A Paradigm Change in Macro Implant Concept: Inverted Body-Shift Design for Extraction Sockets in the Esthetic Zone
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Stephen J. Chu, DMD, MSD, CDT; Jocelyn H.P. Tan-Chu, DDS; Barry P. Levin, DMD; Guido O. Sarnachiaro, DDS; Valentina Lyssova, DDS; and Dennis P. Tarnow, DDS
Abstract: An innovative macro hybrid implant design is aimed at enhancing labial plate dimension and tooth-implant distance while achieving consistent esthetic outcomes. This unique "body-shift" concept in diameter and shape combines a tapered apical portion with a cylindrical coronal portion in a singular implant body design. The overall configuration of the implant is inverted and "convergent" in form toward the implant-abutment interface where bone is thinnest. Conversely, the tapered apical portion is wider where the bone is greatest in volume and vascularity. By reducing the coronal portion of the implant with the inverted body-shift design, a coronal circumferential chamber is created, thereby allowing larger amounts of graft material to be placed labially and interdentally to create a net increased bone dimension. Use of the implant is demonstrated in a case report.
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The concept of immediate implant placement into fresh extraction sockets with immediate provisional restoration in the esthetic zone has existed for several decades and has become a viable and predictable treatment choice, assuming there is proper understanding and execution on the part of the dental team.1-4 Today, the pendulum has swung from the emphasis being on implant survival and osseointegration, though these remain essential, toward treatment outcomes that focus heavily on esthetic results, such as the pink esthetic score.5-7
It has been well-established, understood, and accepted that the thickness of the labial bone plate and soft tissues in the anterior maxilla are extremely thin, ie, ≤1 mm, which increases the risk of esthetic dilemmas.8-11 Consequently, various techniques have been derived to enhance esthetic outcomes at the time of immediate tooth replacement; these include the dual-zone and socket-shield techniques.12-18 Studies employing these treatment strategies have shown they can reduce ridge collapse and recession to tenths of millimeters instead of millimeters, thereby affording good esthetic outcomes.13,14,16
Nonetheless, precautions must be taken with regard to immediate implant placement in anterior extraction sites using straight implant designs, where the probability of apical perforation of the socket is not only real but also extremely high (82%) due to the inherent anatomy of the premaxilla.19-22 Delayed implant placement, cement-retained restorations, angulated screw channel abutments, dynamic or static surgical guides, and subcrestal angle correction (SAC) implants are all proposed solutions to avoid this potential problem.23
From a biologic perspective, thin avascular labial bone ≤1 mm in dimension can survive around natural teeth, because the adjacent periodontal ligament is highly vascular and provides nourishment to this area and to the overlying periosteum.24-26 Equally important, bone surrounding an implant after placement must be adequate in dimension; studies support 1.5 mm to 2 mm in width for biologic reasons that lead to long-term stability.27-29 The danger is that if inadequate bone, ie, ≤1.5 mm, is present around the implant after placement, the implant may not survive and may succumb to avascular necrosis because endosteum or marrow is absent. Also, changes in craniofacial growth and development can cause esthetic issues around implants long-term.30
Hence, although they are less effective in achieving high primary stability than wider-diameter implants, narrower implants must be considered.31-34 Increased length is an alternative strategy, however there is a limit to the amount of apical bone that extends beyond an extraction socket before the floor of the nasal antrum is encroached upon.21 Implant diameter has been shown to be highly effective in achieving primary stability in comparison to length, especially in soft bone where undersizing the osteotomy is an essential and useful clinical approach.31 However, with wider-diameter tapered implant designs, such as those with a divergent wider coronal portion, the labial gap distance is reduced and the tooth-to-implant distance compromised, especially between the central-lateral incisor area, which can lead to interdental papilla loss in extraction sockets.28 The horizontal formation of biologic width even with platform-switched designs and/or pressure necrosis of crestal bone can be causative factors.35-39 The reality is that the requirements of modern-day implants for biologic and ultimately esthetic needs are no longer the same as those in the 1980s when Brånemark first introduced the concept of osseointegration to North America from Sweden and when survival and integration were the principal directives of treatment.
Recent preclinical and clinical studies, respectively, on an innovative macro hybrid implant design (Inverta™, Southern Implants, southernimplants.com) utilizing a paradigm shift in biologic and esthetic thought has been reported.40,41 This unique "body-shift" concept in diameter and shape combines a tapered apical portion with a cylindrical coronal portion in a singular body design (Figure 1). The overall configuration of the implant is inverted and "convergent" in form toward the implant-abutment interface where the bone is thinnest, delicate, and avascular versus divergent (Figure 2). Conversely, the tapered apical portion is wider where the bone is greatest in volume and vascularity. By reducing and shrinking the coronal portion of the implant with the inverted body-shift design, more space is inherently generated, allowing a greater volume of graft material to be placed not only labially but also interdentally into the gap to create a net increased bone dimension. This design also provides a greater tooth-to-implant distance to preserve the interdental attachment of the adjacent natural tooth and, hence, the papillae.
