Commentary Related to this Phase of Treatment
The decision to wait for 6 months until the uncovering was made based on the amount of bone loss present at the time of implant placement as the implant was surrounded by more than 50% of the augmentation material.
For soft tissue grafting the gold standard is an autologous tissue harvested from the palate. There are several techniques for harvesting that will result in different quality and quantity of connective tissue grafts. In this clinical situation, the aim of the connective tissue graft was to ensure proper volume and contours of the soft tissue. In order to achieve this, a high quality of dense connective tissue graft was harvested using the de-epithelized FGG technique from the posterior area of the palate. This type of graft has the potential to increase its volume through the maturation phase and occasionally thereafter. The placement of the connective tissue graft was at the base of both papillae, mesial and distal to the implant, aiming for an increase in volume of the papillae over time.
The use of a transmucosal component such as Connect has several advantages — biologic and prosthetic.
Because the prosthetic platform is 4mm away from the implant head, all of the prosthetic steps can be executed without harming the biologic width that was established during the healing period. Using such a transmucosal extension provides the flexibility of a two-piece implant system (e.g., precise positioning according to the bone anatomy, implant submergence if needed, etc) with the advantages of a tissue-level implant, which include no abutment-implant microgap next to the bone (and, therefore, no bacterial colonization of the abutment-implant junction at the bone level), no micromovement close to the bone, no tissue disruption throughout the prosthetic workflow, and the ability to clearly view and access the implant.
The height of the extension abutment is chosen according to the clinical situation, and this can be replaced if significant tissue alterations occur. In this case, because the extension abutment was never removed after connection, the abutment also adheres to the desirable demand of “one time abutment.”
Phase 6
An impression for a final design for the future restorations was made. The dental technician (Stefano Inglese MDT, Oral Design Pescina, Italy) prepared an ideal diagnostic wax-up and individual provisional crowns for the two central incisors, to be connected during the appointment of preparation and impression making of the adjacent upper maxillary teeth.
Minimally invasive preparations were made through the mock-up and impression for the final restorations were taken.
Commentary Related to this Phase of Treatment
Due to the patient’s desire to improve the overall look of his smile, a decision was taken to treat the adjacent upper maxillary teeth (nos. 5-12). Very conservative preparations were made in order to maintain almost entirely the enamel, by preparing the teeth through the final desired design- mock-up.
Phase 7
Lithium disilicate ceramic veneers and a bi-layered crown (no. 8) (e.max, Ivoclar Vivadent) were made and bonded under proper isolation with rubber dam, following the standard protocol for bonding.
A hybrid screw-retained zirconia crown with e.max veneer was made for the no. 9 implant.
The posterior implants received connected screw-retained zirconia crowns.
Commentary Related to this Phase of Treatment
For very thin ceramic veneers the use of fledsphatic ceramic material will result in excellent esthetics as well. Whenever there is a combination of substrates such as crowns, veneers and implant restorations, for the dental technician it is easier to control the optical characteristics harmony of the restorations when utilizing the same material. For this reason, the design of the implant crown was a hybrid one, having the zirconia abutment design as a prepared tooth for veneer. In this way by working with similar restorative thickness, the overall control of the color and shape is facilitated.
The design of the implant crown was made using the Cervical Contouring Concept – a model-based cervical design in order to create the ideal cervical contour of the definitive crown. An ideal wax-up was duplicated on the working model, and the cervical crown contours were marked on the plaster. Then, the wax crown was removed and the plaster between the marked line and the inner prosthetic platform was gently carved away. Thus, a smooth continuity of the cervical region, from the narrow prosthetic platform (4mm diameter) to the wider diameter of the crown as it emerges from the tissue, was achieved. Also, the implant papillae were thinned and sharpened.
This restorative concept, when referencing the traditional cervical part of an implant crown with its deep and superficial contours (also termed “critical” and “subcritical” contours, respectively) is actually composed of the pre-manufactured narrow Connect abutment as the deep contour, whereas the superficial contour is custom-made as per the cervical contouring concept. This modified cervical region at the model, based on the ideal wax-up, directs the design of the cervical contours of the actual crown. When the crown is connected intraorally the peri-implant mucosa adapts to the crown’s optimal cervical contours and matures by the crown’s superficial contour guidance.