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A randomized crossover study comparing two mandibular repositioning appliances for treatment of obstructive sleep apnea

机译:一项随机交叉研究比较了两种下颌复位装置治疗阻塞性睡眠呼吸暂停的情况

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Purpose: The purpose of this study was to determine whether treatment outcomes vary according to the design of the mandibular repositioning appliance (MRA). Two titratable MRA's were compared. The designs differ in advancement hardware and configuration of acrylic both in bulk and interocclusal contact. Materials and methods: The primary treatment outcome was the Respiratory Disturbance Index (RDI). Other outcomes that were compared included Sleep Apnea Quality of Life Index (SAQLI), Epworth Sleepiness Scale, oxygen saturation, and subjective feedback regarding experiences with the appliances. Twenty-four subjects were recruited from consecutive referrals for MRA therapy following diagnosis of obstructive sleep apnea (OSA) by polysomnography. Subjects were randomly assigned to a treatment arm of the crossover study. Each subject underwent an initial sleep study with a type III home monitor to establish a baseline RDI. Subjects were then treated with one of the two MRAs determined by random assignment. The MRA self-titration phase was monitored until a treatment position was determined, and the home sleep study was repeated. After a 2-week period without any OSA treatment, subjects received the second MRA and the self-titration treatment protocol was repeated. At completion of treatment with each appliance, subjects answered questionnaires and underwent a sleep study with the type III monitor. The outcome data for each appliance were compared using analysis of variance. Results: Eighteen subjects completed the treatment protocol. There were no significant statistical differences in treatment outcomes between the two appliances. There was a statistically significant (p≤0.05) preference for a MRA design with minimal coverage of teeth and palate. The subjects' appliance selection was consistent with a corresponding reduction in SAQLI score for the selected appliance. Conclusion: Although no statistically significant difference was observed between the two appliances in the outcomes measured, there was a trend toward greater improvement with the appliance with less acrylic resin bulk and less interocclusal contact. MRA selection should favor titratable, unobtrusive designs with appropriate construction to promote acceptance and adherence to MRA therapy.
机译:目的:本研究的目的是确定治疗效果是否根据下颌复位装置(MRA)的设计而有所不同。比较了两个可滴定的MRA。这些设计在整体和咬合间接触方面在丙烯酸的先进硬件和配置方面有所不同。材料和方法:主要治疗结果为呼吸障碍指数(RDI)。进行了比较的其他结果包括睡眠呼吸暂停生活质量指数(SAQLI),Epworth睡眠量表,血氧饱和度以及有关使用该设备的经验的主观反馈。通过多导睡眠图诊断出阻塞性睡眠呼吸暂停(OSA)后,从连续转诊中招募了24名受试者进行MRA治疗。将受试者随机分配至交叉研究的治疗组。每个受试者都接受了带有III型家用监护仪的初始睡眠研究,以建立基线RDI。然后用随机分配确定的两个MRA之一治疗受试者。监测MRA自滴定阶段,直到确定治疗位置,并重复进行家庭睡眠研究。在两周的时间内未接受任何OSA治疗后,受试者接受了第二次MRA,并重复了自滴定治疗方案。在完成每种器具的治疗后,受试者回答问卷并使用III型监护仪进行睡眠研究。使用方差分析比较每个设备的结果数据。结果:18名受试者完成了治疗方案。两种矫治器之间的治疗结局无统计学差异。具有MRA设计且牙齿和上颚覆盖率最低的统计学意义(p≤0.05)。对象的器具选择与所选器具的SAQLI分数相应降低相一致。结论:尽管两种器具在测量结果方面均未观察到统计学上的显着差异,但丙烯酸树脂体积较小且咬合间接触较少的器具仍存在改善的趋势。 MRA的选择应支持具有适当结构的可滴定,不引人注目的设计,以促进对MRA治疗的接受和坚持。

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