A novel non-surgical method for mild peri-implantitis- a multicenter consecutive case series
© The Author(s). 2017
Received: 8 April 2017
Accepted: 13 July 2017
Published: 3 August 2017
The aim of the present study was to evaluate the effect on peri-implant mucosal inflammation from the use of a novel instrument made of chitosan in the non-surgical treatment of mild peri-implantitis across several clinical centers.
Materials and methods
In this 6-month multicenter prospective consecutive case series performed in six different periodontal specialist clinics, 63 implants in 63 patients were finally included. The subjects had mild peri-implantitis defined as radiographic bone loss of 1–2 mm, pocket probing depth (PPD) ≥4 mm and a positive bleeding on probing (mBoP) score. The patients were clinically examined at baseline and after 2, 4, 12 and 24 weeks, and radiographs were taken at baseline and at 3 and 6 months. Treatment of the implants with the chitosan brush seated in an oscillating dental drill piece was performed at baseline and at 3 months. Reductions in the clinical parameters (PPD and mBoP) were compared between baseline and the later examination time points.
Significant reductions in both PPD and mBoP were observed at all time points compared with the baseline clinical measurements (p < 0.001). The mean PPD and mBoP at baseline were 5.15 mm (4.97; 5.32) and 1.86 (1.78; 1.93), respectively, whereas the mean PPD and mBoP at 6 months were 4.0 mm (3.91; 4.19) and 0.64 (0.54; 0.75), respectively. Stable reductions in PPD and mBoP were evident up to 6 months after the initial treatment and 3 months after the second treatment. All 63 implants were reported to have stable radiographic levels of osseous support.
This case series demonstrated that an oscillating chitosan brush is safe to use and seems to have merits in the non-surgical treatment of dental implants with mild peri-implantitis. To measure the effectiveness of the method, a multicenter randomized clinical trial needs to be undertaken.
Inflammation and loss of attachment around dental implants (i.e. peri-implantitis) has become a growing concern within the field of dental implantology [1–7]. Peri-implantitis is a microbial infection-driven soft tissue inflammation with loss of bony attachment around an implant. Peri-implant mucositis is the precursor of peri-implantitis, as gingivitis is for periodontitis . It is clearly shown that daily infection control performed by the patient and regular professional maintenance of dental implants is important to prevent the progression of mucositis to peri-implantitis [9–12]. In advanced cases, peri-implantitis may lead to implant loss.
The current view is that most cases of peri-implantitis are unmanageable without surgical intervention. However, the stage of disease progression at which surgery is necessary remains undefined, and limited scientific evidence is available regarding surgical methods that hinder the progression of the disease over time. Because peri-implantitis surgery often involves a high level of patient morbidity, the development of non-surgical and less-invasive treatment methods is of interest for both patients and the dental community. Currently used methods for non-surgical implant debridement include titanium curettes, plastic or carbon fibre curettes, ultrasound, air-polishing and lasers. No particular non-surgical treatment for peri-implantitis resulting in superior outcomes is however supported by sufficient scientific evidence [13, 14]. Furthermore, some procedures have been suggested to cause more problems rather than improving peri-implant health . The crux is to intervene and to treat the inflammation without causing further problems that may contribute to the progression of peri-implant attachment loss. For example, leaving remnants of an instrument could cause a foreign body reaction, which may accelerate disease progression and attachment loss . Similarly, using an ultrasonic steel tip may induce damage to the titanium surface whereas a nylon tip may result in melted material remnants on the implant surface . In a recent study by Eger et al. , it was reported that debridement of titanium surfaces with an ultrasonic device may release titanium particles that was shown to induce a pronounced inflammatory response which caused osteoclastogenesis. The use of ultrasonic devices on titanium surfaces may thus aggravate peri-implantitis rather than resolve the situation.
