Department of Special Care Dentistry, Antwerp University Hospital, Edegem; Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.
Department of Special Care Dentistry, Antwerp University Hospital, Edegem; Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.
Chest. 2013 Nov;144(5):1495-1502. doi: 10.1378/chest.13-0613.
Assessment of the overall therapeutic effectiveness of oral appliance therapy can only be realized through objectively measured compliance. The aims of this study were to assess objectively measured compliance during oral appliance therapy at 1-year follow-up and to compare these data with self-reported use.
Fifty-one eligible patients were enrolled in this 1-year prospective clinical study (men, 61%; mean age, 49 ± 10 years; apnea-hypopnea index, 18.0 ± 11.9 events/h sleep; BMI, 26.6 ± 4.1 kg/m²). Objective compliance during oral appliance therapy at 1-year follow-up was assessed with a microsensor thermometer. Subjective compliance was assessed by self-report. Patients with a mean objectively measured use of ≥ 4 h/night on 70% of nights monitored were considered regular users. The mean disease alleviation was calculated as a measure of overall therapeutic effectiveness.
High agreement between objective and subjective compliance data at 1-year follow-up was reported (intraclass correlation coefficient, 0.8; 95% CI, 0.5-0.9), showing a mean subjective overestimation of 30 min (95% CI, -3.1 to 1.9; P = .02). The discontinuation rate at 1-year follow-up was 9.8%. The objective mean use rate was 6.4 ± 1.7 h/night at 1-year follow-up in continuing users, with a regular use rate of 83%. The mean disease alleviation was 54.9%.
This study is the first to our knowledge to report the 1-year results of objectively measured compliance during oral appliance therapy. In addition, a high agreement between objective and subjective compliance data were reported, with a mean subjective overestimation of 30 min.
ClinicalTrials.gov; No.: NCT01284881; URL: www.clinicaltrials.gov.
评估口腔矫治器治疗的整体疗效只能通过客观测量的依从性来实现。本研究的目的是在 1 年随访时评估口腔矫治器治疗期间的客观测量依从性,并将这些数据与自我报告的使用情况进行比较。
51 名符合条件的患者参与了这项为期 1 年的前瞻性临床研究(男性占 61%;平均年龄为 49 ± 10 岁;睡眠时每小时呼吸暂停低通气指数为 18.0 ± 11.9 次;BMI 为 26.6 ± 4.1 kg/m²)。在 1 年随访时,使用微传感器温度计评估口腔矫治器治疗期间的客观依从性。主观依从性通过自我报告进行评估。将客观测量使用时间≥4 小时/晚,监测到的 70%的夜晚都在使用的患者视为规律使用者。总体治疗效果的衡量标准是平均疾病缓解程度。
在 1 年随访时,客观和主观依从性数据之间的一致性很高(组内相关系数为 0.8;95%置信区间为 0.5-0.9),表明主观估计平均偏高 30 分钟(95%置信区间为-3.1 至 1.9;P=0.02)。1 年随访时的停药率为 9.8%。在继续使用者中,1 年时的客观平均使用率为 6.4 ± 1.7 小时/晚,规律使用率为 83%。平均疾病缓解率为 54.9%。
这是我们首次报道口腔矫治器治疗期间客观测量依从性的 1 年结果。此外,本研究还报告了客观和主观依从性数据之间的高度一致性,平均主观估计偏高 30 分钟。
ClinicalTrials.gov;编号:NCT01284881;网址:www.clinicaltrials.gov。