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International Journal of Implant Dentistry
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Horizontal augmentation techniques in the mandible: a systematic review

International Journal of Implant Dentistry volume 8, Article number: 23 (2022) Cite this article

Abstract

Purpose

Placement of dental implants has evolved to be an advantageous treatment option for rehabilitation of the fully or partially edentulous mandible. In case of extensive horizontal bone resorption, the bone volume needs to be augmented prior to or during implant placement in order to obtain dental rehabilitation and maximize implant survival and success.

Methods

Our aim was to systematically review the available data on lateral augmentation techniques in the horizontally compromised mandible considering all grafting protocols using xenogeneic, synthetic, or allogeneic material. A computerized and manual literature search was performed for clinical studies (published January 1995 to March 2021).

Results

Eight studies ultimately met the inclusion criteria comprising a total of 276 procedures of xenogeneic, allogeneic, or autogenous bone graft applications in horizontal ridge defects. Particulate materials as well as bone blocks were used as grafts with a mean follow-up of 26.0 months across all included studies. Outcome measures, approaches and materials varied from study to study. A gain of horizontal bone width of the mandible with a mean of 4.8 mm was observed in seven of eight studies. All but one study, reported low bone graft failure rates of 4.4% in average.

Conclusions

Only limited data are available on the impact of different horizontal augmentation strategies in the mandible. The results show outcomes for xenogeneic as well as autologous bone materials for horizontal ridge augmentation of the lower jaw. The use of allogeneic bone-block grafts in combination with resorbable barrier membranes must be re-evaluated. Randomized controlled clinical trials are largely missing.

Background

Dental implantology has evolved as an advantageous treatment method for dental rehabilitation and prosthetic restoration of partial or fully edentulous jaws [1, 2]. Sufficient amount and quality of bone remains a determining requirement for successful long-time implant survival and success and to prevent peri-implant disease [3,4,5]. Physiologic bone loss has been reported in various studies as a logical consequence after tooth extraction [6, 7]. In cases of severe bone loss—mostly due to long time interval since tooth removal, unfavorable load, infection, trauma, or other reasons—bone frequently needs to be augmented prior to or during implant placement [8, 9]. Different augmentation techniques have been developed depending on localization, extent, and configuration of the bone defect [10, 11].

If alveolar bone loss is limited, bone splitting and spreading are useful techniques for adaptation to the local conditions, although this may be difficult to apply in strong cortical bone such as the mandible [12]. Narrow diameter implants have also been proven to serve as possible solutions in horizontally compromised bone [13]. However, in cases of severe horizontal bone loss, horizontal augmentation of the mandibular alveolar ridge may be necessary and can be achieved by a variety of surgical approaches [9]. These procedures include insertion of bone grafts or stimulating bone formation in terms of guided bone regeneration [14,15,16,17]. Autologous bone is still regarded as gold standard given its biological properties [9, 18]. However, due to aspects like donor site morbidity, prolonged time of surgery and unpredictable resorption dynamics, a variety of allografts, xenografts and synthetic materials have been introduced into the market and numerous compositions are commercially available. Moreover, these grafts are commonly combined with autologous bone to improve compatibility and combine the advantages of these materials [19]. Additionally, this diversity is extended by different surgical techniques and protocols. Due to the enormous number of materials and techniques, a randomized controlled trial to evaluate and compare all the different approaches would be impossible to conduct. However, there exist scientific reports on the topic that can provide a considerable body of knowledge. For instance, Troeltzsch et al. provide a comprehensive analysis of the available literature for the augmentation of the alveolar ridge [20]. Bone formation in the augmented areas varied from 33.2 ± 14.9% for allogeneic grafts to 56.0 ± 25.6% for mixtures of autogenous and other grafting materials. The authors derive a horizontal gain of 3.7 mm for particulate, compared to 4.5 mm for block grafts. Despite a detailed evaluation of horizontal and vertical dimension, analysis of the donor site (autogenous iliac crest, calvarium, mandible, allogeneic) or the subclassification of the results with regard to the use of membranes and meshes, distinct results for the horizontally compromised lower jaw as recipient site remain elusive.

Furthermore, implant survival and success in concomitantly vs. subsequently placed dental implants are not reported uniformly, so that this aspect remains unclear to date. Thus, the aim of this report was to systematically review the available data and potentially draw conclusions about the efficacy in gaining bone width, implant survival and success rates after or accompanying horizontal ridge augmentation procedures using autologous, xenogeneic, synthetic, or allogeneic materials or combinations of these in cases of bone loss in the lower jaw, which require lateral augmentation. The idea was to systematize approaches and give recommendations on this complex and relevant subject by assessing the efficacy of grafting materials with respect to clinically relevant parameters.

Results

Study characteristics

The initial electronic search identified a total of 15,643 titles (Fig. 1). 890 studies were selected for further assessment of the abstract after screening of the titles. 64 articles were added by manual search. Out of these, a total of 866 were excluded. Subsequently, 88 full-text articles were obtained, and “Materials and methods” and “Results” sections were investigated. Only eight studies ultimately met the inclusion criteria (Fig. 1). The reasons for exclusion are depicted in Table 1.

Fig. 1
figure 1

Tree diagram of exclusion/inclusion of studies for this systematic review

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Table 1 Specification of excluded studies after full-text analysis
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Data synthesis and/or meta-analysis were not performed due to the heterogeneity of the study designs and parameters. Risk of bias of each study is given in Table 2. Information on additional risk of bias across studies is elaborated in “Discussion” section.

Table 2 Assessment of risk of bias according to The Cochrane Collaboration’s tool for RCTs, the ROBINS-I tool was applied for prospective cohorts, and the Checklist for Case Series from the Joanna Briggs Institute
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Efficacy of augmentation procedures in horizontally resorbed ridges

Eight studies met the inclusion criteria containing a total of 276 procedures of xenogeneic, allogeneic, or autogenous bone graft applications in horizontal ridge defects. Outcome measures, approaches and materials varied from study to study. The mean follow-up was 26.0 months across all included studies, with a maximum mean observation period of 40.5 months, and minimum mean observation period of 6 months. Particulate material as well as bone blocks were used as grafts in the studies (see Figs. 2 and 3).

Fig. 2
figure 2

Schematic of horizontal bone loss in the lower jaw after crestal gingival exposure (A). Principle of bone-block grafting and fixation with screws (B). Depiction of lateral augmentation using particulate bone and membrane placement for coverage (C). Gaining of horizontal bone width by surgical splitting of the alveolar ridge (D)

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Fig. 3
figure 3

Clinical example of a 41-year-old female patient presenting with missing tooth 31 and consecutive horizontal bone loss (A). For dental, functional and esthetic rehabilitation, simultaneous implant placement and lateral augmentation was performed. Implantation of Conelog Progressive Line, harvesting of a retromolar bone block from the mandibular angle with a trephine drill, augmentation and microscrew fixation (1.0-mm steel screws) after rounding of the edges with a burr (B). Relining and fitting with particulate bone placement (C). After 5 months of healing time, implant exposure and fixation screw removal, sequential abutment fitting and placement of dental crown were performed (D)

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The autologous block grafts used in the included studies were taken from the mandibular ramus [99, 100] or as bone chips from the posterior mandible/retromolar region [100,101,102]. A combination of autografts with xenografts or allografts was used in four studies. All augmentation sites were covered, either by membranes or platelet-poor plasma. Table 3 shows the variety of outcome measures used in the included studies.

Table 3 Methodological characteristics of the selected studies, the regenerative objective (simultaneous or staged), the types of interventions and measured outcomes
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Even though this review aims to report the results in a standardized way, the wide range of different settings, study protocols and outcome parameters limit conclusions in an evidence-based manner. Hence, only circumscribed quantitative data could be analyzed and this review should be perceived with a narrative approach. The study design ranged from (randomized) controlled clinical trials to pro- and retrospective studies. Particularly, the outcome measures varied extensively in the presented reports. All studies referred to clinical assessment and radiographic imaging when reporting outcome parameters (Table 4).

Table 4 Assessment parameters and study results
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The majority of the included patients were female. Where specified, individuals were 70 women (72.2%) compared to 27 men (27.8%). The inclusion criteria for augmentation procedures and subsequent implant therapy did also vary, as for instance in some studies smokers were explicitly excluded from the study and in other studies smoking status of the patients was only recorded (Table 5). In all studies, the systemic health status was addressed in the inclusion criteria. However, the parameters ranged from patients being “in good health” to listing of specific systemic medical conditions such as “connective tissue diseases” and “immunodeficiencies”.

