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Purpose: To assess the feasibility and success rate of nasal or transnasal implants placed in patients who were affected by severe maxillary anterior atrophy with residual anatomical features that indicate this surgery. Materials and Methods: In this retrospective multicentric study, 52 nasal or transnasal dental implants were placed in 31 maxillary atrophic anterior sites (Cawood and Howell’s class V/VI). All implants were successful after the healing period; 27 nasal implants reached an insertional torque ≥ 50 Ncm², and the threshold value was estimated to be able to support an immediate load. Results: All 52 implants were successful, so the proportion of success was 100%, with a 97.5% one-sided CI of 88.8% to 100%. The success rate was achieved only when at least two of the following criteria were met: (1) a torque > 50 Ncm as a minimum sufficient condition to plan immediate loading; (2) after a healing period of 16 weeks, no coronal bone resorption (this condition allows for successive prosthetic finalization) observed clinically or radiographically; and (3) a possibility of carrying out a full-arch rehabilitation with minimal anterior spread. Insertion torque was < 50 Ncm in 14 patients (45%) and 50 Ncm in 17 patients (55%). Mechanical loading was delayed in the former group of patients and immediate in the latter group of patients. The proportion of torque that was < 50 Ncm was greater in men (69%) than in women (28%; P = .033). Immediate torque was not significantly affected by age. Conclusions: Although the present sample was not extremely numerically significant, it conveyed a clear and significant clinical and surgical meaning that has never been seen before in the literature: nasal or transnasal implants can be very useful in reducing the anterior cantilever and overcoming the anatomical limitations affecting conventional quad zygoma implants. Parole chiave: anterior cantilever prostheses, pterygoid implants, severe atrophy, nasal implants, zygomatic implants

Purpose: To retrospectively evaluate the clinical outcomes of immediately loaded zygomatic implants combined with anterior regular implants (hybrid zygoma) for the fixed rehabilitation of atrophic maxillae. Materials and Methods: A total of 18 patients were enrolled in this study and treated with the hybrid zygoma concept by an experienced surgeon. Follow-up visits were planned after 1 week, 3 weeks, 4 months, 6 months, then annually. At the last follow-up appointment (mean: 36 months after surgery; range: 24 to 52 months), the prostheses were unscrewed and the implants and peri-implant tissues were examined. The primary outcome evaluated was implant success. Following the criteria proposed by Aparicio et al, implant success was classified in five grades, with grade I representing the best condition and grade V representing a failure. At the annual check-up, patients were asked to fill out a questionnaire to evaluate their satisfaction with their oral rehabilitation. Results: A total of 80 implants (34 zygomatic and 46 regular) were inserted. One zygomatic implant was lost in one patient, and two regular implants failed in two other patients. Of the zygomatic implants, 24 (70.6%) presented a success grade I, 9 (26.5%) a success grade II, and 1 (2.9%) a grade V. Sinusitis was the most common biologic complication, occurring in two patients (5.6%). Two patients showed unilateral upper lip paresthesia that was persistent at the last follow-up appointment. According to the annual follow-up visit questionnaire data, 72%, 89%, and 94% of patients declared that they were satisfied with their phonetic ability, chewing ability, and esthetics, respectively. Conclusion: Although zygomatic implants combined with anterior regular implants present a higher risk of complications than traditional implantology, they allow for immediately loaded full-arch fixed rehabilitation of patients with advanced atrophy of the posterior maxilla, which provides satisfactory chewing ability, esthetics, and phonetics. Parole chiave: dental implants, extreme atrophic maxillae, hybrid zygoma, immediate loading, retrospective study, zygomatic implants

The aim of the present report was to evaluate the clinical outcomes of edentulous jaws rehabilitated with the Brånemark Novum protocol over a 16-year period. Between April and November 2001, four patients (three males, one female) were rehabilitated with fixed full-arch rehabilitations supported by three immediately loaded implants following the Brånemark Novum protocol. Cumulative survival rates (CSRs) of the implants and prosthesis, bleeding on probing (BOP), Plaque Index (PI), probing depth (PD), implant stability quotient (ISQ; as measured through resonance frequency analysis [RFA]), and peri-implant bone resorption were evaluated over time, up to the 16-year follow-up. At 16 years of follow-up, no implant failed (CSR 100%) and no prosthesis needed to be substituted (CSR 100%). During the period between the 11th and 16th year of follow-up, bone level (mean: 2.2 mm at 16 years) and RFA values remained stable. At the 16-year follow-up, the implants presented high PI (79.2%) but low BOP (10.4%) values. Mean PD was 3.30 mm (range: 2 to 6 mm). One biologic complication was detected on a central implant (crater-form bone destruction), and several prosthodontic complications occurred during the 16 years (fractures of resin or teeth), the majority of which were registered on the same parafunctional patient. This is the first description of the Brånemark Novum protocol rehabilitation with a 16-year followup. The outcomes demonstrated very good long-term outcomes for this protocol.