Chitosan is a marine biopolymer which is based on chitin derived from the shells of marine crustaceans. The material has been approved for use in surgical bandages, as a haemostatic agent and as a dietary supplement in a wide range of nutritional and health products. Chitosan has also been documented to be non-allergenic and may exhibit anti-inflammatory properties. The material is demonstrated to be completely biocompatible which also recently was verified in an animal experimental study . In a pilot randomized split mouth clinical trial including 11 patients with mucositis, it was demonstrated that debridement with a chitosan device or titanium curettes lead to significant reduction in peri-implant mucositis. A better reduction in parameters of inflammation was however seen at 4 weeks at the implants treated with the chitosan device as compared with titanium curettes (Wohlfahrt et al. submitted for publication).
In the present study, the aim was to evaluate the effect on implant mucosal inflammation from the use of a novel instrument made of chitosan in the non-surgical treatment of mild peri-implantitis across several clinical centers.
Materials and methods
A 6-month multicenter prospective consecutive case series was performed in six different periodontal specialist clinics in Norway, Sweden and Italy.
Ethical approval was provided by the regional ethical review boards of each center (Norway: 2014/852/REK sør-øst; Italy: Sapienza 2011/15, 3547; and Sweden: EPN Lund 2014/695.) Fifteen patients at each center were planned to be included in the study. Patient screening, inclusions and all clinical examinations were performed by board-certified specialists in periodontology. Subjects were included in the study if they had at least one implant that had been in function for more than 12 months and had been diagnosed with mild peri-implantitis defined as 1–2-mm bone loss, pocket probing depth (PPD) ≥4 mm and a positive bleeding on probing score. Patients diagnosed with periodontitis were required to be finished with active periodontal treatment prior to inclusion in the study. All six surfaces of the included implants were free of supragingival visible plaque. Patients were required to have a total plaque score (dichotomous scoring) below 20% prior to inclusion, and baseline measurements were performed after careful oral hygiene instruction on an individual, as-needed basis. Radiographs were taken at baseline and at the 6 months evaluation. Endodontic lesions and dental decay should have been treated prior to inclusion. Clinical examinations were performed at baseline and at 2, 4, 12 and 24 weeks after baseline using a 0.20-N (20-g)-defined force periodontal probe (University of North Carolina, DB764R, AESCULAP, B Braun Germany). PPD and mBoP was recorded at six sites per implant. Bleeding on probing (mBoP) was recorded using a 3-graded index 30 s after probing as follows: A score of 0 represented no bleeding, 1 represented isolated minimal bleeding spots, 2 represented blood forming a confluent red line on the margin and 3 represented heavy or profuse bleeding . The clinical protocol also included scoring of the height of the gingival margin relative to the crown margin.
All patient-related information and clinical recordings were recorded in a web-based clinical research form (VieDoc version 3.24, PCG solutions, Uppsala, Sweden).
Patients under 18 years of age; current smokers; patients who had undergone radiotherapy in the head and neck region, chemotherapy or systemic long-term corticosteroid treatment; patients who were pregnant or nursing; patients receiving medications known to induce gingival hyperplasia; patients with uncontrolled diabetes (HbA1c >6.5); patients who had taken systemic antibiotics less than 6 months prior to baseline; patients receiving bisphosphonate treatment; and patients with prosthetic factors that prevented clinical measurements were excluded from participation in the study. Implants with technical complications, such as loose supraconstructions, cement remnants, ill-fitted crowns with poor marginal contour or any type of prosthetic complication that according to the examiner, would be a local contributing factor to inflammation, were also excluded. Implants that were previously treated surgically for peri-implantitis and implants with overcontoured supraconstructions obstructing access for debridement and clinical measurements of more than three surfaces were also excluded. Before agreeing to participate in this study, all patients were provided with sufficient information via a patient information sheet and a consent form, which was signed prior to final inclusion.
The power calculation was based on data from a pilot clinical study evaluating the same test device performed at the Department of Periodontology, University of Oslo, in 2014. Descriptive statistics were presented for continuous variables (median and interquartile range), and proportions were presented for categorical variables.
