Foreign body granuloma following placement of hard tissue replacement material: a case report

The placement of grafting material in extraction sites for ridge preservation is an increasingly common practice among clinicians. This is a case report of a patient presenting with a symptomatic, foreign body granuloma following the placement of hard tissue replacement (HTR) in extraction sockets. The surgical specimen revealed numerous histiocytes and foreign body type giant cells. The grafting material was surgically removed and the patient's symptoms were alleviated. Although biocompatibility of HTR has previously been shown, specific applications may be contraindicated or some patients may exhibit sensitivity to this material.     

An evaluation of bone induction delivery materials in conjunction with root-form implant placement

The success of bone-inductive cytokines in surgical alveolar defects is greatly dependent upon the ability of carrier materials to effectively deliver the inductive protein to the surgical site. An evaluation of three types of carrier materials was undertaken in six monkeys using an osseous defect of 2.0 cm that was produced by partial resection of the maxilla and mandible and placement of titanium implants in each alveolar quadrant. After 5 months, abutments were placed on the implants, which were allowed to function for an additional 5 months. Intravital labeling with tetracycline was used to evaluate the late healing remodeling processes. The carriers were evaluated by studying (1) the amount of surface osseointegration on the root-form implants; (2) the bone density as related to trabecular pattern and cortex formation; and (3) the quantitative and qualitative thickness of the alveolar bone buccolingually at the implanted sites. Of the three materials, the calcium carbonate coral (BioCoral) produced a decreased amount of bone regeneration in comparison with both the poly(methylethyl methacrylate) material (HTR) and the porous bone mineral (Bio-Oss). Both the HTR and Bio-Oss with rhBMP-2 produced excellent thickness of the repaired alveolar ridge. All three materials produced the same amount of osseointegration with the titanium implant surfaces. Good bone quality, as reflected in thickening of the trabecular bone patterns, was seen with both Bio-Oss and HTR. While all three of these carrier materials appeared to produce good osseointegration with the titanium implants, BioCoral did not effect a quantitative or qualitative restoration of the alveolar bone comparable to that following the use of either HTR or Bio-Oss with rhBMP-2.     

Human clinical and histologic responses to the placement of HTR polymer particles in 11 intrabony lesions

Eleven intrabony periodontal lesions in five volunteer patients received surgical debridement followed by site implantation of a porous particulate polymeric composite (HTR polymer). These patients were observed over time periods varying from 4 weeks to 26 weeks. At the end of the individual observation periods, treated sites were surgically removed in block for histologic analysis. Clinical observations indicated a reduction in pocket depth following treatment which consisted of both gingival recession and gain in clinical closure. No untoward effects were observed clinically in any treated patient during the observation periods. Histologic responses varied from gain in closure by epithelial adhesion to new attachment of varying magnitude. Such varied responses were seen within the same patient and between patients. Graft particles were present at sites from 4 weeks to 26 weeks after implantation and were surrounded by connective tissue capsules. At the periphery of some particles, limited bone formation was present. The alveolar bed was remodeling, at times surrounding specific particles. In our sample, HTR polymer, therefore, appeared to be a well tolerated synthetic graft material when implanted in human intrabony lesions.     

Synthetic bone grafts in peri-implant bone dehiscences: histological results in humans

This study describes the histological results found in three patients treated with osseointegrated implants and Bioplant HTR (Hard Tissue Replacement) synthetic bone graft in peri-implant dehiscences adjacent to implants. This therapy was carried out without the use of barrier membranes. Bioplant HTR is reported to act as its own barrier and prevent gingival soft tissue migration ingrowth. The histologic picture demonstrated that Bioplant HTR is osteoconductive and biocompatible, and can be used both as bone substitute and as a barrier for guided bone regeneration in implant therapy.     

Use of HTR synthetic bone as an augmentation material in conjunction with immediate implant placement: a case report

Immediate placement of dental implants (DI) in fresh extraction sockets is associated with remaining voids around the DI and often a partial dehiscence or thin facial alveolar plate. Bioplant HTR synthetic bone (HTR) was used as a ridge preservation/augmentation material in conjunction with this method of DI placement. A 61-year-old white woman requiring extraction of tooth 12 opted for immediate DI placement. HTR was used to fill the remaining socket void and enhance the facial ridge width, and primary closure was attempted with sutures. DI uncovering was performed at about 6 months. Measurements were taken to the nearest 0.5 mm of the internal socket width and total site width at DI placement and uncovering. The internal socket width was essentially maintained (6.8 vs 6.6 mm), and the total ridge width showed a change from 8.7 to 9.1 mm. The results of this case suggest that HTR is a useful adjunct in the placement of immediate DIs for the preservation of ridge width.     

