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Sökning: L773:0882 2786 > Sennerby Lars

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1.
  • Albrektsson, Tomas, 1945, et al. (författare)
  • On crestal/marginal bone loss around dental implants.
  • 2012
  • Ingår i: The International journal of prosthodontics. - : Quintessence Publishing co inc. - 0893-2174 .- 1139-9791. ; 27:4, s. 736-738
  • Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)
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4.
  • Dahlin, Christer, 1959, et al. (författare)
  • Generation of new bone around titanium implants using a membrane technique: an experimental study in rabbits.
  • 1989
  • Ingår i: The International journal of oral & maxillofacial implants. - 0882-2786. ; 4:1, s. 19-25
  • Tidskriftsartikel (refereegranskat)abstract
    • Insufficient bone volume may be a significant problem in connection with dental implants. In this study, a technique based on the principle of guided tissue regeneration was tested for its ability to generate bone tissue around titanium implants. Implants were inserted in tibiae of rabbits. To create a secluded space for osteogenesis and to prevent soft-tissue ingrowth, a porous Teflon membrane was placed around exposed parts of the implant. Where a membrane had been used, the threads of the implant were completely covered with significant amounts of new bone. This study indicates that the membrane technique is a reconstructive surgical method that may be applicable to create new bone around exposed parts of titanium implants in a clinical setting.
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5.
  • Friberg, Bertil, 1950, et al. (författare)
  • Clinical outcome of Brånemark System implants of various diameters: a retrospective study.
  • 2002
  • Ingår i: The International journal of oral & maxillofacial implants. - 0882-2786. ; 17:5, s. 671-7
  • Tidskriftsartikel (refereegranskat)abstract
    • PURPOSE: The purpose of this study was to evaluate the outcome of the 3 different diameters of Brånemark System implants, with special focus on the 5.0-mm-diameter implant. MATERIALS AND METHODS: Ninety-eight patients (99 jaws) with a mean age of 62 years were included in this retrospective report. The mean follow-up period was 2 years and 8 months. A total of 379 Brånemark System implants (3.75 mm diameter, n = 146; 4.0 mm diameter, n = 76; 5.0 mm diameter, n = 157) were placed in 29 edentulous and 70 partially edentulous jaws. RESULTS: Eight of the 146 implants in the 3.75-mm-diameter group failed (5.5%). The corresponding figures for the 4.0- and 5.0-mm-diameter implants were 3 of 76 (3.9%) and 7 of 157 (4.5%), respectively. DISCUSSION: All failures were recorded in maxillae, ie, 18 of the 298 placed, and the majority of these were found in bone quantity group B and quality group 2. Only 3 implants of 131 failed in bone judged as quality 4. The marginal bone loss was low for the 3 implant diameter groups. CONCLUSION: The favorable outcome in bone of poor quality is ascribed partly to the use of an adapted preparation technique and extended healing periods for achievement of the best primary and secondary implant stability possible.
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6.
  • Hallman, Mats, et al. (författare)
  • A clinical and histologic evaluation of implant integration in the posterior maxilla after sinus floor augmentation with autogenous bone, bovine hydroxyapatite, or a 20:80 mixture.
  • 2002
  • Ingår i: International Journal of Oral & Maxillofacial Implants. - 0882-2786 .- 1942-4434. ; 17:5, s. 635-643
  • Tidskriftsartikel (refereegranskat)abstract
    • PURPOSE: This study was designed to clinically and histologically evaluate the integration of titanium implants in different grafting materials used for maxillary sinus augmentation procedures. MATERIALS AND METHODS: A total of 21 patients and 36 maxillary sinuses were augmented with (1) autogenous particulated bone from the mandibular ramus, (2) bovine hydroxyapatite (BH) with membrane coverage, or (3) an 80/20 mixture of BH and autogenous bone. The grafts were allowed to heal for 6 to 9 months prior to placement of microimplants for histology and standard implants for prosthetic rehabilitation. After another 6 months of healing, when abutments were connected, the microimplants were retrieved for histologic and morphometric analyses. The outcome of the standard implants was clinically evaluated after 1 year of loading. RESULTS: The mean bone-implant contact was 34.6 +/- 9.5%, 54.3 +/- 33.1%, and 31.6 +/- 19.1% for autogenous bone, mixture of 20% autogenous bone/80% BH, and 100% BH, respectively. The corresponding values for the bone area parameter were 37.7 +/- 31.3%, 39.9 +/- 8%, and 41.7 +/- 26.6%. The BH area was found to be 12.3 +/- 8.5% and 11.8 +/- 3.6% for 20% autogenous bone/80% BH and 100% BH, respectively. There were no statistically significant differences for any parameter between any of the groups. After 1 year of loading, 6 of the 33 implants placed in autogenous bone grafts, 2 of the 35 implants placed in the BH/autogenous bone mixture, and 2 of 43 implants placed in BH were lost. There were no statistically significant differences between any of the groups. DISCUSSION: The histomorphometric analysis showed no differences between the 3 groups, indicating that autogenous bone graft can be substituted with bovine hydroxyapatite to 80% or 100% when used for maxillary sinus floor augmentation. The effect of adding autogenous bone remains unclear but may allow for a reduction of the healing time. CONCLUSION: The results from this clinical and histologic study indicate that similar short-term results can be expected when using autogenous bone, BH, or a mixture of them for maxillary sinus floor augmentation and delayed placement of dental implants.
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7.
  • Ivanoff, Carl-Johan, et al. (författare)
  • Influence of variations in implant diameters: a 3- to 5-year retrospective clinical report.
