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The efficacy of systemic antibiotics as an adjunct to surgical treatment of peri-implantitis: a systematic review

BMC Oral Health volume 21, Article number: 666 (2021) Cite this article

Abstract

Background

Microbial biofilm accumulation is the main cause of peri-implantitis. The majority of surgical peri-implantitis treatment protocols suggests adjunctive use of systemic antibiotics to target specific putative bacteria. The aim of this systematic review was to critically evaluate the adjunctive use of systemically administered antibiotics in surgical treatment of peri-implantitis by reviewing previously published systematic reviews and primary studies.

Methods

A systematic literature search was conducted in four electronic databases (MEDLINE, The Cochrane Library, EMBASE, and Web of Science) for randomised controlled trials, cohort studies, case–control studies, and systematic reviews reporting surgical treatment of peri-implantitis with and without adjunctive systemically administered antibiotic therapy. The included systematic reviews and primary studies were qualitatively assessed using AMSTAR and GRADE, respectively. No restrictions were set for date of publication, journal, or language.

Results

The literature search identified 681 papers. Only seven systematic reviews and two primary studies met the inclusion criteria. Four out of seven included systematic reviews concluded that no evidence exists for use of systemic antibiotics to improve the clinical outcomes in surgical treatment of peri-implantitis. One review did not estimate the level of evidence, one did not clearly state any beneficial effect, whereas one reported a limited adjunctive effect. Further, the two included primary studies did not show a long-term significant benefit of adjunctive use of systemically administrated antibiotics. However, one study reported a short-term adjunctive effect in patients with modified surface implants. Due to heterogeneity in study design, low number of included primary studies, and grade of bias, no meta-analysis was performed.

Conclusion

The use of systemically administered antibiotics as an adjunct to surgical interventions of peri-implantitis cannot be justified as a part of a standard treatment protocol. A pervasive problem is the lack of uniform diagnosis criteria for peri-implantitis, deficient information about patient characteristics, absence of high quality long-term randomised controlled trials, and authors’ declaration on conflict of interest.

Peer Review reports

Background

The prescription of systemically administered antibiotics for the prevention of postsurgical complications and/or beneficial surgical outcome effects, has remained a controversial subject for decades [1,2,3,4]. Original protocols for implant placement advocated dogmatic or consensus-based antibiotics prophylaxis and prolongation of antibiotic treatment during the postoperative period [5]. A recently published systematic review concluded that there is no benefit of antibiotic prophylaxis on implant survival in uncomplicated implant surgery in healthy patients [6].

Peri-implantitis is a pathological condition occurring in tissues surrounding dental implants, characterized by inflammation of the peri-implant mucosa and subsequent progressive loss of alveolar bone [7]. This infectious condition affects about two out of 10 patients [7,8,9]. With an estimation of 12 million implants placed annually worldwide by an increasing number of clinicians with varying expertise, there are concerns that peri-implantitis is a growing complication within dentistry [10]. Depending on the case definition applied [11], prevalence of peri-implantitis ranges from 10–22% at implant level [12] and 22–45% at patient level [13, 14].Typically, the development of peri-implantitis appears within the first few years after the implant has been functionally loaded [9].

Numerous peri-implantitis treatment protocols have been advocated, including non-surgical, surgical and combined approaches. Non-surgical treatment alone has shown unpredictable treatment outcomes [15, 16], while long-term data on outcomes following surgical treatment show only minor bone level gain [16, 17]. Nevertheless, access surgery is considered an essential part of the therapy with an impeding effect on the progression of peri-implantitis [16,17,18]. A “gold standard” protocol across the general population or in specific patient groups, has not yet been identified [18, 19]. Surveys of registered specialists in periodontology in Australia, the United Kingdom, and the United States confirm an absence of consensus and standardized therapeutic protocols [20, 21]. One explanation might be lack of high-quality studies limiting the opportunities to perform a meta-analysis on the effects of peri-implantitis treatment [18].

Over decades, it has been assumed that management of peri-implantitis could be adopted from treatment protocols and guidelines for periodontitis. In systemically healthy adult periodontitis cases, adjunctive use of systemic antibiotics is not justified due to minor infection risk following periodontal surgery [22,23,24]. Systemic antibiotic as part of systematic periodontal therapy is recommended only in immunocompromised cases or in cases with aggressive or non-responding periodontitis [22, 23]. Surprisingly, the majority of surgical peri-implantitis treatment protocols suggests adjunctive use of systemic antibiotics to target specific putative bacteria [16, 18, 25]. One argument for adjunctive usage, is that peri-implantitis infections are not confined to the connective tissue compartment and potentially could spread to bone marrow area [26]. Because of diverse microbiomes in peri-implantitis lesions, the use of broad-spectrum antibiotics might be necessary [25]. The drawbacks are not only increased risk of altering normal protective microflora, superinfections, and allergic reactions, but also to potentiate antibiotic resistance [27,28,29].

As there seems to be a lack of controlled clinical trials evaluating the efficacy of systemic antimicrobial therapy as an adjunct to surgical peri-implantitis therapy [30], additional outcome effect still remains questionable [16, 17, 29, 31, 32]. The scarce scientific documentation together with a shortage of treatment guidelines, may lead to excessive usage during surgical treatment of peri-implantitis [28]. Thus, the aim of the present systematic review was to provide knowledge by revisiting the available scientific literature through a two-stage approach consisting of quality appraisal of relevant systematic reviews and assessment of primary studies to critically evaluate the efficacy of systemically administered antibiotics as an adjunct to surgical treatment of peri-implantitis.

Methods

The study protocol was registered in the PROSPERO database (International Prospective Register of Systematic Reviews hosted by the National Institute of Health Research, University of York, Centre for Reviews and Dissemination) with the identification number CRD42020134989 [33]. The manuscript is prepared according to preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines [34].

Focused question

For the identification of relevant studies, the present review aims to address the following focused question: “Does systemically administered antibiotics improve treatment outcomes following surgical intervention of peri-implantitis?”

