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Background:
Systematic Review

Efficacy of Topical Intervention for Recurrent Aphthous Stomatitis: A Network Meta-Analysis

1
College of Stomatology, Chongqing Medical University, Chongqing 400016, China
2
College of Nursing, Chongqing Medical University, Chongqing 400016, China
3
First Clinical College, Chongqing Medical University, Chongqing 400016, China
4
The Center of Experimental Teaching Management, Chongqing Medical University, Chongqing 400016, China
*
Authors to whom correspondence should be addressed.
Medicina 2022, 58(6), 771; https://doi.org/10.3390/medicina58060771
Submission received: 13 May 2022 / Revised: 1 June 2022 / Accepted: 2 June 2022 / Published: 7 June 2022
(This article belongs to the Topic State-of-the-Art Dentistry and Oral Health)

Abstract

:
Background and objectives: To compare the efficacy and safety of topical interventions used for recurrent aphthous stomatitis. Materials and Methods: This network meta-analysis was conducted in accordance with the PRISMA statement. We searched four electronic databases, PubMed, Web of Science (WOS), Cochrane Central Register of Controlled Trials and Embase, for randomized controlled trials reporting efficacy and safety data on topical interventions for recurrent aphthous stomatitis. We performed a quality evaluation using a methodology based on the Cochrane Handbook. Two authors independently extracted data on healing effect, size reduction effect, symptom reduction effect, recurrence and safety assessment. Network meta-analysis was then performed using ADDIS and RevMan. Results: A total of 72 trials (5272 subjects) involving 29 topical interventions were included. Honey, lnsulin liposome gel, laser, amlexanox, glycyrrhiza and triamcinolone had better efficacy performance. Probiotics and chlorhexidine helped to prolong ulcer intervals and reduce recurrence. Doxycycline and penicillin had a high risk of adverse events. Hematologic evaluation showed no preference. The rank possibility of size-reducing effect and symptom-reducing effect supported the short-term effect of laser and the long-term effect of probiotics. Conclusions: We recommend the use of laser as a short-term intervention during the exacerbation phase of RAS and probiotics as a long-term intervention during the exacerbation and remission phases of RAS.

1. Introduction

Recurrent aphthous ulcer (RAU) or recurrent aphthous stomatitis (RAS) is a very common disease of the oral mucosa. The prevalence can range from 1.4% to 21.4% [1,2,3,4,5], according to retrospective population-based studies in different countries and regions. Research on the etiology and pathogenesis of RAS is extensive. Many views have suggested that the oral microbiota may be the culprit [6], with Streptococcus [7], Helicobacter pylori [8], cytomegalovirus [9] and a variety of obscure microorganisms [10] all thought to be potentially important members of the core microbiota responsible for ulcers. Systemic diseases can also have ulcers as an important phenotype [11], adding to the uncertainty of etiologic tracing. In conclusion, the etiology and pathogenesis of RAS are not fully understood, leading to the fact that specific treatments for RAU have not been identified in clinical and basic trials [12]. The current treatment for RAS is still mainly symptomatic, with the main objectives of relieving pain, promoting lesion healing and prolonging the interval period. Topical treatment is considered effective for the treatment of minor recurrent aphthous ulcer (MiRAU) and as an adjunct to the treatment of major recurrent aphthous ulcer (MaRAU). Topical medication, laser, cryotherapy and cautery are currently considered to be effective topical treatments [13]. Topical glucocorticoids are the first-line drug for topical application. They are used for the local treatment of RAS through their anti-inflammatory and immunosuppressive effects, such as dexamethasone and triamcinolone [14]. Tetracyclines and their derivatives (especially doxycycline) are also thought to inhibit ulcer formation and tissue destruction due to lesions. They act by inhibiting matrix metalloproteinases in the inflammatory pathway [15]. Amlexanox has also been repeatedly mentioned in current studies. It is thought to have anti-inflammatory and anti-allergic properties [16]. Biological and laser treatments are new therapeutic techniques for mucosal diseases that are now expected to have high expectations. Recent systematic analyses have affirmed the role of changes in oral flora in the progression of RAS [17], which also provides the basis for topical probiotic interventions. Laser therapy has had a positive effect in accelerating tissue repair and relieving pain [18], with satisfactory responses to the management of RAS. Some traditional treatments such as freezing [19] and cautery [20] have a positive effect on cell metabolism and tissue regeneration which are still heavily used in some areas. Low serum zinc levels have also been shown to be a risk factor for RAS in numerous studies [21]; hence, topical zinc supplementation is also recommended. In addition, some natural extracts such as curcumin [22], glycyrrhiza [23], honey [24], quercetin [25], chitosan [26], aloe [27], berberine gelatin [28], diosmectite [29], allicin [30] and other extracts have been shown in some studies to be promising topical interventions for ulcers.
RAS is a self-limiting disease that can vary in duration and status from one individual to another. Most cases of recurrent Aphthous stomatitis only last a few days and then tend to heal. However, the quality of daily life is severely affected by localized mucosal defects resulting in poor palatability, pain due to chemical-mechanical irritation and recurrent episodes [31]. To date, several authors have conducted traditional meta-analyses of local interventions for RAS [32,33,34]. Their focus has been on whether the interventions studied have a positive effect compared to an ineffective placebo. Such an approach to research dictates that only pairwise comparative estimates of effect can be derived, but the relative efficacy of more than two interventions cannot be compared simultaneously. Which local intervention is most efficacious for RAS remains controversial, and there is a lack of valid research evidence.
Based on a search of relevant databases, no comprehensive systematic evaluation and ranking of multiple local interventions for the treatment of RAS has been identified. Therefore, we reviewed existing studies and included multiple randomized controlled trials (RCTs) in a systematic evaluation study to assess the efficacy and safety of as many as 29 local interventions for the treatment of RAS. Our aim was to provide a reliable reference for the selection of more efficient topical treatment options for patients with RAS.

2. Materials and Methods

2.1. Statement

Network meta-analysis (NMA) is a new type of high-quality analysis method. It is based on the assumptions of homogeneity, transferability and consistency. It fulfils the purpose of allowing simultaneous comparisons between multiple interventions and also provides a possible ranking of the effectiveness of different interventions [35]. As a result, NMA is used in many studies to provide more efficient evidence and to select superior solutions. Our study was carried out in strict accordance with the criteria and requirements for conducting the NMA [36]. Our study was conducted in accordance with the relevant statements. The Addis, Revman, Endnote and other software used in the study complied with the relevant operational requirements. The study was registered in the PROSPERO International Prospective Register of Systematic Reviews in accordance with the relevant requirements prior to implementation (CRD42021251154).

2.2. Data Sources and Search Strategy

Four databases, PubMed, Web of Science (WOS), Cochrane Central Register of Controlled Trials, and Embase, were searched during the study. The search was conducted from the date of creation of the database to 1 October 2021. The search was carried out using the medical terms “Stomatitis, Aphthous”, “Oral Ulcer” and “Clobetasol”. Synonyms and abbreviations such as “Canker sore”, “Corticosteroid” and “LLLT*” were also used as keywords to broaden the search. The search process was carried out by two independent individuals, and Endnote literature management software was used to manage the search results. The search strategy is detailed in Tables S1–S5.

2.3. Selection Criteria

The RCTs included in the study met the following criteria:
(1)
Clinical or histopathological examination confirms a diagnosis of recurrent aphthous ulcers, with ulcer-like lesions visible anywhere on the oral mucosa.
(2)
Simple ulcerative lesions of any undetermined cause such as psychological, nutritional and immunological factors, rather than oral manifestations of systemic diseases such as leukoaraiosis, diabetes mellitus, etc., or specific ulcerative lesions due to trauma, radiotherapy, etc.
(3)
The population enrolled received only local interventions or placebo during the trial and did not receive any other treatment that might alter the RAS prior to or during the trial, such as receiving systemic steroids or immunosuppressants.
(4)
For studies in patients with multiple oral mucosal diseases, we extracted only RAS data. If this was not possible, we excluded the study.

2.4. Outcomes

In this study, clinical efficacy and safety were selected as outcome indicators. Clinical efficacy was assessed by healing efficacy, effect of size reduction and effect of symptom reduction. Healing efficacy was assessed by the time to healing, i.e., the time elapsed from the time the subject was enrolled for the local intervention to the time the ulcer-like lesion was completely healed. The effect of size reduction was assessed by the efficacy index (EI). In this case, EI was calculated by EI = ulcer reduction area (mm2)/ulcer baseline area (mm2). The cumulative reduction in ulcer size on different examination days over the duration of the trial was counted. The effect of symptom reduction was also assessed by the efficacy index (EI). In this case, EI was calculated by EI = reduction in pain score/baseline ulcer pain score. Individual subject’s VAS score or decile scale score of pain level on different examination days. The degree of cumulative pain relief was calculated (VAS score: 10 cm horizontal line, marked 0 = no pain to 10 = worst pain; Decile scale: 0 for no pain, 10 for most pain). Safety was evaluated by the number of adverse events and the blood levels of the intervening drug. The study also extracted an evaluation regarding the effect on RAS recurrence.

2.5. Data Collection and Risk of Bias Assessment

Two researchers independently read and screened the literature against the inclusion and exclusion criteria, evaluated the quality of the literature against the criteria and extracted the information. The above process was completed independently by the two researchers and cross-checked, with any disagreements being resolved by consultation with a third party or discussion. Information extracted included: the first author of included studies, time of publication, country, sample size, gender, age, interventions and outcome indicators. The quality of included studies was assessed using RevMan 5.3 software provided by the Cochrane Collaboration. The evaluation included: (1) random sequence generation; (2) allocation concealment; (3) blinding of participants and personnel; (4) blinding of outcome assessment; (5) incomplete outcome data; (6) selective reporting; (7) other bias. The potential publication bias of the included studies was analyzed using a funnel plotting approach.

