Purpose: To present a case report of autogenous transplant of two impacted mandibular canines.
Materials and methods: A 12-year-old girl, with vestibular impaction of mandibular left and right canines had them extracted and transplanted in the anatomically corrected sites, after an unsuccessful orthodontic treatment including surgical exposure.
Results: After 2 years the teeth are stable and their vitality is maintained.
Conclusions: In this case the transplantation of the mandibular canines was successful and maintained the vitality of the transplanted teeth for at least 2 years. By preserving the periodontal ligament is it possible to re-establish a functional tooth unit, which allows a physiologic growth of the jaws.
{"title":"Autogenous transplant of two impacted mandibular canines: a case report with 2-year follow-up.","authors":"Tiziano Testori, Riccardo Scaini, Tommaso Weinstein, Matteo Deflorian, Silvio Taschieri, Massimo Del Fabbro","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Purpose: </strong>To present a case report of autogenous transplant of two impacted mandibular canines.</p><p><strong>Materials and methods: </strong>A 12-year-old girl, with vestibular impaction of mandibular left and right canines had them extracted and transplanted in the anatomically corrected sites, after an unsuccessful orthodontic treatment including surgical exposure.</p><p><strong>Results: </strong>After 2 years the teeth are stable and their vitality is maintained.</p><p><strong>Conclusions: </strong>In this case the transplantation of the mandibular canines was successful and maintained the vitality of the transplanted teeth for at least 2 years. By preserving the periodontal ligament is it possible to re-establish a functional tooth unit, which allows a physiologic growth of the jaws.</p>","PeriodicalId":49259,"journal":{"name":"European Journal of Oral Implantology","volume":"11 2","pages":"227-232"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36136009","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
This section presents a brief review of articles on dental implants considered of special interest for the reader, in order to encourage the developing of research, the interest for data analysis and the attention to scientific publications. Your comments are welcome. Please contact Dr Michele Nieri at michelenieri@gmail.com.
{"title":"Research in focus.","authors":"","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>This section presents a brief review of articles on dental implants considered of special interest for the reader, in order to encourage the developing of research, the interest for data analysis and the attention to scientific publications. Your comments are welcome. Please contact Dr Michele Nieri at michelenieri@gmail.com.</p>","PeriodicalId":49259,"journal":{"name":"European Journal of Oral Implantology","volume":"11 2","pages":"241-242"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36136010","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Valeria Pistilli, Vittorio Checchi, Filippo De Paolis, Roberto Pistilli, Carlo Barausse
Purpose: To present a case of a woman referred for the management of displacement of one implant in her right posterior mandible that had occurred three days previously.
Materials and methods: After implant placement, the practitioner was no longer able to detect the implant and inserted a second one at the same site without taking a control radiograph. At the end of surgery, when a radiograph was finally taken, the first implant appeared displaced into the mandible body. The patient suffered total paresthesia on the right lower lip and chin. A flap was raised and bone osteotomies were performed on the lateral side of the mandible to create a rectangular cortical bone window that was removed. The implant was stuck by the second implant placed coronally, and only after unscrewing this second implant was it possible to remove the first one.
Results: After 18 months, the patient recovered full sensitivity.
Conclusions: In cases of implant displacement, it is always recommended that appropriate radiographs are performed to visualise where the implants could have been displaced in order to avoid more serious consequences.
