Immediately loaded CAD-CAM manufactured fixed complete dentures using flapless implant placement procedures: A cohort study of consecutive patients

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Statement of problem

Data available regarding the treatment outcome for completely edentulous jaws by means of a prefabricated fixed complete denture placed immediately after flapless implant insertion using a surgical guide are only short term.

Purpose

The purpose of this study was to follow the survival of implants inserted in completely edentulous jaws using a flapless procedure and immediately loaded with prefabricated fixed complete dentures for several years. A second purpose was to investigate whether there is a difference in marginal bone remodeling in smoking (S) and nonsmoking (NS) patients.

Material and methods

During a 5-year period (mean time of follow-up 2.2 years), 30 consecutive patients, 12 women, 38–74 years of age (average 56 years) were treated for complete edentulism in 1 arch in the Department of Periodontology at the University Hospitals in Leuven. The S group included 13 and the NS group 17 patients. Descriptive statistics were used to analyze the data. Two outcome parameters were analyzed: the cumulative survival rate (CSR) of individual implants and the marginal bone remodeling for up to 5 years in the 2 groups.

Results

Nine (4.9%) implants failed. Eight of the failures occurred in 3 smoking patients. The absolute survival rate for all patients was 95%, while the cumulative survival rate (CSR) after 5 years was 91.5%. For the NS group, the CSR was 98.9%, while for the S it was 81.2%. The mean marginal bone resorption was - 2.6 and - 1.2 mm in the S and NS groups, respectively.

Conclusions

The present findings indicate that the treatment protocol described results in good implant survival rate even after several years. Smoking may eventually compromise the efficacy of this treatment concept.

Section snippets

Material and methods

All patients with at least 1 completely edentulous arch who sought rehabilitation with an implant-supported fixed complete denture were considered as possible candidates. The decision for immediate loading of implants, inserted by flapless surgery, using a prefabricated metal and acrylic resin fixed complete denture was made on the basis of medical (to interrupt anticoagulant therapy only once), psychological (fear of surgery), and social (significant scheduling constraints) considerations but

Results

Patients were followed up to a 5-year period with a mean follow-up time of 2.2 years. In 30 consecutive patients, a total of 212 implants were placed. The implant lengths varied between 8.5 and 15 mm and implant diameters were 3.75 (n= 201), 4 (n=3), or 5 mm (n=8). Four patients (29 implants) did not return for further evaluation after initial treatment completion. Thus data for the remaining 26 patients for a total of 183 implants were analyzed. However, when reached by phone all 4 patients

Discussion

Immediate loading seems to be a reasonable alternative to the classical, 2-stage, thoroughly documented protocol. In the present study, a key element to success may be the immediate and rigid connection of the implants by using an acrylic resin and metal fixed complete denture. When excess micromovement occurs, stem cells in the osseous wound differentiate to fibroblasts to form scar tissue around the implant inhibiting osseointegration.11

The present study reports medium term observations in

Conclusions

The use of a prefabricated custom-fit fixed complete denture supported by implants for the completely edentulous patient over 5 years demonstrated similar results for the same implant-supported prosthetic treatment but with delayed loading. Smoking may reduce the favorable outcome but the limited series reported requires further confirmation.

Acknowledgments

The authors thank all referring dentists especially from the Department of Prosthetic Dentistry, who performed the prosthetic treatment of the patients. We also thank Dr Matts Andersson and Izidor Brajnovic of Nobel Biocare for their assistance.

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    This research was partially financed by Nobel Biocare.

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