Skip to main content
International Journal of Biomaterials logoLink to International Journal of Biomaterials
. 2013 Dec 12;2013:307136. doi: 10.1155/2013/307136

Bone Substitutes for Peri-Implant Defects of Postextraction Implants

Pâmela Letícia Santos 1,*, Jéssica Lemos Gulinelli 1, Cristino da Silva Telles 2, Walter Betoni Júnior 2, Roberta Okamoto 3, Vivian Chiacchio Buchignani 1, Thallita Pereira Queiroz 4
PMCID: PMC3876702  PMID: 24454377

Abstract

Placement of implants in fresh sockets is an alternative to try to reduce physiological resorption of alveolar ridge after tooth extraction. This surgery can be used to preserve the bone architecture and also accelerate the restorative procedure. However, the diastasis observed between bone and implant may influence osseointegration. So, autogenous bone graft and/or biomaterials have been used to fill this gap. Considering the importance of bone repair for treatment with implants placed immediately after tooth extraction, this study aimed to present a literature review about biomaterials surrounding immediate dental implants. The search included 56 articles published from 1969 to 2012. The results were based on data analysis and discussion. It was observed that implant fixation immediately after extraction is a reliable alternative to reduce the treatment length of prosthetic restoration. In general, the biomaterial should be used to increase bone/implant contact and enhance osseointegration.

1. Introduction

Although alveolar repair after tooth extraction can be conducted by blood clot, this repair is not complete due to physiological resorption [1]. Studies demonstrated that vertical and horizontal dimensions are reduced around 11–22% and 29–63%, respectively, due to alveolar resorption after 6 months following tooth extraction [2]. This atrophy is more intense in the buccal surface (about 0.8 mm) during the first 3 months [3].

The insertion of immediate implants in atrophic sockets is a challenge to achieve satisfactory esthetics and function [4]. In this sense, in 1976, Schulte and Heimke [5] presented the immediate implants that are placed in fresh sockets.

However, the diastasis observed between bone and implant after dental extraction may influence osseointegration [6]. So, autogenous bone grafts and/or biomaterials have been used in those gaps to correct bone defects and provide appropriate stability.

Considering the importance of stability of immediate implants, this study presented a literature review about the most common biomaterials used for immediate dental implants.

2. Material and Method

The inclusion criteria assumed the studies published in English from 1969 to 2012 searched at Medline (Pubmed) and Bireme databases. The keywords “dental implant,” “osseointegration,” “postextraction,” “bone substitute,” “fresh extraction sockets,” “immediate implant,” “bone repair,” “bone modeling,” “dehiscence,” “dimension,” and “ grafting” were used for searching.

The search was based on scientific researches published in English including systematic reviews and also animal and human studies. The exclusion criteria were case reports and discussion articles. After analysis, 63 studies were selected according to the inclusion criteria. The results were based on data analysis and discussion. (Figure 1)

Figure 1.

Figure 1

Method flowchart.

3. Literature Review

3.1. Gap Dimension

The distance between bone and implant is called peri-implant gap. The fresh socket is wider than the implant diameter, which causes the peri-implant gap that influences stability and osseointegration [6, 7].

In 1977, Schenk and Willenegger [8] conducted a study on rabbits and observed the lack of complete bone formation with peri-implant gaps wider than 1.0 mm. In 1988, Carlsson et al. [9] used the same experimental model to compare 3 values of peri-implant gap between bone and implant (group A—0 mm, group B—0.35 mm, and group C—0.85 mm) and observed residual gaps in groups B and C at 6 and 12 weeks after surgery.

In 1999, Akimoto et al. [10] placed postextraction implants in dogs and evaluated the repair of peri-implant gaps from 0.5 to 1.4 mm after 12 weeks. The results demonstrated that the defect size is inversely proportional to the bone/implant contact. However, Botticelli et al. [6] performed a similar study and found complete bone neoformation and osseointegration in defect with 1.0 mm after 16 weeks.

3.2. Autogenous Bone

Autogenous bone corresponds to bone graft obtained from the same individual. It is considered the gold standard for filling of bone defects since it allows (I) osseointegration: direct contact with bone tissue without fibrous tissue [11]; (II) osteoconduction: support to bone growth [11]; (III) osteoinduction: differentiation of mesenchymal cells of surrounding tissue (receptor site) into osteoblastic cells [12]; and (IV) osteogenesis: bone neoformation by osteoblastic cells present in the graft material [12]. Although few mature osteoblasts survive to grafting, precursor cells are responsible for the osteogenic potential [12].