{"title":"Displacement of a dental implant in the mandible body: an unusual case report.","authors":"Valeria Pistilli, Vittorio Checchi, Filippo De Paolis, Roberto Pistilli, Carlo Barausse","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Purpose: </strong>To present a case of a woman referred for the management of displacement of one implant in her right posterior mandible that had occurred three days previously.</p><p><strong>Materials and methods: </strong>After implant placement, the practitioner was no longer able to detect the implant and inserted a second one at the same site without taking a control radiograph. At the end of surgery, when a radiograph was finally taken, the first implant appeared displaced into the mandible body. The patient suffered total paresthesia on the right lower lip and chin. A flap was raised and bone osteotomies were performed on the lateral side of the mandible to create a rectangular cortical bone window that was removed. The implant was stuck by the second implant placed coronally, and only after unscrewing this second implant was it possible to remove the first one.</p><p><strong>Results: </strong>After 18 months, the patient recovered full sensitivity.</p><p><strong>Conclusions: </strong>In cases of implant displacement, it is always recommended that appropriate radiographs are performed to visualise where the implants could have been displaced in order to avoid more serious consequences.</p>","PeriodicalId":49259,"journal":{"name":"European Journal of Oral Implantology","volume":"11 2","pages":"235-240"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36136011","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Christian M Schmitt, Mayte Buchbender, Rainer Lutz, Friedrich-Wilhelm Neukam
Aim: In this systematic review, we aimed to assess the impact of endosseous implants on the formation of an osteonecrosis of the jaw, as well as implant survival rates for patients under bisphosphonate (BP), antiresorptive and radiation therapy.
Materials and methods: An electronic search was performed using PubMed, Embase, and Medline databases with the logical operators: "dental implant", "antiresorptive", "bisphosphonate", "irradiation", "radiotherapy", "radiation", "necrosis" and "survival". The search was limited to articles published up to 15 December 2016. Recent publications were also searched manually to find any relevant studies that might have been missed using the search criteria noted above. The outcome variables were the implant survival rate and the frequency of osteonecrosis of the jaws.
Results: In total, 18 studies addressing oral implants in patients with BP or antiresorptive therapy and 23 with radiation therapy met the inclusion criteria and were included in this systematic review. Most of the studies had a retrospective design with a level of evidence (LoE) of III (moderately high risk of bias). Implant survival rate ranged from 92.86% to 100% in patients with BP/antiresorptive therapy (all due to osteoporosis) and 38.5% to 97.9% in patients with radiation therapy. For BP patients, osteonecrosis in relation to oral implants more frequently occurred in patients taking BPs due to malignant diseases. In patients with radiation therapy, an "implant triggered" necrosis is also a potential complication. The lack of data in the current literature concerning this issue does not allow a proper risk assessment to date.
Conclusions: Within the limits of this systematic review, implant treatment concepts seem to be a valuable approach in patients with radiation therapy and patients with BP therapy due to an osteoporosis. In patients taking BPs due to a malignant disease, implant treatments are not recommended due to the high number of reported implant-related necrosis in this patient cohort. Outcomes of this review should, however, be regarded with caution due to the low level of evidence of the currently existing data.
{"title":"Oral implant survival in patients with bisphosphonate (BP)/antiresorptive and radiation therapy and their impact on osteonecrosis of the jaws. A systematic review.","authors":"Christian M Schmitt, Mayte Buchbender, Rainer Lutz, Friedrich-Wilhelm Neukam","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Aim: </strong>In this systematic review, we aimed to assess the impact of endosseous implants on the formation of an osteonecrosis of the jaw, as well as implant survival rates for patients under bisphosphonate (BP), antiresorptive and radiation therapy.</p><p><strong>Materials and methods: </strong>An electronic search was performed using PubMed, Embase, and Medline databases with the logical operators: \"dental implant\", \"antiresorptive\", \"bisphosphonate\", \"irradiation\", \"radiotherapy\", \"radiation\", \"necrosis\" and \"survival\". The search was limited to articles published up to 15 December 2016. Recent publications were also searched manually to find any relevant studies that might have been missed using the search criteria noted above. The outcome variables were the implant survival rate and the frequency of osteonecrosis of the jaws.