2.6. Data Synthesis and Statistical Analysis

Traditional meta-analysis was performed using RevMan 5.3 and ADDIS 1.16. Risk difference (RD) was used as an effective indicator for dichotomous variables and mean difference (MD) was used as an effective indicator for continuous variables, and 95% confidence intervals (95% CI) were used for each effect size estimate. I2 was used to quantify the heterogeneity of the test results. If p ≥ 0.1 and I2 ≤ 50%, the heterogeneity among the test results was considered small, and a fixed-effects model was used for combining; if p < 0.1 and I2 > 50%, the heterogeneity among the test results was considered large, and a random-effects model was used for combining, and a subgroup analysis or case-by-case literature exclusion method was used for sensitivity analysis.
A random-effects network within a Bayesian framework model was constructed using ADDIS 1.16 [37]. Networks were constructed according to different outcome indicators in order to include as many local interventions as possible. Direct and indirect comparisons were made between the different interventions to ensure that the results obtained were based on comprehensiveness and completeness considerations. Statistically significant differences were considered at p < 0.05. Ranking probabilities were also estimated in ADDIS 1.16. The MD of each local intervention compared to an arbitrary control was calculated, and the number of iterations of the Markov chain was calculated to evaluate the degree of convergence of the model. Variance calculations and node splitting analyses were also performed to assess inconsistency in the network meta-analysis. Results were considered inconsistent if the random effects variance differed significantly from the inconsistency or if the difference between direct and indirect evidence was judged to be p < 0.05.

3. Results

3.1. Study Selection

A total of 11,962 records were identified by searching the four databases. After removing 2388 duplicate articles, we screened the titles and abstracts of 9574 articles. A total of 9314 articles that did not meet the inclusion criteria were excluded. A full-text review of 260 articles was conducted, and 186 of these were excluded, resulting in 72 eligible studies being used for qualitative and quantitative research (Figure 1).

3.2. Characteristics and Quality of Studies

The 72 included studies are described in Table S6. They included three three-arm studies and two four-arm studies, in addition to one study that subgrouped the adult and child groups, which we also grouped in our study for comparison. The vast majority of subjects included were patients with definite RAS, most with definite minor RAS, and a few studies described the size of the subject’s ulcer, meeting the criteria for inclusion. Subjects were histologically and clinically confirmed, and all had definite symptoms at study entry. The minimum mean age was 6.82, and the oldest subject was 71 years. Most studies had more females than males. Treatment duration ranged from a few days to several months. Intervention forms could be loaded by a mucoadhesive matrix or presented as a paste, liquid, etc. Specific interventions and treatment plans are given in Table S6. The outcomes of the studies are summarized in Tables S7 and S8.
In total, 69 studies were included to measure four evaluation items: (a) healing effect, data from 26 RCTs (1306 participants); (b) size-reducing effect, data from 37 RCTs (3587 participants); (c) symptom-reducing effect, data from 46 RCTs (4020 participants); (d) adverse effect, data from 36 RCTs (2787 participants). The network structure is shown in Figure 2. Three studies, because of incomplete data, only had the information about recurrence outcomes and were evaluated descriptively. In addition, 4 of the 72 studies described hematologic values, which we also evaluated descriptively only. The risk of bias estimates are shown in Figures S1 and S2. The majority of the studies showed a low risk of bias in terms of “incomplete outcome data”, “selective reporting” and “other bias”. Because some of the articles did not detail the specific processes for allocation, randomization, and measurement in the text, the risk estimates for “random sequence generation”, “allocation concealment” and “bling of outcome assessment” were judged as unclear risks. Some studies were single-blinded because of the limitations of interventions such as laser, cauterization and freezing, which did not completely shield participants, and therefore were considered high risk for “blinding of participants and personnel“. However, this does not mean that the quality of the included articles is too low. Using RevMan 5.3 software as an aid, we created funnel plots (Tables S3–S6).

3.3. Pairwise Meta-Analysis

Data from 14 RCTs (n = 820) with seven pairwise comparisons were pooled for healing effect (Chapter S1). Triamcinolone, laser, silver nitrate, and honey all showed a significant preference compared to placebo, while curcumin vs. triamcinolone and triamcinolone vs. placebo did not show a clear preference in the comparison.
Data from 23 RCTs (n = 1807) with eight pairwise comparisons were pooled for size-reducing effect (Chapter S2). Triamcinolone, probiotics, glycyrrhiza and amlexanox were significantly better than placebo, while aloe vs. placebo, curcumin vs. triamcinolone, laser vs. placebo and probiotics vs. triamcinolone did not show a statistically significant difference.
Data from 32 RCTs (n = 2940) with nine pairwise comparisons were pooled for symptom-reducing effect (Chapter S3). Triamcinolone, laser, glycyrrhiza, amlexanox and aloe were considered superior to placebo. Preference was given to laser over triamcinolone. Curcumin vs. triamcinolone, doxycycline vs. placebo, and probiotics vs. placebo were considered indistinguishable.
Data from 22 RCTs (n = 1748) with nine pairwise comparisons were pooled for adverse effects (Chapter S4). There were no statistically significant differences found between any of them.
In addition, there is one point that needs to be added about the two outcome indicators, the size-reducing effect and symptom-reducing effect. Considering that the reporting time of the different studies was not far apart and did not meet the requirement to be divided into long-term and short-term comparisons, we performed pairwise comparisons only at the endpoint of treatment. However, more detailed and precise comparisons of daily changes were also performed, which are shown in Chapters S2 and S3.

3.4. Network Meta-Analysis

3.4.1. Healing Effect

Data from 26 RCTs [20,24,26,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60] with 20 pairwise comparisons among 18 interventions were pooled. The relative effect estimates for honey, insulin liposome gel and laser exhibited shorter healing times and better healing effects relative to placebo. (Estimates values are shown in Table 1). No significant differences were observed in the other comparisons (more details are shown in Chapter S1). From our analysis, we concluded that these 18 local interventions may have consistent or similar performance in terms of healing effect. Compared to placebo, the rank possibility (only the top five are listed in Table 2, more details are shown in Chapter S1) indicates that the best intervention is Insulin-liposomal gel (p-core, 0.24), followed by honey (p-core, 0.15), laser (p-core, 0.11), penicillin (p-core, 0.09) and aloe (p-core, 0.06).

3.4.2. Size-Reducing Effect

Data from 37 RCTs [19,22,25,27,28,29,30,40,42,48,50,55,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84] with 30 pairwise comparisons among 19 interventions were pooled. Network meta-analysis indicated that amlexanox, glycyrrhiza and triamcinolone were more effective than placebo (Table 1). No significant differences in size-reduction effect were shown for the other interventions (Chapter S2). Based on the rank possibility (Table 2, Chapter S2), the optimal solution is quercetin (p-core, 0.27). The other possible efficient interventions in priority order are dexamethasone (p-core, 0.14), amlexanox (p-core, 0.13), glycyrrhiza or laser (p-core, 0.08) and curcumin (p-core, 0.08).
Most studies not only assessed efficacy at the end of the intervention but also performed many measurements during the treatment period. To take full advantage of these data to compare the change in ulcer size for each day of the treatment period, a more detailed ranking was performed (Chapter S2). This ranking uses days as the unit of time rather than the full treatment period. We extracted the probability that each intervention was first-ranked (p-core) and plotted it as a “Time-Rank 1 probability” folding line chart to more accurately reflect the effect of the intervention on ulcer size (Chart 1). We considered laser, glycyrrhiza and zinc to be the most potential to significantly reduce ulcer size in the short term.

3.4.3. Symptom-Reducing Effect

Data from 46 RCTs [20,25,28,29,30,38,43,44,46,48,50,51,52,53,55,61,62,63,64,65,66,67,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91] with 32 pairwise comparisons among 23 interventions were pooled. Amlexanox, laser and triamcinolone have a significant advantage over placebo (Table 1). No statistically significant differences were shown between the other interventions (Chapter S3). Rank possibility (Table 2, Chapter S3) is more in favor of insulin-liposomal gel (p-core, 0.24), followed by N-acetylcysteine or sucralfate (p-core, 0.12), curcumin (p-core, 0.08), laser (p-core, 0.09) and chlorhexidine (p-core, 0.07).
We also plotted the “Time-Rank 1 probability” folding line chart on the symptom reduction effect to reflect the improvement in pain per day during treatment (Chart 2). Laser, insulin-liposomal gel and sucralfate are considered as possible optimal solutions for short-term relief of ulcer-induced pain.

3.4.4. Adverse Effect

Data from 36 RCTs [20,22,24,26,28,29,30,40,41,42,47,48,50,53,54,63,64,65,70,71,75,76,77,80,82,83,85,86,87,88,89,92,93,94,95,96] with 32 pairwise comparisons among 22 interventions were pooled. In terms of possible adverse events, triamcinolone performed better, with none occurring in 259 subjects, compared to amlexanox, chitosan, dexamethasone, doxycycline, penicillin and placebo. Compared to penicillin and doxycycline, dexamethasone also showed a significant improvement with 4 adverse events in 120 subjects, whereas penicillin and doxycycline showed weaknesses compared to placebo (Table 1). The other interventions were not significantly different (Chapter S4). In terms of performance on the rank possibility (Table 2, Chapter S4), triamcinolone (p-core, 0.15) was the optimal choice. The other interventions were berberine gelatin (p-core, 0.08); glycyrrhiza or laser (p-core, 0.07); aloe, honey or probiotics (p-core, 0.06); and curcumin, silver nitrate, triester glycerol oxide or zinc (p-core, 0.06). Possible adverse events are collated and shown in Chapter S4.

3.5. Other Outcome Indicators

3.5.1. Hematologic Values

Four RCTs [30,77,80,82] included in the study reported on the blood levels of the intervention drug or blood laboratory findings (Table 3). There were no valuable results identified. Dexamethasone, aloe, allicin and amlexanox were not associated with hematologic safety hazards.

3.5.2. Relapse

Four RCTs [58,61,97,98] describe considerations regarding RAS recurrence (Table 4). The results involved four interventions probiotics, chlorhexidine, benzydamine and triamcinolone, with outcome indicators including outbreak frequency, number of new ulcers and interval between ulcers. The investigators’ observations were that (a) probiotics helped to reduce the frequency of ulcer outbreaks in children without the same performance in adults; (b) chlorhexidine prolonged the interval between ulcers but did not significantly reduce the number of new ulcers during the trial period; (c) benzydamine was not helpful in reducing the number of new ulcers; (d) both media-based administration or administered in liquid form, the reduction in the number of new ulcers by Triamcinolone was not statistically significant.

