Skip to main content
Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Systemic Antibiotics in Periodontal Treatment of Diabetic Patients: A Systematic Review

Abstract

Aim

To evaluate the effects of systemic antibiotics in combination with scaling and root planing (SRP) on periodontal parameters, tooth loss and oral health-related quality of life in diabetes patients.

Materials and Methods

Two independent reviewers screened for controlled clinical trials with at least 6-month follow-up in six electronic databases, registers of clinical trials, meeting abstracts and four major dental journals. After duplicates removal, electronic and hand searches yielded 1,878 records; 18 full-text articles were independently read by two reviewers. To evaluate the additional effect of antibiotic usage, pooled weighted mean differences and 95% confidence intervals were calculated using a fixed effects model.

Results

Five studies met the inclusion criteria, four of which were included in meta-analyses. The meta-analyses showed a significant effect favouring SRP plus antibiotic for reductions in mean probing depth (PD) (-0.22 mm [-0.34, -0.11]) and mean percentage of bleeding on probing (BoP) (4% [-7, -1]). There was no significant effect for clinical attachment level gain and plaque index reduction. No study reported on tooth loss and oral health-related quality of life.

Conclusion

Adjunctive systemic antibiotic use in diabetic patients provides a small additional benefit in terms of reductions in mean PD and mean percentage of BoP.

Registration

PROSPERO: CRD42013006389.

Introduction

Periodontitis is a biofilm-induced chronic inflammatory disorder of teeth supporting structures [1] that affects over 740 million people worldwide in its severe form [2]. Diabetes mellitus is a group of chronic metabolic disorders characterized by irregular glucose metabolism caused by defects in insulin production and/or action [3]. The International Diabetes Federation estimates that approximately 382 million people have diabetes and a 55% increase in its prevalence is expected by the year 2035 [4].

Several clinical studies have established the relationship between diabetes and periodontitis. This relationship appears to be bidirectional, with diabetes being a risk factor for periodontitis [5] and the severity of periodontitis a factor influencing glycemic control and the development of complications in diabetic patients [6]. In addition, periodontal treatment may have a positive effect on glycemic control in diabetic patients [7, 8].

The clinical benefit of nonsurgical periodontal treatment is well documented in terms of probing depth reduction, bleeding on probing reduction and clinical attachment gain [9]. Nevertheless, whether to use systemic antibiotics as an adjunct therapy for periodontal disease in any patient is still a subject of debate. While there is evidence that the use of antibiotics with nonsurgical periodontal therapy provides some benefit to systemically healthy patients [1012], their use is generally recommended only in specific clinical situations [12]. Also, there is no evidence that there is any additional benefit for smokers with chronic periodontitis [13].

The use of adjunct antibiotics with scaling and root planing in diabetic patients is also a contentious issue [1416]. The results of individual clinical trials are conflicting or inconclusive [1719] and an appropriate summary of their results using a systematic approach would clarify whether the use of antibiotics in periodontal treatment could be beneficial to diabetic patients. The aim of this study was to assess the effects of the adjunctive use of systemic antibiotics in nonsurgical periodontal treatment, compared to nonsurgical periodontal treatment alone, on clinical periodontal parameters, tooth loss and oral health-related quality of life in patients with diabetes.

Materials and Methods

Study design

A systematic review of controlled clinical trials with a follow-up of at least six months.

Participants

Type 1 or type 2 diabetes patients, with a clinical diagnosis of periodontitis, regardless of classification. Chronic and aggressive periodontitis were considered for inclusion with no age restriction. Gestational diabetes was not considered for inclusion.

Interventions

Scaling and root planing (SRP) combined with adjunctive use of systemic antibiotics or sub-antimicrobial doxycycline (SDD) versus SRP alone, with or without a placebo. Quadrant-wise and full-mouth periodontal treatments were considered for inclusion. Any type of systemic antibiotic or combinations of antibiotics, as well as different therapeutic regimens were eligible for inclusion. Studies were excluded when systemic antibiotics were used only in periodontal supportive therapy or with co-interventions such as slow-release devices or subgingival irrigation with antimicrobials.

Outcomes

Changes in periodontal parameters (i.e., clinical attachment level, probing depth, plaque index, and bleeding on probing), tooth loss, and oral health-related quality of life. The occurrence of side effects associated with antibiotics was also investigated.

