Study of Immediate Implants Placed in Mandibular Alveolar Bone Reconstructed with Screw-Guided Bone Regeneration Technique: A 24-Months Follow-Up

Abstract

Aim: Study aimed to test whether implants inserted in posterior mandible sites augmented with screw-guided bone regeneration (S-GBR) technique differ from implants placed in non-grafted sites regarding the success and survival rate. Materials and Methods: 20 edentulous patients (mean age 59.45 ± 15.220) were divided in a test group (S-GBR) (immediate implants placed simultaneously with grafting procedures) and control group (implants placed in naturally healed sites). Primary outcomes (implants success; implants survival) and secondary outcomes (clinical parameters of soft tissues: mPI; mGI; probing depth; keratinized mucosa; marginal-bone-level) were evaluated at 24-months follow-up. Results: Plaque levels were higher (p = 0.046) in S-GBR group (0.97 ± 0.882 mm) when compared with control (0.66 ± 0.695 mm). Keratinized mucosa width was higher in S-GBR group (4.13 ± 1.033 mm) than control (3.34 ± 0.821 mm) (p = 0.000) Probing depth (PD) width was higher in S-GBR group (3.50 ± 1.372 mm) than control (2.56 ± 1.332 mm) (p = 0.000). mGI was higher among implants placed in S-GBR group (0.90 ± 1.020 mm) than control (0.56 ± 0.794 mm) (p = 0.061). The difference between the average bone loss (MBL) for implants placed in grafted sites (Group S-GBR: 2.20 ± 1.867 mm) and for those placed in naturally healed sites (Group B: 1.09 ± 1.678 mm) was statistically significant (p = 0.000). The overall implant success rate after 24-month follow-up was 76.7% in S-GBR group and 90.6% in control group (p = 0.001). The survival rate after 24-month follow-up was 86.7% in S-GBR group and 93.8% in control group (p = 0.182). The reconstruction of the alveolar bone using S-GBR technique and immediate implant placement is a valid guided bone regeneration strategy for mandibular alveolar bone with severe horizontal resorption. The choice of S-GBR technique should be based on specific indications as implants placed in grafted sites recorded worse marginal success rate, survival rate and bone resorption than those placed in non-grafted sites.

1. Introduction

The implant-prosthetic treatment of partially edentulous patients has become in last 20 years a routine treatment procedure with reliable functional and esthetic results. Despite the evolution of implant dentistry, severely resorbed posterior mandible, due to periodontal disease or natural atrophy, remains a challenge even for experienced clinicians. A functional and stable mandibular implant-prosthetic restoration in posterior area can be compromised in the long term due to shape and orientation of the residual alveolar bone, improper sagittal intermaxillary relationships as well as the presence of mandibular inferior nerves. These clinical situations require the enhancement of the alveolar bone volume and quality for long-term success of the implant-prosthetic therapy. However, the high density and low vascularization of the mandibular cortical bone can hinder an effective grafting on the mandible body or regeneration processes of some bone chambers [1].

