Pub Date : 2025-11-28DOI: 10.1038/s41432-025-01194-9
Arash Shahravan
Fatima S, Andrabi S M, Alam S et al. Effect of foraminal enlargement on postoperative pain in primary endodontic treatment: a systematic review and meta-analysis. J Endod 2025; 51: 1536–1548. The purpose of this systematic review and meta-analysis was to investigate how foraminal enlargement (FE) affects postoperative pain following primary endodontic treatment. A systematic literature search was conducted across four major databases— PubMed/MEDLINE, Scopus, Web of Science, and the Cochrane Library—to identify randomized controlled trials evaluating the impact of foraminal enlargement (FE) versus non-foraminal enlargement (NFE) on postoperative pain. The risk of bias in the included studies was evaluated using the Revised Cochrane Risk-of-Bias Tool for Randomized Trials. A meta-analysis was planned to quantitatively assess the impact of foraminal enlargement (FE) on pain during the first 7 days following treatment Eight randomized controlled trials (RCTs) involving a total of 802 participants met the inclusion criteria. The risk-of-bias assessment indicated that two studies were at high risk, four raised some concerns, and two were at low risk. Meta-analysis demonstrated that foraminal enlargement (FE) was associated with significantly greater postoperative pain compared to non-foraminal enlargement (NFE) at 12 h (SMD = 0.79, 95% CI [0.30, 1.28], p = 0.002; I² = 28%), 24 hours (SMD = 0.74, 95% CI [0.12, 1.36], p = 0.02; I² = 89%), and 48 h (SMD = 2.90, 95% CI [0.23, 5.57], p = 0.03; I² = 98%). This meta-analysis indicates that postoperative pain is markedly elevated following foraminal enlargement (FE) compared to non-foraminal enlargement (NFE) during the initial 48-hour period, although such pain is generally mild to moderate and transient. Future investigations are warranted to delineate the impact of FE on essential clinical outcomes, including long-term success rates, and to determine whether its prospective advantages outweigh the attendant short-term increase in discomfort.
评论:Fatima S, Andrabi S M, Alam S等。初级根管治疗中椎间孔扩大对术后疼痛的影响:系统回顾和荟萃分析。[J] end2025;51: 1536 - 1548。目的:本系统综述和荟萃分析的目的是研究椎间孔扩大(FE)如何影响初级根管治疗后的术后疼痛。数据来源:对四个主要数据库(PubMed/MEDLINE、Scopus、Web of Science和Cochrane library)进行了系统的文献检索,以确定评估椎间孔增大(FE)与非椎间孔增大(NFE)对术后疼痛影响的随机对照试验。方法:使用修订后的Cochrane随机试验风险偏倚工具评估纳入研究的偏倚风险。计划进行荟萃分析,定量评估椎间孔扩大(FE)对治疗后前7天疼痛的影响。结果:8项随机对照试验(rct)共涉及802名受试者,符合纳入标准。偏倚风险评估表明,两项研究处于高风险,四项研究引起了一些关注,两项研究处于低风险。meta分析显示,在12小时(SMD = 0.79, 95% CI [0.30, 1.28], p = 0.002; I²= 28%)、24小时(SMD = 0.74, 95% CI [0.12, 1.36], p = 0.02; I²= 89%)和48小时(SMD = 2.90, 95% CI [0.23, 5.57], p = 0.03; I²= 98%),椎间孔增大(FE)与非椎间孔增大(NFE)相比,术后疼痛明显加重。结论:这项荟萃分析表明,在最初的48小时内,椎间孔扩大(FE)术后疼痛明显高于非椎间孔扩大(NFE),尽管这种疼痛通常是轻度至中度和短暂的。未来的研究有必要描述FE对基本临床结果的影响,包括长期成功率,并确定其前景优势是否超过伴随而来的短期不适增加。
{"title":"Unpacking the evidence: a deeper look at foraminal enlargement and postoperative pain outcomes","authors":"Arash Shahravan","doi":"10.1038/s41432-025-01194-9","DOIUrl":"10.1038/s41432-025-01194-9","url":null,"abstract":"Fatima S, Andrabi S M, Alam S et al. Effect of foraminal enlargement on postoperative pain in primary endodontic treatment: a systematic review and meta-analysis. J Endod 2025; 51: 1536–1548. The purpose of this systematic review and meta-analysis was to investigate how foraminal enlargement (FE) affects postoperative pain following primary endodontic treatment. A systematic literature search was conducted across four major databases— PubMed/MEDLINE, Scopus, Web of Science, and the Cochrane Library—to identify randomized controlled trials evaluating the impact of foraminal enlargement (FE) versus non-foraminal enlargement (NFE) on postoperative pain. The risk of bias in the included studies was evaluated using the Revised Cochrane Risk-of-Bias Tool for Randomized Trials. A meta-analysis was planned to quantitatively assess the impact of foraminal enlargement (FE) on pain during the first 7 days following treatment Eight randomized controlled trials (RCTs) involving a total of 802 participants met the inclusion criteria. The risk-of-bias assessment indicated that two studies were at high risk, four raised some concerns, and two were at low risk. Meta-analysis demonstrated that foraminal enlargement (FE) was associated with significantly greater postoperative pain compared to non-foraminal enlargement (NFE) at 12 h (SMD = 0.79, 95% CI [0.30, 1.28], p = 0.002; I² = 28%), 24 hours (SMD = 0.74, 95% CI [0.12, 1.36], p = 0.02; I² = 89%), and 48 h (SMD = 2.90, 95% CI [0.23, 5.57], p = 0.03; I² = 98%). This meta-analysis indicates that postoperative pain is markedly elevated following foraminal enlargement (FE) compared to non-foraminal enlargement (NFE) during the initial 48-hour period, although such pain is generally mild to moderate and transient. Future investigations are warranted to delineate the impact of FE on essential clinical outcomes, including long-term success rates, and to determine whether its prospective advantages outweigh the attendant short-term increase in discomfort.","PeriodicalId":12234,"journal":{"name":"Evidence-based dentistry","volume":"26 4","pages":"166-167"},"PeriodicalIF":2.3,"publicationDate":"2025-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145631507","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-25DOI: 10.1038/s41432-025-01191-y
Soumya Narayani Thirumoorthy, Saumiya Gopal, Darshit Shah