Autogenous grafts are presented as blocks or particles and can be used isolated or associated with allogenic or alloplastic grafts. The donator area can be mentonian region, retromolar area, maxillary tuberosity, iliac crest, rib, cranium, tibia, and fibula [13].

Several studies evaluated peri-implant bone defects filled with autogenous bone. In 2013, Al-Sulaimani et al. [14] evaluated the success rate of immediate implants associated with autogenous bone for filling of the peri-implant gap. In this study, beagle dogs were used for insertion of implants immediately after extraction of right and left maxillary and mandibular lateral incisors. The gaps were filled with blood clot (control) and autogenous bone (experimental) and better results were found for the autogenous bone graft.

Nevertheless, this graft may cause morbidity in the donator area, hematoma, edema, infection, and vascular and nerve lesions. In addition, this technique spends more time for surgical procedure and it is limited for large reconstructions [15]. So, biomaterials have been suggested as an alternative to solve those limitations and reduce the gap between bone and implant.

3.3. Mineralized Bone Tissue

The matrix of mineralized bone tissue is composed by deproteinized bone tissue. It has been widely used for preservation of alveolar ridge dimension after tooth extraction, filling of bone defects near to natural teeth, and also during maxillary sinus lift [1621].

In a study in monkeys, molars and premolar were extracted for fixation of titanium implants after 3 months. Peri-implant defects with 2.5 mm in width and 3.0 mm in height were filled with blood clot, polytetrafluorethylene membrane, Bio-oss, and Bio-oss with membrane. The histological analysis after 6 months revealed that Bio-Oss exhibits osteoconductive capacity and should be used for reconstruction of peri-implant bone defects [17].

Hockers et al. [18] conducted a similar study including one group with autogenous bone and observed that the bone grafts were integrated to the bone tissue.

Caneva et al. [19] used bone substitutes to fill the the gap between bone and implant. The effect of bone fillers (magnesium-enriched hydroxyapatite) on preservation of the alveolar bone around immediate implants was evaluated in a dog study. Implants with a sandblasted acid etched surface were placed into the fresh extraction sockets bilaterally into the dogs' jaws. Magnesium-enriched hydroxyapatite was placed at test sites,while the control sites did not receive augmentation materials. After 4 months of healing, the animals were sacrificed. Histomorphometric evaluations showed that the alveolar bony crest outline was maintained to a higher degree at the buccal bone wall of the test sites (loss: 0.7 mm) compared with the control sites (loss: 1.2 mm), even though this difference did not reach statistical significance.

In another experimental study Caneva et al. [20] explored the effect of GBR based on deproteinized bovine bone mineral on alveolar ridge preservation and the reparation of defects around osseointegrated implants. The authors concluded that the application of DBBM concomitant with a collagene membrane contributed in improving bone regeneration in the defects.

Barone et al. [21] showed that regenerative techniques (GBR) were able to limit resorption of the alveolar crest after implant placement in a fresh extraction socket, tooth extraction.

Hsu et al. [22] in an experimental study instead demonstrated that the placement of implants and deproteinized bovine bone mineral into fresh extraction sockets results in significant buccal bone loss and low osseointegration.

Other clinical studies [2325] used GBR techniques to fill the gap between bone and implant.

3.4. Mineralized Bone Tissue with Addition of 10% Porcine Collagen

This material is composed by mineralized bovine bone matrix with addition of 10% porcine collagen (Bio-oss Collagen, Geistlich). This biomaterial is indicated for filling of extraction sockets, periodontal defects, and maxillary sinus lifting [26].

Araújo et al. [27] conducted an animal study with filling of extraction sockets with Bio-oss collagen. Biopsy and histometric analysis were performed after 3 months and demonstrated that the biomaterial promoted formation of bone tissue, maintained the dimension of alveolar walls, and preserved the alveolar crest profile.

In 2009, the same authors [28] performed a similar study for evaluation after 2 weeks. The results showed delayed alveolar repair with bone neoformation only at apical and lateral walls.

Wong and Rabie [29] conducted a study in rabbits to compare the amount of bone produced by Bio-Oss collagen and collagen matrix. Eighteen bone defects (5.0 mm × 10.0 mm) were created in the parietal bone of the rabbits and filled with Bio-Oss collagen, collagen matrix and blood clot. Biopsies were removed after 14 days for histological analysis. The authors concluded that the Bio-Oss collagen presented better results for bone neoformation in comparison to the collagen matrix while no bone was formed with the blood clot.

