Effect of implant surface properties on peri-implant bone healing: a histological and histomorphometric study in dogs

Aim: The present study aimed to evaluate and compare two types of implants, i.e. grit‐blasted and acid‐etched implants (SLActive^®) with nano‐meter‐scale hydroxyapatite surface‐modified implants (NanoTite^?). Material and methods: For histological and histomorphometrical evaluation, 22 SLActive^® and 22 Nanotite^? implants were inserted in eleven Beagle dogs. The animals were divided into three groups of healing (A: 2 weeks; B: 4 weeks and C: 8 weeks). Two, 4 and 8 weeks after implantation, the animals were sacrificed and bone‐to‐implant contact (BIC %), first implant–bone contact (1st BIC) as well as amount of bone (BV) were assessed. Results: For SLActive^® and Nanotite^? implants, BIC% increased significantly over time. No statistically significant differences in BIC% were found between SLActive^® and Nanotite^? at all the respective implantation times. Moreover, for the different healing periods, no significant differences for BV between SLActive^® and Nanotite^? implants were found. Conclusions: The present study showed that SLActive^® and NanoTite^? implants induce a similar bone response after implantation for 2, 4 and 8 weeks in a non‐submerged position in the mandible of dogs. To cite this article:
Al‐Hamdan K, Al‐Moaber SH, Junker R, Jansen JA. Effect of implant surface properties on peri‐implant bone healing: a histological and histomorphometric study in dogs.
Clin. Oral Impl. Res. 22 , 2011; 399–405.     

Transmucosal healing around peri‐implant defects: crestal and subcrestal implant placement in dogs

Objective: This study was designed to evaluate the transmucosal healing response of implants placed with the junction of the smooth surfaces, either crestal or subcrestal, into simulated extraction defects after healing periods of 1 and 3 months. Materials and methods: A total of 23 Straumann SP ?3.3 mm NN, SLA^® 10 mm implants were placed in the mandibular premolar regions of three greyhound dogs 3 months after the teeth were removed. Five control implants were placed at the crestal bone level, and test implants with surgically created peri‐implant defects of 1.25 mm wide × 5 mm depth were placed either at the crestal (nine implants) or at the 2 mm subcrestal (nine implants) bone level. Implants on the right side were placed 1 month before the dogs were sacrificed, and implants on the left side were placed 3 months before sacrifice. All dogs had daily plaque control following surgery and were sacrificed 3 months after implant placement for histological and histometric analyses. Results: Mesial–distal ground sections of the control and test implant specimens showed a greater %BIC in the coronal defect region after 3 months of healing. This healing response was incomplete for the test implants compared with the control implants after a 1‐month healing period. The histometric measurements for test implants placed at the crestal bone level or 2 mm subcrestal with surgically created peri‐implant defects were more coronal or closer to the implant margin compared with the control implants. Additionally, the degree of osseointegration between the newly formed bone and the implant surface was similar between the test implants. Conclusion: Peri‐implant defects of 1.25 mm width healed with spontaneous bone regeneration around implants placed transmucosally at crestal or 2 mm subcrestal with a high degree of osseointegration after a 3‐month healing period. To cite this article:
Tran BLT, Chen ST, Caiafa A, Davies HMS, Darby IB. Transmucosal healing around peri‐implant defects: crestal and subcrestal implant placement in dogs.
Clin. Oral Impl. Res. 21 , 2010; 794–803.
doi: 10.1111/j.1600‐0501.2010.01911.x     

Bone healing around implants placed in a jaw defect augmented with Bio-Oss. An experimental study in dogs

The present experiment was carried out to study some tissue reactions around implants that were placed in an edentulous ridge which had been augmented with deproteinized natural bovine cancellous bone mineral. In 4 male beagle dogs, the premolars in the right side of the mandible were extracted and a large buccal ridge defect was created by mechanical means. The bone plate at the lingual aspect of the defect was left intact. 5 months later, the distal 2/3 of the defect area was augmented with Bio‐Oss^® (Geistlich Sons Ltd, Wolhusen, Switzerland) mixed with a fibrin sealer (Tisseel^®, Immuno AG, Vienna, Austria). After 3 months of healing, 3 fixtures (Astra Tech AB, Mölndal, Sweden; TiO‐blast; 8×3.5 mm) were installed in the mandible; 2 were placed in the augmented portion and 1 was placed in the non‐augmented portion of the defect. After a healing period of 3 months, abutment connection was performed and a plaque control period initiated. 4 months later, the dogs were sacrificed and each implant region was dissected. The tissue samples were dehydrated, embedded in plastic, sectioned in the bucco‐lingual plane and examined in the light microscope. It was observed that osseointegration failed to occur to implant surfaces within an alveolar ridge portion previously augmented with Bio‐Oss^®. In the augmented portion of the crest, the graft particles were separated from the host tissue as well as from the implant by a well‐defined connective tissue capsule. Although the lingual aspect of all fixtures (test and control) was in contact with hard tissue at the time of installation, after 4 months of function, a deep vertical bone defect frequently had formed at the lingual surface of the implants. It was concluded that in this model (i) Bio‐Oss^® failed to integrate with the host bone tissue and (ii) no osseointegration occurred to the implants within the augmented portion of the crest.     

