment can be developed because geometric information regarding the healing abutment assembly 21 is known, as well as the location of the implant 120 and the angular orientation of the implant's anti-rotational feature 12. The scanning may take place before, during, or after the gingival-healing period.
It should be noted that the kit 100 may not include the dental implant 120, but would be used with a specific type of dental implant. For example, the kit 100 may include a base 122, four healing abutment caps 124a, 124b, 124c, 124d, and a screw 126 that is to be used on a Biomet 3i Certain® 5.0 mm implant system. And the codes provided by the information markers may indicate that the base 122 and the four healing abutment caps 124a, 124b, 124c, 124d are to be used with that specific Biomet 3i implant system. On the other hand, a different kit may include a differently designed base for mating with a different manufacturer's implant system, and the information markers are used to indicate that particular manufacturer's implant system. In other words, the present invention contemplates a plurality of different types of kits, and each type of kit is to be used on a specific type of implant system such that it includes a different base so as to mate with that specific implant. And, in addition to the codes being used to identify information concerning the healing abutment system and the underlying dental implant, the codes would also be used to identify the specific type of underlying implant that is being used. Hence, by scanning the upper surface of the healing cap, the information concerning (i) the healing abutment system, (ii) the location of the dental implant and its structural features, and (iii) the identity of the specific underlying implant (and its manufacturer) would be known.
In summary, the present invention contemplates a plurality of different kits in that different kits are used with different dental implant systems of a single manufacturer (e.g., different style of implant-abutment connection, different sizes of implant, etc.). And, the present invention contemplates a plurality of different kits in that the different kits are used for various dental implant systems from multiple manufacturers. In any event, the coding system on top of the healing abutment can be used to identify the specific type of underlying dental implant.
Thus far, the present invention has been described in terms of a healing abutment that includes the polymeric cap portion containing the information markers.
Referring now to
The temporary abutment 710 has a subgingival region 720 and a supragingival region 730, which are separated by a flange 750. An outer surface 755 of the flange 750 is positioned to engage and aid in forming a patient's gingival tissue during the healing process. The subgingival region 720 includes an anti-rotational feature 722 (e.g., a hexagonal section) for mating with a corresponding anti-rotational feature of an implant (e.g., implant 120 in
The supragingival region 730 includes one or more retention grooves or structures 732 and an anti-rotational structure 734 (e.g., a flat wall or surface). The retention grooves 732 are configured to mate in a snap-type axial holding engagement with corresponding male circumferential features or structures 786 of a temporary abutment cap 780. The one or more retention grooves 732 are configured to mate with the male circumferential features 786 with a retention force between about one and about ten pounds of force. That is, it takes between about one and about ten pounds of force to remove the temporary abutment cap 780 from its snap-fit type engagement with the temporary abutment 710. Alternatively, the supragingival region 730 of the temporary abutment 710 can include male circumferential features that are configured to mate in a snap-type axial holding engagement with corresponding retention grooves on an inside surface of the temporary abutment cap 780.
The anti-rotational structure 734 is configured to mate in a slidable engagement with a corresponding anti-rotational structure 784 to prevent relative rotation of the temporary abutment cap 780 and the temporary abutment 710. In the illustrated implementation, the anti-rotational structure 734 is shown as a polygonal structure that generally extends from a top surface 760 of the temporary abutment 710 toward the flange 750. The anti-rotational structure 734 can be one of a variety of known anti-rotational structures, such as, for example, one or more flat walls, grooves, slots, projections, or any combination thereof. Examples of anti-rotational structures for dental posts are shown in U.S. Pat. Nos. 6,120,293, 6,159,010, and 8,002,547, each of which is commonly owned by the assignee of the present application and is hereby incorporated by reference herein in its entirety. Regardless of the type of anti-rotational structure 734 chosen for the supragingival region 730 of the temporary abutment 710, the temporary abutment cap 780 has a correspondingly shaped structural surface (e.g., anti-rotational structure 784) for engaging the anti-rotational structure 734 so as to prevent relative rotation between the two components. The temporary abutment 710 is generally cylindrical in shape with an internal bore 740 for receiving a screw 770 to removably couple the temporary abutment 710 to the implant 120.
