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- Xhanari, E., et al.
(författare)
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CRESTAL VERSUS LATERAL SINUS LIFT: ONE-YEAR RESULTS FROM A WITHIN- PATIENT RANDOMISED CONTROLLED TRIAL OPEN
- 2019
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Ingår i: Clinical Trials in Dentistry. ; 2019:1, s. 67-78
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Tidskriftsartikel (refereegranskat)abstract
- PURPOSE. To compare the effectiveness of and patient preference for crestal versus la- teral sinus lift. MATERIALS AND METHODS. Fifteen partially edentulous patients missing bilateral maxillary molars and/or premolars and having 2 to 6 mm of residual crestal height below the maxillary sinuses were randomised to receive one to three implants placed in sinuses crestally or laterally lifted with bone substitutes according to a split-mouth design. Implants were submerged and loaded after 6 months with definitive screw-retained metal-ceramic prostheses, and patients were followed-up to 1 year after loading. RESULTS. Twenty crestal implants were placed versus 23 lateral ones. One patient drop- ped out and one lateral implant failed (n = 14; difference = 0.07, 95% CI from -0.28 to 0.13; P = 0.99). No prosthesis failed. Three patients were affected by three complications at crestal versus three patients by four complications at lateral sites. The difference was not statistically significant (n = 14; Diff = 0.07; 95% CI -0.24 to 0.38; P-value = 0.99). Statistically significantly less time was required to place crestal implants (28.2 versus 62.2 minutes on average; Diff = 33.4; SD = 12.1; 95% CI -40.4 to 26.4; P = 0.001). Eight patients preferred the crestal procedure and six had no preference. Crestal implants lost 0.99 mm (SD = 0.55) of peri-implant bone height versus 1.02 mm (SD = 0.57) for lateral ones, the difference being not statistically significant (0.03 mm; 95% CI of difference -0.52 to 0.59; P = 0.89) CONCLUSIONS. Both techniques produced successful outcomes, but the crestal technique required less surgical time and was preferred by patients.
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| 2. |
- Esposito, Marco, 1965, et al.
(författare)
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MACHINED VERSUS CAST ABUTMENTS FOR DENTAL IMPLANTS: A 1-YEAR WITHIN-PATIENT MULTICENTRE RANDOMIZED CONTROLLED TRIAL ASSESSING MARGINAL SEAL CAPACITY AND OUTCOMES
- 2021
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Ingår i: Clinical Trials in Dentistry. - 2784-9015. ; 3:2, s. 19-31
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Tidskriftsartikel (refereegranskat)abstract
- PURPOSE To compare clinical outcomes of machined titanium abutments (machined group) versus cast cobalt-chrome abutments (cast group) and to evaluate in vitro their implant fit. MATERIALS AND METHODS This study comprised two parts. In the in vitro part, the im-plant–abutment fit of 5 cast abutments and 5 machined abutments screwed on with a torque of 30 Ncm was qualitatively and quantitatively evaluated using micro-computed tomography (µ-CT) and AgNO3 to reveal connection gaps. In the clinical part, 31 partially edentulous subjects received two single non-adjacent implant-supported crowns at three centres. At impression taking, three and a half months after implant placement, implants were randomized to receive a machined or cast abutment according to a wi-thin-patient study design. Unfortunately, four patients dropped out and one patient lost one implant before randomization, so only 26 patients had their implants randomized. Outcome measures were: prosthesis and implant failures, any complications, and radiographic peri-implant marginal bone level changes. Patients were followed up to 1 year after loading. RESULTS The fit of the implant–abutment connection was assessed in vitro using µ-CT scans. No gaps were revealed at any of the machined or cast abutments tested. In the clinical part, after randomization, three patients dropped out, no implant failed, but one crown on a cast abutment was replaced. The between-group difference in prosthesis failure was not statistically different (McNemar chi-square test P = 1.0; difference in proportions = 0.039). One complication occurred in each group, the difference not being statistically different (McNemar test P = 1.000; difference in proportions = 0; 95% CI 0.06 to 15.99). Both groups presented statistically significant peri-implant marginal bone loss from implant placement to 1 year after loading, respectively-0.76 ± 1.01 mm for machined and-0.69 ± 0.82 mm for cast abutments, with no statistically significant differences between the two groups (mean difference 0.07 mm; 95% CI-0.54 to 0.67; P = 0.828). Both groups gradually lost marginal peri-implant bone from loading to 1 year after loading but this was not significantly different, respectively-0.06 ± 0.56 mm for machined and-0.10 ± 0.29 mm for cast abutments, with no statistically significant differences between the two groups (P = 0.739; mean difference 0.07 mm; 95% CI-0.12 to 0.16; P = 0.739). CONCLUSIONS Our clinical data suggests that implant prognosis up to 1 year after loading is not affected by using machined or cast abutments. In support of these findings, in vitro analysis proved that both types of abutments allow a tight fit with no gaps. The-refore, for the time being dentists should feel free to choose whichever type they prefer. However, these preliminary results need to be confirmed by larger trials with at least 10 years of follow-up.
