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Abstract Objective This retrospective study aimed to analyze the clinical efficacy of two regenerative surgical methods — Bio-Oss granules combined with barrier membranes and Bio-Oss Collagen alone — and to help clinicians achieve better periodontal regeneration outcomes in the specific periodontal condition. Methodology Patients who underwent periodontal regeneration surgery from January 2018 to April 2022 were retrospectively screened, and their clinical and radiographic outcomes at 6 months postoperatively were analyzed. The probing depth (PD), clinical attachment level (CAL), bleeding on probing (BOP), gingival recession (GR), distance from the cemento-enamel junction to the bottom of the bone defect (CEJ-BD), and depth of intrabony defects (INFRA) were recorded before the operation (T0) and 6 months after it (T1), and subsequently compared. Results In total, 143 patients were included — 77 were placed in the Bio-Oss group and 66 were placed in the Bio-Oss Collagen group. All indicators, including PD and CAL at T1, showed significant differences compared to baseline, for both groups (P<0.001). PD reduction was greater in the group receiving the Bio-Oss Collagen treatment (P=0.042). Furthermore, in cases when the baseline PD range was 7-11 mm and the age range was 35-50 years, PD reduction was more significant for patients receiving the Bio-Oss Collagen treatment (P=0.031, 0.023). A linear regression analysis indicated that postoperative PD and CAL were positively correlated with baseline values, and that the efficacy tended to decrease with increasing age. Conclusion Both the use of Bio-Oss Collagen alone and the use of Bio-Oss granules combined with barrier membranes resulted in significant effects in the treatment of periodontal intrabony defects. The Bio-Oss Collagen treatment generated more improvements in PD than the Bio-Oss granules combined with barrier membranes, particularly within the baseline PD range of 7-11 mm and the 35-50 years age group. Additionally, age was the main factor influencing the effectiveness of regenerative surgery for intrabony defects: older individuals exhibited fewer improvements.
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Introduction: The loss of dental elements can lead to excessive bone loss in the posterior maxillary segments, which can limit the placement of dental implants in that area, the pneumatization of the maxillary sinus and the absence of dental elements to keep the bone active are some of the main causes. Among the wide range of available grafting materials, bovine hydroxyapatite has been extensively studied and has shown excellent clinical and histological results. Materials and methods: A total of 17 maxillary sinus floor elevations were performed (n = 8 Osteodens, n = 9 Bio-Oss). After a healing period of 6 to 8 months, a block of the grafted area was obtained using trephines and analyzed by histomorphometry. Results: The percentage of neoformed bone tissue was higher for Bio-Oss (39.0% ± 11.1) compared to Osteodens (33.4% ± 8.3), while the remaining graft values were slightly lower in Bio-Oss compared to Osteodens (16.3% ± 11.2 and 20.8% ± 12.1, respectively). The proportion of connective tissue was similar in both groups (44.7% Bio-Oss and 45.8% Osteodens). Age, gender, and residual height of the sinus floor did not show statistically significant differences. Conclusions: In this study, both graft materials (Bio-Oss and Osteodens) showed no statistically significant differences in their ability to regenerate suitable bone tissue for implant placement after 6 months of healing. Further studies with a larger sample size are needed to validate these results.
Introducción: La pérdida de elementos dentarios puede provocar una excesiva pérdida ósea en los segmentos maxilares posteriores, lo que puede limitar la colocación de implantes dentarios en esa zona, la neumatización del seno maxilar y la ausencia de elementos dentarios que mantengan el hueso activo son algunas de las principales causas. Entre la amplia gama de materiales de injerto disponibles, la hidroxiapatita bovina ha sido ampliamente estudiada y ha mostrado excelentes resultados clínicos e histológicos. Materiales y métodos: Se realizaron un total de 17 elevaciones del suelo del seno maxilar (n = 8 Osteodens, n = 9 Bio-Oss). Tras un periodo de cicatrización de 6 a 8 meses, se obtuvo un bloque de la zona injertada mediante trépanos y se analizó mediante histomorfometría. Resultados: El porcentaje de tejido óseo neoformado fue mayor en Bio-Oss (39,0% ± 11,1) en comparación con Osteodens (33,4% ± 8,3), mientras que los valores del injerto remanente fueron ligeramente inferiores en Bio-Oss en comparación con Osteodens (16,3% ± 11,2 y 20,8% ± 12,1, respectivamente). La proporción de tejido conjuntivo fue similar en ambos grupos (44,7% Bio-Oss y 45,8% Osteodens). La edad, el sexo y la altura residual del piso sinusal no mostraron diferencias estadísticamente significativas. Conclusiones: En este estudio, ambos materiales de injerto (Bio-Oss y Osteodens) no mostraron diferencias estadísticamente significativas en su capacidad para regenerar tejido óseo adecuado para la colocación de implantes tras 6 meses de cicatrización. Se necesitan más estudios con un tamaño de muestra mayor para validar estos resultados.