Early healing of implants placed into fresh extraction sockets: an experimental study in the beagle dog. De novo bone formation

Objectives: Describe the early phases of tissue integration in implants placed into fresh extraction sockets and test whether a new implant surface nano‐topography (DCD nano‐particles, Nanotite^?) promotes early osseointegration when compared with minimally rough surface implants (DAE, Osseotite^®). Material and Methods: Sixteen beagle dogs received 64 test and control implants randomly installed into the distal socket of ₃P₃ and ₄P₄. Histomorphometric analysis of bone to implant contact (BIC) and bone area was performed at 4 h, 1, 2, 4 and 8 weeks. Results: Wound healing initiated with a coagulum that was substituted by a provisional matrix at 1 week. Bone formation started concomitant to a marked bone resorption. At 2 weeks, woven bone formation was evident and gradually remodelled into lamellar bone at 4 and 8 weeks. BIC increased similarly throughout the study in both groups with a tendency to higher percentages for the test devices at 2 and 4 weeks. The influence of the DCD nano‐particles was more evident at the fourth premolar site. Conclusion: Osseointegration occurred similarly at both implant groups, although the socket dimension appeared to influence bone healing. It is suggested that the enhanced nano‐topography has a limited effect in the immediate implant surgical protocol.     

Effect of grafting materials on osseointegration of dental implants surrounded by circumferential bone defects. An experimental study in the dog

Aims: This study was designed to evaluate the effect of gap width and graft placement on bone healing around implants placed into simulated extraction sockets in the mandibles of four beagle dogs. Materials and methods: Four Ti‐Unite^® implants (13 mm × 3.3 mm) were placed on each side of the mandible. Three implants were surrounded by a 1.35 mm circumferential and a 5 mm deep gap around the coronal portion of the implants. A fourth implant was inserted conventionally into both sides of the mandibles as a positive control. The gaps were filled with either Bio‐Oss^®, autogenous bone or with a blood clot alone. The study design was balanced for animal, side and modality. Ground sections were prepared from biopsies taken at 3 months, and computer‐aided histometric measurements of bone/implant contact and area of bone within threads were made for the coronal 5 mm. Data were analysed using analysis of variance. Results: The mean bone/implant contact was 9.8 mm for the control and ranged from 9.3 to 11.3 mm for the three test modalities. The corresponding values for area within threads were 1 mm² and 1–1.2 mm². Modality had a significant effect on both bone/implant contact (F=16.9; P<0.0001) and area within threads (F=16.7; P<0.0001). Conclusion: The results of this study suggest that both autogenous bone graft and Bio‐Oss^® played an important role in the amount of hard tissue fill and osseointegration occurring within marginal bone defects around implants.     

Flapless Implant Surgery Using a Mini‐Incision

Background: Traditional flapless implant surgery using a soft tissue punch device requires a circumferential excision of keratinized tissue at the implant site. A new flapless implant technique that can submerge implant fixtures is needed. Purpose: This article describes a flapless implant surgery method using a mini‐incision and compares the effects of soft tissue punch and mini‐incision surgery on both the amount of osseointegration and the bone height around the implants using a canine mandible model. Materials and Methods: Bilateral, edentulated, flat alveolar ridges were created in the mandibles of six mongrel dogs. After a 3‐month healing period, two implants were placed on each side of the mandible using either soft tissue punch or mini‐incision procedures. After an additional 3‐month healing period, a second stage surgery and transmucosal abutment attachment was performed for mini‐incision implant cases. Following a 2‐month healing period, the dogs were sacrificed to evaluate the osseointegration and bone height around the implants. Results: Average bone height was 9.6 ± 0.4 mm in the soft tissue punch group and 9.8 ± 0.3 mm in the mini‐incision group (p > .05). Average osseointegration was 70.4 ± 6.3% in the soft tissue punch group and 71.2 ± 7.1% in the mini‐incision group (p > .05). No significant differences were noted between the two groups in vertical alveolar ridge height or bone/implant contact. Conclusions: Our findings support the clinical use of mini‐incision implant surgery at sites where implants need to be protected below the soft tissue during the early phase of healing, particularly for patients with poor bone quality and/or low primary implant stability.     