A various range of bone regenerative bone have been proposed to create conditions for long term success of the implant-prosthetic restorations in mandible posterior areas (guided bone regeneration (GBR), distraction osteogenesis, alveolar ridge splitting techniques, bone expansion techniques, bone grafting techniques) [2,3]. Every surgical technique has advantages and disadvantages, but specialists should give priority to those procedures which are easy-to-use (according to the practical experience of the clinician), less invasive, have lower risk of complications, and allow osteointegration of dental implants within the shortest post-operatory time [4]. Data are controversial regarding the success rate on medium and long term due to low quality of methodology (poor sample size, undefined success criteria, short-term follow-up) [4]. A scientifically validated opinion on which is the best technique and grafting materials is hard to obtain, especially in posterior mandible area. Due to vertical and horizontal bone resorption, augmentation procedures require a minimal surgical technique aiming to avoid soft tissue dehiscence above the bone regeneration compartment. The use of minimally invasive tunneling technique in the reconstruction of horizontally bone defects is associated with difficulty in the positioning and maintenance of the grafted bone in coronal position to increase the area of the peri-implant soft tissues [5]. The success of the lateral ridge augmentation depends on the experience of operator and by ability to stabilize and maintain the graft at the alveolar crest. In large alveolar defects the maintaining of the stability of the grafted areas becomes even more difficult when using this technique [5]. The success of GBR techniques is more predictable when used to patients with mild to moderate horizontal alveolar bone resorption and small edentulous span that allows simultaneous placement of implants. Variants of GBR techniques that use tenting mechanisms can prevent collapse of the soft tissues and bone resorption [5]. Considering these issues, we focused our research on a particular technique used in our dental practice that allows us to obtain excellent results for mandibular edentulous patients with mild-to-moderate atrophy of alveolar bone [6,7]. Screw-guided bone regeneration (S-GBR) is a technique derived from GBR that uses a membrane that delimitates the regenerative bone compartment supported by osteosynthesis screws or dental implants [7]. S-GBR is mostly recommended to the lateral augmentation of the mandibular alveolar bone with moderate or severe horizontal resorption, by using a combination of autograft, xenograft, resorbable or non-resorbable membranes. The significant difference between S-GBR technique and other techniques used in the horizontal augmentation of the alveolar crest is the system used for the maintenance of the regenerative bone space (osteosynthesis screws as space holders, pericardium membrane to protect the graft material from soft tissue invasion), with lower rate of complications. The other techniques use non-resorbable titanium-, zirconium-, or titanium-reinforced membranes (with potential for wound infection following the exposure of e-PTFE membranes) or resorbable membranes (poor space-making ability, fast degradation) [8].

Study aimed to test whether implants inserted in posterior mandible sites augmented with screw-guided bone regeneration (S-GBR) technique differ from implants placed in non-grafted sites regarding success rate, survival rate, interproximal marginal bone level (MBL), and clinical parameters of peri-implant soft tissues.

2. Materials and Method

2.1. Patient Selection and Study Design

The prospective cohort study was conducted at Implant Institute Török (Nuernberg, Germany) between December 2017 and December 2020. The study adhered to the ethical values of the Declaration of Helsinki and received approval of ethics committee of U.M.F. “Grigore T.Popa” Iasi (Romania) (Nr. 10833) Among the patients who visited the dental clinic, 20 edentulous patients (mean age 59.45 ± 15.220) were selected (

Table 1. Characteristics of test and control group.

	Test Group (S-GBR Sites)	Control Group (Non-Grafted Sites)	Total
N of subjects (Ns)	10	10	40
N of sites (Ni)	30	32	124
Mean age (range)	(62.30 ± 16.059)	(56.60 ± 14.159)	(59.45 ± 15.220)
Gender
Men, Ns (Ni)	4 (12)	6 (18)	10 (30)
Women, Ns (Ni)	6 (18)	4 (14)	10 (32)

N, number; Ns, number of subjects; Ni, number of sites (implants).

). All patients involved in study received information about the objectives of the research and gave informed consent. Inclusion criteria (test group) were age >18 years; partially edentulous posterior mandible; severe horizontal resorption of ridges; treatment with fixed implant-supported prosthesis. Additional inclusion criteria for control group: alveolar bone of minimum 10 mm length and minimum 3.8 mm diameter. Exclusion criteria were: insufficient alveolar bone for implant-prosthetic therapy; history of untreated periodontal disease; history of smoking; decompensated metabolic diseases; pregnancy; history of bisphosphonates therapy; severe bruxism; non-collaborative patients.

The selected patients were grouped as follows:

• Test group (n = 10; 30 implants): simultaneous implant placement with ridge augmentation by S-GBR technique.
• Control group (n = 10; 32 implants): implant placement in naturally healed sites (non-grafted).

The components of the study design (population, intervention, comparison, outcomes) are presented in

Table 2. PICO study design.