Santonocito S, Cicciù M, Ronsivalle V. Evaluation of the impact of AI-based chatbot on orthodontic patient education: a preliminary randomized controlled trial. Clin Oral Investig 2025; 29:278. Randomized controlled trial (RCT). A sample of 100 patients was enrolled in the study between June 2023 and August 2024. Participants were randomly allocated into two intervention groups of 50 each, using a computer-generated sequence to maintain a 1:1 ratio. The Chatbot group received oral hygiene (OH) and orthodontic treatment guidance via a chatbot accessed through a QR code, while the control group was given standard educational material by means of information leaflets compiled by the leading scientific societies in orthodontics. Each main group was further divided into two subgroups: Leaflet-fixed therapy (LF, n = 27), Leaflet-aligner (LA, n = 23), Chatbot-fixed therapy (CF, n = 24), and Chatbot-aligner (CA, n = 26). The chatbot was built on the open-source Botpress platform and was refined using expert-reviewed training materials. When the participant opens the chatbot application, the interface displays a menu containing 4 questions, with the 3rd question focusing on home oral hygiene procedures. The evaluation included a clinical examination at baseline (T0) and after 5 weeks of starting orthodontic treatment (T1), along with a questionnaire at T1 assessing participants’ oral hygiene knowledge and compliance. Modified gingival index (MGI) and plaque index (PI) were used for clinical examination of oral hygiene. The questionnaire comprised four domains: Knowledge Evaluation (KE_S), Understanding Scale (US_S), Compliance and Adherence Scale (CAAS_S), and Satisfaction Scale (SS_S). It employed a 5-point Likert scale, with scores ranging from 0 (strongly negative) to 4 (strongly positive), with intermediate values representing negative, neutral, and positive responses. MGI and PI showed a statistically significant increase from T0 to T1 in both groups. While comparing the change in MGI from the start of treatment between the groups, a statistically significant increase was found in the control group than the chatbot group. Further analysis reported statistically lower increase in MGI in the CF and CA groups as compared to the LF and LA subgroups. There were no differences between the control and chatbot groups with respect to questionnaire section scores. The study concluded that the use of an AI-based chatbot positively influences patient compliance with oral hygiene maneuvers. Furthermore, it could not be established whether the AI-based chatbot enhanced the patient’s knowledge, understanding, and satisfaction with the information received compared to the information leaflets.
评论:Santonocito S, Cicciù M, Ronsivalle V.基于ai的聊天机器人对正畸患者教育影响的评估:一项初步随机对照试验。临床口腔调查2025;29:278。设计:随机对照试验(RCT)。病例选择:在2023年6月至2024年8月期间,纳入了100例患者的样本。参与者被随机分配到两个干预组,每组50人,使用计算机生成的顺序保持1:1的比例。聊天机器人组通过聊天机器人通过二维码访问获得口腔卫生(OH)和正畸治疗指导,而对照组通过正畸主要科学学会编制的信息传单获得标准教育材料。每个主组进一步分为两个亚组:leaf -fixed therapy (LF, n = 27)、leaf -aligner (LA, n = 23)、Chatbot-fixed therapy (CF, n = 24)和Chatbot-aligner (CA, n = 26)。这个聊天机器人建立在开源的Botpress平台上,并使用专家审查的培训材料进行了改进。当参与者打开聊天机器人应用程序时,界面显示一个包含4个问题的菜单,其中第三个问题是关于家庭口腔卫生程序的。数据分析:评估包括基线(T0)和开始正畸治疗5周后(T1)的临床检查,以及T1时评估参与者口腔卫生知识和依从性的问卷。采用改良牙龈指数(MGI)和菌斑指数(PI)进行口腔卫生临床检查。问卷由知识评价量表(KE_S)、理解量表(US_S)、依从性与依从性量表(CAAS_S)和满意度量表(SS_S)四个部分组成。它采用李克特5分量表,得分范围从0(强烈消极)到4(强烈积极),中间值代表消极、中性和积极的反应。结果:两组患者MGI、PI从T0到T1均有统计学意义升高。在比较两组治疗开始时MGI的变化时,发现对照组比聊天机器人组有统计学意义上的显著增加。进一步分析报告,与LF和LA亚组相比,CF和CA组MGI的增加在统计学上较低。在问卷部分得分方面,控制组和聊天机器人组之间没有差异。结论:该研究得出结论,使用基于人工智能的聊天机器人对患者遵守口腔卫生操作有积极影响。此外,与信息传单相比,基于ai的聊天机器人是否提高了患者对所接收信息的认识、理解和满意度,这一点也无法确定。
{"title":"Braces meet bots: straight teeth and straight answers?","authors":"Soumya Narayani Thirumoorthy, Saumiya Gopal, Darshit Shah","doi":"10.1038/s41432-025-01191-y","DOIUrl":"10.1038/s41432-025-01191-y","url":null,"abstract":"Santonocito S, Cicciù M, Ronsivalle V. Evaluation of the impact of AI-based chatbot on orthodontic patient education: a preliminary randomized controlled trial. Clin Oral Investig 2025; 29:278. Randomized controlled trial (RCT). A sample of 100 patients was enrolled in the study between June 2023 and August 2024. Participants were randomly allocated into two intervention groups of 50 each, using a computer-generated sequence to maintain a 1:1 ratio. The Chatbot group received oral hygiene (OH) and orthodontic treatment guidance via a chatbot accessed through a QR code, while the control group was given standard educational material by means of information leaflets compiled by the leading scientific societies in orthodontics. Each main group was further divided into two subgroups: Leaflet-fixed therapy (LF, n = 27), Leaflet-aligner (LA, n = 23), Chatbot-fixed therapy (CF, n = 24), and Chatbot-aligner (CA, n = 26). The chatbot was built on the open-source Botpress platform and was refined using expert-reviewed training materials. When the participant opens the chatbot application, the interface displays a menu containing 4 questions, with the 3rd question focusing on home oral hygiene procedures. The evaluation included a clinical examination at baseline (T0) and after 5 weeks of starting orthodontic treatment (T1), along with a questionnaire at T1 assessing participants’ oral hygiene knowledge and compliance. Modified gingival index (MGI) and plaque index (PI) were used for clinical examination of oral hygiene. The questionnaire comprised four domains: Knowledge Evaluation (KE_S), Understanding Scale (US_S), Compliance and Adherence Scale (CAAS_S), and Satisfaction Scale (SS_S). It employed a 5-point Likert scale, with scores ranging from 0 (strongly negative) to 4 (strongly positive), with intermediate values representing negative, neutral, and positive responses. MGI and PI showed a statistically significant increase from T0 to T1 in both groups. While comparing the change in MGI from the start of treatment between the groups, a statistically significant increase was found in the control group than the chatbot group. Further analysis reported statistically lower increase in MGI in the CF and CA groups as compared to the LF and LA subgroups. There were no differences