Efficacy of a bioactive glass–ceramic (Biosilicate®) in the maintenance of alveolar ridges and in osseointegration of titanium implants

Objectives: The aims of this research were to evaluate the efficacy of a bioactive glass–ceramic (Biosilicate^®) and a bioactive glass (Biogran^®) placed in dental sockets in the maintenance of alveolar ridge and in the osseointegration of Ti implants. Material and methods: Six dogs had their low premolars extracted and the sockets were implanted with Biosilicate^®, Biogran^® particles, or left untreated. After the extractions, measurements of width and height on the alveolar ridge were taken. After 12 weeks a new surgery was performed to take the final ridge measurements and to insert bilaterally three Ti implants in biomaterial‐implanted and control sites. Eight weeks post‐Ti implant placement block biopsies were processed for histological and histomorphometric analysis. The percentages of bone–implant contact (BIC), of mineralized bone area between threads (BABT), and of mineralized bone area within the mirror area (BAMA) were determined. Results: The presence of Biosilicate^® or Biogran^® particles preserved alveolar ridge height without affecting its width. No significant differences in terms of BIC, BAMA, and BABT values were detected among Biosilicate^®, Biogran^®, and the non‐implanted group. Conclusions: The results of the present study indicate that filling of sockets with either Biosilicate^® or Biogran^® particles preserves alveolar bone ridge height and allows osseointegration of Ti implants. To cite this article:
Roriz VM, Rosa AL, Peitl O, Zanotto ED, Panzeri H, de Oliveira PT. Efficacy of a bioactive glass–ceramic (Biosilicate^®) in the maintenance of alveolar ridges and in osseointegration of titanium implants.
Clin. Oral Impl. Res. 21 , 2010; 148–155.
doi: 10.1111/j.1600‐0501.2009.01812.x     

Oral implants placed in bone defects treated with Bio‐Oss®, Ostim®‐Paste or PerioGlas: an experimental study in the rabbit tibiae

Objectives: To compare the histological features of bone filled with Bio‐Oss^®, Ostim‐Paste^® or PerioGlas placed in defects in the rabbit tibiae by evaluating bone tissue composition and the integration of titanium implants placed in the grafted bone. Material and methods: Two cylindrical bone defects, about 4 mm in diameter and 6 mm in depth, were created in the tibiae of 10 rabbits. The defects were filled with either Bio‐Oss^®, PerioGlas, Ostim^®‐Paste or left untreated, and covered with a collagen membrane. Six weeks later, one titanium sandblasted and acid‐etched (SLA) implant was inserted at the centre of each previously created defect. The animals were sacrificed after 6 weeks of healing. Results: Implants placed in bone previously grafted with Bio‐Oss^®, PerioGlas or Ostim^®‐Paste obtained a larger extent of osseointegration, although not statistically significant, than implants placed in non‐grafted bone. The three grafting materials seemed to perform in a similar way concerning their contribution towards implant osseointegration. All grafting materials appeared to be osteoconductive, thus leading to the formation of bridges of mineralized bone extending from the cortical plate towards the implants surface through the graft scaffold. Conclusions: Grafting with the above‐mentioned biomaterials did not add any advantage to the osseointegration of titanium SLA implants in a self‐contained defect.     

Healing at fluoride-modified implants placed in wide marginal defects: an experimental study in dogs

OBJECTIVE: To study the healing at fluoride-modified implants placed in wide circumferential defects. MATERIAL AND METHODS: Six mongrel dogs were used. The mandibular premolars and first molars were extracted. Three months later four implants were placed in one side of the mandible of each dog. The control implants (MicroThread) had a TiOblast surface, while the test implants (OsseoSpeed) had a fluoride-modified surface. Two implants of each type were placed. The marginal 50% of the prepared canal was widened using step drills. Following installation a 1 mm wide gap occurred between the implant surface and the bone wall in the defect. All implants were submerged. The installation procedure was repeated in the opposite side of the mandible 4 weeks after the first implant surgery. Two weeks later the animals were euthanized and block biopsies containing the implant and surrounding tissues were prepared for histological analysis. RESULTS: The histological analysis revealed that a significantly larger area of osseointegration was established within the defect at fluoride-modified implants than at implants with a TiOblast surface after 6 weeks of healing. Further, the degree of bone-to-implant contact within the defect area was larger at fluoride-modified implants than at the TiOblast implants. CONCLUSION: It is suggested that the fluoride-modified implant surface promotes bone formation and osseointegration.     

