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Topical tacrolimus orabase versus topical clobetasol propionate orabase in the treatment of symptomatic oral lichen planus: a pilot randomized study. 外用他克莫司奥拉帕斯与外用氯倍他索丙酸酯奥拉帕斯治疗症状性口腔扁平苔藓:一项试验性随机研究。
IF 3.1 2区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2024-09-30 DOI: 10.1007/s00784-024-05943-5
F M M Schroeder, E S Pedraça, V M Palma, V C Carrard, M A T Martins, F L D M Maito, D Q M Lisbôa, Fernanda Visioli

Objectives: This pilot study aimed to compare the efficacy of 0.1% tacrolimus and 0.05% clobetasol propionate in orabase for treating symptomatic oral lichen planus (OLP).

Materials and methods: Pilot, randomized, and controlled study conducted on 21 patients with symptomatic OLP, selected according to the clinical and histopathological criteria of Cheng et al. 2016. Twelve patients received 0.1% tacrolimus, and nine received 0.05% clobetasol, both in orabase for 30 days with a two-month follow-up. The patients were examined for scores of signs (ODSS), symptoms (VAS), quality of life (OHIP-14), anxiety (Beck Anxiety Scale), and treatment satisfaction (Hedonic Scale).

Results: Both treatments were effective in reducing ODSS, VAS, and Beck Anxiety Scale scores and performed well on the hedonic scale, yet without statistical difference between them. However, at the 1-month follow-up, patients in group Clobetasol showed a greater percentage reduction in ODSS score compared to baseline by 50% (p = 0.02) and significantly lower average values (p = 0.03) than those in group Tacrolimus. Longitudinal intragroup analysis revealed significant improvements over time in both groups for ODSS, and only in the tacrolimus group for OHIP-14 and Beck scores.

Conclusions: Both tested protocols were effective over a three-month follow-up. However, due to the lower cost of clobetasol propionate it can be considered the first-choice option. Tacrolimus in orabase formulation may be a promising alternative for refractory lesions that do not respond to topical steroids.

Clinical relevance: Managing symptomatic OLP is challenging. Comparisons between tacrolimus and clobetasol propionate in orabase formulations have not yet been thoroughly explored.

研究目的本试验研究旨在比较0.1%他克莫司和0.05%氯倍他索丙酸酯在奥拉帕斯中治疗症状性口腔扁平苔藓(OLP)的疗效:根据Cheng等人2016年的临床和组织病理学标准,对21例有症状的OLP患者进行了试验性、随机对照研究。12名患者接受0.1%他克莫司治疗,9名患者接受0.05%氯倍他索治疗,两种药物均在奥拉帕斯中使用30天,随访两个月。对患者的体征(ODSS)、症状(VAS)、生活质量(OHIP-14)、焦虑(贝克焦虑量表)和治疗满意度(Hedonic量表)进行了评分:结果:两种疗法都能有效降低 ODSS、VAS 和贝克焦虑量表的评分,在享乐量表上的表现也很好,但两者之间没有统计学差异。然而,在 1 个月的随访中,氯倍他索组患者的 ODSS 评分与基线相比降低了 50%(p = 0.02),平均值也明显低于他克莫司组(p = 0.03)。组内纵向分析显示,随着时间的推移,两组患者的ODSS评分均有显著改善,只有他克莫司组患者的OHIP-14和Beck评分有显著改善:结论:在三个月的随访中,两种测试方案都很有效。结论:两种测试方案在三个月的随访中均有效,但由于氯倍他索丙酸盐的成本较低,可将其作为首选方案。对于外用类固醇类药物无效的难治性皮损,奥拉帕斯制剂中的他克莫司可能是一种很有前途的替代疗法:临床意义:治疗无症状的OLP具有挑战性。对他克莫司和氯倍他索丙酸酯奥拉帕斯制剂的比较尚未进行深入探讨。
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引用次数: 0
Radiographic identification of symptomless mandibular third molars without clinical pericoronitis. 无临床冠周炎的无症状下颌第三磨牙的放射学鉴定。
IF 3.1 2区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2024-09-30 DOI: 10.1007/s00784-024-05953-3
Tommi Vesala, Irja Ventä, Johanna Snäll, Marja Ekholm

Objectives: The aim was to identify radiographic characteristics of mandibular third molars in young adults without symptoms or clinical signs of pericoronal infection.

Materials and methods: An existing cross-sectional material, including records from clinical oral examination and panoramic radiographs (PANs) of university students, was submitted to retrospective analysis. The outcome variable was a symptomless and clinically pericoronitis-free mandibular third molar. Predictor variables for the third molar were clinical eruption level, pathological signs in the follicle, marginal bone level, radiographic depth in bone, inclination, stage of root development, and available space for eruption. Statistics included χ2 and Mann-Whitney U tests.