Criteria for considering studies (PICOT) [35]

The following Participants, Intervention, Comparison, Outcomes, and Time (PICOT) framework was employed to guide the inclusion and exclusion of studies for the focused question:

  • Participants (P): Patients with peri-implantitis who underwent surgical treatment

  • Intervention (I): (A) Surgical treatment of peri-implantitis. (B) Head-to-head comparison of different therapeutic antibiotic compounds or regiments

  • Comparison (C): Surgical treatment of peri-implantitis with and without systemically administered antibiotics, placebo, or other non-antibiotic treatment such as antiseptics rinsing

  • Outcome (0):

    Primary outcome: Radiographic marginal bone level.

    Secondary outcomes: Bleeding on probing (BoP)/suppuration on probing (SoP), probing depth (PD), pain, implant loss, microbial composition, and quality of life (QoL)

  • Time (T): Minimum follow-up of 3 months after surgical intervention

Eligibility criteria

To be eligible for inclusion, studies had to fulfil the following inclusion criteria:

  • Reporting randomized controlled trial (RCT), cohort study, case–control study, or systematic review

  • Include patients being surgically treated for peri-implantitis with and without adjunctive systemically administered antibiotic therapy

  • Abstract available in English language

The following exclusion criteria were applied:

  • In vitro or animal studies

  • Case reports

  • A follow-up less than 3 months

  • Non-surgical peri-implantitis treatment

  • Use of prophylactic antibiotics

  • No clear definition of peri-implantitis

  • Systematic reviews that were followed by more recent systematic reviews by the same author, non-systematic reviews, treatment guidelines, letters, position papers, and consensus statements

Search strategy

A detailed systematic literature search was undertaken by one author (MØ) and one expert reviewer at Medical Library at University of Bergen using the following four electronic databases: The National Library of Medicine (MEDLINE via PubMed), the Cochrane Central Register of Controlled Trials (The Cochrane Library, Wiley), EMBASE via OVID, and Web of Science. Hand-searching included reviewing citation lists of the retrieved full-text articles, and index search in three different journals (Journal of Periodontology, Journal of Clinical Periodontology, and Clinical Oral Implants Research). To detect more recent publications a complementary search was performed September 2021 in the four databases using the same search strategy as in the main search. No restrictions were set for date of publication, journal, or language.

The protocol for the bibliographic research was made on MeSH terms and free text words combined through Boolean Operators (AND, OR). Selection criteria were broad during identification and screening to decrease search specificity (anticipating low agreement between investigators, thus decreasing the risk of omitting relevant articles) and specific during inclusion to increase search precision. The primary search strategy was constructed based on two domains (“peri-implantitis”/“periimplantitis”) AND (“anti-bacterial agents”/ “anti-infective agents”). The search strategy for the various database is summarized in Additional file 1: Table S1.

Study selection

The retrieved list of publications was reviewed by MØ for a crude exclusion of irrelevant publications based on title. In case of uncertainty, a study was retained until next selection step. The remaining titles were screened by all four authors as a group. The abstracts were distributed among the four authors (MØ, KNL, BL, and DFB) who independently screened included abstracts and selected articles that met the inclusion/exclusion criteria. In case of uncertainty, the abstract was read by all four authors and a decision about study eligibility was reached through discussion and consensus among the reviewers. Eligible studies were included in the second round and allocated into primary studies and systematic reviews, which were read in full text independently in duplicates by two teams, respectively MØ/DFB and BL/KNL. Only studies fulfilling the inclusion criteria were reviewed and considered for data extraction. At each stage, disagreement between reviewers were solved through discussion and consensus; if a disagreement persisted, a third reviewer settled the discussion.

Data extraction and method of analysis

The goal of the quantitative assessment was to evaluate and compare the changes in QoL, pain, implant loss, microbial composition, patient characteristics, treatment approaches, and different outcome variables such as radiographic marginal bone level, BoP/SoP, and PD. A predetermined data extraction form based on the aforementioned criteria was used to record data from each included study. However, because of a lack of sufficient data on QoL and pain from the included RCTs, only quantitative analyses on the other variables were conducted. A meta-analysis was not performed because only two primary studies were included, both with moderate risk of bias, displaying heterogeneity in study designs and outcome variables [36].

Quality assessment

The risk of bias of the systematic reviews was assessed using AMSTAR [37]. The reviews were classified according to the criteria showed in Additional file 2: Table S2 as low, moderate, or high risk of bias. The level of bias in the primary studies was assessed using GRADE [38], listed in Table 1.

Table 1 Outcome of quality assessment of the primary studies using GRADE
Full size table

Two teams of reviewers independently evaluated the overall study quality and risk of bias of included reports, using all the checklist items of the respective scales. The articles were graded by the teams. In case of disagreement, consensus was achieved after discussion with the other team.

Results

Literature search

The initial literature search identified a total of 681 articles after de-duplication. The systematic search flow is outlined in Fig. 1. Twelve articles were retrieved through hand-search, whereas no additional articles were found in the grey literature search. Following first-stage screening of titles and abstracts and removal of additional duplicates, 36 articles qualified for full-text screening. Four articles were excluded due to a more recent publication based on the same patient material. Most of the studies included in the primary search was excluded due to lack of control group, being animal studies or testing other forms of peri-implantitis treatment strategies. Altogether 32 studies were included, of which 18 were primary studies and 14 systematic reviews.

Fig. 1
figure 1

Flow chart representing study selection and inclusion

Full size image

Study selection and qualitative assessment

Systematic reviews

Study selection

Following full text reading of the 14 systematic reviews, seven were included (Table 2). The main reasons for exclusion were “out of topic” [39,40,41,42,43], or “not considered as a systematic review” [28, 44]. Table 2 summarizes included and excluded systematic reviews.

Table 2 Included and excluded systematic reviews
Full size table
Quality assessment and data extraction

The quality assessment of the included systematic reviews identified two reports with moderate risk of bias due to lack of information about patient characteristics [18] and conflict of interest [45]. Five were considered as high risk of bias [16, 17, 31, 32, 46] because of shortcomings in study selection (missing flow chart or steps in recommended search strategy for systematic reviews and reporting that the quality assessment was made by only one researcher). No studies were deemed at low risk of bias. Table 3 summarizes the risk of bias in the included systematic reviews.