Search strategy

The following databases were searched from their earliest records through May 2015: The Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE via PubMed, EMBASE, LILACS, BBO (Brazilian Dental Library), and the Brazilian database of theses and dissertations (Banco de Teses CAPES). The strategy was developed for MEDLINE using controlled vocabulary, with words derived from "Medical Subject Headings" (MeSH) associated with free terms considered relevant to the topic in question; the asterisk symbol (*) was used for truncation (S1 Appendix). This strategy was adapted for the other databases without any idiom restrictions.

The following international registers of ongoing trials were also evaluated: ClinicalTrials.gov, Current Controlled Trials, Registro Brasileiro de Ensaios Clínicos (ReBEC), EU Clinical Trials Register, and Australian New Zealand Clinical Trials Registry. Hand searches were performed in the Journal of Clinical Periodontology (since 2003), Journal of Periodontology (since 2003), Journal of Periodontal Research (since 2004), and Journal of Dental Research (since 2004). Searches in journals included in the Cochrane Master List of Journals Being Searched were examined from the last update onward. Likewise, abstracts from the International Association for Dental Research (2001–2014) and the European Federation of Periodontology meetings (EuroPerio 4, 5, 6 and 7) were examined.

Data collection and analysis

Two independent reviewers (CMMLS and RLJ) read the titles and abstracts, when available, of all records identified. Whenever a study seemed to meet the inclusion criteria, but complete information was lacking, the full-text article was obtained. The same reviewers independently extracted the data on characteristics of the study population, interventions, outcomes, and length of follow-up using a data extraction form. Attempts were made to contact authors to check on incomplete data. Disagreements were solved by consulting two other reviewers (BHO and APPS). Studies meeting the inclusion criteria were obtained in full.

We used the Cochrane Collaboration tool for assessing risk of bias in the studies included [20]. The following domains were evaluated as having low, high or unclear risk of bias: sequence generation, allocation concealment, blinding, incomplete outcome data, selective outcome reporting and other biases, such as losses to follow-up (low risk of bias when losses were non-differential and less than 20%), diagnosis reliability (low risk of bias when good) [21], and comparability between groups at baseline (low risk of bias if groups were balanced in terms of age, gender, level of metabolic control and severity of periodontitis).

Meta-analyses of the differences in six-month means were performed. Heterogeneity of studies was assessed by visual inspection of forest plots, Chi-square (χ2) test for heterogeneity and Higgins index (I2). A fixed-effects model was used in the absence of heterogeneity (χ2 with significance level >0.10 and I2 <50%). Post-hoc sensitivity analyses were performed excluding studies restricted to non-smokers and studies restricted to patients with good metabolic control. All analyses were carried out in Stata® 11 (StataCorp LP, College Station, Tex., USA).

Results

The electronic search retrieved 1,983 records. One additional record was found after hand searching an IADR meeting abstract. After excluding duplicates, there were 1,878 records, 1,859 of which did not meet the inclusion criteria, and 19 were selected for full reading, but one full-text could not be obtained. Thus, 18 full-text were read and assessed for eligibility. Five studies met the inclusion criteria and four were used in meta-analyses. Fig 1 describes the studies identified, screened, assessed for eligibility, excluded and included in the review. The list of 12 excluded studies and the reasons for their exclusion are presented in S2 Appendix.

thumbnail
Fig 1. Flow diagram showing the process of identifying, screening, assessing for eligibility, excluding and including the studies retrieved from the electronic and hand searches.

*It was not possible to obtain one full-text article and 1,859 did not meet the inclusion criteria. **One Chinese and one Russian. ***Two articles using the same population were merged and only one article was included.

https://doi.org/10.1371/journal.pone.0145262.g001

The general characteristics of the studies are presented in Table 1. The studies used different antibiotics and/or therapeutic regimens. The Deo et al. (2010) [22] trial used SDD and therefore was not included in the meta-analysis. In that study, a significantly greater PD reduction and CAL gain were found for the group taking SDD (3.06 mm versus 2.54 mm for PD and 2.25 mm versus 1.58 mm for CAL). Deo et al. (2010) [22] described no adverse reactions to SDD therapy.

