Full-Mouth Rehabilitation of a Patient with Sjogren’s Syndrome with Maxillary Titanium-Zirconia and Mandibular Monolithic Zirconia Implant Prostheses Fabricated with CAD/CAM Technology: A Clinical Report

Dental implants have become a well-established treatment modality for the management of complete and partial edentulism. Recent advancements in dental implant systems and CAD/CAM technologies have revolutionized prosthodontic practice by allowing for the predictable, efficient, and faster management of complex dental scenarios. This clinical report describes the interdisciplinary management of a patient with Sjogren’s syndrome and terminal dentition. The patient was rehabilitated using dental implants and zirconia-based prostheses in the maxillary and mandibular arches. These prostheses were fabricated using a combination of CAD/CAM and analog techniques. The successful outcomes for the patient demonstrate the importance of appropriate use of biomaterials and the implementation of interdisciplinary collaboration in treating complex dental cases.


Introduction
Terminal dentition refers to a moment when the dentition is compromised to the point that its predictable restoration is no longer viable; this stage is usually reached after years of periodontal disease or as a result of unfavorable social or pharmacological conditions [1] or, in some situations, autoimmune diseases. Sjogren's syndrome is an autoimmune condition characterized by lymphocyte infiltration and progressive destruction of the exocrine glands. One characteristic of the disease is a reduction in the production of tears and saliva, which has a negative effect on overall oral health and patient well-being and worsens over time. Dry mouth is the key diagnostic sign for this disease and can lead to a wide range of problems, including oral infections, progressive tooth decay, and periodontal breakdown [2]. When patients reach the terminal dentition stage, the restorative dentist faces the challenging task of devising a treatment that meets the patient's esthetic and functional expectations. Traditionally, patients with several non-restorable abutment teeth had no choice but to use complete dentures, which, despite their long history of service,

Materials and Methods
A 69-year-old male patient presented to the Advanced Prosthodontics Dental Clinics at the Ohio State University seeking comprehensive dental care. At the time of the initial examination, the patient stated that he had medically controlled hypertension and Sjogren's syndrome managed with salivary substitutes (Biotene Dry Mouth; GlaxoSmithKline Group, Durham, NC, USA). The extraoral examination revealed anterior metal-ceramic restorations, a positive smile line, and multiple missing anterior teeth (Figure 1). contemporary restorative materials available. The present clinical report presents th comprehensive rehabilitation of a patient with Sjogren's syndrome and terminal dentitio using a maxillary titanium-zirconia complete arch prosthesis and a complete-arch man dibular monolithic zirconia prosthesis fabricated using a combination of analog tech niques and CAD/CAM technologies.