Component	Description
Population (P)	Mandibular edentulous patients requiring bone grafting and dental implants
Intervention (I)	Augmentation of alveolar bone by S-GBR technique. Immediate implant placement in grafted sites
Comparison (C)	Implant placement in non-grafted sites
Outcomes (O)	Primary outcomes: implants success; implants survival Secondary outcomes: clinical parameters of soft tissues: mPI, mGI, probing depth (mm), keratinized mucosa (mm), occurrence of peri-mucositis/peri-implantitis (%); marginal-bone-level (MBL) (mm);

.

2.2. Surgical Procedures

The same surgeon (T.R.), with over 20 years of experience, performed alveolar augmentation and implant procedures. For all patients, systemic antibiotics were given prophylactic preoperatively and at 4 days postoperatively. The procedures of dental implants insertion for test group and control were as follows:

(a)

Dental implants placement simultaneously with alveolar augmentation by SGBR technique (xenograft, or a mixture with autogenous bone; porcine collagen membrane) (test group);

(b)

Standard dental implants placement (control group).

The surgical protocol of S-GBR technique and immediate implant placement is described in

Table 3. Operative protocol in S-GBR technique and immediate implant placement.

No.	Procedure	Instruments and Materials	Role
1.	Local anesthesia	Ultracain DS-Forte (Sanofi, Paris, France)	Comfort of patient and operator
2.	Full-thickness flaps in the resorption bone area	DeveMed GmbH, (Tuttlingen, Germany)	Opening of the surgical field
3.	Immediate implants insertion (3.5–4.5 mm diameter, 10–13 mm length)	BioSTI implants (Tafers, Switzerland) Dentium implants (Seoul, South Korea)
4.	Periosteal incisions on the flaps	AesculapAG (Tuttlingen, Germany)	Promotion of tension-free closure of the flaps
5.	Insertion of the osteosynthesis screws (1.5 mm diameter, 8 mm length) on the buccal face of the alveolar bone (45° angle to the alveolar crest)	Implantology kits Synthes GmbH, (Zuchwil, Switzerland) DeveMed GmbH, (Tuttlingen,Germany)	Maintenance of the space for the grafted area
6.	Covering of the exposed implant bone surface area with a small layer of autologous bone, followed by the placement of xenograft adjacent to the head of osteosynthesis screws. Covering of the grafted area with a resorbable collagen membrane	Xenograft CompactBone, (Dentegris GmbH, Rheinberg, Germany) Porcine pericardial tissue membrane BoneProtect Membrane (Dentegris GmbH)	Isolation and protection of the graft from the gingival tissue. Stimulation of the gingival healing. Protection of the surgical site from gingival dehiscence during the next 3–4 months and Reconstruction of the lateral resorbed bone area
7.	Suture of the surgical site	Non-resorbable sutures (polypropylene 5.0, Hu-Friedy, Chicago, IL, USA)	Protection of grafted bone and peri-implant tissues
8.	Post-operative care (7 days): antibiotherapy, analgesics, rinse of oral cavity with chlorhexidine 0.5%	Augmentin 625 mg, GlaxoSmithKline Pharma, Vienna, Austria) and analgesics (Ibuflam 600, Zentiva, Lichtenstein)	Control of post-operative pain and inflammatory processes
9.	Removal of sutures at 9–11 days after the surgical intervention
10.	Second stage surgery: removal of the osteosynthesis screws at 4 months after the surgical intervention

.

Prosthetic loading was carried out after 14–16 weeks following implants placement in the mandible. Each patient was included in a maintenance program consisting of oral hygiene and recall visit every 6 months.

