Johal A, Arya D, Winchester L J, Venn P J H, Brooks H
Department of Orthodontics, Institute of Dentistry, St. Bartholomew's and The Royal London School of Medicine and Dentistry, New Road, Whitechapel, London E1 1BB.
Br Dent J. 2005 Nov 12;199(9):591-6; discussion 581; quiz 608. doi: 10.1038/sj.bdj.4812903.
This study assessed the effectiveness of a mandibular advancement splint (MAS) in subjects with sleep-related breathing disorders using both objective and subjective outcome measures.
The study was carried out as a retrospective analysis.
The study was conducted within the Sleep Studies Unit at the Queen Victoria Hospital, East Grinstead, between May 1997 and March 2000.
Twenty subjects with obstructive sleep apnoea (OSA) and six with non-apnoeic snoring, diagnosed by overnight polysomnography, were fitted with a monobloc appliance between May 1997 and March 2000.
The subjects were analysed for changes in the respiratory disturbance index (RDI) and Epworth Sleepiness Scale (ESS) scores. In addition each subject completed an outcome questionnaire following fitting of the appliance.
Variability in response measured by the change in the respiratory disturbance index was found with no correlation to the baseline recording. Although median RDI values improved in both groups, significantly so in the obstructive sleep apnoea group (p<0.05), seven subjects exhibited an increased RDI score following mandibular advancement splint therapy. The median Epworth Sleepiness Scale scores decreased in both the OSA group and the non-apnoeic snorers although not significantly. Twenty-one of the 26 subjects completed the outcome questionnaire revealing an 81% reduction in snoring. Side-effects were generally transient and minor. Eighty-six per cent of the subjects' partners reported better quality of sleep as a result of MAS therapy.
The monobloc appliance significantly improved the Respiratory Disturbance Index in the obstructive sleep apnoea group. Some subjects had increased RDI scores following splint therapy. This supports the need for an objective assessment in the follow-up of patients treated with mandibular advancement splints.
本研究采用客观和主观的结果指标,评估下颌前移矫治器(MAS)对睡眠相关呼吸障碍患者的疗效。
本研究为回顾性分析。
研究于1997年5月至2000年3月在东格林斯特德维多利亚女王医院睡眠研究室进行。
通过夜间多导睡眠图诊断出的20名阻塞性睡眠呼吸暂停(OSA)患者和6名非呼吸暂停性打鼾患者,于1997年5月至2000年3月期间佩戴一体式矫治器。
分析受试者的呼吸紊乱指数(RDI)和爱泼沃斯嗜睡量表(ESS)评分的变化。此外,每位受试者在佩戴矫治器后完成一份结果问卷。
发现呼吸紊乱指数变化所衡量的反应存在差异,与基线记录无相关性。尽管两组的RDI中位数均有所改善,阻塞性睡眠呼吸暂停组改善显著(p<0.05),但7名受试者在下颌前移矫治器治疗后RDI评分增加。OSA组和非呼吸暂停性打鼾者的爱泼沃斯嗜睡量表评分中位数均有所下降,尽管不显著。26名受试者中有21名完成了结果问卷,显示打鼾减少了81%。副作用一般为短暂且轻微。86%的受试者伴侣报告MAS治疗后睡眠质量更好。
一体式矫治器显著改善了阻塞性睡眠呼吸暂停组的呼吸紊乱指数。一些受试者在矫治器治疗后RDI评分增加。这支持了对接受下颌前移矫治器治疗的患者进行随访时需要客观评估的观点。