between the control and chatbot groups with respect to questionnaire section scores. The study concluded that the use of an AI-based chatbot positively influences patient compliance with oral hygiene maneuvers. Furthermore, it could not be established whether the AI-based chatbot enhanced the patient’s knowledge, understanding, and satisfaction with the information received compared to the information leaflets.","PeriodicalId":12234,"journal":{"name":"Evidence-based dentistry","volume":"26 4","pages":"162-163"},"PeriodicalIF":2.3,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145603350","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Among various fluoride delivery methods, such as toothpaste, varnishes, and water fluoridation, mouthrinses have gained attention for their versatility, ease of use, and potential to complement other preventive strategies. The aim was to evaluate the effectiveness of mouthrinses in preventing and arresting caries by synthesizing data from existing systematic reviews. Five electronic databases, named PubMed, Cochrane Central Register of Controlled Trials, Cochrane Database of Systematic Reviews, Web of Science and Scopus, were searched to identify systematic reviews that assessed the effect of mouthrinses containing chemical, herbal, or natural agents in comparison to standard oral care, placebo, water, or saline in the development or arrest of crown or root caries. Eligible reviews were selected, and data were extracted and assessed for bias. Three systematic reviews with meta-analysis and four without were included, with a total of eighty-three initial studies (moderate overlap). Supervised regular use of fluoride mouthrinse can reduce coronal and root caries initiation and progression in permanent teeth for an observational period of 6 months to 4 years. The only significant effect was in favor of the fluoride mouthrinse for crown caries at 36 months and root caries at 48 months follow-up time. Mouthrinses effectively reduce the occurrence of crown caries in moderate- and high-risk patients, as well as root caries in older adults. However, their anticaries benefit in populations with additional fluoride exposure remains uncertain. Given the great variability in the design, inclusion criteria set and conduct of the eligible systematic reviews, it is impossible to reach specific conclusions concerning the efficacy of any single product. However, it seems that fluoride mouthrinses are effective in preventing and/or arresting dental caries in moderate and high caries risk patients and may reduce initiation of root caries in older individuals.
目的:在各种氟化物输送方法中,如牙膏、清漆和氟化水,漱口水因其通用性、易用性和补充其他预防策略的潜力而受到关注。目的是通过综合现有系统综述的数据来评估漱口水在预防和抑制龋齿方面的有效性。方法:检索PubMed、Cochrane中央对照试验登记册、Cochrane系统评价数据库、Web of Science和Scopus等5个电子数据库,以确定与标准口腔护理、安慰剂、水或生理盐水相比,含有化学、草药或天然制剂的漱口水在牙冠或牙根龋形成或抑制方面的效果。选择符合条件的综述,提取数据并评估偏倚。结果:纳入了3篇有荟萃分析的系统综述和4篇没有荟萃分析的系统综述,共有83项初始研究(中度重叠)。在6个月至4年的观察期内,在监督下定期使用含氟漱口水可以减少恒牙冠状和根状龋齿的发生和发展。唯一显著的效果是氟化物漱口水在36个月时对冠龋和48个月时对根龋有利。结论:口腔清洁可有效降低中高危患者冠状龋的发生,以及老年人牙根龋的发生。然而,它们的抗药效果在额外接触氟化物的人群中是否有效仍不确定。临床意义:考虑到系统评价的设计、纳入标准设置和实施存在很大的可变性,不可能就任何单一产品的疗效得出具体的结论。然而,氟化物漱口水在预防和/或抑制中、高风险患者的龋齿方面似乎是有效的,并可能减少老年人牙根龋齿的发生。
{"title":"Effectiveness of mouth rinses on caries prevention and arrest: an umbrella review","authors":"Kyriaki Seremidi, Sotiria Davidopoulou, Eleftherios Kaklamanos, Christos Rahiotis, Sotiria Gizani, Panagiotis Koromantzos, Yiorgos Bobetsis, Panagiotis Karakostas, Chrysoula Giota, Konstantinos Papadimitriou, Danae Anastasia Apatzidou, William Papaioannou, Sotiris Kalfas","doi":"10.1038/s41432-025-01188-7","DOIUrl":"10.1038/s41432-025-01188-7","url":null,"abstract":"Among various fluoride delivery methods, such as toothpaste, varnishes, and water fluoridation, mouthrinses have gained attention for their versatility, ease of use, and potential to complement other preventive strategies. The aim was to evaluate the effectiveness of mouthrinses in preventing and arresting caries by synthesizing data from existing systematic reviews. Five electronic databases, named PubMed, Cochrane Central Register of Controlled Trials, Cochrane Database of Systematic Reviews, Web of Science and Scopus, were searched to identify systematic reviews that assessed the effect of mouthrinses containing chemical, herbal, or natural agents in comparison to standard oral care, placebo, water, or saline in the development or arrest of crown or root caries. Eligible reviews were selected, and data were extracted and assessed for bias. Three systematic reviews with meta-analysis and four without were included, with a total of eighty-three initial studies (moderate overlap). Supervised regular use of fluoride mouthrinse can reduce coronal and root caries initiation and progression in permanent teeth for an observational period of 6 months to 4 years. The only significant effect was in favor of the fluoride mouthrinse for crown caries at 36 months and root caries at 48 months follow-up time. Mouthrinses effectively reduce the occurrence of crown caries in moderate- and high-risk patients, as well as root caries in older adults. However, their anticaries benefit in populations with additional fluoride exposure remains uncertain. Given the great variability in the design, inclusion criteria set and conduct of the eligible systematic reviews, it is impossible to reach specific conclusions concerning the efficacy of any single product. However, it seems that fluoride mouthrinses are effective in preventing and/or arresting dental caries in moderate and high caries risk patients and may reduce initiation of root caries in older individuals.","PeriodicalId":12234,"journal":{"name":"Evidence-based dentistry","volume":"26 4","pages":"179-179"},"PeriodicalIF":2.3,"publicationDate":"2025-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145573470","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Wu