Factors influencing resonance frequency analysis assessed by Osstell™mentor during implant tissue integration: I. Instrument positioning,bone structure,implant length

Aim: To monitor longitudinally the development of implant stability of SLA Straumann^® tissue‐level implants using resonance frequency analysis (RFA) and to determine the influence of instrument positioning, bone structure and implant length on the assessment of RFA. Material and methods: Thirty‐two healthy adult patients received either 8 mm, ?4.1 mm Straumann^® Standard Plus tissue‐level implants (n=16: Group A) or 10 mm, ?4.1 mm Straumann^® Standard Plus tissue‐level implants (n=16: Group B). During healing, RFA was performed on Weeks 0,1, 2, 3, 4, 5, 6, 8 and 12. The implants were restored after 10 weeks (impression taking) and 12 weeks. In addition, probing depth, presence of plaque and bleeding on probing were assessed. Implant stability quotient (ISQ) values of Groups A and B were compared using unpaired t‐tests and longitudinally applying paired t‐tests between Week 0 and the subsequent time points. Results: Positioning of the Osstell^?mentor device did not affect the ISQ values. Generally, ISQ values increased continuously during healing from a mean of 65.1 (SD 16.97) to 74.7 (SD 5.17) (significantly from Week 0 to Weeks 6, 8 and 12). Lower bone density (Type III or IV) resulted in significantly lower ISQ values up to Week 8. Implant length affected the increase in ISQ values over time. While no significant increase was observed with 10 mm implants, ISQ values of 8 mm implants increased significantly from Week 0 to Weeks 6, 8 and 12. Conclusions: Using Osstell^?mentor, ISQ values are reproducible irrespective of instrument positioning. ISQ values are affected by the bone structure and implant length. Hence, no predictive values can be attributed to implant stability. To cite this article:
Sim CPC, Lang NP. Factors influencing resonance frequency analysis assessed by Osstell^?mentor during implant tissue integration: I. Instrument positioning, bone structure, implant length.
Clin. Oral Impl. Res. 21 , 2010; 598–604.
doi: 10.1111/j.1600‐0501.2009.01878.x     

Factors influencing resonance frequency analysis assessed by Osstell™mentor during implant tissue integration: II. Implant surface modifications and implant diameter

Objectives: To monitor the development of the stability of Straumann^® tissue‐level implants during the early phases of healing by resonance frequency analysis (RFA) and to determine the influence of implant surface modification and diameter. Material and methods: A total of twenty‐five 10 mm length implants including 12 SLA RN ?4.1 mm implants, eight SLActive RN ?4.1 mm implants and five SLA WN ?4.8 mm implants were placed. Implant stability quotient (ISQ) values were determined with Osstell^?mentor at baseline, 4 days, 1, 2, 3, 4, 6, 8 and 12 weeks post‐surgery. ISQ values were compared between implant types using unpaired t‐tests and longitudinally within implant types using paired t‐tests. Results: During healing, ISQ decreased by 3–4 values after installation and reached the lowest values at 3 weeks. Following this, the ISQ values increased steadily for all implants and up to 12 weeks. No significant differences were noted over time. The longitudinal changes in the ISQ values showed the same patterns for SLA implants, SLActive implants and WB implants. At placement, the mean ISQ values were 72.6, 75.7 and 74.4, respectively. The mean lowest ISQ values, recorded at 3 weeks, were 69.9, 71.4 and 69.8, respectively. At 12 weeks, the mean ISQ values were 76.5, 78.8 and 77.8, respectively. The mean ISQ values at all observation periods did not differ significantly among the various types. Single ISQ values ranged from 55 to 84 during the entire healing period. Pocket probing depths of the implants ranged from 1 to 3 mm and bleeding on probing from 0 to 2 sites/implant post‐surgically. Conclusions: All ISQ values indicated the stability of Straumann^® implants over a 12‐week healing period. All implants showed a slight decrease after installation, with the lowest ISQ values being reached at 3 weeks. ISQ values were restored 8 weeks post‐surgically. It is recommended to monitor implant stability by RFA at 3 and 8 weeks post‐surgically. However, neither implant surface modifications (SLActive) nor implant diameter were revealed by RFA. To cite this article:
Han J, Lulic M, Lang NP. Factors influencing resonance frequency analysis assessed by Osstell^?mentor during implant tissue integration: II. Implant surface modifications and implant diameter.
Clin. Oral Impl. Res. 21 , 2010; 605–611.
doi: 10.1111/j.1600‐0501.2009.01909.x     