All studies presented data on probing depth, clinical attachment level and bleeding on probing. Tsalikis et al. (2014) [19] did not present data on plaque index. For the study by Grossi et al. (1996) [23], additional information on sample size and outcomes were obtained by e-mail. Two studies assessed only type 2 diabetic patients [18, 19]. Follow-up varied from 6 to 12 months. No study evaluated tooth loss and oral health-related quality of life. Fig 2 shows the risk of bias in the included studies. No study had low risk of bias in all domains evaluated.

thumbnail
Fig 2. Ascertainment of the risk of bias in the included studies.

+ = yes;— = no;? = uncertain.

https://doi.org/10.1371/journal.pone.0145262.g002

Meta-analyses showed a significant effect favoring SRP plus antibiotic for reductions in mean PD (-0.22 mm [-0.34, -0.11]) and mean percentage of BoP (-4% [-7, -1]). There was no significant effect for CAL gain and PI reduction (Fig 3). Post-hoc sensitivity analyses showed a significant gain in CAL when studies restricted to non-smokers (-0.24 mm [-0.47, -0.02]) or restricted to well-controlled patients (-0.25 mm [-0.46, -0.05]) were excluded; both results favored SRP plus antibiotic (S3 Appendix).

thumbnail
Fig 3. Forest plots presenting pooled weighted mean differences and 95% confidence intervals for periodontal parameters between test and control groups.

https://doi.org/10.1371/journal.pone.0145262.g003

Three studies reported on side effects related to the use of antibiotics or placebo [1719]. In the Botero et al. (2013) [17] trial, only one control patient reported gastrointestinal discomfort. Miranda et al. (2014) [18] found more side effects in the test group (diarrhea = 7; headache = 4; metallic taste = 4; and nausea/vomiting = 5) than in the control group (diarrhea = 3; headache = 1; metallic taste = 2; and nausea/vomiting = 2). One control patient reported dizziness and difficulty swallowing in the Tsalikis et al. (2014) [19] study.

Discussion

Recent systematic reviews have shown that the use of adjunctive antibiotics may improve periodontal healing in systemically healthy patients with periodontitis [10, 12, 24], although the clinical relevance of this improvement is still subject to debate. To the best of our knowledge, this is the first systematic review of the additional clinical benefit of adjunctive use of systemic antibiotics over SRP alone in diabetic patients. Our results showed an additional 0.22 mm reduction in mean PD and a 4% reduction in mean BoP for SRP plus antibiotic. No additional benefits were observed for mean CAL gain and mean PI reduction.

These findings should be interpreted with great caution. Despite the statistical significance, the clinical relevance of six-month reductions of 0.22 mm in mean PD and of 4% in mean BoP is doubtful. In addition, there is a concern about the increasing use of antibiotics worldwide. From 2000 to 2010, global use of antibiotics increased by 36% [25], contributing to the spread of antimicrobial resistance. Antibiotics prescribed by dentists affect microorganisms beyond the oral cavity [26] and the greater the number or duration of antibiotic courses, the greater the rates of resistance [27]. The prescription of antibiotics by dentists should be balanced against the risks of increasing antimicrobial resistance. Thus, the lack of evidence of a clinically relevant benefit argues against such use in the periodontal treatment of diabetic patients.

Averaging whole mouth PD and CAL may underestimate the benefits of adjunctive antibiotics. The positive results are more pronounced when analyzing deep pockets [12]. Miranda et al. (2014) [18] found increased reduction in numbers of sites with PD ≥ 6 mm in the group taking amoxicillin/metronidazole, which seems to be effective in combination with scaling and root planing in the treatment of chronic periodontitis [10]. Further studies are needed to ascertain the benefit of adjunctive antibiotics based on disease severity.

Our meta-analyses were based on six-month results. In order to be considered a useful intervention, the clinical benefit of antibiotics should remain steady over time. Botero et al. (2013) [17] and Miranda et al. (2014) [18] found stable results 9 and 12 months, respectively, after SRP plus systemic antibiotic. The ideal frequency of antibiotic courses and the extent of the possible long-term benefits of this therapeutic approach remain to be determined.

The decision to use systemic antibiotics should take into consideration, in addition to the other points discussed, whether the clinical benefits outweigh the potential side effects. No study reported serious adverse events related to the use of antibiotics. One study performed a comparative analysis between test and control groups. A higher frequency of side effects was found in the antibiotic group, but the difference was not statistically significant [18].