Mann-Whitney rank sum tests were used to compare changes in the clinical parameters between baseline and subsequent time points. To assess the hierarchical structure of the data (center > patient > site), a linear mixed model using the restricted maximum likelihood method (multilevel logistic models for binary outcomes) was constructed to analyse the PPD, mBoP and suppuration, adjusting for factors such as age, gender and past smoke exposure.
All statistical analyses were performed using Sigma Plot v 13.0 (Systat Software, Inc., San Jose, CA) and Stata 14 (StataCorp, College Station, TX, USA) statistical software.
Range (min; max)
Sweden and Martina
Demographics by center
Number of patients
The mean PPD and mBoP at baseline were 5.15 mm (4.97; 5.32) and 1.86 (1.78; 1.93), respectively, whereas the mean PPD and mBoP at 6 months were 4.0 mm (3.91; 4.19) and 0.64 (0.54; 0.75), respectively (Figs. 2 and 3).
Level of crown margin at the different time points
n = 306
n = 272
n = 267
n = 282
n = 294
Subgingival crown margins
Supragingival crown margins
Baseline to 2 weeks
Baseline to 4 weeks
Baseline to 12 weeks
Baseline to 24 weeks
4 to 12 weeks
12 to 24 weeks
During this study, all 63 implants were reported to have stable radiographic levels of osseous support as validated by the six different local examiners. No adverse events were reported during the study.
Identifying peri-implant disease at an early stage and promptly treating the inflammatory condition is crucial to prevent the progression of peri-implant bone loss and ensure long-term implant survival [23–25]. After completion of active treatment and when the condition is controlled, supportive peri-implant therapy will reduce the risk of disease re-occurrence . A number of scientific reports on various methods for non-surgical peri-implant therapy have been presented, but limited and short-term effects have been reported [26, 27]. Instruments for the removal of submucosal microbial deposits from implant surfaces should obviously be effective without causing damage to the implant. However, clinical devices specifically designed for this purpose are scarce, and the effectiveness and safety of most such devices have rarely been scientifically validated . In a review paper by Schwarz et al. , it was reported that mechanical debridement with, e.g. carbon fibre, titanium or plastic curettes combined with measures of oral hygiene, was effective in the management of peri-implant mucositis and that alternative or adjunctive measures such as lasers, ultrasonic devices or air abrasives with glycine powder may improve the efficacy of the treatment of sites with peri-implantitis. The same group of researchers also performed a systematic review on studies evaluating air-polishing with glycine powder of implants with peri-implantitis and reported that this method may lead to improved reduction in parameters of inflammation as compared to mechanical debridement combined with antiseptic therapy . Chitosan is a completely biocompatible biopolymer which also has been demonstrated to be bacteriostatic and exhibit anti-inflammatory properties [31–33]. A recent in vitro experimental study demonstrated that chitosan inhibits the growth of the periodontal pathogens Porphyromonas gingivalis and Aggregatibacter actinomycetemcomitans and exerts an anti-inflammatory effect by reducing the levels of prostaglandin E-2 (PGE2) . From these perspectives, chitosan may be considered a potential candidate to be used in a device for implant debridement.
In the present study, significant reductions were observed in the clinical parameters of peri-implant inflammation at 2, 4, 12 and 24 weeks relative to baseline after debridement with the chitosan brush seated in an oscillating dental drill piece. No progression in radiographic bone loss was reported at any of the implants at the final evaluation, and the method was thus judged safe to use in cases with mild peri-implantitis.
