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Author: Jou00e3o Carlos Ramos
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Languages : en
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Title Peri-implantitis surgical treatment with implantoplasty: case series Background: Peri-implantitis (PI) has been defined has the presence of radiographic bone loss (RBL)u22653mm and/or probing depth (PD)u22656mm in conjugation with profuse bleeding on probing (BoP). Several surgical treatments have been proposed to treat peri-implantitis but the available evidence does not allow any specific recommendation. Ressective treatment with implantoplasty (IP) allows the decontamination of the infected implant surface. Some clinical studies confirm IP success up to nine years of follow-up.Aim/Hypothesis: To present a 24 months clinical results of peri-implantitis surgical treatment with implantoplasty. Material and Methods (977)Eight patients (17 implants) were diagnosed with peri-implantitis and included in this retrospective case analysis. At baseline the following clinical data were assessed: PD, BoP, suppuration (Sup)(dichotomous) and mucosal recession (MR). After full thickness mucoperiosteal flap and granulation tissue removal implant surface was polished using a sequence of round diamond rotatory burs (200.000 rpm) with the following sequence: blue (40u00b5m) and yellow (15 u00b5m) (Coltu00e8ne/Whaledent AG-Diatech, Switzerland). The final polishing was done with an Arkansas stone. Flaps were repositioned apically and sutured (5/0, Seralonu00ae, Serag-Wiessner, Germany). Sutures were remover at day 15 and controlled every 3 -3 months (1st year) and 6-6 months (2nd year). At 12 and 24 months all clinical data were reassessed. Changes between 0-12 and 12-24 months were analyzed (Wilcoxon test). Statistical analyses used SPSS v24 (SPSS Statistics for Windows, IBM). Significance level of P u2264 .05.Results: There were no clinical complications during the healing period. Implantoplasty allowed the elimination of clinical parameters associated to PI. The clinical parameters at baseline, 12 and 24 months were, respectively: PD (5.16 u00b1 0.47mm/2.81 u00b1 0.36mm/2.83 u00b1 0.50mm), BoP (0.15 u00b1 0.02/0.01 u00b1 0.02/0.02 u00b1 0.01), MR (0.50 u00b1 0.66mm/1.45 u00b1 0.89mm/1.38 u00b1 0.99mm) and Sup (0.01 u00b1 0.01/0.00 u00b1 0.00/0.00 u00b1 0.00).For all clinical parameters than Sup there were statistical significant differences between baseline and 12 months (PD: p=0.012; [2.51; 3.10] / BoP: p=0.011; [0.00; 0.03] / MR: p=0.012; [0.70; 2.19] / Sup: p=0.066; [0.00; 0.00]). No statistical significant differences were found between 12 and 24 months (PD: p=0.389; [2.41; 3.24]/ BoP: p=0.498; [0.01; 0.03]/ MR: p=0.465; [0.56; 2.21]/ Sup: p=1.000; [0.00; 0.00]).None implant was lost.Conclusion and Clinical implications: The clinical signs associated to PI were eliminated by Implantoplasty allowing the pathology stabilization over a period of 24 months. However this method is associated with increased mucosal recession. Itu00b4s fundamental a strict maintenance program.Implantoplasty may be used to eliminate PI. However there are aesthetic considerations to be taken.