</p><p><strong>Results: </strong>In total, 18 studies addressing oral implants in patients with BP or antiresorptive therapy and 23 with radiation therapy met the inclusion criteria and were included in this systematic review. Most of the studies had a retrospective design with a level of evidence (LoE) of III (moderately high risk of bias). Implant survival rate ranged from 92.86% to 100% in patients with BP/antiresorptive therapy (all due to osteoporosis) and 38.5% to 97.9% in patients with radiation therapy. For BP patients, osteonecrosis in relation to oral implants more frequently occurred in patients taking BPs due to malignant diseases. In patients with radiation therapy, an \"implant triggered\" necrosis is also a potential complication. The lack of data in the current literature concerning this issue does not allow a proper risk assessment to date.</p><p><strong>Conclusions: </strong>Within the limits of this systematic review, implant treatment concepts seem to be a valuable approach in patients with radiation therapy and patients with BP therapy due to an osteoporosis. In patients taking BPs due to a malignant disease, implant treatments are not recommended due to the high number of reported implant-related necrosis in this patient cohort. Outcomes of this review should, however, be regarded with caution due to the low level of evidence of the currently existing data.</p>","PeriodicalId":49259,"journal":{"name":"European Journal of Oral Implantology","volume":"11 Suppl 1 ","pages":"S93-S111"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36395104","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Does it still make sense to believe published scientific literature? Editorial.","authors":"Marco Esposito","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":49259,"journal":{"name":"European Journal of Oral Implantology","volume":"11 1","pages":"5-6"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35929000","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pietro Felice, Carlo Barausse, Valeria Pistilli, Maurizio Piattelli, Daniela Rita Ippolito, Marco Esposito
Purpose: To evaluate whether 6 mm long × 4 mm wide dental implants could be an alternative to implants of at least 10 mm long placed in bone augmented with bone substitutes in posterior atrophic jaws.
Materials and methods: A total of 20 patients with bilateral atrophic mandibles, and 20 patients with bilateral atrophic maxillae, having 5 mm to 7 mm of bone height below the maxillary sinus or 6 mm to 8 mm above the mandibular canal, had their side of the jaws randomly allocated according to a split-mouth design. They were allocated to receive one to three 6 mm long × 4 mm wide implants, or implants of at least 10 mm long in augmented bone by two different surgeons at different centres. Mandibles were vertically augmented with interpositional equine bone blocks and resorbable barriers, and implants were placed 3 months later. Maxillary sinuses were augmented with particulated porcine bone via a lateral window and implants were placed simultaneously. After 4 months, all implants were submerged and loaded with provisional prostheses. Four months later, definitive prostheses were delivered. Outcome measures were prosthesis and implant failures, any complication and radiographic peri-implant marginal bone level changes.
Results: Five patients (three treated in mandibles and two in maxillae) dropped out before the 3-year post-loading follow-up. Two short maxillary implants affected by peri-implantitis failed together with their prosthesis vs three mandibular prostheses that could not be placed on implants at least 10 mm long due to graft failures; one was associated with the loss of three implants because of infection. There were no statistically significant differences in implant (difference in proportions = 0.000; 95% CI: -0.140 to 0.140; P = 1.000) and prosthesis failures (difference in proportions = 0.057; 95% CI: -0.094 to 0.216; P = 0.625). In total, 18 complications occurred in 13 patients at augmented sites vs four complications in three patients with 6 mm long implants. Significantly more complications occurred at grafted sites in mandibles (difference in proportions = 0.353; 95% CI: 0.005 to 0.616; P = 0.031), but not in maxillae (difference in proportions = 0.222; 95% CI: -0.071 to 0.486; P = 0.219). In mandibles, patients with 6 mm long implants lost an average of 1.25 mm of peri-implant bone at 3 years vs 1.54 mm in patients with implants of at least 10 mm long. The difference was statistically significant (mean difference = 0.29 mm; 95% CI: 0.08 to 0.51 mm; P = 0.010). In maxillas, patients with 6 mm-long implants lost an average of 1.28 mm of peri-implant bone at 3 years vs 1.50 mm in patients with implants of at least 10 mm long. The difference was statistically significant (mean difference = 0.22 mm; 95% CI: 0.08 to 0.35 mm; P = 0.003).