Y, Jia M, Fang Y, Duangthip D, Chu C H, Gao S S. Use machine learning to predict the treatment outcome of early childhood caries. BMC Oral Health 2025; 25: 389. This was a retrospective secondary analysis of data from a randomized controlled trial published in 2020. No new participants or patient involvement were included. This study used the available data from 880 children, contributing 4157 carious tooth surfaces assessed at 30 months. These data were drawn from an original community-based RCT in Hong Kong (baseline N = 1070) that evaluated fluoride and silver interventions for arresting ECC. Six algorithms were used and compared, including logistic regression (LR), naive Bayes (NB), support-vector machine (SVM), decision tree (DT), random forest (RF), and XGBoost. A surface-level 70:30 train: test split was used. SMOTE was applied to address class imbalance. Models were tuned and evaluated using 1000 bootstrap resamples. Performance metrics were reported as accuracy, recall, precision, F1 score, AUROC, and Brier score. Model interpretability was explored through SHAP analysis to rank variable importance and visualize feature effects. All models achieved acceptable discrimination. Metrics ranged as follows: accuracy 0.674–0.740; recall 0.731–0.809; precision 0.762–0.802; F1 0.741–0.804; AUROC 0.771–0.859 (RF and XGBoost ≈ 0.86); Brier 0.134–0.227. SHAP interpretation indicated that tooth and surface location of caries, newly developed dmfs, baseline dmfs, caregiver-assisted brushing, and visible plaque index contributed most to the model’s predictions, while the fluoride and silver intervention ranked mid-to-low in importance. The original study, however, highlighted tooth and surface location of caries, newly developed dmfs, and daily snack intake as key effect modifiers influencing caries-arrest outcomes. Machine learning models, specifically ensemble tree-based methods, can discriminate which surfaces arrest by 30 months using multidomain inputs spanning clinical, behavioral, and socioeconomic features. However, participant-level splitting was not performed, allowing potential clustering leakage. External validation and detailed calibration analyses were also lacking. These methodological constraints likely inflated model performance and currently limit its generalizability and readiness for clinical implementation.
{"title":"Interpretable machine learning modeling of treatment outcomes for silver and fluoride therapy in early childhood caries","authors":"Mojtaba Mehrabanian, Shahab Kavousinejad, Ebrahim Dastouri","doi":"10.1038/s41432-025-01195-8","DOIUrl":"10.1038/s41432-025-01195-8","url":null,"abstract":"Wu Y, Jia M, Fang Y, Duangthip D, Chu C H, Gao S S. Use machine learning to predict the treatment outcome of early childhood caries. BMC Oral Health 2025; 25: 389. This was a retrospective secondary analysis of data from a randomized controlled trial published in 2020. No new participants or patient involvement were included. This study used the available data from 880 children, contributing 4157 carious tooth surfaces assessed at 30 months. These data were drawn from an original community-based RCT in Hong Kong (baseline N = 1070) that evaluated fluoride and silver interventions for arresting ECC. Six algorithms were used and compared, including logistic regression (LR), naive Bayes (NB), support-vector machine (SVM), decision tree (DT), random forest (RF), and XGBoost. A surface-level 70:30 train: test split was used. SMOTE was applied to address class imbalance. Models were tuned and evaluated using 1000 bootstrap resamples. Performance metrics were reported as accuracy, recall, precision, F1 score, AUROC, and Brier score. Model interpretability was explored through SHAP analysis to rank variable importance and visualize feature effects. All models achieved acceptable discrimination. Metrics ranged as follows: accuracy 0.674–0.740; recall 0.731–0.809; precision 0.762–0.802; F1 0.741–0.804; AUROC 0.771–0.859 (RF and XGBoost ≈ 0.86); Brier 0.134–0.227. SHAP interpretation indicated that tooth and surface location of caries, newly developed dmfs, baseline dmfs, caregiver-assisted brushing, and visible plaque index contributed most to the model’s predictions, while the fluoride and silver intervention ranked mid-to-low in importance. The original study, however, highlighted tooth and surface location of caries, newly developed dmfs, and daily snack intake as key effect modifiers influencing caries-arrest outcomes. Machine learning models, specifically ensemble tree-based methods, can discriminate which surfaces arrest by 30 months using multidomain inputs spanning clinical, behavioral, and socioeconomic features. However, participant-level splitting was not performed, allowing potential clustering leakage. External validation and detailed calibration analyses were also lacking. These methodological constraints likely inflated model performance and currently limit its generalizability and readiness for clinical implementation.","PeriodicalId":12234,"journal":{"name":"Evidence-based dentistry","volume":"26 4","pages":"168-169"},"PeriodicalIF":2.3,"publicationDate":"2025-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145563380","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-20DOI: 10.1038/s41432-025-01192-x
Laura Timms, Zoe Marshman