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Objective@#To evaluate the osteogenic effect of concentrated growth factor (CGF) combined with deproteinated bovine bone mineral (DBBM) in site preservation using clinical and histomorphometric observations.@*Methods @#A total of 26 patients who needed extraction of affected teeth and received staged implantation after site preservation were selected. The patients were randomly divided into the DBBM group (Bio-Oss was implanted simultaneously after extraction) and CGF+DBBM group (CGF+Bio-Oss was implanted simultaneously after extraction), with 13 patients in each group, and both groups were covered with Bio-Gide collagen membrane. Cone beam computed tomography (CBCT) was performed preoperatively and 6 months later to measure the changes in alveolar bone height and width, and the bone specimens were drilled 6 months after site preservation during implant surgery for histological analyses.@*Results@# CBCT showed that the height and width of alveolar bone were absorbed 6 months after site preservation in the CGF+DBBM and DBBM groups, and the reduction in alveolar ridge width in the CGF+DBBM group was statistically less than the DBBM group (P <0.05). The histomorphometry results showed that the percentage of new bone in the CGF+DBBM and DBBM groups were 35.30% ± 3.56% and 26.38% ± 5.04%, respectively, and the amount of new bone in the CGF+DBBM group was statistically higher than the DBBM group (P<0.05). @*Conclusion @#CGF combined with DBBM is superior to DBBM in maintaining the alveolar bone volume and shape in site preservation, which creates favorable conditions for implant restoration.
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BACKGROUND: Dentin particles, tricalcium phosphate/collagen protein composites and Bio-oss particles can repair jaw defects, but the excellent osteogenic effect is not clear. OBJECTIVE: To compare osteogenic effects of three different bone graft materials on mandibular defects in beagle dogs. METHODS: Eight 1-year-old beagles were selected. A boxed bone defect area of 10 mm × 8 mm × 2 mm was prepared at the bilateral mandibular external oblique line and randomly divided into four groups with four bone defect models in each group. Undemineralized dentin particles were implanted in group A; tricalcium phosphate/ collagen protein composite materials were implanted in group B; Bio-oss particles were implanted in group C; and group D was used as blank control. Three months after transplantation, the samples were taken for histological observation. The experimental animals were approved by the Ethics Committee of the Experimental Animal Center of Dalian Medical University. RESULTS AND CONCLUSION: (1) In group A, dentin particles were slightly absorbed, surrounded by new bone tissue; new bone trabeculae and capillaries could be seen, and a large number of fibrous connective tissue surrounded dentin particles in the central area of bone graft. In group B, a small number of new bone trabeculae and osteoblasts could be seen; a large number of powdered β-tricalcium phosphate particles and a small amount of inflammatory cells could be seen in the fibrous connective tissue; and some β-tricalcium phosphate particles were surrounded by new bone tissue. Bone marrow cavity could be seen in the new bone. In group C, some Bio-oss particles were surrounded by new bone tissue; some Bio-oss particles were wrapped by surrounding fibrous connective tissue, and fibers, particles and new bone were intertwined. There was no new bone formation in group D, and many capillaries could be seen in a large number of fibrous connective tissue. (2) The rate of new bone formation in groups A, B and C was higher than that in group D (P < 0.05); the rate in groups A and C was higher than that in group B (P < 0.05). (3) The results show that all the three kinds of bone graft materials can promote the formation of new bone. The short-term osteogenic effects of undecalcified xenogeneic dentin particles and Bio-oss particles are better than tricalcium phosphate/collagen protein composites, but the long-term effects need to be further observed.
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Objective@#To study the clinical outcomes of implanting platelet rich fibrinogen (PRF) mixed with Bio-Oss® in the extraction socket for alveolar ridge preservation and to provide evidence for clinical application. @*Methods@#Thirty-six patients who underwent alveolar ridge preservation were enrolled. Thirty-six extraction sites were divided into two groups: PRF mixed with Bio-Oss® group (test group) and Bio-Oss® alone (control group). Bone dimensional changes in height and width were measured by CBCT before and 6 months after surgery, and early soft tissue healing and postoperative pain sensation were evaluated clinically 1 week after surgery.@* Results @# There was no significant difference in the alveolar bone height (-1.48 ± 0.40) mm between the test group and the control group. The difference in the alveolar bone width between the test group (-1.09 ± 0.42) mm and the control group (-1.35 ± 0.22) mm was statistically significant (z=-2.63, P=0.01). The postoperative pain score of the test group was 2.39 ± 1.20, and that of the control group was 3.39 ± 1.65, the difference was statistically significant (t=-2.083, P=0.045). There was no significant difference in soft tissue healing between the test group and the control group.@*Conclusion @#The use of PRF mixed with Bio-Oss ®in the alveolar ridge preservation procedure can reduce alveolar bone absorption and postoperative pain.