Author: Jou00e3o Carlos Ramos
Publisher:
ISBN:
Category :
Languages : en
Pages :
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Title Peri-implantitis surgical treatment with implantoplasty: case series Background: Peri-implantitis (PI) has been defined has the presence of radiographic bone loss (RBL)u22653mm and/or probing depth (PD)u22656mm in conjugation with profuse bleeding on probing (BoP). Several surgical treatments have been proposed to treat peri-implantitis but the available evidence does not allow any specific recommendation. Ressective treatment with implantoplasty (IP) allows the decontamination of the infected implant surface. Some clinical studies confirm IP success up to nine years of follow-up.Aim/Hypothesis: To present a 24 months clinical results of peri-implantitis surgical treatment with implantoplasty. Material and Methods (977)Eight patients (17 implants) were diagnosed with peri-implantitis and included in this retrospective case analysis. At baseline the following clinical data were assessed: PD, BoP, suppuration (Sup)(dichotomous) and mucosal recession (MR). After full thickness mucoperiosteal flap and granulation tissue removal implant surface was polished using a sequence of round diamond rotatory burs (200.000 rpm) with the following sequence: blue (40u00b5m) and yellow (15 u00b5m) (Coltu00e8ne/Whaledent AG-Diatech, Switzerland). The final polishing was done with an Arkansas stone. Flaps were repositioned apically and sutured (5/0, Seralonu00ae, Serag-Wiessner, Germany). Sutures were remover at day 15 and controlled every 3 -3 months (1st year) and 6-6 months (2nd year). At 12 and 24 months all clinical data were reassessed. Changes between 0-12 and 12-24 months were analyzed (Wilcoxon test). Statistical analyses used SPSS v24 (SPSS Statistics for Windows, IBM). Significance level of P u2264 .05.Results: There were no clinical complications during the healing period. Implantoplasty allowed the elimination of clinical parameters associated to PI. The clinical parameters at baseline, 12 and 24 months were, respectively: PD (5.16 u00b1 0.47mm/2.81 u00b1 0.36mm/2.83 u00b1 0.50mm), BoP (0.15 u00b1 0.02/0.01 u00b1 0.02/0.02 u00b1 0.01), MR (0.50 u00b1 0.66mm/1.45 u00b1 0.89mm/1.38 u00b1 0.99mm) and Sup (0.01 u00b1 0.01/0.00 u00b1 0.00/0.00 u00b1 0.00).For all clinical parameters than Sup there were statistical significant differences between baseline and 12 months (PD: p=0.012; [2.51; 3.10] / BoP: p=0.011; [0.00; 0.03] / MR: p=0.012; [0.70; 2.19] / Sup: p=0.066; [0.00; 0.00]). No statistical significant differences were found between 12 and 24 months (PD: p=0.389; [2.41; 3.24]/ BoP: p=0.498; [0.01; 0.03]/ MR: p=0.465; [0.56; 2.21]/ Sup: p=1.000; [0.00; 0.00]).None implant was lost.Conclusion and Clinical implications: The clinical signs associated to PI were eliminated by Implantoplasty allowing the pathology stabilization over a period of 24 months. However this method is associated with increased mucosal recession. Itu00b4s fundamental a strict maintenance program.Implantoplasty may be used to eliminate PI. However there are aesthetic considerations to be taken.
Author: Paolo Morandi
Publisher:
ISBN:
Category :
Languages : en
Pages :
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Background : Peri-implantitis is a biofilm-related disease characterized by tissues inflammation and bone resorption. Despite the absence of accepted protocols, different therapeutic approaches were proposed as non-surgical therapy, access flap, resective and regenerative surgery associated to various decontamination methods of the implant surface. A beneficial effect was nevertheless reported as a result of implantoplasty in association with a resective or regenerative surgical approach.Aim/Hypothesis : The aim of this study was to observe the clinical effects of implantoplasty applied in different surgical approaches as resective surgery and regenerative surgery.Material and Methods : Fifteen patients with peri-implantitis were enrolled during a period of 30 months; the overall number of implants involved was 34. All patients were initially treated with non-surgical therapy in order to decrease peri-implant tissues inflammation and 6-8 weeks later the surgical treatment was performed. The surgical approach was chosen based on the anatomy of the bone defect. In bone defects with limited infra-bone portion (u2264 4mm) and where the peri-implant ostectomy was an acceptable biologic cost for adjacent teeth or implants a resective surgical approach was chosen and implantoplasty was performed on the resulting exposed implant surface. In deep infra bone defects (> 4mm) and in those defects where the resection of bone wouldnu2019t be acceptable a regenerative surgical approach was chosen. Six months after surgery all patients were reevaluated and probing depth, bone level and peri-implant soft tissues inflammation parameters (redness, bleeding-on-probing, swelling) were recorded.Results : Two implants in two different patients treated with a combination of regenerative surgery and implantoplasty failed due to a lack a primary closure after surgery: one was removed 4 months after surgery, the other implant needed a surgical re-entry three weeks and was then dropped out. Six months after surgery all the other implants showed no signs of peri-implant inflammation, probing depths u2264 5 mm and no further radiographic bone resorptions; mean probing depth (PD) gain was 2,27 mm. No negative side effects linked to the dispersion of metal filing were recorded.Conclusion and Clinical implications : The association of implantoplasty and a surgical treatment of peri-implantitis resulted in an improvement of all clinical parameters regarding the peri-implant tissues and could therefore be considered a safe and effective treatment option.