Zheng F M, Yan I G, Duangthip D, Lo E C M, Gao S S, Chu C H. Randomized clinical trial on caries prevention of silver diamine fluoride. J Dent Res 2025; https://doi.org/10.1177/00220345251363837 . This randomised controlled trial sought to compare the effectiveness of silver diamine fluoride (SDF) to sodium fluoride varnish (NaF) for the prevention of caries in anterior primary teeth for young children. The inclusion criteria were children aged 3–4 years of age. Children were excluded if they had co-operative challenges or were on long-term medications. Children with active caries were included, lesions were considered active if they were soft on probing. The setting was kindergartens in Hong Kong. The children received either 38% SDF or 5% NaF applied to their six upper anterior primary teeth at six-monthly intervals. The primary outcome measure was the mean number of new carious surfaces per child at 30 months follow-up. Intention-to-treat analysis was used with the Mann-Whitney U test applied for the analysis of the primary outcome. Overall, 730 children were randomised, 621 (85%) were followed up and analysed at the 30 months end point for the presence of new carious surfaces (dmfs). Not all children seen at baseline were analysed, however of those that were their caries experience was similar with a mean dmfs of 0.47 ± 1.35 for the SDF group and 0.48 ± 1.53 for the NaF group. At 30 months, there were less new lesions for those in the SDF group (0.35 ± 1.09), than the NaF group (0.54 ± 1.50) (p = 0.048). The authors concluded that SDF was more effective than NaF in preventing new carious surfaces at 30 months for anterior caries in primary teeth of young children.
郑凤梅,闫益刚,段志平,罗春梅,高三生,褚春华。氟化二胺银预防龋齿的随机临床试验。J Dent Res 2025;https://doi.org/10.1177/00220345251363837。设计:本随机对照试验旨在比较氟化二胺银(SDF)和氟化钠清漆(NaF)在预防幼儿前乳牙龋齿方面的有效性。入选标准为3-4岁儿童。如果儿童有合作障碍或长期服用药物,则被排除在外。有活动性龋齿的儿童被包括在内,如果病变在探查时柔软,则认为是活动性的。背景是香港的幼儿园。这些儿童每6个月接受38%的SDF或5%的NaF治疗,用于他们的6颗上前乳牙。主要结局指标是随访30个月时每个儿童新发龋齿表面的平均数量。意向治疗分析采用Mann-Whitney U检验对主要结局进行分析。结果:总体而言,730名儿童被随机分组,621名(85%)接受了随访,并在30个月结束时分析了新龋面(dmfs)的存在。并不是所有在基线时看到的儿童都进行了分析,但是他们的龋病经历相似,SDF组的平均dmfs为0.47±1.35,NaF组的平均dmfs为0.48±1.53。30个月时,SDF组新发病灶数(0.35±1.09)少于NaF组(0.54±1.50)(p = 0.048)。结论:对于30月龄幼儿乳牙前牙,SDF比NaF更有效地预防新的龋面。
{"title":"Is silver diamine fluoride more effective than sodium fluoride varnish at preventing caries in upper anterior primary teeth?","authors":"Laura Timms, Zoe Marshman","doi":"10.1038/s41432-025-01192-x","DOIUrl":"10.1038/s41432-025-01192-x","url":null,"abstract":"Zheng F M, Yan I G, Duangthip D, Lo E C M, Gao S S, Chu C H. Randomized clinical trial on caries prevention of silver diamine fluoride. J Dent Res 2025; https://doi.org/10.1177/00220345251363837 . This randomised controlled trial sought to compare the effectiveness of silver diamine fluoride (SDF) to sodium fluoride varnish (NaF) for the prevention of caries in anterior primary teeth for young children. The inclusion criteria were children aged 3–4 years of age. Children were excluded if they had co-operative challenges or were on long-term medications. Children with active caries were included, lesions were considered active if they were soft on probing. The setting was kindergartens in Hong Kong. The children received either 38% SDF or 5% NaF applied to their six upper anterior primary teeth at six-monthly intervals. The primary outcome measure was the mean number of new carious surfaces per child at 30 months follow-up. Intention-to-treat analysis was used with the Mann-Whitney U test applied for the analysis of the primary outcome. Overall, 730 children were randomised, 621 (85%) were followed up and analysed at the 30 months end point for the presence of new carious surfaces (dmfs). Not all children seen at baseline were analysed, however of those that were their caries experience was similar with a mean dmfs of 0.47 ± 1.35 for the SDF group and 0.48 ± 1.53 for the NaF group. At 30 months, there were less new lesions for those in the SDF group (0.35 ± 1.09), than the NaF group (0.54 ± 1.50) (p = 0.048). The authors concluded that SDF was more effective than NaF in preventing new carious surfaces at 30 months for anterior caries in primary teeth of young children.","PeriodicalId":12234,"journal":{"name":"Evidence-based dentistry","volume":"26 4","pages":"170-171"},"PeriodicalIF":2.3,"publicationDate":"2025-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.nature.comhttps://www.nature.com/articles/s41432-025-01192-x.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145563378","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-12DOI: 10.1038/s41432-025-01186-9
Rafaella Rodrigues da Gama, Lucas Peixoto de Araújo, Evandro Piva, Leandro Perello Duro, Adriana Fernandes da Silva, Wellington Luiz de Oliveira da Rosa
The risk of bias (RoB) assessment is a critical aspect of systematic reviews, yet a lack of standardization in RoB criteria persists in the endodontic literature. This study aimed to evaluate the RoB tools used in systematic reviews (SRs) of in vitro endodontic studies to synthesize the most commonly employed criteria. A comprehensive search of five databases (PubMed, Embase, Web of Science, Scopus, and Cochrane Library) was conducted, identifying SRs with RoB evaluation. Data were extracted independently by two reviewers, focusing on the criteria used for RoB assessment. All SRs were categorized by main objective and the evaluation test. The study protocol was registered in the Open Science Framework ( https://osf.io/azd8u/ ). Of the 10,409 records initially identified, 142 systematic reviews (SRs) published between January 2018 and September 2024 met the inclusion criteria. These SRs employed 36 distinct RoB criteria, with the most common being blinding (40.9%), sample size (34.5%), adequate statistical analysis (31%), randomization (30.3%), and standardized sample preparation and handling (21.8%). Inconsistencies in the application of RoB criteria were evident, with many SRs employing tools adapted from clinical studies that were not fully suitable for the unique methodological requirements of in vitro research. Although some SRs attempted to adapt criteria from other studies, these adaptations often fell short of addressing the specific needs of in vitro studies. The absence of standardized tools compromises the reliability of current SRs and limits their comparability with future research. The observed inconsistencies in RoB assessments across SRs of in vitro endodontic studies highlight the critical need for a standardized tool specifically designed for this context. Such a tool should account for the methodological nuances of in vitro research, including the relevance of criteria like blinding and sample size calculation, to enhance the reliability, reproducibility, and overall relevance of future SRs.