3.6. Consistency and Sensitivity Analysis

We used ADDIS 1.16 software to help assess the consistency and inconsistency of the network meta-analysis. The consistency model, inconsistency model and node split model were adopted for full consideration. The results concluded that statistical heterogeneity within the study was non-existent, with no inconsistency observed in any of the four comparisons healing effect, size-reducing effect, symptom-reducing effect and adverse effect. The inconsistency between direct and indirect comparisons was achieved at the minimum possible level.
In terms of sensitivity analysis, both the method of rejecting literature piece by piece for sensitivity comparison and the method of subgroup analysis based on the time of outcome measurement were used. It can be considered that the optimization was achieved as much as possible.

3.7. Our Perspective

Efficacy and safety are two essential requirements for an intervention capable of being used. In this multi-study, multi-intervention study, we also used efficacy and safety as two important items of comparison. By comparison, we concluded that in terms of safety alone, all interventions included in the study were largely compliant, none exhibiting serious adverse events or hematologic effects. Therefore, efficacy was the first consideration in selecting the interventions. Considering healing promotion, pain reduction and relapse delay as evaluation indicators and, more importantly, the time dimension, we recommend laser as a short-term “shock therapy” intervention and probiotics as a long-term “conditioning” intervention.

4. Discussion

RAS has a self-healing property [99], but by the clinical characteristics of easy recurrence, local tissue loss, and pain [31], interventions are routinely used. However, because the etiology is not clear and the individual tendency is large, the treatment of RAS is limited to symptomatic treatment. Promoting healing, relieving pain and reducing recurrence are the goals of treatment [13]. In patients with minor RAS and major RAS not accompanied by systemic symptoms, local interventions are frequently used [100]. A wide variety of local interventions are available, many of which have demonstrated promising results in clinical trials relative to placebo. However, what is best and what better meets treatment expectations has not been determined. Therefore, there is value in assessing and comparing the efficacy of available topical interventions.
This is the first systematic evaluation and network meta-analysis on topical interventions for RAS, incorporating as many potential options as possible. In this study, both paired analyses and network comparisons were implemented. Descriptive analyses were also necessary for some outcome indicators with small sample sizes and different evaluation metrics. In total, 29 topical interventions were mentioned in this study, including placebo, allicin, aloe, amlexanox, benzydamine, berberine gelatin, chitosan chlorhexidine, clobetasol, cryotherapy, curcumin, dexamethasone, diosmectite, doxycycline, glycyrrhiza, honey, insulin-liposomal gel, laser, minocycline, N-acetylcysteine, penicillin, probiotics, prostaglandin E2, quercetin, silver nitrate, sucralfate, triamcinolone, triester glycerol oxide and zinc (clobetasol and minocycline were evaluated only in adverse events and were not involved in the primary outcome). To obtain as much data as possible, we searched four major databases, also supplemented by gray sources. We established clear inclusion and exclusion criteria, especially for the exclusion of traumatic ulcers, radiological ulcers and ulcers associated with systemic diseases. Seventy-two studies (5272 subjects) were included. We evaluated four efficacy and one safety outcome. The healing effect, size-reducing effect and symptom-reducing effect were the main bases of efficacy evaluation, and relapse was only analyzed descriptively. The safety aspect was more focused on adverse effects, and hematologic values were used as a complement. In addition, rank possibility based on p-score was the tool to help in the screening.
As mentioned in the results, after combining the four efficacy evaluations and an additional safety evaluation, we propose our recommendation to clinicians: use laser as a short-term “shock therapy” during ulcer flare-ups, and use probiotics as a long-term “modifier” during the full ulcer cycle.
The laser, in our opinion, is an absolute landmark in clinical practice for the treatment of oral mucosal diseases. It is remarkable in common oral mucosal diseases and even precancerous lesions, such as oral mucositis due to radiotherapy and chemotherapy [101], oral submucosal fibrosis [102], oral lichen planus [103], oral leukoplakia [104] and burning mouth syndrome [105]. The effect of the laser on the oral mucosa has been interpreted as a stimulating biological effect [106]. Controlled laser light in a specific wavelength and power range is involved in local metabolic events through various physicochemical processes [107,108,109,110], thus exerting analgesic, anti-inflammatory and pro-repair effects without thermal damage. Certainly, the role in the treatment of RAS is gaining attention [111,112,113,114]. The types of lasers used in the current treatment are carbon dioxide laser, crystal laser, diode laser and low-level laser therapy (LLLT). In this evaluation, 14 RCTs with laser interventions were included. Five studies used diode lasers, six used CO2 lasers, one used Er, Cr: YSGG lasers, one used Nd: YAG lasers, and one used LLLT. The modality used, the wavelength of the laser and the power output were different. Whether the different types of laser interventions and the differences in the course and frequency have an impact on the efficacy is under-researched. Due to the scarcity of studies on individual kinds of lasers and the lack of treatment criteria, we grouped different kinds of laser modalities as laser in the study. In the evaluation of efficacy, lasers were considered superior in terms of healing effect, size reduction effect and symptom reduction effect during the full course of treatment. Moreover, in daily evaluations, the laser demonstrated unparalleled short-term explosive power. Laser is also unquestionable in terms of safety considerations. The latest retrospective evaluation was made by Valerie G. A. Suter and co-workers [111]. After reviewing 11 studies, they presented similar expectations for laser interventions in RAS and concerns regarding laser standardization. The advantages of the laser over other topical interventions are: (a) short treatment period: significant results with a single intervention or few interventions apart; (b) superior efficacy: excellent efficiency in promoting defect healing and reducing pain; and (c) reliable safety: several retrospective studies have found no significant safety concerns, including adverse events and hematologic testing. Therefore, laser is a worthwhile option for common cases, steroid-intolerant individuals, and patients with severe ulcers who are forced to undergo systemic treatment. Our recommendation is that laser is used as a short-term intervention during the exacerbation phase of ulcers to promote healing and reduce pain.
The oral cavity is a natural kingdom of microorganisms, and probiotics are one of the important components. The oral microbial community constructed with the participation of various probiotics is an indispensable and important member of oral microecology, which is involved in the balance with pathogenic bacteria through various potential links. This microscopic balance is considered to be essential for maintaining a healthy oral cavity [115,116]. Imbalance is dangerous and may lead to the occurrence of dental caries [117], periodontal disease [118], fungal disease [119], etc. Probiotics alone or supplemented with other drugs to modulate the composition and structure of the dominant flora in disease states, thus intervening in pathological states such as dental caries [120,121,122], periodontal disease [120,123,124] and breath odor [125,126] are supported by many studies. This also applies to RAS. Although the etiology of RAS is unclear, many microbiological and immunological studies have presented evidence for the involvement of microbial factors in the pathogenic process [10,127,128]. Probiotic therapy for RAS was thus pioneered and implemented in many practices [129]. In our study, probiotics were involved in the management of RAS in the form of topical administration. Four RCTs were performed with Lactobacillus and one with Bacillus Clausii probiotic. One was provided as a mouthwash with bacterial product (lactic acid) except for the others, which were solid tablets. The trial period was from 7 days to 90 days. In the early stage, probiotics did not show advantages in terms of healing effect, size reduction effect and symptom reduction effect. In the later stage (day 7), its efficacy in promoting healing began to appear. In the evaluation of recurrence, one study made a valuable contribution. Lotfy Aggour and co-workers [61] used L. acidophilus containing lozenges as an intervention agent for topical interventions in adult subjects and pediatric subjects compared to placebo. They counted the frequency of outbreaks in both groups over a 6-month follow-up period and concluded that the frequency was significantly lower in children using probiotics compared to controls, while the same effect was not seen in adults. More studies on recurrence are missing. The evaluation of safety is satisfactory. Possible mechanisms for the involvement of probiotics in RAS management are: (a) Competition mechanism: compared to pathogenic microorganisms in the oral cavity, probiotics have stronger surface adhesion as well as the ability to organize new aggregation and coaggregation processes [130,131,132]. This would lead to the loss of dominance of old pathogenic microorganisms and the establishment of new harmless or even beneficial biofilms. (b) Pro-repair effects: probiotics and their signaling molecules may help to reduce the levels of pro-inflammatory cytokines, collagenase, elastase and prostaglandin E2 through a series of mechanisms that promote the repair of local damage [133,134]. (c) Regulation of the microenvironment: metabolites and active molecules of probiotics, such as lactic acid, hydrogen peroxide and bacteriocins, and themselves may be involved in the regulation of the local physicochemical environment and immune environments, which facilitates the cessation of RAS progression and promotes tissue resistance and repair [131,133,135]. Based on these several effects, the microenvironment prone to RAS is regulated and is the main reason for the reduction of recurrent effects, and the limited ability to promote healing in the short term may be related to the insufficient number of metabolites and active substances. Our recommendation is that probiotics should be used as a long-term intervention in both the exacerbation and remission phases of ulcers to prolong the inter-episode interval and reduce recurrence.
There are some limitations to our study. First, RCTs on some interventions are scarce, which leads to the credibility of the study being compromised. Second, in our study, we combined different types of lasers, at different wavelengths, into one intervention category and therefore could not explore the differences between them. Studies and standards regarding this area are also lacking. Third, more studies on RAS recurrence are lacking. The evidence is weak for conclusions about probiotics based on non-direct evidence articles and a small number of clinical trials. High-quality studies that include more individuals and uniform criteria for evaluating outcomes are needed in the future.