The top surface of the temporary abutment cap 780 includes four information marker locations 762. The information marker locations 762 are positioned circumferentially around the top surface of the temporary abutment cap 780 at 3 o'clock, 6 o'clock, 9 o'clock, 12 o'clock. Each of the information marker locations 762 is configured to include one or more information markers 764. The information marker 764 is shown as one notch. However, the present disclosure contemplates that the information markers 764 can be positive information markers, negative information markers, raised projections/pimples, recesses or dimples, notches, lines, etching, alphanumeric characters, etc. It is further contemplated that the cross-section of the information markers 764 can be rectangular, triangular, or various other shapes. Further, the information marker locations 762 themselves can act as information markers and provide and/or indicate information.
The information markers 764 are indicative of one or more characteristics of the temporary abutment 710, the temporary abutment cap 780, and/or of the underlying implant 120 to which the temporary abutment 710 and temporary cap 780 are attached. For example, one or more of the information markers 764 can be geometrically aligned with a flat of the non-rotational feature 722 of the temporary abutment 710 and/or a flat on the underlying implant to indicate the rotational orientation of the non-rotational features of the temporary abutment 710 and/or of the underlying implant. It is also contemplated that one or more of the information markers 764 may correspond to the height of the temporary abutment 10 and, hence, a height or vertical position (i.e., z-axis location) of a table or seating surface of the underlying implant. For another example, the information markers 764 can be indicative of the x-y location of the table or seating surface of the underlying implant. For another example, the information markers 764 can be indicative of the angle that the underlying implant rests with respect to vertical within the patient's jawbone (e.g., pitch and yaw). For another example, the information markers 764 can be indicative of the size and/or shape of the temporary abutment 710 and/or the underlying implant. For another example, the information markers 764 can be indicative of the manufacturer of the underlying implant.
The information markers 764 can be part of a binary marking system that identifies unique characteristics of the temporary abutment 710 and/or the underlying implant 120. As is well known, a binary-coded system exists as an array of digits, where the digits are either “1” or “0” that represent two states, respectively, ON and OFF. For each information marking location 762, the presence of an information marker 64 (“ON”) is a 1 and the absence of an information marker 764 (“OFF”) is a 0. By grouping sets of 1's and 0's together starting from a known starting location (e.g., 3 o'clock or the first location in the clockwise direction from the anti-rotational structure 34), information about each temporary abutment 710 is known. For the temporary abutment 710, the four information marker locations 762 can provide sixteen (16) different combinations. Additional details on information markers and the characteristics of the underlying implant and/or the abutment that are identified by the information markers (e.g., information markers 764) can be found in U.S. Pat. No. 7,988,449, which is hereby incorporated by reference herein in its entirety.
The prosthesis assembly includes the temporary abutment 710 and the temporary abutment cap 780 coupled to a temporary prosthesis 790 (e.g., a temporary tooth). The implant 120 is installed in the jawbone (not shown) of a patient, and then the temporary abutment 710 is non-rotationally attached to the implant 120 via the non-rotational feature 722 and the screw 770. The temporary abutment 710 is attached to the implant 120 such that a bottom portion of the flange 750 of the temporary abutment 710 abuts and/or rests upon a table or seating surface of the dental implant 120. The temporary abutment cap 780 is snap-fitted onto the temporary abutment 710 and then the temporary prosthesis 790 is coupled to the temporary abutment cap 780.
The outer surface 781 of the temporary abutment cap 780 is configured to mate with and/or to be bonded with the temporary prosthesis 790. It is contemplated that the temporary prosthesis 790 is coupled to the temporary abutment cap 780 using cement (e.g., dental cement), glue, bonding agent, a press-fit engagement, a snap or click-type engagement, a screw or bolt, or a combination thereof. It is further contemplated that the temporary prosthesis 790 is removably or permanently coupled to the temporary abutment cap 780 such that the temporary prosthesis 790 and the temporary abutment cap 780 can be removed separately or in unison from the temporary abutment 710. Removal of the temporary prosthesis 790 from the temporary abutment cap 780 exposes the information markers 764, which can be scanned directly or indirectly (e.g., from an impression and/or stone/plaster model) to generate scan data that is at least used to determine the location and orientation of the implant 120, which, as explained herein, is used when developing a permanent patient-specific abutment and/or prosthesis.