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Objective@#To research the clinical effect of platelet rich plasma combined with Bio-oss artificial bone meal in repairing bone defects around implants.@*Methods@#From January 2015 to January 2017, 70 cases who completed the implant repair in Lishui People's Hospital, and later confirmed the defects around the implant were selected in the research.They were equally divided into observation group and control group according to admission, with 35 cases in each group.The control group was treated with Bio-oss artificial bone powder.The observation group was treated with platelet rich plasma combined with Bio-oss artificial bone powder.The clinical effects of the two groups were compared and analyzed.@*Results@#Before treatment, the probe depth (PD), clinical attachment loss (CAL), plaque index (PI), gingival sulcus hemorrhage index (SBI) of the observation group and the control group were (7.18±1.31)mm, (5.68±0.87)mm, (1.23±0.31), (2.48±0.34) and (7.22±1.28)mm, (5.74±0.83)mm, (1.27±0.33), (2.53±0.36), respectively, which were significantly higher than those after treatment (all P<0.05). Before treatment, the bone mineral density (BMD) levels of the two groups were (35.48±4.58)g/cm3 and (35.74±4.61)g/cm3, respectively, which were significantly lower than those after treatment (all P<0.05). The levels of PD, CAL, PI and SBI in the observation group at 3 months and 6 months after treatment were (4.48±1.01)mm, (4.27±0.53)mm, (0.68±0.21), (1.12±0.13) and (3.43±0.76)mm, (3.58±0.54)mm, (0.38±0.07), (0.41±0.08), respectively, which were significantly lower than those in the control group [(5.19±0.83)mm, (4.83±0.71)mm, (0.89±0.27), (1.46±0.21) and (4.14±0.98)mm, (4.21±0.62)mm, (0.49±0.11), (0.63±0.13)], the differences were statistically significant (t=3.213, 3.739, 3.632, 8.144 and 3.387, 4.533, 4.991, 8.526, P=0.002, 0.000, 0.000, 0.000, 0.001, 0.000, 0.000, 0.000, 0.000, 0.000). The levels of TA anterior temporalis muscle EMG and MA masseter muscle EMG in the two groups at 6 months after treatment were (76.81±15.17)mV, (67.56±14.43)mV, (74.24±13.28)mV, (68.27±13.03)mV, (66.44±13.28)mV, (58.76±13.07)mV, (65.58±11.55)mV, (59.04±10.76)mV, respectively, which were significantly higher than those before treatment [(46.48±11.15) mV, (38.19±13.04) mV, (54.83±12.57) mV, (56.48±13.13) mV and (45.71±10.98) mV, (38.23±13.11)mV, (55.14±12.69) mV, (56.61±13.08) mV] (all P<0.05). After treatment, the ICP-HB, ICMAP-MC, TA, EMG levels in the observation group were significantly higher than those in the control group, the differences were statistically significant (t=3.042, 2.674, 2.911, 2.994, P=0.003, 0.009, 0.004 and 0.003).@*Conclusion@#The effect of rich plate plasma combined with Bio-oss artificial bone powder on the repair of bone defect around the implant is significant.The platelet rich plasma can speed up and improve the repair speed and repair quality of bone defect around the implant, so that the therapeutic effect of implant repair can be maintained for a long time.
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Objective To research the clinical effect of platelet rich plasma combined with Bio-oss artificial bone meal in repairing bone defects around implants.Methods From January 2015 to January 2017,70 cases who completed the implant repair in Lishui People's Hospital,and later confirmed the defects around the implant were selected in the research.They were equally divided into observation group and control group according to admission,with 35 cases in each group.The control group was treated with Bio-oss artificial bone powder.The observation group was treated with platelet rich plasma combined with Bio-oss artificial bone powder.The clinical effects of the two groups were compared and analyzed.Results Before treatment,the probe depth (PD),clinical attachment loss (CAL),plaque index (PI),gingival sulcus hemorrhage index (SBI) of the observation group and the control group were (7.18 ± 1.31)mm,(5.68 ±0.87)mm,(1.23 ±0.31),(2.48 ±0.34) and (7.22 ± 1.28)mm,(5.74 ±0.83) mm,(1.27 ± 0.33),(2.53 ± 0.36),respectively,which were significantly higher than those after treatment (all P ＜ 0.05).Before treatment,the bone mineral density (BMD) levels of the two groups were (35.48 ± 4.58) g/cm3 and (35.74 ±4.61) g/cm3,respectively,which were significantly lower than those after treatment (all P ＜ 0.05).The levels of PD,CAL,PI and SBI in the observation group at 3 months and 6 months after treatment were (4.48 ± 1.01) mm,(4.27 ±0.53)mm,(0.68 ±0.21),(1.12 ±0.13) and (3.43 ±0.76) mm,(3.58 ±0.54)mm,(0.38 ±0.07),(0.41 ±0.08),respectively,which were significantly lower than those in the control group [(5.19 ± 0.83) mm,(4.83 ±0.71)mm,(0.89 ±0.27),(1.46 ±0.21) and (4.14 ±0.98)mm,(4.21 ±0.62)mm,(0.49 ±0.11),(0.63 ±0.13)],the differences were statistically significant (t =3.213,3.739,3.632,8.144 and 3.387,4.533,4.991,8.526,P =0.002,0.000,0.000,0.000,0.001,0.000,0.000,0.000,0.000,0.000).The levels of TA anterior temporalis muscle EMG and MA masseter muscle EMG in the two groups at 6 months after treatment were (76.81 ± 15.17) mV,(67.56 ±14.43)mV,(74.24 ± 13.28) mV,(68.27 ± 13.03) mV,(66.44 ± 13.28) mV,(58.76 ± 13.07) mV,(65.58 ±11.55) mV,(59.04 ± 10.76) mV,respectively,which were significantly higher than those before treatment [(46.48 ±11.15) mV,(38.19± 13.04) mV,(54.83 ±12.57) mV,(56.48 ±13.13) mV and (45.71 ±10.98) mV,(38.23 ±13.11)mV,(55.14±12.69) mV,(56.61 ± 13.08) mV] (all P ＜0.05).After treatment,the ICP-HB,ICMAP-MC,TA,EMG levels in the observation group were significantly higher than those in the control group,the differences were statistically significant (t =3.042,2.674,2.911,2.994,P =0.003,0.009,0.004 and 0.003).Conclusion The effect of rich plate plasma combined with Bio-oss artificial bone powder on the repair of bone defect around the implant is significant.The platelet rich plasma can speed up and improve the repair speed and repair quality of bone defect around the implant,so that the therapeutic effect of implant repair can be maintained for a long time.
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Objetivo: Bio-Oss is a xenogene bone graft in which all organic components are removed while retaining their natural mineral architecture. Therefore, the aim of this study was to evaluate, through a literature review, the benefits of using Bio-Oss for tissue regenerative treatment prior to implant placement. Materials and methods: a search was performed in Pubmed (Medline) in order to identify articles published in English between January 1, 2000 and June 31, 2018, where the Bio-Oss graft was used prior to implantation of implants in humans. A total of 40 studies were selected for detailed analysis. From this analysis, 18 articles were identified for inclusion in this review. Results: the articles analyzed in the review showed several beneficial effects of this xenograft, such as: positive osteoconductive properties, recovery of bone heights at sites with severe atrophies, slow xenograft reabsorption suggesting long term stability, survival rates and success of implants placed in grafted sites ranging from 91 to 100% in several studies. Conclusion: the use of bio-oss as a bone substitute is a viable alternative in the placement before dental implants, being used in clinical practice and with proved efficacy in several studies, due to its similarity with the bone and its high level of osteoconductivity (AU)
Objetivo: o Bio-Oss é um substituído ósseo xenógeno em que são removidos todos os componentes orgânicos, mantendo sua arquitetura natural. Assim, este trabalho teve como foco avaliar através de uma revisão de literatura os benefícios do uso do Bio-Oss para tratamento regenerativo tecidual previamente a instalação de implantes. Materiais e métodos: realizouse uma busca no Pubmed (Medline) com intuito de se identificar artigos publicados em inglês entre 1 de janeiro de 2000 e 31 de junho de 2018, em que se utilizava o enxerto Bio-Oss previamente a instalação de implantes em humanos. Foram selecionados 40 estudos completos para uma análise detalhada. A partir dessa análise foram identificados 18 artigos para inclusão nessa revisão. Resultados: os artigos analisados na revisão mostraram diversos efeitos benéficos desse xenoenxerto, como: propriedades osteocondutoras positivas, recuperação de alturas ósseas em locais com atrofias graves, reabsorção lenta do xenoenxerto sugerindo estabilidade a longo prazo, taxas de sobrevivência e sucesso de implantes colocados em locais enxertados variando de 91 a 100% em diversas pesquisas. Conclusão: a utilização do biooss como substituto ósseo é uma alternativa viável na colocação previamente ao implante dentário, sendo utilizado na prática clínica e comprovado em diversos estudos sua eficácia, devido sua similaridade com o osso natural e seu alto grau de osteocondutividade (AU)
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Dental Implants , Bone Transplantation , Bone Substitutes , HeterograftsABSTRACT
Objective@#To study the osteogenic potential of recombinant human bone morphogenetic protein 2 (rhBMP-2) combined with Bio-oss bone substitute in the implant restoration of bone defects in the anterior esthetic region. @*Methods@# Twelve patients who underwent the immediate placement of 20 implants with a bone augmentation procedure using rhBMP-2 and Bio-oss were included in this study. Changes in the height and thickness of the buccal bone over 6 months were measured, and the soft tissue was evaluated using the pink esthetic score (PES) after crown placement. @*Results@# All 20 implants were successfully osseointegrated, and the average increase in bone height was 1.9 mm; different degrees of bone height growth were observed for 17 (85%) implants sites. In one case, there was a severe bone fracture on the buccal side before the operation, resulting in bone plate resorption and decreased alveolar bone height. The bone height did not change significantly in 2 cases. The thickness of the buccal bone plate for all implants was greater than 1 mm. The average thickness was 1.9 mm, and the average PES was 9.8 points. @*Conclusion@# rhBMP-2 combined with Bio-oss bone substitute has a preferable effect on the restoration of bone defects in the anterior esthetic area, and can achieve good aesthetic effect.
