Serveur d'exploration sur le patient édenté

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Nonsubmerged and Submerged Implants in the Treatment of the Partially Edentulous Maxilla

Identifieur interne : 008445 ( Main/Exploration ); précédent : 008444; suivant : 008446

Nonsubmerged and Submerged Implants in the Treatment of the Partially Edentulous Maxilla

Auteurs : Per Strand [Suède] ; Bo Engquist [Suède] ; Bengt Anzén [Suède] ; Tom Bergendal [Suède] ; Mats Hallman [Suède] ; Ulf Karlsson [Suède] ; Sven Kvint [Suède] ; Leif Lysell [Suède] ; Torgil Rundcrantz [Suède]

Source :

RBID : ISTEX:111A09FB9131E8A95429495C42397D55ED678F66

English descriptors

Abstract

Background: Dental implants vary in design and surfaces. In addition, different surgical techniques have been used for implant insertion. The ITI Dental Implant System (Straumann AG, Waldenburg, Switzerland) has always required a one‐stage technique, whereas the Brånemark System (Nobel Biocare AB, Gothenburg, Sweden) requires a two‐stage technique. Purpose: The aim of this study is to compare the outcome of fixed partial bridges in the maxilla supported by both ITI and Brånemark implants in a split‐mouth design. Materials and Methods: Twenty‐eight patients with a residual anterior dentition in the maxilla were included in this split‐mouth study. The Brånemark implants were used on one side and the ITI implants on the other side of the residual dentition according to a randomization procedure. A blocking size of four was used, giving equal probability of placing ITI or Brånemark implants in the right or left side of the jaw. The surgical and prosthetic procedures followed the guidelines given by the manufacturers. The prosthetic treatment with the two‐implant systems was performed at the same time, and for that reason the healing period was 6 months for both systems. The observation period for all patients was 1 year after loading. Results: Two Brånemark implants (in one patient) were lost before loading, and one ITI implant was lost 1 year after loading. There was no significant difference in survival rate. Radiographie examination of the bone level was performed at the time of delivery of the bridge and after 1 year. The mean marginal bone level at baseline was situated 1.9 mm from the reference point for the Brånemark implants and 1.5 mm for the ITI implants. With regard to the insertion depth used, these bone levels indicate that bone loss had taken place before baseline. However, between baseline and the 1‐year examination, there was no significant change of the marginal bone (0.2 ± 0.08 mm at the Brånemark implants and 0.1 ± 0.11 mm at the ITI implants). The difference between results with the two implants was not statistically significant. Crater‐form bone destructions were seen at some ITI implants, indicating periimplantitis. However, at only two implants were there clinical signs of periimplantitis. Conclusions: No significant difference in survival rate or in marginal bone change could be demonstrated between the two systems. At some ITI implants (18%), crater‐form bone loss was observed.

Url:
DOI: 10.1111/j.1708-8208.2002.tb00161.x


Affiliations:


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Le document en format XML

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<term>Bone quality</term>
<term>Branemark</term>
<term>Brdnemark implants</term>
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<term>Clin</term>
<term>Clin implant dent relat</term>
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<term>Clinical signs</term>
<term>Corresponding figures</term>
<term>Dental implants</term>
<term>Dentistry</term>
<term>Dentition</term>
<term>Edentulous</term>
<term>Edentulous patients</term>
<term>Healing period</term>
<term>Implant</term>
<term>Implant insertion</term>
<term>Implant systems</term>
<term>Insertion</term>
<term>Insertion depth</term>
<term>Lekholm</term>
<term>Marginal bone level</term>
<term>Maxilla</term>
<term>Maxillofac</term>
<term>Maxillofacial surgery</term>
<term>Nonsubmerged</term>
<term>Oral maxillofac implants</term>
<term>Osseointegrated</term>
<term>Osseointegrated implants</term>
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<term>Prospective study</term>
<term>Prosthesis</term>
<term>Radiograph</term>
<term>Radiographic</term>
<term>Radiographic examination</term>
<term>Reference point</term>
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<term>Residual dentition</term>
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<term>Survival rate</term>
<term>Survival rates</term>
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<term>Brinemark</term>
<term>Brinemark implants</term>
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<term>Corresponding figures</term>
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<term>Implant insertion</term>
<term>Implant systems</term>
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<front>
<div type="abstract" xml:lang="en">Background: Dental implants vary in design and surfaces. In addition, different surgical techniques have been used for implant insertion. The ITI Dental Implant System (Straumann AG, Waldenburg, Switzerland) has always required a one‐stage technique, whereas the Brånemark System (Nobel Biocare AB, Gothenburg, Sweden) requires a two‐stage technique. Purpose: The aim of this study is to compare the outcome of fixed partial bridges in the maxilla supported by both ITI and Brånemark implants in a split‐mouth design. Materials and Methods: Twenty‐eight patients with a residual anterior dentition in the maxilla were included in this split‐mouth study. The Brånemark implants were used on one side and the ITI implants on the other side of the residual dentition according to a randomization procedure. A blocking size of four was used, giving equal probability of placing ITI or Brånemark implants in the right or left side of the jaw. The surgical and prosthetic procedures followed the guidelines given by the manufacturers. The prosthetic treatment with the two‐implant systems was performed at the same time, and for that reason the healing period was 6 months for both systems. The observation period for all patients was 1 year after loading. Results: Two Brånemark implants (in one patient) were lost before loading, and one ITI implant was lost 1 year after loading. There was no significant difference in survival rate. Radiographie examination of the bone level was performed at the time of delivery of the bridge and after 1 year. The mean marginal bone level at baseline was situated 1.9 mm from the reference point for the Brånemark implants and 1.5 mm for the ITI implants. With regard to the insertion depth used, these bone levels indicate that bone loss had taken place before baseline. However, between baseline and the 1‐year examination, there was no significant change of the marginal bone (0.2 ± 0.08 mm at the Brånemark implants and 0.1 ± 0.11 mm at the ITI implants). The difference between results with the two implants was not statistically significant. Crater‐form bone destructions were seen at some ITI implants, indicating periimplantitis. However, at only two implants were there clinical signs of periimplantitis. Conclusions: No significant difference in survival rate or in marginal bone change could be demonstrated between the two systems. At some ITI implants (18%), crater‐form bone loss was observed.</div>
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