首页> 外文期刊>Journal of clinical sleep medicine: JCSM : official publication of the American Academy of Sleep Medicine >Prevalence and prediction of primary sleep disorders in a clinical trial of depressed patients with insomnia.
【24h】

Prevalence and prediction of primary sleep disorders in a clinical trial of depressed patients with insomnia.

机译:失眠抑郁症患者临床试验中原发性睡眠障碍的患病率与预测。

获取原文
获取原文并翻译 | 示例
       

摘要

Insomnia-pharmacology clinical trials routinely exclude primary sleep disorders, such as obstructive sleep apnea (OSA) and periodic limb movement disorder (PLMD), with a single night of polysomnography (PSG). Given the expense of PSG, we examined whether a thorough clinical screening, combined with actigraphy, would successfully identify OSA and PLMD as part of baseline screening for a clinical trial of insomnia treatment in depressed patients. Of the 73 patients with a complete baseline dataset, 12 screened positive for OSA/PLMD (AHI > 15, or PLMAI > 15), while 61 "passed" the PSG screen. The OSA/PLMD+ patients were older (51.4 +/- 10.2 y) and took more naps (2.6 per week) than the OSA/PLMD- patients (41.3 +/- 12.8 y; and 1.1 naps per week). The combination of age and nap frequency produced a "good" receiver operating characteristic (ROC) model for predicting OSA/PLMD+, with the area under the curve of 0.82. There were no other demographic, sleep diary, or actigraphic variables, which differed between OSA/PLM + or -, and no other variable improved the ROC model. Still, the best model misclassified 16 of 73 persons. We conclude that while age and the presence of napping were helpful in identifying OSA and PLM in a well-screened sample of depressed insomniacs, PSG is required to definitively identify and exclude primary sleep disorders in insomnia clinical trials.
机译:失眠药学临床试验常规排除初级睡眠障碍,例如阻塞性睡眠呼吸暂停(OSA)和周期性肢体运动障碍(PLMD),单一的多面体创造(PSG)。鉴于PSG的费用,我们检查了彻底的临床筛查是否与Actigraphy联系,将成功识别OSA和PLMD作为抑郁症患者失眠治疗临床试验的基线筛选的一部分。在73名患者中,完整的基线数据集,12个筛选OSA / PLMD(AHI> 15或PLMAI> 15)呈阳性,而61“通过”PSG屏幕。 OSA / PLMD +患者年龄较大(51.4 +/- 10.2 y),比OSA / PLMD-患者更多的小睡(每周2.6)(41.3 +/- 12.8 y;每周下午1.1小睡)。年龄和午睡频率的组合产生了“良好”的接收器操作特性(ROC)模型,用于预测OSA / PLMD +,该区域在0.82的曲线下。没有其他人口统计学,睡眠日记或戏剧性变量,不同于OSA / PLM +或 - ,并且没有其他可变改善的ROC模型。尽管如此,最好的模型错误分类为73人。我们得出结论,虽然年龄和小睡的存在有助于鉴定OSA和PLM在抑制的失眠症的良好样本中,但PSG是明确识别和排除入侵性临床试验中的主要睡眠障碍。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号