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首页> 外文期刊>American Journal of Orthodontics and Dentofacial Orthopedics >Compliance with removable orthodontic appliances and adjuncts: A systematic review and meta-analysis
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Compliance with removable orthodontic appliances and adjuncts: A systematic review and meta-analysis

机译:符合可拆卸的正畸器具和辅助装置:系统评价和荟萃分析

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摘要

Introduction: The primary aims of this systematic review were to assess objective levels of wear of removable orthodontic appliances and components vs both stipulated and self-reported levels. We also aimed to consider patient experiences and the effectiveness of interventions geared at enhancing compliance. Methods: Electronic databases and reference lists of relevant studies were searched with no language restriction (PROSPERO: CRD42016036059). Randomized and nonrandomized controlled trials, prospective cohort studies, case series, qualitative and mixed-methods studies objectively assessing compliance levels were identified. The quality of the studies was assessed using the Cochrane Collaboration's risk of bias tool, risk of bias in non-randomized studies of interventions (ROBINS-I), or mixed-methods appraisal tool based on their design. Results: Of 4269 records, 80 full texts were obtained, with 24 studies meeting the selection criteria. Of these, 11 were included in the quantitative synthesis. A weighted estimate of objectively assessed compliance levels in relation to stipulated wear time was calculated with the discrepancy highest in the headgear group (5.81 hours per day, 95% confidence interval, 4.98, 6.64) based on 6 studies. The mean discrepancy between self-reported and objectively assessed headgear wear was 5.02 hours per day (95% confidence interval, 3.64, 6.40). Compliance level was not directly related to appliance type (P = 0.211). Thematic synthesis was not undertaken because of the limited number of qualitative studies. Conclusions: Compliance with removable orthodontic appliances and adjuncts is suboptimal, and patients routinely overestimate duration of wear. Techniques for improving compliance have promise but require further evaluation in high-level research.
机译:介绍:该系统审查的主要目标是评估可拆卸正畸器具和组件的客观水平与规定和自我报告的水平。我们还旨在考虑患者的经验和加强遵守情况的干预措施的有效性。方法:没有语言限制搜索相关研究的电子数据库和参考列表(Prospero:CRD42016036059)。鉴定了随机和非扫描控制试验,预期队列研究,案例系列,定性和混合方法客观评估合规水平。使用Cochrane协作的偏置工具的风险评估研究质量,干预措施(Robins-I)的非随机研究中的偏差风险或基于其设计的混合方法评估工具。结果:4269条记录,获得了80个全文,24项研究符合选定标准。其中,11种包含在定量合成中。基于6项研究,通过头盔组中的差异(每天5.81小时,95%置信区间,4.98,6.64)计算了对规定的磨损时间相关的客观评估的合规水平的加权估计。自我报告和客观评估的头带磨损之间的平均差异为每天5.02小时(95%置信区间,3.64,6.40)。合规级别与器具类型无直接相关(P = 0.211)。由于有限数量的定性研究,未进行主题合成。结论:遵守可拆卸的正畸器具和辅助次疗,患者经常高估磨损持续时间。提高遵守的技术具有承诺,但需要进一步评估高级研究。

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