Background
The discovery of osseointegration by Branemark in 1969 [
1] opened up a multitude of new possibilities for restoring health, esthetics, and function in edentulous patients and those with extensive damage to their dentition. Therefore, implant therapy has revolutionized dental practice. Along with the implant ad modum Branemark, intramobile cylinder implants (IMZs) were among the first fixtures used in implant therapy. The IMZ implant system was particularly popular in the 1980s and the early 1990s, before it was replaced by the Camlog implant system in the late 1990s. The key component of the IMZ implant system is the intramobile element (IME), whose purpose is to simulate the viscoelasticity of the periodontal ligament and reduce the forces transmitted to the marginal bone–implant interface [
2]. Since the implant and IME are rigidly connected, the IME serves to reduce the displacement differential between the osseointegrated implant and a natural tooth while also impeding the intrusion of natural teeth, which can occur if a nonrigid interlock is used [
3]. Several previous studies have reported excellent results on survival rate and radiographic and clinical data [
3‐
7]. However, to date, longitudinal studies with a follow-up period greater than 10 years are scarce. Previous prospective studies with a follow-up period of up to 10 years have reported findings on the IMZ Implant system [
6,
8,
9]. There are also a few additional retrospective studies reporting on IMZ implants after a period of more than 10 years, but as implants of significantly lower age were also included in those studies, the overall mean observation time was considerably shorter [
7,
10]. A literature search in MEDLINE on the IMZ Implant system regarding follow-ups with a mean observational period of at least 5 years reveals a total of four studies of heterogenous design shown in Table
1. Further, additional three studies report results after up to 13 years of follow-up without specifying the mean observation time. Although all authors report on implant survival or success rates, data on peri-implant conditions such as marginal bone loss is hardly mentioned [
2‐
11]. While existing data indicate high survival rates of over 90% and minimal marginal bone-level changes of less than 2 mm after a period of 10 years [
6], the long-term outcome of the IMZ implant system is still unknown, as there are no studies reporting data after at least 20 years.
Table 1
Publications providing medium- and long-term data on the IMZ Implant System
Kirsch & Ackermann 1989 | Retrospective | Not specified (1–10 years) | Patients with sufficient horizontal and vertical residual bone | SC, FDP, RDP | 1401/3088 | ?/334 (?/10.8%) | Not specified | Not specified | 97.8% (excluding drop out) |
Spiekermann et al. 1995 | Prospective | 5.7 | No special features | RDP | 125/264 | Not specified | 2–6 (depending on IMZ-implant type) | Not specified | > 90% (cumulative after 5 years) |
Noack et al. 1999 | Retrospective | Not specified (1–13 years) | Treatment between 1984 and 1997 | SC, FDP, RDP | 527/1250 | Not specified | Not specified | Not specified | 81% (cumulative, after 10 years) |
Willer et al. 2003 | Prospective | Not specified (1–13 years) | No special features | SC, FDP, RDP | 541/1250 | 89/136 (16.5%/10.9%) | Not specified | Not specified | 82.4% (cumulative, after 10 years) |
Meijer et al. 2003 | Prospective | 10 | - Edentulousness for at least one year - Problems with retention and stability of the lower denture | RDP | 29/58 | 1/2 (3.4%) | No mean values reported | Not specified | 93% (percentage implants lost) |
Meijer et al. 2009 | Prospective | 10 | - Severely reduced mandible -Edentulousness - Problems with retention and stability of the lower denture | RDP | 30/60 | 1/2 (3.3%) | 1.4 ± 1.1 | Not specified | 93% (percentage implants lost) |
Visser et al. (2016) | Prospective | 15 | - Treated between 1996 and 1999 -Edentulousness for at least 2 years - Functional problems | RDP | 40/160 | 20/80 (50%) | Not specified | Not specified | 88.7%-98.7% (percentage implants lost, range between subgroups) |
Our Findings | Retrospective | 28.3 | - Treated between 1981–1995 - Availability of baseline radiographs | SC, FDP, RDP | 94/199 | 79/167 (84%/83.9%) | 2.5 ± 1.8 | 9.4% | 79.5% |
Notably, middle-aged or younger patients with multiple agenesis are often treated with endosseous implants and are reliant on the function of their implants for many decades. Considering these patients’ age, longer observation periods than those typically seen in 5- to 10-year follow-up periods are appropriate and needed. While many aspects of implant design have changed over the years, the overall principle and structure of endosseous implants have remained unaltered. Importantly, data on older implant systems might provide valuable insights into long-term implant therapy, even with the current systems. Therefore, the aims of the present retrospective study were: 1) to examine the feasibility of implant therapy follow-up examinations after a mean observation time of at least 20 years; 2) to investigate the outcome of IMZ implant therapy providing clinical and radiographical long-term results.