目的:偏倚风险(RoB)评估是系统评价的一个关键方面,然而在牙髓学文献中仍然缺乏标准化的RoB标准。本研究旨在评估体外牙髓研究系统评价(SRs)中使用的RoB工具,以合成最常用的标准。方法:综合检索PubMed、Embase、Web of Science、Scopus、Cochrane Library等5个数据库,采用RoB评价法对ssr进行鉴定。数据由两位审稿人独立提取,重点关注用于RoB评估的标准。根据主要目标和评价方法对所有的SRs进行分类。研究方案已在开放科学框架(https://osf.io/azd8u/)中注册。结果:在最初确定的10409条记录中,2018年1月至2024年9月期间发表的142篇系统评价(SRs)符合纳入标准。这些SRs采用36个不同的RoB标准,其中最常见的是盲法(40.9%)、样本量(34.5%)、充分的统计分析(31%)、随机化(30.3%)和标准化的样品制备和处理(21.8%)。讨论:RoB标准应用的不一致性很明显,许多SRs采用的工具改编自临床研究,并不完全适合体外研究的独特方法学要求。尽管一些SRs试图适应其他研究的标准,但这些适应往往不能满足体外研究的特定需求。标准化工具的缺乏损害了当前SRs的可靠性,并限制了它们与未来研究的可比性。结论:在体外根管研究中观察到的不同SRs的RoB评估的不一致性突出了对专门为这种情况设计的标准化工具的迫切需要。这样的工具应该考虑到体外研究方法上的细微差别,包括盲法和样本量计算等标准的相关性,以提高未来SRs的可靠性、可重复性和总体相关性。
{"title":"Mapping risk of bias criteria in systematic reviews of in vitro endodontic studies: an umbrella review","authors":"Rafaella Rodrigues da Gama, Lucas Peixoto de Araújo, Evandro Piva, Leandro Perello Duro, Adriana Fernandes da Silva, Wellington Luiz de Oliveira da Rosa","doi":"10.1038/s41432-025-01186-9","DOIUrl":"10.1038/s41432-025-01186-9","url":null,"abstract":"The risk of bias (RoB) assessment is a critical aspect of systematic reviews, yet a lack of standardization in RoB criteria persists in the endodontic literature. This study aimed to evaluate the RoB tools used in systematic reviews (SRs) of in vitro endodontic studies to synthesize the most commonly employed criteria. A comprehensive search of five databases (PubMed, Embase, Web of Science, Scopus, and Cochrane Library) was conducted, identifying SRs with RoB evaluation. Data were extracted independently by two reviewers, focusing on the criteria used for RoB assessment. All SRs were categorized by main objective and the evaluation test. The study protocol was registered in the Open Science Framework ( https://osf.io/azd8u/ ). Of the 10,409 records initially identified, 142 systematic reviews (SRs) published between January 2018 and September 2024 met the inclusion criteria. These SRs employed 36 distinct RoB criteria, with the most common being blinding (40.9%), sample size (34.5%), adequate statistical analysis (31%), randomization (30.3%), and standardized sample preparation and handling (21.8%). Inconsistencies in the application of RoB criteria were evident, with many SRs employing tools adapted from clinical studies that were not fully suitable for the unique methodological requirements of in vitro research. Although some SRs attempted to adapt criteria from other studies, these adaptations often fell short of addressing the specific needs of in vitro studies. The absence of standardized tools compromises the reliability of current SRs and limits their comparability with future research. The observed inconsistencies in RoB assessments across SRs of in vitro endodontic studies highlight the critical need for a standardized tool specifically designed for this context. Such a tool should account for the methodological nuances of in vitro research, including the relevance of criteria like blinding and sample size calculation, to enhance the reliability, reproducibility, and overall relevance of future SRs.","PeriodicalId":12234,"journal":{"name":"Evidence-based dentistry","volume":"26 4","pages":"179-180"},"PeriodicalIF":2.3,"publicationDate":"2025-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145502629","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
This systematic review evaluated experimental evidence on how incorporating flowable dental composites affects the bond strength of dental cementation. This systematic review, following PRISMA guidelines, assessed in vitro studies (2003–2025) on the effect of flowable composites on cementation bond strength using a comprehensive database search, QUIN Tool for bias assessment, Begg’s and Egger’s tests for publication bias, and random-effects meta-analysis with SMD and I² statistics. This systematic review included eight in vitro studies published between 2003 and 2025. The meta-analysis found no statistically significant differences among the various bond strength test methods. Although the shear bond strength (SBS) test demonstrated a significant effect, the high heterogeneity among studies limits the reliability of this result. Etchable ceramics showed favourable effect sizes, but again, the high heterogeneity reduces the certainty of this finding. No significant difference was observed between self-etch and self-adhesive resin cements; however, self-etch resin cements tended to perform better in terms of bond strength. Nevertheless, the substantial heterogeneity in both adhesive groups indicates notable variability across studies. For the dual-cured group, a statistically significant standardized mean difference was observed, suggesting a positive effect of the dual-cured luting cement compared to the light-cured luting cement. Flowable dental composites generally perform comparably to conventional resin cements, with dual-cured and self-etch resin cements showing a tendency toward improved bond strength. However, variability across studies limits the certainty of these results. Further standardized in vitro studies are needed to confirm these findings and guide clinical application.
