Prevalence, risk indicators, and clinical characteristics of peri-implant mucositis and peri-implantitis for an internal conical connection implant system: A multicenter cross-sectional study.

BACKGROUND: Peri-implant disease prevalence is associated with a multifactorial etiology and distinct clinical characteristics of inflammation. METHODS: The present study aimed to assess the prevalence of peri-implant diseases, identify related risk indicators, and associate specific clinical characteristics to peri-implant biological complications in the medium term. Peri-implant diseases were classified according to established case criteria. Patients' data, implant and/or prosthetic features, and maintenance records were collected. Clinical characteristics such as bleeding on probing (BOP), suppuration (SUPP), keratinized mucosa (KM), probing depth (PD), marginal recession (MR), and modified plaque index (mPI) were recorded. RESULTS: Ninety-nine patients with 266 implants with a mean functional duration of 30.26 months were evaluated. Peri-implant mucositis and peri-implantitis prevalence totaled to 49.5% and 15.15% (patient level), respectively. Peri-implant mucositis was associated with osteoporosis (odds ratio [OR] 6.09), age (OR 0.97), diabetes mellitus (OR 3.09), cemented-retained prosthesis (OR 3.81), and partial prosthesis (OR 2.21). Peri-implantitis was associated with osteoporosis (OR 7.74) and periodontitis (OR 2.74), cemented prosthesis (OR 10.12), partial and full arch prostheses (OR 12.35 and 19.86), implant diameter (OR 3.64), abutment transmucosal height (OR 3.39), and hygiene difficulty (OR 3.14). Furthermore, mPI score 3 (OR 3.27) and PD scores (OR 1.64) were associated with peri-implant mucositis, while mPI score 3 (OR 16.42), KM (OR 1.53), PD (OR 1.81), MR (OR 2.61), and the relationship between KM and PD (OR 0.63) were associated with peri-implantitis. CONCLUSION: In the medium term, peri-implant diseases were correlated with factors inherent to the patient's conditions, presurgical treatment plan, and hygiene maintenance care. The knowledge of the mentioned factors and featured clinical characteristics can be crucial for disease prevention and establishment of a superior implant therapy prognosis.

Clinical and Radiographic Outcomes of Resective Surgery with Adjunctive Implantoplasty Over a 6- to 11-Year Follow-up: A Case Series.

OBJECTIVES: The aim of the present case series is to exhibit the long-term clinical and radiographic outcomes of resective surgery with adjunctive implantoplasty over a 6-to-11-year follow-up. MATERIALS AND METHODS: Four patients presenting 4 implants diagnosed with peri-implantitis according a to an established case definition were included in the present case series. Subjects underwent resective surgery, a modified implantoplasty approach, and implant surface decontamination. Clinical and radiographic outcomes such as bleeding on probing (BOP), suppuration on probing (SoP), probing depth (PD), marginal recession (MR), modified plaque index (mPI), and marginal bone levels (MBL) were recorded over a long-term following surgical therapy. RESULTS: Over 6-to-11-year follow-up, mean BOP, PD, and SoP scores amounted to 17 ±24%, 2.5 ±1.26 mm, and 0%, respectively. BOP scores were reduced in 17%, PD values in 2.5mm, and SoP scores in 100%. Radiographic analysis revealed a mean radiographic bone gain of 3.1 ± 1.84 mm. Peri-implant marginal bone loss surface area decreased by 5.7±3.77mm2 over the long-term follow-up. CONCLUSION: Resective therapy with adjunctive implantoplasty promoted favorable clinical and radiographic outcomes at peri-implantitis treated sites over a long-term period. CLINICAL RELEVANCE: Diverse surgical approaches such as resective, reconstructive, and combined therapy have been proposed towards peri-implantitis treatment. A resective surgical approach with an adjunctive "modified" implantoplasty refers to the modification of the implant body into a constricted area to mimic a "waist" silhouette. This modified technique conforms an adequate concave smooth area that may favor the outcomes of resective surgical therapy for soft tissue adaptation, biofilm control, and possible peri-implant bone gain over the long term.

Evaluation of Behavior of Castable versus Machined Solid Abutments for Morse Tapper Implant Connection: A Clinical Retrospective Study.