The study of Araújo et al. [30] is the only study evaluating peri-implant defects filled with Bio-oss collagen. In this paper, dogs were used to evaluate bone repair after fixation of immediate implants and insertion of mineralized bovine bone with addition of 10% porcine collagen. Biopsies were obtained after 6 months for histological analysis. The authors found that the presence of Bio-oss collagen changed the healing process of hard tissue, which improved bone/implant contact.

3.5. Beta-Tricalcium Phosphate

The β-tricalcium phosphate has been considered a material with excellent results since it is absorbable, osteoconductive, and nonosteoinductive [1]. Animal [26, 3133] and human [34] studies demonstrated that this material supported bone neoformation.

In 2013, Daif [35] conducted a study to evaluate the influence of β-tricalcium phosphate on bone density surrounding immediate dental implants using helical computer tomography. Twenty-eight patients were selected and divided into two groups: (I) no filling and (II) filling with beta-TCP in the peri-implant defect. Tomography was obtained after 3 and 6 months and showed that the β-tricalcium phosphate increased bone density in the bone defect of immediate dental implants.

Recently, some industries developed a synthetic bone substitute composed by a homogeneous mixture of 60% of hydroxyapatite (HA) and 40% of beta-tricalcium phosphate [36]. Although the HA is resistant to physiological resorption [37], its osteoconductive capacity remains uncertain [38, 39]. On the other hand, the β-tricalcium phosphate is absorbed slowly and it is considered an osteoconductive material [40]. Thus, the HA maintains the gap while the β-tricalcium phosphate is absorbed to promote bone regeneration simultaneously [41].

In 2004, Boix et al. [42] evaluated the efficacy of this material in peri-implant defects in dogs and concluded that the biomaterial generated significant increase in bone regeneration surrounding the dental implant.

4. Discussion

The extraction socket is usually wider than the implant diameter, which results in a gap between the cervical region of the implant and the bone tissue (Figures 2, 3, and 4). Although this gap can be restored by maintenance of blood clot [43], the use of biomaterials is indicated to preserve alveolar ridge dimensions and promote repair [36] (Figure 5). In addition, the insertion of biomaterials simultaneously to the implant fixation improves functional and esthetic restoration of the stomatognathic system (Figures 6 and 7).

Figure 2.

Figure 2

Initial panoramic radiograph.

Figure 3.

Figure 3

Initial computed tomography.

Figure 4.

Figure 4

Peri-implant defect.

Figure 5.

Figure 5

Peri-implant defect filled with biomaterial.

Figure 6.

Figure 6

Esthetic restoration.

Figure 7.

Figure 7

Final computed tomography.

Several animal [6, 7, 30, 44, 45] and human [34, 39, 4654] studies were conducted to evaluate the reconstruction of the peri-implant gap with biomaterials through clinical follow-up, histology, imaging, and immunohistochemistry. However, few of the literature reviews about biomaterials for peri-implant defects were found [55].

The ideal bone graft should present limited source, lack of morbidity in the donator site, no risk to disease transmission, efficient bone repair, immediate stability, versatility, easy manipulation, appropriate lifetime, and accessible cost [56].

The autogenous bone is considered the first option for bone reconstruction in implantology since it presents characteristics of the ideal graft. However, this approach requires longer surgical procedure and may not obtain enough bone volume [57]. So, alternative treatments have been suggest for peri-implant reconstruction.

Jensen et al. [33] compared the performance of autogenous bone, β-tricalcium phosphate, and anorganic bovine bone by histological and histomorphometric analyses in pigs. The authors observed greater efficacy for the autogenous bone in comparison to the other grafts.

On the other hand, Hockers et al. [18] compared grafting with autogenous bone and demineralized bovine bone for reconstruction of peri-implant defects in dogs and found similar integration for both materials. Similarly, Santis et al. [58] concluded that the autogenous bone and demineralized bovine bone provided a high level of bone regeneration and satisfactory bone/implant contact for osseointegration.

In 2009, Benić et al. [59] performed a human study to assess the success rate of peri-implant defects reconstruction with autogenous bone, demineralized bovine bone, and association of both materials. No difference was observed between the groups after a 5-year follow-up.

Han et al. [60] compared bone regeneration in peri-implant defects of dogs according to the following groups: (I) no filling, (II) autogenous bone, (III) Bio-Oss collagen, (IV) Bio-Oss, (V) no filling and collagen membrane, (VI) autogenous bone and collagen membrane, (VII) Bio-Oss collagen and collagen membrane, and (VIII) Bio-Oss and collagen membrane. The authors concluded that reconstruction of peri-implant defect with bone substitutes associated with membrane or not increases the percentage of bone/implant contact.