Results: Analysis included 345 mandibular third molars in 189 participants (20% men, 80% women; mean age 20.7 years; SD ± 0.6). Symptomless and clinically pericoronitis-free mandibular third molars were characterized as follows: clinically unerupted in 78% of teeth, associated with reduced marginal bone level in 70%, located deeper in the bone in 87%, mesially inclined in 73%, and stage of root development incomplete in 68% (p ≤ 0.001 for all).

Conclusions: Radiographic characteristics of symptomless mandibular third molars without clinical pericoronitis in young adults can be assessed from a PAN with 68-87% certainty.

Clinical relevance: These findings may prove useful when trying to exclude non-pathological mandibular third molars from diseased teeth.

目的旨在确定无冠周炎症状或临床表现的青壮年下颌第三磨牙的放射学特征:回顾性分析现有的横断面材料,包括临床口腔检查记录和大学生的全景X光片(PAN)。结果变量为无症状、无临床冠周炎的下颌第三磨牙。第三磨牙的预测变量包括临床萌出水平、牙泡中的病理征象、边缘骨水平、放射学显示的骨深度、倾斜度、牙根发育阶段和可用于萌出的空间。统计方法包括χ2检验和曼-惠特尼U检验:分析包括 189 名参与者(20% 为男性,80% 为女性;平均年龄 20.7 岁;SD ± 0.6)的 345 颗下颌第三磨牙。无症状和临床上无冠周炎的下颌第三磨牙的特征如下:78%的牙齿临床上未萌出,70%的牙齿边缘骨水平降低,87%的牙齿位于牙槽骨较深的位置,73%的牙齿向中线倾斜,68%的牙齿牙根发育不完全(所有数据的P≤0.001):结论:无临床冠周炎的无症状下颌第三磨牙的影像学特征可通过 PAN 进行评估,确定性为 68-87%:临床相关性:这些发现可能有助于将非病理性下颌第三磨牙从病牙中排除。
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引用次数: 0
Accuracy of polyether and vinylpolysiloxane impressions when using different types of 3D-printed impression trays - an in vitro study. 使用不同类型 3D 打印印模托盘时聚醚和乙烯基聚硅氧烷印模的准确性 - 一项体外研究。
IF 3.1 2区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2024-09-30 DOI: 10.1007/s00784-024-05962-2
Stefan Rues, David Depré, Thomas Stober, Peter Rammelsberg, Andreas Zenthöfer

Objectives: To investigate dimensional accuracy of polyether (PE) and vinylpolysiloxane (VPS) impressions taken with manually fabricated and 3D-printed trays.

Materials and methods: To evaluate impression accuracy, highly precise digital data of a metallic lower jaw model with prepared teeth (regions 34 and 36), an implant (region 47) and three precision balls placed occlusally along the dental arch served as reference. PE (Impregum, 3M Oral Care) and VPS (Aquasil, Dentsply Sirona) impressions (n = 10/group) were taken with trays fabricated using different materials and manufacturing techniques (FDM: filament deposition modeling, material: Arfona Tray, Arfona; printer: Pro2, Raise3D; DLP: digital light processing, material: V-Print Tray, VOCO, printer: Max, Asiga; MPR: manual processing with light-curing plates, material: LC Tray, Müller-Omicron) including an open implant impression. Scans of resulting stone models were compared with the reference situation. Global distance and angular deviations as well as local trueness and precision for abutment teeth and scan abutment were computed. Possible statistical effects were analyzed using ANOVA.

Results: Clinically acceptable global accuracy was found (all mean absolute distance changes < 100 μm) and local accuracy for single abutments was excellent. All factors (abutment type, impression material, tray material) affected global accuracy (p < 0.05). In particular with PE impressions, MPR trays led to the best accuracies, both in horizontal and vertical direction.

Conclusions: Within the limitations of this in vitro study, impression accuracy was high in use of both polyether and vinylpolysiloxane combined with different 3D-printed and customized trays making them recommendable for at least impressions for smaller fixed dental prostheses. Manually fabricated trays were overall still the best choice if utmost precision is required.

Clinical relevance: Based on the results of this study, use of innovative CAD-CAM fabrication of individual impression trays fulfills the perquisites to be a viable option for impression making. In the sense of translational research, performance should be proved in a clinical setting.