Use of HTR synthetic bone grafts in conjunction with immediate dental implants

Immediate placement of dental implants in fresh extraction sockets is associated with remaining voids around the implants and often a partial dehiscence or thinning of the facial alveolar plate. Nine patients had Bioplant HTR synthetic bone used as a ridge preservation/augmentation material in conjunction with immediate placement of 10 implants. Hard tissue replacement (HTR) was used to fill the remaining socket void and enhance the facial ridge width, and the wound closed as completely as possible. Dental implants were uncovered at approximately 6 months. Measurements taken of the internal socket width and total ridge width at the implant placement and uncovering showed the mean internal socket width was maintained (7.2 mm vs 6.9 mm), and the total ridge width exhibited a mean change from 9.6 mm to 8.8 mm. Of the 10 implant sites, 7 showed a net increase, 2 no change, and 1 a decrease in overall ridge width. All 10 implants were restored for at least 6 months. These clinical results suggest that HTR is a useful adjunct in the placement of immediate dental implants for the preservation of ridge width and provides a good base for functional and esthetic prosthetic reconstruction.     

Alveolar ridge repair using resorbable membranes and autogenous bone particles with simultaneous placement of implants: an experimental pilot study in dogs

The aim of this experimental study was to evaluate the use of autogenous bone harvested during preparation of implant sites in combination with resorbable membranes for vertical ridge augmentation under 2 different defect site conditions. Combined vertical/horizontal alveolar bone defects were created by experimentally induced periodontal infections around all premolar teeth in the mandibles of 3 dogs (group 1). In another 3 dogs, fresh surgical defects were created after extraction of all premolar teeth in the mandibles (group 2). In all dogs, 2 implants were placed on each side of the mandible into the defect areas. One implant on each side of the mandible received augmentation with autogenous bone particles, and both implants on one side of the mandible were covered with polylactic acid membranes. After 5 months, the material was evaluated histologically. There was a small but significant increase in bone regeneration in the defects augmented with bone particles with and without membrane coverage in group 1. In group 2, no significant difference was seen between the controls and the augmented sites. The major limiting effect for bone regeneration appeared to be insufficient stability of the bone material to withstand the overlying soft tissue pressure. It was concluded that the placement of autogenous bone particles, either with or without membrane coverage, had little effect on the regeneration of peri-implant bone defects.     

Placement of implants into ridges grafted with bioplant HTR synthetic bone: histological long-term case history reports

Following alveolar ridge grafting procedures for ridge preservation, for example, the immediate filling of extraction sockets, and ridge augmentation, for example, the building up of the atrophic jawbone, punch biopsies were obtained at various times postextraction prior to the placement of endosseous root-form implants. These histological sections provided an opportunity to study the bony regenerative response to an osteoconductive synthetic graft material and longer term interactions over a period from 8 months to 12 years. The formation and remodeling of healthy dense lamina of bone in areas where bone voids previously existed either from healed or immediate extraction sockets or where there was jawbone atrophy resulting from multiple tooth loss was observed. The grafting procedures enabled dentists to place implants into sites that would have been impossible if not for these preimplant grafting procedures. The jawbone areas studied involved grafted single sites and quadrants as well as full arch augmentation with a calcified microporous copolymer (Bioplant HTR Synthetic Bone, Bioplant Inc, South Norwalk, Conn) graft material. Retrospective case reports of 24 patients were followed radiographically and clinically to 12 years post-alveolar-ridge grafting and subsequently to 5 years after implants were placed into these augmented ridges. Implant and grafting histories from 4.7 months to 17 years are reported for three of these patients. General applications of synthetic bone grafting before implant placement are recommended.     

Clinical comparison of microporous biocompatible composite of PMMA, PHEMA and calcium hydroxide grafts and expanded polytetrafluoroethylene barrier membranes in human mandibular molar Class II furcations. A case series.

