Assessment of potential tooth movement and bite changes with a hard-acrylic sleep appliance: A 2-year clinical study.

Allen Lee Khai, N. Vranješ, K. Schulze, G. Santucci, D. Kuhns
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引用次数: 1

Abstract

Study Objectives: The objective of this study was to test a proprietary hard-acrylic computer-aided design/computer-aided manufacturing (CAD/CAM) oral appliance with “retainer-like fit” and determine whether it resulted in tooth movement upon regular wear over a minimum 2-year period. Additionally, this study focused on determining patient acceptance of said device considering any reported side effects. Methods: The 2-year clinical study reports on selected patients in whom sleep apnea has been diagnosed (n=18) recruited from The Snore Center in Calgary. Patients were fitted with a ProSomnus® Sleep Appliance. Impressions were taken at baseline, after approximately 1 year, and after 2 years of use with the oral appliance. Models were marked, scanned, and scored; upper and lower anterior teeth crowding was assessed; and overjet and overbite were measured independently at the University of Pacific. Patients were surveyed on compliance, satisfaction with the appliance, and quality of life using the Sleep Apnea Quality of Life Index (SAQLI-10). Results: This study shows a rigid OA made with proprietary CAD/CAM technology demonstrated no significant change in tooth position during the 2.3-year test period, or in bite changes per maximum intercuspation (MIP), as measured by overjet and overbite. At 2 years, the mean change in Little Irregularity Index for the lower anterior teeth was 0.007 mm (95% confidence interval = [-0.03, 0.05]), which was not statistically different from zero (P>0.05). Patients were highly satisfied with the device and considered it beneficial. Conclusions: A key component to any treatment is patient's acceptance of the appliance and the willingness to wear the OA long term. When patient compliance is observed, hard-acrylic sleep appliances have little effect on tooth movement and MIP bite changes as shown by overjet/overbite. Clinical Trial Registration: Health Research Ethics Board of Alberta: CTC-16-0108
使用硬质丙烯酸睡眠矫治器评估潜在的牙齿移动和咬合变化:一项为期2年的临床研究。
研究目的:本研究的目的是测试一种专有的硬丙烯酸计算机辅助设计/计算机辅助制造(CAD/CAM)口腔矫治器,该矫治器具有“类似固位器的配合”,并确定在至少2年的时间内,它是否会在定期磨损时导致牙齿移动。此外,考虑到任何报告的副作用,本研究的重点是确定患者对所述设备的接受程度。方法:这项为期2年的临床研究报告了从卡尔加里Snore中心招募的被诊断为睡眠呼吸暂停的选定患者(n=18)。患者安装了ProSomnus®睡眠设备。在使用口腔矫治器的基线、大约1年后和2年后进行印模。对模型进行标记、扫描和评分;评估上下前牙拥挤程度;太平洋大学对覆盖层和覆层进行了独立测量。使用睡眠呼吸暂停生活质量指数(SAQLI-10)对患者的依从性、对矫治器的满意度和生活质量进行调查。结果:这项研究表明,在2.3年的测试期内,使用专有CAD/CAM技术制造的刚性OA的牙齿位置没有显著变化,也没有通过覆盖和覆牙测量的每次最大咬合间隔(MIP)的咬合变化。2年时,下前牙的小不规则指数平均变化为0.007mm(95%置信区间=[0.03,0.05]),与零无统计学差异(P>0.05)。患者对该装置非常满意,认为它是有益的。结论:任何治疗的关键因素是患者对矫治器的接受程度和长期佩戴OA的意愿。当观察到患者的依从性时,硬质丙烯酸睡眠用具对牙齿移动和MIP咬合变化的影响很小,如覆盖/覆盖所示。临床试验注册:阿尔伯塔省健康研究伦理委员会:CTC-16-108
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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