Discussion
Of the 94 preselected and possible participants in this study, 30.9% passed away, and 27.6% were unavailable, leading to a positive response rate of 41.5% (CG). A further 25.5% of these patients had to be excluded for the various reasons listed in Table
5, ultimately leaving 16% of the patients from our original cohort who were examined after a mean observation time of 28.3 years. Comparable long-term studies with observation periods of up to 25 years showed dropout rates ranging from 31.6–71.7%, which is significantly lower than the 84% dropout rate in our study [
16‐
26]. Variations in observation periods may be a decisive factor for this discrepancy, as our study had a longer mean observation time. Thus, on average, patients in our study cohort were older, leading to a higher number of deaths (Table
5). Only one previous study by Bakker et al. (2019) included a cohort whose average age (85.5 + years) significantly surpassed the mean age found in our study, as patients younger than 60 years at baseline were excluded [
17]. Consequently, the proportion of patient deaths (62.3%) in this cohort was the highest, leading to a dropout rate of 71.7%. The relatively small number of “unavailable” patients compared to our study might be explained by its prospective study design, since those patient cohorts have been meticulously followed up several times over the course of the last 20 years [
17]. Generally, dropout rates are very high, with most studies observing at best, about 30%, and more often about 60% after 20 years, regardless of the study design. Importantly, cutting out such a large proportion of potential information limits the validity of the collected data.
Table 5
Follow-up studies providing data on implant therapy after more than 15 years
Dierens et al. (2011) | Retrospective | 18.4 | - Treated between 1987 and 1993 - Availability of peri-apical radiographs - Availability of original patient file | Branemark | Single crown (SC) | 134/166 | 84/104 (62.7%/62.7%) | - Deceased (4) - No contact information (9) - Moved away (11) - Did not answer phone (2) - Loss of all original implants (7) - Unwilling to attend clinical examination (51) | 42.4 | 91.5% (cumulative, contact group) |
Frisch et al. (2020) | Retrospective | 25.4 | - Treated between 1991 and 1996 - Availability of radiographs after ≥ 20 years | Ankylos, Branemark, IMZ, ITI Bonefit | SC, FDP, RDP | 62/? | 36/? (58.1%/?) | - Deceased or serious disease (24) - No participation in supportive implant therapy program (SIT) (7) - No radiographs (1) - Reason not known (4) | 74.6 | 94.7% (percentage implants lost) |
Astrand et al. (2008) | Prospective | 20 | - Original study cohort - Edentulous patients in one or two jaws | Branemark | RDP | 48/? | 27/146 (56.3%/?) | - Deceased (19) - Age/sickness (8) | 61–94 (range) | 99.2% (percentage implants lost) |
Lekholm et al. (2006) | Retrospective | 20 | - Treated between 1983 and 1985 - Treated and followed by one surgeon - Availability of baseline radiographs | Branemark | SC, FDP | 27/112 | 10/43 (37%/38.4%) | - Deceased (6) - Moved away (3) - Unwilling to attend follow-up (1) | 68 | 91% (cumulative, including drop out) |
Jokstad et al. (2017) | Retrospective | 17.5 | - Implant treatment before 2002 | Branemark | SC, FDP | 298/? | 177/? (59.4%/?) | - Could not be located (92) - Deceased (23) - Moved away (21) - Age/illness (14) - Unwilling to attend follow-up (23) - Loss of original implant(s) (4) | 62 | 94% (percentage implants lost) |
Chappuis et al. (2013) | Prospective | 20 | - Original study cohort - Partially edentulous patients | Bonefit | FDP | 98/145 | 31/50 (31.6%/34.5%) | - Deceased (11) - Moved away, age, illness (20) | 66.3 | 89.5% (percentage implants lost) |
Bakker et al. (2019) | Prospective | 20 | - Original study cohorts (Batenburg et al., 1998; Heydenrijk et al., 2002) - Edentulous patients - Patient’s age > 60 years at the time of implant placement | Branemark, IMZ, ITI | RDP | 53/106 | 38/76 (71.7%) | - Deceased (33) - Moved away (5) | 85.5 | 92.5% (percentage implants lost, including drop out) |