The risk of bias in the studies included is also worth noting. Among the trials included in the meta-analyses, one had high risk of bias [19] and three were at unclear risk of bias [17, 18, 23]. Deo et al. (2010) [22] had high risk of bias.

Only one study [22] used SDD, which does not have anti-microbial effects and is used as host-modulator agent [28], hence it was not included in our meta-analysis. Although this study found positive results favoring SDD therapy for PD and CAL, no definite conclusion can be drawn due to the small number of participants and unclear risk of bias.

One limitation of our meta-analyses was the inclusion of different types and regimens of antibiotics. Recently, Keestra et al. (2015) [12] reported that no type of antibiotic was superior to any other. However, when analyzing moderate and deep pockets, they found a trend suggesting that amoxicillin/metronidazole is more effective. Our PD and BoP results were largely influenced by Miranda et al. (2014) [18], the only study using the amoxicillin/metronidazole combination.

Another limitation was the diversity in tobacco exposure and the level of metabolic control across the studies. It is well known that smoking has a negative influence on the outcome of periodontal therapy [29] and level of metabolic control is an important mediator of the relationship between diabetes and periodontitis [30]. Although baseline severity of periodontal disease was similar in all studies, we performed sensitivity analyses excluding studies restricted to non-smokers [18, 19] and studies restricted to patients with good metabolic control [19]. When studies restricted to non-smokers were excluded, statistical significance remained unchanged for PI and PD. However, the confidence interval for BoP became wider, suggesting no evidence that the adjunctive use of antibiotics provides any benefit. On the other hand, the pooled estimate for CAL became statistically significant, favoring the adjunctive use of antibiotics (S3 Appendix). When the only study that was restricted to patients with good metabolic control was excluded, results for BoP and PD did not change. Again, the pooled estimate for CAL became statistically significant, favoring the adjunctive use of antibiotics (S3 Appendix). These uncertainties around the effect estimates reinforce the need for better evidence on this subject in order to inform clinical practice.

Despite differences in types and regimens of antibiotics, inclusion of smokers, type of diabetes and levels of metabolic control, no evidence of statistical heterogeneity was found. Due to the small number of studies included, it was not possible to perform meta-regression to evaluate the potential modifier effect of covariates. One study has included topical irrigation with water in both groups [23]. Although we have excluded studies using co-interventions, water irrigation was accepted since no additional benefit in PD reduction and CAL gain has been shown due to its use in diabetic patients [31].

Unfortunately, we did not find any trial that provided data on true outcome measures, such as tooth loss, adverse events, oral health-related quality of life and bacterial resistance. Cunha-Cruz et al. (2008) [32], in a large retrospective cohort study, found no association between systemic antibiotics prescribed for dental or medical reasons and lower incidence of tooth loss. Well-designed clinical trials with large sample sizes, longer follow-up periods and true outcome measures need to be given high priority. Also, as compliance with antibiotic regimen is important to treatment outcomes, all studies should report data on it.

This study indicates that adjunctive systemic antibiotic use provides statistically significant benefits in terms of reductions in mean probing depth and mean percentage of bleeding on probing, but no improvement in CAL gain. However, the widespread use of systemic antibiotics in periodontal treatment of diabetics should not be encouraged, since the clinical relevance of these findings has yet to be shown. The risk of bias of included studies should also be taken into account when translating the results into clinical practice.

Based on the results of this systematic review, we consider that it is still appropriate to adopt a conservative approach in the prescription of systemic antibiotics for the treatment of chronic periodontitis in diabetic patients, in line with what is currently recommended to other chronic periodontal patients [33].

Supporting Information

S1 Appendix. Search strategy for MEDLINE via PubMed.

https://doi.org/10.1371/journal.pone.0145262.s001

(PDF)

S2 Appendix. List of excluded studies and the reasons for exclusion.

https://doi.org/10.1371/journal.pone.0145262.s002

(PDF)

Author Contributions

Conceived and designed the experiments: CMMLS RLJ RGF APPS BHO. Performed the experiments: CMMLS RLJ APPS BHO. Analyzed the data: CMMLS RLJ RGF APPS BHO. Wrote the paper: CMMLS RLJ RGF APPS BHO.