Objective: The primary objective of the present retrospective clinical study was to evaluate and compare the clinical performance presented by castable abutments developed for the MT system versus intermediate machined abutments, specifically regarding prosthetic or implant fractures/loss; the secondary objective was to verify the looseness of the abutments and the behavior of the peri-implant soft tissues. Methods: This clinical retrospective study was conducted on patients rehabilitated between 2019 and 2020. Inclusion criteria were patients in good general health, with an implants-supporting single crown; with solid machined abutments (control group) or castable UCLA abutments; with a connection portion (base) machined in cobalt-chrome (test group) over Morse taper DuoCone implants in the posterior mandible area; and at least two years in function. Clinical assessment was carried out by the same professional, considering the following parameters: (A) prosthetic: (i) loosening of the fixation screw, (ii) fracture of the screw and (iii) the number of times the patient had some type of complication after the installation of the prostheses were evaluated; (B) biological: (i) without keratinized mucosa (KM), (ii) 1 mm or less, (iii) between 1 and 2 mm and (iv) greater than 2 mm of KM width; and the presence or absence of mucositis. Furthermore, radiographic evaluation was performed in order to assess the marginal bone loss. These evaluations permitted to compare the groups analyzed and patients enrolled. Data were statistically analyzed, with the level of significance set at α = 0.05. Results: 79 patients with 120 MT implants were evaluated (80 castable UCLA abutments and 40 machined solid abutments). The follow-up was from 2 to 4 years. There was a 100% implant survival rate. Therefore, the control group showed two fractured abutments (5%) and no abutment loosening (95% for prosthetic survival rate), whereas the test group showed no abutment fracture but nine loosening screws (11.3%) (100% for prosthetic survival rate). Keratinized mucosa was considered thin or absent in 19 implants in the control group (47.5%) and 42 in the test group (52.5%). Mucositis was found in 11 implants in the control group (27.5%) and 27 in the test group (33.8%). A positive correlation was observed between the width of keratinized mucosa and mucositis (r = 0.521, p = 0.002). The mean marginal bone loss was 2.3 mm, ranging from 1.1 to 5.8 mm. No correlation was observed when considering marginal bone loss versus the three parameters (implant diameter, implant length and time of the prosthesis in function). Conclusions: The results suggest that UCLA-type abutments are a viable option for rehabilitating implants with Morse taper connections, suggesting lower fracture risk. Further research is necessary to confirm these findings and thoroughly evaluate the clinical performance and long-term outcomes.

Marginal Bone Level and Biomechanical Behavior of Titanium-Indexed Abutment Base of Conical Connection Used for Single Ceramic Crowns on Morse-Taper Implant: A Clinical Retrospective Study.

The goal of this retrospective clinical study was to evaluate the behavior of Morse-taper indexed abutments by analyzing the marginal bone level (MBL) after at least 12 months of function. Patients rehabilitated with single ceramic crowns between May 2015 and December 2020 received single Morse-taper connection implants (DuoCone implant) with two-piece straight abutment baseT used for at least 12 months, presenting periapical radiograph immediately after crown installation were enrolled. The position of the rehabilitated tooth and arch (maxilla or mandible), crown installation period, implant dimensions, abutment transmucosal height, installation site (immediate implant placement or healed area), associated with bone regeneration, immediate provisionalization, and complications after installation of the final crown were analyzed. The initial and final MBL was evaluated by comparing the initial and final X-rays. The level of significance was α = 0.05. Seventy-five patients (49 women and 26 men) enrolled had a mean period of evaluation of 22.7 ± 6.2 months. Thirty-one implant-abutment (IA) sets had between 12-18 months, 34 between 19-24 months, and 44 between 25-33 months. Only one patient failed due to an abutment fracture after 25 months of function. Fifty-eight implants were placed in the maxilla (53.2%) and 51 in the mandible (46.8%). Seventy-four implants were installed in healed sites (67.9%), and 35 were in fresh socket sites (32.1%). Thirty-two out of these 35 implants placed in fresh sockets had the gap filled with bone graft particles. Twenty-six implants received immediate provisionalization. The average MBL was -0.67 ± 0.65 mm in mesial and -0.70 ± 0.63 mm in distal (p = 0.5072). The most important finding was the statistically significant difference comparing the values obtained for MBL between the abutments with different transmucosal height portions, which were better for abutments with heights greater than 2.5 mm. Regarding the abutments' diameter, 58 had 3.5 mm (53.2%) and 51 had 4.5 mm (46.8%). There was no statistical difference between them, with the following means and standard deviation, respectively, -0.57 ± 0.53 mm (mesial) and -0.66 ± 0.50 mm (distal), and -0.78 ± 0.75 mm (mesial) and -0.746 ± 0.76 mm (distal). Regarding the implant dimensions, 24 implants were 3.5 mm (22%), and 85 implants (78%) had 4.0 mm. In length, 51 implants had 9 mm (46.8%), 25 had 11 mm (22.9%), and 33 implants were 13 mm (30.3%). There was no statistical difference between the abutment diameters (p > 0.05). Within the limitations of this study, it was possible to conclude that better behavior and lesser marginal bone loss were observed when using abutment heights greater than 2.5 mm of transmucosal portion and when placed implants with 13 mm length. Furthermore, this type of abutment showed a little incidence of failures within the period analyzed in our study.

