Primeau Michelle, Gershon Anda, Talbot Lisa, Cotto Isabelle, Lotspeich Linda, Hardan Antonio, Hallmayer Joachim, O'Hara Ruth
Palo Alto Medical Foundation, Department of Sleep Medicine, Sunnyvale, CA.
Stanford University Department of Psychiatry and Behavioral Sciences, Stanford, CA.
J Clin Sleep Med. 2016 Mar;12(3):357-62. doi: 10.5664/jcsm.5584.
Polysomnography (PSG) is the gold standard for the assessment of sleep, yet the extensive apparatus required for monitoring with PSG can be difficult to tolerate, particularly in children. Clinical populations, such as those with anxiety or tactile sensitivity, may have even greater difficulty tolerating the PSG equipment. This study evaluated an innovative protocol for obtaining full PSG in individuals diagnosed autism spectrum disorders (ASD) or developmental delay (DD), as well as typically developing controls (TD). The primary aim was to assess whether this protocol was equally successful for obtaining PSG between these groups.
One hundred sixty-one individuals were recruited for participation; 93 with a diagnosis of ASD, 23 with a diagnosis of DD, and 45 TD. The participants and families were instructed on a procedure of systematic desensitization to the ambulatory PSG equipment; PSG was performed in the home of the participant.
PSG was successfully attained in 144 (89.4%) participants. There was no difference in completion rate by diagnosis (p = 0.1), though younger age (p = 0.018) and duration of desensitization (p = 0.024) did predict PSG failure. Further, it was found that individuals with ASD took longer to desensitize to the equipment (16.08 d), than those with DD (8.04 d) or TD (0.98 d).
Systematic desensitization to PSG equipment, in combination with PSG completed in the home, allows for individuals with ASD to be equally successful in completing PSG, though they do take longer to acclimate to the equipment.
多导睡眠图(PSG)是评估睡眠的金标准,但使用PSG进行监测所需的大量设备可能难以耐受,尤其是在儿童中。临床人群,如患有焦虑症或触觉敏感的人群,可能更难以耐受PSG设备。本研究评估了一种创新方案,用于在诊断为自闭症谱系障碍(ASD)或发育迟缓(DD)的个体以及发育正常的对照组(TD)中获得完整的PSG。主要目的是评估该方案在这些组中获得PSG是否同样成功。
招募了161名个体参与研究;93名被诊断为ASD,23名被诊断为DD,45名TD。参与者及其家人接受了对便携式PSG设备进行系统脱敏的程序指导;PSG在参与者家中进行。
144名(89.4%)参与者成功完成了PSG。按诊断分组的完成率没有差异(p = 0.1),但年龄较小(p = 0.018)和脱敏持续时间(p = 0.024)确实预测了PSG失败。此外,发现患有ASD的个体对设备脱敏所需的时间(16.08天)比患有DD的个体(8.04天)或TD的个体(0.98天)更长。
对PSG设备进行系统脱敏,结合在家庭中完成PSG,使患有ASD的个体在完成PSG方面同样成功,尽管他们需要更长时间来适应设备。