Guerra et al. [61] conducted a study on rabbits to compare grafting with bovine bone, bovine bone associated with platelet-rich plasma, bovine bone protected by membrane, and blood clot. A higher percentage of bone/implant contact with bovine bone protected by collagen membrane was observed.

Jensen et al. used immunohistochemistry in dogs to evaluate the performance of Bio-Oss collagen and Bone-Ceramic and found that both biomaterials are great osteoconductive materials for bone repair [33]. However, Antunes et al. [62] evaluated repair with blood clot, autogenous bone, Bio-Oss, and Bone-Ceramic in dogs and observed lower stability with Bio-Oss after 2 months.

Wang and Lang [63] evaluated the more recent studies in animal and human about this topic and they concluded that implants placed into the fresh extraction sockets do not prevent the resorption of the alveolar bone. In the research that was conducted bone regeneration with implant post-extractive implants would notice minor alveolar bone resorption. Moreover, other bone substitutes were tested: magnesium-enriched hydroxyapatite, human demineralized bone matrix, and deproteinized bovine bone mineral have been shown to be effective in ridge preservation. Applying the guided bone regeneration principle using bone substitutes together with a collagen membrane has shown clear effects on preserving alveolar ridge height as well as ridge width. Soft tissue grafts or primary closure did not show a beneficial effect on preserving the alveolar bone.

5. Conclusions

Considering this literature review, the fixation of implants immediately after tooth extraction is a reliable alternative to reduce the treatment length for patient's rehabilitation. In general, this treatment requires the use of a biomaterial to increase bone/implant contact and enhance osseointegration.