Conclusions: Results at 3 years after loading indicate that 6 mm long implants with a conventional diameter of 4
{"title":"Posterior atrophic jaws rehabilitated with prostheses supported by 6 mm long × 4 mm wide implants or by longer implants in augmented bone. 3-year post-loading results from a randomised controlled trial.","authors":"Pietro Felice, Carlo Barausse, Valeria Pistilli, Maurizio Piattelli, Daniela Rita Ippolito, Marco Esposito","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Purpose: </strong>To evaluate whether 6 mm long × 4 mm wide dental implants could be an alternative to implants of at least 10 mm long placed in bone augmented with bone substitutes in posterior atrophic jaws.</p><p><strong>Materials and methods: </strong>A total of 20 patients with bilateral atrophic mandibles, and 20 patients with bilateral atrophic maxillae, having 5 mm to 7 mm of bone height below the maxillary sinus or 6 mm to 8 mm above the mandibular canal, had their side of the jaws randomly allocated according to a split-mouth design. They were allocated to receive one to three 6 mm long × 4 mm wide implants, or implants of at least 10 mm long in augmented bone by two different surgeons at different centres. Mandibles were vertically augmented with interpositional equine bone blocks and resorbable barriers, and implants were placed 3 months later. Maxillary sinuses were augmented with particulated porcine bone via a lateral window and implants were placed simultaneously. After 4 months, all implants were submerged and loaded with provisional prostheses. Four months later, definitive prostheses were delivered. Outcome measures were prosthesis and implant failures, any complication and radiographic peri-implant marginal bone level changes.</p><p><strong>Results: </strong>Five patients (three treated in mandibles and two in maxillae) dropped out before the 3-year post-loading follow-up. Two short maxillary implants affected by peri-implantitis failed together with their prosthesis vs three mandibular prostheses that could not be placed on implants at least 10 mm long due to graft failures; one was associated with the loss of three implants because of infection. There were no statistically significant differences in implant (difference in proportions = 0.000; 95% CI: -0.140 to 0.140; P = 1.000) and prosthesis failures (difference in proportions = 0.057; 95% CI: -0.094 to 0.216; P = 0.625). In total, 18 complications occurred in 13 patients at augmented sites vs four complications in three patients with 6 mm long implants. Significantly more complications occurred at grafted sites in mandibles (difference in proportions = 0.353; 95% CI: 0.005 to 0.616; P = 0.031), but not in maxillae (difference in proportions = 0.222; 95% CI: -0.071 to 0.486; P = 0.219). In mandibles, patients with 6 mm long implants lost an average of 1.25 mm of peri-implant bone at 3 years vs 1.54 mm in patients with implants of at least 10 mm long. The difference was statistically significant (mean difference = 0.29 mm; 95% CI: 0.08 to 0.51 mm; P = 0.010). In maxillas, patients with 6 mm-long implants lost an average of 1.28 mm of peri-implant bone at 3 years vs 1.50 mm in patients with implants of at least 10 mm long. The difference was statistically significant (mean difference = 0.22 mm; 95% CI: 0.08 to 0.35 mm; P = 0.003).</p><p><strong>Conclusions: </strong>Results at 3 years after loading indicate that 6 mm long implants with a conventional diameter of 4 ","PeriodicalId":49259,"journal":{"name":"European Journal of Oral Implantology","volume":"11 2","pages":"175-187"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36136985","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Purpose: To evaluate the effect of sub-mucosal mechanical instrumentation following supra-mucosal plaque removal in the treatment of peri-implant mucositis.
Materials and methods: A total of 44 patients, 27 from a specialist clinic in Sweden, and 17 from a Japanese one, were included. The 44 patients had a total of 175 implants of which 84 (48%) had clinical signs of mucositis (bleeding on probing [BoP]) and no radiographic bone loss. At baseline, the 44 patients received professional supra-mucosal plaque removal and oral hygiene instruction and motivation. Following the 1-month examination, sub-mucosal instrumentation was initiated using ultrasonic and hand instruments. Patients were then examined at 4 and 7 months. Presence of plaque, marginal bleeding, BoP and probing pocket depth (PPD) changes were recorded at each examination in an unblinded manner.
Results: One month following supra-mucosal plaque removal, the number of treated implants with BoP was reduced from 84 to 44 (48% reduction) with a concomitant decrease of the mean PPD of 0.6 mm (95% CI: -0.5 to -0.7), from 4.4 ± 1.0 mm (mean ± SD) to 3.8 ± 1.0 mm, P < 0.0001. Following sub-mucosal instrumentation, a further reduction of 9% (from 44% to 36%) of BoP was recorded, with a concomitant reduction of the mean PPD of 0.3 mm (95% CI: -0.1 to -0.4) at the 7-month examination.