In comparison, a randomized clinical trial by Sahm et al.  compared amino acid glycine powder versus mechanical debridement using carbon curettes and antiseptic therapy with chlorhexidine digluconate. At the 6-month final evaluation, PPD reductions of 0.6 and 0.5 mm, respectively, were reported. Similarly, Renvert et al.  performed a randomized clinical trial comparing an air-abrasive device and an Er:yttrium aluminium garnet (YAG) laser in the non-surgical treatment of peri-implantitis and reported mean PPD reductions of 0.9 and 0.8 mm, respectively, in the two groups. In the present study, a mean PPD reduction of 1.1 mm was determined at the final evaluation at 6 months which is comparable to findings reported in other studies.
A study by Riben-Grundstrom and co-workers  compared the use of glycine powder air-polishing and the ultrasonic treatment of peri-implant mucositis and utilized inclusion criteria comparable to those used in the present study for mild peri-implantitis. The inclusion criteria were (1) the presence of one or more sites diagnosed with peri-implant mucositis. The diagnostic criteria used were a probing depth ≥4 mm combined with bleeding with or without suppuration and (2) bone loss ≤2 mm assessed from the implant shoulder subsequent to the bone healing and remodelling process. They used dichotomous values for BoP and observed reductions of 27% in the air-polishing group and 31% in the ultrasonic group after 6 months.
When pooling the index scores to dichotomous values in the present study, the mBoP score was found to have decreased from 2 or 3 to 0 or 1 in 55% of the samples. Although the complete absence of inflammation was difficult to achieve in most implants, significant and stable reductions in the parameters of inflammation were demonstrated in most sites up to 6 months after treatment with the chitosan brush. Nicotine interferes with the bleeding response in soft tissues and may, consequently, lead to false negatives for the BoP; therefore, to avoid positively skewing the results due to smoking, we decided to exclude current smokers from this study. According to the literature, bleeding on probing has low sensitivity as a predictor for active peri-implant disease because of the high frequency of false-positive responses, but it has a high level of specificity as no bleeding on probing indicates peri-implant health . Due to the absence of perpendicular periodontal fibres in dental implants, a lighter probing force should be used than when probing the gingival crevice in teeth. Similarly, the standardization of the examiners’ technique is critical . A pressure-sensitive periodontal probe was used to record PPD and mBoP. We also used a 3-graded bleeding index to further distinguish between true disease and bleeding from the base of the pocket as the result of excessive pressure and rupture of the junctional epithelium. Scores of 1 and 0 and scores of 2 and 3 were pooled to create a more rigid, dichotomous score. This strengthens the positive results because significant differences were obtained when both the graded and dichotomous BoP scores were analysed. However, previous smokers were included but the outcomes in this patient group did not differ from finding in never smokers. Similarly, patients taking anticoagulants were excluded to avoid false-positive bleeding scores because of the increased bleeding response caused by the medication. Salvi and co-workers  studied the reduction in experimental peri-implant mucositis and revealed that 3 weeks of reinstituted plaque control did not yield pre-experimental levels of peri-implant health. While infection control was carefully installed prior to baseline, and the included implants were plaque free, we found significant reductions in the parameters of inflammation as early as 2 weeks after treatment with the chitosan brush. These results were stable up to 6 months after treatment, indicating a fast and stable response. More of the crown margins were exposed 2 weeks after debridement with the brush and the levels were thereafter stable. The more apical position the crown margins is most probably related to reduction in the soft tissue oedema from the inflammation.
The chitosan brush used in this study is made of a material that is soft with the aim to make a device optimized for removal of the biofilm within the implant threads. The soft bristles on the contrary make the device suboptimal for removal of hard deposits, such as calculus and cement remnants. It has been reported that such cement remnants are a common finding around dental implants , and in hindsight, it would have been beneficial for the analysis to record this. We did not record or analyse on cement- or screw-retained supraconstructions, and it may well be that some of the implants with cement-retained crowns and bridges had subgingival and non-visible cement remnants contributing to the mucosal inflammation. It can thus be hypothesized that combining the brush with an instrument for the removal of potential hard deposits would have yielded even better results. One such instrument for surgical use on titanium surfaces is a rotating titanium brush. The disadvantage with such a rigid metal brush is that the metal bristles may potentially cause injure to the mucosa if used non-surgically. Once active peri-implantitis treatment is finished with a positive response verified and the long-term and regular supportive treatment phase initiated, it could be argued that avoiding instruments that may damage the implant surface is preferable . The consecutive case series presented here does only show the potential merits of a chitosan brush on reducing peri-implant mucosal inflammation. No control group was included in this study, and to test the clinical efficacy of this novel device in the non-surgical treatment of peri-implantitis, a randomized clinical trial will be required. It is also important with a long-term follow-up to study if the use of this novel device will prevent progression of peri-implant bone loss over time, potentially causing implant loss.