Materials and Methods
A 69-year-old male patient presented to the Advanced Prosthodontics Dental Clinic at the Ohio State University seeking comprehensive dental care. At the time of the initial ex amination, the patient stated that he had medically controlled hypertension and Sjogren's syn drome managed with salivary substitutes (Biotene Dry Mouth; GlaxoSmithKline Group Durham, NC, USA). The extraoral examination revealed anterior metal-ceramic restora tions, a positive smile line, and multiple missing anterior teeth (Figure 1). Intraorally, all the remaining teeth except for the mandibular incisors had complete coverage extracoronal restorations, the majority with secondary decay. A sinus tract wa noticed on the buccal mucosa of tooth number 4.1, and tooth number 1.1 presented a hor izontal fracture above the gingival margin ( Figure 2). Additionally, clinical features typ cal of Sjogren's syndrome, including minimal salivary flow and generalized bleeding o probing, were also noted during the examination.
The clinical findings were corroborated radiographically since multiple radiolucen lesions were noticed on the margins of the restorations, thus confirming the compromise state of the dentition. Additionally, a radiopaque mass was noticed on the anterior of th right mandibular angle ( Figure 3).
After asking the patient, he explained that it was an osseous exostosis of benig origin that was frequently monitored by his primary care physician. Maxillary and man dibular preliminary impressions were taken with irreversible hydrocolloid (Geltrate Dentsply Sirona North America, York, PA, USA) and were used to fabricate maxillary an mandibular diagnostic casts with type III dental stone (Buff Stone; Whip Mix Corp., Lou isville, KY, USA). Additionally, a diagnostic cone-beam computerized tomograph (CBCT) was taken at the end of the appointment. Intraorally, all the remaining teeth except for the mandibular incisors had completecoverage extracoronal restorations, the majority with secondary decay. A sinus tract was noticed on the buccal mucosa of tooth number 4.1, and tooth number 1.1 presented a horizontal fracture above the gingival margin ( Figure 2). Additionally, clinical features typical of Sjogren's syndrome, including minimal salivary flow and generalized bleeding on probing, were also noted during the examination.  The clinical findings were corroborated radiographically since multiple radiolucent lesions were noticed on the margins of the restorations, thus confirming the compromised state of the dentition. Additionally, a radiopaque mass was noticed on the anterior of the right mandibular angle (Figure 3). Figure 2. Frontal intraoral photograph taken at the initial appointment. After evaluating the information gathered during the clinical examination, multipl treatment options involving removable and fixed dental prostheses were presented to th patient. Once the treatment options were reviewed, the patient stated that he preferre not to undergo extensive restorative procedures to keep his teeth. He explained that fixe partial dentures never restored his smile nor his masticatory function since they deve oped decay and failed within a few months post-delivery. Removable partial denture were not considered since the patient had had issues related to difficult maintenance, poo function, and discomfort with these prostheses in the past. After evaluating these factor and analyzing the patient's expectations, complete-arch implant-supported prosthese were considered a feasible, definitive treatment capable of improving the patient's overa quality of life in addition to restoring esthetics and function. The advantages and limita tions of complete arch dental prostheses supported by dental implants were discussed After the treatment duration (including the number of appointments), finances, an After asking the patient, he explained that it was an osseous exostosis of benign origin that was frequently monitored by his primary care physician. Maxillary and mandibular preliminary impressions were taken with irreversible hydrocolloid (Geltrate; Dentsply Sirona North America, York, PA, USA) and were used to fabricate maxillary and mandibular diagnostic casts with type III dental stone (Buff Stone; Whip Mix Corp., Louisville, KY, USA). Additionally, a diagnostic cone-beam computerized tomography (CBCT) was taken at the end of the appointment.
After evaluating the information gathered during the clinical examination, multiple treatment options involving removable and fixed dental prostheses were presented to the patient. Once the treatment options were reviewed, the patient stated that he preferred not to undergo extensive restorative procedures to keep his teeth. He explained that fixed partial dentures never restored his smile nor his masticatory function since they developed decay and failed within a few months post-delivery. Removable partial dentures were not considered since the patient had had issues related to difficult maintenance, poor function, and discomfort with these prostheses in the past. After evaluating these factors and analyzing the patient's expectations, complete-arch implant-supported prostheses were considered a feasible, definitive treatment capable of improving the patient's overall quality of life in addition to restoring esthetics and function. The advantages and limitations of complete arch dental prostheses supported by dental implants were discussed. After the treatment duration (including the number of appointments), finances, and expectations were discussed, the patient decided to proceed with a treatment plan consisting of 4 maxillary and 4 mandibular implants with complete-arch Zirconia-based prostheses.
Maxillary and mandibular diagnostic teeth arrangements were fabricated with denture teeth (Blue-Line; Ivoclar Vivadent Schaan, Liechtenstein, Switzerland) and visible-light cure (VLC) denture bases (Triad VLC Denture Base Material; Dentsply Sirona North America, York, PA, USA) to establish the desired incisal edge position and future occlusal plane ( Figure 4A). Additionally, the distance from the incisal edges to the lower border of the upper lip during a maximum smile was recorded and inscribed on the diagnostic casts to plan the position of the maxillary implants so that they would be 4 mm above the upper lip during function and smiling to ensure the concealment of the future prosthesis-tissue junction [33,34]. Subsequently, the diagnostic casts and diagnostic artificial teeth arrangements were scanned using a benchtop 3D scanner (E3 Scanner; 3Shape A/S, Copenhagen, Denmark) and were merged with the patient's CBCT data in an implant planning computer program (BlueSky Plan V4; Blue Sky Bio, Libertyville, IL, USA) ( Figure 4B). The placement of four standard-diameter dental implants (Tapered Screw Vent 4.1 × 10; Zimmer Biomet, Parsippany, NJ, USA) for the maxillary arch and four standard-diameter dental implants (Tapered Screw Vent 4.1 × 1 1.5 and 4.1 × 10 mm; Zimmer Biomet, Parsippany, NJ, USA) for the mandibular arch was planned digitally ( Figure 4C), and a surgical template was designed in the same computer program. Subsequently, maxillary and mandibular bone reduction guides and bone-supported surgical templates were manufactured using a clear photopolymer (Surgical Guide V2; FormLabs, Somerville, MA, USA) in