Purpose: To compare clinical outcomes of immediate vs delayed implant loading in edentulous maxillae with full-arch fixed prostheses. Materials and Methods: Two patient groups were identified for this study: (1) the test group (TG), which included 34 patients (19 women, 15 men; mean age 56.7 years) treated with the Columbus Bridge Protocol with 4 to 6 postextractive implants loaded within 24 hours (163 implants total); and (2) the control group (CG), which included 15 patients (6 women, 9 men; mean age 59.96 years) treated with a traditional two-stage delayed loading rehabilitation using 6 to 9 implants inserted in healed sites (97 implants total). All patients were rehabilitated with full-arch fixed prostheses in the maxilla. Results: At the 10-year follow-up, no difference in the implant cumulative survival rate between the TG (93.25%) and CG (94.85%) was found. Mean bone loss was significantly lower in the TG (mean: 2.11 mm) compared to the CG (mean: 2.65 mm). All original prostheses were maintained and functioning satisfactorily. Conclusion: Maxillary full-arch immediate loading represents a valid alternative to the traditional delayed loading rehabilitation.

Purpose: The aim of this study was to analyze through a three-dimensional finite element analysis (3D-FEA) stress distribution on four implants supporting a fullarch implant-supported fixed prosthesis (FFP) using different prosthesis designs. Materials and Methods: A 3D edentulous maxillary model was created and four implants were virtually placed into the maxilla and splinted, simulating an FFP without framework, with a cast metal framework, and with a carbon fiber framework. An occlusal load of 150 N was applied, stresses were transmitted into peri-implant bone, and prosthodontic components were recorded. Results: 3D-FEA revealed higher stresses on the implants (up to +55.16%), on peri-implant bone (up to +56.93%), and in the prosthesis (up to +70.71%) when the full-acrylic prosthesis was simulated. The prosthesis with a carbon fiber framework showed an intermediate behavior between that of the other two configurations. Conclusion: This study suggests that the presence of a rigid framework in full-arch fixed prostheses provides a better load distribution that decreases the maximum values of stress at the levels of implants, prosthesis, and maxillary bone.

Purpose: The aim of this split-mouth, double-blind, randomized study is to evaluate if pulsed electromagnetic fields treatment can improve swelling and pain management after a full-arch immediate loading implant surgery. Materials and methods: Eleven patients were selected for the study. Each patient received four implants in the upper or lower jaw using distal tilted implants and underwent a full-arch immediate loading rehabilitation. After surgery two pulsed electromagnetic fields (PEMF) devices were applied on the right and the left cheek of each patient. Randomly one PEMF device was switched on (test side), applying the other one as a placebo (control side). 48 hours after surgery clinicians estimated the postoperative swelling through photographic documentation, comparing the condition prior and after surgery, while pain was assessed using a verbal rating scale. Patient's comfort degree in relation to PEMF devices was analyzed by questionnaires using a numerical rating scale. Results: No statistically significant difference was observed between the test side and the control one as regards to swelling and pain (p>0.05). Most of patients did not present swelling or pain 48 hours after surgery, without distinction between PEMF device activated and not. Variable outcomes emerged from comfort evaluation. Conclusion: Within the limits of this study, PEMF does not reduce postoperative swelling and pain after immediate loading implant surgery. Parole chiave: immediate loading, implant surgery, pulsed electromagnetic field, PEMF, postoperative swelling, pain

This prospective study reports the 6-year outcomes for patients rehabilitated with an immediate loading protocol of the maxilla (Columbus Bridge Protocol). In this study, 164 implants were inserted in 37 patients and loaded within 24 to 36 hours. Four implants failed during the first 6 months. At the 6-year follow-up, a mean bone loss of 1.52 mm was found. Significantly (P .0083) less bone loss was found next to tapered implants compared with cylindric implants and next to machined collar implants compared with full acid-etched implants (P .0083). No significant differences in bone loss were found in tilted versus upright implants or in mesial versus distal implant sites. In addition, there were no significant differences relating to either the degree of abutment angulation or the reason for tooth loss.

