Division of Orthodontics, The Ohio State University College of Dentistry, Room 4088, 305 W 12th Ave., Columbus, OH, 43210, USA.
Former resident Division of Orthodontics, The Ohio State University College of Dentistry, Private practice, Lexington, KY, USA.
Sleep Breath. 2022 Dec;26(4):1739-1745. doi: 10.1007/s11325-021-02548-0. Epub 2022 Jan 11.
Obstructive sleep apnea (OSA) is a common chronic condition, associated with several conditions that account for leading causes of mortality. Adherence to treatment of a chronic condition is, along with treatment efficacy, a major determinant of treatment outcome. The aim of this study was to test whether or not a multifactorial intervention in addition to standard care increases adherence rates in patients using a titratable oral appliance for OSA.
All subjects were 18 years old or older, had a diagnosis of OSA, and were treated with an oral appliance with an embedded sensor to measure appliance wear time objectively. The control group received routine care, while the experimental subjects received an additional multifactorial intervention. Comparison of adherence was at 30 days (Phase I) and 90 days (Phase II) after appliance delivery.
Data are reported for 82 subjects in Phase I (control 43; experimental 39) and 66 subjects in Phase II (control 36; experimental 30). There were no significant differences for age, sex, body mass index, and apnea-hypopnea index (p > 0.05) between groups. In both Phase I and Phase II, the mean number of nights the appliance was worn 4 or more hours and the mean time the appliance was worn nightly were significantly greater in the experimental than in the control group (p < 0.05).
Interventions were well received by subjects and can be carried out by auxiliary personnel. The experimental interventions resulted in clinically important and statistically significant improvements in patient adherence to treatment.
阻塞性睡眠呼吸暂停(OSA)是一种常见的慢性疾病,与几种导致主要死亡原因的疾病有关。慢性疾病治疗的依从性与治疗效果一样,是治疗结果的主要决定因素。本研究的目的是测试在标准治疗的基础上增加多因素干预是否会增加使用可滴定口腔器具治疗 OSA 的患者的依从率。
所有受试者年龄在 18 岁或以上,诊断为 OSA,并使用带有嵌入式传感器的口腔器具进行治疗,以客观测量器具佩戴时间。对照组接受常规护理,而实验组接受额外的多因素干预。在器具交付后 30 天(第 I 阶段)和 90 天(第 II 阶段)比较依从性。
第 I 阶段(对照组 43 例,实验组 39 例)和第 II 阶段(对照组 36 例,实验组 30 例)分别报告了 82 例和 66 例数据。两组之间的年龄、性别、体重指数和呼吸暂停低通气指数无显著差异(p>0.05)。在第 I 阶段和第 II 阶段,实验组佩戴器具 4 小时或以上的夜间平均数量和每晚佩戴器具的平均时间均明显大于对照组(p<0.05)。
干预措施受到受试者的欢迎,并可由辅助人员实施。实验组的干预措施导致患者对治疗的依从性有了临床重要和统计学显著的改善。