Conclusions: The improvement of the clinical condition (absence of marginal bleeding, BoP and PPD reduction at treated implants) following non-surgical treatment of mucositis appeared to be in great part because of supra-mucosal plaque removal, while the sub-mucosal instrumentation seemed to have only a minor additional effect. Deep implant position compared to neighbouring teeth/implant was associated with persisting mucositis following treatment. The presence of deep pockets following treatment was associated with BoP, screw-retained prostheses without abutment and sub-mucosal crown margins.
目的:评价粘膜上斑块去除后粘膜下机械器械在种植体周围粘膜炎治疗中的效果。材料与方法:共纳入44例患者,其中27例来自瑞典一家专科诊所,17例来自日本一家专科诊所。44例患者共植入175个种植体,其中84例(48%)有黏膜炎的临床症状(探查出血[BoP]),无影像学骨质流失。在基线时,44名患者接受了专业的粘膜上菌斑清除和口腔卫生指导和激励。检查1个月后,开始使用超声和手动仪器进行粘膜下仪器检查。然后在4个月和7个月时对患者进行检查。在每次检查中以非盲方式记录斑块、边缘出血、防喷器和探测袋深度(PPD)的变化。结果:粘膜上斑块去除1个月后,BoP处理的种植体数量从84个减少到44个(减少48%),同时平均PPD下降0.6 mm (95% CI: -0.5至-0.7),从4.4±1.0 mm (mean±SD)下降到3.8±1.0 mm, P < 0.0001。在粘膜下检查后,记录到BoP进一步降低9%(从44%降至36%),同时在7个月的检查中,PPD平均降低0.3 mm (95% CI: -0.1至-0.4)。结论:非手术治疗粘膜炎后临床状况的改善(无边缘出血,治疗后种植体BoP和PPD降低)似乎在很大程度上是因为粘膜上斑块的清除,而粘膜下内固定似乎只有很小的额外效果。与邻近牙齿/种植体相比,深层种植体的位置与治疗后持续的黏膜炎有关。治疗后出现的深囊与BoP、无基台的螺钉保留假体和粘膜下冠缘有关。
{"title":"Non-surgical mechanical treatment of peri-implant mucositis: the effect of sub-mucosal mechanical instrumentation following supra-mucosal plaque removal. A 7-month prospective single cohort study.","authors":"Giovanni Serino, Masahiro Wada","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Purpose: </strong>To evaluate the effect of sub-mucosal mechanical instrumentation following supra-mucosal plaque removal in the treatment of peri-implant mucositis.</p><p><strong>Materials and methods: </strong>A total of 44 patients, 27 from a specialist clinic in Sweden, and 17 from a Japanese one, were included. The 44 patients had a total of 175 implants of which 84 (48%) had clinical signs of mucositis (bleeding on probing [BoP]) and no radiographic bone loss. At baseline, the 44 patients received professional supra-mucosal plaque removal and oral hygiene instruction and motivation. Following the 1-month examination, sub-mucosal instrumentation was initiated using ultrasonic and hand instruments. Patients were then examined at 4 and 7 months. Presence of plaque, marginal bleeding, BoP and probing pocket depth (PPD) changes were recorded at each examination in an unblinded manner.</p><p><strong>Results: </strong>One month following supra-mucosal plaque removal, the number of treated implants with BoP was reduced from 84 to 44 (48% reduction) with a concomitant decrease of the mean PPD of 0.6 mm (95% CI: -0.5 to -0.7), from 4.4 ± 1.0 mm (mean ± SD) to 3.8 ± 1.0 mm, P < 0.0001. Following sub-mucosal instrumentation, a further reduction of 9% (from 44% to 36%) of BoP was recorded, with a concomitant reduction of the mean PPD of 0.3 mm (95% CI: -0.1 to -0.4) at the 7-month examination.</p><p><strong>Conclusions: </strong>The improvement of the clinical condition (absence of marginal bleeding, BoP and PPD reduction at treated implants) following non-surgical treatment of mucositis appeared to be in great part because of supra-mucosal plaque removal, while the sub-mucosal instrumentation seemed to have only a minor additional effect. Deep implant position compared to neighbouring teeth/implant was associated with persisting mucositis following treatment. The presence of deep pockets following treatment was associated with BoP, screw-retained prostheses without abutment and sub-mucosal crown margins.</p>","PeriodicalId":49259,"journal":{"name":"European Journal of Oral Implantology","volume":"11 4","pages":"455-466"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36750755","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Marzio Todisco, Luca Sbricoli, Daniela Rita Ippolito, Marco Esposito
Purpose: To compare the clinical outcome (in particular of marginal peri-implant bone level changes) between immediately loaded straight implants which had definitive abutments placed at implant placement and never removed versus implants which had no intermediate abutments.