Table 5 Patient characteristics and implant specification
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The horizontal mandibular bone serving as indication for augmentation procedures in the studies was also reported in various ways. The reported projected bone increase needed for implant placement was 3 mm of bone width [103]. Other groups performed lateral augmentation in case of residual width from < 4 mm [102, 104] to < 6 mm [105]. The article of Schwarz-Arad et al. proposed a need for augmentation if an implant of 6 mm in height could not be placed without the risk of damaging anatomical structures. The horizontal gain of bone width after the healing process was evaluated radiographically in seven studies. A gain of horizontal bone width was reported in seven of eight studies, with a mean of 4.8 mm, ranging from 3.2 to 5.7 mm (Table 4).

No significant difference was found regarding the outcome variables due to the heterogeneity of reporting the data. The use of rhPDGF-BB in one study significantly limited the resorption of augmented bone [101]. This observation was true for both the group having been augmented with corticocancellous allograft of the iliac bone and the control group of bone chips from the retromolar region. Marginal bone loss during the healing period was evaluated in four studies, with a mean of 0.5 mm, and values between 0.2 and 1.1 mm. Histologic findings were reported in three studies [102, 104, 105]. In the study conducted by Urban et al., a xenograft was combined with autologous bone and the mandible was augmented using particulated material. Histological results showed autologous bone in 31.0%, ABBM, remaining xenograft in 25.8% and marrow space in 43.2% of the derived samples. Di Stefano et al. and Silva et al. quantified newly formed bone at 35.0% and 31.8%, respectively. None of the studies reported on implant success rates. Implant survival rates were shown to be above 92.5% in the included studies at 36 months of last follow-up (Table 4). Four studies reported on crestal incision techniques with an implant survival rate ranging from 92.5 to 100.0% at 18.9 to 37 months of follow-up. One study group used a lateral incision for the augmentation and the surgical approach was not specified in the remainder of the reports. The declared implant survival rate was 96% to 100% with a mean follow-up of 10 to 40.5 months.

One study reported up to 3.6% complications concerning the grafted site at the follow-up [101]. Although data of horizontal and combined horizontal–vertical expansion of the atrophic mandible have not been reported separately in the investigated work by Schwartz-Arad et al., the total complication rate of mandibular augmentation was found to be 6.1%. However, only two of the seven complications occurred in solely horizontal augmented sites. Failure of one graft [6.3%] was reported in the study by Urban et al., when looking at the data of mandibular augmented sites. A comparatively high failure rate of six bone grafts was observed in the study by Nissan et al. [20.7%]. Although distinct failure rates in the horizontally augmented mandible are missing, most of the allograft failures [71.0%] in this study occurred in the posterior mandible. Barbu and colleagues reported graft exposure 2 weeks after the augmentation in one patient. Another week later clinical signs of necrosis led to removal of the graft resulting in a failure rate of 4.2% [100]. In conjunction with bone graft failure rates of 0.0% in four reports, the overall average amounts to 4.4% across all studies.

Discussion

Successful long-time survival and success of dental implants depend on sufficient amount and quality of bone. In case of severe horizontal bone loss, horizontal ridge augmentation of the mandibular ridge can provide optimum conditions for successful implant placement. However, the jaw recipient site (maxilla or mandible) has been shown to influence graft resorption [106]. Therefore, the aim of the present review was to systematically examine the clinical efficacy of augmentation procedures in horizontally resorbed mandibular ridges in terms of horizontal bone gain, implant success and survival after a follow-up period of at least 6 months. The results of this systematic review indicate a high variability in types of interventions to gain horizontal bone width. However, all techniques were able to create a sufficient horizontal bone gain. Implant survival was very good with results exceeding 92.5% between 12 and 36 months of follow-up.

Even though the present review aims to report the results in a standardized way, the wide range of different settings, study protocols and outcome parameters prevent drawing conclusions in an evidence-based manner. Only eight studies met the inclusion criteria and could be considered for this review, which is one of the main limitations of this study. However, the authors chose not to further modify the inclusion criteria to provide sufficient evidence. Additional inherent limitations are different study designs, different materials used, different assessment methods and prominently different outcome measures throughout. Therefore, comparisons from study to study are limited and comprehensive statistical analysis was not feasible. Augmentation procedures always included the use of membranes. In all studies, combinations of materials (autologous bone combined with xenografts or allografts) were used. The minimum bone width to include patients was either not specified or differed from study to study. Only three of the evaluated studies were randomized [100, 101, 103]. None of the studies reported on implant success rates. This results in the demand of further studies particularly focusing on how implants survive. This also includes the claim on reporting prosthetic data that were proposed at the 4th EAO Consensus Conference [107].

As case reports or case series with less than five patients did not meet the criteria for inclusion in this review, a considerable part of the pre-selected publications (19 in total) had to be dismissed in the process of data extraction. An observation period falling below 6 months after augmentation was reported in eight studies and considered too short to evaluate augmentation procedure and implant success. A major shortcoming during thorough data extraction was whether the horizontal ridge augmentation took place in the upper or lower jaw. As it has been reported that the augmentation procedure in the mandible may be correlated with higher complication rates and thus might be less predictable, the need for reporting the data in this distinctive way remains high [108].

Overall results show that all bone grafts that were used in the included studies have the potential to increase horizontal bone width. Even though no analysis could be carried out due to the lack of homogeneous data and outcome results, the descriptive data suggest a slightly better performance of bone blocks for horizontal augmentation of the lower alveolar ridge than for particulate material. In contrast, Urban and colleagues found comparable results on bone block augmentations using particulate autologous bone grafts in combination with allogeneic material (horizontal bone gain of 5.3 mm in mean).

Troeltzsch et al. conducted a comprehensive pooled analysis with regard to clinical efficacy of grafting materials in alveolar ridge augmentation over a weighted mean follow-up of 27.4 months (range 3–168 months) [20]. In this review, the mean follow-up was 26.0 months across all included studies, with a maximum mean observation period of 40.5 months, and minimum mean observation period of 6 months. After augmentation, the weighted mean horizontal gain for all particulate grafting materials was 3.7 ± 1.2 mm, with variation between 2.2 ± 1.2 mm (synthetic) and 4.5 ± 1.0 mm (mixtures of autogenous bone with allogeneic/xenogeneic grafting material) without statistical significance in the work of Troeltzsch et al. The authors derive a horizontal gain of 4.5 ± 1.2 mm for block grafts. Limited to the inclusion criteria of our review, a gain of horizontal bone width of the mandible in seven of eight studies, with a mean of 4.8 mm, ranging from 3.2 to 5.7 mm was observed. All but one study, reported low bone graft failure rates of 4.4% in average. One group of authors, that used bone-block allografts combined with particulate mineralized freeze-dried bone allograft or particulate bovine bone xenografts, reported a failure rate of 20.7% [103]. The reasons were only discussed marginally, and the authors suggested a relation to the localization of the augmentation as all failures had occurred in the posterior mandible. However, a successful use of allografts was stated in further studies that did not meet the inclusion criteria of this review. This suggests that other reasons than the use of allografts might be responsible for the high failure rate in the above-mentioned study [105, 109].

The augmentation procedure and subsequent complication rates may also be associated with the surgical approach. Horizontal ridge augmentation techniques in the mandible have been shown to be very efficient and safe. However, the method of placing narrow-diameter implants in horizontally resorbed alveolar ridges provides an alternative approach when bone loss is limited. Studies showed that results of narrow-diameter implants placed to support single crowns in the posterior region of the jaw did not differ from results of regular implants regarding the outcome parameters of marginal bone level, implant survival and success rates [110]. Moreover, recent studies suggest that narrow-diameter implants (2.75 to 3.25 mm) can successfully be used as minimally invasive alternative to horizontal bone augmentation in the posterior mandible with implant survival rates exceeding 97% [111]. A recent clinical trial over 2 years showed that patients receiving mini implants with shorter diameters of 1.8–2.4 mm had clinical outcomes similar to those of patients receiving conventional dental implants to support overdenture prostheses [112]. These results must be taken into account when considering horizontal ridge augmentation procedures in the mandible. To appropriately evaluate lateral augmentation techniques in the mandible, other approaches like the split bone block technique had to be excluded in the present review. Given the lack of information provided in the studies, no recommendation can be given concerning the surgical approach.