BACKGROUND: Class II furcations present difficult treatment problems. Several treatment approaches to obtain furcation fill have been used with varying success. METHODS: The response of mandibular Class II furcations to treatment with either a microporous biocompatible composite of PMMA (poly-methyl-methacrylate), PHEMA (poly-hydroxyl-ethyl methacrylate) and calcium hydroxide graft synthetic bone (HTR) replacement graft material; ePTFE barrier membrane; or a combination of the two was evaluated in trios of mandibular molars with Class II furcations in 8 patients with moderate to advanced periodontitis. Following initial preparation, full-thickness flaps were raised in the areas being treated, the bone and furcation defects debrided of granulomatous tissue, and the involved root surfaces mechanically prepared and chemically conditioned. By random allocation, HTR, ePTFE, or a combination of both was placed into and/or fitted over the furcations, packed and/or secured in place, and the host flap replaced or coronally positioned with sutures. Postsurgical deplaquing was performed every 10 days leading up to ePTFE removal at approximately 6 weeks. Continuing periodontal maintenance therapy was provided until surgical reentry at 6 months for documentation and any further necessary treatment. RESULTS: Direct clinical measurements demonstrated essentially similar clinical results with all 3 treatments for bone and soft tissue changes. There were no statistically or clinically significant differences except for better horizontal amount and percent defect fill with HTR alone. Four of 8 furcations became Class I clinically with HTR alone, 5 of 8 became Class I with ePTFE alone, and 5 of 8 with combination treatment. The only complete furcation closure occurred with HTR. CONCLUSION: The findings of this study suggest essentially equal clinical results with HTR bone replacement graft material alone, ePTFE barrier alone, and a combination of the two in mandibular molar Class II furcations. However, a real difference may not have been detected based on the small number of subjects in the study.     

Evaluation of a bone substitute prepared from alpha-tricalcium phosphate and an acid polysaccharide solution.

Tissue response to a readily consolidating material prepared by mixing alpha-tricalcium phosphate (alpha-TCP) powder with a glycolic acid dextran solution and to this consolidating material combined with particulate hydroxylapatite (HA) was studied after implantation in the subperiosteal space of the mandible in rabbits. Active new bone formation comparable to that seen on HA implants was observed around the two compounds. The newly formed bone was in direct contact with the HA as well as the readily consolidated material and little adverse effect resulting from the glycolic acid and dextran was observed. Because the readily consolidating material was firm and could be contoured into any shape during the process of consolidation, it may be quite useful as a bone substitute and as an adherent for HA particles for reconstructive bone surgery, overcoming the disadvantages inherent to the particulate form of HA.     

HTR polymer grafts in human periodontal osseous defects. I. 6-month clinical results

HTR polymer was evaluated as a grafting material in periodontal osseous defects in 21 adult patients. Following initial preparation and pre-surgical documentation with standardized measurements, radiographs, and photographs, vertical osseous defects were treated with surgical open flap debridement alone (DEBR) or with DEBR plus placement of HTR polymer graft material. Patients were followed with frequent recalls until surgical re-entry at about 6 months for documentation and any needed remedial therapy. Re-entry data show that use of HTR polymer grafts resulted in significantly better mean defect fill of 2.2 mm (60.8%) compared to 1.0 mm (32.2%) with DEBR alone (P less than .001). Other hard tissue findings such as residual defect depth, crestal resorption, and percent defect resolution showed similar clinically superior results with the use of HTR polymer. Soft tissue findings showed significant differences in favor of HTR for decrease in probing depth and gain in clinical attachment. These results are similar to those reported with other graft materials. Over a 6-month period, HTR polymer was found to show promise for the repair of periodontal osseous defects.     

Clinical and radiographic evaluation of the effects of guided tissue regeneration using resorbable membranes after extraction of impacted mandibular third molars

The aim of this investigation was to evaluate the healing following guided tissue regeneration of bone defects distal to the mandibular second molars after surgical extraction of soft tissue-impacted, mesioangularly inclined third molars. After the impacted third molars were extracted, 15 sites were treated with polyglycolic acid/polylactic acid bioresorbable membranes plus scaling and root planing (SRP) of the distal surface of the second molars (test sites); 15 sites were treated with SRP alone (control sites) according to a split-mouth design. At 12 months after surgery, the placement of barrier material was shown to have resulted in statistically significant differences in clinical attachment level and bone gain compared to control sites.     

Human histologic evaluation of HTR polymer and freeze-dried bone allograft

Abstract This case report compares the results of placement of HTR^TM (Hard Tissue Replacement Synthetic Bone^TM) and freeze-dried bone allograft (FDBA) in the same patient. 2 notches were made in each of 6 teeth, 1 at the gingival margin and the other at the most apical level of calculus. Soft tissue reponses with both materials included probing depth reduction, gingival shrinkage and gain in clinical attachment. Histological sections of block extraction sites 30 months after placement of either material showed no signs of new attachment. Little or no inflammation was present with both materials. There was also an absence of all FDBA particles which assumes complete resorption of this material prior to 30 months. Gingival shrinkage resulted in the exposure of the gingival and calculus notch in all FDBA treated sites. Gingival epithelium was found adjacent to the gingival notch in all HTR^TM treated sites. The calculus notch in HTR^TM treated sites was lined by junctional epithelium with connective tissue and bone opposing the adhesion. HTR^TM particles were present and surrounded by connective tissue or bone. HTR^TM appears to serve as a scaffold for new bone formation when in close contact with alveolar bone.     