Table 3 Data extraction and risk of bias in the systematic reviews
Full size table
Estimated level of evidence

Four out of seven included systematic reviews concluded that no evidence exists indicating that systemic antibiotics improved the clinical outcomes of surgical treatment of peri-implantitis [18, 31, 32, 46]. One review did not estimate the level of evidence [16], one did not clearly state any beneficial effect [45], whereas one reported a limited adjunctive effect [17].

Primary studies

Study selection

A total of 18 primary studies were read in full text. Only two studies met the inclusion criteria [47, 48]. The main reasons for exclusion were lack of control groups [49,50,51,52,53,54], and/or that all included subjects received systemic antibiotics [55,56,57,58,59,60]. One study was excluded as a more recent report was published on the same material [61], one reported outcomes of non-surgical treatment [62], one adjunctive use of locally administered antibiotics [52], whereas one was a case report [63]. Table 4 summarizes included and excluded primary studies.

Table 4 Included and excluded primary studies
Full size table

In the case of two publications reporting on the same cohort at different follow-up intervals, it was decided to pool all relevant details as a single report providing more comprehensive data for inclusion in the qualitative and quantitative analyses. Insufficient volume of quantitative outcome data from only two included RCTs, precluded the use of meta-analysis [64].

Quality assessment and data extraction

Quality assessment of the two included studies rendered an estimated medium risk of bias for both [47, 48]. The main features of the two studies are shown in Table 5; population characteristics; peri-implantitis case definition; surgical protocol; and supportive care during follow-ups.

Table 5 Data characteristics in the primary studies
Full size table

Carcuac et al. compared surgical treatment of peri-implantitis with and without adjunctive use of amoxicillin in four groups of patients [48]. They followed 100 subjects with 179 implants over 3 years, with a participant mean age of 66.3 (21–90 years). In patient group 1 and 2, a 10-d systemic antibiotic regimen (amoxicillin 2 × 750 mg daily) started 3 days prior to surgery. Patients in group 3 and 4 did not receive systemic antibiotics. Hallström et al. compared treatment outcomes following surgical treatment with and without adjunctive use of Zithromax® (Sandoz AS, Copenhagen, Denmark) [47]. They followed 39 subjects with 39 implants for 1 year, with a participant mean age of 70.5 (26–86 years). The test group received Zithromax® 250 mg × 2 at the day of surgery, and 250 mg × 1 per day during 4 additional days. The 19 patients in the control group were treated with open flap debridement, whereas the 20 test individuals received open flap debridement and systemic antibiotics.

For both studies [47, 48], the treatment was performed by trained periodontists in a university stetting or at a hospital, but none of the studies provided detailed information about a supportive care protocol. The evaluations of each bias item for the included studies are summarized in Table 1.

Outcome

Additional file 3: Table S8 summarizes the effects of adjunctive use of systemic antibiotic following surgical treatment of peri-implantitis. From baseline to 3 years, Carcuac et al. reported a radiographic bone level gain of 0.32 ± 1.35 mm in the groups receiving systemic antibiotics (AB+), whereas a radiographic bone level loss of 0.51 ± 1.87 was observed in the non-antibiotic groups (AB−) [47]. However, the positive effect of systemic antibiotics faded after 1 year. From year 1 to year 3, a minor mean bone loss was detected in all four groups: Group 1 and 2 (AB+) and Group 3 and 4 (AB−) 0.21 ± 0.94 and 0.06 ± 1.37, respectively. Compared with baseline, increased PD (> 5 mm) was noted at 35% of the implants at 3 years. Systemic antibiotics decreased the probability for PD > 5 mm at implants with modified surfaces from 58 to 34%. An opposite effect was observed at non-modified implants (AB−: 9%; AB+: 22%). At 3 years, systemic antibiotics had no effect in terms of reduced BoP/SoP.

Of 121 implants included, 69% were successfully treated according to the authors (no bone loss > 0.5 mm). Totally, 20 implants were explanted (six at year 1) during the observation period. Predicted probability of a successful outcome varied between 91% (AB−) and 89% (AB+) for non-modified surface implants and between 32% (AB−) and 78% (AB+) for modified surface implants. Benefits of systemic antibiotics were limited to implants with modified surfaces (0.3 mm (AB+) and − 1.3 mm (AB−) and to the first year of follow-up [48].

At 1 year, Hallström et al. reported a non-significant bone level gain of 0.6 mm in patients receiving systemic antibiotics (+ 0.6 mm) and 0.4 mm in the control group without systemic antibiotics (+ 0.4 mm) [47]. In this study, successful clinical outcome was defined as PD ≤ 5 mm, no suppuration, no BoP at the implant site, and bone loss ≤ 0.5 mm at 1 year. A successful study outcome was identified in seven individuals (46.7%) in the test and four individuals (25%) in the control group. Carcuac et al. did not define successful clinical outcome, but analysed clinical and radiographic changes at baseline, at 1 and 3 years [47]. None of the studies evaluated patient-related outcomes. Sample size calculation to estimate the minimal number of individuals needed to detect a significant positive treatment outcome between groups, was only reported in the Hallström’s study.

Discussion

Summary of main results and clinical relevance

By reviewing original studies and systematic reviews, the present review shows that there is at best, limited evidence for a sustained adjunctive effect of systemically administered antibiotics in surgical treatment of peri-implantitis. Systemic antibiotics might be beneficial as adjunct to surgical treatment in specific group of patients and implants with specific surface modifications. Previous clinical studies have major shortcomings as lack of information about patient characteristics, absence of high-quality long-term (> 3 years of follow-up) RCTs, and authors’ declaration on conflict of interest. The impact of these shortcomings is discussed in the present systematic review.

An included systematic review from 2002, concluded that the evidence for a consistent and clinically relevant advantage using systemically administered antibiotics can be questioned [32]. Special attention was drawn to the problem with no standardized protocol in treatment of peri-implantitis and the lack of RCT’s with a low grade of bias. This perception is supported by all included systematic reviews, and particularly highlighted in the latest review from 2019, stating that there is a need for well-designed RCTs with sufficient power to evaluate surgical non-regenerative treatment of peri-implantitis [11]. When pooling data from the seven included systematic reviews, 69% of the included primary studies used systemically or locally administered antimicrobial therapy as a part of the surgical treatment protocol of peri-implantitis. This documents that adjunctive use of antimicrobials is a general trend more than an exception.