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The purpose of this animal study is to evaluate, by histomorphometric analysis, bone regeneration in rabbit's maxillary sinuses with blood clots alone, Bio-Oss, β-tricalcium phosphate (β-TCP), and demineralized tooth dentin (DTD) grafting. Bilateral sinus augmentation procedures were performed in 18 adult male rabbits. Rectangular replaceable bony windows were made with a piezoelectric thin saw insert. In the group 1, blood clots were filled; group 2, anorganic bovine graft (Bio-Oss) was grafted; group 3, β-TCP was grafted; group 4, DTD was grafted, and covered by replaceable bony windows. Animals were sacrificed at 2, 4, and 8 weeks after surgical procedure. The augmented sinuses were evaluated by histomorphometric analysis using hematoxylin and eosin and Masson's trichrome stains. Histologically, new bone formation was revealed along the elevated sinus membrane and all graft materials. The new bone area of the group 2 was significantly greater than the group 1, and of the group 3 was significantly greater than the group 2, and of the group 4 was significantly greater than the group 3 at 8 weeks with P < 0.05. The bone marrow area of group 1 was significantly greater than other groups at 8 weeks. The DTD area was significantly lesser than Bio-Oss or β-TCP particles area at 8 weeks. This present study suggests that DTD can be effective graft materials for bone regeneration of the maxillary sinus augmentation.
Subject(s)
Adult , Animals , Humans , Male , Rabbits , Bone Marrow , Bone Regeneration , Coloring Agents , Dentin , Eosine Yellowish-(YS) , Hematoxylin , Maxillary Sinus , Membranes , Osteogenesis , Tooth , TransplantsABSTRACT
Para tentar preservar as dimensões teciduais (ósseas e de tecido mole) do alvéolo até o momento da instalação do implante pode-se lançar mão de técnicas de preservação de alvéolos dentários imediatamente após a exodontia. Dentre as diversas técnicas e biomateriais existentes, a associação de um substituto ósseo (Bio-Oss® Collagen) com um selador do alvéolo (Mucograft® Seal) vem apresentando resultados satisfatórios na literatura. O objetivo do presente trabalho é apresentar uma breve revisão de literatura e um relato de caso clínico usando essa abordagem. Os principais achados da revisão de literatura é que a utilização desses substitutos mucosos e ósseos são a redução do tempo cirúrgico e diminuição da morbidade e desconforto pós-operatório do paciente, já que não necessita da área doadora. No relato de caso, os resultados clínicos de 15 e 60 dias de pós-operatório mostraram que essa abordagem foi eficaz em manter as dimensões ósseas e de tecido queratinizado do alvéolo. (AU)
In an effort to preserve the alveolar tissue dimensions (bone and soft tissue) until the time of implant installation can make use of ridge preservation techniques after the dental extraction. Among the many techniques and biomaterials the association of a bone substitute (Bio-Oss® Collagen) with an alveolar sealer (Mucograft® Seal) has shown satisfactory results in the literature.The objective of this study is present a brief literature review and a clinical case report using this approach. The main findings of the literature review are that the use of these mucosal and bone substitutes are the reduction of surgical time and decrease of the postoperative morbidity and discomfort of the patient, since it does not need the donor area. In the case reportthe clinical results of 15 and 60 days postoperatively showed that this approach was effective in maintaining bone dimensions and keratinized alveolar tissue (AU)
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Humans , Female , Middle Aged , Biocompatible Materials , Tooth SocketABSTRACT