Author: João Carlos Ramos
Publisher:
ISBN:
Category :
Languages : en
Pages : 0
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Title Peri-implantitis surgical treatment with implantoplasty: case series Background: Peri-implantitis (PI) has been defined has the presence of radiographic bone loss (RBL)u22653mm and/or probing depth (PD)u22656mm in conjugation with profuse bleeding on probing (BoP). Several surgical treatments have been proposed to treat peri-implantitis but the available evidence does not allow any specific recommendation. Ressective treatment with implantoplasty (IP) allows the decontamination of the infected implant surface. Some clinical studies confirm IP success up to nine years of follow-up.Aim/Hypothesis: To present a 24 months clinical results of peri-implantitis surgical treatment with implantoplasty. Material and Methods (977)Eight patients (17 implants) were diagnosed with peri-implantitis and included in this retrospective case analysis. At baseline the following clinical data were assessed: PD, BoP, suppuration (Sup)(dichotomous) and mucosal recession (MR). After full thickness mucoperiosteal flap and granulation tissue removal implant surface was polished using a sequence of round diamond rotatory burs (200.000 rpm) with the following sequence: blue (40u00b5m) and yellow (15 u00b5m) (Coltu00e8ne/Whaledent AG-Diatech, Switzerland). The final polishing was done with an Arkansas stone. Flaps were repositioned apically and sutured (5/0, Seralonu00ae, Serag-Wiessner, Germany). Sutures were remover at day 15 and controlled every 3 -3 months (1st year) and 6-6 months (2nd year). At 12 and 24 months all clinical data were reassessed. Changes between 0-12 and 12-24 months were analyzed (Wilcoxon test). Statistical analyses used SPSS v24 (SPSS Statistics for Windows, IBM). Significance level of P u2264 .05.Results: There were no clinical complications during the healing period. Implantoplasty allowed the elimination of clinical parameters associated to PI. The clinical parameters at baseline, 12 and 24 months were, respectively: PD (5.16 u00b1 0.47mm/2.81 u00b1 0.36mm/2.83 u00b1 0.50mm), BoP (0.15 u00b1 0.02/0.01 u00b1 0.02/0.02 u00b1 0.01), MR (0.50 u00b1 0.66mm/1.45 u00b1 0.89mm/1.38 u00b1 0.99mm) and Sup (0.01 u00b1 0.01/0.00 u00b1 0.00/0.00 u00b1 0.00).For all clinical parameters than Sup there were statistical significant differences between baseline and 12 months (PD: p=0.012; [2.51; 3.10] / BoP: p=0.011; [0.00; 0.03] / MR: p=0.012; [0.70; 2.19] / Sup: p=0.066; [0.00; 0.00]). No statistical significant differences were found between 12 and 24 months (PD: p=0.389; [2.41; 3.24]/ BoP: p=0.498; [0.01; 0.03]/ MR: p=0.465; [0.56; 2.21]/ Sup: p=1.000; [0.00; 0.00]).None implant was lost.Conclusion and Clinical implications: The clinical signs associated to PI were eliminated by Implantoplasty allowing the pathology stabilization over a period of 24 months. However this method is associated with increased mucosal recession. Itu00b4s fundamental a strict maintenance program.Implantoplasty may be used to eliminate PI. However there are aesthetic considerations to be taken.
Author: Boyd J. Tomasetti
Publisher: Springer Nature
ISBN: 3030441997
Category : Medical
Languages : en
Pages : 334
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This comprehensive guide to short implants will take the reader through their research and development, explain the clinical indications, evaluate the outcomes achieved with various implants, and explore restorative and laboratory considerations. Short implants have steadily gained greater market share in the last decade as practitioners sought alternatives to traditional length implants in order to avoid grafting procedures. Current manufacturers offer a variety of implant lengths and widths, allowing surgeons and restorative dentists the ability to select the best implant for each clinical circumstance. Cutting edge information is provided on the research and clinical results achieved utilizing a range of implants, specifically those developed by Nobel Biocare, Straumann, Jack Hahn, and Bicon. Readers will also find an extensive description of the role of ultra-short implants involving reconstruction in both cleft patients and cancer patients who have lost portions of their mandible and/or maxilla. This book is a must-have for those interested in learning how the use of short and ultra-short implants offers both surgeons and restorative dentists an opportunity to stand out from those that use only the traditional length implants.