In the included primary studies, there were limited information about patient characteristics. Hallström et al. registered smoking status [47], but neither Carcuac et al. nor Hallström et al. discussed the potential impact of patient characteristics on the treatment outcomes [47, 48]. On the other hand, Carcuac et al. reported that implant surface characteristics may impact peri-implantitis susceptibility and resolution of inflammation [48]. At 3 years, treatment success was more frequent observed at implants with a non-modified (“turned”) surface compared with implants with modified surface [48]. This indicates that the effect of adjunctive systemic antibiotics in the surgical treatment of peri-implantitis may be dependent on patient as well as implant surface characteristics.

In 2016 The World Health Organization (WHO) decided to prioritize the development of evidence-based recommendations for use of antibiotics in surgical therapy [65]. WHO does not recommend prolonged surgical antibiotic prophylaxis after completion of the surgery for the purpose of preventing site infections. The recommendation of these drugs in oral medicine should follow the same precepts as those of general medicine [22]. However, lack of treatment guidelines, slow adoption of guidelines, a varied skill set of the average dentist, and pressure from the patients, might contribute to unnecessary antibiotics prescriptions [66]. The awareness among dentists and administrative personnel of their responsibility for the increasing antibiotic resistance should therefore be highlighted.

Management of antimicrobial resistance requires the implementations of two processes: infection control practices to limit spread of resistant microorganisms and hospital policies of good antimicrobial use stewardship, which may include antimicrobial usage control [67]. Generally, multidrug resistant bacteria are a growing global concern most likely caused by frequent and inappropriate use of antibiotics [68,69,70,71]. Data from the United States show that up to 60% of the microorganisms isolated from infected surgical wounds was antibiotic resistant [65]. Concerns have also been raised that an extensive use of systemic antibiotics in periodontal therapy, particularly when administered to counterbalance incomplete mechanical instrumentation or poor oral hygiene, could contribute substantially to the development of bacterial antimicrobial resistance [72,73,74]. Similar concerns should be expressed to peri-implantitis treatment protocol comprising systemically administered antibiotics. A recently published systematic review found that most of the 18 included primary studies did not report full-mouth plaque scores [45]. Nevertheless, 13 of the 18 studies used systemically administered antibiotics as part of the surgical treatment protocol.

Comparison with other studies

Treatment of peri-implantitis aims to re-establish and maintain peri-implant health around implants with reduced bone support [75]. The main goal is to mechanically remove or disturb the bacterial biofilm contaminating the exposed implant surface. Long-term data attained from the included systematic reviews, reveal only minor changes in quantitative parameters such as BoP, SoP, radiographic bone level gain, and reduction in PD following systemically administered antibiotics as an adjunct to surgical treatment of peri-implantitis. Studies reporting superior treatment outcomes are exceptions, and their quality assessments have categorized the risk of bias as high [18, 31].

None of the included systematic reviews discussed microbiological changes before and after surgical treatment and only one of the primary studies investigated bacterial composition. Hallström et al. failed to find any statistical differences in bacterial load between the two treatment groups in their RCT [47]. Trends of decreasing bacterial loads were found between baseline, 2 and 4 weeks in both the experimental and the control group. Regarding periodontitis, Haffajee found that the short-term benefit of adjunctive systemic antibiotic treatment was not critical for the long term survival of teeth [72]. A bone gain of 0.3 mm would be equivalent to reversing 4–7 years of disease progression in a well-maintained population. Similarly, the included RCTs and systematic reviews indicate that on average, systemically administered antibiotics contribute to therapeutic short time success in the treatment of peri-implantitis but fails to generate the long-term benefit.

The wide heterogeneity of peri-implant disease definition has also been a problem in the field of peri-implantitis research. All included systematic reviews reported wide heterogeneity of peri-implant disease definition. Until World Workshop of Periodontitis 2017 [9], no uniform clinical definition of peri-implantitis existed. Although bone loss and clinical manifestation of inflammation are the most important diagnostic criteria of peri-implantitis, a significant crestal bone loss over time must be verified to distinguish between peri-implant mucositis and peri-implantitis. The large variations in case-definitions make it inapplicable to compare different study outcomes following treatment of peri-implantitis. This partly reflects the wide heterogeneity of conclusions in former systematic reviews and lack of treatment standards founded in meta-analysis [76]. The majority of the included systematic reviews highlight this point in the discussion and conclusion section.

Strength and limitation of the study

A common denominator trough all included systematic reviews was that no conclusion could be drawn due to lack of high-quality studies. The present review specified inclusion criteria as minimum follow-up time of 3 months, presence of control group, and low or moderate level of bias. The primary search included 681 studies on surgical treatment of peri-implantitis. Of these, only two RCTs fulfilled the criteria [47, 48]. The lack of high-quality studies might be related to high research costs and ethical issues when designing and testing pharmacological drugs in RCT. Research bias towards publishing positive and encouraging results is another dilemma [77].

The market for dental implants keeps growing, and the size of the global market for dental implants had a value of USD 3.6 billion in 2020 [78]. Interestingly, the main sponsorship of major national and international conferences has been carried out by implant and biomaterial industries [79]. The leading implant companies may focus on functionality rather than biological complications and environmental dilemmas with overuse of antibiotics. Detailed information on potential conflict of interest and sponsorship are pivotal for an adequate understanding and appropriate interpretation of the reported study outcomes. Not only financial conflict of interest (COI), but also academical. In five of the included systematic reviews a COI statement was not included. One systematic review found that only four of 18 included studies reported on funding [45]. Another review of RCT`s, showed that seven out of nine included studies were funded by industry directly involved in the product being tested; one study did not receive funding, and one reported unclear funding [80]. The prevalence of COI statements/sections seems to be more underreported (32.1%) in dental journals compared with other medical journals (13.6%) [81]. However, a systematic review that compared sponsored and non-sponsored RCT assessing different implant systems, found no significant difference in marginal bone loss related to sponsorship status [82].