a stereolithographic (SLA) 3D printer (Form2; FormLabs, Somerville, MA, USA). Additionally, maxillary and mandibular interim complete dentures were fabricated by compression molding using heat polymerized polymethylmethacrylate (PMMA) denture base resin (Lucitone 199; Dentsply Sirona North America, York, PA, USA). On the day of the surgery, the dental implants were placed uneventfully using the computer-generated surgical templates, and the mandibular prosthesis was immediately loaded ( Figure 4D). ture teeth (Blue-Line; Ivoclar Vivadent Schaan, Liechtenstein, Switzerland) and visible light cure (VLC) denture bases (Triad VLC Denture Base Material; Dentsply Sirona Nort America, York, PA, USA) to establish the desired incisal edge position and future occlusa plane ( Figure 4A). Additionally, the distance from the incisal edges to the lower border o the upper lip during a maximum smile was recorded and inscribed on the diagnostic cast to plan the position of the maxillary implants so that they would be 4 mm above the uppe lip during function and smiling to ensure the concealment of the future prosthesis-tissu junction [33,34]. Subsequently, the diagnostic casts and diagnostic artificial teeth arrange ments were scanned using a benchtop 3D scanner (E3 Scanner; 3Shape A/S, Copenhagen Denmark) and were merged with the patient's CBCT data in an implant planning com puter program (BlueSky Plan V4; Blue Sky Bio, ,Libertyville,IL,USA) ( Figure 4B). Th placement of four standard-diameter dental implants (Tapered Screw Vent 4.1 × 10; Zim mer Biomet, Parsippany, NJ, USA) for the maxillary arch and four standard-diameter den tal implants (Tapered Screw Vent 4.1 × 1 1.5 and 4.1 × 10 mm; Zimmer Biomet, Parsippany NJ, USA) for the mandibular arch was planned digitally (Figure 4C), and a surgical tem plate was designed in the same computer program. Subsequently, maxillary and mandib ular bone reduction guides and bone-supported surgical templates were manufacture using a clear photopolymer (Surgical Guide V2; FormLabs, Somerville, MA, USA) in stereolithographic (SLA) 3D printer (Form2; FormLabs, Somerville, MA, USA). Addition ally, maxillary and mandibular interim complete dentures were fabricated by compres sion molding using heat polymerized polymethylmethacrylate (PMMA) denture bas resin (Lucitone 199; Dentsply Sirona North America, York, PA, USA). On the day of th surgery, the dental implants were placed uneventfully using the computer-generated sur gical templates, and the mandibular prosthesis was immediately loaded ( Figure 4D). After 4 months of healing, the maxillary implants were uncovered, and tapered abut ments were installed (straight, 15°, and 30° tapered abutment systems; Zimmer Biome Dental). Definitive impressions were taken using custom impression trays (Triad Tr Tray; Dentsply Sirona North America, York, PA, USA) and medium-bodied polyether im pression material (Impregum Penta; 3M America, Saint Paul, MN, USA), and maxillar After 4 months of healing, the maxillary implants were uncovered, and tapered abutments were installed (straight, 15 • , and 30 • tapered abutment systems; Zimmer Biomet Dental). Definitive impressions were taken using custom impression trays (Triad Tru Tray; Dentsply Sirona North America, York, PA, USA) and medium-bodied polyether impression material (Impregum Penta; 3M America, Saint Paul, MN, USA), and maxillary and mandibular definitive casts were fabricated with low-expansion type IV dental stone (New Fuji Rock IMP; GC America Inc., St. Alsip, IL, USA). Subsequently, verification devices were fabricated using low-shrinkage PMMA resin (Pattern Resin LS; GC America Inc., St. Alsip, IL, USA) and were used to verify the accuracy of the definitive casts ( Figure 5A). During the same appointment, occlusion rims were fabricated to record the maxillomandibular relationships, aided by the verification devices [35] (Figure 5B-D). and mandibular definitive casts were fabricated with low-expansion type IV dental ston (New Fuji Rock IMP; GC America Inc., St. Alsip, IL, USA). Subsequently, verification de vices were fabricated using low-shrinkage PMMA resin (Pattern Resin LS; GC Americ Inc., St. Alsip, IL, USA) and were used to verify the accuracy of the definitive casts (Figur 5A). During the same appointment, occlusion rims were fabricated to record the maxillo mandibular relationships, aided by the verification devices [35] (Figure 5B-D).   The definitive casts were articulated in a semi-adjustable articulator (Denar Omni-Track; Whip Mix Corp., Louisville, KY, USA), and maxillary and mandibular artificial tooth arrangements were fabricated ( Figure 6). and mandibular definitive casts were fabricated with low-expansion type IV dental ston (New Fuji Rock IMP; GC America Inc., St. Alsip, IL, USA). Subsequently, verification de vices were fabricated using low-shrinkage PMMA resin (Pattern Resin LS; GC Americ Inc., St. Alsip, IL, USA) and were used to verify the accuracy of the definitive casts (Figur 5A). During the same appointment, occlusion rims were fabricated to record the maxillo mandibular relationships, aided by the verification devices [35] (Figure 5B-D).   The artificial tooth arrangements were tried intraorally, and their esthetics, phonetics, vertical dimension, and centric relation were evaluated and deemed satisfactory (Figure 7). The artificial tooth arrangements were tried intraorally, and their esthetics, phonetics, vertical dimension, and centric relation were evaluated and deemed satisfactory (Figure 7). The contours and occlusal relationships of the maxillary and mandibular tooth arrangements were used as blueprints for the manufacture of the definitive maxillary complete-arch implant-supported prostheses. The maxillary prosthesis consisted of a titanium framework with a cementable 3 mm-thick zirconia overlay (AccuFrame 360; Cagenix Inc., Memphis, TN, USA) ( Figure 8A,B), and the mandibular prosthesis was a monolithic zirconia prosthesis (BarZero; Cagenix Inc., Memphis, TN, USA). It is worth mentioning that, preceding the fabrication of the definitive prostheses, printed prototypes were ordered and tried intraorally to refine the occlusion and esthetics and verify the centric relation ( Figure 8C). At this stage, a custom incisal guide table was manufactured to ensure the accurate reproduction of the anterior guidance established with the prototypes in the definitive prostheses [36] (Figure 8D).  The contours and occlusal relationships of the maxillary and mandibular tooth arrangements were used as blueprints for the manufacture of the definitive maxillary complete-arch implant-supported prostheses. The maxillary prosthesis consisted of a titanium framework with a cementable 3 mm-thick zirconia overlay (AccuFrame 360; Cagenix Inc., Memphis, TN, USA) ( Figure 8A,B), and the mandibular prosthesis was a monolithic zirconia prosthesis (BarZero; Cagenix Inc., Memphis, TN, USA). It is worth mentioning that, preceding the fabrication of the definitive prostheses, printed prototypes were ordered and tried intraorally to refine the occlusion and esthetics and verify the centric relation ( Figure 8C). At this stage, a custom incisal guide table was manufactured to ensure the accurate reproduction of the anterior guidance established with the prototypes in the definitive prostheses [36] ( Figure 8D).