Materials and methods: Thirty-two edentulous patients had one of their jaws rehabilitated with a provisional screw-retained resin reinforced cross-arch fixed prosthesis supported by four immediately loaded implants: two central straight implants and two either tilted or straight distal implants. The two central straight implants were randomly allocated in two equal groups to receive or not an intermediate abutment (Multi-Unit Abutment, MUA) according to a parallel group design. To be immediately loaded implants had to be inserted with a minimum torque of 30 Ncm, which was achieved by all implants. After 4 months, definitive screw-retained metal-ceramic prostheses were delivered and patients were followed-up to 5 years after loading. Prostheses were removed every 8 months to facilitate professionally delivered maintenance. Outcome measures were prosthesis and implant failures, complications, peri-implant marginal bone level changes and bleeding on probing (BoP).
Results: Five-years after loading one patient dropped out from each group. No implant or prosthetic failure occurred. Three patients of the abutment group versus one of the no-abutment group were affected by complications (risk difference = 0.125; 95% CI: -0.13 to 0.37; Fisher exact test, P = 0.600). At 5 years, both groups lost marginal bone in a statistically significant way (0.32 ± 0.40 mm for patients of the abutment group and 0.35 ± 0.29 mm for patients of the no-abutment group), with no difference in bone loss between groups at patient levels (difference = 0.03 mm; 95% CI: -0.23 to 0.29 mm; P = 0.809). At 5 years, BoP was significantly higher in the no-abutment group than in the abutment group (difference between medians = 25%; 95% CI: 12.5% to 25%; P < 0.001). By considering only the average of the two central study implants per patient with and without intermediate abutments, there were no differences in bone loss (difference: -0.05 mm; 95% CI: -0.41 to 0.31 mm; P = 0.763), while marginal bleeding was significantly higher in the no-abutment group (difference between medians = 25%; 95% CI: 0% to 50%; P = 0.004).
Conclusions: The present results suggest that intermediate abutments may not be needed at immediately loaded cross-arch screw-retained prostheses, unless there is the necessity to correct implant angulation.