Author: Carrara Clara
Publisher:
ISBN:
Category :
Languages : en
Pages :
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Background and aim: The treatment of peri-implantitis has been challenging in the past years.u2028Non-surgical procedures are considered to be fundamental in the treatment of peri-implant diseases, in order to reduce the inflammatory parameters. However, there is limited evidence on its efficacy in the complete resolution of peri-implantitis and a surgical access may be needed. The aim of this case series was to evaluate the clinical results of a non-surgical treatment protocol that includes supra-mucosal and sub-mucosal decontamination with erythritol powder air polishing, topical doxycycline and chlorhexidine.Materials and methods: A total of 22 implants in 7 patients affected by peri-implantitis were included in the study.u2028Peri-implantitis was defined as probing depth (PD) of at least 5 mm, bleeding on probing and a radiographic bone loss of at least 2 mm. All implants were treated with the following non-surgical protocol. T0: supra-mucosal mechanical debridement with rubber plugs and topical application of chlorhexidine 1% gel, that was repeated by the patients twice a day for 7 days. T1 (7 days after T0): sub-mucosal debridement with teflon curettes and air-polishing with erythritol powder (Air-Flow Powder Plus, eMS, Nyon). T2 (2 days after T1): sub-mucosal application of topical 14% doxycycline gel (Ligosan, Heraeus Kulzer, Hanau) around the infected implant. T3 (2 weeks after T2): second application of topical doxycycline. T4 (6 weeks after T3): re-evaluation. PD, recession, bleeding index (BI), plaque index (PI) and suppuration were recorded at T0, T1, T4. Peri-apical radiographs were taken at T0 and T4. Results: All the included implants had external connection (Nobel Speedy Groovy, Nobel Biocare, Zurich) with a moderately rough surface. In all the treated implants it was possible to remove the prosthesis in order to perform each phase of the treatment.u2028No implant failure were recorded.Considering the totality of the sites, the implants have an average PD of 4.95 mm (SD2.06) at t0, 4.72 mm (SD 2.21) at t1 and 3.57 mm (SD 1.07) at t4. Considering only the sites with PD at t0 greater than 4 mm, an average PD value of 6.10 mm was recorded at t0, 5.72 mm at t1 and 3.52 mm at t4 (Graph 1).The number of implants with suppuration were 13 at t0 and 2 at t4 (Graph 3).u2028In both cases there is a significant difference between the values of PD at t0 and t4 and between t1 and t4 (p0.05). The decrease in BI among t0, t1 and t4 (Graph 2) and the decrease suppuration (Graph 3) between t0-t4 and t1-t4 were statistically significant (p0.05). No significant radiographic bone loss was found in any implant at t4 compared to t0. Conclusion: Within the limitations of the present study, the proposed protocol showed good short-term efficacy, in both reduction of PD and BI, greater than what described in the literature by other non-surgical treatment methods.u2028Further studies with a larger sample and medium and long term results are needed to be able to evaluate its efficacy, better understand possible risk factors and predict the therapy outcome.
Author: Lisa J. A. Heitz-Mayfield
Publisher: Quintessenz Verlag
ISBN: 3868676171
Category : Medical
Languages : en
Pages : 411
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Dental implants are used routinely throughout the world to replace missing teeth. With the broadening of treatment options and an increasing number of clinicians that provide implant therapy, it is important to ensure that the treatment methods used meet the highest clinical standards. The ITI Treatment Guide series is a compendium of evidence-based implant-therapy techniques in daily practice. Written by renowned clinicians and supported by contributions from expert practitioners, the ITI Treatment Guides provide a comprehensive overview of the various indicated treatment options. The management of different clinical situations is discussed with an emphasis on sound diagnostics, evidence-based treatment concepts, and predictable treatment outcomes with minimal risk to the patient. Volume 13 of the ITI Treatment Guide series provides clinicians with the latest evidence-based information on the prevention and management of peri-implant diseases. This information is based in part on the proceedings of the 6th ITI Consensus Conference held in Amsterdam in 2018, as well as on a review of the current literature. Seventeen clinical cases presented by experienced clinicians from all over the world illustrate the diagnosis and treatment of peri-implant diseases.
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A prospective case series was performed to examine the clinical andradiographic changes of peri-implant tissues 2 years after resective treatment ofperi-implantitis, including an apically positioned flap, osteoplasty andimplantoplasty. In total, 25 patients with 40 titanium implants from multiplebrands and advanced peri-implantitis were included in this study. After 2 years,all implants survived, mean probing pocket depth reduced from 8.7mm to3.3mm and bone level remained stable in 92.5% of the implants. Findingssuggest the approach of an apically positioned flap combined with osteoplastyand implantoplasty as an effective and reliable strategy against peri-implantitis.