目的研究使用手工制造和三维打印托盘制作的聚醚(PE)和乙烯基聚硅氧烷(VPS)印模的尺寸精度:为了评估印模的准确性,以金属下颌模型的高精度数字数据为参考,该模型包含准备好的牙齿(34 和 36 区)、种植体(47 区)和沿牙弓咬合方向放置的三个精密球。在使用不同材料和制造技术(FDM:长丝沉积建模,材料:Arfona Tray,Arfona,Dentsply Sirona)制作的托盘上取 PE(Impregum,3M Oral Care)和 VPS(Aquasil,Dentsply Sirona)印模(n = 10/组):Arfona托盘,Arfona;打印机:Pro2,Raise3D;DLP:数字光处理,材料:V-Print托盘,VOCO,打印机:Max,Asiga;MPR:使用光固化板进行手动加工,材料:LC Tray,Müller,Asiga;打印机:Pro2,Raise3D:LC托盘,Müller-Omicron),包括开放式种植体印模。将生成的结石模型的扫描结果与参考情况进行比较。计算了基牙和扫描基台的整体距离和角度偏差以及局部真实度和精度。使用方差分析对可能的统计影响进行了分析:结果:发现了临床上可接受的整体精度(所有平均绝对距离变化结论):在这项体外研究的局限性范围内,聚醚和乙烯基聚硅氧烷与不同的 3D 打印和定制托盘结合使用时,印模准确性都很高,因此至少在较小的固定义齿印模中值得推荐。如果需要最高精度,手工制作的托盘总体上仍是最佳选择:根据这项研究的结果,使用创新的 CAD-CAM 制作个人印模托盘符合印模制作的前提条件。就转化研究而言,其性能应在临床环境中得到验证。
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引用次数: 0
Five-year survival of class II restorations with and without base bulk-fill composite: a retrospective cohort study. 使用和不使用基底填充复合材料的二级修复体的五年存活率:一项回顾性队列研究。
IF 3.1 2区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2024-09-30 DOI: 10.1007/s00784-024-05965-z
Jukka Leinonen, Hannu Vähänikkilä, Remo Luksepp, Vuokko Anttonen

Objective: This study aimed to determine the survival of class II composite restorations in premolars and molars with and without base bulk-fill composite in general dental practice.

Materials and methods: We collected data from the electronic patient files of the Public Dental Services in the City of Oulu, Finland. The timespan of data collection was from August 15th, 2002, to August 9th, 2018. The data consisted of class II composite restorations both with and without base bulk-fill composite. We compared the survival of these restorations using Kaplan-Meier survival curves, the log-rank test, survival rates, and the Wilcoxon signed ranks test.

Results: We observed 297 restorations in 96 patients. The five-year survival rates for restorations with and without base bulk-fill composite were comparable in premolars (77.5% and 77.4%, respectively) but different in molars (69.9% and 57.8%, respectively, p = 0.069). In molars, the restorations with base bulk-fill composite exhibited a higher survival rate in 14 patients, whereas in 11 patients the restorations without base bulk-fill composites exhibited a higher survival rate. In 24 patients the survival rates were similar for restorations with and without the base bulk-fill composite (p = 0.246).

Conclusions: The restorations with and without base bulk-fill composite had similar longevity.

Clinical relevance: Base bulk-fill composites are safe to use in general practice due to their similar survival rates compared to conventional composites.

研究目的本研究旨在确定普通牙科诊所中使用或不使用基底大量填充复合材料的前磨牙和磨牙二类复合材料修复体的存活率:我们从芬兰奥卢市公共牙科服务机构的电子患者档案中收集数据。数据收集的时间跨度为 2002 年 8 月 15 日至 2018 年 8 月 9 日。数据包括使用和不使用基底填充复合材料的二类复合材料修复体。我们使用 Kaplan-Meier 生存曲线、对数秩检验、生存率和 Wilcoxon 符号行列检验比较了这些修复体的存活率:结果:我们观察了 96 名患者的 297 次修复。在前磨牙中,使用和不使用基底填充复合材料的修复体的五年存活率相当(分别为 77.5%和 77.4%),但在磨牙中却不同(分别为 69.9%和 57.8%,p = 0.069)。在磨牙中,14 名患者的基底填充复合材料修复体的存活率较高,而 11 名患者的无基底填充复合材料修复体的存活率较高。在 24 名患者中,使用和不使用基底填充复合材料的修复体的存活率相似(p = 0.246):结论:有基底填充复合材料和没有基底填充复合材料的修复体寿命相似:临床意义:由于基底填充复合材料的存活率与传统复合材料相似,因此在普通临床中使用是安全的。
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引用次数: 0
Direct versus fully digital indirect bracket bonding: a split-mouth randomized clinical trial on accuracy. 直接与全数字化间接支架粘接:关于准确性的分口随机临床试验。
IF 3.1 2区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2024-09-28 DOI: 10.1007/s00784-024-05950-6
Pauline M J Hoekstra-van Hout, Jan Willem M Hoekstra, Robin Bruggink, Ewald M Bronkhorst, Edwin M Ongkosuwito

Objectives: The primary aim is to assess differences in accuracy of orthodontic bracket positioning between fully digital indirect bracket bonding (IDB) and conventional direct bracket bonding (DBB). The secondary aims are to assess differences in bracket bonding failures, bracket repositioning need, clinician experience and patient satisfaction.

Materials and methods: This prospective study was designed as a split-mouth randomized clinical trial. In total, 35 patients were analyzed with a six month follow-up period. Translational and orientational deviations from the planned bracket position were determined. Clinician experience and patient satisfaction were evaluated by means of a survey.

Results: The difference in translation was 0.34 mm (95% CI: 0.238-0.352, p = 0.017), the difference in orientation was 4.80˚ (95% CI: 3.858-5.727, p < 0.001), both in favour of IDB. IDB showed significantly more immediate (IDB: 3.9%, DBB: 0%) and late (IDB: 5.4%, DBB: 2.5%, p = 0.008) bonding failures. Clinicians and patients experienced a shorter clinical chair time with indirect bonding over direct bonding.