Clinical and CBCT aspects of patient from the test group, describing the stages of S-GBR technique and implant-prosthetic stage, are presented in Figure 1, Figure 2, Figure 3, Figure 4, Figure 5, Figure 6, Figure 7, Figure 8, Figure 9, Figure 10 and Figure 11. CBCT exam allows the evaluation of the horizontal alveolar bone defect and the position of the mandibular alveolar nerf (Figure 1A,B). Figure 1C,D show cross-sectional CBCT aspects of the implant sites. Figure 2 shows the narrowed mandibular alveolar bone with horizontal resorption. Figure 3 shows the exposed buccal surface of the alveolar ridge with severe horizontal resorption, after flap opening. The inserted implants (4.5 mm diameter, 11.5 mm length) and osteosynthesis screws (45° from the occlusal plan) are shown in Figure 4A. The placement of graft (autologous bone and xenograft) and collagen membrane is shown in Figure 4B. Figure 5A shows tension-free sutures, due to periosteal incisions alveolar ridge. Figure 5B shows clinical aspect at 7 months after surgery, with gingival tissue adherent on the reconstructed alveolar ridge. Figure 6 shows OPG aspect at follow-up of 7 months, with osseointegration of the dental implants. Figure 7A shows clinical aspect before osteosynthesis screws removal. Figure 7B shows clinical aspect after osteosynthesis screws removal. Figure 8A shows healthy peri-implant soft tissues. Figure 8B shows repositioning key for perfect position of abutments. Figure 10A,B show clinical aspects of implant-supported prosthetic restoration. Figure 11A,B show CBCT aspects of Osseo integrated dental implants at 24 months follow-up.

2.3. Results Analysis

The clinical and radiographic analysis of the parameters related to the primary outcomes and secondary outcomes was performed by one investigator (T.B) at 24-months post-loading. Criteria for the success of S-GBR grafting procedure were: absence of fistula, flow out from mucosal dehiscence of the particles of the graft material, or the chronic inflammation. Buser criteria, used to define the implant success, are as follows: the absence of pain, the absence of implant mobility, the absence of recurrent peri-implant infection, the absence of peri-implant radiolucency at 6 months and 24 months post-loading [9].

Diagnostic of peri-implant mucositis [10,11]:

(1)

Clinical inflammation signs (erythema, swelling, bleeding on probing at force not overpassing 0.25 N, and/or suppuration) [12]

(2)

Mild increase of probing depth.

(3)

Absence of peri-implant bone loss (after post-loading stage of bone remodeling).

Diagnostic of peri-implantitis [10,11]:

(1)

Clinical inflammation signs (erythema, swelling, bleeding on probing and/or suppuration);

(2)

Probing depth >3 mm, and/or recession of the mucosal margin.

(3)

Loss of peri-implant bone >3 mm (from implant shoulder).

Indices mPI and mGI were used to evaluate the status of the peri-implant soft tissues (

Table 4. mPI Indice (peri-implant bacterial plaque accumulation).

Score	Description
0	Undetected bacterial plaque
1	Bacterial plaque detected by peri-implant probing
2	Bacterial plaque detected by visual inspection
3	Peri-implant abundant white materia

and

Table 5. mGI Indice (peri-implant soft tissues status).

Score	Description
0	No bleeding when the periodontal probe is passed along the peri-implant mucosal margin
1	Isolated bleeding spots
2	Bleeding line on mucosal margin
3	Heavy bleeding; profuse bleeding

) [13,14,15]. Probing Depth (PD) (mm) was evaluated with periodontal probe (Click-Probe^®, Kerr, Bioggio, Switzerland).

Keratinized Mucosa (KM) (mm) was measured with periodontal probe (Click-Probe^®, Kerr) as the distance between the mucogingival junction and the most coronal point of the keratinized mucosa in the center of the implant-prosthetic restoration

The marginal bone loss at buccal area (MBL) at 24-months follow-up was measured on CBCT as the distance between the connection implant-abutment and the peri-implant MBL.

2.4. Statistical Analysis

Using the statistical software G*Power (Version 3.1.9, Heinrich-Heine-University, Düsseldorf, Germany), a sample of 9 subjects in each group was calculated as minimum number required to determine a significant statistical difference in marginal bone level loss, success rate and survival rate of implants (80% power, 5% confidence level). Considering a dropout rate of 10% during the study period, 10 subjects were included in each group.