J. Funct. Biomater. 2023, 13, x FOR PEER REVIEW 7 of 13
The artificial tooth arrangements were tried intraorally, and their esthetics, phonetics, vertical dimension, and centric relation were evaluated and deemed satisfactory (Figure 7). The contours and occlusal relationships of the maxillary and mandibular tooth arrangements were used as blueprints for the manufacture of the definitive maxillary complete-arch implant-supported prostheses. The maxillary prosthesis consisted of a titanium framework with a cementable 3 mm-thick zirconia overlay (AccuFrame 360; Cagenix Inc., Memphis, TN, USA) ( Figure 8A,B), and the mandibular prosthesis was a monolithic zirconia prosthesis (BarZero; Cagenix Inc., Memphis, TN, USA). It is worth mentioning that, preceding the fabrication of the definitive prostheses, printed prototypes were ordered and tried intraorally to refine the occlusion and esthetics and verify the centric relation ( Figure 8C). At this stage, a custom incisal guide table was manufactured to ensure the accurate reproduction of the anterior guidance established with the prototypes in the definitive prostheses [36] (Figure 8D).  Subsequently, the definitive maxillary and mandibular prostheses were fabricated ( Figure 9) and tried intraorally.
The passivity and accuracy of the fit were assessed clinically and radiographically (Figure 10), and the abutment screws were tightened to the recommended manufacturer's recommended torque values.
Subsequently, home maintenance instructions and interdental brushes (ProxaBrush Go-Betweens Wide; GUM Sunstar America, Schaumbaum, IL, USA) were provided, and a hygiene program consisting of recall appointments every 6 months was established on the day of delivery. At the subsequent appointments, overall hygiene was reassessed and deemed adequate. Additionally, during these appointments, the patient expressed satisfaction with the function, esthetics, and confidence provided by the definitive prostheses ( Figure 12). Subsequently, the definitive maxillary and mandibular prostheses were fabricated ( Figure 9) and tried intraorally. The passivity and accuracy of the fit were assessed clinically and radiographically (Figure 10), and the abutment screws were tightened to the recommended manufacturer's recommended torque values. Vertical dimension, centric occlusion, protrusive, and laterotrusive excursive movements were assessed and refined (Figure 11). Additionally, cleanability, esthetics, with PMMA overlay and mandibular prototype (D), and maxillary and mandibular prototypes mounted after intraoral adjustments with custom incisal guide table.
Subsequently, the definitive maxillary and mandibular prostheses were fabricated ( Figure 9) and tried intraorally. The passivity and accuracy of the fit were assessed clinically and radiographically (Figure 10), and the abutment screws were tightened to the recommended manufacturer's recommended torque values. Vertical dimension, centric occlusion, protrusive, and laterotrusive excursive movements were assessed and refined (Figure 11). Additionally, cleanability, esthetics, and comfort were deemed adequate by the patient (Figure 11).  Subsequently, home maintenance instructions and interdental brushes (ProxaBrush Go-Betweens Wide; GUM Sunstar America, Schaumbaum, IL, USA) were provided, and a hygiene program consisting of recall appointments every 6 months was established on the day of delivery. At the subsequent appointments, overall hygiene was reassessed and deemed adequate. Additionally, during these appointments, the patient expressed satisfaction with the function, esthetics, and confidence provided by the definitive prostheses ( Figure 12).