{"title":"Do we need abutments at immediately loaded implants supporting cross-arch fixed prostheses? Results from a 5-year randomised controlled trial.","authors":"Marzio Todisco, Luca Sbricoli, Daniela Rita Ippolito, Marco Esposito","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Purpose: </strong>To compare the clinical outcome (in particular of marginal peri-implant bone level changes) between immediately loaded straight implants which had definitive abutments placed at implant placement and never removed versus implants which had no intermediate abutments.</p><p><strong>Materials and methods: </strong>Thirty-two edentulous patients had one of their jaws rehabilitated with a provisional screw-retained resin reinforced cross-arch fixed prosthesis supported by four immediately loaded implants: two central straight implants and two either tilted or straight distal implants. The two central straight implants were randomly allocated in two equal groups to receive or not an intermediate abutment (Multi-Unit Abutment, MUA) according to a parallel group design. To be immediately loaded implants had to be inserted with a minimum torque of 30 Ncm, which was achieved by all implants. After 4 months, definitive screw-retained metal-ceramic prostheses were delivered and patients were followed-up to 5 years after loading. Prostheses were removed every 8 months to facilitate professionally delivered maintenance. Outcome measures were prosthesis and implant failures, complications, peri-implant marginal bone level changes and bleeding on probing (BoP).</p><p><strong>Results: </strong>Five-years after loading one patient dropped out from each group. No implant or prosthetic failure occurred. Three patients of the abutment group versus one of the no-abutment group were affected by complications (risk difference = 0.125; 95% CI: -0.13 to 0.37; Fisher exact test, P = 0.600). At 5 years, both groups lost marginal bone in a statistically significant way (0.32 ± 0.40 mm for patients of the abutment group and 0.35 ± 0.29 mm for patients of the no-abutment group), with no difference in bone loss between groups at patient levels (difference = 0.03 mm; 95% CI: -0.23 to 0.29 mm; P = 0.809). At 5 years, BoP was significantly higher in the no-abutment group than in the abutment group (difference between medians = 25%; 95% CI: 12.5% to 25%; P < 0.001). By considering only the average of the two central study implants per patient with and without intermediate abutments, there were no differences in bone loss (difference: -0.05 mm; 95% CI: -0.41 to 0.31 mm; P = 0.763), while marginal bleeding was significantly higher in the no-abutment group (difference between medians = 25%; 95% CI: 0% to 50%; P = 0.004).</p><p><strong>Conclusions: </strong>The present results suggest that intermediate abutments may not be needed at immediately loaded cross-arch screw-retained prostheses, unless there is the necessity to correct implant angulation.</p>","PeriodicalId":49259,"journal":{"name":"European Journal of Oral Implantology","volume":"11 4","pages":"397-407"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36750850","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Purpose: To compare the outcome of immediately loaded and one-stage conventionally loaded variable-thread tapered implants in the posterior maxilla.
Materials and methods: This study was designed as a split-mouth randomised controlled trial. Twenty-six patients missing teeth bilaterally in the posterior maxilla received three to four implants in each of the posterior sextants. Bone quality was recorded based on Misch criteria (D1-D4) and insertion torque values were measured using a manual wrench. The implants on one side were immediately loaded with a temporary resin fixed partial denture on definitive multi-unit abutments. The implants in the contralateral side received definitive multi-unit abutments according to the one-stage unloaded protocol. Three to 3.5 months following implant placement, the implants were restored with metal-ceramic fixed prostheses. Outcome measures were implant and prosthesis failure rates, complications, and peri-implant bone level changes at 1 year following delivery of the definitive prostheses.
Results: Two patients dropped out prior to the delivery of definitive prostheses. Four implants supporting a four-unit immediately loaded prosthesis failed in one patient, 3 months following delivery of the definitive prostheses. None of the conventionally loaded implants or prostheses failed. There were no significant differences in the proportions of implant and prosthesis failures (difference = 4.2%; 95% CI -4.2 to 12.6%; P = 0.999). In the immediately loaded group, four early prosthetic complications occurred during the provisionalization phase (three small resin chippings and one prosthetic screw loosening). No other complications were reported. The difference in the rate of complications between the two interventions was not statistically significant (difference = 16.7%; 95% CI -1.2% to 35.6%; P = 0.125). The 1-year peri-implant marginal bone level changes were evaluated in 23 patients (77 immediately loaded and 76 conventionally loaded implants). On average, patients lost 0.42 mm at the immediately loaded and 0.46 mm at the conventionally loaded implants, the difference being statistically not significant (difference = 0.044 mm; 95% CI -0.27 to 0.18 mm; P = 0.701).
Conclusions: Immediate loading of 3- to 4-unit fixed partial prostheses supported by variable-thread implants in the posterior maxilla can yield good and similar 1-year results to one-stage conventionally loaded implants.
