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首页> 外文期刊>BMC Oral Health >A 12-month randomized controlled trial evaluating erythritol air-polishing versus curette/ultrasonic debridement of mandibular furcations in supportive periodontal therapy
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A 12-month randomized controlled trial evaluating erythritol air-polishing versus curette/ultrasonic debridement of mandibular furcations in supportive periodontal therapy

机译:12个月的随机对照试验评估赤藓糖醇空气抛光与卷曲/超声波清记,在支持性牙周治疗中的下颌毛刺

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Due to complex morphology and limited access, the cleaning of the furcation area is extremely challenging. Therefore, novel therapeutic approaches need to be tested to potentially overcome debridement limitations. The aim of the present prospective 12-month study was to compare clinical and microbiological effects following erythritol air-polishing versus conventional mechanical debridement of furcation defects in a cohort of periodontal maintenance patients. Twenty patients with grade II mandibular molar furcation defects volunteered to enroll in this single-centre, examiner masked, randomized controlled trial. In a split-mouth study design, two furcation sites in each patient were randomly assigned to either receive subgingival debridement using erythritol air-polishing (test) or conventional ultrasonic/curette debridement (control) at baseline, and at 3, 6, 9 and 12?months. Probing depth, clinical attachment level and bleeding on probing were recorded at 3-month intervals. Subgingival microbiological samples obtained at baseline, 6 and 12?months were analyzed using checkerboard DNA–DNA hybridization. Discomfort from treatment was scored at 12?months using a visual analogue scale. The differences between treatments, and time-points, were tested using multilevel analysis (mixed effect models and robust variance estimates). A significant reduction in probing depth took place following both treatments (p??0.001). Control sites experienced a significant mean gain in clinical attachment level of 0.5?mm (±?0.2) (p?=?0.004), whereas a non-significant gain of 0.4?mm (±?0.3) was observed at test sites (p?=?0.119). At 6?months, a significant between-treatment difference of 0.8?mm (±?0.4) was observed in favor of the control (p?=?0.032). No significant between-treatment differences were observed in microbial load or composition. Notably, at 12?months patients experienced significantly less discomfort following air-polishing compared with control (p?=?0.001). The 12-month observations indicate that erythritol air-polishing and conventional mechanical debridement both support clinical improvements. A significant between-treatment difference in clinical attachment level was, however, detected in favour of control debridement at 6?months. In terms of patient comfort, erythritol air-polishing is superior. Trial Registration: The clinical trial was retrospectively registered in ClinicalTrial.gov with registration NCT04493398 (07/28/2020).
机译:由于复杂的形态和有限的访问,浮雕区域的清洁极具挑战性。因此,需要测试新的治疗方法以潜在地克服清卓界限。目前预期的12个月的目的的目的是比较季节性维持患者队列中红细胞空气抛光与常规机械缺陷的常规机械缺陷后的临床和微生物作用。二十岁患者二级下颌摩尔毛细血管缺陷志愿参加该单一中心,审查员蒙面,随机对照试验。在一个分裂的研究设计中,每位患者的两个突发位点被随机分配给在基线的赤藓糖醇空气抛光(测试)或常规超声/刮匙子(对照)在3,6,9和3,6,9和3,6,9和12个月。探测深度,临床附着水平和探测的出血以3个月的间隔记录。使用棋盘DNA-DNA杂交分析在基线,6和12的潜在微生物学样品。使用视觉模拟量表的12个月,治疗的不适被评分。使用多级分析(混合效果模型和鲁棒方差估计)测试治疗和时间点之间的差异。探测深度的显着降低在治疗后发生(p≤≤0.001)。控制位点在临床附着水平为0.5Ω·mm(±0.2)(p≤0.004),而在试验部位观察到非显着增益0.4ΩΩmm(±0.3)(P. ?=?0.119)。在6个月,观察到治疗差异为0.8Ωmm(±0.4),有利于对照(p?= 0.032)。在微生物载荷或组合物中没有观察到治疗差异没有显着的治疗差异。值得注意的是,在12个月的患者中,与对照相比,在空气抛光后经历了显着不适(p?= 0.001)。 12个月的观察结果表明赤藓糖醇空气抛光和常规机械清卓人均支持临床改进。然而,临床附着水平的治疗差异有显着的治疗差异,以便在6个月内有利于控制清创。就患者舒适而言,赤藓糖醇空气抛光优异。试验注册:临床试验在ClinCORICLTIAL.GOV中回顾性注册NCT04493398(07/28/2020)。

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