Results
In the present clinical report, complete-arch implant-supported prostheses permitted the predictable rehabilitation of a patient with severely decayed terminal dentition. CAD/CAM technology is a valuable resource for restorative dentists since it enhances communication between the different members of the restorative team and permits the fabrication of complex prosthetic designs that maximize functionality and retrievability while minimizing complications.  Subsequently, home maintenance instructions and interdental brushes (ProxaBrush Go-Betweens Wide; GUM Sunstar America, Schaumbaum, IL, USA) were provided, and a hygiene program consisting of recall appointments every 6 months was established on the day of delivery. At the subsequent appointments, overall hygiene was reassessed and deemed adequate. Additionally, during these appointments, the patient expressed satisfaction with the function, esthetics, and confidence provided by the definitive prostheses ( Figure 12).

Results
In the present clinical report, complete-arch implant-supported prostheses permitted the predictable rehabilitation of a patient with severely decayed terminal dentition. CAD/CAM technology is a valuable resource for restorative dentists since it enhances communication between the different members of the restorative team and permits the fabrication of complex prosthetic designs that maximize functionality and retrievability while minimizing complications.

Results
In the present clinical report, complete-arch implant-supported prostheses permitted the predictable rehabilitation of a patient with severely decayed terminal dentition. CAD/CAM technology is a valuable resource for restorative dentists since it enhances communication between the different members of the restorative team and permits the fabrication of complex prosthetic designs that maximize functionality and retrievability while minimizing complications.