Xenograft versus extraction alone for ridge preservation after tooth removal: a clinical and histomorphometric study

BACKGROUND: The preservation of bone volume immediately after tooth removal might be necessary to optimize the success of implant placement in terms of esthetics and function. The objectives of this randomized clinical trial were two-fold: 1) to compare the bone dimensional changes following tooth extraction with extraction plus ridge preservation using corticocancellous porcine bone and a collagen membrane; and 2) to analyze and compare histologic and histomorphometric aspects of the extraction-alone sites to the grafted sites. METHODS: Forty subjects who required tooth extraction and implant placement were enrolled in this study. Using a computer-generated randomization list, the subjects were randomly assigned to the control group (EXT; extraction alone) or to the test group (RP; ridge-preservation procedure with corticocancellous porcine bone and collagen membrane). The following parameters were assessed immediately after extraction and 7 months prior to implant placement: plaque index, gingival index, bleeding on probing, horizontal ridge width, and vertical ridge changes. A bone biopsy was taken from the control and test sites 7 months after the surgical treatment. Histologic and histomorphometric analyses were also performed. RESULTS: A significantly greater horizontal reabsorption was observed at EXT sites (4.3+/-0.8 mm) compared to RP sites (2.5+/-1.2 mm). The ridge height reduction at the buccal side was 3.6+/-1.5 mm for the extraction-alone group, whereas it was 0.7+/-1.4 mm for the ridge-preservation group. Moreover, the vertical change at the lingual sites was 0.4 mm in the ridge-preservation group and 3 mm in the extraction-alone group. Forty biopsies were harvested from the experimental sites (test and control sites). The biopsies harvested from the grafted sites revealed the presence of trabecular bone, which was highly mineralized and well structured. Particles of the grafted material could be identified in all samples. The bone formed in the control sites was also well structured with a minor percentage of mineralized bone. The amount of connective tissue was significantly higher in the extraction-alone group than in the ridge-preservation group. CONCLUSIONS: The ridge-preservation approach using porcine bone in combination with collagen membrane significantly limited the resorption of hard tissue ridge after tooth extraction compared to extraction alone. Furthermore, the histologic analysis showed a significantly higher percentage of trabecular bone and total mineralized tissue in ridge-preservation sites compared to extraction-alone sites 7 months after tooth removal.     

牙周炎患者即刻种植修复的临床观察

目的 评价重度牙周炎患者拔牙后种植治疗并行即刻修复的临床效果.方法 选择在中山大学光华口腔医学院·附属口腔医院种植科就诊的需行义齿修复的重度牙周炎患者12例.术前行完善的牙周治疗,术中拔除余留牙,彻底清创,植入种植体并于手术当日完成树脂临时修复,6个月后行永久修复.术后l、6、12、24个月复诊,评价种植体和修复体存留率及软硬组织状态.结果 植入种植体84枚,上颌50枚、下颌34枚,其中32枚为即刻植入新鲜拔牙窝.3例(4枚)种植体失败,种植体两年存留率为95％,其中上颌92％( 46/50),下颌为100％ (34/34);修复成功率为100％.所有的种植失败均发生在手术后6个月内.即刻种植体植入拔牙窝和种植体植入正常牙槽骨两组在植入扭矩及牙槽骨吸收水平方面差异无统计学意义.结论 本组牙周炎患者行完善牙周治疗后全口种植即刻修复取得满意的修复效果.     

Quantitative evaluation of extraction socket healing following the use of autologous platelet-rich fibrin matrix in humans

Platelet-rich fibrin matrix (PRFM) is an autologous biologic material created by centrifugation of blood. This study quantified ridge changes associated with the healing of 21 extraction sites using PRFM alone as a graft. Standardized measurements of ridge width and height were recorded at extraction, after graft placement, and after 4 months of healing. Mean width resorption 3 and 5 mm apical to the crest was 0.32 mm (4.71% loss) and 0.57 mm (7.38% loss), respectively. Mean height resorption was 0.67 mm (7.13% loss). Sites grafted with PRFM alone displayed rapid clinical healing, minimal flap reopening, and excellent bone density. Advantages of PRFM alone include less surgical time, elimination of techniques and potential healing difficulties associated with membranes, and less resorption during healing, as compared to guided bone regeneration procedures.     