In this multicenter case series of implants affected by mild peri-implantitis, significant reductions in the clinical parameters of inflammation were demonstrated at all time points after the initial treatment with a chitosan brush. The use of an oscillating chitosan device appears to be safe and has potential merits for the treatment of mild peri-implantitis and for the maintenance of dental implants. To measure the effectiveness of the method, a multicenter randomized clinical trial needs to be undertaken.
This study was funded by a grant from the Norwegian Research Council FORNY Study number 234524. A short case series reporting on the results from one of the centers (Sapienza) has been accepted for publication in Minerva Stomatologica.
JCW, BJE, BZ, HJ, AP, AMR-J, AMA, MK and OCK participated in the design and undertaking of the study as well as drafting of the manuscript. GLDT carried out the statistics section and drafting of the manuscript. All authors read and approved the final manuscript.
J.C. Wohlfahrt is the inventor and patent holder of BioClean and is a shareholder in LABRIDA AS. B.J. Evensen, B. Zeza, H. Jansson, A. Pilloni, A.M. Roos-Jansåker, G.L. Di Tanna, A.M. Aass, M. Klepp and O.C. Koldsland state that there were no conflicts of interests during the undertaking of the study.
Ethics approval and consent to participate
Ethical approval was provided by the regional ethical review boards of each center (Norway: 2014/852/REK sør-øst; Italy: Sapienza 2011/15, 3547; and Sweden: EPN Lund 2014/695). A written informed consent was signed by all patients prior to final inclusion.
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- Koldsland OC, Scheie AA, Aass AM. Prevalence of peri-implantitis related to severity of the disease with different degrees of bone loss. J Periodontol. 2010;81(2):231–8.View ArticlePubMedGoogle Scholar
- Roos-Jansaker AM, et al. Nine- to fourteen-year follow-up of implant treatment. Part II: presence of peri-implant lesions. J Clin Periodontol. 2006;33(4):290–5.View ArticlePubMedGoogle Scholar
- Derks J, et al. Effectiveness of implant therapy analyzed in a Swedish population: prevalence of peri-implantitis. J Dent Res. 2016;95(1):43–9.View ArticlePubMedGoogle Scholar
- Ogata Y, Nakayama Y, Tatsumi J, Kubota T, Sato S, Nishida T, Takeuchi Y, Onitsuka T, Sakagami R, Nozaki T, Murakami S, Matsubara N, Tanaka M, Yoshino T, Ota J, Nakagawa T, Ishihara Y, Ito T, Saito A, Yamaki K, Matsuzaki E, Hidaka T, Sasaki D, Yaegashi T, Yasuda T, Shibutani T, Noguchi K, Araki H, Ikumi N, Aoyama Y, Kogai H, Nemoto K, Deguchi S, Takiguchi T, Yamamoto M, Inokuchi K, Ito T, Kado T, Furuichi Y, Kanazashi M, Gomi K, Takagi Y, Kubokawa K, Yoshinari N, Hasegawa Y, Hirose T, Sase T, Arita H, Kodama T, Shin K, Izumi Y, Yoshie H. Prevalence and risk factors for peri-implant diseases in Japanese adult dental patients. J Oral Sci. 2017;59(1):1-11. doi:10.2334/josnusd.16-0027. Epub 2016 Oct 7.