Finally, some additional study limitations should be acknowledged. (1) Lack of uniform diagnostic criteria. (2) Different implant surface modifications. (3) Variation in length of follow-up and treatment modalities. (4) The included RCTs are from the same country, published the same year, and in the same journal. (5) Restricted inclusion criteria. RCTs were only included if the primary outcome was comparison of surgical therapy of peri-implantitis with and without adjunctive systemically administered antibiotics and if the bias rate was low or moderate. (6) Only including two RCTs resulting in data scarcity and heterogeneity precluding meta-analysis. (7) None of the included studies were considered at low risk of bias, indicating a strict interpretation in the use of GRADE and AMSTAR guidelines.

Conclusions

The use of systemically administered antibiotics as an adjunct to surgical interventions of peri-implantitis cannot be justified as a part of a standard treatment protocol. Considering the pathological pattern of peri-implantitis, systemic antibiotics might be beneficial as adjunct to surgical treatment in specific patient groups and implants with specific surface characteristics. In these cases, benefit versus harm analysis including considerations on the overall use of antibiotics for the individual patient and public health must be considered. This systematic review shows that there is limited evidence for adjunctive use of systemic antibiotics due to scarcity of published high-quality clinical studies. Future studies evaluating the efficacy of systemically administered antibiotics as an adjunct to surgical treatment of peri-implantitis in high-quality long-term RCT are warranted.

Availability of data and materials

Not applicable.

Abbreviations

PICOT:

Participants, intervention, comparison, outcomes, and time

BoP:

Bleeding on probing

SoP:

Suppuration on probing

QoL:

Quality of life

RCT:

Randomized controlled trial

COI:

Conflict of interest

References

  1. Cervino G, Cicciu M, Biondi A, Bocchieri S, Herford AS, Laino L, et al. Antibiotic prophylaxis on third molar extraction: systematic review of recent data. Antibiotics. 2019;8(2):53.

    Article  PubMed Central  Google Scholar 

  2. Esposito M, Grusovin MG, Worthington HV. Interventions for replacing missing teeth: antibiotics at dental implant placement to prevent complications. Cochrane Database Syst Rev. 2013;2013(7):CD004152.

    PubMed Central  Google Scholar 

  3. Ahmad N, Saad N. Effects of antibiotics on dental implants: a review. J Clin Med Res. 2012;4(1):1–6.

    PubMed  PubMed Central  Google Scholar 

  4. Schwartz AB, Larson EL. Antibiotic prophylaxis and postoperative complications after tooth extraction and implant placement: a review of the literature. J Dent. 2007;35(12):881–8.

    Article  PubMed  Google Scholar 

  5. Adell R, Lekholm U, Rockler B, Branemark PI. A 15-year study of osseointegrated implants in the treatment of the edentulous jaw. Int J Oral Surg. 1981;10(6):387–416.

    Article  PubMed  Google Scholar 

  6. Lund B, Hultin M, Tranaeus S, Naimi-Akbar A, Klinge B. Complex systematic review—perioperative antibiotics in conjunction with dental implant placement. Clin Oral Implants Res. 2015;26(Suppl 11):1–14.

    Article  PubMed  Google Scholar 

  7. Schwarz F, Derks J, Monje A, Wang H-L. Peri-implantitis. J Clin Periodontol. 2018;45(S20):S246–66.

    Article  PubMed  Google Scholar 

  8. Lindhe J, Meyle J, Group DoEWoP. Peri-implant diseases: consensus report of the sixth European workshop on periodontology. J Clin Periodontol. 2008;35(8 Suppl):282–5.

    Article  PubMed  Google Scholar 

  9. Renvert S, Persson GR, Pirih FQ, Camargo PM. Peri-implant health, peri-implant mucositis, and peri-implantitis: case definitions and diagnostic considerations. J Clin Periodontol. 2018;45(Suppl 20):S278–85.

    Article  PubMed  Google Scholar 

  10. Klinge B, Klinge A, Bertl K, Stavropoulos A. Peri-implant diseases. Eur J Oral Sci. 2018;126(Suppl 1):88–94.

    Article  PubMed  Google Scholar 

  11. Tomasi C, Derks J. Clinical research of peri-implant diseases—quality of reporting, case definitions and methods to study incidence, prevalence and risk factors of peri-implant diseases. J Clin Periodontol. 2012;39(Suppl 12):207–23.

    Article  PubMed  Google Scholar 

  12. Salvi GE, Cosgarea R, Sculean A. Prevalence of periimplant diseases. Implant Dent. 2019;28(2):100–2.

    Article  PubMed  Google Scholar 

  13. Derks J, Tomasi C. Peri-implant health and disease. A systematic review of current epidemiology. J Clin Periodontol. 2015;42(Suppl 16):S158–71.

    Article  PubMed  Google Scholar 

  14. Derks J, Schaller D, Hakansson J, Wennstrom JL, Tomasi C, Berglundh T. Effectiveness of implant therapy analyzed in a Swedish population: prevalence of peri-implantitis. J Dent Res. 2016;95(1):43–9.

    Article  PubMed  Google Scholar 

  15. Faggion CM Jr, Chambrone L, Listl S, Tu YK. Network meta-analysis for evaluating interventions in implant dentistry: the case of peri-implantitis treatment. Clin Implant Dent Relat Res. 2013;15(4):576–88.

    Article  PubMed  Google Scholar 

  16. Renvert S, Polyzois I, Claffey N. Surgical therapy for the control of peri-implantitis. Clin Oral Implants Res. 2012;23(Suppl 6):84–94.

    Article  PubMed  Google Scholar 

  17. Keeve PL, Koo KT, Ramanauskaite A, Romanos G, Schwarz F, Sculean A, et al. Surgical treatment of periimplantitis with non-augmentative techniques. Implant Dent. 2019;28(2):177–86.

    Article  PubMed  Google Scholar 

  18. Heitz-Mayfield LJ, Mombelli A. The therapy of peri-implantitis: a systematic review. Int J Oral Maxillofac Implants. 2014;29(Suppl):325–45.