References

  • 1.Brkovic BMB, Prasad HS, Rohrer MD, et al. Beta-tricalcium phosphate/type I collagen cones with or without a barrier membrane in human extraction socket healing: clinical, histologic, histomorphometric, and immunohistochemical evaluation. Clinical Oral Investigations. 2012;16(2):581–590. doi: 10.1007/s00784-011-0531-1. [DOI] [PubMed] [Google Scholar]
  • 2.Tan WL, Wong TLT, Wong MCM, Lang NP. A systematic review of post-extractional alveolar hard and soft tissue dimensional changes in humans. Clinical Oral Implants Research. 2012;23(5):1–21. doi: 10.1111/j.1600-0501.2011.02375.x. [DOI] [PubMed] [Google Scholar]
  • 3.Schropp L, Wenzel A, Kostopoulos L, Karring T. Bone healing and soft tissue contour changes following single-tooth extraction: a clinical and radiographic 12-month prospective study. International Journal of Periodontics and Restorative Dentistry. 2003;23(4):313–323. [PubMed] [Google Scholar]
  • 4.Shi B, Zhou Y, Wang YN, Cheng XR. Alveolar ridge preservation prior to implant placement with surgical-grade calcium sulfate and platelet-rich plasma: a pilot study in a canine model. The International Journal of Oral & Maxillofacial Implants. 2007;22(4):656–665. [PubMed] [Google Scholar]
  • 5.Schulte W, Heimke G. The Tübinger immediate implant. Die Quintessenz. 1976;27(6):17–23. [PubMed] [Google Scholar]
  • 6.Botticelli D, Berglundh T, Buser D, Lindhe J. The jumping distance revisited: an experimental study in the dog. Clinical Oral Implants Research. 2003;14(1):35–42. doi: 10.1034/j.1600-0501.2003.140105.x. [DOI] [PubMed] [Google Scholar]
  • 7.Botticelli D, Renzi A, Lindhe J, Berglundh T. Implants in fresh extraction sockets: a prospective 5-year follow-up clinical study. Clinical Oral Implants Research. 2008;19(12):1226–1232. doi: 10.1111/j.1600-0501.2008.01620.x. [DOI] [PubMed] [Google Scholar]
  • 8.Schenk RK, Willenegger HR. Histology of primary bone healing: modifications and limits of recovery of gaps in relation to extent of the defect. Unfallheilkunde. 1977;80(5):155–160. [PubMed] [Google Scholar]
  • 9.Carlsson L, Rostlund T, Albrektsson B, Albrektsson T. Implant fixation improved by close fit. Cylindrical implant-bone interface studied in rabbits. Acta Orthopaedica Scandinavica. 1988;59(3):272–275. doi: 10.3109/17453678809149361. [DOI] [PubMed] [Google Scholar]
  • 10.Akimoto K, Becker W, Persson R, Baker DA, Rohrer MD, O’Neal RB. Evaluation of titanium implants placed into simulated extraction sockets: a study in dogs. The International Journal of Oral & Maxillofacial Implants. 1999;14(3):351–360. [PubMed] [Google Scholar]
  • 11.Costantino PD, Friedman CD. Synthetic bone graft substitutes. Otolaryngologic Clinics of North America. 1994;27(5):1037–1074. [PubMed] [Google Scholar]
  • 12.Cypher TJ, Grossman JP. Biological principles of bone graft healing. Journal of Foot and Ankle Surgery. 1996;35(5):413–417. doi: 10.1016/s1067-2516(96)80061-5. [DOI] [PubMed] [Google Scholar]
  • 13.Coradazzi LF, Garcia IR, Jr., Manfrin TM. Evaluation of autogenous bone grafts, particulate or collected during osteotomy with implant burs: histologic and histomorphometric analysis in rabbits. The International Journal of Oral & Maxillofacial Implants. 2007;22(2):201–207. [PubMed] [Google Scholar]
  • 14.Al-Sulaimani A, Mokeem SA, Anil S. Peri-implant defect augmentation with autogenous bone: a study in beagle dogs. Journal of Oral Implantology. 2013;39:30–36. doi: 10.1563/AAID-JOI-D-10-00132. [DOI] [PubMed] [Google Scholar]
  • 15.Trejo PM, Weltman R, Caffesse R. Treatment of intraosseous defects with bioabsorbable barriers alone or in combination with decalcified freeze-dried bone allograft: a randomized clinical trial. Journal of Periodontology. 2000;71(12):1852–1861. doi: 10.1902/jop.2000.71.12.1852. [DOI] [PubMed] [Google Scholar]
  • 16.Hürzeler MB, Quiñones CR, Kirsch A, et al. Maxillary sinus augmentation using different grafting materials and dental implants in monkeys. Part I. Evaluation of anorganic bovine-derived bone matrix. Clinical Oral Implants Research. 1997;8(6):476–486. doi: 10.1034/j.1600-0501.1997.080606.x. [DOI] [PubMed] [Google Scholar]
  • 17.Hämmerle CHF, Chiantella GC, Karring T, Lang NP. The effect of a deproteinized bovine bone mineral on bone regeneration around titanium dental implants. Clinical Oral Implants Research. 1998;9(3):151–162. doi: 10.1034/j.1600-0501.1998.090302.x. [DOI] [PubMed] [Google Scholar]