The outer surface of the temporary prosthesis 790 and/or the outer surface 755 of the flange 750 are configured to be suitable for replicating the gingival emergence profile formed by a natural tooth (e.g., in a non-round shape). As such, after the temporary prosthesis 790 is installed, the patient's gingiva is permitted to heal around the temporary prosthesis 790 and/or the temporary abutment 710. Such a prosthesis assembly results in a gingival emergence profile approximating that of what would be around a natural tooth and/or that of what a clinician determined to be most appropriate for the given implant installation site (e.g., an ovular shape). In other words, the prosthesis assembly also acts as a gingival healing abutment. This is advantageous because, after the patient's mouth has an opportunity to heal and is ready to be processed (e.g., intra-oral direct scanning, impression scanning, or scanning of a model formed from the impression) for creating a permanent patient-specific abutment and prosthesis, the temporary prosthesis 790 and the temporary abutment cap 780 are removed to reveal the temporary abutment 710 and the resulting emergence profile of the adjacent gingiva. Because the resulting emergence profile approximates that of a natural tooth, the permanent patient-specific abutment and prosthesis can be accurately created from the scan data and/or from known data associated with the temporary abutment 10 (e.g., the known contours of the outer surface 55 of the flange 50 of the temporary abutment 10). For example, the permanent patient-specific abutment and prosthesis can be created and attached to the underlying implant 120 such that the permanent patient-specific abutment and prosthesis (not shown) are highly aesthetic and fit closely within the gingiva emergence profile adjacent to the implant 120 that was formed by the prosthesis assembly 100.
It is further contemplated that a kit or package of temporary abutment caps 780, where each temporary abutment cap 780 includes an outer surface with an anatomically shaped tooth (not shown), can be supplied and/or packaged together for use by, for example, clinicians. In such alternatives, the clinician is supplied with a variety of temporary abutment caps including different anatomically shaped teeth that can be attached to the temporary abutment 710 as described herein and used directly as temporary prostheses without further modification or attachment of additional components. In each of these alternatives, the temporary abutment 10 is still useful for scanning The information markers 764 can be placed on a lateral side of the abutment cap 780 such that they are not visible (e.g., lingual side). Again, the information markers 764 can be provided in a binary arrangement to provide information regarding the cap 780, the abutment 710, and/or implant.
Referring to
Referring to
Additionally, the temporary abutment cap 880 includes an aperture 883 that provides a path for the screw 870 to mate with the implant 120 through the internal bore 840 of the temporary abutment 810, thereby securing the temporary abutment cap 880 and the temporary abutment 810 onto the implant 120 in a non-rotational fashion, as best shown in
Referring to
Optionally, a temporary prosthesis 890 is coupled to the temporary abutment cap 880. In such an alternative implementation, the information marker locations 862 and/or the information markers 864 can also mate with correspondingly shaped internal surfaces (not shown) of the temporary prosthesis 890 to provide for anti-rotation between the temporary abutment cap 880 and the temporary prosthesis 890. In the case that the temporary prosthesis 890 is not coupled to the temporary abutment cap 880, the temporary abutment cap 880 itself can have an anatomically shaped tooth structure and act as a temporary prosthesis. In that case, the gingiva engages the temporary abutment cap 880 and the temporary abutment 810 to define an emergence profile, such that the combination of these components acts as a healing abutment (as noted above) in addition to serving other functions.
The various methods of creating the permanent patient-specific abutment from the systems of
While the illustrated embodiments have been primarily described with reference to the development of a patient-specific abutment for a single tooth application, it should be understood that the present invention is also useful in multiple-tooth applications, such as bridges and bars for supporting full or partial dentures. In those situations, the patient-specific abutment would not necessarily need a non-rotational feature for engaging the underlying implant(s) because the final prosthesis would also be supported by another structure in the mouth (e.g., one or more additional underlying implants), which would inherently achieve a non-rotational aspect to the design. In any event, using a scanning process to obtain the necessary information about the emergence profile shape of the gingiva and the dimensional and/or positional information for the implant(s) (via information markers in the temporary prosthetic assembly) can lead to the development of an aesthetically pleasing multiple-tooth system.
While the present invention has been described with reference to one or more particular embodiments, those skilled in the art will recognize that many changes may be made thereto without departing from the spirit and scope of the present invention. Each of these embodiments and obvious variations thereof is contemplated as falling within the spirit and scope of the present invention, which is set forth in the claims that follow.
This application is a continuation-in-part of co-pending U.S. Ser. No. 13/473,202, filed on May 16, 2012, entitled “Temporary Abutment with Combination of Scanning Features and Provisionalization Features,” which is hereby incorporated by reference in its entirety.
Number | Date | Country | |
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61486630 | May 2011 | US |
Number | Date | Country | |
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Parent | 13473202 | May 2012 | US |
Child | 13798894 | US |