    Article  PubMed  Google Scholar 

  19. Claffey N, Clarke E, Polyzois I, Renvert S. Surgical treatment of peri-implantitis. J Clin Periodontol. 2008;35(8 Suppl):316–32.

    Article  PubMed  Google Scholar 

  20. Papathanasiou E, Finkelman M, Hanley J, Parashis AO. Prevalence, etiology and treatment of peri-implant mucositis and peri-implantitis: a survey of periodontists in the United States. J Periodontol. 2016;87(5):493–501.

    Article  PubMed  Google Scholar 

  21. Mattheos N, Collier S, Walmsley AD. Specialists’ management decisions and attitudes towards mucositis and peri-implantitis. Br Dent J. 2012;212(1):E1.

    Article  PubMed  Google Scholar 

  22. Feres M, Figueiredo LC, Soares GMS, Faveri M. Systemic antibiotics in the treatment of periodontitis. Periodontol 2000. 2015;67(1):131–86.

    Article  PubMed  Google Scholar 

  23. Jepsen K, Jepsen S. Antibiotics/antimicrobials: systemic and local administration in the therapy of mild to moderately advanced periodontitis. Periodontol 2000. 2016;71(1):82–112.

    Article  PubMed  Google Scholar 

  24. Seymour RA, Hogg SD. Antibiotics and chemoprophylaxis. Periodontol 2000. 2000;2008(46):80–108.

    Google Scholar 

  25. Heitz-Mayfield LJA, Salvi GE, Mombelli A, Faddy M, Lang NP. Anti-infective surgical therapy of peri-implantitis. A 12-month prospective clinical study. Clin Oral Implants Res. 2012;23(2):205–10.

    Article  PubMed  Google Scholar 

  26. Lindhe J, Berglundh T, Ericsson I, Liljenberg B, Marinello C. Experimental breakdown of peri-implant and periodontal tissues. A study in the beagle dog. Clin Oral Implants Res. 1992;3(1):9–16.

    Article  PubMed  Google Scholar 

  27. Nibali L, Koidou VP, Hamborg T, Donos N. Empirical or microbiologically guided systemic antimicrobials as adjuncts to non-surgical periodontal therapy? A systematic review. J Clin Periodontol. 2019;46(10):999–1012.

    Article  PubMed  Google Scholar 

  28. Verdugo F, Laksmana T, Uribarri A. Systemic antibiotics and the risk of superinfection in peri-implantitis. Arch Oral Biol. 2016;64:39–50.

    Article  PubMed  Google Scholar 

  29. Enersen M, Hultin M, Kønønen E, Poulsen A, Simm R. Antibiotics in the treatment of periodontal and peri-implant infections. NorTannlegeforen Tid. 2019;109:224–35.

    Google Scholar 

  30. Renvert S, Polyzois I. Treatment of pathologic peri-implant pockets. Periodontol 2000. 2018;76(1):180–90.

    Article  PubMed  Google Scholar 

  31. Heitz-Mayfield LJ, Lang NP. Antimicrobial treatment of peri-implant diseases. Int J Oral Maxillofac Implants. 2004;19(Suppl):128–39.

    PubMed  Google Scholar 

  32. Klinge B, Gustafsson A, Berglundh T. A systematic review of the effect of anti-infective therapy in the treatment of peri-implantitis. J Clin Periodontol. 2002;29(Suppl 3):213–25 (discussion 32–3).

    Article  PubMed  Google Scholar 

  33. www.crd.york.ac.uk/PROSPERO. Accessed 28/04/2020.

  34. Liberati A, Altman DG, Tetzlaff J, Mulrow C, Gotzsche PC, Ioannidis JP, et al. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration. J Clin Epidemiol. 2009;62(10):e1-34.

    Article  PubMed  Google Scholar 

  35. Stillwell SB, Fineout-Overholt E, Melnyk BM, Williamson KM. Evidence-based practice, step by step: asking the clinical question: a key step in evidence-based practice. Am J Nurs. 2010;110(3):58–61.

    Article  PubMed  Google Scholar 

  36. Moher D, Pham B, Jones A, Cook DJ, Jadad AR, Moher M, et al. Does quality of reports of randomised trials affect estimates of intervention efficacy reported in meta-analyses? Lancet. 1998;352(9128):609–13.

    Article  PubMed  Google Scholar 

  37. Shea BJ, Reeves BC, Wells G, Thuku M, Hamel C, Moran J, et al. AMSTAR 2: a critical appraisal tool for systematic reviews that include randomised or non-randomised studies of healthcare interventions, or both. BMJ. 2017;358:j4008.

    Article  PubMed  PubMed Central  Google Scholar 

  38. 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 

  39. Chan HL, Lin GH, Suarez F, MacEachern M, Wang HL. Surgical management of peri-implantitis: a systematic review and meta-analysis of treatment outcomes. J Periodontol. 2014;85(8):1027–41.

    Article  PubMed  Google Scholar 

  40. Esposito M, Grusovin MG, Worthington HV. Interventions for replacing missing teeth: treatment of peri-implantitis. Cochrane Database Syst Rev. 2012;1:CD004970.

    PubMed  Google Scholar 

  41. Kotsovilis S, Karoussis IK, Trianti M, Fourmousis I. Therapy of peri-implantitis: a systematic review. J Clin Periodontol. 2008;35(7):621–9.

    Article  PubMed  Google Scholar 

  42. Naujokat H, Kunzendorf B, Wiltfang J. Dental implants and diabetes mellitus—a systematic review. Int J Implant Dent. 2016;2(1):5.

    Article  PubMed  PubMed Central  Google Scholar 

  43. Schwarz F, Schmucker A, Becker J. Efficacy of alternative or adjunctive measures to conventional treatment of peri-implant mucositis and peri-implantitis: a systematic review and meta-analysis. Int J Implant Dent. 2015;1(1):22.

    Article  PubMed  PubMed Central  Google Scholar 

  44. Schou S, Berglundh T, Lang NP. Surgical treatment of peri-implantitis. Int J Oral Maxillofac Implants. 2004;19:140–9.