  • 18.Hockers T, Abensur D, Valentini P, Legrand R, Hammerle CHF. The combined use of bioresorbable membranes and xenografts or autografts in the treatment of bone defects around implants: a study in beagle dogs. Clinical Oral Implants Research. 1999;10(6):487–498. doi: 10.1034/j.1600-0501.1999.100607.x. [DOI] [PubMed] [Google Scholar]
  • 19.Caneva M, Botticelli D, Stellini E, Souza SLS, Salata LA, Lang NP. Magnesium-enriched hydroxyapatite at immediate implants: a histomorphometric study in dogs. Clinical Oral Implants Research. 2011;22(5):512–517. doi: 10.1111/j.1600-0501.2010.02040.x. [DOI] [PubMed] [Google Scholar]
  • 20.Caneva M, Botticelli D, Pantani F, Baffone GM, Rangel IG, Jr., Lang NP. Deproteinized bovine bone mineral in marginal defects at implants installed immediately into extraction sockets: an experimental study in dogs. Clinical Oral Implants Research. 2012;23(1):106–112. doi: 10.1111/j.1600-0501.2011.02202.x. [DOI] [PubMed] [Google Scholar]
  • 21.Barone A, Ricci M, Calvo-Guirado JL, Covani U. Bone remodelling after regenerative procedures around implants placed in fresh extraction sockets: an experimental study in Beagle dogs. Clinical Oral Implants Research. 2011;22(10):1131–1137. doi: 10.1111/j.1600-0501.2010.02084.x. [DOI] [PubMed] [Google Scholar]
  • 22.Hsu KM, Choi BH, Ko CY, Kim HS, Xuan F, Jeong SM. Ridge alterations following immediate implant placement and the treatment of bone defects with Bio-Oss in an animal model. Clinical Implant Dentistry and Related Research. 2012;14(5):690–695. doi: 10.1111/j.1708-8208.2010.00316.x. [DOI] [PubMed] [Google Scholar]
  • 23.Cafiero C, Annibali S, Gherlone E, et al. Immediate transmucosal implant placement in molar extraction sites: a 12-month prospective multicenter cohort study. Clinical Oral Implants Research. 2008;19(5):476–482. doi: 10.1111/j.1600-0501.2008.01541.x. [DOI] [PubMed] [Google Scholar]
  • 24.Matarasso S, Salvi GE, Iorio Siciliano V, Cafiero C, Blasi A, Lang NP. Dimensional ridge alterations following immediate implant placement in molar extraction sites: a six-month prospective cohort study with surgical re-entry. Clinical Oral Implants Research. 2009;20(10):1092–1098. doi: 10.1111/j.1600-0501.2009.01803.x. [DOI] [PubMed] [Google Scholar]
  • 25.Siciliano VI, Salvi GE, Matarasso S, Cafiero C, Blasi A, Lang NP. Soft tissues healing at immediate transmucosal implants placed into molar extraction sites with buccal self-contained dehiscences. A 12-month controlled clinical trial. Clinical Oral Implants Research. 2009;20(5):482–488. doi: 10.1111/j.1600-0501.2008.01688.x. [DOI] [PubMed] [Google Scholar]
  • 26.Artzi Z, Kozlovsky A, Nemcovsky CE, Weinreb M. The amount of newly formed bone in sinus grafting procedures depends on tissue depth as well as the type and residual amount of the grafted material. Journal of Clinical Periodontology. 2005;32(2):193–199. doi: 10.1111/j.1600-051X.2005.00656.x. [DOI] [PubMed] [Google Scholar]
  • 27.Araújo M, Linder E, Wennström J, Lindhe J. The influence of Bio-Oss collagen on healing of an extraction socket: an experimental study in the dog. International Journal of Periodontics and Restorative Dentistry. 2008;28(2):123–135. [PubMed] [Google Scholar]
  • 28.Araújo M, Linder E, Lindhe J. Effect of a xenograft on early bone formation in extraction sockets: an experimental study in dog. Clinical Oral Implants Research. 2009;20(1):1–6. doi: 10.1111/j.1600-0501.2008.01606.x. [DOI] [PubMed] [Google Scholar]
  • 29.Wong RWK, Rabie ABM. Effect of Bio-Oss collagen and collagen matrix on bone formation. Open Biomedical Engineering Journal. 2010;4:71–76. doi: 10.2174/1874120701004010071. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Araújo MG, Linder E, Lindhe J. Bio-Oss Collagen in the buccal gap at immediate implants: a 6-month study in the dog. Clinical Oral Implants Research. 2011;22(1):1–8. doi: 10.1111/j.1600-0501.2010.01920.x. [DOI] [PubMed] [Google Scholar]
  • 31.Fujita R, Yokoyama A, Nodasaka Y, Kohgo T, Kawasaki T. Ultrastructure of ceramic-bone interface using hydroxyapatite and β-tricalcium phosphate ceramics and replacement mechanism of β-tricalcium phosphae in bone. Tissue and Cell. 2003;35(6):427–440. doi: 10.1016/s0040-8166(03)00067-3. [DOI] [PubMed] [Google Scholar]
  • 32.Schwarz F, Herten M, Ferrari D, et al. Guided bone regeneration at dehiscence-type defects using biphasic hydroxyapatite + beta tricalcium phosphate (Bone Ceramic) or a collagen-coated natural bone mineral (BioOss Collagen): an immunohistochemical study in dogs. International Journal of Oral and Maxillofacial Surgery. 2007;36(12):1198–1206. doi: 10.1016/j.ijom.2007.07.014. [DOI] [PubMed] [Google Scholar]