All studies included the use of a barrier membrane. Due to missing control groups without membranes, a beneficial effect of this procedure on horizontal ridge preservation techniques accompanying augmentation is conceivable but cannot be evaluated. However, literature regarding the reconstruction of peri-implant dehiscence defects suggests a beneficial effect of barrier membranes on the degree of defect filling [20]. Long-term follow-up data based on imaging results are not consistently provided. According to the guidelines of Albrektsson et al., the majority of crestal bone remodeling occurs during the first 2 years following implant-loading, therefore long-term (at least 2 years) follow-up of implants inserted in the augmented sites would be advisable [3]. Furthermore, bleeding and deep peri-implant pockets with crestal bone loss are closely related to the faith of newly formed hard tissues, which are reconstructed via GBR. Thus, implant success rate, which depends on change of crestal bone level and the lack of inflammatory signs, may represent a more relevant evaluation method of GBR efficacy than implant survival rate during long-term follow-ups.

Considering the limited number of included studies and the various approaches that were used, it is not possible to give concise recommendations for horizontal ridge augmentation procedures. Data of prospective randomized and controlled clinical trials regarding different horizontal ridge augmentation techniques including longer follow-up intervals, standardized outcome measures and distinguished results for the upper and lower jaw are missing. As implant success was not evaluated in any of the present studies, further investigations must be conducted including data on how implants and prosthetic reconstructions survive over time.

The role of growth factors in horizontal ridge augmentation must be outlined in a more specific manner. Two of the included studies did in fact work with growth factors—rhPDGF and PRP/PPP, respectively. As the present review is not designed to outline the role of growth factors, no evidence-based conclusion can be drawn from the present data. However, it must be kept in mind that these growth factors present a bias in the present study, which must be considered when interpreting the results.

It is obvious that different surgeons prefer different surgical techniques according to their individual expertise. Therefore, a comparison of distinct GBR procedures in studies with a single surgeon in a split-mouth design hardly represents comparable data. Thus, randomized controlled trials might represent an objective approach with clinically relevant results if the procedures are performed by two different surgeons practicing their favorable techniques after randomization. This would filter the advantages against the individual skillset of the surgeon.

The primary objective can be concluded based on quantitative data, but from the secondary objectives only implant survival rate can be answered. It is of high interest whether the biological behavior of augmented sites is similar to pristine bone or not. Furthermore, bone block alone or bone block supported GBR techniques are compared with GBR techniques based on particulate bone and xenograft (composite graft). Due to the difficulties of these procedures, but also due to different extent and morphology of bone defects, it is very likely that the superiority of one therapy cannot be easily concluded. However, a standardized follow-up protocol with particular timing and assessment methods is needed for getting clear results regarding techniques and long-term implant success.

Data extraction and assessment were performed by two authors to reduce reviewer bias. However, this kind of bias cannot be ruled out completely. As there is a possibility that only studies were published with favorable outcomes or significant findings, a publication bias might exist. Accordingly, studies with a follow-up of less than 6 months could have been so-called “cancelled studies” due to a poor outcome and therefore are not recorded by the mentioned search strategy [80, 81]. As the data extraction is based solely on reported outcomes in the present studies, a reporting bias and incomplete outcome data might have been influenced the data assessment. Predominantly, in five of eight studies multiple biases exist regarding randomization and blinding within each study. Only one study by Amorfini et al. is reported to be a randomized clinical trial on the research topic, whereas the study by Nissan et al. uses randomization only for parameters like deficiency filling and the use of membranes [101, 103]. Barbu and colleagues divided patients between the use of particulate graft composition and membrane and the data were de-identified before research analysis [100]. No further specifics on blinding and randomization can be found. Possible risks of bias according to the Cochrane Collaboration’s tool for randomized controlled trials, as well as the ROBINS-I tool for prospective cohorts, and the Checklist for Case Series from the Joanna Briggs Institute are given in Table 2.

Materials and methods

Focused question and PICO

Does the outcome of horizontal mandibular augmentation using xenogeneic, synthetic, or allogeneic material differ from the outcome of autologous bone grafts with regard to gained quantity of bone width, implant survival, success and complication rate in patients that underwent resorption of the horizontal alveolar ridge? The PICO Question is depicted in Table 6.

Table 6 PICO Question
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Search strategy

A computerized literature search (Medline/PubMed and Cochrane Central Register of Controlled Trials (CENTRAL)) was performed for clinical studies, including articles published from January 1st, 1995, up to March 31st, 2021. Additionally, manual search was carried out in: International Journal of Oral and Maxillofacial Surgery, Journal of Oral and Maxillofacial Surgery, Journal of Craniomaxillofacial Surgery, Journal of Clinical Periodontology, Journal of Periodontology, Clinical Oral Implants Research, International Journal of Oral Maxillofacial Implants, Clinical Implant Dentistry and Related Research, Journal of Implantology, Journal of Biomedical Materials Research. Furthermore, full-text articles of reviews published between January 2012 and March 2021 were obtained. An additional manual search was performed on these reviews to identify relevant studies. The language was limited to English. Risk of bias for RCTs was assessed in agreement with the Cochrane Collaboration’s tool [113, 114]. For non-randomized studies, the ROBINS-I tool was applied, and the Checklist for Case Series from the Joanna Briggs Institute [115]. The study followed the PRISMA guidelines (see Additional file 1: Table S1) [116] and was prospectively registered in the international prospective register of systematic reviews (PROSPERO) under registration number CRD42018082149 (www.crd.york.ac.uk/PROSPERO/). No contact was made to acquire additional data from the authors of the study. Any data report and subsequent conclusions are made based solely on published reports.

Search terms

The following search terms were applied: (“xenogeneic bone substitute” OR “synthetic bone substitute” OR “allogeneic bone graft” OR “xenograft” OR “allograft” OR “synthetic material” OR “lateral space” OR “bone graft” OR “guided bone regeneration” OR “alveolar ridge augmentation” OR “dental augmentation” OR “ridge atrophy” OR “GBR” OR “horizontal augmentation success” OR “horizontal ridge augmentation” OR “bone substitute” OR “alveolar bone graft” OR “alveolar bone loss” OR “alveolar resorption”). The search was limited to “human trial”. Accordingly, the MESH Terms “clinical study”, “clinical trial”, “controlled clinical trial”, “randomized controlled trial” were used.


AND

(“dental implants” OR “lower jaw” OR “alveolar ridge” OR “implant site” OR “mandible”). The search was limited to the MESH Terms “Humans” and “Clinical Trial”.

Inclusion criteria

Publications were considered when all of the following criteria were applicable:

  1. 1.

    Human, clinical trials with a minimum of five patients reported upon.

  2. 2.

    Horizontal augmentation with bone grafts or substitute materials prior to or accompanying implant placement.

  3. 3.

    Follow-up of at least 6 months in mean.

  4. 4.

    Metric outcome measures following surgical intervention.

Exclusion criteria

Publications limited to (1–4) or containing (5–13) the following were excluded:

  1. 1.

    In vitro studies

  2. 2.

    Animal (preclinical) studies

  3. 3.

    Cadaver studies

  4. 4.

    Case reports and reports based on interviews and charts

  5. 5.

    Vascularized free bone grafts

  6. 6.

    Only soft tissue augmentation

  7. 7.

    Distraction osteogenesis

  8. 8.

    Socket preservation techniques

  9. 9.

    Augmentation procedures after removal of malignant or benign tumors

  10. 10.

    Patients receiving radio- or chemotherapy

  11. 11.

    Results of patients that had been presented in prior studies of the authors

  12. 12.

    Only vertical augmentation procedures

  13. 13.

    Other bone preservation procedures, e.g., splitting or spreading.

Selection of studies

Two researchers (CK and LM) independently screened the publications derived from the online search based on the inclusion criteria. Subsequently, the abstracts of the selected titles were obtained and screened for meeting the inclusion criteria. If an abstract was not available in the database, the abstract of the printed article was used. Full-text articles of the selected abstracts were obtained. Again, a selection was made based on the inclusion criteria for the full-text articles. For this purpose, “Materials and methods” and “Results” sections of these studies were investigated. No additional data were obtained other than data included in the articles.