Deporter et al. (2014) | Prospective | 20 | -Original study cohort (Deporter et al. 1992) -Edentulous patients with advanced mandibular resorption | SPS | RDP | 52/156 | 30/103 (57.7%/66%) | -All implants lost within the first 2 years (2) - Deceased (11) -Age, Illness (17) | Not specified | 73.4% (cumulative, including drop out except the 2 patients with early loss of all implants) |
Jacobs et al. (2010) | Prospective | 16 | -Original study cohort (van Steenberghe et al. 2000) -Patients with bilateral tooth loss (Kennedy Class 1) -Treated between 1993 and 1994 | Astra, Branemark | FDP | 18/95 | 6/48 (33.3%/50.5%) | -Deceased (1) -Moved away (3) -Age (2) | Not specified | 97.7%-100% (cumulative success rate, including drop out, range between subgroups) |
Jung et al. (2021) | Prospective, comparative | 22–24 (mean value not described) | -Original study cohort (Zitzmann et al. 2001) -Treated from 1994–1996 | Branemark, Biomed 3i, IMZ | Fixed, removable | 72/265 | 33/118 (45.8%/44.5%) | -Deceased (23) -Moved away, illness (10) | 75.8 | 89.3–93.8% (cumulative, range between subgroups) |
Donati et al. (2018) | Prospective, comparative | 20 | -Original study cohort (Wennström et al. 2004) | Astra | FDP | 51/148 | 26/84 (51%/56.8%) | -Deceased (19) -Moved away, illness (7) | Not specified | 87.8% (percentage implants lost) |
Our findings | Retrospective | 28.3 | - Treated between 1981–1995 - Availability of baseline radiographs | IMZ | FDP, RDP | 94/199 | 79/167 (84%/83.9%) | - Deceased (29) - Unavailable (26) - Loss of all original implants (13) - Age/illness (5) - Moved away (4) - No up-to-date radiographs (2) | 75.3 | 79.5% (contact group) |
Owing to steadily evolving implant technology, the lack of sufficient long-term data is an issue, especially for outdated implant systems, as the benefit of data on those systems is arguable. Furthermore, the presented studies indicate that the feasibility of long-term follow-up studies spanning 20 years or longer is complicated due to high patient dropout rates [
16‐
18,
20,
22,
24,
26].
The present study showed a relatively high survival rate of 79.5% after a mean observation time of 28 years. However, it falls short of the survival rates of follow-up studies with comparable observation periods, ranging from a survival rate between 87.8. and 100% [
16‐
18,
20‐
26]. Interestingly, studies exclusively examining Branemark implants have reported the highest survival rates, regardless of the study design. On the other hand, Frisch et al. (2020) observed excellent survival rates in a cohort of patients with various implant types, who were part of a permanent supportive implant therapy program [
22]. Nevertheless, due to the heterogeneity of study designs and the generally high dropout rates described in all studies to date, the results should be interpreted with caution.
Regarding the radiographic analysis, we found a mean marginal bone loss of 2.5 mm after an average observation time of 28.3 years. While slightly higher, our results are comparable to those of previous studies [
16,
17,
20,
22‐
26] reporting mean marginal bone loss in the range of 0.02–2.5 mm analyzing predominantly Branemark implants (Table
6). Regarding clinical outcomes, we recorded an average probing pocket depth of 2.4 mm. In relation to the mean pocket probing depths ranging from 2.5 to 4.0 mm in comparable studies (Table
6), our results stand out in a positive way. Owing to the variability of PPD which depends on the width of the peri-implant mucosa, information on the progression or stagnation of PPD is essential for peri-implant diagnostics. In addition, our favorable findings can be explained by the reduced accessibility of the peri-implant pocket due to the geometry of the implant’s suprastructure [
27], as in our study the implant suprastructures were not removed for clinical evaluation.