Discussion
In the present clinical report, a patient with Sjogren's syndrome and terminal dentition was predictably rehabilitated with complete-arch implant-supported prostheses composed of two functional biomaterials: titanium and zirconia. For decades, titanium has been the material of choice for dental implants due to its availability, machinability, biocompatibility, and favorable elastic modulus [27]. Similarly, dental professionals have embraced high-strength polycrystalline zirconia ceramics as restorative materials since they allow the consistent manufacture of highly-esthetic, tooth-colored restorations with remarkable flexural strength [27,28] and biocompatibility [27,29]. Nowadays, thanks to the advances in CAD/CAM technologies, the best features of these completely different materials can be merged into a single prosthetic design, and multi-material complete-arch implantsupported prostheses can be designed and manufactured digitally [13]. However, as with any other dental prosthesis, the success and adequate function of these complex prostheses lie in an adequate design and careful clinical refinement.
Since fixed complete dentures were introduced as a treatment for edentulism, significant changes have been made to the design of complete-arch implant-supported prostheses. For zirconia-based rehabilitations, limiting the application of porcelain to the gingival region, reducing the extension of cantilevers, and ensuring adequate prosthetic space have been advised to prevent biological and mechanical complications [31,32,37]. In the present clinical report, the maxillary zirconia overlay accurately copied the occlusal relationships and anterior guidance established intraorally with the prototypes and was supported by a titanium bar with 25 mm 2 of cross-sectional area. The decision to use a prosthesis composed of two different materials was based on the presence of bilateral 10 mm-long distal cantilevers, which could create unfavorable flexural stresses in the ceramic overlay [27], although there is no clear evidence indicating a detrimental effect of distal cantilevers when their extension is small [37,38]. This design was selected over a monolithic alternative for the maxillary arch since it would permit retrieving and replacing the overlay portion of the prostheses if any complications occurred. On the other hand, for the mandibular definitive prostheses, the implant distribution and prosthetic space available permitted designing a prosthesis of dimensions that permitted adequate esthetics and function without compromising structural durability; therefore, a completely monolithic design was used.
Regardless of the significant progress in contemporary biomaterials and CAD/CAM technologies, there are aspects of prosthetic and implant dentistry that need further consideration. Substantial research has been done evaluating several restorative alternatives for complete-arch implant-supported restorations, and aspects such as retrievability, passivity, and occlusion have been researched [18][19][20]. Recently, alternative retention mechanisms and prosthetic designs involving high-performance polymers and novel ceramic-reinforced materials have been implemented to rehabilitate patients with complex dental needs and craniofacial conditions [16,39,40]. In the present clinical report, the combination of CAD/CAM and contemporary biomaterials permitted restoring the confidence, esthetics, and function of a patient exhausted by failing restorations. Research suggests that dental implants are a feasible modality to rehabilitate patients with terminal dentition caused by Sjogren's syndrome. Satisfactory survival rates, low marginal bone loss, and biological complications comparable to those in healthy patients have been reported in the literature [41]. A systematic review of the topic suggests that, to ensure optimum outcomes, a hygienic prosthetic design and regular maintenance regime should be established on the day of delivery [40]. With satisfactory maintenance, implant-supported rehabilitations in patients with Sjogren's syndrome can perform satisfactorily for many years, with case reports describing up to 13 years of service available in the literature [42,43]. In a similar way, a cohort study reported high satisfaction levels for this treatment modality, and 97% of the candidates would recommend dental implants to other patients with Sjogren's syndrome [44,45]. However, it is worth noting that the majority of research available describes the clinical performance of traditional prosthetic designs such as traditional fixed complete dentures or porcelain-fused to metal complete arch rehabilitations. Therefore, research on the clinical performance of newer prosthetic designs and functional biomaterials in patients with Sjogren's syndrome is needed.
Finally, this clinical report presents limitations related to the lack of cytologic, morphometric, and prospective clinical evaluation of the interaction of the biomaterials used with the tissues of the patient. Prosthetic factors such as passivity, restitution of phonetics, reestablishment of occlusion, and anterior guidance were assessed clinically throughout the different stages of the treatment, and osseointegration was evaluated radiographically. The lack of quantitative analysis is a common limitation of clinical reports, where time and patient factors play an important role. For these reasons, the materials used in the prostheses were not examined in greater depth in this clinical report. However, since their introduction as restorative materials, zirconia and titanium have demonstrated their biomechanical adequacy for complete arch rehabilitations when masticatory dynamics are considered [27,31,32]. Therefore, although the present clinical report lacks quantitative analysis, the gratitude of the patient and his favorable adaptation to the prostheses suggest the achievement of functionality and satisfaction, two of the greatest indicators of success in any restorative treatment.

Conclusions
A patient with Sjogren's syndrome and terminal dentition was successfully rehabilitated using complete-arch implant-supported prostheses and dental implants. Completearch implant-supported rehabilitations manufactured using CAD/CAM technologies can be designed with multiple components made of different materials to ensure the prostheses have satisfactory biomechanics, esthetics, and occlusion.

Institutional Review Board Statement:
The study was conducted in accordance with the Declaration of Helsinki for studies involving humans.

Informed Consent Statement:
Written informed consent has been obtained from the patient to publish this paper. Data Availability Statement: Not applicable.