Bio-Oss collagen in the buccal gap at immediate implants: a 6-month study in the dog

Background: Following tooth extraction and immediate implant installation, the edentulous site of the alveolar process undergoes substantial bone modeling and the ridge dimensions are reduced. Objective: The objective of the present experiment was to determine whether the process of bone modeling following tooth extraction and immediate implant placement was influenced by the placement of a xenogenic graft in the void that occurred between the implant and the walls of the fresh extraction socket. Material and methods: Five beagle dogs about 1 year old were used. The 4th premolar in both quadrants of the mandible (₄P₄) were selected and used as experimental sites. The premolars were hemi‐sected and the distal roots removed and, subsequently, implants were inserted in the distal sockets. In one side of the jaw, the marginal buccal‐approximal void that consistently occurred between the implant and the socket walls was grafted with Bio‐Oss^® Collagen while no grafting was performed in the contra‐lateral sites. After 6 months of healing, biopsies from each experimental site were obtained and prepared for histological analyses. Results: The outline of the marginal hard tissue of the control sites was markedly different from that of the grafted sites. Thus, while the buccal bone crest in the grafted sites was comparatively thick and located at or close to the SLA border, the corresponding crest at the control sites was thinner and located a varying distance below SLA border. Conclusions: It was demonstrated that the placement of Bio‐Oss^® Collagen in the void between the implant and the buccal‐approximal bone walls of fresh extraction sockets modified the process of hard tissue healing, provided additional amounts of hard tissue at the entrance of the previous socket and improved the level of marginal bone‐to‐implant contact. To cite this article:
Araújo MG, Linder E, Lindhe J. Bio‐Oss^® Collagen in the buccal gap at immediate implants: a 6‐month study in the dog.
Clin. Oral Impl. Res. 22 , 2011; 1–8.
doi: 10.1111/j.1600‐0501.2010.01920.x     

Deproteinized bovine bone mineral in marginal defects at implants installed immediately into extraction sockets: an experimental study in dogs

Aim: To evaluate the influence of deproteinized bovine bone mineral (DBBM) particles concomitant with the placement of a collagen membrane on alveolar ridge preservation and on osseointegration of implants placed into alveolar sockets immediately after tooth extraction. Material and methods: The pulp tissue of the mesial roots of ₃P₃ was removed in six Labrador dogs and the root canals were filled. Flaps were elevated in the right side of the mandible, and the buccal and lingual alveolar bony plates were exposed. The third premolar was hemi‐sectioned and the distal root was removed. A recipient site was prepared and an implant was placed lingually. After implant installation, defects of about 0.6 mm wide and 3.1 mm depth resulted at the buccal aspects of the implant, both at the test and at the control sites. The same surgical procedures and measurements were performed on the left side of the mandible. However, DBBM particles with a size of 0.25–1 mm were placed into the remaining defect concomitant with the placement of a collagen membrane. Results: All implants were integrated into mature bone. No residual DBBM particles were detected at the test sites after 4 months of healing. Both the test and the control sites showed buccal alveolar bone resorption, 1.8±1.1 and 2.1±1 mm, respectively. The most coronal bone‐to‐implant contact at the buccal aspect was 2±1.1 an 2.8±1.3 mm, at the test and the control sites, respectively. This difference in the distance was statistically significant. Conclusion: The application of DBBM concomitant with a collagen membrane to fill the marginal defects around implants placed into the alveolus immediately after tooth extraction contributed to improved bone regeneration in the defects. However, with regard to buccal bony crest preservation, a limited contribution of DBBM particles was achieved. To cite this article:
Caneva M, Botticelli D, Pantani F, Baffone GM, Rangel IG Jr, Lang NP. Deproteinized bovine bone mineral in marginal defects at implants installed immediately into extraction sockets: an experimental study in dogs.
Clin. Oral Impl. Res. 23 , 2012; 106–112.
doi: 10.1111/j.1600‐0501.2011.02202.x     