References

  1. 1. Pihlstrom BL, Michalowicz BS, Johnson NW. Periodontal diseases. Lancet. 2005;366(9499):1809–20. pmid:16298220
  2. 2. Kassebaum NJ, Bernabe E, Dahiya M, Bhandari B, Murray CJ, Marcenes W. Global burden of severe periodontitis in 1990–2010: a systematic review and meta-regression. Journal of dental research. 2014;93(11):1045–53. pmid:25261053
  3. 3. Kahn CR. Banting Lecture. Insulin action, diabetogenes, and the cause of type II diabetes. Diabetes. 1994;43:1066–84. pmid:8039601
  4. 4. International Diabetes Federation. IDF Diabetes Atlas 2013.
  5. 5. Chavarry NG, Vettore MV, Sansone C, Sheiham A. The relationship between diabetes mellitus and destructive periodontal disease: a meta-analysis. Oral health & preventive dentistry. 2009;7(2):107–27.
  6. 6. Lalla E, Papapanou PN. Diabetes mellitus and periodontitis: a tale of two common interrelated diseases. Nature reviews Endocrinology. 2011;7(12):738–48. pmid:21709707
  7. 7. Liew AK, Punnanithinont N, Lee YC, Yang J. Effect of non-surgical periodontal treatment on HbA1c: a meta-analysis of randomized controlled trials. Australian dental journal. 2013;58(3):350–7. pmid:23981218
  8. 8. Simpson TC, Needleman I, Wild SH, Moles DR, Mills EJ. Treatment of periodontal disease for glycaemic control in people with diabetes. The Cochrane database of systematic reviews. 2010;(5):CD004714. pmid:20464734
  9. 9. Lowenguth RA, Greenstein G. Clinical and microbiological response to nonsurgical mechanical periodontal therapy. Periodontology 2000. 1995;9:14–22. pmid:9567975
  10. 10. Sgolastra F, Gatto R, Petrucci A, Monaco A. Effectiveness of systemic amoxicillin/metronidazole as adjunctive therapy to scaling and root planing in the treatment of chronic periodontitis: a systematic review and meta-analysis. Journal of periodontology. 2012;83(10):1257–69. pmid:22220767
  11. 11. Herrera D, Sanz M, Jepsen S, Needleman I, Roldán S. A systematic review on the effect of systemic antimicrobials as an adjunct to scaling and root planing in periodontitis patients. Journal of clinical periodontology. 2002;29(Suppl 3):136–59. pmid:12787214
  12. 12. Keestra JA, Grosjean I, Coucke W, Quirynen M, Teughels W. Non-surgical periodontal therapy with systemic antibiotics in patients with untreated chronic periodontitis: a systematic review and meta-analysis. Journal of periodontal research. 2015;50(3):294–314. pmid:25142259
  13. 13. Angaji M, Gelskey S, Nogueira-Filho G, Brothwell D. A systematic review of clinical efficacy of adjunctive antibiotics in the treatment of smokers with periodontitis. Journal of periodontology. 2010;81(11):1518–28. pmid:20583918
  14. 14. Grossi SG, Skrepcinski FB, DeCaro T, Robertson DC, Ho AW, Dunford RG, et al. Treatment of periodontal disease in diabetics reduces glycated hemoglobin. Journal of periodontology. 1997;68(8):713–9. pmid:9287060
  15. 15. Llambes F, Silvestre FJ, Hernandez-Mijares A, Guiha R, Caffesse R. Effect of non-surgical periodontal treatment with or without doxycycline on the periodontium of type 1 diabetic patients. Journal of clinical periodontology. 2005;32(8):915–20. pmid:15998278
  16. 16. Rodrigues DC, Taba MJ, Novaes AB, Souza SL, Grisi MF. Effect of non-surgical periodontal therapy on glycemic control in patients with type 2 diabetes mellitus. Journal of periodontology. 2003;74(9):1361–7. pmid:14584871
  17. 17. Botero JE, Yepes FL, Ochoa SP, Hincapie JP, Roldan N, Ospina CA, et al. Effects of periodontal non-surgical therapy plus azithromycin on glycemic control in patients with diabetes: a randomized clinical trial. Journal of periodontal research. 2013;48(6):706–12. pmid:23441920