    PubMed  Google Scholar 

  45. Roccuzzo M, Layton DM, Roccuzzo A, Heitz-Mayfield LJ. Clinical outcomes of peri-implantitis treatment and supportive care: a systematic review. Clin Oral Implants Res. 2018;29(Suppl 16):331–50.

    Article  PubMed  Google Scholar 

  46. Mombelli A, Moene R, Decaillet F. Surgical treatments of peri-implantitis. Eur J Oral Implantol. 2012;5(Suppl):S61-70.

    PubMed  Google Scholar 

  47. Hallström H, Persson GR, Lindgren S, Renvert S. Open flap debridement of peri-implantitis with or without adjunctive systemic antibiotics: a randomized clinical trial. J Clin Periodontol. 2017;44(12):1285–93.

    Article  PubMed  Google Scholar 

  48. Carcuac O, Derks J, Abrahamsson I, Wennström JL, Petzold M, Berglundh T. Surgical treatment of peri-implantitis: 3-year results from a randomized controlled clinical trial. J Clin Periodontol. 2017;44(12):1294–303.

    Article  PubMed  Google Scholar 

  49. Bianchini MA, Galarraga-Vinueza ME, Apaza-Bedoya K, De Souza JM, Magini R, Schwarz F. Two to six-year disease resolution and marginal bone stability rates of a modified resective-implantoplasty therapy in 32 peri-implantitis cases. Clin Implant Dent Relat Res. 2019;21(4):758–65.

    PubMed  Google Scholar 

  50. Charalampakis G, Rabe P, Leonhardt A, Dahlen G. A follow-up study of peri-implantitis cases after treatment. J Clin Periodontol. 2011;38(9):864–71.

    Article  PubMed  Google Scholar 

  51. Khoury F, Buchmann R. Surgical therapy of peri-implant disease: a 3-year follow-up study of cases treated with 3 different techniques of bone regeneration. J Periodontol. 2001;72(11):1498–508.

    Article  PubMed  Google Scholar 

  52. Maximo MB, de Mendonca AC, Renata Santos V, Figueiredo LC, Feres M, Duarte PM. Short-term clinical and microbiological evaluations of peri-implant diseases before and after mechanical anti-infective therapies. Clin Oral Implants Res. 2009;20(1):99–108.

    Article  PubMed  Google Scholar 

  53. Mercado F, Hamlet S, Ivanovski S. Regenerative surgical therapy for peri-implantitis using deproteinized bovine bone mineral with 10% collagen, enamel matrix derivative and Doxycycline-A prospective 3-year cohort study. Clin Oral Implants Res. 2018;29(6):583–91.

    Article  PubMed  Google Scholar 

  54. Serino G, Turri A. Outcome of surgical treatment of peri-implantitis: results from a 2-year prospective clinical study in humans. Clin Oral Implants Res. 2011;22(11):1214–20.

    Article  PubMed  Google Scholar 

  55. Heitz-Mayfield LJA, Salvi GE, Mombelli A, Faddy M, Lang NP. Implant complication Res G. Anti-infective surgical therapy of peri-implantitis. A 12-month prospective clinical study. Clin Oral Implants Res. 2012;23(2):205–10.

    Article  PubMed  Google Scholar 

  56. Heitz-Mayfield LJA, Salvi GE, Mombelli A, Loup PJ, Heitz F, Kruger E, et al. Supportive peri-implant therapy following anti-infective surgical peri-implantitis treatment: 5-year survival and success. Clin Oral Implant Res. 2018;29(1):1–6.

    Article  Google Scholar 

  57. Jepsen K, Jepsen S, Laine ML, Anssari Moin D, Pilloni A, Zeza B, et al. Reconstruction of peri-implant osseous defects: a multicenter randomized trial. J Dent Res. 2016;95(1):58–66.

    Article  PubMed  Google Scholar 

  58. Mombelli A, Lang NP. Antimicrobial treatment of peri-implant infections. Clin Oral Implants Res. 1992;3(4):162–8.

    Article  PubMed  Google Scholar 

  59. Roos-Jansaker AM, Lindahl C, Persson GR, Renvert S. Long-term stability of surgical bone regenerative procedures of peri-implantitis lesions in a prospective case-control study over 3 years. J Clin Periodontol. 2011;38(6):590–7.

    Article  PubMed  Google Scholar 

  60. Roccuzzo M, Pittoni D, Roccuzzo A, Charrier L, Dalmasso P. Surgical treatment of peri-implantitis intrabony lesions by means of deproteinized bovine bone mineral with 10% collagen: 7-year-results. Clin Oral Implants Res. 2017;28(12):1577–83.

    Article  PubMed  Google Scholar 

  61. Carcuac O, Derks J, Charalampakis G, Abrahamsson I, Wennström J, Berglundh T. Adjunctive systemic and local antimicrobial therapy in the surgical treatment of peri-implantitis: a randomized controlled clinical trial. J Dent Res. 2016;95(1):50–7.

    Article  PubMed  Google Scholar 

  62. Buchter A, Meyer U, Kruse-Losler B, Joos U, Kleinheinz J. Sustained release of doxycycline for the treatment of peri-implantitis: randomised controlled trial. Br J Oral Maxillofac Surg. 2004;42(5):439–44.

    Article  PubMed  Google Scholar 

  63. Verdugo F. Risk of superinfection in peri-implantitis after systemic broad spectrum antibiotics. Int J Periodont Rest. 2018;38(3):443–50.

    Google Scholar 

  64. Gurevitch J, Koricheva J, Nakagawa S, Stewart G. Meta-analysis and the science of research synthesis. Nature. 2018;555(7695):175–82.

    Article  PubMed  Google Scholar 

  65. Allegranzi B, Bischoff P, de Jonge S, Kubilay NZ, Zayed B, Gomes SM, et al. New WHO recommendations on preoperative measures for surgical site infection prevention: an evidence-based global perspective. Lancet Infect Dis. 2016;16(12):e276–87.

    Article  PubMed  Google Scholar 

  66. Durkin MJ, Hsueh K, Sallah YH, Feng Q, Jafarzadeh SR, Munshi KD, et al. An evaluation of dental antibiotic prescribing practices in the United States. J Am Dent Assoc. 2017;148(12):878-86.e1.