- Gurgel BC, et al. Frequency of peri-implant diseases and associated factors. Clin Oral Implants Res. 2016;Google Scholar
- Ferreira CF, et al. Prevalence of peri-implant diseases: analyses of associated factors. Eur J Prosthodont Restor Dent. 2015;23(4):199–206.PubMedGoogle Scholar
- Fransson C, et al. Prevalence of subjects with progressive bone loss at implants. Clin Oral Implants Res. 2005;16(4):440–6.View ArticlePubMedGoogle Scholar
- Jepsen S, et al. Primary prevention of peri-implantitis: managing peri-implant mucositis. J Clin Periodontol. 2015;42(Suppl 16):S152–7.View ArticlePubMedGoogle Scholar
- Costa FO, et al. Peri-implant disease in subjects with and without preventive maintenance: a 5-year follow-up. J Clin Periodontol. 2012;39(2):173–81.View ArticlePubMedGoogle Scholar
- Serino G, Strom C. Peri-implantitis in partially edentulous patients: association with inadequate plaque control. Clin Oral Implants Res. 2009;20(2):169–74.View ArticlePubMedGoogle Scholar
- Tonetti MS, et al. Primary and secondary prevention of periodontal and peri-implant diseases: introduction to, and objectives of the 11th European Workshop on Periodontology consensus conference. J Clin Periodontol. 2015;42(Suppl 16):S1–4.View ArticlePubMedGoogle Scholar
- Rokn A, et al. Prevalence of peri-implantitis in patients not participating in well-designed supportive periodontal treatments: a cross-sectional study. Clin Oral Implants Res. 2017;28(3):314–9.View ArticlePubMedGoogle Scholar
- Faggion CM Jr, et al. A systematic review and Bayesian network meta-analysis of randomized clinical trials on non-surgical treatments for peri-implantitis. J Clin Periodontol. 2014;41(10):1015–25.View ArticlePubMedGoogle Scholar
- Mellado-Valero A, et al. Decontamination of dental implant surface in peri-implantitis treatment: a literature review. Med Oral Patol Oral Cir Bucal. 2013;18(6):e869–76.View ArticlePubMedPubMed CentralGoogle Scholar
- Eger M, et al. Scaling of titanium implants entrains inflammation-induced osteolysis. Sci Rep. 2017;7:39612.View ArticlePubMedPubMed CentralGoogle Scholar
- van Velzen FJ, et al. Dental floss as a possible risk for the development of peri-implant disease: an observational study of 10 cases. Clin Oral Implants Res. 2016;27(5):618–21.View ArticlePubMedGoogle Scholar
- Mann M, et al. Effect of plastic-covered ultrasonic scalers on titanium implant surfaces. Clin Oral Implants Res. 2012;23(1):76–82.View ArticlePubMedGoogle Scholar
- Ramaglia L, et al. Profilometric and standard error of the mean analysis of rough implant surfaces treated with different instrumentations. Implant Dent. 2006;15(1):77–82.View ArticlePubMedGoogle Scholar
- Ruhling A, et al. Treatment of subgingival implant surfaces with Teflon-coated sonic and ultrasonic scaler tips and various implant curettes. An in vitro study. Clin Oral Implants Res. 1994;5(1):19–29.View ArticlePubMedGoogle Scholar
- Mengel R, et al. An in vitro study of the treatment of implant surfaces with different instruments. Int J Oral Maxillofac Implants. 1998;13(1):91–6.PubMedGoogle Scholar
- Villa O, et al. Suture materials affect peri-implant bone healing and implant osseointegration. J Oral Sci. 2015;57(3):219–27.View ArticlePubMedGoogle Scholar
- Roos-Jansaker AM, et al. Submerged healing following surgical treatment of peri-implantitis: a case series. J Clin Periodontol. 2007;34(8):723–7.View ArticlePubMedGoogle Scholar
- Salvi GE, Cosgarea R, Sculean A. Prevalence and mechanisms of peri-implant diseases. J Dental Res. 2016;Google Scholar