Purpose: This study compared the surgical protocol efficacy of immediate and delayed implant loading in edentulous maxillae opposed by natural or restored mandibular dentitions over an observational period of 6 years or longer. The selected outcome determinants included individual implant survival data, progressive measurements of peri-implant bone resorption, prosthodontic survival and success data, and report of complications. Materials and Methods: A convenience sample of 49 patients requiring fixed implant-supported maxillary prostheses was split into two groups. The test group (34 patients) was treated according to the Columbus Bridge Protocol, which prescribes the insertion of four to six implants, including distally tilted implants, and load within 24 hours. The control group (15 patients) was treated via a two-stage surgical protocol of 6 to 9 straight implants that were loaded a mean 8.75 months after stage-one implant surgery. Two hundred sixty implants (test: n = 163, control: n = 97) were placed, and all subjects were ultimately treated with screw-retained full-arch prostheses. Results: Two patients dropped out (one in the test group and one in the control group) by the time of the scheduled sixth annual visit. The other patients were followed up for 75.2 months (range: 72 to 90 months). At the 6-year follow-up, no differences in implant cumulative survival rates were found between groups. Significantly less bone loss was found in the test group (mean: 1.62 mm) compared with the control group (mean: 2.44 mm). All of the original prostheses were maintained throughout the study's observation period and were functioning satisfactorily at each patient's last recall appointment. Conclusion: Patients who received immediate and delayed implant loading in their edentulous maxillae demonstrated similar survival outcomes. However, less marginal bone loss was recorded around the immediately loaded implants over the study's 6-year follow-up period.

Background: Reducing the risk of overloading is mandatory to achieve a predictable osseointegration in immediate loading protocols. Purpose: The aim of this study was to analyse through a three-dimensional Finite Element Analysis (3D-FEA) stress distribution on four implants supporting a full-arch implant-supported fixed bridge (FFB) using different prosthesis design. Materials and Methods: A 3-D edentulous maxillary model was created using a customized computer software. Four implants were virtually placed into the maxilla and splinted with a FFB of 12 masticatory units. 3 different configurations were evaluated: (1) full acrylic resin prosthesis without framework, (2) acrylic resin veneering material with cast metal framework, (3) acrylic resin veneering material with a carbon fibre framework. An occlusal load of 150 N was applied on the left most distal portion of the bridge and stresses transmitted into peri-implant bone, to the implants and to the prosthodontic components were recorded. Results: 3D-FEA revealed higher stresses on the implants (up to +58,27%), on peri-implant bone (up to +56,93%) and in the prosthesis (up to +91,43%) when the full-acrylic denture was simulated. Conclusions: FEA simulating a maxillary rehabilitation revealed that FFBs endowed with a stiff framework decrease stresses on implants, prosthesis and on the peri-implant bone providing a better load distribution compared with all-acrylic prostheses. Parole chiave: Dental implants, Framework, Dental materials, Finite Element Analysis, In vitro study, Prosthodontics

Purpose: This systematic review considers possible etiologic factors and definitions of peri-implantitis as reported in the recent literature. Materials and Methods: An electronic search of databases plus a hand search of the most relevant journals published between January 2005 and September 2012 were performed. Results: The electronic and manual searches yielded 640 and 14 titles, respectively. From the independent doublecheck of the titles and abstracts, 24 full texts were downloaded (18 clinical studies and 6 animal studies). After reading the full texts, 10 articles (4 clinical studies and 6 animal studies) were included in this review. None of the human articles selected provided sufficient evidence to address the research question, and no human clinical evidence is available to support a cause-effect relationship between peri-implantitis and bacterial accumulation and/or occlusal overload. The animal literature is also not unanimous regarding a specific peri-implantitis etiology. However, a correlation between periodontitis and smoking histories was cited as contributing to a higher incidence of peri-implantitis. Conclusion: The available scientific literature is characterized by an absence of a unanimous consensus regarding the etiology of peri-implantitis and its specific relationship to periodontitis. Furthermore, both the choice of the term peri-implantitis and its definition remain controversial. Int J Prosthodont 2014;27:15-25. doi: 10.11607/ijp.3785