    Article  PubMed  PubMed Central  Google Scholar 

  67. Shlaes DM, Gerding DN, John JF Jr, Craig WA, Bornstein DL, Duncan RA, et al. Society for Healthcare Epidemiology of America and Infectious Diseases Society of America Joint Committee on the Prevention of Antimicrobial Resistance: guidelines for the prevention of antimicrobial resistance in hospitals. Infect Control Hosp Epidemiol. 1997;18(4):275–91.

    Article  PubMed  Google Scholar 

  68. Tacconelli E, Sifakis F, Harbarth S, Schrijver R, van Mourik M, Voss A, et al. Surveillance for control of antimicrobial resistance. Lancet Infect Dis. 2018;18(3):e99–106.

    Article  PubMed  Google Scholar 

  69. WHO. Antimicrobial resistance: global report on surveillance 2014. WHO; 2014. p. 257.

    Google Scholar 

  70. Roca I, Akova M, Baquero F, Carlet J, Cavaleri M, Coenen S, et al. The global threat of antimicrobial resistance: science for intervention. New Microbes New Infect. 2015;6:22–9.

    Article  PubMed  PubMed Central  Google Scholar 

  71. European Antimicrobial Resistance Surveillance Network (EARS-Net). https://ecdc.europa.eu/en/about-us/partnerships-and-networks/disease-and-laboratory-networks/ears-net.

  72. Haffajee AD. Systemic antibiotics: to use or not to use in the treatment of periodontal infections. That is the question. J Clin Periodontol. 2006;33(5):359–61.

    Article  PubMed  Google Scholar 

  73. Mombelli A, Cionca N, Almaghlouth A. Does adjunctive antimicrobial therapy reduce the perceived need for periodontal surgery? Periodontol 2000. 2011;55:205–16.

    Article  PubMed  Google Scholar 

  74. van Winkelhoff AJ, Winkel EG. Antibiotics in periodontics: right or wrong? J Periodontol. 2009;80(10):1555–8.

    Article  PubMed  Google Scholar 

  75. Caton JG, Armitage G, Berglundh T, Chapple ILC, Jepsen S, Kornman KS, et al. A new classification scheme for periodontal and peri-implant diseases and conditions—introduction and key changes from the 1999 classification. J Periodontol. 2018;89(Suppl 1):S1–8.

    PubMed  Google Scholar 

  76. Ramanauskaite A, Daugela P, Juodzbalys G. Treatment of peri-implantitis: meta-analysis of findings in a systematic literature review and novel protocol proposal. Quintessence Int. 2016;47(5):379–93.

    PubMed  Google Scholar 

  77. Wu X, Yan Q, Fang X, Hua F, Shi B, Tu YK. Spin in the abstracts of randomized controlled trials in periodontology and oral implantology: a cross-sectional analysis. J Clin Periodontol. 2020;47:1079–86.

    Article  Google Scholar 

  78. Research GV. Dental implant market size, share & trends analysis report by implants type (titanium, zirconium), by region (North America, Europe Asia Pacific, Latin America, MEA), and segment forecasts. Research GV; 2021. p. 2021–8.

    Google Scholar 

  79. Matarese G, Ramaglia L, Fiorillo L, Cervino G, Lauritano F, Isola G. Implantology and periodontal disease: the panacea to problem solving? Open Dent J. 2017;11:460–5.

    Article  PubMed  PubMed Central  Google Scholar 

  80. Esposito M, Grusovin MG, Worthington HV. Treatment of peri-implantitis: what interventions are effective? A cochrane systematic review. Eur J Oral Implantol. 2012;5(Suppl):S21-41.

    PubMed  Google Scholar 

  81. Faggion CM, Pandis N, Cardoso GC, Rodolfo B, Morel LL, Moraes RR. Reporting of conflict of interest and sponsorship in dental journals. J Dent. 2020;102:103452.

    Article  PubMed  Google Scholar 

  82. Dos Santos MBF, Agostini BA, de Moraes RR, Schwendicke F, Sarkis-Onofre R. Industry sponsorship bias in clinical trials in implant dentistry: systematic review and meta-regression. J Clin Periodontol. 2019;46(4):510–9.

    Article  PubMed  Google Scholar 

  83. Cha JK, et al. Surgical therapy of peri-implantitis with local minocycline: a 6-month randomized controlled clinical trial. J Dent Res. 2019;98(3):288–95.

    Article  PubMed  Google Scholar 

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Acknowledgements

The authors would like to acknowledge the Medical Library at University of Bergen, for skillful assistance during the literature search and Professor Einar Berg for reviewing the manuscript.

Funding

The study was self-funded by the authors and their institutions.

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Authors and Affiliations

  1. Department of Clinical Dentistry – Periodontics, Faculty of Medicine, University of Bergen, Aarstadveien 19, 5009, Bergen, Norway

    Malene Øen, Knut N. Leknes & Dagmar F. Bunæs

  2. Division of Oral Diagnostics and Oral Rehabilitation, Department of Dental Medicine, Karolinska Institutet and Medical Unit for Reconstructive Plastic- and Craniofacial Surgery, Karolinska University Hospital, Stockholm, Sweden

    Bodil Lund

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  1. Malene Øen
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  3. Bodil Lund
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Contributions

All authors have made substantial contributions to conception and design of the study. MØ collected the data. MØ, DFB, KNL and BL have been involved in data interpretation, drafting the manuscript, and revising it critically and have given final approval of publishing. All authors read and approved the final manuscript.

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Supplementary Information

Additional file 1: Table S1.

Strategy for the literature search.

Additional file 2: Table S2.

Quality assessment of the systematic reviews.

Additional file 3: Table S8.

Outcome variables in the primary studies.

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Øen, M., Leknes, K.N., Lund, B. et al. The efficacy of systemic antibiotics as an adjunct to surgical treatment of peri-implantitis: a systematic review. BMC Oral Health 21, 666 (2021). https://doi.org/10.1186/s12903-021-02020-1

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BMC Oral Health

ISSN: 1472-6831

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