Magnesium-enriched hydroxyapatite at immediate implants: a histomorphometric study in dogs

Aim: To evaluate the influence of magnesium‐enriched hydroxyapatite (MHA) (SintLife^®) on bone contour preservation and osseointegration at implants placed immediately into extraction sockets. Material and methods: In the mandibular pre‐molar region, implants were installed immediately into extraction sockets of six Labrador dogs. MHA was placed at test sites, while the control sites did not receive augmentation materials. Implants were intended to heal in a submerged mode. After 4 months of healing, the animals were sacrificed, and ground sections were obtained for histomorphometric evaluation. Results: After 4 months of healing, one control implant was not integrated leaving n=5 test and control implants for evaluation. Both at the test and the control sites, bone resorption occurred. While the most coronal bone‐to‐implant contact was similar between test and control sites, the alveolar bony crest outline was maintained to a higher degree at the buccal aspect of the test sites (loss: 0.7 mm) compared with the control sites (loss: 1.2 mm), even though this difference did not reach statistical significance. Conclusions: The use of MHA to fill the defect around implants placed into the alveolus immediately after tooth extraction did not contribute significantly to the maintenance of the contours of the buccal alveolar bone crest. To cite this article:
Caneva M, Botticelli D, Stellini E, Souza SLS, Salata LA, Lang NP. Magnesium‐enriched hydroxyapatite at immediate implants: a histomorphometric study in dogs.
Clin. Oral Impl. Res. 22 , 2011; 512–517
doi: 10.1111/j.1600‐0501.2010.02040.x     

Bone healing pattern in surgically created circumferential defects around submerged implants: an experimental study in dog

Objective: To describe the healing of marginal defects below or above 1 mm of dimension around submerged implants in a dog model. Material and methods: In 12 Labrador dogs, all mandibular premolars and first molars were extracted bilaterally. After 3 months of healing, full‐thickness flaps were elevated in the edentulous region of the right side of the mandible. Two recipient sites were prepared and the marginal 5 mm were widened to such an extent to obtain, after implant installation, a marginal gap of 0.5 mm at the mesial site (small defect) and of 1.25 mm at the distal site (large defect). Titanium healing caps were affixed to the implants and the flaps were sutured allowing a fully submerged healing. The experimental procedures were subsequently performed in the left side of the mandible. The timing of the experiments and sacrifices were planned in such a way to obtain biopsies representing the healing after 5, 10, 20 and 30 days. Ground sections were prepared and histomorphometrically analyzed. Results: The filling of the defect with newly formed bone was incomplete after 1 month of healing in all specimens. Bone formation occurred from the base and the lateral walls of the defects. A larger volume of new bone was formed in the large compared with the small defects. Most of the new bone at the large defect was formed between the 10‐ and the 20‐day period of healing. After 1 month of healing, the outline of the newly formed bone was, however, located at a similar distance from the implant surface (about 0.4 mm) at both defect types. Only minor newly formed bone in contact with the implant, starting from the base of the defects, was seen at the large defects (about 0.8 mm) while a larger amount was detected at the small defects (about 2.2 mm). Conclusion: Marginal defects around titanium implants appeared to regenerate in 20–30 days by means of a distance osteogenesis. The bone fill of the defects was, however, incomplete after 1 month. To cite this article:
Rossi F, Botticelli D, Pantani F, Pereira FP, Salata LA, Lang NP. Bone healing pattern in surgically created circumferential defects around submerged implants: an experimental study in dog.
Clin. Oral Impl. Res 23 , 2012; 41–48.
doi: 10.1111/j.1600‐0501.2011.02170.x     

A 2-year prospective study on immediate loading with fluoride-modified implants in the edentulous mandible

