E-Book, Englisch, 216 Seiten
Reihe: ITI Treatment Guide Series
Treatment Options
E-Book, Englisch, 216 Seiten
Reihe: ITI Treatment Guide Series
ISBN: 978-1-85097-346-1
Verlag: Quintessenz Verlag
Format: EPUB
Kopierschutz: Adobe DRM (»Systemvoraussetzungen)
Autoren/Hrsg.
Weitere Infos & Material
2 Proceedings of the Third ITI Consensus Conference: Implants in Post-Extraction Sites
The International Team for Implantology (ITI) is an independent academic network that unites professionals from all fields of implant dentistry and related tissue regeneration. It is active in the fields of research, development, and continuing education, and is dedicated to the promotion and spread of knowledge about all aspects of implant dentistry and related tissue regeneration for the benefit of patients. To date, the ITI unites about 5000 Fellows and Members in more than 40 countries. The ITI regularly draws up and publishes treatment guidelines that are based on comprehensive clinical studies and supported by long-term clinical results. The results of this commitment include, for instance, publications such as the ITI Treatment Guide and the ITI Consensus Papers. The ITI organizes consensus conferences at five-year intervals to discuss relevant topics in implant dentistry. The first and second ITI Consensus Conferences in 1993 and 1997 (Proceedings of the ITI Consensus Conference 2000) primarily discussed basic surgical and prosthetic issues in implant dentistry. The third ITI Consensus Conference was convened in 2003. For this conference, the ITI Education Committee decided to focus the discussion on four special topics that had received much attention in recent years, “Implants in Extraction Sockets” (current terminology: post-extraction sites) being one of them (Proceedings of the Third ITI Consensus Conference, International Journal of Oral and Maxillofacial Implants, 2004. Vol 19, Supplement). The objectives of the ITI Consensus Conference were to review the current literature in peer-reviewed journals and to discuss where sufficient evidence was available for specific clinical procedures and where evidence was lacking. A working group was elected for the exploration of each topic. Working Group 1,under the leadership of Professor Christoph H. F. Hämmerle, was asked to review relevant literature, focus on, and find consensus relating to implants in post-extraction sites. The participants of Working Group 1 were:
Gil Alcoforado
Jay R. Beagle
Jean-Pierre Bernard
Stephen T. Chen
Anthony Dickinson
Paul Fugazzotto
Erik Hjørting-Hansen
Louis Antonio Lima
Jan Lindhe
Thomas Oates
Mario Roccuzzo
James Ruskin
Thomas von Arx
Gerhard Wahl
Thomas G. Wilson Jr. 2.1 Consensus Statements and Recommended Clinical Procedures Regarding the Placement of Implants in Post-Extraction Sites
The group was asked to develop evidence-based reviews on topics related to various placement protocols for dental implants. The following material was presented to the group for review and discussion: Stephen T. Chen, Thomas G. Wilson Jr., and Christoph H. F. Hämmerle: “Immediate or Early Placement of Implants Following Tooth Extraction: Review of Biologic Basis, Clinical Procedures, and Outcomes” (Chen and coworkers, 2004) The aim of this article was to review the current literature with regard to survival and success rates, along with the clinical procedures and outcomes associated with immediate and delayed implant placement. The consensus statements and proposed clinical approaches defined by Working Group 1 on the topic of “Implants in Extraction Sockets”, as listed in Chapters 2.1.1 and 2.1.2 are intended to serve as a guide to clinicians in the diagnosis, treatment planning, and management of patients requiring dental implant therapy. With the consensus statements as guidelines, it is hoped that clinicians will be better prepared to make informed surgical and prosthodontic treatment decisions to further enhance the quality of care and predictability of treatment outcome for their patients. 2.1.1 Consensus Statements
Socket Healing Results of clinical, radiologic, and histologic studies indicate that bony healing of extraction sites proceeds with external resorption of the original socket walls and a varying degree of bone fill within the socket. Bone Regeneration Studies in humans and animals have demonstrated that at implant sites with a horizontal defect dimension (HDD; i.e. the peri-implant space) of 2 mm or less, spontaneous bone healing and osseointegration of implants with a rough titanium surface takes place. In sites with HDDs larger than 2 mm and or non-intact socket walls, techniques utilizing barrier membranes and/or membrane-supporting materials have been shown to be effective in regenerating bone and allowing osseointegration. Although scarce, the majority of the comparative data regarding the success of bone regeneration at peri-implant defects suggests no differences between Type 1, 2, and 3 procedures. Further comparative analyses of different methods of bone augmentation with regard to successful bone formation and stability over time are required. Long-term analysis of the stability of the regenerated bone is focused almost exclusively on radiographic assessments of the interproximal bone and implant survival. There is a need for studies to evaluate the fate of the buccal bone plate – whether regenerated or not – over time. Adjunctive Medication In most studies reviewed, broad-spectrum systemic antibiotics were used in conjunction with implant placement Type 1, 2, and 3. Controlled studies evaluating the effect of systemic antibiotics on treatment outcomes are needed. Survival of Implants The survival rate of immediately placed implants (Type 1) was reported in numerous studies to be similar to that of implants placed into healed ridges (Type 4). In the few studies available, short-term survival rates of implants placed in conjunction with Type 2 and 3 procedures appear similar to those placed in Type 1 and 4 approaches. There have been relatively few reports on the subject of Type 2 and 3 implant procedures, and only 2 of them were randomized with respect to timing of placement and augmentation methods used. Longitudinal studies of greater than 3 years’ duration were limited to 2 reports. There is evidence to suggest that the survival rate for implants placed immediately following extraction of teeth associated with local pathology is similar to that of implants placed into healed ridges. Further controlled studies are required to provide definitive information about the management of these situations. Esthetic Outcomes Esthetically pleasing treatment outcomes have received considerable attention in recent years; however, there are no controlled studies available on esthetic treatment outcomes in Type 1, 2, and 3 procedures. 2.1.2 Proposed Clinical Approaches
Patient Assessment All candidates for extraction-site implants should meet the same general screening criteria as regular implant patients, regardless of the timing of implant placement. Antibiotics The literature is inconclusive regarding antibiotic use in conjunction with implant therapy. There is general agreement that the use of antibiotics is advantageous when augmentation procedures are performed. Tooth Extraction Extraction techniques that result in minimal trauma to hard and soft tissue should be used. The sectioning of multi-rooted teeth is advised. All granulation tissue should be removed from the socket. Site Evaluation Site evaluation is critical to the determination of appropriate treatment modalities. Factors of concern include: Overall patient treatment plan Esthetic expectations of the patient Soft tissue quality, quantity, and morphology Bone quality, quantity, and morphology Presence of pathology Condition of adjacent teeth and supporting structures Primary Implant Stability The implant should not be placed at the time of tooth removal if the residual ridge morphology precludes attainment of primary stability of an appropriately sized implant in an ideal restorative position. Thin Biotype When treating patients with a thin, scalloped tissue biotype – even those with an intact buccal plate – concomitant augmentation therapies at the time of implant placement (Type 1) are recommended because of the high risk of buccal plate resorption and marginal tissue recession. If buccal plate integrity is lost, implant placement is not recommended at the time of tooth removal. Rather, augmentation therapy is performed, and a Type 3 or 4 approach is...