Conclusions: IDB bracket positioning leads to significant smaller translation and orientation deviations from digital IDB planning, than DBB bracket positioning. However, IDB leads to more immediate bonding failures than DBB. The majority of patients preferred IDB over DBB, due to a shorter clinical chair time.

Clinical relevance: This study adds to the knowledge of IDB in orthodontics and contributes to evidence on this technique. This evidence is applicable in everyday orthodontics, with respect to patient satisfaction and technical limits of IDB. The trial was registered in the Dutch Trial Register and the International Clinical Trials Registry Platform (ICTRP) of the World Health Organization (WHO), number NL9411.

目的:主要目的是评估全数字化间接托槽粘接(IDB)与传统直接托槽粘接(DBB)在正畸托槽定位精度方面的差异。次要目的是评估托槽粘结失败率、托槽重新定位需求、临床医生经验和患者满意度的差异:这项前瞻性研究设计为分口随机临床试验。共对 35 名患者进行了为期 6 个月的随访分析。确定了与计划托槽位置的横向和纵向偏差。通过调查对临床医生的经验和患者的满意度进行了评估:结果:平移偏差为 0.34 毫米(95% CI:0.238-0.352,p = 0.017),方向偏差为 4.80˚(95% CI:3.858-5.727,p 结论:IDB 托槽定位可显著缩小患者的矫治范围:与 DBB 托槽定位相比,IDB 托槽定位导致的平移和方向偏差明显小于数字 IDB 规划。然而,与 DBB 相比,IDB 会导致更多的即刻粘接失败。与 DBB 相比,大多数患者更愿意选择 IDB,因为临床治疗椅时间更短:临床相关性:这项研究增加了正畸学中 IDB 的知识,并为这项技术提供了证据。在患者满意度和 IDB 技术限制方面,这些证据适用于日常正畸。该试验已在荷兰试验注册中心和世界卫生组织(WHO)的国际临床试验注册平台(ICTRP)注册,编号为NL9411。
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引用次数: 0
Two versus three magnesium screws for osteosynthesis of mandibular condylar head fractures: a finite element analysis. 下颌骨髁状头骨折截骨术中使用两颗镁螺钉还是三颗镁螺钉:有限元分析。
IF 3.1 2区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2024-09-27 DOI: 10.1007/s00784-024-05927-5
Daphne Schönegg, Günter T Müller, Michael Blumer, Harald Essig, Maximilian E H Wagner

Objectives: Previous finite element analyses (FEA) have shown promising results for using two titanium screws in treating mandibular condylar head fractures but limited mechanical stability of a two-screw osteosynthesis with magnesium screws. Given the potential benefits of magnesium screws in terms of biocompatibility and resorption, this study aimed to compare two- and three-screw osteosynthesis solutions for a right condylar head fracture (AO CMF type p) with magnesium screws with a FEA.

Materials and methods: A previously validated finite element model simulating a 350 N bite on the contralateral molars was used to analyze von Mises stress within the screws, fragment deformation, and fracture displacement. All screws were modeled with uniform geometric specifications mirroring the design of Medartis MODUS® Mandible Hexadrive cortical screws.

Results: The three-screw configuration demonstrated lower values for all three parameters compared to the two-screw scenario. There was a 30% reduction in maximum von Mises stress for the top screw and a 46% reduction for the bottom screw.

Conclusions: Fracture treatment with three magnesium screws could be a valuable and sufficiently stable alternative to the established treatment with titanium screws. Further studies on screw geometry could help improve material stability under mechanical loading, enhancing the performance of magnesium screws in clinical applications.

Clinical relevance: The use of magnesium screws for osteosynthesis of mandibular condylar head fractures offers the benefit of reducing the need for second surgery for hardware removal. Clinical data is needed to determine whether the advantages of resorbable screw materials outweigh potential drawbacks in condylar head fracture treatment.

目的:以往的有限元分析(FEA)显示,使用两根钛螺钉治疗下颌骨髁状头骨折的效果很好,但使用镁螺钉进行双螺钉骨合成的机械稳定性有限。鉴于镁螺钉在生物相容性和吸收方面的潜在优势,本研究旨在通过有限元分析比较使用镁螺钉治疗右髁头骨折(AO CMF p型)的双螺钉和三螺钉骨合成方案:使用先前验证的有限元模型模拟对侧臼齿 350 N 的咬合,分析螺钉内的 von Mises 应力、碎片变形和骨折位移。所有螺钉均采用与 Medartis MODUS® Mandible Hexadrive 皮质螺钉设计一致的几何规格进行建模:结果:与双螺钉方案相比,三螺钉配置的所有三个参数值都较低。顶部螺钉的最大 von Mises 应力降低了 30%,底部螺钉降低了 46%:结论:使用三根镁制螺钉进行骨折治疗是一种有价值且足够稳定的方法,可替代现有的钛制螺钉治疗方法。对螺钉几何形状的进一步研究有助于提高材料在机械负荷下的稳定性,从而提高镁螺钉在临床应用中的性能:临床相关性:使用镁螺钉对下颌骨髁状头骨折进行骨合成,可减少二次手术取出硬件的需要。需要临床数据来确定可吸收螺钉材料在髁状头骨折治疗中的优势是否大于潜在的缺点。
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引用次数: 0
Prosthesis choice in the adult USA population with partial edentulism. 美国成人部分缺牙症患者的假牙选择。
IF 3.1 2区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2024-09-27 DOI: 10.1007/s00784-024-05934-6
Jiale Li, Zhaohua Ji, Zhe Zhao, Fu Wang, Min Tian