Comparative analysis of the mechanical limits of resistance in implant/abutment set of a new implant design: An in vitro study.

OBJECTIVE: The aim of the present in vitro study was to evaluate the resistance on quasi-static forces and in the fatigue mechanical cycling of a new implant design compared to two other conventional implant designs. MATERIALS AND METHODS: Eighty-eight implants with their respective abutments were tested and distributed into four groups (n = 22 per group): Morse taper connection implant (MT group), conventional external hexagon implant (EH con group), new Collo implant of external hexagon with the smooth portion out of the bone insertion (EH out group), and new Collo implant of external hexagon with the implant platform inserted to the bone level (EH bl group). All the sets were subjected to quasi-static loading in a universal testing machine, and we measured the maximum resistance force supported by each sample. Another 12 samples from each group were submitted to the cyclic fatigue test at 4 intensities of forces (n = 3 per force): 80%, 60%, 40%, and 20%. The number of cycles supported by each sample at each force intensity was evaluated. RESULTS: The three groups of implants with external hexagon connection had similar maximum strength values of the sets (p > 0.05). Meanwhile, samples from the MT group showed the highest resistance values in comparison to the other three groups (p < 0.05). In the fatigue test, the Collo out group supported a smaller number of cycles that led to the fracture than the other 3 groups proposed at loads of 80%, 60%, and 40%, and only at the load value of 20% all groups had the same performance. CONCLUSIONS: Within the limitations of the present in vitro study, the results showed that the new Collo implant performs better when installed at bone level.

Increasing the Thickness of the Collagen Xenogeneic Matrix Prevents Early Matrix Degradation and Improves the Proliferation, Adhesion, and Viability of Human Gingival Fibroblasts and Mesenchymal Stem Cells.

Using autogenous grafts in mucogingival surgeries is related to postoperative morbidity and limited tissue availability, and thus xenogeneic matrices are increasingly used. This in vitro study evaluated the influence of xenogeneic collagen matrix thickness on cell adhesion, morphology, viability, proliferation, and matrix degradation. Matrices were divided into three groups: SLC: single layer of Lumina Coat, as commercially available (2-mm thickness); DLC: double layer of SLC (Lumina Coat); and MG: single layer of Mucograft, as commercially available (4-mm thickness). SEM was used to evaluate the matrix surface topographies. To evaluate the cell viability, proliferation, adhesion, and morphology, human gingival fibroblasts (HGF) and stem cells from human exfoliated deciduous teeth (SHED) were used. Cell viability was evaluated through MTS colorimetric method evaluating HGF and SHED on days 1, 3, and 7. Cell proliferation was assessed by PicoGreen assay, evaluating HGF and SHED on days 3 and 7. Sample degradation was evaluated on days 1, 3, 7, 14, 21, 28, and 35. All groups were biocompatible for HGF and SHED, showing viabilities > 70% on days 1, 3, and 7. DCL promoted HGF viabilities similar to MG (P = .2828) and the highest SHED viability (P < .0001) on day 1. DLC also demonstrated HGF and SHED proliferations higher than the positive control (MG; P < .05) on day 7. SLC was completely degraded on day 14, while DLC and MG presented 48.41% and 20.52% of their initial mass, respectively, on day 35. Increasing the matrix thickness improved HGF and SHED viability and proliferation and prevented early matrix degradation. DLC demonstrated better results than SLC and MG concerning matrix degradation and HGF and SHED viability and proliferation.

Histologic and histomorphometric analysis of two biomaterials of xenogenous origin for maxillary sinus elevation: a clinical study.

