Fava Maurizio, Asnis Gregory M, Shrivastava Ram, Lydiard Bruce, Bastani Bijan, Sheehan David, Roth Thomas
Depression Clinical and Research Program, Massachusetts General Hospital, Boston, MA 02114-2696, USA.
J Clin Psychopharmacol. 2009 Jun;29(3):222-30. doi: 10.1097/JCP.0b013e3181a390ba.
A multicenter, double-blind, parallel-group study was designed to assess the efficacy and safety of zolpidem extended-release coadministered with escitalopram in patients with insomnia and comorbid generalized anxiety disorder. Patients (N = 383) received open-label escitalopram 10 mg/d and were randomized to either adjunct zolpidem extended-release 12.5 mg or placebo. The primary efficacy measure was change from baseline to week 8 in subjective total sleep time. Secondary efficacy measures included subjective sleep onset latency, number of awakenings, wake time after sleep onset, sleep quality, the Hamilton Rating Scale for Anxiety, the Beck Anxiety Inventory, the Sleep Impact Scale, the Massachusetts General Hospital Cognitive and Physical Functioning Questionnaire, and the Sheehan Disability Scale. The last-observation-carried-forward method was used to impute missing values for most efficacy measures. Safety was monitored at each visit. At week 8 and all time points, there was a significant improvement in the zolpidem extended-release/escitalopram group compared with placebo/escitalopram for total sleep time (P < 0.0001). Most of the secondary efficacy measures also significantly favored zolpidem at most visits (P < 0.0001). The most common treatment-emergent adverse events in both groups were nausea, dizziness, headache, fatigue, and dry mouth. Concurrent zolpidem extended-release/escitalopram, compared with placebo/escitalopram, significantly improved insomnia and sleep-related next-day symptoms, but not anxiety symptoms, in patients with comorbid insomnia and generalized anxiety disorder.
一项多中心、双盲、平行组研究旨在评估唑吡坦缓释剂与艾司西酞普兰联合使用对伴有共病广泛性焦虑症的失眠患者的疗效和安全性。患者(N = 383)接受开放标签的艾司西酞普兰10 mg/d,并被随机分为接受唑吡坦缓释剂12.5 mg辅助治疗或安慰剂组。主要疗效指标是从基线到第8周主观总睡眠时间的变化。次要疗效指标包括主观入睡潜伏期、觉醒次数、睡眠后觉醒时间、睡眠质量、汉密尔顿焦虑量表、贝克焦虑量表、睡眠影响量表、麻省总医院认知和身体功能问卷以及希恩残疾量表。对于大多数疗效指标,采用末次观察结转法推算缺失值。每次访视时监测安全性。在第8周及所有时间点,唑吡坦缓释剂/艾司西酞普兰组与安慰剂/艾司西酞普兰组相比,总睡眠时间有显著改善(P < 0.0001)。在大多数访视中,大多数次要疗效指标也显著有利于唑吡坦(P < 0.0001)。两组中最常见的治疗中出现的不良事件是恶心、头晕、头痛、疲劳和口干。对于伴有共病失眠和广泛性焦虑症的患者,唑吡坦缓释剂/艾司西酞普兰与安慰剂/艾司西酞普兰相比,显著改善了失眠和与睡眠相关的次日症状,但未改善焦虑症状。