The frequencies distributions were calculated for qualitative variables, while the averages and standard deviations for the quantitative ones. The normality of data distribution was checked by Shapiro–Wilks test. The comparison of the quantitative variables between test group and control was performed by using t-test and Mann-Whitney test. The comparison of the qualitative variables between test group and control was performed by using Chi-squared test. The significance level was set at p < 0.05. Statistical analysis was performed using SPSS version 27.0 for Windows (IBM, Armonk, NY. USA).

3. Results

Plaque levels (mPI) were significantly higher (p = 0.046) in S-GBR group (0.97 ± 0.882 mm) when compared with control (0.66 ± 0.695 mm) (

Table 6. Clinical parameters and radiographic results at 24-months follow-up.

	S-GBR Group	Control	p-Value
Mean Plaque Index (mPI) (mm)	0.97 ± 0.882 (SD)	0.66 ± 0.695 (SD)	0.046 *
Keratinized mucosa (KM)	4.13 ± 1.033 (SD)	3.34 ± 0.821 (SD)	0.000 **
Probing Depth (PD) (mm)	3.50 ± 1.372 (SD)	2.56 ± 1.332 (SD)	0.000 **
Mean mGI	0.90 ± 1.020 (SD)	0.56 ± 0.794 (SD)	0.061
mGI (scores)			0.075
Score 0	43.3%	56.3%
Score 1	36.7%	37.5%
Score 2	6.7%	0.0%
Score 3	13.3%	6.3%
MBL (mm)	2.20 ± 1.867 (SD)	1.09 ± 1.678 (SD)	0.000 **

* Statistically significant, p < 0.05; ** Statistically highly significant, p < 0.01.

).

Keratinized mucosa width (KM) was higher in S-GBR group (4.13 ± 1.033 mm) than control (3.34 ± 0.821 mm), with statistically significant differences (p = 0.000) (Table 6).

Probing depth (PD) width was higher in S-GBR group (3.50 ± 1.372 mm) than control (2.56 ± 1.332 mm), with statistically significant differences (p = 0.000) (Table 6).

Modified gingival index (mGI) was higher among implants placed in S-GBR group (0.90 ± 1.020 mm) than control (0.56 ± 0.794 mm), although differences were not statistically significant between groups (p-0.061) (Table 6).

The difference between the average bone loss (MBL) for implants in Group S-GBR (2.20 ± 1.867 mm) and for implants placed in non-grafted sites (Group B: 1.09 ± 1.678 mm) was statistically significant (p = 0.000) (Table 6).

The success rate and the survival rate were higher for control when compared with S-GBR group after 24-months follow-up (

Table 7. Success rate and survival rate at 24-months follow-up.

	S-GBR Group	Control	p-Value
Success rate	76.7%	90.6%	0.001 **
Survival rate	86.7%	93.8%	0.182

** Statistically highly significant, p < 0.01.

).

The overall implant success rate at 24-month follow-up was 76.7% in S-GBR group and 90.6% in control group, with significant differences between groups (p = 0.001).

The survival rate after 24-month follow-up was 86.7% in S-GBR group and 93.8% in control group, without statistically significant differences although differences between groups (p = 0.182).

4. Discussion

This study compared clinical and radiographic parameters of the implant-supported fixed restorations, following immediate implants placement in sites grafted by the S-GBR technique.