Objectives: This study aimed to estimate the prevalence of prostheses and investigate how demographic and socioeconomic characteristics influence choices of restoration types in the adult population of the United States over 20 years of age.

Materials and methods: The study utilized data from the National Health and Nutrition Examination Surveys (NHANES) conducted from 2017 to March 2020 Pre-Pandemic Data. We examined demographic and socioeconomic variables, dentition status, and restoration types among participants with partial edentulism. The percentage of categorical variables between restoration types was compared using chi-square tests. Multinomial logistic regression models were employed to explore the relationship between prosthetic choices and demographic and socioeconomic factors, both unadjusted and adjusted for all characteristics, including the number of missing teeth.

Results: Out of 15,560 participants, 7,805 eligible individuals with a mean age of 47.8 and a male percentage of 48.4% were included in the analysis. The results indicated that individuals who were younger, male, of Mexican American or non-Hispanic Black ethnicity, possessed lower educational attainment, were never married, had a low income-to-poverty ratio, held private insurance, or were unemployed were more inclined to choose no restoration. Further, males, non-Hispanic Black individuals, those with lower educational attainment, lower income-to-poverty ratios, and those who were unemployed or retired were more likely to choose RPDs over FPDs. Furthermore, never-married individuals and those with private insurance were likelier to choose FPDs in the maxilla (p < 0.01).

Conclusions: Significant differences were observed among restoration types, demographic and socioeconomic variables, and dentition status in both the upper and lower jaws.

Clinical relevance: This study underscores the significance of socioeconomic variables in the restoration of partial edentulism.

目的:本研究旨在估算美国 20 岁以上成年人的修复率,并调查人口和社会经济特征如何影响修复类型的选择:本研究旨在估算美国 20 岁以上成年人的假肢使用率,并调查人口和社会经济特征如何影响修复类型的选择:该研究利用了 2017 年至 2020 年 3 月进行的美国国家健康与营养调查(NHANES)的大流行前数据。我们研究了部分缺牙症参与者的人口统计学和社会经济变量、牙齿状况和修复类型。修复类型之间的分类变量百分比采用卡方检验进行比较。采用多项式逻辑回归模型来探讨修复体选择与人口和社会经济因素之间的关系,既包括未调整的因素,也包括对所有特征(包括缺失牙齿数量)进行调整的因素:在 15,560 名参与者中,7,805 名符合条件的人被纳入分析,他们的平均年龄为 47.8 岁,男性比例为 48.4%。结果显示,年龄较小、男性、墨西哥裔美国人或非西班牙裔黑人、教育程度较低、从未结过婚、收入与贫困比例较低、持有私人保险或失业的人更倾向于选择不修复。此外,男性、非西班牙裔黑人、教育程度较低、收入与贫困比率较低、失业或退休人员更倾向于选择 RPD 而不是 FPD。此外,未婚者和有私人保险的人更倾向于选择上颌的FPD(p 结论):在上颌和下颌的修复类型、人口统计学和社会经济变量以及牙齿状况之间观察到了显著差异:本研究强调了社会经济变量在部分缺牙修复中的重要性。
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引用次数: 0
Systemic ozone therapy as an adjunctive treatment in guided bone regeneration: a histomorphometrical and immunohistochemical study in rats. 全身臭氧疗法作为引导骨再生的辅助疗法:大鼠组织形态计量学和免疫组织化学研究。
IF 3.1 2区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2024-09-27 DOI: 10.1007/s00784-024-05961-3
Ana Maira Pereira Baggio, Vinícius Ferreira Bizelli, Izabela Fornazari Delamura, Arthur Henrique Alecio Viotto, Allice Santos Cruz Veras, Giovana Rampazzo Teixeira, Leonardo Perez Faverani, Ana Paula Farnezi Bassi

Objectives: To assess the effectiveness of ozone therapy in guided bone regeneration (GBR) for critical size calvarial defects in rats.

Materials and methods: 96 male Wistar rats were divided into four groups (n = 6 each). An 8 mm critical defect was created in the calvaria of each rat. The groups were: BIO (porcine collagen membrane, BioGide®), BIO + OZ (membrane with systemic ozone therapy every 2 days), COA + OZ (blood clot with ozone therapy), and COA (blood clot only). Evaluations at 7, 15, 30, and 60 days included histological, histomorphometric, inflammatory profile, Micro-CT, and immunohistochemical analyses. Statistical analysis involved two-factor ANOVA with Tukey's post-hoc test for general data, and one-factor ANOVA with Holm-Sidak post-hoc test for Micro-CT data.