  • 33.Jensen SS, Broggini N, Hjørting-Hansen E, Schenk R, Buser D. Bone healing and graft resorption of autograft, anorganic bovine bone and β-tricalcium phosphate. A histologic and histomorphometric study in the mandibles of minipigs. Clinical Oral Implants Research. 2006;17(3):237–243. doi: 10.1111/j.1600-0501.2005.01257.x. [DOI] [PubMed] [Google Scholar]
  • 34.Zerbo IR, Bronckers ALJJ, de Lange GL, van Beek GJ, Burger EH. Histology of human alveolar bone regeneration with a porous tricalcium phosphate. A report of two cases. Clinical Oral Implants Research. 2001;12(4):379–384. doi: 10.1034/j.1600-0501.2001.012004379.x. [DOI] [PubMed] [Google Scholar]
  • 35.Daif ET. Effect of a multiporous beta- tricalicum phosphate on bone density around dental. Journal of Oral Implantology. 2013;39(3):339–344. doi: 10.1563/AAID-JOI-D-11-00079. [DOI] [PubMed] [Google Scholar]
  • 36.Mardas N, Chadha V, Donos N. Alveolar ridge preservation with guided bone regeneration and a synthetic bone substitute or a bovine-derived xenograft: a randomized, controlled clinical trial. Clinical Oral Implants Research. 2010;21(7):688–698. doi: 10.1111/j.1600-0501.2010.01918.x. [DOI] [PubMed] [Google Scholar]
  • 37.Govindaraj S, Costantino PD, Friedman CD. Current use of bone substitutes in maxillofacial surgery. Facial Plastic Surgery. 1999;15(1):73–81. doi: 10.1055/s-2008-1064302. [DOI] [PubMed] [Google Scholar]
  • 38.Beirne OR, Curtis TA, Greenspan JS. Mandibular augmentation with hydroxyapatite. The Journal of Prosthetic Dentistry. 1986;55(3):362–367. doi: 10.1016/0022-3913(86)90121-6. [DOI] [PubMed] [Google Scholar]
  • 39.Stahl SS, Froum SJ. Histologic and clinical responses to porous hydroxylapatite implants in human periodontal defects. Three to twelve months postimplantation. Journal of Periodontology. 1987;58(10):689–695. doi: 10.1902/jop.1987.58.10.689. [DOI] [PubMed] [Google Scholar]
  • 40.Breitbart AS, Staffenberg DA, Thorne CHM, et al. Tricalcium phosphate and osteogenin: a bioactive onlay bone graft substitute. Plastic and Reconstructive Surgery. 1995;96(3):699–708. doi: 10.1097/00006534-199509000-00024. [DOI] [PubMed] [Google Scholar]
  • 41.Mardas N, D’Aiuto F, Mezzomo L, Arzoumanidi M, Donos N. Radiographic alveolar bone changes following ridge preservation with two different biomaterials. Clinical Oral Implants Research. 2011;22(4):416–423. doi: 10.1111/j.1600-0501.2010.02154.x. [DOI] [PubMed] [Google Scholar]
  • 42.Boix D, Gauthier O, Guicheux J, et al. Alveolar bone regeneration for immediate implant placement using an injectable bone substitute: an experimental study in dogs. Journal of Periodontology. 2004;75(5):663–671. doi: 10.1902/jop.2004.75.5.663. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Misch CE, Dietsh F. Bone-grafting materials in implant dentistry. Implant Dentistry. 1993;2(3):158–167. doi: 10.1097/00008505-199309000-00003. [DOI] [PubMed] [Google Scholar]
  • 44.Botticelli D, Berglundh T, Lindhe J. Resolution of bone defects of varying dimension and configuration in the marginal portion of the peri-implant bone: an experimental study in the dog. Journal of Clinical Periodontology. 2004;31(4):309–317. doi: 10.1111/j.1600-051X.2004.00502.x. [DOI] [PubMed] [Google Scholar]
  • 45.Botticelli D, Persson LG, Lindhe J, Berglundh T. Bone tissue formation adjacent to implants placed in fresh extraction sockets: an experimental study in dogs. Clinical Oral Implants Research. 2006;17(4):351–358. doi: 10.1111/j.1600-0501.2006.01270.x. [DOI] [PubMed] [Google Scholar]
  • 46.Gelb DA. Immediate implant surgery: three-year retrospective evaluation of 50 consecutive cases. The International Journal of Oral & Maxillofacial Implants. 1993;8(4):388–399. [PubMed] [Google Scholar]
  • 47.Brägger U, Hämmerle CHF, Lang NP. Immediate transmucosal implants using the principle of guided tissue regeneration (II). A cross-sectional study comparing the clinical outcome 1 year after immediate to standard implant placement. Clinical Oral Implants Research. 1996;7(3):268–276. doi: 10.1034/j.1600-0501.1996.070309.x. [DOI] [PubMed] [Google Scholar]
  • 48.Schwartz-Arad D, Chaushu G. Placement of implants into fresh extraction sites: 4 to 7 years retrospective evaluation of 95 immediate implants. Journal of Periodontology. 1997;68(11):1110–1116. doi: 10.1902/jop.1997.68.11.1110. [DOI] [PubMed] [Google Scholar]
