Purpose. To evaluate the outcomes of a new computer-guided surgical approach for prosthetically - and aesthetically - driven implant insertion in horizontally atrophic ridges using a double template concept and one-stage guided bone regeneration (GBR) procedure at 1 year and half after loading.
Materials and methods. This study was designed as a prospective case series. Patients in need of rehabilitation with an implant-supported restoration between the upper premolars, Cawood-Howell Class III defects and residual horizontal bone width of less than 6 mm and more than 4 mm were treated with computer-guided implant placement using two templates and simultaneous GBR, and, in cases of bone fenestration with autologous bone, anorganic bovine bone arranged in layers, or in cases of thin buccal bone, using a mix of 20% autologous bone and 80% anorganic bovine bone protected with a resorbable collagen membrane. After 6 months of healing, implants were fitted with temporary screw-retained acrylic resin crowns, and 6 months later permanent screw-retained zirconia-ceramic crowns. Outcome measures were: implant and prosthesis failures, complications, marginal bone level (MBL) changes, periodontal parameters, and pink aesthetic score (PES).
Results. Twenty-one consecutive patients (mean age 39.2 years) received one computer-guided GBR procedure each, with contemporary placement of 25 conical-connection implants. No implants or prostheses failed, and only two minor complications were observed. Mean marginal bone loss fom implant placement up to 18 months after loading was 0.71±0.23 mm (95% CI 0.59 to 0.83 mm); mean BoP was 1.12±0.88 (95% CI 0.77 to 1.47) percent of sites, mean PPD was 2.54±0.49 mm (95% CI 2.35 to 2.73 mm), and mean PES was 11.2±1.2 (95% CI 10.3 to 12.1).
Conclusions. Acknowledging the limitations of this study, the high survival rate and PES seem to validate the use of a double-template approach in association with one-stage GBR and implant placement in atrophic aesthetic areas. Randomised controlled trials are needed to properly evaluate the utility of this technique versus simple free-hand implant placement with no augmentation procedures.
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