Objectives: Chemically modified surfaces were introduced during the last decade to improve indications for implant treatment. The fluoride‐modified implant (Osseospeed^®) was launched in 2004 and clinical studies suggest a more rapid bone formation and stronger bone to implant contact. However, limited clinical data are available on marginal bone loss and the outcome after >1 year under immediate loading conditions is not fully understood. Hence, the purpose of this prospective study was to present implant survival and marginal bone level data when fluoride‐modified implants are supporting a fully functional rehabilitation from the day after surgery in the completely edentulous mandible. Materials and methods: Twenty‐five patients, completely edentulous in the mandible, were consecutively treated with five fluoride‐modified implants that were functionally loaded with a provisional screw retained restoration. Marginal bone loss was measured from day of surgery to 3, 6, 12 and 24 months. Implants were considered successful after 24 months if radiographic bone loss did not exceed 1 mm and no pain or mobility was caused under a torque of 20 N cm. Statistical analysis was carried out on both patient and implant levels. Results: All implants survived and mean bone loss on implant level after 3, 6, 12 and 24 months was 0.14, 0.13, 0.11 and 0.11 mm, respectively. Bone loss was only statistically significant between baseline and 3 months (P<0.001) and remained unchanged afterward. None of the implants lost >1 mm of bone after 2 years. On the patient level, the mean bone loss after 2 years was 0.12 mm (SD 0.14; range ?0.06 to 0.55) with probing pocket depth 2.45 mm (SD 0.43; range 1.3–3.1) and bleeding index 0.55% (SD 0.34; range 0–1). Conclusion: Immediate loading of fluoride‐modified implants is a predictable treatment yielding a high survival and success rate after 2 years. To cite this article:
Collaert B, Wijnen L, De Bruyn H. A 2‐year prospective study on immediate loading with fluoride‐modified implants in the edentulous mandible.
Clin. Oral Impl. Res. 22 , 2011; 1111–1116.
doi: 10.1111/j.1600‐0501.2010.02077.x     

Prefabricated zirconium dioxide implant abutments for single‐tooth replacement in the posterior region: evaluation of peri‐implant tissues and superstructures after 12 months of function

Aim: In the present study, prefabricated abutments made of zirconium dioxide Y‐TZP (tetragonal zirconia polycrystals) were inserted into the posterior region under controlled clinical conditions. The aim was to test whether abutments made of zirconium dioxide are suitable for this indication. Investigation parameters included reactions of peri‐implant tissue and the structural integrity of the all‐ceramic superstructures on the implants. Results after 12 months in function are reported in this article. Material and methods: Forty implants of the XiVE^® S plus screw‐type implants (DENTSPLY Friadent) were inserted into the posterior region of 24 patients. After the healing period, the implants were provided with all‐ceramic abutments made of zirconium dioxide Y‐TZP (FRIADENT^® CERCON^® Abutment; DENTSPLY Friadent). All‐ceramic crowns (CERCON^® smart ceramics; DENTSPLY DeguDent) were used as superstructures and cemented using the conventional method. The following parameters were used to document the state of soft tissue: modified plaque index (mPI), sulcus fluid flow rate (SFFR, Periotron; Oraflow Inc), modified sulcus bleeding index (mSBI) and pocket depth (ST). Mesial and distal bone levels were determined on radiographs during the prosthetic treatment and at the 12‐month recall. The Periotest^? (Medizintechnik Gulden) was used to determine implant stability. Results: All implants could be followed up after 12 months in function. In the presence of good oral hygiene (mPI: 0.5), the parameters SFFR (18) and mSBI (0.5) were indicative of stable and healthy soft tissue. ST was highest at the distal points of measurement (2.3 mm) and was generally at a low level. Compared with the baseline situation, proximal bone defects were reduced from ?1.1 to ?1 mm during the 12‐month period of functioning. The mean Periost^? values at the 12‐month recall were ?1.9 in the maxilla and ?3.8 in the mandible. Neither implant loss nor crown fractures occurred. Chipping of parts of the veneering ceramic was registered in four cases (10%). Conclusion: After 12 months of wear, no mechanical failure was registered in any of the all‐ceramic abutments. On clinical investigation, the peri‐implant hard and soft tissues were largely healthy and devoid of inflammation. To cite this article:
Nothdurft F, Pospiech P. Prefabricated zirconium dioxide implant abutments for single‐tooth replacement in the posterior region: evaluation of peri‐implant tissues and superstructures after 12 months of function.
Clin. Oral Impl. Res. 21 , 2010; 857–865.
doi: 10.1111/j.1600‐0501.2009.01899.x     

The role of bone debris in early healing adjacent to hydrophilic and hydrophobic implant surfaces in man