  18. 18. Miranda TS, Feres M, Perez-Chaparro PJ, Faveri M, Figueiredo LC, Tamashiro NS, et al. Metronidazole and amoxicillin as adjuncts to scaling and root planing for the treatment of type 2 diabetic subjects with periodontitis: 1-year outcomes of a randomized placebo-controlled clinical trial. Journal of clinical periodontology. 2014;41(9):890–9. pmid:24930639
  19. 19. Tsalikis L, Sakellari D, Dagalis P, Boura P, Konstantinidis A. Effects of doxycycline on clinical, microbiological and immunological parameters in well-controlled diabetes type-2 patients with periodontal disease: a randomized, controlled clinical trial. Journal of clinical periodontology. 2014;41(10):972–80. pmid:25041182
  20. 20. Higgins JP, Altman DG. Assessing risk of bias in included studies. In: Higgins JP, Green S, editors. Cochrane Handbook for Systematic Reviews of Intervention 2008. p. 187–241.
  21. 21. Altman DG. Some common problems in medical research. In: Altman DG, editor. Practical Statistics for Medical Research: Chapman & Hall; 1991. p. 396–439.
  22. 22. Deo V, Gupta S, Bhongade ML, Jaiswal R. Evaluation of subantimicrobial dose doxycycline as an adjunct to scaling and root planing in chronic periodontitis patients with diabetes: a randomized, placebo-controlled clinical trial. Journal of contemporary dental practice. 2010;11(3):009–16. pmid:20461319
  23. 23. Grossi SG, Skrepcinski FB, DeCaro T, Zambon JJ, Cummins D, Genco RJ. Response to periodontal therapy in diabetics and smokers. Journal of periodontology. 1996;67(10 Suppl):1094–102. pmid:8910828
  24. 24. Sgolastra F, Severino M, Petrucci A, Gatto R, Monaco A. Effectiveness of metronidazole as an adjunct to scaling and root planing in the treatment of chronic periodontitis: a systematic review and meta-analysis. Journal of periodontal research. 2014;49(1):10–9. pmid:23668676
  25. 25. Van Boeckel TP, Gandra S, Ashok A, Caudron Q, Grenfell BT, Levin SA, et al. Global antibiotic consumption 2000 to 2010: an analysis of national pharmaceutical sales data. The Lancet Infectious diseases. 2014;14(8):742–50. pmid:25022435
  26. 26. Sweeney LC, Dave J, Chambers PA, Heritage J. Antibiotic resistance in general dental practice—a cause for concern? The Journal of antimicrobial chemotherapy. 2004;53(4):567–76. pmid:14985274
  27. 27. Costelloe C, Metcalfe C, Lovering A, Mant D, Hay AD. Effect of antibiotic prescribing in primary care on antimicrobial resistance in individual patients: systematic review and meta-analysis. BMJ. 2010;340:c2096. pmid:20483949
  28. 28. Golub LM, Ciancio S, Ramamamurthy NS, Leung M, McNamara TF. Low-dose doxycycline therapy: effect on gingival and crevicular fluid collagenase activity in humans. Journal of periodontal research. 1990;25(6):321–30. pmid:2177499
  29. 29. Labriola A, Needleman I, Moles DR. Systematic review of the effect of smoking on nonsurgical periodontal therapy. Periodontology 2000. 2005;37:124–37. pmid:15655029
  30. 30. Tsai C, Hayes C, Taylor GW. Glycemic control of type 2 diabetes and severe periodontal disease in the US adult population. Community dentistry and oral epidemiology. 2002;30(3):182–192. pmid:12000341
  31. 31. Al-Mubarak S, Ciancio S, Aljada A, Mohanty P, Ross C, Dandona P. Comparative evaluation of adjunctive oral irrigation in diabetics. Journal of clinical periodontology. 2002;29(4):295–300. pmid:11966926
  32. 32. Cunha-Cruz J, Hujoel PP, Maupome G, Saver B. Systemic antibiotics and tooth loss in periodontal disease. Journal of dental research. 2008;87(9):871–6. pmid:18719216
  33. 33. Smiley CJ, Tracy SL, Abt E, Michalowicz BS, John MT, Gunsolley J, et al. Evidence-based clinical practice guideline on the nonsurgical treatment of chronic periodontitis by means of scaling and root planing with or without adjuncts. Journal of the american dental association. 2015;146(7):525–35. pmid:26113100