Objective: This study analyzed two xenogenous biomaterials based on deproteinized bovine bone mineral applied for maxillary sinus elevation. Method and materials: Fourteen patients were submitted to maxillary sinus augmentation with one of the following biomaterials: Criteria Lumina Bone Porous (test group) or Geistlich Bio-Oss (control group), both of large granules (1 to 2 mm). After 6 months, trephine biopsies were collected at the time of implant placement: 27 samples (11 patients) in the test group; 7 samples (3 patients) in the control group. Biopsies were analyzed by descriptive histology and histomorphometry, in which the percentages of newly formed bone, residual biomaterial particles, and connective tissue were evaluated. Results: Histomorphometry showed means for test and control groups, respectively, of 32.41% ± 9.42% and 26.59% ± 4.88% for newly formed bone, 22.89% ± 4.58% and 25.00% ± 4.81% for residual biomaterial, and 44.70% ± 9.54% and 48.41% ± 3.36% for connective tissue. There were no differences between groups (P > .05). Conclusion: This study concluded that Criteria Lumina Bone Porous presented similar histologic and histomorphometric characteristics to Geistlich Bio-Oss 6 months after sinus elevation surgery, identifying the tested biomaterial as an interesting alternative for bone augmentation in the maxillary sinus.

Effect of Flavonoid Supplementation on Alveolar Bone Healing-A Randomized Pilot Trial.

We investigated the effects of two common dietary supplements on bone healing in dental extraction sockets in humans. In this randomized pilot trial, male subjects took Grape Seed Extract [GSE] or Grapefruit Extract [GFE] starting two weeks prior to dental extraction and maintained this regimen for sixty days after surgery. Extraction sockets were filled with a collagen plug. After 24 h, a socket sample was collected and processed for quantitative real-time reverse transcription polymerase chain reaction (qRT-PCR) and an 84-gene wound healing assay. Sixty days after tooth extraction, a core of newly formed bone was obtained prior to dental implant placement and processed for histology. qRT-PCR revealed that GFE led to a significant decrease in platelet-derived growth factor and interleukin (IL)1-ß compared to GSE, and a significant decrease in IL-6 and CXCL2 compared to control. GSE led to a significant increase in coagulation factor Von Willebrand and inflammatory marker IL1-ß compared to GFE. WISP1 and CXCL5 were upregulated in both groups. Overall, GFE showed a downregulation of inflammation and GSE led to a decrease in collagen density and increased osteoclasts. This pilot trial highlights the need for further investigation on the mechanism of action of such supplements on bone healing and oral health.

Implantoplasty Enhancing Peri-implant Bone Stability Over a 3-Year Follow-up: A Case Series.

Implantoplasty has been claimed as a promising strategy to treat peri-implantitis and prevent progressive peri-implant bone loss. Consequently, the aim of the present case series is to exhibit the clinical outcomes of a 3-year-follow-up resective and implantoplasty therapy applying a novel platform-switch concept to preserve peri-implant tissue integrity and counteract progressive bone loss. Four patients who underwent dental implant therapy and were diagnosed with peri-implantitis were treated through access flap surgery, a modified implantoplasty, bone recontouring, and surface decontamination. The radiographic and clinical parameters recorded before and during the 3-year follow-up were: marginal bone loss (MBL) as the primary endpoint, bleeding on probing index (BOP), probing depth (PD), presence of suppuration, pain, mobility, and fracture. The 3-year follow-up exhibited peri-implant bone stability in all cases (100%) showing radiographically an MBL reduction (mean) of 0.8 ± 0.5 mm (mesial) and 0.5 ± 0.3 mm (distal). Mean PD reduction was 4.75 ± 1 mm and mean BOP was reduced by 71%. Pain and suppuration were resolved in all cases. None of the cases reported implant fracture or mobility after the modified implantoplasty therapy. The present case series demonstrated that this modified implantoplasty can be more than a surface decontamination therapy where the narrow and smooth exposed implant surface can counteract peri-implantitis alterations providing favorable biologic conditions to maintain stability of peri-implant tissues.

Evaluation of the Effect of Air Polishing With Different Abrasive Powders on the Roughness of Implant Abutment Surface: An In Vitro Study.

The aim of this in vitro study was to evaluate the effect of air polishing on the implant abutment surface using different abrasive powders: sodium bicarbonate and amino acid glycine. Fifteen grade III machined surface titanium disks with 8-mm diameter and 2-mm thickness were divided in 3 groups of 5 samples each and subjected to air polishing for 20 seconds with an Ultrajet Flex air-abrasive device and a distinct prophylaxis protocol: air and water (G1); air, water, and sodium bicarbonate (G2); and air, water; and amino acid glycine (G3). After the air polishing, the average roughness (Ra) of the samples was measured using an optical profilometer, and the obtained data were statistically analyzed. We found that G1 and G3 had similar Ra, while Ra values for G2 were significantly higher. This study demonstrated that air-polishing powders containing glycine had less of an effect on the roughness of the surface of titanium disks compared with sodium bicarbonate powders. Future in vivo studies will be conducted to investigate the clinical relevance of the present results.