Data extraction and method of analysis

Two researchers independently analyzed all data using data extraction tables (CK and LM). Information on the following parameters was extracted: author(s), year of publication, study setting and study design, patient cohort (age range, mean age, gender, drop outs), follow-up (mean time and range), type of grafting material (autologous, allogeneic, xenogeneic, synthetic), type of fixation, type of graft preparation (particulate vs. block graft), type of barrier material used (collagen based, PTFE, polymer, titanium, none), the regenerative objective (two-staged vs. simultaneous), test/control groups, information on smoking or systemic conditions of the patients as well as the timing of implant placement, the assessment method and complications during or after surgery.

Outcome parameters

Metric data and clinical outcome on the following parameters were extracted, as indicated:

  • horizontal width (mm)

  • horizontal gain (mm)

  • loss of augmented bone width (%)

  • complication rate of surgical and post-surgical complications (%)

  • bone formation (%)

  • implant survival rate (%).

The data extraction was defined as follows:

  • Complications (%): complication rate in the augmented sites occurring during the observation period in percent.

  • Implant survival (%): survival rate of implants in the augmented area in percent.

  • Horizontal width I (mm): horizontal bone width before augmentation in mm.

  • Horizontal width II (mm): entire horizontal bone width at the end of the observation period in mm.

  • Horizontal gain (mm): horizontal result of gained bone in mm at the end of the observation period.

  • Loss (mm)/(%): difference between the initially augmented bone width and the entire horizontal bone width in millimeters/percent.

  • Bone formation (%): the bone formation rate is the mineral apposition rate multiplied with the surface area undergoing bone formation. Amount of newly formed bone in the defect area was calculated in percent.

Conclusions

A variety of approaches and materials exist for the reconstruction of bone width of the mandible. Only limited evidence with risk of bias is available on the impact of using particular grafts or bone blocks for horizontal augmentation in the lower jaw. The results of this review show outcomes for xenogeneic as well as autologous bone materials for horizontal ridge augmentation of the lower jaw. The use of allogeneic bone-block grafts in combination with resorbable barrier membranes must be re-evaluated. Data of randomized controlled clinical trials indicating superiority of specific horizontal ridge augmentation procedures in the lower jaw are still missing and worthwhile being investigated.

Availability of data and materials

Not applicable.

Abbreviations

ABBM:

Anorganic bovine bone-derived mineral

BOP:

Bleeding on probing

BV:

Bone volume changes

CAL:

Peri-implant clinical attachment level

CCT:

Controlled clinical trial

CENTRAL:

Cochrane Central Register of Controlled Trials

ePTFE:

Expanded polytetrafluoroethylene

EX:

Exposure

EXH:

Exposed site height

EXW:

Exposed site width

GBR:

Guided bone regeneration

HA:

Histological assessment

IS:

Implant survival

mBL:

Mean marginal bone loss

ME:

Membrane exposure

PGF:

Partial graft failure

PI:

Peri-implant plaque index

PICO:

Population, Intervention, Comparison, Outcome variable

PPD:

Peri-implant probing depth

PRF:

Platelet-rich fibrin

RA:

Radiographic assessment

POP:

Penetration of the probe

PRP:

Platelet-rich plasma

RCT:

Randomized controlled trial

rh-BMP2:

Recombinant human bone morphogenic protein 2

rhPDGF-BB:

Recombinant human platelet-derived growth factor-BB

SP:

Success rate procedure

TGF:

Total graft failure

WG:

Width gain

WR:

Width reduction

References

  1. Buser D, Sennerby L, De Bruyn H. Modern implant dentistry based on osseointegration: 50 years of progress, current trends and open questions. Periodontol 2000. 2017;73(1):7–21.

    Article  PubMed  Google Scholar 

  2. Srinivasan M, Meyer S, Mombelli A, Muller F. Dental implants in the elderly population: a systematic review and meta-analysis. Clin Oral Implants Res. 2017;28(8):920–30.

    Article  PubMed  Google Scholar 

  3. Albrektsson T, Chrcanovic B, Ostman PO, Sennerby L. Initial and long-term crestal bone responses to modern dental implants. Periodontol 2000. 2017;73(1):41–50.

    Article  PubMed  Google Scholar 

  4. Chrcanovic BR, Albrektsson T, Wennerberg A. Bone quality and quantity and dental implant failure: a systematic review and meta-analysis. Int J Prosthodont. 2017;30(3):219–37.

    Article  PubMed  Google Scholar 

  5. Smeets R, Henningsen A, Jung O, Heiland M, Hammacher C, Stein JM. Definition, etiology, prevention and treatment of peri-implantitis—a review. Head Face Med. 2014;10:34.

    Article  PubMed  PubMed Central  Google Scholar 

  6. Araujo MG, Lindhe J. Dimensional ridge alterations following tooth extraction. An experimental study in the dog. J Clin Periodontol. 2005;32(2):212–8.

    Article  PubMed  Google Scholar 

  7. Vignoletti F, Discepoli N, Muller A, de Sanctis M, Munoz F, Sanz M. Bone modelling at fresh extraction sockets: immediate implant placement versus spontaneous healing: an experimental study in the beagle dog. J Clin Periodontol. 2012;39(1):91–7.

    Article  PubMed  Google Scholar 

  8. Lutz R, Neukam FW, Simion M, Schmitt CM. Long-term outcomes of bone augmentation on soft and hard-tissue stability: a systematic review. Clin Oral Implants Res. 2015;26(Suppl 11):103–22.

    Article  PubMed  Google Scholar 

  9. Sanz-Sanchez I, Ortiz-Vigon A, Sanz-Martin I, Figuero E, Sanz M. Effectiveness of lateral bone augmentation on the alveolar crest dimension: a systematic review and meta-analysis. J Dent Res. 2015;94(9 Suppl):128S-S142.

    Article  PubMed  Google Scholar 

  10. Aghaloo TL, Misch C, Lin GH, Iacono VJ, Wang HL. Bone augmentation of the edentulous maxilla for implant placement: a systematic review. Int J Oral Maxillofac Implants. 2016;31(Suppl):s19-30.

    PubMed  Google Scholar 

  11. Elnayef B, Monje A, Gargallo-Albiol J, Galindo-Moreno P, Wang HL, Hernandez-Alfaro F. Vertical ridge augmentation in the atrophic mandible: a systematic review and meta-analysis. Int J Oral Maxillofac Implants. 2017;32(2):291–312.

    Article  PubMed  Google Scholar 

  12. Bassetti MA, Bassetti RG, Bosshardt DD. The alveolar ridge splitting/expansion technique: a systematic review. Clin Oral Implants Res. 2016;27(3):310–24.

    Article  PubMed  Google Scholar 

  13. Klein MO, Schiegnitz E, Al-Nawas B. Systematic review on success of narrow-diameter dental implants. Int J Oral Maxillofac Implants. 2014;29(Suppl):43–54.

    Article  PubMed  Google Scholar 

  14. Windisch P, Orban K, Salvi GE, Sculean A, Molnar B. Vertical-guided bone regeneration with a titanium-reinforced d-PTFE membrane utilizing a novel split-thickness flap design: a prospective case series. Clin Oral Investig. 2020;25(5):2969–80.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Hashemipoor M, Asghari N, Mohammadi M, Kalantari M, Arabsolghar M, Ranjbar H. Radiological and histological evaluation of horizontal ridge augmentation using corticocancellous freeze-dried bone allograft with and without autogenous bone: a randomized controlled clinical trial. Clin Implant Dent Relat Res. 2020;22(5):582–92.

    Article  PubMed  Google Scholar 

  16. Mendoza-Azpur G, de la Fuente A, Chavez E, Valdivia E, Khouly I. Horizontal ridge augmentation with guided bone regeneration using particulate xenogenic bone substitutes with or without autogenous block grafts: a randomized controlled trial. Clin Implant Dent Relat Res. 2019;21(4):521–30.

    PubMed  Google Scholar 

  17. Meloni SM, Jovanovic SA, Urban I, Baldoni E, Pisano M, Tallarico M. Horizontal ridge augmentation using GBR with a native collagen membrane and 1: 1 ratio of particulate xenograft and autologous bone: a 3-year after final loading prospective clinical study. Clin Implant Dent Relat Res. 2019;21(4):669–77.