Objective: To evaluate morphologically and morphometrically the sequential healing and osseointegration events at moderately rough implant surfaces with and without chemical modification. Particularly the role of bone debris in initiating bone formation was emphasized. Material and methods: Solid, screw‐type cylindrical titanium implants (SSI) (n=49), 4 mm long and 2.8 mm wide, with either chemically modified (SLActive^®) or sandblasted and acid‐etched (SLA^®) surface configurations were surgically installed in the retromolar region of 28 human volunteers. After 7, 14, 28 and 42 days of submerged healing, the devices were retrieved with a trephine. Histologic ground sections were prepared and histomorphometrically analyzed. Linear measurements determined fractions of old bone (OBIC), new bone (NBIC), soft tissue (ST) and bone debris (BD) in contact with the SSI surfaces. Results: Healing was uneventful at all installation sites. Sixty‐one percent of all devices were suitable for morphometric analyses. All implant surfaces were partially coated with bone debris and new bone formation was observed as early as 7 days after installation. There was a gradual increase in NBIC, whereas OBIC, ST and BD progressively decreased over time. NBIC after 2 and 4 weeks was higher on SLActive^® than on SLA^® surfaces, albeit statistically not significant. The BD : ST ratio changed significantly from 7 to 42 days (from 50 : 50 to 10 : 90 for SLActive^®; from 38: 62 to 10 : 90 for SLA^®) (Fisher's exact test, P<0.01). Conclusion: Both SLActive^® and SLA^® devices became progressively osseointegrated, while old bone on the device surface was gradually resorbed. The decrease in BD : ST ratio suggests that bone debris, created during implant installation and adhering to moderately rough surfaces, significantly contributed to the initiation of bone deposition and mediated the connection between the old bone and the new bone on the implant surface. To cite this article:
Bosshardt DD, Salvi GE, Huynh‐Ba G, Ivanovski S, Donos N, Lang, NP. The role of bone debris in early healing adjacent to hydrophilic and hydrophobic implant surfaces in man.
Clin. Oral Impl. Res. 22 , 2011; 357–364.     

Comparative study of the osseointegration of dental implants after different bone augmentation techniques: vascularized femur flap, non-vascularized femur graft and mandibular bone graft

Objectives: The purpose of this study was to evaluate the osseointegration of the dental implants placed into the mandible augmented with different techniques in pigs. Material and methods: Four adult domestic pigs were used. Horizontal augmentation of the mandible was performed in animals by using vascularized femur flap (VFF), non‐vascularized femur graft (NVFG) and monocortical mandibular block graft (MG). After 5 months of healing 10 dental implants were placed into each augmented site. The pigs were sacrificed after 3 months of healing. Undecalcified sections were prepared for histomorphometric analysis. Results: Mean bone–implant contact (BIC) values for implants placed into MG, NVFG and VFF were 57.38 ± 11.97%, 76.5 ± 7.88%, 76.53 ± 8.15%, respectively. The BIC values of NVFG and VFF group were significantly greater than MG group (P<0.001). On the other hand, there was not statistically significant difference between NVFG group and VFF group (P=0.999). Conclusion: NVFG as well as VFF can be considered as a promising method for augmentation of alveolar defects and the placement of the implants. The selection of non‐vascularized graft or vascularized flap depends on the condition of the recipient site. To cite this article:
Benlidayi ME, Gaggl A, Bürger H, Brandner C, Kurkcu M, Ünlügenç H. Comparative study of the osseointegration of dental implants after different bone augmentation techniques: vascularized femur flap, non‐vascularized femur graft and mandibular bone graft.
Clin. Oral Impl. Res. 22 , 2011; 594–599
doi: 10.1111/j.1600‐0501.2010.02013.x     

The jumping distance revisited: An experimental study in the dog

Following tooth extraction, a socket often presents dimensions that may be considerably greater that the diameter of a conventional implant. The present experiment was performed to study the healing that occurred adjacent to implants placed in recipient sites with a wide marginal defect. Four Labrador dogs were used. In the right side of the mandible, four experimental sites were prepared to receive titanium implants [sandblasted, large-grit, acid-etched (SLA) surface]. Traditional implant installation (control) was performed in one site. In the remaining three sites (test), a step drill was used to widen the marginal 5 mm of the canal. Following placement of an implant in a test site, a circumferential gap about 1-1.25 mm wide and 5 mm deep was present lateral to the implant. A resorbable barrier membrane was used to cover the implant and the bone tissue of two sites, while one site was left uncovered. Four months following implant installation, block biopsies of each implant site were obtained and prepared for ground sectioning. After 4 months of healing, the large marginal defect had been filled with newly formed bone. The degree of bone-to-implant contact between the newly formed tissue and the SLA surface was at all test sites high and similar to that obtained at control sites. The placement of a barrier membrane following implant installation did not improve the outcome of healing. We conclude that a marginal defect wider than 1 mm may heal with new bone and a high degree of osseointegration to an implant designed with a SLA surface.