Mechanical Complications Related to the Retention Screws of Prefabricated Metal Abutments With Different Angulations: A Retrospective Study With 916 Implants.

OBJECTIVES: The present retrospective study assessed the clinical performance of abutment screws from prefabricated metal abutments and compared technical complication rates between straight and angled abutments. MATERIALS AND METHODS: Dental charts were selected for patients with dental implant rehabilitations delivered between 1998 and 2012. Abutment angulation, prosthetic screw type, and presence of complications that occurred during the selected time period were collected. Technical complications registered included abutment screw loosening and/or fractures detected during clinical and radiographic examinations. The chi-square test was used for statistical analysis. RESULTS: Abutment angulations were divided into 2 groups: G1) prefabricated straight abutments and G2) prefabricated angled conical mini UCLA-type abutments. A total of 916 implants (799 straight and 117 angled conical mini UCLA-type abutments) were evaluated. G1 showed 91.1% had absence of failures, which were clinically defined as any screw loosening or fracture; and 8.9% reported some type of technical complication. G2 showed 92.3% and 7.7%, with and without technical complications, respectively. CONCLUSIONS: No significant differences were observed between abutment angulation and technical complications.

Risk indicators for Peri-implantitis. A cross-sectional study with 916 implants.

OBJECTIVES: The aim of this study was to identify systemic and local risk indicators associated with peri-implantitis. MATERIAL AND METHODS: One hundred eighty-three patients treated with 916 osseointegrated titanium implants, in function for at least 1 year, were included in the present study. The implants were installed at the Foundation for Scientific and Technological Development of Dentistry (FUNDECTO) - University of Sao Paulo (USP) - from 1998 to 2012. Factors related to patient's systemic conditions (heart disorders, hypertension, smoking habits, alcoholism, liver disorders, hepatitis, gastrointestinal disease, diabetes mellitus I and II, hyperthyroidism or hypothyroidism, radiation therapy, chemotherapy, menopause, osteoporosis, active periodontal disease, history of periodontal disease and bruxism), implant's characteristics (location, diameter, length, connection, shape, and antagonist), and clinical parameters (wear facets, periodontal status on the adjacent tooth, plaque accumulation on the adjacent tooth, modified plaque index, sulcus bleeding index, probing depth, bleeding on probing, width of keratinized tissue and marginal recession). RESULTS: An increased risk of 2.2 times for history of periodontal disease (PD), 3.6 times for cemented restorations compared to screw-retained prostheses, 2.4 times when wear facets were displayed on the prosthetic crown and 16.1 times for total rehabilitations when compared to single rehabilitations were found. Logistic regression analysis did not show any association between the implant's characteristics and peri-implantitis. CONCLUSIONS: A history of periodontal disease, cemented prostheses, presences of wear facets on the prosthetic crown and full mouth rehabilitations were identified as risk indicators for peri-implantitis. Implants' characteristics were not related to the presence of peri-implantitis.

Efeito de partículas metálicas liberadas dos implantes dentários sobre os tecidos peri-implantares / The effect of metallic particles released from dental implants on peri-implant tissues

Objetivo: realizar uma revisão da literatura sobre os efeitos das partículas metálicas liberadas nos tecidos peri-implantares, como consequência do uso de técnicas terapêuticas empregadas no tratamento de doenças peri-implantares e/ou pela degradação do implante. Material e métodos: foi efetuado um levantamento bibliográfico através de pesquisas em livros, textos e base de dados PubMed entre o período de 1977 a 2015. Os seguintes termos foram explorados: "titanium wear e dental implant", "titanium corrosion e dental implant", "bio-tribocorrosion", "peri-implantitis", "treatment of peri-implantitis", "titanium particles release e dental implant", "titanium ion release e dental implant", e "tratamento da peri-implantite". Foram selecionados 91 artigos científicos, definidos como os mais relevantes sobre o tema. Resultados: há liberação de citocinas pró-inflamatórias, infiltrado de células de resposta inflamatória e ativação dos osteoclastos nos tecidos peri-implantares, em contato com partículas e íons metálicos. Ainda, foram reportadas alterações degenerativas em macrófagos, e neutrófilos que fagocitaram micropartículas de titânio, bem como mutações em células humanas em cultura contendo nanopartículas de TiO2. Conclusão: partículas metálicas liberadas a partir do sistema de implantes têm potencial citotóxico e genotóxico, e são capazes de induzir resposta inflamatória nos tecidos peri-implantares.