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| 3. |
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| 4. |
- Tallarico, M., et al.
(författare)
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Computer-guided vs freehand placement of immediately loaded dental implants: 5-year postloading results of a randomised controlled trial
- 2018
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Ingår i: European Journal of Oral Implantology. - 1756-2406. ; 11:2, s. 203-213
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Tidskriftsartikel (refereegranskat)abstract
- Purpose: To compare planning and patient rehabilitation using 3D implant planning software and dedicated surgical templates with conventional freehand implant placement for the rehabilitation of partially or fully edentulous patients using flapless or mini-flap procedures and immediate loading. Materials and methods: Patients requiring at least two implants to be restored with a single prosthesis, having at least 7 mm of bone height and 4 mm in bone width were consecutively enrolled. Patients were randomised according to a parallel group study design into two groups: computerguided group or conventional freehand group. Implants were loaded immediately with a provisional prosthesis, replaced by a definitive prosthesis 4 months later. Outcome measures assessed by a blinded independent assessor were: implant and prosthesis failures, any complications, marginal bone levels, number of treatment sessions, duration of treatment, post-surgical pain and swelling, consumption of pain killers, surgical and prosthetic time, time required to solve complications, and patient satisfaction. Patients were followed up to 5 years after loading. Results: Ten patients (32 implants) were randomised to the computer-guided group and 10 patients (30 implants) were randomised to the freehand group. At the 5-year follow-up examination one patient of the computer-guided group and one of the freehand group dropped-out (both moved to another country). No prostheses failed during the entire follow-up. Two implants failed in the conventional group (6.6%) vs none in the computer-guided group (P = 0.158). Ten patients (five in each group) experienced 11 complications (six in the computer-guided group and five in the freehand group), that were successfully solved. Differences between groups for implant failures and complications were not statistically significant. Five years after loading, the mean marginal bone loss was 0.87 mm ± 0.40 (95% CI: 0.54 to 1.06 mm) in the computer-guided group and 1.29 mm ± 0.31 (95% CI: 1.09 to 1.51 mm) in the freehand group. The difference was statistically significant (difference 0.42 mm ± 0.54; 95% CI: 0.05 to 0.75; P = 0.024). Patient self-reported post-surgical pain (P = 0.037) and swelling (P = 0.007) were found to be statistically significant higher in patients in the freehand group. Number of sessions from patient's recruitment to delivery of the definitive prosthesis, number of days from the initial CBCT scan to implant placement, consumption of painkillers, averaged surgical, prosthetic, and complication times, were not statistically significant different between the groups. At the 5-year followup, all the patients were fully satisfied with the function and aesthetics of their definitive prostheses. Conclusions: Both approaches achieved successful results over the 5-year follow-up period. Statistically higher post-operative pain and swelling were experienced at sites treated freehand with flap elevation. Less marginal bone loss (0.4 mm) was observed in the computer-guided group, at 5 years follow-up. © Quintessenz.
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