5. Conclusions

This new consideration-based and comprehensive network meta-analysis concluded that most of the local interventions did not show significant differences in the efficacy evaluation and safety evaluation. Based on the currently available evidence, we recommend the use of laser as a short-term intervention to promote healing and reduce pain during the exacerbation phase of RAS and probiotics as a long-term intervention to prolong the inter-episode period and reduce recurrence during the exacerbation and remission phases of RAS. We call for more large-scale RCTs based on trustworthy standards.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/medicina58060771/s1, Table S1: Search Strategy; Table S2–S5: Search terms of PubMed, Web of Science, Cochrane Central Register of Controlled Trials and EMBASE; Table S6: Characteristics of included studies; Table S7: Outcomes of included studies; Table S8–S10: Details information of studies for each outcome in network meta-analysis; Table S11: PRISMA NMA Checklist of Items; Chapter S1: Healing effect; Chapter S2: Size-reducing effect; Chapter S3: Symptom-reducing effect; Chapter S4: Safety outcomes; Chapter S5: Relapse; Chart S1: “Time-Rank 1 probability” folding line chart; Figure S1: Risk of bias graph; Figure S2: Risk of bias summary for individual studies; Figure S3: Funnel plot for healing effect; Figure S4: Funnel plot for size-reducing effect; Figure S5: Funnel plot for symptom-reducing effect; Figure S6: Funnel plot for adverse effect; Figure S7: Network structure of sensitivity analysis.

Author Contributions

Conceptualization, H.L. and L.C.; methodology, H.L.; software, H.L.; validation, H.L., L.T. and G.F.; formal analysis, H.L.; investigation, H.L.; resources, L.C. and H.T.; data curation, L.T.; writing—original draft preparation, H.L.; writing—review and editing, H.L.; visualization, H.L.; supervision, L.C. and H.T.; project administration, L.C.; funding acquisition, L.C. and H.T. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by The project of Tutorial System of Medical Undergraduate in Lab Teaching and Management Center at Chongqing Medical University (Grant No. LTMCMTS202114).

Data Availability Statement

All data generated or analyzed during this study were taken from the published study. The data are included in this article and supporting file.

Conflicts of Interest

The authors state they have no conflict of interest.