Table 6
Mean values for MBL, PPD, plaque, and Bleeding Index as well as the corresponding peri-implantitis rate, as described by the authors in Table
5
Dierens et al. (2011) | 1.7 ± 0.88 (from baseline) | 3.9 ± 1.27 | 0.25 ± 0.35 (acc. to Loe, 1967) | Not specified | Not specified |
Frisch et al. (2020) | 1.8 ± 1.2 (bone level) | 3.69 ± 1.06 | Not specified | 36.6% (implants with BOP) | 7%, 40% (incidence) |
Astrand et al. (2008) | 1.72 ± 0.16 (from baseline) | 3.4 | Not specified | Not specified | 2.4% |
Lekholm et al. (2006) | 1.0 (from baseline) | Not specified | Not specified | Not specified | Not specified |
Jokstad et al. (2017) | 1.52 ± 1.57 (bone level) | 2.5 ± 1.3 | 0.8 ± 0.98 (acc. to Mombelli, 1987) | 0.92 ± 0.83 (acc. to Mombelli, 1987) | 5.1% |
Chappuis et al. (2013) | 3.04 (bone level, median) | 3.14 ± 0.95 | 0.44 ± 0.64 (acc. to Mombelli, 1987) | 0.11 ± 0.41 (acc. to Mombelli, 1987) | 13.7% (incidence) |
Bakker et al. (2019) | 1.14 ± 0.85 (from baseline) | 3.5 (median) | 2 (median, acc. To Mombelli, 1987) | 1 (median, acc. to Mombelli, 1987) | Not specified |
Deporter et al. (2014) | 0.67 (bone level) | Not specified | Not specified | Not specified | Not specified |
Jacobs et al. (2010) | 0.02 ± 0.45–0.31 ± 0.69 (from baseline) | Not specified | Not specified | Not specified | Not specified |
Jung et al. (2021) | 2.0 ± 1.4–2.5 ± 1.5 (from baseline) | 2.9 ± 1.1–3.3 ± 1.1 | 6–21% (acc. to O’Leary) | 34–41% (BOP) | Not specified |
Donati et al. (2018) | 0.41 ± 1.25–0.83 ± 1.59 (from baseline) | 3.7 ± 1.03–4.0 ± 1.3 | 14.8–25.9% (index not specified) | 11.1–25.9% (BOP) | 10.9% |
Our findings | 2.5 ± 1.8 (from baseline) | 2.4 ± 1.5 | 1.0 ± 1.2 (acc. to Mombelli, 1987) | 40.6% (implants with BOP) | 9.4% |
Comparing the MBL of the IMZ implants among the FDPs and RDPs groups, we found significantly less bone-level changes in the FDPs group (1.7 mm and 3.2 mm, respectively). To date, no studies have analyzed bone-level changes in IMZ implants in fixed dental prostheses. Regarding the MBL of IMZ implants in removable prostheses, we observed significantly higher bone loss than the 1.4 mm described by Meijer et al. (2009) after 10 years. Therefore, owing to the vast differences in observation times, comparisons must be performed with caution. Notably, based on differences observed in MBL between the FDPs and RDPs groups, Berglundh et al. (2002) concluded, that the percentage of implants showing MBL of at least 2.5 mm is notably higher (4.76%) in overdentures than in FDPs or single-implant restorations (1.01% and 1.28%, respectively) [
28]. These results confirm our findings. The increased bone loss might be explained by the unfavorable bending forces that are applied to the implants due to the free-ending saddles typically used in RDPs [
29].
Of the 32 implants included in our study, 3 (9.4%) were diagnosed as peri-implantitis, which is a slightly higher prevalence rate than that reported in comparable studies ranging from 2.4–7% [
16,
22,
24]. However, the value is in accordance with the 10% proportion of peri-implant diseased implants reported in the review by Mombelli et al. (2012) after an observation time of 5–10 years [
30]. As pointed out in the review by Mombelli et al. (2012), a wide range of different disease-defining criteria were used in the selected studies, so the comparability of peri-implantitis rates is generally difficult. For example, according to Astrand et al. (2008), a crater or beaker-like type of bone loss is required to diagnose peri-implantitis [
16], while Jokstad et al. (2017) defined diseased implants as unsuccessful implants according to the criteria of Buser et al. (1990) [
24,
31].