- Monje A, et al. Impact of maintenance therapy for the prevention of peri-implant diseases: a systematic review and meta-analysis. J Dental Res. 2016;95(4):372–9.View ArticleGoogle Scholar
- Gay IC, et al. Role of supportive maintenance therapy on implant survival: a university-based 17 years retrospective analysis. Int J Dental Hygiene. 2016;14(4):267–71.View ArticleGoogle Scholar
- Muthukuru M, et al. Non-surgical therapy for the management of peri-implantitis: a systematic review. Clin Oral Implants Res. 2012;23(Suppl 6):77–83.View ArticlePubMedGoogle Scholar
- 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.PubMedGoogle Scholar
- Armitage GC, Xenoudi P. Post-treatment supportive care for the natural dentition and dental implants. Periodontol. 2016;71(1):164–84.View ArticleGoogle Scholar
- 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.View ArticlePubMedPubMed CentralGoogle Scholar
- Schwarz F, Becker K, Renvert S. Efficacy of air polishing for the non-surgical treatment of peri-implant diseases: a systematic review. J Clin Periodontol. 2015;42(10):951–9.View ArticlePubMedGoogle Scholar
- Costa EM, et al. Evaluation and insights into chitosan antimicrobial activity against anaerobic oral pathogens. Anaerobe. 2012;18(3):305–9.View ArticlePubMedGoogle Scholar
- Choi BK, et al. In vitro antimicrobial activity of a chitooligosaccharide mixture against Actinobacillus actinomycetemcomitans and Streptococcus mutans. Int J Antimicrob Agents. 2001;18(6):553–7.View ArticlePubMedGoogle Scholar
- Sarasam AR, et al. Antibacterial activity of chitosan-based matrices on oral pathogens. Journal of materials science. Mat Med. 2008;19(3):1083–90.View ArticleGoogle Scholar
- Arancibia R, et al. Effects of chitosan particles in periodontal pathogens and gingival fibroblasts. J Dental Res. 2013;92(8):740–5.View ArticleGoogle Scholar
- Sahm N, et al. Non-surgical treatment of peri-implantitis using an air-abrasive device or mechanical debridement and local application of chlorhexidine: a prospective, randomized, controlled clinical study. J Clin Periodontol. 2011;38(9):872–8.View ArticlePubMedGoogle Scholar
- Renvert S, et al. Treatment of peri-implantitis using an Er:YAG laser or an air-abrasive device: a randomized clinical trial. J Clin Periodontol. 2011;38(1):65–73.View ArticlePubMedGoogle Scholar
- Riben-Grundstrom C, et al. Treatment of peri-implant mucositis using a glycine powder air-polishing or ultrasonic device: a randomized clinical trial. J Clin Periodontol. 2015;42(5):462–9.View ArticlePubMedGoogle Scholar
- Lang NP, et al. Histologic probe penetration in healthy and inflamed peri-implant tissues. Clin Oral Implants Res. 1994;5(4):191–201.View ArticlePubMedGoogle Scholar
- Schou S, et al. Probing around implants and teeth with healthy or inflamed peri-implant mucosa/gingiva. A histologic comparison in cynomolgus monkeys (Macaca fascicularis). Clin Oral Implants Res. 2002;13(2):113–26.View ArticlePubMedGoogle Scholar
- Salvi GE, et al. Reversibility of experimental peri-implant mucositis compared with experimental gingivitis in humans. Clin Oral Implants Res. 2012;23(2):182–90.View ArticlePubMedGoogle Scholar
- Korsch M, Obst U, Walther W. Cement-associated peri-implantitis: a retrospective clinical observational study of fixed implant-supported restorations using a methacrylate cement. Clin Oral Implants Res. 2014;25(7):797–802.View ArticlePubMedGoogle Scholar