References

  1. Kaur, R.; Behl, A.B.; Punia, R.S.; Nirav, K.; Singh, K.B.; Kaur, S. Assessment of Prevalence of Recurrent Aphthous Stomatitis in the North Indian Population: A Cross-Sectional Study. J. Pharm. Bioallied Sci. 2021, 13, S363–S366. [Google Scholar] [CrossRef] [PubMed]
  2. Darjani, A.; Joukar, F.; Naghipour, M.; Asgharnezhad, M.; Mansour-Ghanaei, F. Lifetime prevalence of recurrent aphthous stomatitis and its related factors in Northern Iranian population: The PERSIAN Guilan Cohort Study. Clin. Oral. Investig. 2021, 25, 711–718. [Google Scholar] [CrossRef] [PubMed]
  3. Xu, K.; Zhou, C.; Huang, F.; Duan, N.; Wang, Y.; Zheng, L.; Wang, X.; Wang, W. Relationship between dietary factors and recurrent aphthous stomatitis in China: A cross-sectional study. J. Int. Med. Res. 2021, 49, 675888644. [Google Scholar] [CrossRef]
  4. Hariyani, N.; Bramantoro, T.; Nair, R.; Singh, A.; Sengupta, K. Depression symptoms and recurrent aphthous stomatitis—Evidence from a population-based study in Indonesia. Oral Dis. 2020, 26, 948–954. [Google Scholar] [CrossRef] [PubMed]
  5. Queiroz, S.; Silva, M.; Medeiros, A.; Oliveira, P.T.; Gurgel, B.; Silveira, É. Recurrent aphthous ulceration: An epidemiological study of etiological factors, treatment and differential diagnosis. An. Bras. Dermatol. 2018, 93, 341–346. [Google Scholar] [CrossRef] [PubMed]
  6. Gasmi, B.A.; Noor, S.; Menzel, A.; Gasmi, A. Oral Aphthous: Pathophysiology, Clinical Aspects and Medical Treatment. Arch. Razi Inst. 2021, 76, 1155–1163. [Google Scholar]
  7. Bankvall, M.; Sjöberg, F.; Gale, G.; Wold, A.; Jontell, M.; Östman, S. The oral microbiota of patients with recurrent aphthous stomatitis. J. Oral Microbiol. 2014, 6, 25739. [Google Scholar] [CrossRef] [Green Version]
  8. Kazanowska-Dygdała, M.; Duś, I.; Radwan-Oczko, M. The presence of Helicobacter pylori in oral cavities of patients with leukoplakia and oral lichen planus. J. Appl. Oral Sci. 2016, 24, 18–23. [Google Scholar] [CrossRef] [Green Version]
  9. Irani, S. New Insights into Oral Cancer-Risk Factors and Prevention: A Review of Literature. Int. J. Prev. Med. 2020, 11, 202. [Google Scholar] [CrossRef]
  10. Slebioda, Z.; Szponar, E.; Kowalska, A. Etiopathogenesis of recurrent aphthous stomatitis and the role of immunologic aspects: Literature review. Arch. Immunol. Ther. Exp. 2014, 62, 205–215. [Google Scholar] [CrossRef] [Green Version]
  11. Ludovichetti, F.S.; Signoriello, A.G.; Girotto, L.; Del Dot, L.; Piovan, S.; Mazzoleni, S. Oro-dental lesions in paediatric patients with coeliac disease: An observational retrospective clinical study. Rev. Esp. Enferm. Dig. 2022; Online ahead of print. [Google Scholar] [CrossRef] [PubMed]
  12. Scully, C.; Porter, S. Oral mucosal disease: Recurrent aphthous stomatitis. Br. J. Oral Maxillofac. Surg. 2008, 46, 198–206. [Google Scholar] [CrossRef] [PubMed]
  13. Saikaly, S.K.; Saikaly, T.S.; Saikaly, L.E. Recurrent aphthous ulceration: A review of potential causes and novel treatments. J. Dermatolog. Treat. 2018, 29, 542–552. [Google Scholar] [CrossRef] [PubMed]
  14. Ahluwalia, A. Topical glucocorticoids and the skin—Mechanisms of action: An update. Mediat. Inflamm. 1998, 7, 183–193. [Google Scholar] [CrossRef] [PubMed]
  15. Golub, L.M.; Ramamurthy, N.S.; Mcnamara, T.F.; Greenwald, R.A.; Rifkin, B.R. Tetracyclines inhibit connective tissue breakdown: New therapeutic implications for an old family of drugs. Crit. Rev. Oral Biol. Med. 1991, 2, 297–321. [Google Scholar] [CrossRef]
  16. Baccaglini, L.; Lalla, R.V.; Bruce, A.J.; Sartori-Valinotti, J.C.; Latortue, M.C.; Carrozzo, M.; Rogers, R.R. Urban legends: Recurrent aphthous stomatitis. Oral Dis. 2011, 17, 755–770. [Google Scholar] [CrossRef] [Green Version]
  17. Yuan, H.; Qiu, J.; Zhang, T.; Wu, X.; Zhou, J.; Park, S. Quantitative changes of Veillonella, Streptococcus, and Neisseria in the oral cavity of patients with recurrent aphthous stomatitis: A systematic review and meta-analysis. Arch. Oral Biol. 2021, 129, 105198. [Google Scholar] [CrossRef] [PubMed]
  18. Da Silva, J.P.; Da Silva, M.A.; Almeida, A.P.; Lombardi, J.I.; Matos, A.P. Laser therapy in the tissue repair process: A literature review. Photomed. Laser Surg. 2010, 28, 17–21. [Google Scholar] [CrossRef] [PubMed]
  19. Arikan, O.K.; Birol, A.; Tuncez, F.; Erkek, E.; Koc, C. A prospective randomized controlled trial to determine if cryotherapy can reduce the pain of patients with minor form of recurrent aphthous stomatitis. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. Endod. 2006, 101, E1–E5. [Google Scholar] [CrossRef]
  20. Soylu Özler, G. Silver nitrate cauterization: A treatment option for aphthous stomatitis. J. Cranio-Maxillofac. Surg. 2014, 42, e281–e283. [Google Scholar] [CrossRef] [PubMed]
  21. Al-Maweri, S.A.; Halboub, E.; Al-Sharani, H.M.; Shamala, A.; Al-Kamel, A.; Al-Wesabi, M.; Albashari, A.; Al-Sharani, A.; Abdulrab, S. Association between serum zinc levels and recurrent aphthous stomatitis: A meta-analysis with trial sequential analysis. Clin. Oral Investig. 2021, 25, 407–415. [Google Scholar] [CrossRef]
  22. Manifar, S.; Obwaller, A.; Gharehgozloo, A.; Boorboor Shirazi Kordi, H.R.; Akhondzadeh, S. Curcumin gel in the treatment of minor aphthous ulcer: A randomized, placebo-controlled trial. J. Med. Plants 2012, 11, 40–45. [Google Scholar]
  23. Martin, M.D.; Sherman, J.; Van Der Ven, P.; Burgess, J. A controlled trial of a dissolving oral patch concerning glycyrrhiza (licorice) herbal extract for the treatment of aphthous ulcers. Gen. Dent. 2008, 56, 206–210. [Google Scholar] [PubMed]
  24. El-Haddad, S.A.; Asiri, F.Y.; Al-Qahtani, H.H.; Al-Ghmlas, A.S. Efficacy of honey in comparison to topical corticosteroid for treatment of recurrent minor aphthous ulceration: A randomized, blind, controlled, parallel, double-center clinical trial. Quintessence Int. 2014, 45, 691–701. [Google Scholar]
  25. Pandya, M.; Kalappanavar, A.N.; Annigeri, R.G.; Rao, D.S. Relative Efficacy of Quercetin Compared with Benzydamine Hydrochloride in Minor Aphthae: A Prospective, Parallel, Double Blind, Active Control, Preliminary Study. Int. J. Dent. 2017, 2017, 7034390. [Google Scholar] [CrossRef] [Green Version]
  26. Rahmani, F.; Moghadamnia, A.A.; Kazemi, S.; Shirzad, A.; Motallebnejad, M. Effect of 0.5% Chitosan mouthwash on recurrent aphthous stomatitis: A randomized double-blind crossover clinical trial. Electron. Physician 2018, 10, 6912–6919. [Google Scholar] [CrossRef]
  27. Babaee, N.; Zabihi, E.; Mohseni, S.; Moghadamnia, A.A. Evaluation of the therapeutic effects of Aloe vera gel on minor recurrent aphthous stomatitis. Dent. Res. J. 2012, 9, 381–385. [Google Scholar]
  28. Jiang, X.W.; Zhang, Y.; Zhu, Y.L.; Zhang, H.; Lu, K.; Li, F.F.; Peng, H.Y. Effects of berberine gelatin on recurrent aphthous stomatitis: A randomized, placebo-controlled, double-blind trial in a Chinese cohort. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. 2013, 115, 212–217. [Google Scholar] [CrossRef] [PubMed]
  29. Jiang, X.W.; Zhang, Y.; Zhang, H.; Lu, K.; Yang, S.K.; Sun, G.L. Double-blind, randomized, controlled clinical trial of the effects of diosmectite and basic fibroblast growth factor paste on the treatment of minor recurrent aphthous stomatitis. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. 2013, 116, 570–575. [Google Scholar] [CrossRef]
  30. Jiang, X.W.; Zhang, Y.; Song, G.D.; Li, F.F.; Peng, H.Y.; Yang, S.K.; Sun, G.L. Clinical evaluation of allicin oral adhesive tablets in the treatment of recurrent aphthous ulceration. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. 2012, 113, 500–504. [Google Scholar] [CrossRef] [PubMed]
  31. Al-Omiri, M.K.; Karasneh, J.; Alhijawi, M.M.; Zwiri, A.M.; Scully, C.; Lynch, E. Recurrent aphthous stomatitis (RAS): A preliminary within-subject study of quality of life, oral health impacts and personality profiles. J. Oral Pathol. Med. 2015, 44, 278–283. [Google Scholar] [CrossRef]
  32. Cheng, B.; Zeng, X.; Liu, S.; Zou, J.; Wang, Y. The efficacy of probiotics in management of recurrent aphthous stomatitis: A systematic review and meta-analysis. Sci. Rep. 2020, 10, 21181. [Google Scholar] [CrossRef]
  33. Al-Maweri, S.A.; Halboub, E.; Ashraf, S.; Alqutaibi, A.Y.; Qaid, N.M.; Yahya, K.; Alhajj, M.N. Single application of topical doxycycline in management of recurrent aphthous stomatitis: A systematic review and meta-analysis of the available evidence. BMC Oral Health 2020, 20, 231. [Google Scholar] [CrossRef] [PubMed]
  34. Cheng, L.L. Limited Evidence Suggests That Patients with Recurrent Aphthous Stomatitis May Benefit from Using Sodium Lauryl Sulfate-free Dentifrices. J. Evid. Based Dent. Pract. 2019, 19, 101349. [Google Scholar] [CrossRef]
  35. Watt, J.; Tricco, A.C.; Straus, S.; Veroniki, A.A.; Naglie, G.; Drucker, A.M. Research Techniques Made Simple: Network Meta-Analysis. J. Invest. Dermatol. 2019, 139, 4–12. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  36. Hutton, B.; Salanti, G.; Caldwell, D.M.; Chaimani, A.; Schmid, C.H.; Cameron, C.; Ioannidis, J.P.; Straus, S.; Thorlund, K.; Jansen, J.P.; et al. The PRISMA extension statement for reporting of systematic reviews incorporating network meta-analyses of health care interventions: Checklist and explanations. Ann. Intern. Med. 2015, 162, 777–784. [Google Scholar] [CrossRef] [Green Version]
  37. van Valkenhoef, G.; Tervonen, T.; Zwinkels, T.; de Brock, B.; Hillege, H. ADDIS: A decision support system for evidence-based medicine. Decis. Support Syst. 2013, 55, 459–475. [Google Scholar] [CrossRef] [Green Version]
  38. Huo, X.; Han, N.; Liu, L. Effect of different treatments on recurrent aphthous stomatitis: Laser versus medication. Lasers Med. Sci. 2021, 36, 1095–1100. [Google Scholar] [CrossRef]