Bacterial Persistence in Dentoalveolar Bone Following Extraction: A Microbiological Study and Implications for Dental Implant Treatment

Background: The microbiological status of apparently healed alveolar bone implant sites is unknown. Implant success may be compromised by site‐specific persistence of bacterial biofilm co‐aggregations contaminating healed alveolar bone. Purpose: The purpose of the present study was to investigate whether extraradicular infection can persist in apparently healed alveolar bone and to develop a surgical debridement strategy that favors implant osseointegration. Materials and Methods: The study was conducted on 32 private practice patients. Seventy‐seven microbiological samples were taken from 16 pre‐implant extraction sockets, 56 healed post‐extraction osteotomies at fixture placement, and five failed fixtures. Two of the healed osteotomy samples were healed retreatment sites. Tissue fluid and bone samples were analyzed by either anaerobic/aerobic culturing or DNA molecular techniques. All patients were treated ad modum Brånemark, with a two‐stage sterile surgical procedure. A search of the medical and dental literature revealed no evidence‐based or best practice recommendations for the use of debridement in implant therapy. Thus, we developed a new technique for the debridement of alveolar bone found to be contaminated by persistent biofilm or planktonic bacteria. Results: The results of the microbiological analysis of 77 bone and effusion samples from 47 implant sites of the 32 patients showed that overall, 32% (n = 25) had bacteria present in the sample. In 16 pre‐implant extraction sockets, 69% of samples were positive for the presence of bacteria (n = 11). Of 56 osteotomies with a minimum 3‐month healing at fixture placement, 21% revealed a positive culture (n = 12). Two‐stage failed fixtures had 100% positive cultures (n = 5) and it was evident from radiographs that all of these failed fixtures had the apical ends close to the former tooth root end. Based on these findings, we have developed a microbiologically based surgical debridement strategy to successfully re‐treat early infective failures and to place successful two‐stage fixtures. Conclusion: Bacteria can persist as a contaminant in apparently healed alveolar bone following extraction of teeth with apical or radicular pathosis. A new technique for surgical debridement to reduce and limit this bacterial contamination has been described.     

Preservation of the postextraction alveolar ridge: a clinical and histologic study

The aim of this investigation was to assess the possibility of preserving the buccal and lingual plates of a postextraction socket from resorption using bone filler after tooth extraction. In 10 patients, 10 single extraction sites in the posterior area received a bone substitute. The osteoconductive material was covered by a collagen membrane in all cases. Contour changes of the alveolar process were evaluated intraorally using a surgical caliper over a 4-month period. Four months after extraction, a specimen was harvested from the area previously augmented with bone filler, and histologic analysis was performed. The results demonstrated that it was possible to preserve about 85% of the initial ridge dimensions, allowing for correct implant placement. From a histologic point of view, new bone formation was detected in all sites, with a 25% average residual presence of the graft particles. This investigation confirms the benefit of augmenting an extraction socket with bone substitutes.     

PRF联合GBR在前牙即刻种植中的应用1例

目的:评价富血小板纤维蛋白(Platelet Rich-Fibrin,PRF)在前牙即刻种植修复中应用的临床效果。方法:前牙即刻种植,PRF联合GBR修复种植体周围骨缺损。结果:种植体周围骨结合良好,软组织充足。结论:PRF联合GBR在前牙即刻种植中引导组织再生的临床效果显著。[关键词] PRF 即刻种植 骨缺损     

Alveolar ridge preservation of an extraction socket using autogenous tooth bone graft material for implant site development: prospective case series

This case series evaluated the clinical efficacy of autogenous tooth bone graft material (AutoBT) in alveolar ridge preservation of an extraction socket. Thirteen patients who received extraction socket graft using AutoBT followed by delayed implant placements from Nov. 2008 to Aug. 2010 were evaluated. A total of fifteen implants were placed. The primary and secondary stability of the placed implants were an average of 58 ISQ and 77.9 ISQ, respectively. The average amount of crestal bone loss around the implant was 0.05 mm during an average of 22.5 months (from 12 to 34 months) of functional loading. Newly formed tissues were evident from the 3-month specimen. Within the limitations of this case, autogenous tooth bone graft material can be a favorable bone substitute for extraction socket graft due to its good bone remodeling and osteoconductivity.