    PubMed  Google Scholar 

  18. Spin-Neto R, Stavropoulos A, Dias Pereira LA, Marcantonio E Jr, Wenzel A. Fate of autologous and fresh-frozen allogeneic block bone grafts used for ridge augmentation. A CBCT-based analysis. Clin Oral Implants Res. 2013;24(2):167–73.

    Article  PubMed  Google Scholar 

  19. Maiorana C, Beretta M, Salina S, Santoro F. Reduction of autogenous bone graft resorption by means of bio-oss coverage: a prospective study. Int J Periodontics Restor Dent. 2005;25(1):19–25.

    Google Scholar 

  20. Troeltzsch M, Troeltzsch M, Kauffmann P, Gruber R, Brockmeyer P, Moser N, et al. Clinical efficacy of grafting materials in alveolar ridge augmentation: a systematic review. J Craniomaxillofac Surg. 2016;44(10):1618–29.

    Article  PubMed  Google Scholar 

  21. Bell RB, Blakey GH, White RP, Hillebrand DG, Molina A. Staged reconstruction of the severely atrophic mandible with autogenous bone graft and endosteal implants. J Oral Maxillofac Surg. 2002;60(10):1135–41.

    Article  PubMed  Google Scholar 

  22. Cotter CJ, Maher A, Gallagher C, Sleeman D. Mandibular lower border: donor site of choice for alveolar grafting. Br J Oral Maxillofac Surg. 2002;40(5):429–32.

    Article  PubMed  Google Scholar 

  23. Ella B, Laurentjoye M, Sedarat C, Coutant JC, Masson E, Rouas A. Mandibular ridge expansion using a horizontal bone-splitting technique and synthetic bone substitute: an alternative to bone block grafting? Int J Oral Maxillofac Implants. 2014;29(1):135–40.

    Article  PubMed  Google Scholar 

  24. Elo JA, Herford AS, Boyne PJ. Implant success in distracted bone versus autogenous bone-grafted sites. J Oral Implantol. 2009;35(4):181–4.

    Article  PubMed  Google Scholar 

  25. Hu GH, Froum SJ, Alodadi A, Nose F, Yu YP, Suzuki T, et al. A three-stage split-crest technique: case series of horizontal ridge augmentation in the atrophic posterior mandible. Int J Periodontics Restor Dent. 2018;38(4):565–73.

    Article  Google Scholar 

  26. Huang HY, Ogata Y, Hanley J, Finkelman M, Hur Y. Crestal bone resorption in augmented bone using mineralized freeze-dried bone allograft or pristine bone during submerged implant healing: a prospective study in humans. Clin Oral Implants Res. 2016;27(2):e25–30.

    Article  PubMed  Google Scholar 

  27. Keith JD Jr, Petrungaro P, Leonetti JA, Elwell CW, Zeren KJ, Caputo C, et al. Clinical and histologic evaluation of a mineralized block allograft: results from the developmental period (2001–2004). Int J Periodontics Restor Dent. 2006;26(4):321–7.

    Google Scholar 

  28. Stellingsma K, Raghoebar GM, Meijer HJ, Stegenga B. The extremely resorbed mandible: a comparative prospective study of 2-year results with 3 treatment strategies. Int J Oral Maxillofac Implants. 2004;19(4):563–77.

    PubMed  Google Scholar 

  29. Stellingsma K, Raghoebar GM, Visser A, Vissink A, Meijer HJ. The extremely resorbed mandible, 10-year results of a randomized controlled trial on 3 treatment strategies. Clin Oral Implants Res. 2014;25(8):926–32.

    Article  PubMed  Google Scholar 

  30. Sohn DS, Lee HJ, Heo JU, Moon JW, Park IS, Romanos GE. Immediate and delayed lateral ridge expansion technique in the atrophic posterior mandibular ridge. J Oral Maxillofac Surg. 2010;68(9):2283–90.

    Article  PubMed  Google Scholar 

  31. Rachmiel A, Emodi O, Aizenbud D, Rachmiel D, Shilo D. Two-stage reconstruction of the severely deficient alveolar ridge: bone graft followed by alveolar distraction osteogenesis. Int J Oral Maxillofac Surg. 2018;47(1):117–24.

    Article  PubMed  Google Scholar 

  32. Thalmair T, Fickl S, Schneider D, Hinze M, Wachtel H. Dimensional alterations of extraction sites after different alveolar ridge preservation techniques—a volumetric study. J Clin Periodontol. 2013;40(7):721–7.

    Article  PubMed  Google Scholar 

  33. Torres J, Tamimi F, Alkhraisat MH, Manchon A, Linares R, Prados-Frutos JC, et al. Platelet-rich plasma may prevent titanium-mesh exposure in alveolar ridge augmentation with anorganic bovine bone. J Clin Periodontol. 2010;37(10):943–51.

    Article  PubMed  Google Scholar 

  34. Thanasrisuebwong P, Kiattavorncharoen S, Deeb GR, Bencharit S. Implant site preparation application of injectable platelet-rich fibrin for vertical and horizontal bone regeneration: a clinical report. J Oral Implantol. 2020;48(1):43–50.

    Article  Google Scholar 

  35. Guo Z, Chen L, Ning Y, Ding X, Gao Y, Zhou L, et al. Split-crest technique with inlay bone block grafts for narrow posterior mandibles: a retrospective clinical study with a 3-year follow-up. Am J Transl Res. 2020;12(8):4628–38.

    PubMed  PubMed Central  Google Scholar 

  36. Chaushu L, Chaushu G, Kolerman R, Vered M, Naishlos S, Nissan J. Anterior atrophic mandible restoration using cancellous bone block allograft. Clin Implant Dent Relat Res. 2019;21(5):903–9.

    Article  PubMed  Google Scholar 

  37. Bazrafshan N, Darby I. Retrospective success and survival rates of dental implants placed with simultaneous bone augmentation in partially edentulous patients. Clin Oral Implants Res. 2014;25(7):768–73.

    Article  PubMed  Google Scholar 

  38. Beitlitum I, Artzi Z, Nemcovsky CE. Clinical evaluation of particulate allogeneic with and without autogenous bone grafts and resorbable collagen membranes for bone augmentation of atrophic alveolar ridges. Clin Oral Implants Res. 2010;21(11):1242–50.

    Article  PubMed  Google Scholar 

  39. Buser D, Ingimarsson S, Dula K, Lussi A, Hirt HP, Belser UC. Long-term stability of osseointegrated implants in augmented bone: a 5-year prospective study in partially edentulous patients. Int J Periodontics Restor Dent. 2002;22(2):109–17.

    Google Scholar 

  40. Chappuis V, Cavusoglu Y, Buser D, von Arx T. Lateral ridge augmentation using autogenous block grafts and guided bone regeneration: a 10-year prospective case series study. Clin Implant Dent Relat Res. 2017;19(1):85–96.

    Article  PubMed  Google Scholar 

  41. Dahlin C, Simion M, Hatano N. Long-term follow-up on soft and hard tissue levels following guided bone regeneration treatment in combination with a xenogeneic filling material: a 5-year prospective clinical study. Clin Implant Dent Relat Res. 2010;12(4):263–70.

    Article  PubMed  Google Scholar 

  42. de Lacerda PE, Pelegrine AA, Teixeira ML, Montalli VA, Rodrigues H, Napimoga MH. Homologous transplantation with fresh-frozen bone for dental implant placement can induce HLA sensitization: a preliminary study. Cell Tissue Bank. 2016;17(3):465–72.

    Article  PubMed  Google Scholar 

  43. Hellem S, Astrand P, Stenstrom B, Engquist B, Bengtsson M, Dahlgren S. Implant treatment in combination with lateral augmentation of the alveolar process: a 3-year prospective study. Clin Implant Dent Relat Res. 2003;5(4):233–40.

    Article  PubMed  Google Scholar 

  44. Jung RE, Benic GI, Scherrer D, Hammerle CH. Cone beam computed tomography evaluation of regenerated buccal bone 5 years after simultaneous implant placement and guided bone regeneration procedures—a randomized, controlled clinical trial. Clin Oral Implants Res. 2013;26(1):28–34.

    Article  PubMed  Google Scholar 

  45. Miyamoto I, Funaki K, Yamauchi K, Kodama T, Takahashi T. Alveolar ridge reconstruction with titanium mesh and autogenous particulate bone graft: computed tomography-based evaluations of augmented bone quality and quantity. Clin Implant Dent Relat Res. 2012;14(2):304–11.