  39. Shi, Y.; Wei, K.; Lu, J.; Wei, J.; Hu, X.; Chen, T. A Clinic Trial Evaluating the Effects of Aloe Vera Fermentation Gel on Recurrent Aphthous Stomatitis. Can. J. Infect. Dis. Med. Microbiol. 2020, 2020, 8867548. [Google Scholar] [CrossRef]
  40. Ibrahim, S.A.; Elkot, R.A.; Soliman, H.E. Lactic acid 5% mouth wash vs Kenalog in Orabase 0.1% for treatment and prophylaxis of recurrent aphthous ulcer. J. Cosmet. Dermatol. 2020, 19, 964–969. [Google Scholar] [CrossRef]
  41. Owlia, M.B.; Mirzadeh, M.; Mehrpoor, G. Penicillin in oral aphthosis, new insight for an old drug: A randomized, double-blind, controlled clinical trial. J. Res. Med. Sci. 2020, 25, 95. [Google Scholar]
  42. Raman, P.; Pitty, R.; Krithika, C.L.; Anand, S.P.N.; Subramani, G.P. Topical Curcumin and Triamcinolone Acetonide in Recurrent Minor Aphthous Ulcers: A Pilot Trial. J. Contemp. Dent. Pract. 2020, 21, 884–890. [Google Scholar]
  43. Halboub, E.; Alkadasi, B.; Alakhali, M.; Alkhairat, A.; Mdabesh, H.; Alkahsah, S.; Abdulrab, S. N-acetylcysteine versus chlorhexidine in treatment of aphthous ulcers: A preliminary clinical trial. J. Dermatol. Treat. 2019, 32, 649–653. [Google Scholar] [CrossRef] [PubMed]
  44. El-Wakeel, N.M.; Dawoud, M.H.S. Topical insulin-liposomal formulation in management of recurrent aphthous ulcers: A randomized placebo-controlled trial. J. Investig. Clin. Dent. 2019, 10, e12437. [Google Scholar] [CrossRef]
  45. Tavangar, A.; Aslani, A.; Nikbakht, N. Comparative Study of Punica granatum Gel and Triadent Oral Paste Effect on Recurrent Aphthous Stomatitis, a Double Blind Clinical Trial. J. Dent. 2019, 20, 184–189. [Google Scholar]
  46. Zeini, J.N.; Ghapanchi, J.; Pourshahidi, S.; Zahed, M.; Ebrahimi, H. Clinical Evaluation of High and Low-Level Laser Treatment (CO2vsInGaAlP Diode Laser) for Recurrent Aphthous Stomatitis. J. Dent. 2017, 18, 17–23. [Google Scholar]
  47. Rodríguez-Archilla, A.; Raissouni, T. Randomized clinical trial of the effectiveness of complementary therapies for recurrent aphthous stomatitis. Med. Clin. 2017, 149, 55–60. [Google Scholar] [CrossRef]
  48. Raeesi, V.; Arbabi-Kalati, F.; Akbari, N.; Hamishekar, H. Comparison effectiveness of the bioadhesive paste containing licorice 5% with bioadhesive paste without drug in the management of recurrent aphthous stomatitis. Acta Med. Mediterr. 2015, 31, 1331–1335. [Google Scholar]
  49. Aggarwal, H.; Pal Singh, M.; Nahar, P.; Mathur, H.; Sowmya, G.V. Efficacy of low-level laser therapy in treatment of recurrent aphthous ulcers—A sham controlled, split mouth follow up study. J. Clin. Diagn. Res. 2014, 8, 218–221. [Google Scholar] [CrossRef]
  50. Deshmukh, R.A.; Bagewadi, A.S. Comparison of effectiveness of curcumin with triamcinolone acetonide in the gel form in treatment of minor recurrent aphthous stomatitis: A randomized clinical trial. Int. J. Pharm. Investig. 2014, 4, 138–141. [Google Scholar] [CrossRef] [Green Version]
  51. Soylu, Ö.G.; Okuyucu, Ş.; Akoğlu, E. The Efficacy of Sucralfate and Chlorhexidine as an Oral Rinse in Patients with Recurrent Aphthous Stomatitis. Adv. Med. 2014, 2014, 986203. [Google Scholar]
  52. Prasad, R.S.; Pai, A. Assessment of immediate pain relief with laser treatment in recurrent aphthous stomatitis. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. 2013, 116, 189–193. [Google Scholar] [CrossRef] [PubMed]
  53. Vijayabala, G.S.; Kalappanavar, A.N.; Annigeri, R.G.; Sudarshan, R.; Shettar, S.S. Single application of topical doxycycline hyclate in the management of recurrent aphthous stomatitis. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. 2013, 116, 440–446. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  54. Zand, N.; Fateh, M.; Ataie-Fashtami, L.; Djavid, G.E.; Fatemi, S.M.; Shirkavand, A. Promoting wound healing in minor recurrent aphthous stomatitis by non-thermal, non-ablative CO2 laser therapy: A pilot study. Photomed. Laser Surg. 2012, 30, 719–723. [Google Scholar] [CrossRef] [PubMed]
  55. Moghadamnia, A.A.; Motallebnejad, M.; Khanian, M. The efficacy of the bioadhesive patches containing licorice extract in the management of recurrent aphthous stomatitis. Phytother. Res. 2009, 23, 246–250. [Google Scholar] [CrossRef]
  56. Garnick, J.J.; Singh, B.; Winkley, G. Effectiveness of a medicament containing silicon dioxide, aloe, and allantoin on aphthous stomatitis. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. Endod. 1998, 86, 550–556. [Google Scholar] [CrossRef]
  57. Taylor, L.J.; Walker, D.M.; Bagg, J. A clinical trial of prostaglandin E2 in recurrent aphthous ulceration. Brit. Dent. J. 1993, 175, 125–129. [Google Scholar] [CrossRef]
  58. Hunter, L.; Addy, M. Chlorhexidine gluconate mouthwash in the management of minor aphthous ulceration. A double-blind, placebo-controlled cross-over trial. Brit. Dent. J. 1987, 162, 106–110. [Google Scholar] [CrossRef] [PubMed]
  59. Addy, M.; Carpenter, R.; Roberts, W.R. Management of recurrent aphthous ulceration. A trial of chlorhexidine gluconate gel. Br. Dent. J. 1976, 141, 118–120. [Google Scholar] [CrossRef]
  60. Addy, M.; Tapper-Jones, L.; Seal, M. Trial of astringent and antibacterial mouthwashes in the management of recurrent aphthous ulceration. Br. Dent. J. 1974, 136, 452–455. [Google Scholar] [CrossRef]
  61. Aggour, R.L.; Mahmoud, S.H.; Abdelwhab, A. Evaluation of the effect of probiotic lozenges in the treatment of recurrent aphthous stomatitis: A randomized, controlled clinical trial. Clin. Oral Invest. 2021, 25, 2151–2158. [Google Scholar] [CrossRef]
  62. Kavita, K.; Singh, R.; Singh, R.; Gonuguntla, S.; Luke, A.M.; Jois, H.S. Assessment of efficacy of 5% topical amlexanox and 0.1% topical triamcinolone acetonide in management of recurrent aphthous stomatitis. J. Pharm. Bioallied Sci. 2020, 12, S444–S447. [Google Scholar]
  63. Shao, Y.; Zhou, H. Clinical evaluation of an oral mucoadhesive film containing chitosan for the treatment of recurrent aphthous stomatitis: A randomized, double-blind study. J. Dermatol. Treat. 2020, 31, 739–743. [Google Scholar] [CrossRef]
  64. Ghorbani, A.; Akbari, J.; Boorboor, M.; Nekoukar, Z.; Eslami, G. Evaluation of zinc sulfate mucoadhesive formulation on recurrent aphthous stomatitis: A randomized double-blind, placebo-controlled clinical trial. BMC Oral Health 2020, 20, 212. [Google Scholar] [CrossRef] [PubMed]
  65. Kia, S.J.; Mansourian, A.; Basirat, M.; Akhavan, M.; Mohtasham-Amiri, Z.; Moosavi, M.S. New concentration of curcumin orabase in recurrent aphthous stomatitis: A randomized, controlled clinical trial. J. Herb. Med. 2020, 22, 100336. [Google Scholar] [CrossRef]
  66. Bardellini, E.; Veneri, F.; Amadori, F.; Conti, G.; Majorana, A. Photobiomodulation therapy for the management of recurrent aphthous sto-matitis in children: Clinical effectiveness and parental satisfaction. Med. Oral Patol. Oral 2020, 25, e549–e553. [Google Scholar] [CrossRef] [PubMed]
  67. Seyyedi, S.A.; Olyaee, P.; Fekrazad, R.; Partovi, S.; Baghizadeh, F.M. The Effect of Carbon Dioxide Laser on Aphthous stomatitis Treatment: A Double-Blind Randomized Clinical Trial. J. Lasers Med. Sci. 2020, 11, S67–S72. [Google Scholar] [CrossRef] [PubMed]
  68. Nirmala, M.; Smitha, S.G.; Kamath, G.J. A Study to Assess the Efficacy of Local Application of Oral Probiotic in Treating Recurrent Aphthous Ulcer and Oral Candidiasis. Indian J. Otolaryngol. Head Neck Surg. 2019, 71, 113–117. [Google Scholar] [CrossRef] [PubMed]
  69. Soliman, H.A.; Mostafaa, D. Clinical evaluation of 660 nm diode laser therapy on the pain, size and functional disorders of recurrent aphthous stomatitis. Open Access Maced. J. Med. Sci. 2019, 7, 1516–1522. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  70. Sharma, R.; Pallagatti, S.; Aggarwal, A.; Sheikh, S.; Singh, R.; Gupta, D. A Randomized, Double-Blind, Placebo-Controlled Trial on Clinical Efficacy of Topical Agents in Reducing Pain and Frequency of Recurrent Aphthous Ulcers. Open Dent. J. 2018, 12, 700–713. [Google Scholar] [CrossRef] [PubMed]
  71. Ofluoglu, D.; Ergun, S.; Warnakulasuriya, S.; Namdar-Pekiner, F.; Tanyeri, H. An evaluation of the efficacy of a topical gel with Triester Glycerol Oxide (TGO) in the treatment of minor recurrent aphthous stomatitis in a turkish cohort: A randomized, double-blind, placebo-controlled clinical trial. Med. Oral Patol. Oral Cir. Bucal 2017, 22, e159–e166. [Google Scholar] [CrossRef] [Green Version]
  72. Nasry, S.A.; El Shenawy, H.M.; Mostafa, D.; Ammar, N.M. Different modalities for treatment of recurrent aphthous stomatitis. A randomized clinical trial. J. Clin. Exp. Dent. 2016, 8, e517–e522. [Google Scholar] [CrossRef]
  73. Abbasi, F.; Raoof, M.; Khatami, R.; Shadman, N.; Borjian-Boroojeni, F.; Nazari, F. Effectiveness of Amlexanox and Adcortyl for the treatment of recurrent aphthous ulcers. J. Clin. Exp. Dent. 2016, 8, e368–e372. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  74. Andishe Tadbir, A.; Pourshahidi, S.; Ebrahimi, H.; Hajipour, Z.; Memarzade, M.R.; Shirazian, S. The effect of Matricaria chamomilla (chamomile) extract in Orabase on minor aphthous stomatitis, a randomized clinical trial. J. Herb. Med. 2015, 5, 71–76. [Google Scholar] [CrossRef]
  75. Mansour, G.; Ouda, S.; Shaker, A.; Abdallah, H.M. Clinical efficacy of new aloe vera- and myrrh-based oral mucoadhesive gels in the management of minor recurrent aphthous stomatitis: A randomized, double-blind, vehicle-controlled study. J. Oral Pathol. Med. 2014, 43, 405–409. [Google Scholar] [CrossRef]
  76. Bhat, S.; Sujatha, D. A clinical evaluation of 5% amlexanox oral paste in the treatment of minor recurrent aphthous ulcers and comparison with the placebo paste: A randomized, vehicle controlled, parallel, single center clinical trial. Indian J. Dent. Res. Off. Publ. Indian Soc. Dent. Res. 2013, 24, 593–598. [Google Scholar] [CrossRef]