  • 49.Grunder U, Polizzi G, Goené R, et al. A 3-year prospective multicenter follow-up report on the immediate and delayed-immediate placement of implants. The International Journal of Oral & Maxillofacial Implants. 1999;14(2):210–216. [PubMed] [Google Scholar]
  • 50.Lekholm U, Wannfors K, Isaksson S, Adielsson B. Oral implants in combination with bone grafts: a 3-year retrospective multicenter study using the Brånemark implant system. International Journal of Oral and Maxillofacial Surgery. 1999;28(3):181–187. [PubMed] [Google Scholar]
  • 51.Artzi Z, Tal H, Dayan D. Porous bovine bone mineral in healing of human extraction sockets. Part 1. Histomorphometric evaluations at 9 Months. Journal of Periodontology. 2000;71(6):1015–1023. doi: 10.1902/jop.2000.71.6.1015. [DOI] [PubMed] [Google Scholar]
  • 52.Froum S, Cho S-C, Rosenberg E, Rohrer M, Tarnow D. Histological comparison of healing extraction sockets implanted with bioactive glass or demineralized freeze-dried bone allograft: a pilot study. Journal of Periodontology. 2002;73(1):94–102. doi: 10.1902/jop.2002.73.1.94. [DOI] [PubMed] [Google Scholar]
  • 53.Carmagnola D, Adriaens P, Berglundh T. Healing of human extraction sockets filled with Bio-Oss. Clinical Oral Implants Research. 2003;14(2):137–143. doi: 10.1034/j.1600-0501.2003.140201.x. [DOI] [PubMed] [Google Scholar]
  • 54.Norton MR, Odell EW, Thompson ID, Cook RJ. Efficacy of bovine bone mineral for alveolar augmentation: a human histologic study. Clinical Oral Implants Research. 2003;14(6):775–783. doi: 10.1046/j.0905-7161.2003.00952.x. [DOI] [PubMed] [Google Scholar]
  • 55.Ortega-Martínez J, Pérez-Pascual T, Mareque-Bueno S, Hernández-Alfaro F, Ferrés-Padró E. Immediate implants following tooth extraction. A systematic review. Medicina Oral, Patologia Oral y Cirugia Bucal. 2012;17(2):e251–e261. doi: 10.4317/medoral.17469. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.Eppley BL, Pietrzak WS, Blanton MW. Allograft and alloplastic bone substitutes: a review of science and technology for the craniomaxillofacial surgeon. Journal of Craniofacial Surgery. 2005;16(6):981–989. doi: 10.1097/01.scs.0000179662.38172.dd. [DOI] [PubMed] [Google Scholar]
  • 57.McAllister DR, Joyce MJ, Mann BJ, Vangsness CT., Jr. Allograft update: the current status of tissue regulation, procurement, processing, and sterilization. The American Journal of Sports Medicine. 2007;35(12):2148–2158. doi: 10.1177/0363546507308936. [DOI] [PubMed] [Google Scholar]
  • 58.de Santis E, Botticelli D, Pantani F, Pereira FP, Beolchini M, Lang NP. Bone regeneration at implants placed into extraction sockets of maxillary incisors in dogs. Clinical Oral Implants Research. 2011;22(4):430–437. doi: 10.1111/j.1600-0501.2010.02122.x. [DOI] [PubMed] [Google Scholar]
  • 59.Benić GI, Jung RE, Siegenthaler DW, Hämmerle CHF. Clinical and radiographic comparison of implants in regenerated or native bone: 5-year results. Clinical Oral Implants Research. 2009;20(5):507–513. doi: 10.1111/j.1600-0501.2008.01583.x. [DOI] [PubMed] [Google Scholar]
  • 60.Han J-Y, Shin S-I, Herr Y, Kwon Y-H, Chung J-H. The effects of bone grafting material and a collagen membrane in the ridge splitting technique: an experimental study in dogs. Clinical Oral Implants Research. 2011;22(12):1391–1398. doi: 10.1111/j.1600-0501.2010.02127.x. [DOI] [PubMed] [Google Scholar]
  • 61.Guerra I, Morais Branco F, Vasconcelos M, Afonso A, Figueiral H, Zita R. Evaluation of implant osseointegration with different regeneration techniques in the treatment of bone defects around implants: an experimental study in a rabbit model. Clinical Oral Implants Research. 2011;22(3):314–322. doi: 10.1111/j.1600-0501.2010.02002.x. [DOI] [PubMed] [Google Scholar]
  • 62.Antunes AA, Oliveira Neto P, de Santis E, Caneva M, Botticelli D, Salata LA. Comparisons between Bio-Oss and Straumann Bone Ceramic in immediate and staged implant placement in dogs mandible bone defects. Clinical Oral Implants Research. 2013;24:135–142. doi: 10.1111/j.1600-0501.2011.02385.x. [DOI] [PubMed] [Google Scholar]
  • 63.Wang RE, Lang NP. Ridge preservation after tooth extraction. Clinical Oral Implants Research. 2012;23(6):147–156. doi: 10.1111/j.1600-0501.2012.02560.x. [DOI] [PubMed] [Google Scholar]

Articles from International Journal of Biomaterials are provided here courtesy of Wiley

RESOURCES