Objective: to review the literature regarding the effect of metallic particles released at the peri-implant tissues, as a consequence of therapeutic techniques to treat peri-implant diseases and/or by implant degradation. Material and methods: a search was made at the PubMed from 1977 to 2015. The following terms were combined: titanium wear and dental implant", "titanium corrosion and dental implant", "bio-tribocorrosion", "peri-implantitis", "treatment of peri-implantitis", "titanium particles release and dental implant", "titanium ion release and dental implant", and "peri-implant treatment". 91 scientific articles were selected to define the most relevant topics. Results: there is pro-infl ammatory cytokine release, inflammatory cell infiltrate and osteoclast activation over the peri-implant tissues contacting particles and metallic ions. Also, degenerative changes on macrophages and neutrophils engulfing titanium microparticles were reported, as well as mutations on culture human cells containing TiO2 nanoparticles. Conclusion: metallic particles released from the dental implant system can be cytotoxic and genotoxic in nature and to induce inflammatory response at the peri-implant tissues.

Analysis of Effectiveness of Different Rotational Instruments in Implantoplasty: An In Vitro Study.

OBJECTIVE: To analyze the temperature increase in the implant, adjacent bone, procedure time, and roughness provided by different rotatory instruments in the implantoplasty procedure. MATERIAL AND METHODS: Three types of rotational instruments were used to evaluate the implant surface wear, divided according to their surface features: Group 1 (G1) diamond, Group 2 (G2) tungsten carbide, and Group 3 (G3) multilaminar. For the roughness test, a control group was included for comparison with the test groups. RESULTS: The temperature variation was statistically significant in the implant (P < 0.05) where G2 showed the lowest variation. There was no statistically significant difference between the 3 groups regarding the temperature increase measured in the bone (P > 0.05). The difference of wear time was statistically significant (P < 0.05) with faster results for G3. In the surface roughness analyses, there was a statistically significant difference (P < 0.05) between the control group and the test groups. Among the 3 test groups, the difference between measurements was not statistically significant (P > 0.05). CONCLUSION: All tested rotatory instruments performed the same level of surface roughness in the implantoplasty. The tungsten carbide bur caused a minor change in the implant temperature. The multilaminar bur performed a faster wear time. More in vivo studies are necessary to conclude which is the best rotatory instrument for implantoplasty.

As características protéticas das reabilitações implantossuportadas podem influenciar no sangramento a sondagem? Um estudo retrospectivo em 916 implantes / Does the prosthesis type over implant-supported rehabilitations can infl uence on bleeding on probing? A retrospective study with 916 dental implants

Objetivos: avaliar se a união entre implantes e/ou a presença de gengiva artifi cial infl uencia no sangramento a sondagem dos tecidos peri-implantares. Material e métodos: foram incluídos pacientes tratados com implantes de titânio (Implacil De Bortoli, São Paulo, Brasil), instalados no período de 1998 a 2012, na Universidade de São Paulo (USP). Os implantes foram examinados para avaliação do sangramento a sondagem, sendo divididos de acordo com o tipo de prótese: unitárias (n=167), parciais (n=522) e totais (n=227); e de acordo com a ausência (n=674) ou presença (n=242) de gengiva artifi cial. O teste estatístico com equação de estimativa generalizada foi usado para testar possíveis associações. Resultados: foram examinados 183 pacientes reabilitados com 916 implantes em função, pelo menos por um ano. Ao menos um ponto de sangramento a sondagem foi detectado em 85 (50,9%), 304 (58,2%) e 129 (56,8%) implantes das próteses unitárias, parciais e totais, respectivamente. Em relação à gengiva artificial, 378 (56,1%) dos implantes sem e 140 (57,9%) dos implantes com esta característica apresentaram sangramento a sondagem. Não foram verificadas diferenças significativas entre os grupos. Conclusão: a união dos implantes ou a presença de gengiva artificial não foram associadas com os resultados de sangramento a sondagem nos implantes em função.

Objective: to evaluate whether the prosthesis type (single, partial, complete) and/or the presence of artifi cial gingiva can influence on bleeding on probing of peri-implant tissues. Material and methods: patients treated with titanium dental implants (Implacil De Bortoli, São Paulo, Brazil) between 1998 to 2012 at the University of Sao Paulo (USP) were included in this study. The implants were divided according the following prosthodontic types: single (n=167), partial (n=522), and complete (n=277), and also regarding the presence (n=674) or absence (n=242) or artificial gingiva. The generalized estimating equation test was used to verify possible associations. Results: 183 patients and 916 implants at least 1 year in function were screened. At least one bleeding point was detected in 85 (50.9%), 304 (58.2%), and 129 (56.8%) implants for single, partial, and complete prostheses, respectively. 378 (56.1%) and 140 (57.9%) implant from groups without and with artificial gingiva presented bleeding on probing. No significant differences were identified among groups. Conclusion: the prosthesis design and/or artifi cial gingiva were not associated to bleeding on probing for dental implants in function.