  77. Bhalang, K.; Thunyakitpisal, P.; Rungsirisatean, N. Acemannan, a polysaccharide extracted from aloe vera, is effective in the treatment of oral aphthous ulceration. J. Altern. Complem. Med. 2013, 19, 429–434. [Google Scholar] [CrossRef]
  78. Halim, D.S.; Khalik, N.I.B.A.; Taib, H.; Pohchi, A.; Hassan, A.; Alam, M.K. Novel material in the treatment of minor oral recurrent aphthous stomatitis. Int. Med. J. 2013, 20, 392–394. [Google Scholar]
  79. Sattayut, S.; Trivibulwanich, J.; Pipithirunkarn, N.; Danvirutai, N. A clinical efficacy of using CO2 laser irradiating to transparent gel on aphthous stomatitis patients. Laser Ther. 2013, 22, 283–289. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  80. Liu, C.; Zhou, Z.; Liu, G.; Wang, Q.; Chen, J.; Wang, L.; Zhou, Y.; Dong, G.; Xu, X.; Wang, Y.; et al. Efficacy and safety of dexamethasone ointment on recurrent aphthous ulceration. Am. J. Med. 2012, 125, 292–301. [Google Scholar] [CrossRef]
  81. Galal, M.; Nasry, S.A.; Mostafa, D.M.; Ammar, N.M. Therapeutic Efficacy of Herbal Formulations for Recurrent Aphthous Ulcer. Correlation with Salivary Epidermal Growth Factor. Life Sci. J. 2012, 9, 2398–2406. [Google Scholar]
  82. Meng, W.; Dong, Y.; Liu, J.; Wang, Z.; Zhong, X.; Chen, R.; Zhou, H.; Lin, M.; Jiang, L.; Gao, F.; et al. A clinical evaluation of amlexanox oral adhesive pellicles in the treatment of recurrent aphthous stomatitis and comparison with amlexanox oral tablets: A randomized, placebo controlled, blinded, multicenter clinical trial. Trials 2009, 10, 30. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  83. Liu, J.; Zeng, X.; Chen, Q.; Cai, Y.; Chen, F.; Wang, Y.; Zhou, H.; Lin, M.; Shi, J.; Wang, Z.; et al. An evaluation on the efficacy and safety of amlexanox oral adhesive tablets in the treatment of recurrent minor aphthous ulceration in a Chinese cohort: A randomized, double-blind, vehicle-controlled, unparallel multicenter clinical trial. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. Endod. 2006, 102, 475–481. [Google Scholar] [CrossRef]
  84. Khandwala, A.; Van Inwegen, R.G.; Alfano, M.C. 5% amlexanox oral paste, a new treatment for recurrent minor aphthous ulcers: I. Clinical demonstration of acceleration of healing and resolution of pain. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. Endod. 1997, 83, 222–230. [Google Scholar] [CrossRef]
  85. Pedersen, A.M.L.; Bukkehave, K.H.; Bennett, E.P.; Twetman, S. Effect of Lozenges Containing Lactobacillus reuteri on the Severity of Recurrent Aphthous Ulcers: A Pilot Study. Probiotics Antimicrob. Proteins 2020, 12, 819–823. [Google Scholar] [CrossRef] [PubMed]
  86. Yilmaz, H.G.; Albaba, M.R.; Caygur, A.; Cengiz, E.; Boke-Karacaoglu, F.; Tumer, H. Treatment of recurrent aphthous stomatitis with Er,Cr:YSGG laser irradiation: A randomized controlled split mouth clinical study. J. Photochem. Photobiol. B Biol. 2017, 170, 1–5. [Google Scholar] [CrossRef]
  87. Tezel, A.; Kara, C.; Balkaya, V.; Orbak, R. An evaluation of different treatments for recurrent aphthous stomatitis and patient perceptions: Nd:YAG laser versus medication. Photomed. Laser Surg. 2009, 27, 101–106. [Google Scholar] [CrossRef]
  88. Skulason, S.; Holbrook, W.P.; Kristmundsdottir, T. Clinical assessment of the effect of a matrix metalloproteinase inhibitor on aphthous ulcers. Acta Odontol. Scand. 2009, 67, 25–29. [Google Scholar] [CrossRef]
  89. Zand, N.; Ataie-Fashtami, L.; Djavid, G.E.; Fateh, M.; Alinaghizadeh, M.R.; Fatemi, S.M.; Arbabi-Kalati, F. Relieving pain in minor aphthous stomatitis by a single session of non-thermal carbon dioxide laser irradiation. Laser. Med. Sci. 2009, 24, 515–520. [Google Scholar] [CrossRef] [PubMed]
  90. Ylikontiola, L.; Sorsa, T.; Häyrinen-Immonen, R.; Salo, T. Doxymycine-cyanoacrylate treatment of recurrent aphthous ulcers. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. Endod. 1997, 83, 329–333. [Google Scholar] [CrossRef]
  91. Miles, D.A.; Bricker, S.L.; Razmus, T.F.; Potter, R.H. Triamcinolone acetonide versus chlorhexidine for treatment of recurrent stomatitis. Oral Surg. Oral Med. Oral Pathol. 1993, 75, 397–402. [Google Scholar] [CrossRef]
  92. Albrektson, M. Recurrent aphthous stomatitis and pain management with low-level laser therapy: A randomized controlled trial. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. 2014, 117, 590–594. [Google Scholar] [CrossRef]
  93. Trinchieri, V.; Di Carlo, S.; Bossu’, M.; Polimeni, A. Use of lozenges containing Lactobacillus brevis CD2 in recurrent aphthous stomatitis: A double-blind placebo-controlled trial. Ulcers 2011, 2011, 439425. [Google Scholar] [CrossRef] [Green Version]
  94. Gorsky, M.; Epstein, J.; Raviv, A.; Yaniv, R.; Truelove, E. Topical minocycline for managing symptoms of recurrent aphthous stomatitis. Spec. Care Dent. 2008, 28, 27–31. [Google Scholar] [CrossRef] [PubMed]
  95. Rodríguez, M.; Rubio, J.A.; Sanchez, R. Effectiveness of two oral pastes for the treatment of recurrent aphthous stomatitis. Oral Dis. 2007, 13, 490–494. [Google Scholar] [CrossRef] [PubMed]
  96. Greer, R.O., Jr.; Lindenmuth, J.E.; Juarez, T.; Khandwala, A.; Kaugars, G.E. A double-blind study of topically applied 5% amlexanox in the treatment of aphthous ulcers. J. Oral Maxillofac. Surg. 1993, 51, 243–249. [Google Scholar] [CrossRef]
  97. Matthews, R.W.; Scully, C.M.; Levers, B.G.H.; Hislop, W.S. Clinical evaluation of benzydamine, chlorhexidine, and placebo mouthwashes in the management of recurrent aphthous stomatitis. Oral Surg. Oral Med. Oral Pathol. 1987, 63, 189–191. [Google Scholar] [CrossRef]
  98. Browne, R.M.; Fox, E.C.; Anderson, R.J. Topical triamcinolone acetonide in recurrent aphthous stomatitis. A clinical trial. Lancet 1968, 1, 565–567. [Google Scholar] [CrossRef]
  99. Diegelmann, R.F.; Evans, M.C. Wound healing: An overview of acute, fibrotic and delayed healing. Front. Biosci. 2004, 9, 283–289. [Google Scholar] [CrossRef]
  100. Manfredini, M.; Guida, S.; Giovani, M.; Lippolis, N.; Spinas, E.; Farnetani, F.; Dattola, A.; Di Matteo, E.; Pellacani, G.; Giannetti, L. Recurrent Aphthous Stomatitis: Treatment and Management. Dermatol. Pract. Concept. 2021, 11, e2021099. [Google Scholar] [CrossRef]
  101. Daugėlaitė, G.; Užkuraitytė, K.; Jagelavičienė, E.; Filipauskas, A. Prevention and Treatment of Chemotherapy and Radiotherapy Induced Oral Mucositis. Medicina 2019, 55, 25. [Google Scholar] [CrossRef] [Green Version]
  102. Gondivkar, D.; Gadbail, D.; Sarode, D.; Gondivkar, D.; Patil, S.; Gaikwad, D.; Dinh-Toi, C.; Yuwanati, D.M. Treatment outcomes of laser therapy in oral submucous fibrosis—A systematic review. J. Oral Biol. Craniofac. Res. 2020, 10, 253–258. [Google Scholar] [CrossRef]
  103. García-Pola, M.J.; González-Álvarez, L.; Garcia-Martin, J.M. Treatment of oral lichen planus. Systematic review and therapeutic guide. Med. Clin. 2017, 149, 351–362. [Google Scholar] [CrossRef]
  104. Lodi, G.; Franchini, R.; Warnakulasuriya, S.; Varoni, E.M.; Sardella, A.; Kerr, A.R.; Carrassi, A.; Macdonald, L.C.; Worthington, H.V. Interventions for treating oral leukoplakia to prevent oral cancer. Cochrane Database Syst. Rev. 2016, 7, D1829. [Google Scholar] [CrossRef]
  105. Matos, A.L.; Silva, P.U.; Paranhos, L.R.; Santana, I.T.; Matos, F.R. Efficacy of the laser at low intensity on primary burning oral syndrome: A systematic review. Med. Oral Patol. Oral Cir. Bucal 2021, 26, e216–e225. [Google Scholar] [CrossRef] [PubMed]
  106. Figueiredo, A.L.; Lins, L.; Cattony, A.C.; Falcão, A.F. Laser therapy in the control of oral mucositis: A meta-analysis. Rev. Assoc. Med. Bras. 2013, 59, 467–474. [Google Scholar] [CrossRef] [Green Version]
  107. Lino, M.D.; Carvalho, F.B.; Oliveira, L.R.; Magalhães, E.B.; Pinheiro, A.L.; Ramalho, L.M. Laser phototherapy as a treatment for radiotherapy-induced oral mucositis. Braz. Dent. J. 2011, 22, 162–165. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  108. Silveira, P.C.; Streck, E.L.; Pinho, R.A. Evaluation of mitochondrial respiratory chain activity in wound healing by low-level laser therapy. J. Photochem. Photobiol. B 2007, 86, 279–282. [Google Scholar] [CrossRef] [PubMed]
  109. Karu, T.I.; Kolyakov, S.F. Exact action spectra for cellular responses relevant to phototherapy. Photomed. Laser Surg. 2005, 23, 355–361. [Google Scholar] [CrossRef] [Green Version]
  110. Medrado, A.R.; Pugliese, L.S.; Reis, S.R.; Andrade, Z.A. Influence of low level laser therapy on wound healing and its biological action upon myofibroblasts. Lasers Surg. Med. 2003, 32, 239–244. [Google Scholar] [CrossRef]
  111. Suter, V.; Sjölund, S.; Bornstein, M.M. Effect of laser on pain relief and wound healing of recurrent aphthous stomatitis: A systematic review. Lasers Med. Sci. 2017, 32, 953–963. [Google Scholar] [CrossRef]
  112. Han, M.; Fang, H.; Li, Q.L.; Cao, Y.; Xia, R.; Zhang, Z.H. Effectiveness of Laser Therapy in the Management of Recurrent Aphthous Stomatitis: A Systematic Review. Scientifica 2016, 2016, 9062430. [Google Scholar] [CrossRef]
  113. Najeeb, S.; Khurshid, Z.; Zohaib, S.; Najeeb, B.; Qasim, S.B.; Zafar, M.S. Management of recurrent aphthous ulcers using low-level lasers: A systematic review. Medicina 2016, 52, 263–268. [Google Scholar] [CrossRef]
  114. Pavlić, V.; Vujić-Aleksić, V.; Aoki, A.; Nežić, L. Treatment of recurrent aphthous stomatitis by laser therapy: A systematic review of the literature. Vojnosanit. Pregl. 2015, 72, 722–728. [Google Scholar] [CrossRef]
  115. Bizzini, B.; Pizzo, G.; Scapagnini, G.; Nuzzo, D.; Vasto, S. Probiotics and oral health. Curr. Pharm. Des. 2012, 18, 5522–5531. [Google Scholar] [CrossRef]
  116. Bandara, H.; Panduwawala, C.P.; Samaranayake, L.P. Biodiversity of the human oral mycobiome in health and disease. Oral Dis. 2019, 25, 363–371. [Google Scholar] [CrossRef]
  117. Nyvad, B.; Crielaard, W.; Mira, A.; Takahashi, N.; Beighton, D. Dental caries from a molecular microbiological perspective. Caries Res. 2013, 47, 89–102. [Google Scholar] [CrossRef] [PubMed]