  • 1999
  • Ingår i: The International journal of oral & maxillofacial implants. - 0882-2786. ; 14:2, s. 173-80
  • Tidskriftsartikel (refereegranskat)abstract
    • Sixty-seven patients ranging in age from 16 to 86 years were included in this 3- to 5-year retrospective report focusing on implant survival and marginal bone remodeling in relation to implant diameter. A total of 299 Brånemark implants (3.75-mm diameter: 141; 4.0-mm diameter: 61; 5.0-mm diameter: 97) were placed in 16 completely and 51 partially edentulous arches. Seven of the 141 implants in the 3.75-mm-diameter group failed (5%). The corresponding value for the 4.0-mm-wide implants was 2 of 61 (3%). The highest failure rate, 18% (17/97), was seen for the 5.0-mm-diameter implants. The least favorable cumulative survival rates were seen in mandibles after 5 years and involving 4.0-mm- and 5.0-mm-diameter implants (84.8% and 73.0%, respectively). The marginal bone loss was generally low over the 5-year period. When the data were evaluated by the Cox regression analysis, a relationship was found between implant failure and implant diameter (P < .05), with a higher failure rate for the 5.0-mm-diameter implant. However, no relationship could be seen between implant failure and jaw type, or bone quality and quantity (P > .05). Neither was any relationship seen between marginal bone loss and bone quality and quantity, implant diameter, or jaw type when tested by multiple linear regression analysis (P > .05). A learning curve, poor bone quality, and changed implant design were suggested as possible reasons for the less positive outcome seen for the 5.0-mm-diameter implant. The fact that this implant was often used as a rescue implant when the standard ones were not considered suitable or did not reach initial stability was another plausible explanation.
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8.
  • Jensen, O T, et al. (författare)
  • Histologic analysis of clinically retrieved titanium microimplants placed in conjunction with maxillary sinus floor augmentation.
  • 1998
  • Ingår i: The International journal of oral & maxillofacial implants. - 0882-2786. ; 13:4, s. 513-21
  • Tidskriftsartikel (refereegranskat)abstract
    • In this study, a new approach involving placement and subsequent retrieval of titanium microimplants was employed for the histologic investigation of the implant-tissue interface in conjunction with maxillary sinus floor augmentation. Nine patients scheduled for sinus floor augmentation and simultaneous placement of Brånemark implants were included in the study. After a sinus graft procedure and placement of implants, an additional microimplant was placed into the graft through the lateral wall of the sinus. At abutment connection, the microimplants were retrieved using a 3- or 5-mm-wide trephine drill. Six specimens were retrieved after 6 to 14 months from sites augmented with particulate radiated mineralized cancellous allograft. Another six implants were retrieved after 6 to 12 months from maxillary sinuses augmented with particulate autogenous bone grafts. The histologic analysis showed distinct differences between the two types of grafts. The sites with autogenous bones grafts displayed a normal morphology of bone and bone marrow, including formation of bone on the surfaces of the grafted particles and remodeling of newly formed as well as grafted bone. The bone was more mature after 11 to 14 months than at 6 months. The allografted sites had a mixed morphologic appearance of newly formed bone and nonviable allograft particles (about 75% of the total bone area) in loose connective tissue. Significantly more bone was found at the autografted than at the allografted implants. The use of autogenous bone for augmentation of the maxillary sinus floor resulted in a greater amount of viable bone surrounding the implant; however, simultaneous placement of implants apparently resulted in a low proportion of bone-implant contact after 6 to 14 months irrespective of graft type.
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9.
  • Johansson, C B, et al. (författare)
  • A removal torque and histomorphometric study of bone tissue reactions to commercially pure titanium and Vitallium implants.
  • 1991
  • Ingår i: The International journal of oral & maxillofacial implants. - 0882-2786. ; 6:4, s. 437-41
  • Tidskriftsartikel (refereegranskat)abstract
    • Screw-shaped commercially pure (CP) titanium and Vitallium implants were inserted in the rabbit tibial metaphysis. After a healing period of 3 months, it was demonstrated that a higher torque was needed to remove the CP titanium implants (average 24.9 Ncm) compared to Vitallium implants (average 11.7 Ncm). The histomorphometric part of the study revealed more bone-to-metal contact for the CP titanium implants (average 34.7%) compared to the Vitallium implants (average 21.7%). The results obtained in this study could be explained by differences in the topography or in biocompatibility of the metals, or a combination of these two factors.
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10.
  • Lekholm, Ulf, 1944, et al. (författare)
  • Soft tissue and marginal bone conditions at osseointegrated implants that have exposed threads: a 5-year retrospective study.
  • 1996
  • Ingår i: The International journal of oral & maxillofacial implants. - 0882-2786. ; 11:5, s. 599-604
  • Tidskriftsartikel (refereegranskat)abstract
    • The purpose of this retrospective clinical investigation was to study possible soft tissue complications and marginal bone resorption related to exposed threads of osseointegrated Brånemark oral implants during a 5-year period. Group 1 comprised 27 patients with 38 test implants that had not become completely covered with bone at implant placement. Thirty control implants in 25 of the patients were each next to a test implant and had no exposed threads initially. Group 2 comprised 51 patients with 107 test implants that had developed marginal bone loss beyond the second thread, as judged radiographically at the first annual checkup. Forty-eight control implants showed no or minor marginal bone resorption up to the first thread. Initial marginal defects and fenestrations at Brånemark implants (group 1) did not lead to mucosal problems or progressive marginal bone resorption during the first 5 years of function. Moreover, bone resorption, seen after the first year of loading at initially completely bone-covered implants, did not lead to any specific soft tissue problems, nor did it result in any further progressive bone resorption during a subsequent 4-year period. Based on the observed low incidence of soft tissue pathology at implants with exposed threads, it is suggested that bone augmentation techniques in the situations studied be used with restriction.
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