Results: The BIO + OZ group demonstrated superior bone regeneration with well-organized, mature bone tissue and significant bone formation at 30 and 60 days. The COA + OZ group showed early angiogenesis and reduced inflammation, resulting in complete defect closure by 30 days. The BIO group had good regeneration, but less mature tissue compared to BIO + OZ. The COA group exhibited limited bone formation and higher porosity.

Conclusion: Ozone therapy positively influences bone regeneration by enhancing cell proliferation and the healing response.

Clinical relevance: Improving regenerative processes with auxiliary therapies like ozone therapy can be significant for advancing dental reconstructions.

目的:评估臭氧疗法对大鼠临界大小腓骨缺损的引导骨再生(GBR)效果:材料与方法:96 只雄性 Wistar 大鼠分为四组(每组 6 只)。每只大鼠的腓骨上都有一个 8 毫米的临界缺损。各组分别为BIO组(猪胶原膜,BioGide®)、BIO + OZ组(猪胶原膜,每两天进行一次全身臭氧治疗)、COA + OZ组(血凝块,臭氧治疗)和COA组(仅血凝块)。7、15、30 和 60 天的评估包括组织学、组织形态计量学、炎症特征、Micro-CT 和免疫组化分析。统计分析包括一般数据的双因素方差分析和Tukey's事后检验,以及Micro-CT数据的单因素方差分析和Holm-Sidak事后检验:30 天和 60 天后,BIO + OZ 组显示出良好的骨再生效果,骨组织组织有序、成熟,骨形成显著。COA + OZ 组显示出早期血管生成,炎症减少,30 天后缺损完全闭合。BIO 组再生良好,但成熟组织少于 BIO + OZ 组。COA组的骨形成有限,孔隙率较高:结论:臭氧疗法通过促进细胞增殖和愈合反应对骨再生产生积极影响:临床意义:利用臭氧疗法等辅助疗法改善再生过程对牙科重建具有重要意义。
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引用次数: 0
Qualitative somatosensory evaluation of recipient and donor sites of subepithelial connective tissue grafts: a preliminary study. 上皮下结缔组织移植受体和供体部位的定性体感评估:初步研究。
IF 3.1 2区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2024-09-27 DOI: 10.1007/s00784-024-05933-7
Esther Belotti do Nascimento, Talyta Sasaki Jurkevicz, Leonardo Rigoldi Bonjardim, Adriana Campos Passanezi Sant' Ana, Carla Andreotti Damante, Mariana Schutzer Ragghianti Zangrando

Objectives: The subepithelial connective tissue graft (SCTG) plus coronal advanced flap is commonly evaluated by clinical parameters, but potential sensory changes (patients' perception of painful or painless sensations) need to be further explored. This preliminary study aimed to qualitatively evaluate the somatosensory profile of recipient and palatal donor sites of SCTG.

Materials and methods: Sensory tests were applied at SCTG recipient and donor sites at baseline, after 3 and 6 months. A single calibrated examiner applied Douleur Neuropathique 4 questionnaire (DN4), qualitative sensory test (QualST), discriminating the areas as hypersensitive, hyposensitive or normosensitive, and two-point acuity test. Descriptive statistics, non-parametric Kruskal Wallis test for QualST evaluation and ANOVA for Two-point test (p < 0.05) were used.

Results: QualST revealed that recipient areas presented no significant differences in tactile, pressure and thermal tests. Brush test revealed hyposensitivity after 3 months (p = 0.03). In donor areas, only thermal evaluation showed a significant difference (p = 0.01), being hypersensitive after 3 months and hyposensitive after 6 months. At baseline, all evaluations in recipient and donor areas were normosensitive. According to DN4, no patient reported pain in recipient and donor sites. Non-painful sensory perception was reported as numbness in recipient (3.14% of patients) and donor (18.4%) areas. No significant differences were found for two-point acuity test values.

Conclusions: Somatosensory variations were observed in donor and recipient areas using qualitative tests, with no detection of painful sensations, only non-painful sensations of numbness and electric shock.

Clinical relevance: This preliminary study demonstrated that alterations of hypo- and hypersensitivity may occur in donor and recipient areas of gingival grafts. However, when present, these alterations were non-painful and did not impact oral functions.

Clinical registration: ReBEC #RBR-7zz3b6p.