La elevación del piso del seno maxilar or medio de injertos óseos es un procedimiento predecible y frecuente para el tratamiento del reborde alveolar superior atrófico. El mateiççrial de injerto debe poseer propiedades mecánicas y biológicas que promuevan la osteoconducción y una buena estabilidad de los implantes colocados en dicho injerto. Objetivo: evaluar el efecto del tamaño de las partículas (pequeñas 0,25-1 mm o grandes 1-2 mm) de hidroxiapatita natural macroporosa de origen bovino, usadas en procedimientos de relleno de seno maxilar humano, sobre el coeficiente de estabilidad de los implantes (ISQ) que se coloquen en el injerto, obtenidos a través de análisis de frecuencia de resonancia. Material y método: se midió el coeficiente de estabilidad de 30 implantes colocados en 15 pacientes (8 varones y 7 mujeres), tratados con procedimientos de relleno de seno maxilar, usando como material de injerto hidroxiapatita natural macroporosa de origen bovino (Bio-Oss), de partículas grandes o de partículas pequeñas (11 y 7 respectivamente). Las mediciones se realizaron en el momento de la cirugía de colocación de los implantes a través de análisis de frecuencia de resonancia. El período de cicatrización de las elevaciones de seno maxilar fue de 8 a 9 meses. Los datos fueron analizados con estadística no paramétrica. Resultados: no se detectaron diferencias significativas en los varones de ISQ de los implantes colocados en senos rellenados con partículas pequeñas og randes (P<0,05). Los valores de desvío estándar de RFA fueron numéricamente mayores en partículas grandes (+- 13,46 ISQ) que en las pequeñas (+- 5,23 ISQ). Conclusión: dentro de las limitaciones de este estudio realizado en senos maxilares humanos, se concluye que el diferente tamaño de las partículas de hidroxiapatita natural macroporosa de origen bovino, no tiene un efecto diferencial en los valores de ISQ de los implantes dentales colocados en los senos tratados...
Subject(s)
Humans , Cattle , Dental Implantation, Endosseous , Alveolar Bone Loss/surgery , Maxillary Sinus/surgery , Bone Transplantation/instrumentation , Biocompatible Materials , Durapatite/therapeutic use , Osseointegration/physiology , Particulate Matter , Data Interpretation, Statistical , Statistics, NonparametricABSTRACT
Objective:To compare the outcomes of guide bone regeneration by calcined bovine bone and Bio-Oss graft material in alveolar ridge preservation after tooth extraction.Methods:280 patients were divided into two groups randomly.Each patient had single tooth extracted.The sockets were filled with calcined bovine bone in 140 patients and Bio-Oss graft in another 140 patients. After shaping,all the sockets were covered with Bio-Gide membrane.Buccal mucoperiosteal flap was released and sutured to close the alveolar sockets.The patients were regularly examined at the 1st,12th and 24th week after surgery.Physical examination and X-ray evaluation were applied to compare the outcomes of the two materials in alveolar ridge preservation.Results:No infection and re-jection occurred.The radiographic results showed the width and height of the alveolar bone were preserved well at the 12th and 24th weeks.No statistically difference was found in the two groups at the 1st and 24th weeks(P>0.05).Conclusion:The two graft ma-terials can effectively preserve alveolar bone after tooth extraction.
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Objective To histomorphometricly assess changes occurred in the alveolar ridge following different methods of socket preservation and to compare them against natural healing without interventions. Methods The second、 third and fourth mandibular premolars were extracted from six beagles. Six extraction sites in each dog were randomly assigned to three treatments as follows:natural healing (T1), Bio-Oss Collagen (T2) and immediate implant with Bio-Oss (T3). Six month after surgery, the dogs were euthanized and tissue samples were sectioned, fixed and mounted, then were stained with toluidine blue. The histologic studies and morphological measurements were performed by using an optical microscope and a digital image software. Results Reabsorption in the buccal aspect of the alveolar crest of ridge was showed in all groups. With respect to the mean vertical bone loss of the buccal bone plate, T3 is lower than T1 and T2(P<0.001 ), while no significant differences were observed between T1 and T2. With regard to horizontal dimension of the alveolar process , a statistical significance could be found at 3mm and 4mm below the crest of ridge in group T1 and T3(P=0.017, P=0.042), while no statistical differences were found between other groups. Conclusions Both techniques of alveolar ridge preservation were not able to completely preserve the original bone volume after tooth extraction. Immediate implant placement in combination with Bio-Oss seems to have the potential to limit the reabsorption of the alveolar process efficiently , but the bone preserving effect of Bio-Oss Collagen is undesirable.