    Article  PubMed  Google Scholar 

  46. Penarrocha-Diago M, Aloy-Prosper A, Penarrocha-Oltra D, Guirado JL, Penarrocha-Diago M. Localized lateral alveolar ridge augmentation with block bone grafts: simultaneous versus delayed implant placement: a clinical and radiographic retrospective study. Int J Oral Maxillofac Implants. 2013;28(3):846–53.

    Article  PubMed  Google Scholar 

  47. Proussaefs P, Lozada J. Use of titanium mesh for staged localized alveolar ridge augmentation: clinical and histologic-histomorphometric evaluation. J Oral Implantol. 2006;32(5):237–47.

    Article  PubMed  Google Scholar 

  48. Santana RB, Santana CM. A clinical comparison of guided bone regeneration with platelet-derived growth factor-enhanced bone ceramic versus autogenous bone block grafting. Int J Oral Maxillofac Implants. 2015;30(3):700–6.

    Article  PubMed  Google Scholar 

  49. Sbordone L, Toti P, Menchini-Fabris G, Sbordone C, Guidetti F. Implant survival in maxillary and mandibular osseous onlay grafts and native bone: a 3-year clinical and computerized tomographic follow-up. Int J Oral Maxillofac Implants. 2009;24(4):695–703.

    PubMed  Google Scholar 

  50. Spin-Neto R, Stavropoulos A, Coletti FL, Faeda RS, Pereira LA, Marcantonio E Jr. Graft incorporation and implant osseointegration following the use of autologous and fresh-frozen allogeneic block bone grafts for lateral ridge augmentation. Clin Oral Implants Res. 2014;25(2):226–33.

    Article  PubMed  Google Scholar 

  51. Wessing B, Emmerich M, Bozkurt A. Horizontal ridge augmentation with a novel resorbable collagen membrane: a retrospective analysis of 36 consecutive patients. Int J Periodontics Restor Dent. 2016;36(2):179–87.

    Article  Google Scholar 

  52. Hattingh A, De Bruyn H, Van Weehaeghe M, Hommez G, Vandeweghe S. Contour changes following immediate placement of ultra-wide implants in molar extraction sockets without bone grafting. J Clin Med. 2020;9(8):2504.

    Article  PubMed Central  Google Scholar 

  53. Blanco J, Alonso A, Sanz M. Long-term results and survival rate of implants treated with guided bone regeneration: a 5-year case series prospective study. Clin Oral Implants Res. 2005;16(3):294–301.

    Article  PubMed  Google Scholar 

  54. Buser D, Dula K, Lang NP, Nyman S. Long-term stability of osseointegrated implants in bone regenerated with the membrane technique. 5-year results of a prospective study with 12 implants. Clin Oral Implants Res. 1996;7(2):175–83.

    Article  PubMed  Google Scholar 

  55. Chiapasco M, Abati S, Romeo E, Vogel G. Clinical outcome of autogenous bone blocks or guided bone regeneration with e-PTFE membranes for the reconstruction of narrow edentulous ridges. Clin Oral Implants Res. 1999;10(4):278–88.

    Article  PubMed  Google Scholar 

  56. De Boever AL, De Boever JA. Guided bone regeneration around non-submerged implants in narrow alveolar ridges: a prospective long-term clinical study. Clin Oral Implants Res. 2005;16(5):549–56.

    Article  PubMed  Google Scholar 

  57. Eskan MA, Greenwell H, Hill M, Morton D, Vidal R, Shumway B, et al. Platelet-rich plasma-assisted guided bone regeneration for ridge augmentation: a randomized, controlled clinical trial. J Periodontol. 2014;85(5):661–8.

    Article  PubMed  Google Scholar 

  58. Hammerle CH, 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 Implants Res. 2008;19(1):19–25.

    PubMed  Google Scholar 

  59. Merli M, Moscatelli M, Mariotti G, Pagliaro U, Breschi L, Mazzoni A, et al. Membranes and bone substitutes in a one-stage procedure for horizontal bone augmentation: a histologic double-blind parallel randomized controlled trial. Int J Periodontics Restor Dent. 2015;35(4):463–71.

    Article  Google Scholar 

  60. Mordenfeld A, Johansson CB, Albrektsson T, Hallman M. A randomized and controlled clinical trial of two different compositions of deproteinized bovine bone and autogenous bone used for lateral ridge augmentation. Clin Oral Implants Res. 2014;25(3):310–20.

    Article  PubMed  Google Scholar 

  61. Novell J, Novell-Costa F, Ivorra C, Farinas O, Munilla A, Martinez C. Five-year results of implants inserted into freeze-dried block allografts. Implant Dent. 2012;21(2):129–35.

    Article  PubMed  Google Scholar 

  62. Pendarvis WT, Sandifer JB. Localized ridge augmentation using a block allograft with subsequent implant placement: a case series. Int J Periodontics Restor Dent. 2008;28(5):509–15.

    Google Scholar 

  63. Proussaefs P, Lozada J. The use of resorbable collagen membrane in conjunction with autogenous bone graft and inorganic bovine mineral for buccal/labial alveolar ridge augmentation: a pilot study. J Prosthet Dent. 2003;90(6):530–8.

    Article  PubMed  Google Scholar 

  64. Proussaefs P, Lozada J, Kleinman A, Rohrer MD, McMillan PJ. The use of titanium mesh in conjunction with autogenous bone graft and inorganic bovine bone mineral (bio-oss) for localized alveolar ridge augmentation: a human study. Int J Periodontics Restor Dent. 2003;23(2):185–95.

    Google Scholar 

  65. Soehardi A, Meijer GJ, Strooband VF, de Koning M, Stoelinga PJ. The potential of the horizontal ramus of the mandible as a donor site for block and particular grafts in pre-implant surgery. Int J Oral Maxillofac Surg. 2009;38(11):1173–8.

    Article  PubMed  Google Scholar 

  66. Strietzel FP, Reichart PA, Graf HL. Lateral alveolar ridge augmentation using a synthetic nano-crystalline hydroxyapatite bone substitution material (Ostim): preliminary clinical and histological results. Clin Oral Implants Res. 2007;18(6):743–51.

    Article  PubMed  Google Scholar 

  67. von Arx T, Kurt B. Implant placement and simultaneous ridge augmentation using autogenous bone and a micro titanium mesh: a prospective clinical study with 20 implants. Clin Oral Implants Res. 1999;10(1):24–33.

    Article  Google Scholar 

  68. Zita Gomes R, Paraud Freixas A, Han CH, Bechara S, Tawil I. Alveolar ridge reconstruction with titanium meshes and simultaneous implant placement: a retrospective, multicenter clinical study. Biomed Res Int. 2016;2016:5126838.

    Article  PubMed  PubMed Central  Google Scholar 

  69. Landsberg C, Moses O. Ridge augmentation using customized allogeneic bone block: a 3-year follow-up of two case reports. Int J Periodontics Restor Dent. 2020;40(6):881–9.

    Article  Google Scholar 

  70. Zhou M, Li SY, Terheyden H, Cao SS, Che YJ, Geng YM. Particulate coral hydroxyapatite sheltered by titanium mesh for localized alveolar rehabilitation after onlay graft failure: a case report. J Oral Implantol. 2018;44(2):147–52.

    Article  PubMed  Google Scholar 

  71. Mello BF, de Carvalho Formiga M, de Souza da Silva LF, Dos Santos Coura G, Shibli JA. Horizontal ridge augmentation using a xenograft bone substitute for implant-supported fixed rehabilitation: a case report with four years of follow-up. Case Rep Dent. 2020;2020:6723936.

    PubMed  PubMed Central  Google Scholar 

  72. Acocella A, Ercoli C, Geminiani A, Feng C, Billi M, Acocella G, et al. Clinical evaluation of immediate loading of electroeroded screw-retained titanium fixed prostheses supported by tilted implant: a multicenter retrospective study. Clin Implant Dent Relat Res. 2012;14(Suppl 1):e98-108.

    Article  PubMed  Google Scholar 

  73. D’Amato S, Tartaro G, Itro A, Nastri L, Santagata M. Block versus particulate/titanium mesh for ridge augmentation for mandibular lateral incisor defects: clinical and histologic analysis. Int J Periodontics Restor Dent. 2015;35(1):e1-8.