目的:上皮下结缔组织移植(SCTG)加冠状先进皮瓣通常通过临床参数进行评估,但潜在的感觉变化(患者对疼痛或无痛感觉的感知)需要进一步探讨。本初步研究旨在定性评估 SCTG 受体和腭供体部位的体感特征:在基线、3 个月后和 6 个月后对 SCTG 受体和供体部位进行感觉测试。由一名经过校准的检查员进行Douleur Neuropathique 4问卷调查(DN4)、定性感觉测试(QualST)(区分高敏感区、低敏感区或正常敏感区)和两点敏锐度测试。对 QualST 评估采用描述性统计、非参数 Kruskal Wallis 检验,对两点测试采用方差分析(P 结果):QualST显示,受体区域在触觉、压力和热测试中没有明显差异。刷子测试显示 3 个月后受体敏感性降低(p = 0.03)。在供体区,只有热敏评估显示出显著差异(p = 0.01),3 个月后敏感度降低,6 个月后敏感度降低。基线时,受体和供体区域的所有评估结果均正常。根据 DN4,没有患者报告受体和供体部位出现疼痛。受体(3.14% 的患者)和供体(18.4% 的患者)部位的非疼痛感觉为麻木。两点敏锐度测试值无明显差异:通过定性测试观察到供体和受体区域的躯体感觉变化,未发现疼痛感觉,仅发现麻木和电击等非疼痛感觉:这项初步研究表明,牙龈移植的供体区和受体区可能会出现超敏反应和过敏反应的改变。然而,即使出现这些改变,也不会引起疼痛,也不会影响口腔功能:临床注册:ReBEC #RBR-7zz3b6p。
{"title":"Qualitative somatosensory evaluation of recipient and donor sites of subepithelial connective tissue grafts: a preliminary study.","authors":"Esther Belotti do Nascimento, Talyta Sasaki Jurkevicz, Leonardo Rigoldi Bonjardim, Adriana Campos Passanezi Sant' Ana, Carla Andreotti Damante, Mariana Schutzer Ragghianti Zangrando","doi":"10.1007/s00784-024-05933-7","DOIUrl":"https://doi.org/10.1007/s00784-024-05933-7","url":null,"abstract":"<p><strong>Objectives: </strong>The subepithelial connective tissue graft (SCTG) plus coronal advanced flap is commonly evaluated by clinical parameters, but potential sensory changes (patients' perception of painful or painless sensations) need to be further explored. This preliminary study aimed to qualitatively evaluate the somatosensory profile of recipient and palatal donor sites of SCTG.</p><p><strong>Materials and methods: </strong>Sensory tests were applied at SCTG recipient and donor sites at baseline, after 3 and 6 months. A single calibrated examiner applied Douleur Neuropathique 4 questionnaire (DN4), qualitative sensory test (QualST), discriminating the areas as hypersensitive, hyposensitive or normosensitive, and two-point acuity test. Descriptive statistics, non-parametric Kruskal Wallis test for QualST evaluation and ANOVA for Two-point test (p < 0.05) were used.</p><p><strong>Results: </strong>QualST revealed that recipient areas presented no significant differences in tactile, pressure and thermal tests. Brush test revealed hyposensitivity after 3 months (p = 0.03). In donor areas, only thermal evaluation showed a significant difference (p = 0.01), being hypersensitive after 3 months and hyposensitive after 6 months. At baseline, all evaluations in recipient and donor areas were normosensitive. According to DN4, no patient reported pain in recipient and donor sites. Non-painful sensory perception was reported as numbness in recipient (3.14% of patients) and donor (18.4%) areas. No significant differences were found for two-point acuity test values.</p><p><strong>Conclusions: </strong>Somatosensory variations were observed in donor and recipient areas using qualitative tests, with no detection of painful sensations, only non-painful sensations of numbness and electric shock.</p><p><strong>Clinical relevance: </strong>This preliminary study demonstrated that alterations of hypo- and hypersensitivity may occur in donor and recipient areas of gingival grafts. However, when present, these alterations were non-painful and did not impact oral functions.</p><p><strong>Clinical registration: </strong>ReBEC #RBR-7zz3b6p.</p>","PeriodicalId":10461,"journal":{"name":"Clinical Oral Investigations","volume":null,"pages":null},"PeriodicalIF":3.1,"publicationDate":"2024-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142342893","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Efficacy of botulinum neurotoxin A in persistent idiopathic dentoalveolar pain: a case series. A 型肉毒杆菌神经毒素对顽固性特发性牙槽骨疼痛的疗效:一个病例系列。
IF 3.1 2区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2024-09-25 DOI: 10.1007/s00784-024-05935-5
Katia Rupel, Florian Martina, Ottaviani Giulia, Di Lenarda Roberto, Manganotti Paolo, Rizzo Roberto

Objectives: Persistent idiopathic dentoalveolar pain (PIDP) is a challenging clinical entity associated with both physical and emotional consequences. Currently, the management is symptom-based and includes both topical and/or systemic treatments. More recently, botulinum neurotoxin-A (BONT-A) has been suggested as a treatment option.

Materials and methods: We present a case series of 9 patients (5 female) with mean age 56 ± 15 diagnosed with PIDP. All patients reported prior experience with systemic drugs without a sufficient pain-relieving effect. BONT-A (BOTOX, Allergan) 100 U diluted with saline solution was used and the dose ranged from 20U to 50U distributed in 3 sites (intraoral and/or extraoral) per session. Patients underwent further injections (50U) monthly if pain severity measured using a Numerical Rating Scale (NRS 0-10) was still > 3 for 3 months. Pain severity and characteristics were recorded at baseline (T0), after 1 month (T1), 2 months (T2) and 3 months (T3).

