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Ridge augmentation by applying bioresorbable membranes and deproteinized bovine bone mineral: a report of twelve consecutive cases

Identifieur interne : 003967 ( Istex/Corpus ); précédent : 003966; suivant : 003968

Ridge augmentation by applying bioresorbable membranes and deproteinized bovine bone mineral: a report of twelve consecutive cases

Auteurs : Christoph H. F. H Mmerle ; Ronald E. Jung ; Duygu Yaman ; Niklaus P. Lang

Source :

RBID : ISTEX:7484C968E8ADD83E9DA44891147A79E729ED4FFD

English descriptors

Abstract

Objective: Lateral ridge augmentations are traditionally performed using autogenous bone grafts to support membranes for guided bone regeneration (GBR). The bone‐harvesting procedure, however, is accompanied by considerable patient morbidity.

Url:
DOI: 10.1111/j.1600-0501.2007.01407.x

Links to Exploration step

ISTEX:7484C968E8ADD83E9DA44891147A79E729ED4FFD

Le document en format XML

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Lateral ridge augmentations are traditionally performed using autogenous bone grafts to support membranes for guided bone regeneration (GBR). The bone‐harvesting procedure, however, is accompanied by considerable patient morbidity.</p>
<p>
<hi rend="bold">Aim: </hi>
The aim of the present study was to test whether or not resorbable membranes and bone substitutes will lead to successful horizontal ridge augmentation allowing implant installation under standard conditions.</p>
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<hi rend="bold">Material and methods: </hi>
Twelve patients in need of implant therapy participated in this study. They revealed bone deficits in the areas intended for implant placement. Soft tissue flaps were carefully raised and blocks or particles of deproteinized bovine bone mineral (DBBM) (Bio‐Oss
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<p>
<hi rend="bold">Results: </hi>
All sites in the 12 patients healed uneventfully. No flap dehiscences and no exposures of membranes were observed. Nine to 10 months following augmentation surgery, flaps were raised in order to visualize the outcomes of the augmentation. An integration of the DBBM particles into the newly formed bone was consistently observed. Merely on the surface of the new bone, some pieces of the grafting material were only partly integrated into bone. However, these were not encapsulated by connective tissue but rather anchored into the newly regenerated bone. In all of the cases, but one, the bone volume following regeneration was adequate to place implants in a prosthetically ideal position and according to the standard protocol with complete bone coverage of the surface intended for osseointegration. Before the regenerative procedure, the average crestal bone width was 3.2 mm and to 6.9 mm at the time of implant placement. This difference was statistically significant (
<hi rend="italic">P</hi>
<0.05, Wilcoxon's matched pairs signed‐rank test).</p>
<p>
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After a healing period of 9–10 months, the combination of DBBM and a collagen membrane is an effective treatment option for horizontal bone augmentation before implant placement.</p>
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Clinic for Fixed and Removable Prosthodontics
Center for Dental and Oral Medicine and
Cranio‐Maxillofacial Surgery
University of Zurich
Plattenstrasse 11
8032 Zurich
Switzerland
Tel.: +49 44 6343 259
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<b>Objective: </b>
Lateral ridge augmentations are traditionally performed using autogenous bone grafts to support membranes for guided bone regeneration (GBR). The bone‐harvesting procedure, however, is accompanied by considerable patient morbidity.</p>
<p>
<b>Aim: </b>
The aim of the present study was to test whether or not resorbable membranes and bone substitutes will lead to successful horizontal ridge augmentation allowing implant installation under standard conditions.</p>
<p>
<b>Material and methods: </b>
Twelve patients in need of implant therapy participated in this study. They revealed bone deficits in the areas intended for implant placement. Soft tissue flaps were carefully raised and blocks or particles of deproteinized bovine bone mineral (DBBM) (Bio‐Oss
<sup>®</sup>
) were placed in the defect area. A collagenous membrane (Bio‐Gide
<sup>®</sup>
) was applied to cover the DBBM and was fixed to the surrounding bone using poly‐lactic acid pins. The flaps were sutured to allow for healing by primary intention.</p>
<p>
<b>Results: </b>
All sites in the 12 patients healed uneventfully. No flap dehiscences and no exposures of membranes were observed. Nine to 10 months following augmentation surgery, flaps were raised in order to visualize the outcomes of the augmentation. An integration of the DBBM particles into the newly formed bone was consistently observed. Merely on the surface of the new bone, some pieces of the grafting material were only partly integrated into bone. However, these were not encapsulated by connective tissue but rather anchored into the newly regenerated bone. In all of the cases, but one, the bone volume following regeneration was adequate to place implants in a prosthetically ideal position and according to the standard protocol with complete bone coverage of the surface intended for osseointegration. Before the regenerative procedure, the average crestal bone width was 3.2 mm and to 6.9 mm at the time of implant placement. This difference was statistically significant (
<i>P</i>
<0.05, Wilcoxon's matched pairs signed‐rank test).</p>
<p>
<b>Conclusion: </b>
After a healing period of 9–10 months, the combination of DBBM and a collagen membrane is an effective treatment option for horizontal bone augmentation before implant placement.</p>
<!--

To cite this article:

Hämmerle CHF, Jung RE, Yaman D, Lang NP. Ridge augmentation by applying bioresorbable membranes and deproteinized bovine bone mineral: a report of twelve consecutive cases.

Clin. Oral Impl. Res. 19, 2008; 19–25

doi: 10.1111/j.1600-0501.2007.01407.x

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<abstract>Material and methods: Twelve patients in need of implant therapy participated in this study. They revealed bone deficits in the areas intended for implant placement. Soft tissue flaps were carefully raised and blocks or particles of deproteinized bovine bone mineral (DBBM) (Bio‐Oss®) were placed in the defect area. A collagenous membrane (Bio‐Gide®) was applied to cover the DBBM and was fixed to the surrounding bone using poly‐lactic acid pins. The flaps were sutured to allow for healing by primary intention.</abstract>
<abstract>Results: All sites in the 12 patients healed uneventfully. No flap dehiscences and no exposures of membranes were observed. Nine to 10 months following augmentation surgery, flaps were raised in order to visualize the outcomes of the augmentation. An integration of the DBBM particles into the newly formed bone was consistently observed. Merely on the surface of the new bone, some pieces of the grafting material were only partly integrated into bone. However, these were not encapsulated by connective tissue but rather anchored into the newly regenerated bone. In all of the cases, but one, the bone volume following regeneration was adequate to place implants in a prosthetically ideal position and according to the standard protocol with complete bone coverage of the surface intended for osseointegration. Before the regenerative procedure, the average crestal bone width was 3.2 mm and to 6.9 mm at the time of implant placement. This difference was statistically significant (P<0.05, Wilcoxon's matched pairs signed‐rank test).</abstract>
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