    Article  Google Scholar 

  74. Friedmann A, Strietzel FP, Maretzki B, Pitaru S, Bernimoulin JP. Histological assessment of augmented jaw bone utilizing a new collagen barrier membrane compared to a standard barrier membrane to protect a granular bone substitute material. Clin Oral Implants Res. 2002;13(6):587–94.

    Article  PubMed  Google Scholar 

  75. Fu JH, Oh TJ, Benavides E, Rudek I, Wang HL. A randomized clinical trial evaluating the efficacy of the sandwich bone augmentation technique in increasing buccal bone thickness during implant placement surgery: I. Clinical and radiographic parameters. Clin Oral Implants Res. 2014;25(4):458–67.

    Article  PubMed  Google Scholar 

  76. Geurs NC, Korostoff JM, Vassilopoulos PJ, Kang TH, Jeffcoat M, Kellar R, et al. Clinical and histologic assessment of lateral alveolar ridge augmentation using a synthetic long-term bioabsorbable membrane and an allograft. J Periodontol. 2008;79(7):1133–40.

    Article  PubMed  Google Scholar 

  77. Peleg M, Sawatari Y, Marx RN, Santoro J, Cohen J, Bejarano P, et al. Use of corticocancellous allogeneic bone blocks for augmentation of alveolar bone defects. Int J Oral Maxillofac Implants. 2010;25(1):153–62.

    PubMed  Google Scholar 

  78. Buser D, Dula K, Hirt HP, Schenk RK. Lateral ridge augmentation using autografts and barrier membranes: a clinical study with 40 partially edentulous patients. J Oral Maxillofac Surg. 1996;54(4):420–32 (discussion 32–3).

    Article  PubMed  Google Scholar 

  79. Atef M, Osman AH, Hakam M. Autogenous interpositional block graft vs onlay graft for horizontal ridge augmentation in the mandible. Clin Implant Dent Relat Res. 2019;21(4):678–85.

    Article  PubMed  Google Scholar 

  80. Ortiz-Vigon A, Suarez I, Martinez-Villa S, Sanz-Martin I, Bollain J, Sanz M. Safety and performance of a novel collagenated xenogeneic bone block for lateral alveolar crest augmentation for staged implant placement. Clin Oral Implants Res. 2018;29(1):36–45.

    Article  PubMed  Google Scholar 

  81. Angermair J, Bosshardt DD, Nelson K, Flügge TV, Stricker A, Fretwurst T. Horizontal bone grafting using equine-derived cancellous bone blocks is associated with severe complications: a prospective clinical and histological pilot study. Clin Oral Implants Res. 2020;31(11):1149–58.

    Article  PubMed  Google Scholar 

  82. Chiapasco M, Colletti G, Romeo E, Zaniboni M, Brusati R. Long-term results of mandibular reconstruction with autogenous bone grafts and oral implants after tumor resection. Clin Oral Implants Res. 2008;19(10):1074–80.

    Article  PubMed  Google Scholar 

  83. Khojasteh A, Hassani A, Motamedian SR, Saadat S, Alikhasi M. Cortical bone augmentation versus nerve lateralization for treatment of atrophic posterior mandible: a retrospective study and review of literature. Clin Implant Dent Relat Res. 2016;18(2):342–59.

    Article  PubMed  Google Scholar 

  84. Lenzen C, Meiss A, Bull HG. Augmentation of the extremely atrophied maxilla and mandible by autologous calvarial bone transplantation. Mund Kiefer Gesichtschir. 1999;3(Suppl 1):S40–2.

    Article  PubMed  Google Scholar 

  85. Nissan J, Marilena V, Gross O, Mardinger O, Chaushu G. Histomorphometric analysis following augmentation of the posterior mandible using cancellous bone-block allograft. J Biomed Mater Res A. 2011;97(4):509–13.

    Article  PubMed  Google Scholar 

  86. Ozkan Y, Ozcan M, Varol A, Akoglu B, Ucankale M, Basa S. Resonance frequency analysis assessment of implant stability in labial onlay grafted posterior mandibles: a pilot clinical study. Int J Oral Maxillofac Implants. 2007;22(2):235–42.

    PubMed  Google Scholar 

  87. Sbordone L, Toti P, Menchini-Fabris GB, Sbordone C, Piombino P, Guidetti F. Volume changes of autogenous bone grafts after alveolar ridge augmentation of atrophic maxillae and mandibles. Int J Oral Maxillofac Surg. 2009;38(10):1059–65.

    Article  PubMed  Google Scholar 

  88. Teng F, Zhang Q, Wu M, Rachana S, Ou G. Clinical use of ridge-splitting combined with ridge expansion osteotomy, sandwich bone augmentation, and simultaneous implantation. Br J Oral Maxillofac Surg. 2014;52(8):703–8.

    Article  PubMed  Google Scholar 

  89. Toscano N, Holtzclaw D, Mazor Z, Rosen P, Horowitz R, Toffler M. Horizontal ridge augmentation utilizing a composite graft of demineralized freeze-dried allograft, mineralized cortical cancellous chips, and a biologically degradable thermoplastic carrier combined with a resorbable membrane: a retrospective evaluation of 73 consecutively treated cases from private practices. J Oral Implantol. 2010;36(6):467–74.

    Article  PubMed  Google Scholar 

  90. Urban IA, Nagursky H, Lozada JL. Horizontal ridge augmentation with a resorbable membrane and particulated autogenous bone with or without anorganic bovine bone-derived mineral: a prospective case series in 22 patients. Int J Oral Maxillofac Implants. 2011;26(2):404–14.

    PubMed  Google Scholar 

  91. Van Assche N, Michels S, Naert I, Quirynen M. Randomized controlled trial to compare two bone substitutes in the treatment of bony dehiscences. Clin Implant Dent Relat Res. 2013;15(4):558–68.

    Article  PubMed  Google Scholar 

  92. Viscioni A, Rigo L, Franco M, Brunelli G, Avantaggiato A, Sollazzo V, et al. Reconstruction of severely atrophic jaws using homografts and simultaneous implant placement: a retrospective study. J Oral Implantol. 2010;36(2):131–9.

    Article  PubMed  Google Scholar 

  93. Korzh DG, Haritonov DY, Stepanov IV, Podoprigora AV. Evaluation of autogenous mandibular bone block resorption in horizontal alveolar ridge augmentation. Stomatologiia (Mosk). 2019;98(6):30–2.

    Google Scholar 

  94. Li L, Su W, Xie X, Lei L, Bao J, He S, et al. A novel in situ bone elevation method to achieve vertical periodontal augmentation in dogs: a pilot study. J Oral Rehabil. 2019;46(8):756–64.

    Article  PubMed  PubMed Central  Google Scholar 

  95. Jeon YT, Han SJ. Comparative study of the effect of paranasal augmentation with autologous bone in orthognathic surgery. J Oral Maxillofac Surg. 2019;77(10):2116–24.

    Article  PubMed  Google Scholar 

  96. Sanz-Martin I, Ferrantino L, Vignoletti F, Nuñez J, Baldini N, Duvina M, et al. Contour changes after guided bone regeneration of large non-contained mandibular buccal bone defects using deproteinized bovine bone mineral and a porcine-derived collagen membrane: an experimental in vivo investigation. Clin Oral Investig. 2018;22(3):1273–83.

    Article  PubMed  Google Scholar 

  97. Wang S, Wu W, Liu Y, Wang X, Tang L, You P, et al. Bone augmentation of peri-implant dehiscence defects using multilaminated small intestinal submucosa as a barrier membrane: an experimental study in dogs. Biomed Res Int. 2019;2019:8962730.

    PubMed  PubMed Central  Google Scholar 

  98. Lee JT, Cha JK, Kim S, Jung UW, Thoma DS, Jung RE. Lateral onlay grafting using different combinations of soft-type synthetic block grafts and resorbable collagen membranes: an experimental in vivo study. Clin Oral Implants Res. 2020;31(4):303–14.

    Article  PubMed  Google Scholar 

  99. Schwartz-Arad D, Ofec R, Eliyahu G, Ruban A, Sterer N. Long term follow-up of dental implants placed in autologous onlay bone graft. Clin Implant Dent Relat Res. 2016;18(3):449–61.