Results: Mean pain intensity at baseline was NRS 6 (4-10). Latency before analgesic effect was at least 5-10 days after injection. Minor adverse effects were sickness and muscular hypotonia. Pain significantly reduced to NRS 4 (0-8) at T1, to NRS 2 (0-8) at T2 and to NRS 2 (NRS 0-8) at T3. Patients' functional variables (discomfort while chewing, talking, swallowing) were also recorded.

Conclusions: BONT-A is widely used and although the exact mechanism of action remains unclear, it can be used effectively in reducing pain for a variety of conditions including PIDP.

Clinical relevance: Our results suggest that BONT-A seems to be an alternative therapeutic approach for patients with PIDP.

目的:顽固性特发性牙槽骨痛(PIDP)是一种具有挑战性的临床症状,会对患者的身体和情绪造成影响。目前,治疗方法以对症治疗为主,包括局部治疗和/或系统治疗。最近,有人建议将肉毒杆菌神经毒素-A(BONT-A)作为一种治疗选择:我们对 9 名患者(5 名女性)(平均年龄 56 ± 15 岁)进行了病例系列研究,这些患者被诊断为 PIDP。所有患者均表示曾使用过系统性药物,但止痛效果不佳。患者使用了用生理盐水稀释的 100U BONT-A(BOTOX,Allergan 公司),每次剂量从 20U 到 50U 不等,分布在 3 个部位(口内和/或口外)。如果使用数字评分量表(NRS 0-10)测量的疼痛严重程度在 3 个月内仍大于 3,则患者每月接受一次注射(50U)。记录基线(T0)、1 个月(T1)、2 个月(T2)和 3 个月(T3)后的疼痛严重程度和特征:基线时的平均疼痛强度为 NRS 6(4-10)。注射后至少 5-10 天才能产生镇痛效果。轻微的不良反应是恶心和肌肉张力减退。疼痛明显减轻,T1时为NRS 4(0-8),T2时为NRS 2(0-8),T3时为NRS 2(NRS 0-8)。此外,还记录了患者的功能变量(咀嚼、说话、吞咽时的不适感):BONT-A被广泛使用,尽管其确切的作用机制仍不清楚,但它可以有效减轻包括PIDP在内的多种疾病的疼痛:临床意义:我们的研究结果表明,BONT-A 似乎是治疗 PIDP 患者的另一种方法。
{"title":"Efficacy of botulinum neurotoxin A in persistent idiopathic dentoalveolar pain: a case series.","authors":"Katia Rupel, Florian Martina, Ottaviani Giulia, Di Lenarda Roberto, Manganotti Paolo, Rizzo Roberto","doi":"10.1007/s00784-024-05935-5","DOIUrl":"https://doi.org/10.1007/s00784-024-05935-5","url":null,"abstract":"<p><strong>Objectives: </strong>Persistent idiopathic dentoalveolar pain (PIDP) is a challenging clinical entity associated with both physical and emotional consequences. Currently, the management is symptom-based and includes both topical and/or systemic treatments. More recently, botulinum neurotoxin-A (BONT-A) has been suggested as a treatment option.</p><p><strong>Materials and methods: </strong>We present a case series of 9 patients (5 female) with mean age 56 ± 15 diagnosed with PIDP. All patients reported prior experience with systemic drugs without a sufficient pain-relieving effect. BONT-A (BOTOX, Allergan) 100 U diluted with saline solution was used and the dose ranged from 20U to 50U distributed in 3 sites (intraoral and/or extraoral) per session. Patients underwent further injections (50U) monthly if pain severity measured using a Numerical Rating Scale (NRS 0-10) was still > 3 for 3 months. Pain severity and characteristics were recorded at baseline (T0), after 1 month (T1), 2 months (T2) and 3 months (T3).</p><p><strong>Results: </strong>Mean pain intensity at baseline was NRS 6 (4-10). Latency before analgesic effect was at least 5-10 days after injection. Minor adverse effects were sickness and muscular hypotonia. Pain significantly reduced to NRS 4 (0-8) at T1, to NRS 2 (0-8) at T2 and to NRS 2 (NRS 0-8) at T3. Patients' functional variables (discomfort while chewing, talking, swallowing) were also recorded.</p><p><strong>Conclusions: </strong>BONT-A is widely used and although the exact mechanism of action remains unclear, it can be used effectively in reducing pain for a variety of conditions including PIDP.</p><p><strong>Clinical relevance: </strong>Our results suggest that BONT-A seems to be an alternative therapeutic approach for patients with PIDP.</p>","PeriodicalId":10461,"journal":{"name":"Clinical Oral Investigations","volume":null,"pages":null},"PeriodicalIF":3.1,"publicationDate":"2024-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142342968","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Clinical Oral Investigations
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