目的:比较即刻加载和一期常规加载可变螺纹锥形种植体在上颌骨后牙的效果。材料与方法:本研究采用裂口随机对照试验。26例双侧后上颌缺牙的患者在每个后六分体上接受了三到四个种植体。根据Misch标准(D1-D4)记录骨质量,使用手动扳手测量插入扭矩值。一侧种植体即刻在确定多单元基牙上装载临时树脂固定局部义齿。对侧种植体根据一期卸载方案接受确定的多单元基台。种植体放置后3 ~ 3.5个月,用金属-陶瓷固定假体修复种植体。结果测量是种植体和假体的失败率、并发症和植入假体后1年的种植体周围骨水平变化。结果:2例患者在最终义肢交付前退出。在最终假体交付3个月后,1例患者4个种植体支持4个单元立即加载的假体失败。没有一个传统的植入物或假体失败。种植体和假体失败的比例差异无统计学意义(差异= 4.2%;95% CI -4.2至12.6%;P = 0.999)。即刻加载组在预备阶段发生了4例早期假体并发症(3例小树脂碎裂和1例假体螺钉松动)。无其他并发症报道。两种干预措施的并发症发生率差异无统计学意义(差异= 16.7%;95% CI -1.2%至35.6%;P = 0.125)。对23例患者(77例即刻加载,76例常规加载)1年内种植体周围边缘骨水平变化进行了评估。即刻加载组患者平均损失0.42 mm,常规加载组患者平均损失0.46 mm,差异无统计学意义(差异= 0.044 mm;95% CI -0.27 ~ 0.18 mm;P = 0.701)。结论:上颌后牙即刻加载3- 4单元固定部分假体与一期常规加载假体相比,可获得良好且相似的1年效果。
{"title":"Immediate vs conventional loading of variable-thread tapered implants supporting three- to four-unit fixed partial dentures in the posterior maxilla: 1-year interim results of a split-mouth randomised controlled trial.","authors":"Habib Abi-Aad, Fadi Daher, Hani Dimassi, Giampiero Cordioli, Zeina Majzoub","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Purpose: </strong>To compare the outcome of immediately loaded and one-stage conventionally loaded variable-thread tapered implants in the posterior maxilla.</p><p><strong>Materials and methods: </strong>This study was designed as a split-mouth randomised controlled trial. Twenty-six patients missing teeth bilaterally in the posterior maxilla received three to four implants in each of the posterior sextants. Bone quality was recorded based on Misch criteria (D1-D4) and insertion torque values were measured using a manual wrench. The implants on one side were immediately loaded with a temporary resin fixed partial denture on definitive multi-unit abutments. The implants in the contralateral side received definitive multi-unit abutments according to the one-stage unloaded protocol. Three to 3.5 months following implant placement, the implants were restored with metal-ceramic fixed prostheses. Outcome measures were implant and prosthesis failure rates, complications, and peri-implant bone level changes at 1 year following delivery of the definitive prostheses.</p><p><strong>Results: </strong>Two patients dropped out prior to the delivery of definitive prostheses. Four implants supporting a four-unit immediately loaded prosthesis failed in one patient, 3 months following delivery of the definitive prostheses. None of the conventionally loaded implants or prostheses failed. There were no significant differences in the proportions of implant and prosthesis failures (difference = 4.2%; 95% CI -4.2 to 12.6%; P = 0.999). In the immediately loaded group, four early prosthetic complications occurred during the provisionalization phase (three small resin chippings and one prosthetic screw loosening). No other complications were reported. The difference in the rate of complications between the two interventions was not statistically significant (difference = 16.7%; 95% CI -1.2% to 35.6%; P = 0.125). The 1-year peri-implant marginal bone level changes were evaluated in 23 patients (77 immediately loaded and 76 conventionally loaded implants). On average, patients lost 0.42 mm at the immediately loaded and 0.46 mm at the conventionally loaded implants, the difference being statistically not significant (difference = 0.044 mm; 95% CI -0.27 to 0.18 mm; P = 0.701).</p><p><strong>Conclusions: </strong>Immediate loading of 3- to 4-unit fixed partial prostheses supported by variable-thread implants in the posterior maxilla can yield good and similar 1-year results to one-stage conventionally loaded implants.</p>","PeriodicalId":49259,"journal":{"name":"European Journal of Oral Implantology","volume":"11 3","pages":"337-350"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36514162","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}