Due to these different definitions, the 2017 Consensus Conference established a uniform standard. Consequently, the new definition for peri-implantitis was used in the current study. As one of the latest long-term follow-ups on implant therapy Frisch et al. (2020) also followed this new standard allowing a more concise comparison of the presented per-implantitis rates [
22]. Frisch et al. (2020) observed a prevalence of peri-implantitis of 7% in a cohort of patients participating in a strict supportive implant therapy program. In contrast, a peri-implantitis incidence rate of 40% was observed among patients that were not part of a supportive structured implant therapy program but instead kept control examination appointments on their own initiative. In contrast to these data, the results of our study seem very favorable, even if on our patient cohort a strict supportive implant therapy program was not performed. Further, because of the absence of previous examinations in contrast to Frisch et al. (2020) we had to rely on the thresholds proposed in the Consensus report [
13] limiting the comparability between the presented peri-implantitis rates. Due to the geometry of the implant’s suprastructure, the access to the peri-implant pocket was reduced possibly leading to a more positive outcome, as suprastructures were not removed in our study [
27]. Nevertheless, a recent systematic review also observed significant differences in the prevalence of peri-implantitis between patients who participated regularly in a prophylaxis program (9.0%) and those without regular preventive maintenance care (18.8%). These findings confirm a tendency towards an increased risk for developing peri-implantitis in patients with a lack of prophylaxis on a medium level of evidence [
32]. Although several studies have found a strong tendency to favor peri-implantitis in smokers, patients with periodontitis and patients with diabetes [
30,
32], our study failed to show a significant connection between these risk factors and the development of peri-implantitis. As we predominantly relied on self-reported medical history, it is most likely that many patients did not know or remember the exact reason for their teeth loss leading to implant therapy. In our study, 46.7% of the patients had previously suffered from periodontitis, although the actual number might be greater, considering that the fifth German oral health study reported that 65% of elderly people suffer from periodontal disease, which is considerably higher than that observed in our study [
33]. With regard to osteoporosis as a potential risk factor for peri-implantitis, neither our study nor the systematic review by Dreyer et al. (2018) found any significant associations [
32].
Our literature search in MEDLINE did not reveal any meta-analysis nor systematic review on implant survival and marginal bone loss after an observation time of 15 years or longer. This applies not only to IMZ implants but also in general to other implant systems. Latest systematic reviews on this topic present data on implant therapy after 10 years, while studies with longer follow-up periods were occasionally included [
34,
35]. In these studies, implant survival ranges from 73.4 to 100% with a cumulative mean value of 94.6% [
35].
According to the aims of the presented study, we compiled publications analyzing patient drop out, implant survival and peri-implant conditions with long-term data after more than 15 years (Tables
5,
6). We included all studies with a prospective as well as retrospective design. Publications not providing a distinct description of patient drop out were excluded. The selected studies partially providing detailed investigation on long-term implant therapy suggest that a systematic review and meta-analysis on this topic in a dedicated publication is meaningful.
The major limiting factor of our study was the small number of patients, who attended the follow-up appointment. Of the 94 patients with 199 implants, 15 patients with 32 implants agreed to undergo clinical and radiographic examinations. This was equivalent to a dropout rate of 84%. Since most of the dropped-out patients were deceased or unavailable, and the patient’s status was considered independent of the condition of the implants, we assume that our contact group is representative of the original patient pool. However, it is arguable whether patients with CEG were generally healthier and therefore more compliant than patients who were not available for a follow-up appointment because of senility or death. Additionally, as the clinical and radiographical data of lost implants could not be considered, our results are probably based on a positive selection of largely successful implants. Despite these assumptions, the influence of a largely reduced study population accompanied by a corresponding loss of information is unclear and could equally lead to false-positive or false-negative outcomes, which is why the results of our study should be interpreted with caution. This applies especially to the results from the radiographic analysis. Although differences in the reported bone loss across all the studies mentioned are minimal, strict comparisons are difficult, and exact conclusions cannot be drawn. As seen in our study, the number of patients examined at follow-up after 10–20 years was comparably small. Hence, individual findings and statistical outliers could drastically affect the results, leading to greater variability in the reported outcomes.
In addition, one major problem in analyzing the radiographs was the rather difficult identification of the reference points of the implant according to our definition. Since it was not possible to remove the implant suprastructures for examination, the radiographic reference points were often overlaid by the intramobile connector (IMC). In addition, radiographic superimposition and motion blur led to varying image quality and in some cases, the position of the radiographic reference point had to be gauged. The bone-level measurements were performed by two individual examiners with the help of optical magnification, thus any possible deviations between the estimated and actual reference points should be minor and clinically irrelevant.
Due to the retrospective nature of this study, combined with missing or incomplete patient files, no statements on changes in clinical parameters could be made, as no baseline data were reported. In addition, we often had to rely on self-reported medical history, limiting the validity of the presented analysis of risk factors, as the senescence of the patients has to be considered. The lack of memory and understanding for their anamnesis could explain the relatively small number of patients with a history of periodontitis found in our study.
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