  118. Dye, B.A. Global periodontal disease epidemiology. Periodontol. 2000 2012, 58, 10–25. [Google Scholar] [CrossRef]
  119. Telles, D.R.; Karki, N.; Marshall, M.W. Oral Fungal Infections: Diagnosis and Management. Dent. Clin. North Am. 2017, 61, 319–349. [Google Scholar] [CrossRef]
  120. Gruner, D.; Paris, S.; Schwendicke, F. Probiotics for managing caries and periodontitis: Systematic review and meta-analysis. J. Dent. 2016, 48, 16–25. [Google Scholar] [CrossRef] [PubMed]
  121. Laleman, I.; Teughels, W. Probiotics in the dental practice: A review. Quintessence Int. 2015, 46, 255–264. [Google Scholar] [PubMed]
  122. Laleman, I.; Detailleur, V.; Slot, D.E.; Slomka, V.; Quirynen, M.; Teughels, W. Probiotics reduce mutans streptococci counts in humans: A systematic review and meta-analysis. Clin. Oral Investig. 2014, 18, 1539–1552. [Google Scholar] [CrossRef] [Green Version]
  123. Laleman, I.; Yilmaz, E.; Ozcelik, O.; Haytac, C.; Pauwels, M.; Herrero, E.R.; Slomka, V.; Quirynen, M.; Alkaya, B.; Teughels, W. The effect of a streptococci containing probiotic in periodontal therapy: A randomized controlled trial. J. Clin. Periodontol. 2015, 42, 1032–1041. [Google Scholar] [CrossRef]
  124. Shimauchi, H.; Mayanagi, G.; Nakaya, S.; Minamibuchi, M.; Ito, Y.; Yamaki, K.; Hirata, H. Improvement of periodontal condition by probiotics with Lactobacillus salivarius WB21: A randomized, double-blind, placebo-controlled study. J. Clin. Periodontol. 2008, 35, 897–905. [Google Scholar] [CrossRef] [PubMed]
  125. Wylleman, A.; Vuylsteke, F.; Dekeyser, C.; Teughels, W.; Quirynen, M.; Laleman, I. Alternative therapies in controlling oral malodour: A systematic review. J. Breath Res. 2021, 15, 026009. [Google Scholar] [CrossRef]
  126. Georgiou, A.C.; Laine, M.L.; Deng, D.M.; Brandt, B.W.; van Loveren, C.; Dereka, X. Efficacy of probiotics: Clinical and microbial parameters of halitosis. J. Breath Res. 2018, 12, 46010. [Google Scholar] [CrossRef] [PubMed]
  127. Hernández-Olivos, R.; Muñoz, M.; Núñez, E.; Camargo-Ayala, P.A.; Garcia-Huidobro, J.; Pereira, A.; Nachtigall, F.M.; Santos, L.S.; Rivera, C. Salivary proteome of aphthous stomatitis reveals the participation of vitamin metabolism, nutrients, and bacteria. Sci. Rep. 2021, 11, 15646. [Google Scholar] [CrossRef]
  128. Koybasi, S.; Parlak, A.H.; Serin, E.; Yilmaz, F.; Serin, D. Recurrent aphthous stomatitis: Investigation of possible etiologic factors. Am. J. Otolaryngol. 2006, 27, 229–232. [Google Scholar] [CrossRef]
  129. Cappello, F.; Rappa, F.; Canepa, F.; Carini, F.; Mazzola, M.; Tomasello, G.; Bonaventura, G.; Giuliana, G.; Leone, A.; Saguto, D.; et al. Probiotics Can Cure Oral Aphthous-Like Ulcers in Inflammatory Bowel Disease Patients: A Review of the Literature and a Working Hypothesis. Int. J. Mol. Sci. 2019, 20, 5026. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  130. Piwat, S.; Sophatha, B.; Teanpaisan, R. An assessment of adhesion, aggregation and surface charges of Lactobacillus strains derived from the human oral cavity. Lett. Appl. Microbiol. 2015, 61, 98–105. [Google Scholar] [CrossRef]
  131. Takahashi, N. Oral Microbiome Metabolism: From “Who Are They?” to “What Are They Doing?”. J. Dent. Res. 2015, 94, 1628–1637. [Google Scholar] [CrossRef]
  132. Twetman, S. Are we ready for caries prevention through bacteriotherapy? Braz. Oral Res. 2012, 26 (Suppl. S1), 64–70. [Google Scholar] [CrossRef] [Green Version]
  133. Maldonado, G.C.; Cazorla, S.I.; Lemme, D.J.; Vélez, E.; Perdigón, G. Beneficial Effects of Probiotic Consumption on the Immune System. Ann. Nutr. Metab. 2019, 74, 115–124. [Google Scholar] [CrossRef] [PubMed]
  134. Haukioja, A. Probiotics and oral health. Eur. J. Dent. 2010, 4, 348–355. [Google Scholar] [CrossRef] [Green Version]
  135. Stamatova, I.; Meurman, J.H. Probiotics: Health benefits in the mouth. Am. J. Dent. 2009, 22, 329–338. [Google Scholar]
Figure 1. Flow chart of the study selection process.
Figure 1. Flow chart of the study selection process.
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Figure 2. Network plots for the main outcomes considered in the review. (a) Healing effect; (b) size-reducing effect; (c) symptom-reducing effect; (d) adverse effect. Nodes and edges are weighted according to volume of studies, including that treatment or comparison.
Figure 2. Network plots for the main outcomes considered in the review. (a) Healing effect; (b) size-reducing effect; (c) symptom-reducing effect; (d) adverse effect. Nodes and edges are weighted according to volume of studies, including that treatment or comparison.
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Chart 1. “Time-Rank 1 probability” folding line chart of side-reducing effect.
Chart 1. “Time-Rank 1 probability” folding line chart of side-reducing effect.
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Chart 2. “Time-Rank 1 probability” folding line chart of symptom-reducing effect.
Chart 2. “Time-Rank 1 probability” folding line chart of symptom-reducing effect.
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Table 1. Significantly different estimates for healing effect.
Table 1. Significantly different estimates for healing effect.
Healing Effect
ComparisonHoney vs. placeboInsulin-liposomal gel vs. placeboLaser vs. placebo
Relative effect estimate−3.55 (−5.90, −1.13)−3.90 (−7.53, −0.23)−3.08 (−4.81, −1.19)
Size-reducing Effect
ComparisonAmlexanox vs. placeboGlycyrrhiza vs. placeboTriamcinolone vs. placebo
Relative effect estimate35.29 (15.53, 54.72)29.07 (3.58, 54.49)25.83 (7.91, 45.48)
Symptom-Reducing Effect
ComparisonAmlexanox vs. placeboLaser vs. placeboTriamcinolone vs. placebo
Relative effect estimate23.26 (4.15, 42.15)32.21 (16.39, 48.08)28.45 (10.36, 46.76)
Adverse Effect
ComparisonTriamcinolone vs. amlexanoxTriamcinolone vs. chitosan Triamcinolone vs. dexamethasone
Relative effect estimate0.00 (0.00, 0.00)0.00 (0.00, 0.08)0.00 (0.00, 0.00)
ComparisonDexamethasone vs. penicillinPlacebo vs. doxycyclineTriamcinolone vs. doxycycline
Relative effect estimate0.00 (0.00, 0.10)0.00 (0.00, 0.06)0.00 (0.00, 0.00)
ComparisonTriamcinolone vs. penicillinTriamcinolone vs. placeboPlacebo vs. penicillin
Relative effect estimate0.00 (0.00, 0.00)0.00 (0.00, 0.00)0.00 (0.00, 0.14)
ComparisonDexamethasone vs. doxycycline
Relative effect estimate0.00 (0.00, 0.06)
Table 2. Outcome p-cores for the best five interventions.
Table 2. Outcome p-cores for the best five interventions.
Healing EffectSize-Reducing EffectSymptom-Reducing EffectAdverse Effect
RankTreatmentp-CoreRankTreatmentp-CoreRankTreatmentp-CoreRankTreatmentp-Core
18Insulin-liposomal gel0.241Quercetin0.271Insulin-liposomal gel0.2422Triamcinolone0.15
17Honey0.152Dexamethasone0.142N-acetylcysteine
or sucralfate
0.1221Berberine gelatin0.08
16Laser0.113Amlexanox0.133Curcumin0.0820Glycyrrhiza
or laser
0.07
15Penicillin0.094Glycyrrhiza
or laser
0.084Laser0.0919Aloe or honey
or probiotics
0.06
14Aloe0.065Curcumin0.085Chlorhexidine0.0718Curcumin, silver nitrate, triester glycerol oxide or zinc0.06
Table 3. Hematologic values.
Table 3. Hematologic values.
InterventionsTotalHematologic Values
Dexamethasone114Blood level < 0.502 ng/mL
Aloe60No significant differences between the blood test values before and after 7 days of application
Allicin48None of the hematologic values on day 6 were considered clinically abnormal
Amlexanox108None of the hematologic values were considered clinically abnormal
Table 4. Recurrence and statistical significance.
Table 4. Recurrence and statistical significance.
InterventionsTotalRelapseStatistical Significance
ProbioticsAdult group: 30
Children group: 30
Adult group:
(Outbreak frequency/6 months)
Probiotics: 3.33 (0.64)
Placebo: 3.65 (0.32)
Children group:
(Outbreak frequency/6 months)
Probiotics: 2.65 (0.54)
Placebo: 3.65 (0.62)
Adult group:
No change in outbreak frequency was reported within the 6 months next to treatment (p > 0.05).
Children group:
A statistically significant decrease in outbreak frequency was reported for probiotics group within the 6 months next to treatment. The change was significantly different from placebo group (p < 0.05).
Chlorhexidine38Total ulcer numbers (6 weeks):
Chlorhexidine: 7.54 ± 6.52
Placebo: 8.32 ± 5.52
Interval between ulcers (6 weeks):
Chlorhexidine: 7.26 ± 8.61
Placebo:3.86 ± 2.05
Total ulcer numbers:
NA
Interval between ulcers:
Chlorhexidine significantly increased the interval between successive ulcers (p < 0.05). For the total group, the increase was from 3.86 days with the placebo to 7.26 days with chlorhexidine.
Benzydamine18Number of new ulcers (3 months)
Benzydamine: 7 (2–33)
Placebo: 8 (2–20)
p = 0.07
Chlorhexidine18Number of new ulcers (3 months)
Chlorhexidine: 6.5 (3–20)
Placebo: 8 (2–20)
p = 0.27
Triamcinolone26No. of new ulcers (8 months)
Placebo: 7.81
Triamcinolone acetonide in orabase: 7.00
Triamcinolone acetonide in watery base: 6.42
Although there was a slight reduction in the number of new ulcers during treatment with both steroid preparations, this was not statistically significant.
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Liu, H.; Tan, L.; Fu, G.; Chen, L.; Tan, H. Efficacy of Topical Intervention for Recurrent Aphthous Stomatitis: A Network Meta-Analysis. Medicina 2022, 58, 771. https://doi.org/10.3390/medicina58060771

AMA Style

Liu H, Tan L, Fu G, Chen L, Tan H. Efficacy of Topical Intervention for Recurrent Aphthous Stomatitis: A Network Meta-Analysis. Medicina. 2022; 58(6):771. https://doi.org/10.3390/medicina58060771

Chicago/Turabian Style

Liu, Hao, Lei Tan, Gege Fu, Ling Chen, and Hua Tan. 2022. "Efficacy of Topical Intervention for Recurrent Aphthous Stomatitis: A Network Meta-Analysis" Medicina 58, no. 6: 771. https://doi.org/10.3390/medicina58060771

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