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PURPOSE: The purpose of this prospective study was to evaluate the effectiveness of newly developed autogenous tooth bone graft material (AutoBT)application for sinus bone graft procedure. MATERIALS AND METHODS: The patients with less than 5.0 mm of residual bone height in maxillary posterior area were enrolled. For the sinus bone graft procedure, Bio-Oss was grafted in control group and AutoBT powder was grafted in experimental group. Clinical and radiographic examination were done for the comparison of grafted materials in sinus cavity between groups. At 4 months after sinus bone graft procedure, biopsy specimens were analyzed by microcomputed tomography and histomorphometric examination for the evaluation of healing state of bone graft site. RESULTS: In CT evaluation, there was no difference in bone density, bone height and sinus membrane thickness between groups. In microCT analysis, there was no difference in total bone volume, new bone volume, bone mineral density of new bone between groups. There was significant difference trabecular thickness (0.07 microm in Bio-Oss group Vs. 0.08 microm in AutoBT group) (P=.006). In histomorphometric analysis, there was no difference in new bone formation, residual graft material, bone marrow space between groups. There was significant difference osteoid thickness (8.35 microm in Bio-Oss group Vs. 13.12 microm in AutoBT group) (P=.025). CONCLUSION: AutoBT could be considered a viable alternative to the autogenous bone or other bone graft materials in sinus bone graft procedure.
Subject(s)
Humans , Biopsy , Bone Density , Bone Marrow , Membranes , Osteogenesis , Prospective Studies , Tooth , Transplants , X-Ray MicrotomographyABSTRACT
Procedimentos de levantamento do seio maxilar têm sido realizados para aumentar o volume ósseo e promover a estabilidade do implante, na região posterior de maxilas severamente atrofiadas. Ao longo dos anos, resultados de vários estudos demonstraram que alguns substitutos ósseos podem suportar implantes em função, após o levantamento de seio maxilar, igual ou melhor quando utilizado o osso autógeno. Neste estudo, foi avaliado o comportamento de um substituto ósseo completamente biodegradável (OsteoScaf) no modelo experimental de levantamento de seio maxilar em coelhos. Além disso, ele foi comparado com o osso autógeno e outros dois substitutos ósseos, não totalmente biodegradáveis, disponíveis comercialmente (Bio-Oss® e BoneCeramic®). Avaliação clínica, tomografia computadorizada por feixe cônico, microtomografia computadorizada, análises microscópicas e análise molecular, através da técnica de PCR, foram realizadas após 2, 4 e 8 semanas de cirurgia. O levantamento de seio maxilar utilizando o osso autógeno demonstrou maior reabsorção, ao longo do tempo, comparado aos substitutos ósseos, os quais revelaram maior neoformação óssea após 8, 4 e 2 semanas, respectivamente. O grupo Bio-Oss® apresentou maior neoformação óssea, ao longo do tempo, quando comparado aos grupos Osteoscaf e BoneCeramic®, os quais foram qualitativamente emelhantes. O grupo BoneCeramic® mostrou uma resposta celular de células gigantes até 8 semanas. Concluiu-se que os substitutos ósseos, neste estudo, obtiveram melhor desempenho do que o osso autógeno, e o OsteoScaf demonstrou maior reabsorção do que os outros grupos, em todos períodos.
Maxillary sinus augmentation procedures have been applied to increase bone volume and to promote stability of implants in the severely atrophied posterior maxilla. Over the years, the outcomes of several studies have demonstrated that some bone substitutes can support implants in function after sinus augmentation as well as, or better than those with autogenous bone. Our experimental model evaluated the behavior of a fully biodegradable bone substitute (OsteoScaf) in a rabbit sinus lift procedure. We compared this with autogenous bone and other two available non-biodegradable bone substitutes (Bio-Oss® and BoneCeramic®). Clinical evaluation, Cone Beam Computed Tomography, Microcomputed Tomography, microscopic and molecular evaluation were used for data analysis at 2, 4 and 8 weeks after sinus augmentation. Autogenous bone was more resorbed over time than the other materials. All bone substitutes showed more bone formation at 8, 4 and 2 weeks, respectively. Bio-Oss® showed more bone formation/timepoint than Osteoscaf and Boneceramic®, which were similar. Boneceramic® showed a florid giant cell response up to 8 weeks. We concluded that the bone graft materials all performed better than autogenous bone and OsteoScaf showed comparative bone growth yet greater degradation than the other two materials.
Subject(s)
Animals , Male , Rabbits , Models, Animal , Maxillary Sinus/surgery , Bone Substitutes/therapeutic use , Cone-Beam Computed Tomography , Materials Testing , Reproducibility of Results , Time Factors , Treatment OutcomeABSTRACT
Procedimentos de levantamento do seio maxilar têm sido realizados para aumentar o volume ósseo e promover a estabilidade do implante, na região posterior de maxilas severamente atrofiadas. Ao longo dos anos, resultados de vários estudos demonstraram que alguns substitutos ósseos podem suportar implantes em função, após o levantamento de seio maxilar, igual ou melhor quando utilizado o osso autógeno. Neste estudo, foi avaliado o comportamento de um substituto ósseo completamente biodegradável (OsteoScaf) no modelo experimental de levantamento de seio maxilar em coelhos. Além disso, ele foi comparado com o osso autógeno e outros dois substitutos ósseos, não totalmente biodegradáveis, disponíveis comercialmente (Bio-Oss® e BoneCeramic®). Avaliação clínica, tomografia computadorizada por feixe cônico, microtomografia computadorizada, análises microscópicas e análise molecular, através da técnica de PCR, foram realizadas após 2, 4 e 8 semanas de cirurgia. O levantamento de seio maxilar utilizando o osso autógeno demonstrou maior reabsorção, ao longo do tempo, comparado aos substitutos ósseos, os quais revelaram maior neoformação óssea após 8, 4 e 2 semanas, respectivamente. O grupo Bio-Oss® apresentou maior neoformação óssea, ao longo do tempo, quando comparado aos grupos Osteoscaf e BoneCeramic®, os quais foram qualitativamente emelhantes. O grupo BoneCeramic® mostrou uma resposta celular de células gigantes até 8 semanas. Concluiu-se que os substitutos ósseos, neste estudo, obtiveram melhor desempenho do que o osso autógeno, e o OsteoScaf demonstrou maior reabsorção do que os outros grupos, em todos períodos.
