Manber Rachel, Rush A John, Thase Michael E, Amow Bruce, Klein Dan, Trivedi Madhukar H, Korenstein Susan G, Markowitz John C, Dunner David L, Munsaka Melvin, Borian Fran E, Keller B
Department of Psychiatry and Behavioral Sciences, Stanford University, CA 94305, USA.
Sleep. 2003 Mar 15;26(2):130-6. doi: 10.1093/sleep/26.2.130.
The purpose of the study was to compare the effects of psychotherapy, nefazodone, and their combination on subjective measures of sleep in patients with chronic forms of major depression.
Participants were randomized to receive 12 weeks of treatment with one of the three interventions.
The study was conducted in parallel at 12 academic institutions and was approved by the Human Subjects Committee at each site.
484 adult outpatients (65.29% female) who met DSM-IV criteria for one of three chronic forms of major depression.
Psychotherapy (16-20 sessions) was provided by certified therapists following a standardized treatment manual for Cognitive Behavioral Analysis System of Psychotherapy (CBASP), a variant of cognitive psychotherapy developed for chronic depression. Pharmacotherapy consisted of open-label nefazodone, 300-600 mg per day in two divided doses prescribed by psychiatrists. The clinical management visits were limited to 15-20 minutes and followed a standardized protocol. Combination treatment consisted of both therapies.
Depression outcome was determined by the 24-item Hamilton Rating Scale for Depression and the 30-item Inventory of Depressive Symptomatology-Self Rating. Sleep outcome was measured prospectively with daily sleep diaries that were completed a week prior to HRSD assessments at baseline and after 1, 2, 3, 4, 8, and 12 weeks of treatment. Although nefazodone alone and CBASP alone had comparable impact on global measures of depression outcome, only monotherapy with nefazodone improved early morning awakening and total sleep time. Significant improvements in sleep quality, time awake after sleep onset, latency to sleep onset, and sleep efficiency were present in each of the three treatment groups. These improvements, however, occurred earlier in the course of treatment for participants receiving nefazodone, alone or in combination with CBASP.
Nefazodone therapy may have a direct impact on disturbed sleep associated with depression beyond what would be expected if the improvements were all a consequence of improved depression.
本研究旨在比较心理治疗、奈法唑酮及其联合应用对慢性重度抑郁症患者睡眠主观指标的影响。
参与者被随机分配接受三种干预措施之一的12周治疗。
该研究在12个学术机构并行开展,并获得了每个研究点人类受试者委员会的批准。
484名成年门诊患者(65.29%为女性),符合三种慢性重度抑郁症形式之一的DSM-IV标准。
心理治疗(16 - 20次疗程)由认证治疗师按照标准化治疗手册提供,该手册用于认知行为分析心理治疗系统(CBASP),这是一种为慢性抑郁症开发的认知心理治疗变体。药物治疗包括开放标签的奈法唑酮,由精神科医生每天分两次开具300 - 600毫克的处方。临床管理访视限制在15 - 20分钟,并遵循标准化方案。联合治疗包括两种疗法。
抑郁结果由24项汉密尔顿抑郁评定量表和30项抑郁症状自评量表确定。睡眠结果通过每日睡眠日记进行前瞻性测量,这些日记在基线时以及治疗1、2、3、4、8和12周后,在HRSD评估前一周完成。尽管单独使用奈法唑酮和单独使用CBASP对抑郁结果的整体测量有相当的影响,但只有奈法唑酮单一疗法改善了早醒和总睡眠时间。三个治疗组在睡眠质量、入睡后清醒时间、入睡潜伏期和睡眠效率方面均有显著改善。然而,对于接受奈法唑酮单独治疗或与CBASP联合治疗的参与者,这些改善在治疗过程中出现得更早。
奈法唑酮治疗可能对与抑郁症相关的睡眠障碍有直接影响,这种影响超出了如果所有改善都是抑郁症改善的结果所预期的范围。