Author: Maria Elisa Galarraga-Vinueza
Publisher:
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Languages : en
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Several surgical therapies have been proposed to counteract peri-implantitis (PI) and stop the progression of peri-implant bone loss. Implantoplasty has been claimed as a promising strategy to treat peri-implant disease and prevent progressive bone loss. The aim of the present retrospective study is to evaluate the success rate and clinical outcomes of 23 peri-implantitis cases treated through a combined surgical resective/implantoplasty therapy applying a novel u201cplatform switchu201d technique to preserve peri-implant tissues integrity and counteract progressive bone loss in a 2 year follow-up period.23 patients who underwent dental implant therapy, were diagnosed with peri-implantitis, and were treated through access flap surgery, a modified implantoplasty applying a platform switch design, bone recontouring, and surface decontamination. Implantoplasty success rate was determined by radiographic and clinical parameters recorded before and over the 2-year follow-up. Marginal bone loss (MBL) as the primary endpoint, presence of suppuration, pain, mobility, and implant fracture were evaluated through clinical and radiographic analysis before(T0), after the surgical treatment(T1), and after 2-years follow-up(T2). The 2-year follow-up exhibited peri-implant bone stability in 21 cases (91.3%) showing radiographically a MBL reduction(mean) of 0.2mm/SD:0.1 (mesial) and 0.04mm/SD:0.1 (distal). 3(13%) treated implants showed radiographically a mesial bone gain of (1.6 /SD: 0.1mm). Only one implant showed progressive bone loss (4.3%) of 1.5mm (mesial) after the 24-month follow- up, however the implant did not show any other clinical signs or symptoms. One implant was lost after one year of treatment due to mobility, presenting a failure rate of 4.3%. Pain and suppuration were resolved in 22 cases (96%) and none of the cases reported implant fracture or mobility after the modified implantoplasty was performed. Considering there is no u201cgold standardu201d treatment for PI, the relevant 2-year follow-up success rate of combined surgical resective and novel u201cplatform switchu201d implantoplasty therapy shows that this modified technique is promising since it counteracted progressive bone loss and eliminated PI signs and symptoms in more than 90% of the cases. Importantly, this therapy showed bone gain in smoothened surfaces in 13%, which is the desired goal of PI treatment. Consequently, further clinical studies are need to consolidate the efficiency and relevance of this novel technique for PI treatment.
Author: Mario Roccuzzo
Publisher: Quintessenz Verlag
ISBN: 3868675590
Category : Medical
Languages : en
Pages : 503
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Popular demand for dental implants as a reliable long-term option to replace missing teeth has risen dramatically. However, situations remain that pose challenges to practitioners and the treatment process. Written by renowned clinicians and supported by cases contributed by expert practitioners, the present volume of the ITI Treatment Guide series highlights the integration and management of peri-implant soft tissues. It discusses soft-tissue management before and during implant placement and during supportive peri-implant therapy and addresses the techniques and materials used for peri-implant soft-tissue augmentation and replacement and for the treatment of peri-implant soft-tissue dehiscences. Volume 12 of the ITI Treatment Guides series offers clinicians a comprehensive overview of various evidence-based techniques and treatment approaches for use in daily practice, with a focus on current techniques and materials.
Author: Ramanauskaite Ausra
Publisher:
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Languages : en
Pages :
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Clinical outcomes following treatment of peri-implantitis at formerly graftet implant sites.Ramanauskaite A, Becker K, and Schwarz FDepartment of Oral Surgery, Heinrich Heine University, Du00fcsseldorf, GermanyThe aim: This retrospective analysis aimed at comparing the clinical outcomes following nonsurgical and surgical therapy of peri-implantitis at formerly grafted and non-grafted (i.e. pristine) implant sites.M&M: A total of 29 patients with established peri-implantitis (i.e. 27 implants placed at grafted and 19 implants at non-grafted sites) were included. Each subject had received either nonsurgical (i.e. mechanical, Er:YAG laser or photodynamic therapy (PDT)) (grafted sites: 13 implants, non-grafted sites: 4 implants) or combined (i.e. implantoplasty +/- augmentative therapy) surgical (grafted sites: 14 implants, non-grafted sites: 15 implants) treatment procedures at respective implants. A chi - squared test was used to assess whether the initial grafting procedure did affect the treatment outcomes (i.e. disease resolution, bleeding on probing u2013 BOP, probing pocket depths - PD). The mean follow-up period was 176.75u00b1135 weeks.Results: At the patient level, disease resolution (i.e. absence of BOP and PDu22656 mm) following nonsurgical and surgical treatment was obtained in 6/9 (67%) and 5/9 (56%) at grafted and in 2/2 (100%) and 7/12 (58%) at non-grafted sites respectively (p=0.673). BOP reductions following nonsurgical and surgical treatment amounted to 40.09u00b152.02% and 59.19u00b145.68% at grafted and 52.83u00b14.0% and 68.08u00b135.82% at non-grafted sites (p=0.575). PD reductions following nonsurgical and surgical treatment amounted to 1.24u00b12.08 mm and 0.90u00b11.47 mm at grafted and 0.33u00b12.36 mm and 2.0u00b13.14 mm at non-grafted sites (p=0.728). Conclusions: The effectiveness of nonsurgical and surgical treatment of peri-implantitis was comparable at both formerly grafted and non-grafted implant sites.