Maxillary sinus augmentation procedures have been applied to increase bone volume and to promote stability of implants in the severely atrophied posterior maxilla. Over the years, the outcomes of several studies have demonstrated that some bone substitutes can support implants in function after sinus augmentation as well as, or better than those with autogenous bone. Our experimental model evaluated the behavior of a fully biodegradable bone substitute (OsteoScaf) in a rabbit sinus lift procedure. We compared this with autogenous bone and other two available non-biodegradable bone substitutes (Bio-Oss® and BoneCeramic®). Clinical evaluation, Cone Beam Computed Tomography, Microcomputed Tomography, microscopic and molecular evaluation were used for data analysis at 2, 4 and 8 weeks after sinus augmentation. Autogenous bone was more resorbed over time than the other materials. All bone substitutes showed more bone formation at 8, 4 and 2 weeks, respectively. Bio-Oss® showed more bone formation/timepoint than Osteoscaf and Boneceramic®, which were similar. Boneceramic® showed a florid giant cell response up to 8 weeks. We concluded that the bone graft materials all performed better than autogenous bone and OsteoScaf showed comparative bone growth yet greater degradation than the other two materials.
Subject(s)
Animals , Male , Rabbits , Models, Animal , Maxillary Sinus/surgery , Bone Substitutes/therapeutic use , Cone-Beam Computed Tomography , Materials Testing , Reproducibility of Results , Time Factors , Treatment OutcomeABSTRACT
Objective: To evaluate the osteogenic activities of Bio-oss after combining with fibrin glue in reconstruction of canine mandibular defects. Methods: The second and fourth premolar teeth and the second molar teeth were extracted bilaterally, in 9 hibrid canines, resulting in 6 bone defects (1 cm × 1 cm) in each canine. Bio-oss, Bio-oss+FG and FG were implanted into the bone defects of the second, fourth premolar teeth and the second molar teeth, respectively. Canines were executed in group of 3 after 4, 8, and 12 weeks to observe the healing of soft tissues. The bone density was assessed by X-ray, the property of Bio-oss were observed via gross specimen, and the morphology of the newly-formed bone was observed by tissue sections. The proportion of newly-formed bone was obtained by computer image analysis (SAS software, analysis of variance). Results: Stage I healing of soft tissues was achieved in all animals. The bone densities were not significantly different between Bio-oss+FG and Bio-oss groups. The bone in FG group had transparent area. We also found that the bone in Bio-oss+FG group was closely combined and there were sccatered Bio-oss dusts in the soft tissues of the Bio-oss group. The newly-formed bone in the FG group was only found in the border between the defects and FG. The proportion of newly-formed bone was less in the Bio-oss+FG group than in the Bio-oss group at 4, 8, and 12 weeks after extraction(P<0.05). Conclusion: Fibrin glue can well shape the Bio-oss and has satisfactory biocompatibility, but it reduces the new bone forming.
ABSTRACT
Maxillary sinus lift and bone graft are used to reconstruct atrophic maxilla molar area for endosseous dental implants. Many different grafting materials and techniques can be used for maxillary sinus bone graft. Bio-Oss(R) has been proposed as bone substitute and successfully utilized as osteoconductive filler. Platelet rich plasma (PRP) is an autologous material with many growth factors, such as PDGF, TGF-beta, IGF, VEGF, facilitating bone healing process. And Platelet poor plasma (PPP) is the by-product in procedure of producing PRP. Six rabbits were used as experimental animal. Both maxillary sinus were grafted with Bio-Oss(R) and PRP, and Bio-Oss(R) and PPP. Rabbits were sacrificed at 4, 8 and 12 weeks. The grafting sites were evaluated by histomorphometric analysis. As a result, using PRP showed excellent bone formation in the early stage, but no further significant effect after that. In late stage, the ability of bone formation of using PRP was even worse than using PPP. The further studies need to be considered in this case.