{"title":"Bond strength of flowable dental composites in the cementation of indirect restorations: a systematic review and meta-analysis","authors":"Baharan Ranjbar Omidi, Soolmaz Heidari, Armin Izadpanah","doi":"10.1038/s41432-025-01187-8","DOIUrl":"10.1038/s41432-025-01187-8","url":null,"abstract":"This systematic review evaluated experimental evidence on how incorporating flowable dental composites affects the bond strength of dental cementation. This systematic review, following PRISMA guidelines, assessed in vitro studies (2003–2025) on the effect of flowable composites on cementation bond strength using a comprehensive database search, QUIN Tool for bias assessment, Begg’s and Egger’s tests for publication bias, and random-effects meta-analysis with SMD and I² statistics. This systematic review included eight in vitro studies published between 2003 and 2025. The meta-analysis found no statistically significant differences among the various bond strength test methods. Although the shear bond strength (SBS) test demonstrated a significant effect, the high heterogeneity among studies limits the reliability of this result. Etchable ceramics showed favourable effect sizes, but again, the high heterogeneity reduces the certainty of this finding. No significant difference was observed between self-etch and self-adhesive resin cements; however, self-etch resin cements tended to perform better in terms of bond strength. Nevertheless, the substantial heterogeneity in both adhesive groups indicates notable variability across studies. For the dual-cured group, a statistically significant standardized mean difference was observed, suggesting a positive effect of the dual-cured luting cement compared to the light-cured luting cement. Flowable dental composites generally perform comparably to conventional resin cements, with dual-cured and self-etch resin cements showing a tendency toward improved bond strength. However, variability across studies limits the certainty of these results. Further standardized in vitro studies are needed to confirm these findings and guide clinical application.","PeriodicalId":12234,"journal":{"name":"Evidence-based dentistry","volume":"26 4","pages":"178-179"},"PeriodicalIF":2.3,"publicationDate":"2025-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145471024","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-08DOI: 10.1038/s41432-025-01184-x
Celine Raseekaanthan, Pirashani Umassudan
Mohamed M H, Abouauf E A, Mosallam R S. Clinical performance of class II MOD fiber reinforced resin composite restorations: an 18-month randomized controlled clinical trial. BMC Oral Health 2025;25: 159. https://doi.org/10.1186/s12903-025-05521-5 . A double blinded 18-month randomised controlled trial was carried out to compare the clinical performance of fibre reinforced resin composites compared to conventional nanohybrid resin composites in restoring Class II MOD cavities. Participants were allocated to one of three groups: Group 1 with short glass fibre reinforced resin composite, Group 2 with polyethylene fibre reinforced resin composite and Group 3 with conventional nanohybrid resin composite. A principal investigator carried out the restorative procedures for all participants. Participants in the study were enrolled from the educational clinic in Cairo University, Egypt. A total of 45 participants with a mean age of 32.3 ± 7.3 years were included. All participants had class II MOD carious lesions in vital posterior teeth with ICDAS scores of 3,4 or 5. Additionally only those with good oral hygiene, a healthy periodontal status and normal occlusion were included. The study excluded pregnant patients, as well as those with systemic disease or evidence of parafunctional habits. Patients with hypersensitivity, allergy to materials used, secondary caries or delayed response to sensibility testing were also excluded. Outcomes were assessed by two examiners at the baseline and at the following time intervals: 3, 6, 12, 18 months using Modified USPHS criteria. The primary outcome assessed was marginal adaptation, followed by gross fracture, marginal discolouration, colour match and recurrent caries. The clinical significance was determined based on relative risk. The chi-Square test compared between groups with significance set at P ≤ 0.016, and Cochran’s Q test compared within groups with significance at P ≤ 0.005, both adjusted using Bonferroni correction. The study was conducted with a 95% confidence level and an 80% statistical power. The study had a 97.7% retention rate with all but one patient successfully completing the 18 month follow up period. Colour match was the only outcome that showed a statistically significant difference between the groups, with short glass fibre reinforced restorations displaying some colour discrepancies. Other outcomes such as marginal adaptation, marginal discoloration, recurrent caries and gross fracture showed no significant differences between groups. Age, gender and tooth distribution also showed no significant statistical differences. The clinical performance of fibre-reinforced resin composite restorations are similar and comparable to nanohybrid composite restorations over an 18-month duration. Short glass fibre-reinforced restorations displayed variations in colour match, indicating that aesthetic outcomes should be carefully considered.