Tratamento cirúrgico de peri-implantite û relato de caso com 3 anos de acompanhamento / Surgical treatment for peri-implantitis û case report with 3-years follow-up

A peri-implantite (PI), doença peri-implantar causada pelo desequilíbrio entre a colonização bacteriana ao redor dos implantes e a resposta do hospedeiro, é caracterizada pela perda óssea e profundidade de sondagem aumentada com sangramento e/ou supuração. Este artigo relata um caso clínico de tratamento cirúrgico de peri-implantite em área estética da maxila e descreve o acompanhamento longitudinal da paciente, num período de 3 anos após cirurgia. A paciente compareceu ao Centro de Ensino e Pesquisa em Implantes Dentários (CEPID), no Departamento de Odontologia da Universidade Federal de Santa Catarina (UFSC) (Florianópolis/Brasil) para tratamento de doença peri-implantar na região do dente 11. Após diagnóstico de PI e tratamento não cirúrgico local, a terapia cirúrgica foi indicada. A coroa parafusada foi removida e o osso foi exposto através de uma incisão de espessura total. O tecido de granulação foi removido através de raspagem manual e a osteoplastia foi realizada ao redor do implante com cinzéis, de forma manual, buscando preservar ao máximo o osso próximo aos dentes vizinhos à região. Ácido cítrico a 3% foi aplicado com o intuito de promover a descontaminação química e, também, o condicionamento do osso para reinserção dos tecidos. O manejo da PI permanece sem um protocolo de tratamento definido, porém, as opções terapêuticas adotadas foram suficientes para limitar os danos da doença e restabelecer a saúde dos tecidos peri-implantares no caso apresentado...

Peri-implantitis (PI), a peri-implant disease caused by an imbalance between bacterial colonization around the implant and host response, is characterized by bone loss and increased probing depths with bleeding and/or suppuration. This paper reports a clinical case of surgical treatment of PI in aesthetic area of the maxilla and describes the longitudinal follow-up of the patient over a period of 3 years after surgery. The patient searched the Center of Education and Research on Dental Implants (CEPID), Department of Dentistry of the Federal University of Santa Catarina (UFSC) (Florianopolis/Brazil), for peri-implant disease treatment in the 11 tooth region. After diagnosis of PI and local non-surgical treatment, surgical therapy was indicated. The screwed crown was removed and the bone exposed through a full thickness incision. Granulation tissue was removed by manual curettage and osteoplasty was performed manually around the implant with chisels, as an attempt to preserve bone near the adjacent teeth. In order to promote chemical decontamination and bone conditioning for tissue reinsertion, citric acid at 3% was applied. PI management remains without a defined treatment protocol, however in the present case the adopted therapeutic options were sufficient to limit the damage of the disease and restore health of peri-implant tissues...

Implantoplastia no tratamento da peri-implantite û relato de caso / Use of Implantoplasty in the treatment of peri-implantitis û case report

A Implantoplastia é uma terapia cirúrgica utilizada com sucesso no tratamento da peri- -implantite. A técnica consiste no alisamento e polimento das roscas expostas do implante, que sofreu perda óssea e contaminação por micro-organismos patogênicos. Este artigo objetiva demonstrar, a partir de um relato de caso clínico, a execução do procedimento de Implantoplastia, bem como seu resultado e acompanhamento. O controle do caso ocorreu com 7 dias, 14 dias e 6 meses...

Implantoplasty is a surgical therapy successfully used in the treatment of peri-implantitis. The technique consists of smoothing and polishing the exposed implant surfaces, which has suffered bone loss and contamination by pathogenic microorganisms. This article aims to demonstrate, with a case report, the Implantoplasty technique as well as its result and monitoring. Follow-up was performed at 7 days, 14 days, and six months...

