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Träfflista för sökning "L773:0882 2786 srt2:(2000-2004)"

Sökning: L773:0882 2786 > (2000-2004)

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  • Ellingsen, Jan Eirik, et al. (författare)
  • Improved Retention and Bone-to-Implant Contact with Fluoride-Modified Titanium Implants
  • 2004
  • Ingår i: International Journal of Oral & Maxillofacial Implants. - Chicago, Ill.] : Quintessence Pub. Co.. - 0882-2786 .- 1942-4434. ; 19:5, s. 659-666
  • Tidskriftsartikel (refereegranskat)abstract
    • Purpose: The purpose of the present study was to investigate whether a fluoride modification of the titanium surface would have an effect on bone response after implantation. Materials and Methods: Titanium-oxide–blasted titanium implants with and without fluoride modification were investigated in a rabbit tibia model. Quantitative analysis of surface roughness, biomechanical interlocking, and in vivo tissue reactions in rabbit bone at 1 and 3 months after placement were compared. Results: The fluoride-modified test implants had a slightly smoother surface (Sa: 0.91 ± 0.14 µm) than the unmodified control implants (Sa: 1.12 ± 0.24 µm). Significantly higher removal torque values (85 ± 16 Ncm vs 54 ± 12 Ncm) and shear strength between bone and implants (23 ± 9 N/mm2 vs 15 ± 5 N/mm2) were measured for the fluoride-modified implants after 3 months. The histomorphometric evaluations demonstrated higher bone-to-implant contact for test implants at 1 month (35% ± 14% vs 26% ± 8%) and 3 months (39% ± 11% vs 31% ± 6%) after placement. Discussion: Implant surface modification with fluoride may result in morphologic and physiochemical phenomena that are of significance for the bone response. Another possible explanation for the findings in the present study is that a surface modification changes the surface chemical structures to be more suitable for bone bonding. Conclusion: Based on the biomechanical and histomorphometric data, the fluoride-modified titanium implants demonstrated a firmer bone anchorage than the unmodified titanium implants. These implants achieved greater bone integration than unmodified titanium implants after a shorter healing time. (More than 50 references.)
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  • Ellingsen, Jan Eirik, et al. (författare)
  • Improved retention and bone-tolmplant contact with fluoride-modified titanium implants.
  • 2004
  • Ingår i: International Journal of Oral & Maxillofacial Implants. - 0882-2786. ; 19:5, s. 659-66
  • Tidskriftsartikel (refereegranskat)abstract
    • PURPOSE: The purpose of the present study was to investigate whether a fluoride modification of the titanium surface would have an effect on bone response after implantation. MATERIALS AND METHODS: Titanium-oxide-blasted titanium implants with and without fluoride modification were investigated in a rabbit tibia model. Quantitative analysis of surface roughness, biomechanical interlocking, and in vivo tissue reactions in rabbit bone at 1 and 3 months after placement were compared. RESULTS: The fluoride-modified test implants had a slightly smoother surface (Sa: 0.91 +/- 0.14 microm) than the unmodified control implants (Sa: 1.12 +/- 0.24 microm). Significantly higher removal torque values (85 +/- 16 Ncm vs 54 +/- 12 Ncm) and shear strength between bone and implants (23 +/- 9 N/mm2 vs 15 +/- 5 N/mm2) were measured for the fluoride-modified implants after 3 months. The histomorphometric evaluations demonstrated higher bone-to-implant contact for test implants at 1 month (35% +/- 14% vs 26% +/- 8%) and 3 months (39% +/- 11% vs 31% +/- 6%) after placement. DISCUSSION: Implant surface modification with fluoride may result in morphologic and physiochemical phenomena that are of significance for the bone response. Another possible explanation for the findings in the present study is that a surface modification changes the surface chemical structures to be more suitable for bone bonding. CONCLUSION: Based on the biomechanical and histomorphometric data, the fluoride-modified titanium implants demonstrated a firmer bone anchorage than the unmodified titanium implants. These implants achieved greater bone integration than unmodified titanium implants after a shorter healing time.
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  • 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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  • 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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  • Ivanoff, Carl-Johan, et al. (författare)
  • Histologic evaluation of bone response to oxidized and turned titanium micro-implants in human jawbone
  • 2003
  • Ingår i: International Journal of Oral & Maxillofacial Implants. - 0882-2786 .- 1942-4434. ; 18:3, s. 341-348
  • Tidskriftsartikel (refereegranskat)abstract
    • PURPOSE: To evaluate the human bone tissue response to 2 surfaces (oxidized or turned) on commercially available titanium implants. MATERIALS AND METHODS: Screw-type turned (control) and oxidized (test) micro-implants were manufactured in the same manner as commercially available turned and oxidized (TiUnite, Brånemark System) implants. The thickness of the oxide layer of the test implants was on average 10 microm, corresponding to the oxide thickness of the apical part of the TiUnite implant. Twenty patients received 1 test and 1 control micro-implant each during implant surgery. Before placement, the surface topography of the implants was characterized with an optical confocal laser profilometer. After a mean healing period of 6.6 months in the maxilla and 3.5 months in the mandible, the micro-implants and surrounding tissue were removed with a trephine bur. Histologic sections were produced, and the specimens were analyzed histomorphometrically. RESULTS: Surface roughness and enlargement were greater for the oxidized implants than for the turned implants. All micro-implants, except for 2 controls, were found to be clinically stable at the time of retrieval. Histomorphometric evaluation demonstrated significantly higher bone-to-implant contact for the oxidized implants, whether placed in the maxilla or in the mandible. Significantly more bone was found inside the threaded area for the oxidized implants placed in the mandible and maxilla, but there was no difference between implants with regard to position (maxilla or mandible). DISCUSSION: The stronger bone response to the oxidized implants may have contributed to the fact that 2 control implants but no test implants were lost. The reason for these findings may depend on one or multiple differences of the surfaces between test and control implants: (1) the thicker oxide layer itself, (2) increased surface roughness, (3) different surface morphology in terms of porosity, or (4) change in crystal structure. CONCLUSION: The present histologic study in human jawbone demonstrated a significantly higher bone response for anodic oxidized titanium implants than for implants with a turned surface.
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