The aforementioned preclinical animal study showed no evidence of apical pressure necrosis with consistent insertion torque values of 100 Ncm on roughly three-quarters of the implants placed.40 The results of this histomorphometric study showed that high insertion torque of 100 Ncm will not cause pressure necrosis because the apical portion of the extraction socket possesses not only the greatest amount of bone volume but also is rich in marrow, which has excellent potential for wound healing. The clinical study on 33 implants in the same number of patients showed that a labial bone dimension of 1.6 mm to 2 mm, interdental distance of 2.4 mm to 2.6 mm, and a pink esthetic score of 12.5 was achieved up to 1-year follow-up.41
A 25-year-old African American male patient presented with a fractured maxillary left central incisor with a pre-existing periapical lesion (Figure 3 and Figure 4). A fistula tract was evident over the apex of the tooth (No. 9) as a result of prior endodontic therapy that was failing (Figure 3), and the periapical radiograph of tooth No. 9 showed crestal bone loss, a decemented post/core foundation restoration, and residual apical radiolucency (Figure 4). The patient was given pretreatment antibiotics. The supragingival fibers were severed with sharp dissection using a 15c scalpel, and the clinical crown and residual root segment were removed in toto atraumatically without flap elevation (Figure 5).42
After thorough socket debridement with a surgical spoon excavator it was noted that a slight dentoalveolar dehiscence defect of the labial plate was present involving the coronal one-third of the extraction socket. This would be addressed during socket grafting using a cross-linked collagen membrane. The osteotomy was precisely created with the use of extended-length solid shank drills, because only the apical part of the implant was providing primary stability. The incisal edge position was used as a point of reference when drilling the osteotomy and during placement (Figure 6).
Because the bone quality was type III, a decision was made to undersize the osteotomy to 4.5 mm diameter instead of 5 mm. Subsequently, a 13 mm length implant was placed that had an inverted body-shift design with a 5 mm diameter apical portion roughly half the implant length and a 4 mm coronal cylindrical portion about 40% in extent with a subcrestal angle correction feature (Inverta IV-DC4012d-5013) to enable a screw-retained restoration (Figure 7). This implant had a 12-degree angle correction of the implant-abutment interface and, therefore, was premounted with a counter-matching holder (Figure 8). The inherent SAC feature redirected the restorative position of the prosthetic screw to the cingulum of the tooth. An alignment groove on the facial aspect of the implant mount helped orient the implant into the proper position (Figure 9).
A screw-retained acrylic provisional restoration attached to a polyetheretherkeytone (PEEK) temporary cylinder was made with full labial restorative contour to support the peri-implant soft tissues (Figure 10 and Figure 11). A flat non-contoured healing abutment was placed to mitigate graft material from entering the implant-abutment connection, and a cross-linked collagen membrane was placed within the residual socket walls on the facial aspect to cover the bony defect in its entirety to the level of the free gingival margin facially, thereby converting a type 2 socket into a type 1 scenario (Figure 12). The provisional restoration was then replaced after dual-zone socket grafting to contain and protect the graft during the healing phase (Figure 13).12 The provisional restoration was re-evaluated to make sure it was not in occlusal contact during maximum intercuspal position or lateral excursive movements. This is a critical step in treatment to ensure implant survival with extraction socket implants.
A cone-beam computed tomography (CBCT) scan was taken immediate post-treatment and revealed a labial bone plate thickness of 2.4 mm at the implant-abutment interface (Figure 14). A periapical radiograph revealed a tooth-to-implant distance of 3.1 mm at the distal aspect of the central incisor implant between the central and lateral incisors (Figure 15).
The patient continued the antibiotic regiment for 1-week post-treatment and was instructed to not brush the surgical site for 5 to 7 days. At the first postoperative appointment the following week, the wound healing was evaluated and occlusion re-checked. The implant was allowed to heal for 6 months before the first abutment disconnection and final impression making (Figure 16 and Figure 17). After seating an analog implant-level impression coping, flowable composite or pattern resin may be used to register the submergence profile of the peri-implant soft tissues.
A soft-tissue gypsum cast made in the laboratory enabled fabrication of a screw-retained metal-ceramic implant crown. A mesial indirect composite veneer also was created to manage the size and space discrepancy between the two central incisors (Figure 18). The color, texture, and form of the restoration was made to mimic that of the contralateral tooth in one surgical intervention, and the patient was highly accepting of and pleased with the outcome (Figure 19 and Figure 20).
The use of an inverted body-shift macro hybrid implant design not only can enhance labial plate dimension and tooth-implant distance ≥1.5 mm for biologic purposes, but also is conducive to consistent esthetic outcomes in modern-day implant dentistry. This macro change in diameter and shape at the coronal aspect of the implant body at roughly one-half its length may have additional biologic and esthetic implications in not only extraction sockets but also edentulous sites where osteoinduction in situ may occur spontaneously.
Dr. Chu has been a consultant and has a financial interest in products that he has developed for Southern Implants.
Stephen J. Chu, DMD, MSD, CDT
Adjunct Clinical Professor, New York University, College of Dentistry, New York, New York; Private Practice, New York, New York
Jocelyn H.P. Tan-Chu, DDS
Private Practice, New York, New York
Barry P. Levin, DMD
Clinical Associate Professor, Department of Graduate Periodontology, University of Pennsylvania, Philadelphia, Pennsylvania; Diplomate, American Board of Periodontology; Private Practice, Jenkintown, Pennsylvania
Guido O. Sarnachiaro, DDS
Assistant Clinical Professor, Department of Prosthodontics, New York University, College of Dentistry, New York, New York
Valentina Lyssova, DDS
Private Practice, New York, New York
Dennis P. Tarnow, DDS
Clinical Professor, Department of Periodontology, Director of Implant Education, Columbia University, College of Dental Medicine, New York, New York