Mohamed M H, Abouauf E A, Mosallam R s。ⅱ类MOD纤维增强树脂复合材料修复体的临床性能:18个月随机对照临床试验。BMC口腔健康2025;25: 159。https://doi.org/10.1186/s12903 - 025 - 05521 - 5。设计:进行了一项为期18个月的双盲随机对照试验,比较纤维增强树脂复合材料与传统纳米混合树脂复合材料在修复II类MOD腔中的临床性能。参与者被分配到三组中的一组:第一组使用短玻璃纤维增强树脂复合材料,第二组使用聚乙烯纤维增强树脂复合材料,第三组使用常规纳米混合树脂复合材料。一名首席研究员对所有参与者进行了修复程序。病例选择:研究的参与者来自埃及开罗大学的教育诊所。共纳入45名参与者,平均年龄为32.3±7.3岁。所有参与者都有II级MOD龋齿病变,ICDAS评分为3,4或5。此外,仅包括口腔卫生良好、牙周健康、咬合正常的患者。该研究排除了怀孕患者,以及那些有全身性疾病或有不良习惯的患者。对所用材料过敏、继发性龋齿或敏感性测试反应延迟的患者也被排除在外。数据分析:结果由两名审查员在基线和以下时间间隔进行评估:3、6、12、18个月,使用修改的USPHS标准。评估的主要结果是边缘适应,其次是大体骨折、边缘变色、颜色匹配和复发性龋齿。临床意义是根据相对风险来确定的。卡方检验组间比较P≤0.016,科克伦Q检验组内比较P≤0.005,均采用Bonferroni校正。该研究的置信度为95%,统计效力为80%。结果:该研究的保留率为97.7%,除1例患者外,其余患者均成功完成18个月的随访期。颜色匹配是两组之间唯一有统计学差异的结果,短玻璃纤维增强修复体显示出一些颜色差异。其他结果如边缘适应、边缘变色、复发性龋齿和大体骨折在两组间无显著差异。年龄、性别、牙齿分布差异无统计学意义。结论:在18个月的时间内,纤维增强树脂复合材料修复体的临床性能与纳米复合材料修复体相似且相当。短玻璃纤维增强修复体在颜色匹配上表现出变化,表明应该仔细考虑美学结果。
{"title":"Fibre or facade? Do fibre reinforced composites really hold up in Class II restorations?","authors":"Celine Raseekaanthan, Pirashani Umassudan","doi":"10.1038/s41432-025-01184-x","DOIUrl":"10.1038/s41432-025-01184-x","url":null,"abstract":"Mohamed M H, Abouauf E A, Mosallam R S. Clinical performance of class II MOD fiber reinforced resin composite restorations: an 18-month randomized controlled clinical trial. BMC Oral Health 2025;25: 159. https://doi.org/10.1186/s12903-025-05521-5 . A double blinded 18-month randomised controlled trial was carried out to compare the clinical performance of fibre reinforced resin composites compared to conventional nanohybrid resin composites in restoring Class II MOD cavities. Participants were allocated to one of three groups: Group 1 with short glass fibre reinforced resin composite, Group 2 with polyethylene fibre reinforced resin composite and Group 3 with conventional nanohybrid resin composite. A principal investigator carried out the restorative procedures for all participants. Participants in the study were enrolled from the educational clinic in Cairo University, Egypt. A total of 45 participants with a mean age of 32.3 ± 7.3 years were included. All participants had class II MOD carious lesions in vital posterior teeth with ICDAS scores of 3,4 or 5. Additionally only those with good oral hygiene, a healthy periodontal status and normal occlusion were included. The study excluded pregnant patients, as well as those with systemic disease or evidence of parafunctional habits. Patients with hypersensitivity, allergy to materials used, secondary caries or delayed response to sensibility testing were also excluded. Outcomes were assessed by two examiners at the baseline and at the following time intervals: 3, 6, 12, 18 months using Modified USPHS criteria. The primary outcome assessed was marginal adaptation, followed by gross fracture, marginal discolouration, colour match and recurrent caries. The clinical significance was determined based on relative risk. The chi-Square test compared between groups with significance set at P ≤ 0.016, and Cochran’s Q test compared within groups with significance at P ≤ 0.005, both adjusted using Bonferroni correction. The study was conducted with a 95% confidence level and an 80% statistical power. The study had a 97.7% retention rate with all but one patient successfully completing the 18 month follow up period. Colour match was the only outcome that showed a statistically significant difference between the groups, with short glass fibre reinforced restorations displaying some colour discrepancies. Other outcomes such as marginal adaptation, marginal discoloration, recurrent caries and gross fracture showed no significant differences between groups. Age, gender and tooth distribution also showed no significant statistical differences. The clinical performance of fibre-reinforced resin composite restorations are similar and comparable to nanohybrid composite restorations over an 18-month duration. Short glass fibre-reinforced restorations displayed variations in colour match, indicating that aesthetic outcomes should be carefully considered.","PeriodicalId":12234,"journal":{"name":"Evidence-based dentistry","volume":"26 3","pages":"144-145"},"PeriodicalIF":2.3,"publicationDate":"2025-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145023149","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-05DOI: 10.1038/s41432-025-01183-y
Mona Nasser
{"title":"We still need to bridge the gap","authors":"Mona Nasser","doi":"10.1038/s41432-025-01183-y","DOIUrl":"10.1038/s41432-025-01183-y","url":null,"abstract":"","PeriodicalId":12234,"journal":{"name":"Evidence-based dentistry","volume":"26 3","pages":"121-122"},"PeriodicalIF":2.3,"publicationDate":"2025-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.nature.comhttps://www.nature.com/articles/s41432-025-01183-y.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145006026","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}