A condition of the implants success rate when placed in grafted sites is the absence of post-operatory early complications due to exposure or improper stabilization of bone graft as well as to post-operatory infection. In our study, post-grafting complications, that could interfere with implants osseointegration processes, were absent. The absence of the risk factors (due to the selection criteria of patients) could contribute significantly in maximizing the rate of the grafting procedures success [16]. However, Dastaran et al. found that the implant survival rate is not influenced by alveolar bone augmentation, despite higher complications rate for implants inserted in sites with vertical and horizontal resorption [17]. The S-GBR technique was performed using mixed grafts (autologous bone and bovine bone). Based on reviewed studies, with a follow-up of minimum 3–5 years, Ellakia et al. recommend the replacement of allografts and xenografts with autologous bone in the implant sites with medium and severe bone resorption [18]. Xenografts can delay bone formation in comparison to the naturally healed sites, but also preserve the alveolar ridge and stimulate bone formation as to enable placement of implants with high success rate in mandibular implant-prosthetic restorations [19]. Our study investigated the success rate and survival rate of immediate implants placed in alveolar bone reconstructed by S-GBR technique. Immediate implant placement simultaneously with alveolar bone grafting had been well investigated in some systematic review. One study reported, at 20-months follow-up, the absence of statistically significant differences regarding various clinical parameters of the peri-implant soft tissue and peri-implant marginal bone loss, between the immediate implants and delayed implants [20]. In our study we found higher probing depth (p = 0.000), mGI index (p = 0.061), and average bone loss (p = 0.000) for immediate implants placed in grafted sites, when compared with naturally healed sites at 24-month follow-up. However, implant placement simultaneous with horizontal ridge augmentation is recommended when possible as implant survival rates are similar to subsequent implant placement [21]. We found after 24-months follow-up an implant success rate of 76.7% in S-GBR group, while the survival rate was 86.7%. The statistical analysis revealed the lack of significant statistical differences regarding the survival rate, but statistically significant differences for success rate when comparing S-GBR sites and non-grafted sites. According to a comprehensive review of studies, implants placed with GBR techniques had a mean 95.5% rate of survival for follow-ups of 5–74 months [22]. The survival rate of the implants inserted in augmented sites, irrespective of the surgical technique, ranged from 91.7% to 100%, while survival rates for non-grafted sites ranged between 93.2% and 100% at follow-up periods of 1–5 years [23]. A review of studies with 1–3 years follow-up, found non-significant changes of peri-implant soft tissues clinical parameters and marginal bone levels, when lateral bone augmentation techniques are used [24]. The implant survival rate for the alveolar bone submitted to lateral ridge augmentation was 97% to 100% at 6–12 months of follow-up [25].

At 24 months follow-up the probing depth and the peri-implant marginal bone loss are higher than control group. This result is correlated with higher resorption rate of the augmented alveolar area when compared with the implants placed in naturally healed alveolar bone. However, S-GBR is an augmentation technique with very low rate of complications [7]. The only complication could be the exposure of the osteosynthesis screw, managed by taking out the screw without any need of anesthesia.

An interesting research issue would be the comparison of the results obtained with S-GBR technique and immediate implantation when used in combination with different graft materials. Further studies will be published by our research group to report the influence of the graft material on the success and survival rate of dental implants placed in mandibular alveolar bone.

S-GBR technique is an easy method to regenerate the bone around implants and can be used in the daily work by every practitioner. The big advantage of this method is the low complication rate and the protection offered by the osteosynthesis screws to the augmented side against the compression forces in the oral cavity.

The comparison and interpretation of the results with those reported by literature must be done with caution as various factors impact the long-term success of the implant-prosthetic restorations [26,27,28,29].

Literature data is scarce in studies investigating the results of the implant-prosthetic treatments in simultaneous approach (augmentation technique combined with immediate implantation). Also, the success of the dental implants following immediate implantation in mandibular sites reconstructed with S-GBR technique, was not yet investigated.

Further studies can highlight the benefits and limits of this augmentation technique and can establish specific clinical situations when this technique can be recommended.

The limitations of this study are related to insufficient follow-up which is not enough to establish long-term survival rate of the implants, low sample size, and possible subjective bias of the investigators.

5. Conclusions

The reconstruction of the alveolar bone using S-GBR technique and immediate implant placement is a valid guided bone regeneration strategy for mandibular alveolar bone with severe horizontal resorption. The selection of S-GBR technique should be based on specific indications as implants placed in grafted sites recorded worse marginal success rate, survival rate and bone resorption than those placed in non-grafted sites.