Failure of prosthetic screws on 971 implants

Abstract Aim: To evaluate the presence of failures in prosthetic screws and whether these failures are related to the type of prosthesis, abutment angulation and presence or not of intermediate. Methods: Two-hundred and sixty-seven patients were evaluated at the Federal University of Santa Catarina, totaling 971 external hexagonal implants in place for at least one year. A Tobit regression model for censored variables was used and the explanatory variables were subjected to percentage analysis. Results: The results demonstrated a relationship between the failure in prosthetic screws and the investigated factors with a significance of F=0.003 and p<0.05. The percentage analysis showed that the prosthetic screw failed in 8.82% of 238 unitary prostheses and 10.1% of 773 multiple prostheses. Among 912 abutments, 9.43% failed and in the 59 angled abutments, failures appeared in 15.25%. A total of 200 prostheses were placed over the implant platform and 13% failed. A total of 771 prostheses were made over abutment and 8.95% of these screws failed. Conclusions: Through multiple linear regression it could be concluded that the type of prosthesis showed no significant influence on the prosthetic screw failure, but other variables were related to this mechanical failure. There was a significant relationship among the variables, demonstrating the need for greater attention in choosing the type of prosthesis, the abutment angulation and whether the prosthesis will be placed directly on the implant platform or on the abutment.

Implante imediato com estética imediata, definitiva e acompanhamento tomográfico da tábua óssea vestibular û relato de caso / Immediate implant, immediate aesthetic and final restoration with tomographic follow-up of the buccal plate û case report

O resultado da terapia com implantes osseointegrados não é apenas mensurado pela taxa de sobrevivência, mas também pela estabilidade/ integridade estética e funcional dos tecidos peri-implantares a longo prazo. A técnica do implante imediato tornou-se uma opção viável para a manutenção da arquitetura peri-implantar, além de reduzir significantemente o tempo do tratamento. O presente caso clínico descreve a resolução de um único elemento dentário maxilar anterior perdido (elemento 22), através da instalação de implante imediato pós-exodontia sem retalho, estética imediata e definitiva, com acompanhamento tomográfico de 6 meses e 1 ano das alterações da tábua óssea vestibular. Este tipo de abordagem de tratamento diminui o número de intervenções cirúrgicas, bem como o tempo de instalação da restauração protética final, aumentando a satisfação estética e funcional do paciente. É evidente que o sucesso desta técnica requer a seleção correta dos casos, exodontia atraumática e estabilidade primária.

The outcome of the therapy with osseointegrated implants is not only measured through survival rate, but also through aesthetic and function stability of the peri-implant tissue during long-term. Immediate implants technique has become an option for maintaining the peri-implant architecture and reduce the time of treatment. This case report presents the complete resolution of a single anterior maxillary tooth loss (element 22), by installing an implant immediately after tooth extraction without flap, immediate and definitive aesthetic, with 6 months and 1 year CT scan follow-up to analyze alterations on the buccal bone plate. This type of approach reduces the number of surgical interventions, as well as the installation time of final prosthetic restoration, increasing functional and aesthetic satisfaction of the patient. It is evident that the success of this technique requires proper selection of cases, atraumatic extraction of the tooth and primary stability of the implant.

Conditioned medium of demineralized freeze-dried bone activates gene expression in periodontal fibroblasts in vitro.

BACKGROUND: Demineralized bone matrix (DBM) is used for the treatment of osseous defects. Conditioned medium from native bone chips can activate transforming growth factor (TGF)-ß signaling in mesenchymal cells. The aim of this study is to determine whether processing of native bone into DBM affects the activity of the conditioned medium. METHODS: Porcine cortical bone blocks were subjected to defatting, different concentrations of hydrochloric acid, and various temperatures. DBM was lyophilized, ground, and placed into culture medium. Human gingiva and periodontal fibroblasts were exposed to the respective conditioned medium obtained from DBM (DBCM). Changes in the expression of TGF-ß target genes were determined. RESULTS: DBCM altered the expression of TGF-ß target genes (e.g., adrenomedullin, pentraxin 3, KN motif and ankyrin repeat domains 4, interleukin 11, NADPH oxidase 4, and BTB [POZ] domain containing 11) by at least five-fold. The response was observed in fibroblasts from both sources. Defatting lowered the activity of DBCM. The TGF-ß receptor type I kinase inhibitor SB431542 [4-(4-(benzo[d][1,3]dioxol-5-yl)-5-(pyridin-2-yl)-1H-imidazol-2-yl)benzamide] but not the inhibitor of bone morphogenetic protein receptor dorsomorphin, blocked the effects of DBCM on gene expression. Moreover, conditioned medium obtained from commercial human DBM modulated the expression of TGF-ß target genes. CONCLUSION: The findings suggest that the DBCM can activate TGF-ß signaling in oral fibroblasts.