    Article  PubMed  Google Scholar 

  100. Barbu HM, Andreescu CF, Lorean A, Kolerman R, Moraru L, Mortellaro C, et al. Comparison of two techniques for lateral ridge augmentation in mandible with ramus block graft. J Craniofac Surg. 2016;27(3):662–7.

    Article  PubMed  Google Scholar 

  101. Amorfini L, Migliorati M, Signori A, Silvestrini-Biavati A, Benedicenti S. Block allograft technique versus standard guided bone regeneration: a randomized clinical trial. Clin Implant Dent Relat Res. 2014;16(5):655–67.

    Article  PubMed  Google Scholar 

  102. Urban IA, Nagursky H, Lozada JL, Nagy K. Horizontal ridge augmentation with a collagen membrane and a combination of particulated autogenous bone and anorganic bovine bone-derived mineral: a prospective case series in 25 patients. Int J Periodontics Restor Dent. 2013;33(3):299–307.

    Article  Google Scholar 

  103. Nissan J, Ghelfan O, Mardinger O, Calderon S, Chaushu G. Efficacy of cancellous block allograft augmentation prior to implant placement in the posterior atrophic mandible. Clin Implant Dent Relat Res. 2011;13(4):279–85.

    Article  PubMed  Google Scholar 

  104. Di Stefano DA, Artese L, Iezzi G, Piattelli A, Pagnutti S, Piccirilli M, et al. Alveolar ridge regeneration with equine spongy bone: a clinical, histological, and immunohistochemical case series. Clin Implant Dent Relat Res. 2009;11(2):90–100.

    Article  PubMed  Google Scholar 

  105. Silva ER, Ferraz EP, Neto EC, Chaushu G, Chaushu L, Xavier SP. Volumetric stability of fresh frozen bone blocks in atrophic posterior mandible augmentation. J Oral Implantol. 2017;43(1):25–32.

    Article  PubMed  Google Scholar 

  106. Naenni N, Lim HC, Papageorgiou SN, Hämmerle CHF. Efficacy of lateral bone augmentation prior to implant placement: a systematic review and meta-analysis. J Clin Periodontol. 2019;46(Suppl 21):287–306.

    Article  PubMed  Google Scholar 

  107. Klinge B, Flemming T, Cosyn J, De Bruyn H, Eisner BM, Hultin M, et al. The patient undergoing implant therapy. Summary and consensus statements. The 4th EAO consensus conference 2015. Clin Oral Implants Res. 2015;26(Suppl 11):64–7.

    Article  PubMed  Google Scholar 

  108. Bahat O, Fontanessi RV. Efficacy of implant placement after bone grafting for three-dimensional reconstruction of the posterior jaw. Int J Periodontics Restor Dent. 2001;21(3):220–31.

    Google Scholar 

  109. Ahmadi RS, Sayar F, Rakhshan V, Iranpour B, Jahanbani J, Toumaj A, et al. Clinical and histomorphometric assessment of lateral alveolar ridge augmentation using a corticocancellous freeze-dried allograft bone block. J Oral Implantol. 2017;43(3):202–10.

    Article  PubMed  Google Scholar 

  110. de Souza AB, Sukekava F, Tolentino L, Cesar-Neto JB, Garcez-Filho J, Araujo MG. Narrow- and regular-diameter implants in the posterior region of the jaws to support single crowns: a 3-year split-mouth randomized clinical trial. Clin Oral Implants Res. 2017;29(1):100–7.

    Article  PubMed  Google Scholar 

  111. Grandi T, Svezia L, Grandi G. Narrow implants (2.75 and 3.25 mm diameter) supporting a fixed splinted prostheses in posterior regions of mandible: one-year results from a prospective cohort study. Int J Implant Dent. 2017;3(1):43.

    Article  PubMed  PubMed Central  Google Scholar 

  112. Temizel S, Heinemann F, Dirk C, Bourauel C, Hasan I. Clinical and radiological investigations of mandibular overdentures supported by conventional or mini-dental implants: a 2-year prospective follow-up study. J Prosthet Dent. 2017;117(2):239-46.e2.

    Article  PubMed  Google Scholar 

  113. Higgins JP, Altman DG, Gotzsche PC, Juni P, Moher D, Oxman AD, et al. The Cochrane Collaboration’s tool for assessing risk of bias in randomised trials. BMJ. 2011;343: d5928.

    Article  PubMed  PubMed Central  Google Scholar 

  114. Sterne JA, Savović J, Page MJ, Elbers RG, Blencowe NS, Boutron I, et al. RoB 2: a revised tool for assessing risk of bias in randomised trials. BMJ. 2019. https://doi.org/10.1136/bmj.l4898.

    Article  PubMed  PubMed Central  Google Scholar 

  115. Sterne JA, Hernán MA, McAleenan A, Reeves BC, Higgins JP. Assessing risk of bias in a non-randomized study. In: Cochrane handbook for systematic reviews of interventions. London: Cochrane Collaboration; 2019. p. 621–41.

    Chapter  Google Scholar 

  116. Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ. 2021;372: n71.

    Article  PubMed  PubMed Central  Google Scholar 

  117. Beitlitum I, Sebaoun A, Nemcovsky CE, Slutzkey S. Lateral bone augmentation in narrow posterior mandibles, description of a novel approach, and analysis of results. Clin Implant Dent Relat Res. 2018;20(2):96–101.

    Article  PubMed  Google Scholar 

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Acknowledgements

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Funding

This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors.

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Author notes

  1. Ralf Smeets and Levi Matthies contributed equally to this work

Authors and Affiliations

  1. Department of Oral and Maxillofacial Surgery, University Medical Center Hamburg-Eppendorf, Hamburg, Germany

    Ralf Smeets, Levi Matthies, Martin Gosau, Anders Henningsen & Christian Knipfer

  2. Division of “Regenerative Orofacial Medicine”, Department of Oral and Maxillofacial Surgery, University Medical Center Hamburg-Eppendorf, Hamburg, Germany

    Ralf Smeets

  3. Mildred Scheel Cancer Career Center HaTriCS4, University Medical Center Hamburg-Eppendorf, Hamburg, Germany

    Levi Matthies

  4. Department of Periodontology, Faculty of Dentistry, Semmelweis University, Budapest, Hungary

    Peter Windisch

  5. Department of Prosthetics and Dental Material Science, Center for Dentistry, Zürich University, Zurich, Switzerland

    Ronald Jung

  6. Periodontics LLC, Chicago, USA

    Nadine Brodala

  7. Department of Biomedical and Neuromotor Sciences, Bologna University, Bologna, Italy

    Martina Stefanini

  8. Department of Oral and Maxillofacial Surgery, University Medical Center Münster, Münster, Germany

    Johannes Kleinheinz

  9. Department of Oral Surgery and Orthodontics, Medical University Graz, Graz, Austria

    Michael Payer

  10. Department of Oral and Maxillofacial Surgery, Plastic Operations, Mainz University Medical Center, Mainz, Germany

    Bilal Al-Nawas

Authors
  1. Ralf Smeets
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  2. Levi Matthies
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  9. Michael Payer
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  10. Anders Henningsen
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  11. Bilal Al-Nawas
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  12. Christian Knipfer
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Contributions

LM and CK screened, analyzed, and interpreted the data and wrote the original manuscript draft. AH and RS provided conceptualization and validation of the data. MG contributed resources and project administration. PW, RJ, NB, MS, JK and MP reviewed and edited the manuscript substantially. BAN provided project supervision and correspondence with the journal. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Bilal Al-Nawas.

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Not applicable.

Competing interests

Dr. Smeets reports grants and lecture fees from CAMLOG Biotechnologies AG, lecture fees from Straumann, Dentsply and Botiss, outside the submitted work. Dr. Jung reports grants from CAMLOG Biotechnologies AG, during the conduct of the study and receiving grants, lecture fees from the following industrial companies: Geistlich, Straumann, Vita, Dentsply, Henry Schein. Dr. Al-Nawas reports grants and personal fees from Geistlich, Straumann, and Dentsply, grants from Nobel Biocare, outside the submitted work.

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Supplementary Information

Additional file 1: Table S1.

PRISMA 2020 checklist.

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Smeets, R., Matthies, L., Windisch, P. et al. Horizontal augmentation techniques in the mandible: a systematic review. Int J Implant Dent 8, 23 (2022). https://doi.org/10.1186/s40729-022-00421-7

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